AU2022241074A1

AU2022241074A1 - A component for an article for use in an aerosol provision system

Info

Publication number: AU2022241074A1
Application number: AU2022241074A
Authority: AU
Inventors: Andrei GRISHCHENKO
Original assignee: Nicoventures Trading Ltd
Current assignee: Nicoventures Trading Ltd
Priority date: 2021-03-15
Filing date: 2022-03-15
Publication date: 2023-10-05
Also published as: BR112023018779A2; EP4307931A1; CN117750893A; WO2022195271A1; IL305723A; JP2024510470A; GB202109118D0; CA3212175A1; KR20230157422A; GB202103577D0; US20240156155A1; MX2023010748A

Abstract

A component for an article for use in or as a non-combustible aerosol provision system includes a body of material extending in a longitudinal direction, where the body of material comprises sheet material having fibres having a length in the range 2 mm to 6 mm. The body of material can have a density in the range between about o.i and 0.25 mg/mnT-. An article for use in or as a non-combustible aerosol provision system is also provided including an aerosol generating material and a downstream portion downstream of the aerosol generating material, the downstream portion including the component. A non-combustible aerosol provision system and a method for forming a component for an article for use in a non-combustible aerosol provision system are also described.

Description

A component for an article for use in an aerosol provision system Technical Field

The present disclosure relates to a component for an article for use in or as a non- combustible aerosol provision system, an article for use in or as a non-combustible aerosol provision system and a method for forming a component for an article for use in or as a non-combustible aerosol provision system.

Background Certain tobacco industry products produce an aerosol during use, which is inhaled by a user. For example, tobacco heating devices heat an aerosol generating substrate such as tobacco to form an aerosol by heating, but not burning, the substrate. Such tobacco industry products commonly include mouthpieces through which the aerosol passes to reach the user’s mouth.

Summary

In accordance with embodiments described herein, according to a first aspect, there is provided a component for an article for use in or as a non-combustible aerosol provision system, the component comprising a body of material extending in a longitudinal direction, wherein the body of material comprises sheet material comprising fibres having a length in the range 2 mm to 6 mm and wherein the body of material has a density in the range between about o.i and 0.25 mg/mms.

In accordance with embodiments described herein, according to a second aspect, there is provided component for an article for use in or as a non-combustible aerosol provision system, the component comprising a body of material extending in a longitudinal direction, wherein the body of material comprises sheet material comprising fibres having a length in the range 2 mm to 6 mm and wherein the body of material has a density in the range between about 0.1 and 0.25 mg/mms.

In accordance with embodiments described herein, according to a third aspect, there is provided an article for use in or as a non-combustible aerosol provision system, the article comprising an aerosol generating material and a downstream portion downstream of the aerosol generating material, the downstream portion comprising a component according to the first or second aspect above. In accordance with embodiments described herein, according to a fourth aspect there is provided a non-combustible aerosol provision system comprising an article according to the third aspect above. In accordance with embodiments described herein, according to a fifth aspect there is provided a method for forming a component for an article for use in a non-combustible aerosol provision system, the method comprising forming a sheet material into a body of material, wherein the sheet material comprises fibres having a length in the range 2 mm to 6 mm and wherein the body of material has a density in the range between about o.i and 0.25 mg/mm3.

Brief Description of the Drawings

Embodiments of the invention will now be described, by way of non-limiting examples only, with reference to the accompanying drawings, in which: Figure 1 is a side-on cross sectional view of an article for use with a non-combustible aerosol provision device, the article including a body of material formed from a sheet material;

Figure 2A is a cross-sectional end view of the body of material of the article of Figure 1, along the line A-A of Figure 1; Figure 2B is a side-on view of the sheet material forming the body of material of Figure 2A;

Figure 3 is a side-on cross sectional view of an article for use with a non-combustible aerosol provision device;

Figure 4 is a side-on cross sectional view of an article for use with a non-combustible aerosol provision device;

Figure 5 is a side-on cross sectional view of an article for use with a non-combustible aerosol provision device;

Figure 6 is a side-on cross sectional view of a multiple length rod for manufacture of a body of material of the article of Figure 5; Figure 7 is a perspective illustration of a non-combustible aerosol provision device;

Figure 8 illustrates the device of Figure 7 with the outer cover removed and without an article present;

Figure 9 is a side view of the device of Figure 8 in partial cross-section;

Figure 10 is an exploded view of the device of Figure 8, with the outer cover omitted; Figure 11A is a cross sectional view of a portion of the device of Figure 8; and Figure 11B is a close-up illustration of a region of the device of Figure 11A. Detailed Description

According to the present disclosure, an “aerosol provision system” includes both combustible aerosol provision systems and non-combustible aerosol provision systems.

According to the present disclosure, a “combustible” aerosol provision system is one where a constituent aerosol-generating material of the aerosol provision system (or component thereof) is combusted or burned during use in order to facilitate delivery of at least one substance to a user.

According to the present disclosure, a “non-combustible” aerosol provision system is one where a constituent aerosol-generating material of the aerosol provision system (or component thereof) is not combusted or burned in order to facilitate delivery of at least one substance to a user.

In some embodiments, the delivery system is a non-combustible aerosol provision system, such as a powered non-combustible aerosol provision system.

In some embodiments, the non-combustible aerosol provision system is an electronic cigarette, also known as a vaping device or electronic nicotine delivery system (END), although it is noted that the presence of nicotine in the aerosol-generating material is not a requirement.

In some embodiments, the non-combustible aerosol provision system is an aerosol- generating material heating system, also known as a heat-not-burn system. An example of such a system is a tobacco heating system.

In some embodiments, the non-combustible aerosol provision system is a hybrid system to generate aerosol using a combination of aerosol-generating materials, one or a plurality of which may be heated. Each of the aerosol-generating materials may be, for example, in the form of a solid, liquid or gel and may or may not contain nicotine.

In some embodiments, the hybrid system comprises a liquid or gel aerosol-generating material and a solid aerosol-generating material. The solid aerosol-generating material may comprise, for example, tobacco or a non-tobacco product. Typically, the non-combustible aerosol provision system may comprise a non combustible aerosol provision device and a consumable for use with the non combustible aerosol provision device. In some embodiments, the disclosure relates to consumables comprising aerosol generating material and configured to be used with non-combustible aerosol provision devices. These consumables are sometimes referred to as articles throughout the disclosure. In some embodiments, the non-combustible aerosol provision system, such as a non combustible aerosol provision device thereof, may comprise a power source and a controller. The power source may, for example, be an electric power source or an exothermic power source. In some embodiments, the exothermic power source comprises a carbon substrate which may be energised so as to distribute power in the form of heat to an aerosol-generating material or to a heat transfer material in proximity to the exothermic power source.

In some embodiments, the non-combustible aerosol provision system may comprise an area for receiving the consumable, an aerosol generator, an aerosol generation area, a housing, a mouthpiece, a filter and/ or an aerosol-modifying agent.

In some embodiments, the consumable for use with the non-combustible aerosol provision device may comprise aerosol-generating material, an aerosol-generating material storage area, an aerosol-generating material transfer component, an aerosol generator, an aerosol generation area, a housing, a wrapper, a filter, a mouthpiece, and/ or an aerosol-modifying agent.

In some embodiments, the substance to be delivered comprises an active substance. The active substance as used herein may be a physiologically active material, which is a material intended to achieve or enhance a physiological response. The active substance may for example be selected from nutraceuticals, nootropics, psychoactives. The active substance may be naturally occurring or synthetically obtained. The active substance may comprise for example nicotine, caffeine, taurine, theine, vitamins such as B6 or B12 or C, melatonin, cannabinoids, or constituents, derivatives, or combinations thereof. The active substance may comprise one or more constituents, derivatives or extracts of tobacco, cannabis or another botanical.

In some embodiments, the active substance comprises nicotine. In some embodiments, the active substance comprises caffeine, melatonin or vitamin B12.

As noted herein, the active substance may comprise or be derived from one or more botanicals or constituents, derivatives or extracts thereof. As used herein, the term "botanical" includes any material derived from plants including, but not limited to, extracts, leaves, bark, fibres, stems, roots, seeds, flowers, fruits, pollen, husk, shells or the like. Alternatively, the material may comprise an active compound naturally existing in a botanical, obtained synthetically. Example botanicals are tobacco, eucalyptus, star anise, hemp, cocoa, cannabis, fennel, lemongrass, peppermint, spearmint, rooibos, chamomile, flax, ginger, ginkgo biloba, hazel, hibiscus, laurel, licorice (liquorice), matcha, mate, orange skin, papaya, rose, sage, tea such as green tea or black tea, thyme, clove, cinnamon, coffee, aniseed (anise), basil, bay leaves, cardamom, coriander, cumin, nutmeg, oregano, paprika, rosemary, saffron, lavender, lemon peel, mint, juniper, elderflower, vanilla, wintergreen, beefsteak plant, curcuma, turmeric, sandalwood, cilantro, bergamot, orange blossom, myrtle, cassis, valerian, pimento, mace, damien, marjoram, olive, lemon balm, lemon basil, chive, carvi, verbena, tarragon, geranium, mulberry, ginseng, theanine, theacrine, maca, ashwagandha, damiana, guarana, chlorophyll, baobab or any combination thereof. The mint maybe chosen from the following mint varieties: Mentha Arventis, Mentha c.v., Mentha niliaca, Mentha piperita, Mentha piperita citrata c.v., Mentha piperita c.v, Mentha spicata crispa, Mentha cardifolia, Memtha longifolia, Mentha suaveolens variegata, Mentha pulegium, Mentha spicata c.v. and Mentha suaveolens

In some embodiments, the active substance comprises or is derived from one or more botanicals or constituents, derivatives or extracts thereof and the botanical is tobacco.

In some embodiments, the active substance comprises or derived from one or more botanicals or constituents, derivatives or extracts thereof and the botanical is selected from eucalyptus, star anise, cocoa and hemp. In some embodiments, the active substance comprises or derived from one or more botanicals or constituents, derivatives or extracts thereof and the botanical is selected from rooibos and fennel. In some embodiments, the substance to be delivered comprises a flavour.

As used herein, the terms "flavour" and "flavourant" refer to materials which, where local regulations permit, maybe used to create a desired taste, aroma or other somatosensorial sensation in a product for adult consumers. They may include naturally occurring flavour materials, botanicals, extracts of botanicals, synthetically obtained materials, or combinations thereof (e.g., tobacco, cannabis, licorice (liquorice), hydrangea, eugenol, Japanese white bark magnolia leaf, chamomile, fenugreek, clove, maple, matcha, menthol, Japanese mint, aniseed (anise), cinnamon, turmeric, Indian spices, Asian spices, herb, wintergreen, cherry, berry, red berry, cranberry, peach, apple, orange, mango, clementine, lemon, lime, tropical fruit, papaya, rhubarb, grape, durian, dragon fruit, cucumber, blueberry, mulberry, citrus fruits, Drambuie, bourbon, scotch, whiskey, gin, tequila, rum, spearmint, peppermint, lavender, aloe vera, cardamom, celery, cascarilla, nutmeg, sandalwood, bergamot, geranium, khat, naswar, betel, shisha, pine, honey essence, rose oil, vanilla, lemon oil, orange oil, orange blossom, cherry blossom, cassia, caraway, cognac, jasmine, ylang- ylang, sage, fennel, wasabi, piment, ginger, coriander, coffee, hemp, a mint oil from any species of the genus Mentha, eucalyptus, star anise, cocoa, lemongrass, rooibos, flax, ginkgo biloba, hazel, hibiscus, laurel, mate, orange skin, rose, tea such as green tea or black tea, thyme, juniper, elderflower, basil, bay leaves, cumin, oregano, paprika, rosemary, saffron, lemon peel, mint, beefsteak plant, curcuma, cilantro, myrtle, cassis, valerian, pimento, mace, damien, marjoram, olive, lemon balm, lemon basil, chive, carvi, verbena, tarragon, limonene, thymol, camphene), flavour enhancers, bitterness receptor site blockers, sensorial receptor site activators or stimulators, sugars and/or sugar substitutes (e.g., sucralose, acesulfame potassium, aspartame, saccharine, cyclamates, lactose, sucrose, glucose, fructose, sorbitol, or mannitol), and other additives such as charcoal, chlorophyll, minerals, botanicals, or breath freshening agents. They maybe imitation, synthetic or natural ingredients or blends thereof. They may be in any suitable form, for example, liquid such as an oil, solid such as a powder, or gas. In some embodiments, the flavour comprises menthol, spearmint and/or peppermint. In some embodiments, the flavour comprises flavour components of cucumber, blueberry, citrus fruits and/or redberry. In some embodiments, the flavour comprises eugenol. In some embodiments, the flavour comprises flavour components extracted from tobacco. In some embodiments, the flavour comprises flavour components extracted from cannabis.

In some embodiments, the flavour may comprise a sensate, which is intended to achieve a somatosensorial sensation which are usually chemically induced and perceived by the stimulation of the fifth cranial nerve (trigeminal nerve), in addition to or in place of aroma or taste nerves, and these may include agents providing heating, cooling, tingling, numbing effect. A suitable heat effect agent may be, but is not limited to, vanillyl ethyl ether and a suitable cooling agent may be, but not limited to eucolyptol, WS-3.

Aerosol-generating material is a material that is capable of generating aerosol, for example when heated, irradiated or energized in any other way. Aerosol-generating material may, for example, be in the form of a solid, liquid or gel which may or may not contain an active substance and/or flavourants. In some embodiments, the aerosol - generating material may comprise an “amorphous solid”, which may alternatively be referred to as a “monolithic solid” (i.e. non-fibrous). In some embodiments, the amorphous solid may be a dried gel. The amorphous solid is a solid material that may retain some fluid, such as liquid, within it. In some embodiments, the aerosol generating material may for example comprise from about 50wt%, 6owt% or 70wt% of amorphous solid, to about 90wt%, 95wt% or ioowt% of amorphous solid.

The aerosol-generating material may comprise one or more active substances and/or flavours, one or more aerosol-former materials, and optionally one or more other functional material.

The aerosol-former material may comprise one or more constituents capable of forming an aerosol. In some embodiments, the aerosol-former material may comprise one or more of glycerine, glycerol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 1,3-butylene glycol, erythritol, meso-Erythritol, ethyl vanillate, ethyl laurate, a diethyl suberate, triethyl citrate, triacetin, a diacetin mixture, benzyl benzoate, benzyl phenyl acetate, tributyrin, lauryl acetate, lauric acid, myristic acid, and propylene carbonate.

The one or more other functional materials may comprise one or more of pH regulators, colouring agents, preservatives, binders, fillers, stabilizers, and/or antioxidants.

The material may be present on or in a support, to form a substrate. The support may, for example, be or comprise paper, card, paperboard, cardboard, reconstituted material, a plastics material, a ceramic material, a composite material, glass, a metal, or a metal alloy. In some embodiments, the support comprises a susceptor. In some embodiments, the susceptor is embedded within the material. In some alternative embodiments, the susceptor is on one or either side of the material. A consumable is an article comprising or consisting of aerosol-generating material, part or all of which is intended to be consumed during use by a user. A consumable may comprise one or more other components, such as an aerosol-generating material storage area, an aerosol-generating material transfer component, an aerosol generation area, a housing, a wrapper, a mouthpiece, a filter and/ or an aerosol-modifying agent. A consumable may also comprise an aerosol generator, such as a heater, that emits heat to cause the aerosol-generating material to generate aerosol in use. The heater may, for example, comprise combustible material, a material heatable by electrical conduction, or a susceptor. A susceptor is a material that is heatable by penetration with a varying magnetic field, such as an alternating magnetic field. The susceptor may be an electrically-conductive material, so that penetration thereof with a varying magnetic field causes induction heating of the heating material. The heating material may be magnetic material, so that penetration thereof with a varying magnetic field causes magnetic hysteresis heating of the heating material. The susceptor may be both electrically-conductive and magnetic, so that the susceptor is heatable by both heating mechanisms. The device that is configured to generate the varying magnetic field is referred to as a magnetic field generator, herein. An aerosol-modifying agent is a substance that is configured to modify the aerosol generated, for example by changing the taste, flavour, acidity or another characteristic of the aerosol. The aerosol-modifying agent may be provided in an aerosol-modifying agent release component, that is operable to selectively release the aerosol-modifying agent The aerosol-modifying agent may, for example, be an additive or a sorbent. The aerosol-modifying agent may, for example, comprise one or more of a flavourant, a colourant, water, and a carbon adsorbent. The aerosol-modifying agent may, for example, be a solid, a liquid, or a gel. The aerosol-modifying agent maybe in powder, thread or granule form. The aerosol-modifying agent may be free from filtration material.

An aerosol generator is an apparatus configured to cause aerosol to be generated from the aerosol-generating material. In some embodiments, the aerosol generator is a heater configured to subject the aerosol-generating material to heat energy, so as to release one or more volatiles from the aerosol-generating material to form an aerosol.

In some embodiments, the aerosol generator is configured to cause an aerosol to be generated from the aerosol-generating material without heating. For example, the aerosol generator maybe configured to subject the aerosol-generating material to one or more of vibration, increased pressure, or electrostatic energy.

Articles, for instance those in the shape of rods, are often named according to the product length: “regular” (typically in the range 68 - 75 mm, e.g. from about 68 mm to about 72 mm), “short” or “mini” (68 mm or less), “king-size” (typically in the range 75 - 91 mm, e.g. from about 79 mm to about 88 mm), “long” or “super-king” (typically in the range 91 - 105 mm, e.g. from about 94 mm to about 101 mm) and “ultra-long”

(typically in the range from about 110 mm to about 121 mm).

They are also named according to the product circumference: “regular” (about 23 - 25 mm), “wide” (greater than 25 mm), “slim” (about 22 - 23 mm), “demi-slim” (about 19 - 22 mm), “super-slim” (about 16 - 19 mm), and “micro-slim” (less than about 16 mm).

Accordingly, an article in a king-size, super-slim format will, for example, have a length of about 83 mm and a circumference of about 17 mm. Each format may be produced with mouthpieces of different lengths. The mouthpiece length will be from about 30mm to 50 mm. A tipping paper connects the mouthpiece to the aerosol generating material and will usually have a greater length than the mouthpiece, for example from 3 to 10 mm longer, such that the tipping paper covers the mouthpiece and overlaps the aerosol generating material, for instance in the form of a rod of substrate material, to connect the mouthpiece to the rod.

Articles and their aerosol generating materials and mouthpieces described herein can be made in, but are not limited to, any of the above formats.

The terms ‘upstream’ and ‘downstream’ used herein are relative terms defined in relation to the direction of mainstream aerosol drawn though an article or device in use.

The filamentary tow material described herein can comprise cellulose acetate fibre tow. The filamentary tow can also be formed using other materials used to form fibres, such as polyvinyl alcohol (PVOH), polylactic acid (PLA), polycaprolactone (PCL), poly(i-4 butanediol succinate) (PBS), poly(butylene adipate-co-terephthalate)(PBAT), starch based materials, cotton, aliphatic polyester materials and polysaccharide polymers or a combination thereof. The filamentary tow may be plasticised with a suitable plasticiser for the tow, such as triacetin where the material is cellulose acetate tow, or the tow may be non-plasticised. The tow can have any suitable specification, such as fibres having a Ύ’ shaped or other cross section such as ‘X’ shaped, filamentary denier values between 2.5 and 15 denier per filament, for example between 8.0 and 11.0 denier per filament and total denier values of 5,000 to 50,000, for example between 10,000 and 40,000. As used herein, the term “tobacco material” refers to any material comprising tobacco or derivatives or substitutes thereof. The term “tobacco material” may include one or more of tobacco, tobacco derivatives, expanded tobacco, reconstituted tobacco or tobacco substitutes. The tobacco material may comprise one or more of ground tobacco, tobacco fibre, cut tobacco, extruded tobacco, tobacco stem, tobacco lamina, reconstituted tobacco and/ or tobacco extract.

In the figures described herein, like reference numerals are used to illustrate equivalent features, articles or components. Figure 1 is a side-on cross sectional view of an article 1 for use as part of a non combustible aerosol provision system. The article 1 includes a cylindrical rod of aerosol generating material 3, in the present case tobacco material, and a downstream portion, in the present case referred to as a mouthpiece 2, connected to the aerosol generating material 3 such that it is downstream of the aerosol generating material 3. The aerosol generating material 3 provides an aerosol when heated, for instance within a non-combustible aerosol provision device as described herein, for instance a non-combustible aerosol provision device comprising a coil, forming a system. In other embodiments, the article 1 can include its own heat source, forming an aerosol provision system without requiring a separate aerosol provision device.

The aerosol generating material 3, also referred to herein as an aerosol generating substrate 3, comprises at least one aerosol-former material. In the present example, the aerosol-former material is glycerol. In alternative examples, the aerosol-former material can be another material as described herein or a combination thereof, for instance propylene glycol.

In the present example, the mouthpiece includes a tubular portion 4a, in the present example formed by a hollow tube, also referred to as a cooling element. The mouthpiece 2, in the present example, includes a component including a body of material 6 downstream of the tubular portion 4a. In the present example, the body of material 6 is adjacent to and in an abutting relationship with the tubular portion 4a. The body of material 6 and tubular portion 4a each define a substantially cylindrical overall outer shape and share a common longitudinal axis. The body of material 6 comprises a sheet material.

The sheet material comprises fibres having a length in the range 2 mm to 6 mm. Such fibres have the benefit that they result in a material which is less likely to absorb and hold an aerosol former (e.g. glycerol, as in the present example) and/or an aerosol-modifying agent (e.g. menthol). Hence, a body of material including such fibres may allow a greater amount of aerosol former and/ or aerosol-modifying agent to pass through the body of material to the user. In some embodiments, the body of material comprises fibres having a length in the range 2 mm to 5 mm, 2 mm to 4 mm, or 2 mm to 3 mm. The body of material can comprise fibres having one or more of the following lengths: about 2 mm, about 2.5 mm, about 3 mm, about 3.5 mm, about 4 mm, about 4.5 mm, about 5 mm, about 5.5 mm and about 6 mm. The fibre length can be measured in accordance with an appropriate standard and the fibre lengths set out above can be the length-weighted mean value of fibre lengths. Selection of appropriate fibre lengths can be made based, for instance, on the source of material, such as the type of wood, used to provide pulp for the sheet material paper production process. The fibre length can be, for instance, selected based on the form of cellulosic material used to form the sheet material. For instance, species of pine generally result in wood pulp having an average fibre length in the range of about 3.5mm to 4.4mm , whereas species of ash may result in wood pulp having an average fibre length between about 1.05mm and 1.20mm. The average fibre length in the sheet material can, for instance, be determined by scanning electron microscopy or other techniques known to those in the art. At least 70% of the fibres, for instance, can have a length in the range 2 mm to 6 mm, or at least 80% or 90%.

In the present example, the body of material 6 of the component is formed from sheet material which is crimped. In the present example, the body of material comprises crimped sheet material formed having a crimp pattern comprising a series of substantially parallel ridges and grooves, and the average spacing between adjacent ridges is greater than about 0.3 mm. In addition, in the present example, the crimp amplitude is less than about 0.7 mm. In other examples, the sheet material can include either an average spacing between adjacent ridges of greater than about 0.3 mm or a crimp amplitude of less than about 0.7 mm. In any of these examples, the average density of said body of material can be between about 0.1 and about 0.25 mg/mm3. Alternatively, the crimp amplitude can be greater than 0.7mm, for instance between 0.7mm and 1.2mm. The crimp amplitude (also known as “crimping factor”) refers to the depth of the grooves the crimping forms in the sheet material forming the body. That is, crimping the sheet material produces a plurality of peaks and troughs in the sheet material when viewed from a first side of the sheet material, as shown in Figure 2B, wherein the crimp amplitude ‘A’ is the depth of the troughs, measured from their peak. The crimping may form a ‘Zig-Zag’ formation or another shape. In some embodiments, adjacent grooves of the crimped sheet material are spaced by a distance, or have a pitch ‘P’, in the range of 0.3 to 2 mm and, preferably, in the range of 0.4 to 1 mm. In some embodiments, adjacent grooves of the crimped sheet material are spaced by a distance of at least 0.4 mm or at least 0.5, 0.6, 0.7 or 0.8 mm. In some embodiments, adjacent grooves of the crimped sheet material 10 are spaced by a distance of at most 1.5 mm, and preferably, at most, 1.4, 1.3, 1.2, 1.1 or 1.0 mm. For instance, the sheet material can have a crimp with a crimp amplitude of less than distance of 500 pm and spacing between peaks (or troughs) of at least 300 pm, at least 400 pm or at least 500 pm.

In some embodiments, the sheet material 10 is heated as it is crimped. For example, the sheet material 10 may be passed between crimping rollers, wherein one or both of the crimping rollers is heated.

Advantageously, sheet material, for instance paper, having the above crimp pitch and/ or amplitude has been found to exhibit improved performance when used in components of aerosol provision systems. In particular, these relatively low levels of crimp pitch and amplitude surprisingly result in a body of material having a lower pressure drop compared to bodies formed from sheet material with higher levels of crimping. In the present example, the density of the body of material 6 is about 0.19 mg/mm3. In some embodiments, the body 6 has a density of at least 0.1 mg/mm3, 0.12 mg/mm3 or 0.15 mg/ mm3. Alternatively or in addition, the body of material 6 can have a density of less than about 0.3 mg/mm3, less than about 0.25 mg/mm3 or less than about 0.22 mg/ mm3. Advantageously, the density of the body of material can be between about 0.1 or 0.15 mg/mm3 and about 0.25 mg/mm3. These values include any additives included within the body of material 6. Before being crimped and formed into the body of material, the sheet material can have a density of between about 0.2 and 0.5 mg/mm3, for instance about 0.25, 0.30 or 0.35 mg/mm3. The body of material 6 may be formed from a continuous web of sheet material 6A. In the present example, the sheet material 6A is gathered to form the body of material 6 is a similar manner to a ‘crepe filter’. The sheet material 6A maybe manufactured using a CU-20 filter making machine manufactured by Decoufle (TM). However, a skilled person will appreciate that other machines may be used to manufacture the body of material 6. In the present example, the sheet material 6A comprises cellulose. In the present example, the sheet material 6A is paper.

In some embodiments, the continuous web of sheet material 6A has a width of at least 60 mm, at least 70 mm, at least 80 mm, at least 90 mm, at least 100 mm, at least 110 mm, or at least 120 mm.

In some embodiments, the continuous web of sheet material 6A has a width of at most 240 mm, at most 230 mm, at most 220 mm, at most 210 mm, at most 200 mm or at most 190 mm.

In some embodiments, the sheet material has a width in the range of 120 mm to 200 mm, in the range of 150 mm to 190 mm, in the range of 160 mm to 190 mm, or in the range of 160 mm to 180 mm.

The sheet material can have a thickness of between about 50 and about 100 pm, or between about 60 and about 90 pm. In one example, the sheet material is paper having a thickness of between 60 and 70 pm and a basis weight of between 30 and 40 grams/m².

The sheet material 6A may additionally or alternatively comprise a different material. For example, in some embodiments the sheet material 6A comprises reconstituted tobacco that is formed into a sheet material 6A that is arranged to form the body of material 6. The reconstituted tobacco comprises cellulose. In another embodiment (not shown), the reconstituted tobacco is manufactured into a uniform plug of material that forms the body 6. The reconstituted tobacco may optionally be paper reconstituted tobacco.

In some embodiments, the sheet material 6A comprises paper with a basis weight in the range of 15 gm to 80 gsm, or in the range of 20 gsm to 50 gsm.

In some embodiments, the sheet material 6A has a basis weight of at least 15 gsm, at least 20 gsm, at least 25 gsm or at least 30 gsm. In some embodiments, the sheet material has a basis weight of 100 gsm or less, 90 gsm or less, 80 gsm or less or 70 gsm or less. Preferably, the sheet material has a basis weight of 60 gsm or less, 50 gsm or less, or 40 gsm or less. In some embodiments, the sheet material has a basis weight in the range of 20 gsm to 40 gsm, in the range of 24 gsm to 36 gsm, or in the range of 30 gsm to 40 gsm.

The body of material 6 is wrapped in a first plug wrap 7. In the present example, the tubular portion 4a and body of material 6 are combined using a second plug wrap 9 which is wrapped around both sections. A tipping paper 5 is wrapped around the full length of the mouthpiece 2 and over part of the rod of aerosol generating material 3 and has an adhesive on its inner surface to connect the mouthpiece 2 and rod 3.

In the present example, the tubular portion 4a is formed from a plurality of layers of paper which are parallel wound, with butted seams, to form a hollow tube. In the present example, first and second paper layers are provided in a two-ply tube, although in other examples 3, 4 or more paper layers can be used forming 3, 4 or more ply tubes. Other constructions can be used, such as spirally wound layers of paper, cardboard tubes, tubes formed using a papier-mache type process, moulded or extruded plastic tubes or similar.

In some embodiments, the tubular portion has a wall thickness of at least about 150 pm and up to about 2 mm, between 200 pm and 1.5 mm, or between 250 pm and 1 mm. In the present example, the tubular portion has a wall thickness of about 300 pm. The "wall thickness" of the tubular portion corresponds to the thickness of the wall of the tubular portion in a radial direction. This may be measured, for example, using a caliper.

The article 1 has a ventilation level of about 75% of the aerosol drawn through the article. In alternative embodiments, the article can have a ventilation level of between 50% and 80% of aerosol drawn through the article, for instance between 65% and 75%. Ventilation at these levels helps to slow down the flow of aerosol drawn through the mouthpiece 2 and thereby enable the aerosol to cool sufficiently before it reaches a downstream end 2b of the mouthpiece 2. The ventilation is provided directly into the mouthpiece 2 of the article 1. In the present example, the ventilation is provided into the tubular portion 4a, which has been found to be particularly beneficial in assisting with the aerosol generation process. The ventilation is provided via first and second parallel rows of ventilation holes 12, in the present case formed as laser perforations, at positions 13.925 mm and 14.625 mm respectively from the downstream, mouth-end 2b of the mouthpiece 2. These ventilation holes 12 pass though the tipping paper 5, second plug wrap 9 and tubular portion 4a. In alternative embodiments, the ventilation can be provided into the mouthpiece at other locations. For example, the ventilation may be provided into the body of material 6.

Alternatively, the ventilation can be provided via a single row of ventilation holes, for instance laser perforations, into the portion of the article in which the tubular body 4a is located. This has been found to result in improved aerosol formation, which is thought to result from the airflow through the ventilation holes being more uniform than with multiple rows of ventilation holes, for a given ventilation level. In some examples, the aerosol generating material 3 described herein is a first aerosol generating material and the tubular portion 4a may include a second aerosol generating material. In one example, wall 4b of tubular portion 4a comprises the second aerosol generating material. For example, the second aerosol generating material can be disposed on an inner surface of wall 4b of the tubular portion 4a.

The second aerosol generating material comprises at least one aerosol former material, and may also comprise at least one aerosol modifying agent, or other sensate material. The aerosol former material and/ or aerosol modifying agent can be any aerosol former material or aerosol modifying agent as described herein, or a combination thereof.

As the aerosol generated from aerosol generating material 3, referred to herein as the first aerosol, is drawn through the tubular portion 4a of the mouthpiece, heat from the first aerosol may aerosolise the aerosol forming material of the second aerosol generating material, to form a second aerosol. The second aerosol may comprise a flavourant, which can be any of the flavourants described herein, and which may be additional or complementary to the flavour of the first aerosol.

Providing a second aerosol generating material on the tubular body 4a can result in generation of a second aerosol which boosts or complements the flavour or visual appearance of the first aerosol. In the present example, the article 1 has an outer circumference of about 21 mm (i.e. the article is in the demi-slim format). In some embodiments, the article 1 has a rod of aerosol generating material having a circumference greater than 19 mm. This has been found to provide a sufficient circumference to generate an improved and sustained aerosol over a usual aerosol generation session preferred by consumers. As the article is heated, heat transfers through the rod of aerosol generating material 3 to volatise components of the rod, and circumferences greater than 19 mm have been found to be particularly effective at producing an aerosol in this way. Since the article is to be heated to release an aerosol, improved heating efficiency can be achieved using articles having circumferences of less than about 23 mm. To achieve improved aerosol via heating, while maintaining a suitable product length, rod circumferences of greater than 19 mm and less than 23 mm are suitable. In some examples, the rod circumference can be between 20 mm and 22 mm, which has been found to provide a good balance between providing effective aerosol delivery while allowing for efficient heating.

The outer circumference of the mouthpiece 2 is substantially the same as the outer circumference of the rod of aerosol generating material 3, such that there is a smooth transition between these components. In the present example, the outer circumference of the mouthpiece 2 is about 20.8 mm.

In some examples, the tipping paper 5 comprises citrate, such as sodium citrate or potassium citrate. In such examples, the tipping paper 5 may have a citrate content of 2% by weight or less, or 1% by weight or less. Reducing the citrate content of the tipping paper 5 is thought to assist with reducing the charring effect which may occur during use.

In the present example, the tipping paper 5 extends 5 mm over the rod of aerosol generating material 3 but it can alternatively extend between 3 mm and 10 mm over the rod 3, or between 4 mm and 6 mm, to provide a secure attachment between the mouthpiece 2 and rod 3. The tipping paper 5 can have a basis weight which is higher than the basis weight of plug wraps used in the article 1, for instance a basis weight of 40 gsm to 80 gsm, or between 50 gsm and 70 gsm, and in the present example 58 gsm. These ranges of basis weights have been found to result in tipping papers having acceptable tensile strength while being flexible enough to wrap around the article 1 and adhere to itself along a longitudinal lap seam on the paper. The outer circumference of the tipping paper 5, once wrapped around the mouthpiece 2, is about 21 mm.

In some embodiments, the first plug wrap 7 has a basis weight of less than 50 gsm, for instance between about 20 gsm and 40 gsm. However, it should be recognised that the basis weight of the first plug wrap 7 may be higher to increase the hardness of the mouthpiece. For instance, the basis weight of the first plug wrap 7 maybe at least 50 gsm, at least 60 gsm, at least 70 gsm, at least 80 gsm, at least 90 gsm or at least 100 gsm. In some embodiments, the basis weight of the first plug wrap 7 is in the range of 50 gsm to 110 gsm, or in the range of 60 gsm to 100 gsm.

In some embodiments, the first plug wrap 7 has a basis weight of at least 20 gsm or at least 30 gsm. In some embodiments, the first plug wrap 7 has a basis weight of at most 120 gsm, 110 gsm or too gsm. In some embodiments, the first plug wrap 7 has a basis weight in the range of 20 gsm to 120 gsm, or in the range of 30 to too gsm.

In some embodiments, the first plug wrap 7 has a thickness of between 30 pm and 60 pm, or between 35 pm and 45 pm. However, it should be recognised that the thickness weight of the first plug wrap 7 may be higher to increase the hardness of the mouthpiece. In some embodiments, for example, the thickness of the first plug wrap 7 maybe at least 40 microns, 50 microns, 60 microns, 70 microns, 80 microns, 90 microns or too microns. In some embodiments, the thickness of the first plug wrap 7 is in the range of 40 microns to 120 microns, or in the range of 50 to too microns. In some embodiments, the first plug wrap 7 is a non-porous plug wrap, for instance having a permeability of less than too Coresta units, for instance less than 50 Coresta units. However, in other embodiments, the first plug wrap 7 can be a porous plug wrap, for instance having a permeability of greater than 200 Coresta Units. In some embodiments, the length of the body of material 6 is less than about 20 mm. In the present example, the length of the body of material 6 is about 12 mm.

In some embodiments, the axial length of the body of material 6 is in the range of 10 mm to 20 mm. In some embodiments, an aerosol-former material is applied to the body of material 6. For example, the aerosol-former material may be applied to the sheet material 6A prior to the sheet material 6A being folded to form the body of material 6. The aerosol- former material may be sprayed on to the sheet material 6A or applied by a brush or by dipping the sheet material 6A in aerosol-former material.

In some embodiments, the aerosol-former material may comprise one or more of glycerine, glycerol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 1,3-butylene glycol, erythritol, meso-Erythritol, ethyl vanillate, ethyl laurate, a diethyl suberate, triethyl citrate, triacetin, a diacetin mixture, benzyl benzoate, benzyl phenyl acetate, tributyrin, lauryl acetate, lauric acid, myristic acid, and propylene carbonate. For instance, the aerosol-former material can comprise triacetin and/or triethyl citrate. In some embodiments, at least 0.02 mg of aerosol-former material is applied to the body of material per 1 mm axial length of the body of material. In some embodiments, at least 0.03 mg, at least 0.04 mg or at least 0.05 mg of aerosol-former material is applied to the body of material per 1 mm axial length of the body of material. In some embodiments, 0.5 mg or less of aerosol-former material is applied to the body of material per 1 mm axial length of the body of material. In some embodiments, 0.4 mg or less or 0.3 mg or less of aerosol-former material is applied to the body of material per 1 mm axial length of the body of material. At least some of the aerosol-former material is combined with the aerosol as it passes through the body of material 6 and helps to make the aerosol feel less dry within the user’s mouth.

In some embodiments, the body of material 6 has an outer volume of at least 115 mm3. In the present example, the body of material 6 is generally cylindrical and thus has a generally cylindrical outer volume. It should be recognised that in other embodiments the body of material 6 may have an outer volume that is smaller than 115 mm3.

In the present example, the width Wi of the body of material 6 (which in the present example corresponds to the diameter of the body of material 6) is about 6.36 mm and the axial length Li of the body of material 6 is 12 mm. Thus, the outer volume of the body of material 6 is about 381 mm3.

It has been found that a body of material 6A comprising cellulose and having a volume of at least 115mm³ helps to remove moisture from aerosol generated by the aerosol generating material 3 as the aerosol passes through the body of material 6A of the mouthpiece 2. That is, the cellulose containing sheet material 6A absorbs water from the aerosol. Removing moisture from the aerosol makes the aerosol feel cooler in the user’s mouth.

In some embodiments, the body of material 6 has a volume of at least 19 mm3 per mm axial length of the body of material, at least 25 mm3 per mm axial length, or at least 30 mm³ per mm axial length. For instance, if the body of material 6 has a volume of 19 mm³ per mm axial length, and a length Li of 10 mm, then the volume of the body of material would be 190 mm³.

A larger volume of body of material 6A will generally be more effective at removing moisture from the aerosol. In some examples, the outer volume of the body of material 6 is at least 200 mm³, at least 300 mm³, at least 400 mm³, at least 500 mm³, at least 600 mm³, at least 700 mm³, at least 800 mm³, at least 900 mm³ or at least 1000 mm³.

In some embodiments, the axial length Li of the body of material 6 is at least 4 mm, at least 5 mm, at least 6 mm, at least 7 mm, at least 8 mm, at least 9 mm, or at least 10 mm.

In some embodiments, the axial length Li of the body of material 6 is in the range of 5 mm to 20 mm, 6 mm to 15 mm, or 8 mm to 14 mm.

In some embodiments, the width Wi of the body of material 6 is at least 4 mm, at least 5 mm, at least 6 mm, at least 7 mm, at least 8 mm or at least 9 mm.

In some embodiments, the circumference of the body of material 6 is at least 16 mm, at least 18 mm, at least 20 mm, at least 22 mm, at least 25 mm or at least 26 mm. In some embodiments, the pressure drop across the body of material 6 is at least 2 mmH₂0, at least 3 mmH₂0, or at least 4 mmH₂0. The pressure drop across the body of material may be at least 5 mmH₂0, at least 6 mmH₂0, at least 7 mmH₂0, at least 8 mmH₂0, at least 9 mmH₂0, at least 10 mmH₂0 or at least 11 mmH₂0.

In some embodiments, the pressure drop across the body of material 6 is less than 30 mmH₂0, less than 28 mmH₂0 or less than 25 mmH₂0.

In some embodiments, the pressure drop across the body of material 6 is about 20 mmH₂0, 23 mmH₂0 or 28 mmH₂0. In some embodiments, the pressure drop across the body of material 6 is in the range of 10 mmH₂0 to 30 mmH₂0, or in the range of 15 mmH₂0 to 25 mmH₂0.

In some embodiments, the pressure drop across the body of material 6 is at least 1.0 mmH₂0 per mm axial length of the body of material 6. In some embodiments, the pressure drop across the body of material 6 is at least 1.2 mmH₂0, 1.5 mmH₂0, or 1.8 mmH₂0 per mm axial length of the body of material 6.

In some embodiments, the pressure drop across the body of material 6 is less than 3.0 mmH₂0, 2.8 mmH₂0, or 2.6 mmH₂0 axial length of the body of material 6. In some embodiments, the pressure drop across the body of material 6 is less than 2.5 mmH₂0,

2.4 mmH₂0 or 2.3 mmH₂0 per mm of axial length of the body of material 6.

In some embodiments, the pressure drop across the body of material 6 is in the range of

1.5 mmH₂0 to 2.5 mmH₂0 per mm axial length of the body of material 6, or in the range of 1.6 to 2.4 mmWG per mm axial length of the body of material 6.

In some of the embodiments, the mass of body of material 6 is at least 50 mg, at least 60 mg or at least 70 mg. It has been advantageously found that providing a higher mass of the body of material 6 increases the amount of moisture that is absorbed form the aerosol. In the present example, the mass of the body of material is about 75 mg.

In some of the embodiments, the mass of body of material 6 is less than 150 mg, less than too mg, less than 85 mg or less than 80 mg. In some embodiments, the body of material 6 has a weight of at least 2 mg per mm axial length of the body of material. In some embodiments, the body of material 6 has a weight of at least 3 mg per mm axial length or at least 4 mg per mm axial length. In the present example, the body of material 6 has a weight of about 6 mg per mm. That is, if the body of material 6 has an axial length Li of 12 mm, as in the present example, then the total mass of the body of material 6 would be about 74 mg.

In some embodiments, the body of material 6 is a solid cylindrical body of material.

In some embodiments, the mouthpiece 2 has a hardness in the range of about 80% to 95%, or in the range of about 85% to 90%. The hardness of the mouthpiece 2 may be at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91% or at least 92%.

The hardness of the mouthpiece 2 may be measured according to the following protocol. Where the hardness of a section is referred to herein, the hardness is that as determined by the following measurement process. Any suitable device may be used for performing the measurement, such as the Borgwaldt Hardness Tester H10.

Hardness is defined as the ratio between the height ho of a body and the height hi of the body under a defined load, stated as a percentage of ho. Hardness may be expressed as: Hardness = (hi/ho)xioo

For an individual body, or a body contained in a multi-section rod, the hardness measurement is performed at the longitudinal centre point of the body. A load bar is used to apply the defined load to the body. The length of the load bar should be significantly higher than that of the specimen to be measured. Prior to the hardness measurement, the body to be measured is conditioned according to ISO 3402 for a minimum of 48 hours, and is maintained in environmental conditions according to ISO 3402 during the measurement. To perform the hardness measurement, a body is placed into the Hardness Tester Hio, a pre-load of 2 g is applied to the body, and after 1 s the initial height ho of the body under the 2 g pre-load is recorded. The pre-load is then removed and a load bar bearing a load of 150 g is lowered onto the sample at a rate of 0.6 mm/s, after 5 s the height hi of the body under the 150 g load is measured.

The hardness of the mouthpiece is determined as the average hardness of at least 20 mouthpieces measured according to this protocol. The hardness of the body of material 6 circumscribed by the first plug wrap 7

(hereinafter together referred to as the “component” for the purposes of determining the hardness) may also be determined using the above protocol, by carefully cutting the article to remove the body of material 6 surrounded by the first plug wrap 7. The hardness of the component maybe at least 80%, at least 81%, at least 82%, at least at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91% or at least 92%.

The expression “roundness” refers to the percentage conformity of the cross-sectional shape of the article/component to a perfect circle. The roundness is calculated according to Equation 1 below:

[Equation 1] To determine the roundness of the article 1 the maximum external diameter “X” of the component is measured using a calliper and the minimum external diameter “Y” of the article is measured using a calliper (the diameters being perpendicular to the central axis of the article 1). The less deviation between the maximum external diameter X and minimum external diameter Y of the article 1, the higher the roundness, which indicates that the cross-sectional shape of the article 1 is closer to a perfect circle.

In some embodiments, the roundness of the article 1 is at least 90%, at least 91%, at least 92%, at least 93%, at least 94% or at least 95%. The hardness of the body of material 6 circumscribed by the first plug wrap 7 (hereinafter together referred to as the “component” for the purposes of determining the roundness) may also be determined using the above protocol, by carefully cutting the article to remove the body of material 6 surrounded by the first plug wrap 7.

To determine the roundness of the body of material 6 circumscribed by the first plug wrap 7 (hereinafter together referred to as “the component” for the purposes of determining the roundness) the maximum external diameter “X” of the component is measured using a calliper and the minimum external diameter “Y” of the component is measured using a calliper (the diameters being perpendicular to the central axis of the component). The less deviation between the maximum external diameter X and minimum external diameter Y of the component, the higher the roundness, which indicates that the cross-sectional shape of the component is closer to a perfect circle. In some embodiments, the roundness of the component (i.e. the roundness of the body of material 6 circumscribed by the first plug wrap 7) is at least 90%, at least 91%, at least 92%, at least 93%, at least 94% or at least 95%.

The increased roundness of the article/component helps to ensure that the downstream portion can be processed, as otherwise a downstream portion that is too oval may become jammed or misaligned in the manufacturing machinery.

The first and/or second plug wraps 7, 9 can be adhered around the component(s) of the article by adhesive applied to a lap seam extending longitudinally along the first and/or second plug wraps. The first and/or second plug wraps 7, 9 can alternatively or in addition be adhered directly to the underlying component(s) using an adhesive. In both cases, the adhesive can be selected to be a water soluble adhesive to aid degradation of the component(s). Additionally or alternatively, the first and/ or second plug wraps 7, 9 can themselves be formed from paper or other material having improved degradability, for instance improved dispersibility when exposed to water.

Biodegradability can be measured according to the procedure set out under ISO 14855. Components as described herein can achieve a biodegradation of greater than 50% in 30 days when exposed to either fresh or marine water.

In some embodiments, the length of the tubular portion 4a is less than about 50 mm. In some embodiments, the length of the tubular portion 4a is less than about 40 mm. In some embodiments, the length of the tubular portion 4a is less than about 35 mm. In addition, or as an alternative, the length of the tubular portion 4a is at least about 10 mm. In some embodiments, the length of the tubular portion 4a is at least about 15 mm.

In some embodiments, the length of the tubular portion 4a is from about 15 mm to about 35 mm, from about 20 mm to about 30 mm, from about 23 to about 29 mm, or about 25 mm or about 29 mm. In the present example, the length of the tubular portion 4a is 25 mm.

In some embodiments, the second plug wrap 9 has a basis weight of less than 50 gsm.

In some embodiments, the second plug wrap 9 has a basis weight between about 20 gsm and 45 gsm. However, it should be recognised that the basis weight of the second plug wrap 9 may be higher to increase the hardness of the mouthpiece. For instance, the basis weight of the second plug wrap 9 maybe at least 50 gsm, at least 60 gsm, at least 70 gsm, at least 80 gsm, at least 90 gsm or at least too gsm. In some embodiments, the basis weight of the second plug wrap 9 is in the range of 50 gsm to 110 gsm, or in the range of 60 gsm to too gsm.

In some embodiments, the second plug wrap 9 has a basis weight of at least 10 gsm, at least 15 gsm, at least 20 gsm or at least 25 gsm.

In some embodiments, the second plug wrap 9 has a basis weight of less than 40 gsm, less than 35 gsm or less than 30 gsm.

In some embodiments, the second plug wrap 9 has a basis weight in the range of 10 to 40 gsm, in the range of 15 to 35 gsm, in the range of 20 to 30 gsm, or in the range of 25 to 30 gsm. In some embodiments, the basis weight of the second plug wrap 9 is about 27 gsm.

In some embodiments, the second plug wrap 9 has a thickness of between 30 pm and 60 pm, or between 35 pm and 45 pm. However, it should be recognised that the thickness of the second plug wrap 9 may be higher to increase the hardness of the mouthpiece. In some embodiments, for example, the thickness of the second plug wrap 9 maybe at least 40 microns, at least 50 microns, at least 60 microns, at least 70 microns, at least 80 microns, at least 90 microns or at least 100 microns. In some embodiments, the thickness of the second plug wrap 9 is in the range of 40 microns to 120 microns, or in the range of 50 microns to 100 microns. In some embodiments, the second plug wrap 9 is a non-porous plug wrap having a permeability of less than 100 Coresta Units, for instance less than 50 Coresta Units. However, in alternative embodiments, the second plug wrap 9 can be a porous plug wrap, for instance having a permeability of greater than 200 Coresta Units. The tubular portion 4a is located around and defines an air gap within the mouthpiece 2 which acts as a cooling segment. The air gap provides a chamber through which heated volatilised components generated by the aerosol generating material 3 flow.

The tubular portion 4a is hollow to provide a chamber for aerosol accumulation yet rigid enough to withstand axial compressive forces and bending moments that might arise during manufacture and whilst the article 1 is in use. The tubular portion 4a provides a physical displacement between the aerosol generating material 3 and the body of material 6. The physical displacement provided by the tubular portion 4a will provide a thermal gradient across the length of the tubular portion 4a. In some embodiments, the mouthpiece 2 comprises a cavity having an internal volume greater than 450 mm3. Providing a cavity of at least this volume has been found to enable the formation of an improved aerosol. Such a cavity size provides sufficient space within the mouthpiece 2 to allow heated volatilised components to cool, therefore allowing the exposure of the aerosol generating material 3 to higher temperatures than would otherwise be possible, since they may result in an aerosol which is too warm. In the present example, the cavity is formed by the tubular portion 4a, but in alternative arrangements it could be formed within a different part of the mouthpiece 2. In some embodiments, the mouthpiece 2 comprises a cavity, for instance formed within the tubular portion 4a, having an internal volume greater than 500 mm3, for instance greater than 550 mm³, allowing further improvement of the aerosol. In some embodiments, the internal cavity comprises a volume of between about 550 mm³ and about 850 mm³, or between about 600 mm³ and about 800 mm³. In the present example, the internal cavity of the tubular portion 4a has a volume of about 762 mm³. The tubular portion 4a can be configured to provide a temperature differential of at least 40 degrees Celsius between a heated volatilised component entering a first, upstream end of the tubular portion 4a and a heated volatilised component exiting a second, downstream end of the tubular portion 4a. In some embodiments, the tubular portion 4a is configured to provide a temperature differential of at least 60 degrees Celsius, at least 80 degrees Celsius, or at least 100 degrees Celsius between a heated volatilised component entering a first, upstream end of the tubular portion 4a and a heated volatilised component exiting a second, downstream end of the tubular portion 4a. This temperature differential across the length of the tubular portion 4a protects the temperature sensitive body of material 6 from the high temperatures of the aerosol generating material 3 when it is heated.

In alternative articles, the tubular portion 4a can be replaced with an alternative cooling element, for instance an element formed from a body of material which allows aerosol to pass through it longitudinally, and which also performs the function of cooling the aerosol.

The mouthpiece 2 of the article 1 comprises an upstream end 3a adjacent to the aerosol generating substrate 3 and a downstream end 2b distal from the aerosol generating substrate 3. The pressure drop or difference (also referred to as resistance to draw) across the mouthpiece, for instance the part of the article 1 downstream of the aerosol generating material 3, is less than about 40 mmH₂0. Such pressure drops have been found to allow sufficient aerosol, including desirable compounds such as flavour compounds, to pass through the mouthpiece 2 to the consumer. In some embodiments, the pressure drop across the mouthpiece 2 is less than about 20 mmH₂0. In some embodiments, particularly improved aerosol has been achieved using a mouthpiece 2 having a pressure drop of less than 15 mmH₂0, for instance about 6 mmH₂0, about 10 mmH₂o or about 14 mmH₂0. Alternatively or additionally, the mouthpiece pressure drop can be at least 3 mmH₂0, at least 4 mmH₂0 or at least 5 mmH₂0. In some embodiments, the mouthpiece pressure drop can be between about 5 mmH₂0 and 20 mmH₂0 or between 5 mmH₂0 and 15 mmH₂0. These values enable the mouthpiece 2 to slow down the aerosol as it passes through the mouthpiece 2 such that the temperature of the aerosol has time to reduce before reaching the downstream end 2b of the mouthpiece 2. In the present example, the aerosol generating material 3 is wrapped in a wrapper 10. The wrapper 10 can, for instance, be a paper or paper-backed foil wrapper. In the present example, the wrapper 10 is substantially impermeable to air. In alternative embodiments, the wrapper 10 has a permeability of less than 100 Coresta Units, or less than 60 Coresta Units. It has been found that using low permeability wrappers, for instance having a permeability of less than 100 Coresta Units, or less than 60 Coresta Units, results in an improvement in the aerosol formation in the aerosol generating material 3. Without wishing to be bound by theory, it is hypothesised that this is due to reduced loss of aerosol compounds through the wrapper 10. The permeability of the wrapper 10 can be measured in accordance with ISO 2965:2009 concerning the determination of air permeability for materials used as cigarette papers, filter plug wrap and filter joining paper.

In the present embodiment, the wrapper 10 comprises aluminium foil. Aluminium foil has been found to be particularly effective at enhancing the formation of aerosol within the aerosol generating material 3. In the present example, the aluminium foil has a metal layer having a thickness of about 6 pm. In the present example, the aluminium foil has a paper backing. However, in alternative arrangements, the aluminium foil can be other thicknesses, for instance between 4 pm and 16 pm in thickness. The aluminium foil also need not have a paper backing, but could have a backing formed from other materials, for instance to help provide an appropriate tensile strength to the foil, or it could have no backing material. Metallic layers or foils other than aluminium can also be used. The total thickness of the wrapper is between 20 pm and 60 pm, or between 30 pm and 50 pm, which can provide a wrapper having appropriate structural integrity and heat transfer characteristics. The tensile force which can be applied to the wrapper before it breaks can be greater than 3,000 grams force, for instance between 3,000 and 10,000 grams force or between 3,000 and 4,500 grams force.

In some examples, the wrapper 10 surrounding the aerosol generating material 3 has a high level of permeability, for example greater than about 1000 Coresta Units, or greater than about 1500 Coresta Units, or greater than about 2000 Coresta Units. The permeability of the wrapper 10 can be measured in accordance with ISO 2965:2009 concerning the determination of air permeability for materials used as cigarette papers, filter plug wrap and filter joining paper. The wrapper 10 may be formed from a material with a high inherent level of permeability, an inherently porous material, or may be formed from a material with any level of inherent permeability where the final level of permeability is achieved by providing the wrapper 10 with a permeable zone or area. Providing a permeable wrapper 10 provides a route for air to enter the article. The wrapper 10 can be provided with a permeability such that the amount of air entering through the rod of aerosol generating material is relatively more than the amount of air entering the article through the ventilation holes 12 in the mouthpiece. An article having this arrangement may produce a more flavoursome aerosol which may be more satisfactory to the user.

In the present example, the aerosol-former material added to the aerosol generating substrate 3 comprises 14% by weight of the aerosol generating substrate 3. In some embodiments, the aerosol-former material comprises at least 5% by weight of the aerosol generating substrate, or at least 10% by weight of the aerosol generating substrate. In some embodiments, the aerosol-former material comprises less than 25% by weight of the aerosol generating substrate, or less than 20%, for instance between 10% and 20%, between 12% and 18% or between 13% and 16%.

In some embodiments, the aerosol generating material 3 is provided as a cylindrical rod of aerosol generating material. Irrespective of the form of the aerosol generating material, it can have a length of about 10 mm to too mm. In some embodiments, the length of the aerosol generating material is in the range about 25 mm to 50 mm, in the range about 30 mm to 45 mm, or in the range about 30 mm to 40 mm. In some examples, the article 1 may be configured such that there is a separation (i.e. a minimum distance) between a heater of the non-combustible aerosol provision device too and the tubular body 4a. This prevents heat from the heater from damaging the material forming the tubular body 4a. The minimum distance between a heater of the non-combustible aerosol provision device too and the tubular body 4a may be 3 mm or greater. In some examples, minimum distance between the heater of the non-combustible aerosol provision device too and the tubular body 4a may be in the range 3 mm to 10 mm, for example 3 mm, 4 mm, 5 mm, 6 mm, 7 mm, 8 mm, 9 mm or 10 mm. The separation between the heater of the non-combustible aerosol provision device 100 and the tubular body 4a may be achieved by, for example, adjusting the length of the rod of aerosol generating material 3. The volume of aerosol generating material 3 provided can vary from about 200 mm31₀ about 4300 mm3, from about 500 mm3 t_{0 1}500 mm3, ₀r from about 1000 mm3 1₀ about 1300 mm³. The provision of these volumes of aerosol generating material, for instance from about 1000 mm³ to about 1300 mm³, has been advantageously shown to achieve a superior aerosol, having a greater visibility and sensory performance compared to that achieved with volumes selected from the lower end of the range.

The mass of aerosol generating material 3 provided can be greater than 200 mg, for instance from about 200 mg to 400 mg, from about 230 mg to 360 mg, or from about 250 mg to 360 mg. It has been advantageously found that providing a higher mass of aerosol generating material results in improved sensory performance compared to aerosol generated from a lower mass of tobacco material.

In some embodiments, the aerosol generating material or substrate is formed from tobacco material as described herein, which includes a tobacco component.

In the tobacco material described herein, the tobacco component may contain paper reconstituted tobacco. The tobacco component may also contain leaf tobacco, extruded tobacco, and/or bandcast tobacco. The aerosol generating material 3 can comprise reconstituted tobacco material having a density of less than about 700 milligrams per cubic centimetre (mg/cc). Such tobacco material has been found to be particularly effective at providing an aerosol generating material which can be heated quickly to release an aerosol, as compared to denser materials. For instance, the inventors tested the properties of various aerosol generating materials, such as bandcast reconstituted tobacco material and paper reconstituted tobacco material, when heated. It was found that, for each given aerosol generating material, there is a particular zero heat flow temperature below which net heat flow is endothermic, in other words more heat enters the material than leaves the material, and above which net heat flow is exothermic, in other words more heat leaves the material than enters the material, while heat is applied to the material. Materials having a density less than 700 mg/ cc had a lower zero heat flow temperature. Since a significant portion of the heat flow out of the material is via the formation of aerosol, having a lower zero heat flow temperature has a beneficial effect on the time it takes to first release aerosol from the aerosol generating material. For instance, aerosol generating materials having a density of less than 700 mg/cc were found to have a zero heat flow temperature of less than I64°C, as compared to materials with a density over 700 mg/ cc, which had zero heat flow temperatures greater than I64°C.

The density of the aerosol generating material also has an impact on the speed at which heat conducts through the material, with lower densities, for instance those below 700 mg/ cc, conducting heat more slowly through the material, and therefore enabling a more sustained release of aerosol.

The aerosol generating material 3 may comprise reconstituted tobacco material having a density of less than about 700 mg/cc, for instance paper reconstituted tobacco material. In some embodiments, the aerosol generating material 3 comprises reconstituted tobacco material having a density of less than about 600 mg/cc. Alternatively or in addition, the aerosol generating material 3 may comprise reconstituted tobacco material having a density of at least 350 mg/cc, which is considered to allow for a sufficient amount of heat conduction through the material.

The tobacco material maybe provided in the form of cut rag tobacco. The cut rag tobacco can have a cut width of at least 15 cuts per inch (about 5.9 cuts per cm, equivalent to a cut width of about 1.7mm). In some embodiments, the cut rag tobacco has a cut width of at least 18 cuts per inch (about 7.1 cuts per cm, equivalent to a cut width of about 1.4mm) or at least 20 cuts per inch (about 7.9 cuts per cm, equivalent to a cut width of about 1.27mm). In one example, the cut rag tobacco has a cut width of 22 cuts per inch (about 8.7 cuts per cm, equivalent to a cut width of about 1.15mm). The cut rag tobacco may have a cut width at or below 40 cuts per inch (about 15.7 cuts per cm, equivalent to a cut width of about 0.64mm). Cut widths between 0.5 mm and 2.0 mm, for instance between 0.6 mm and 1.5 mm, or between 0.6 mm and 1.7mm have been found to result in tobacco material which is suitable in terms of surface area to volume ratio, particularly when heated, and the overall density and pressure drop of the substrate 3. The cut rag tobacco can be formed from a mixture of forms of tobacco material, for instance a mixture of one or more of paper reconstituted tobacco, leaf tobacco, extruded tobacco and bandcast tobacco. In some embodiments, the tobacco material comprises paper reconstituted tobacco or a mixture of paper reconstituted tobacco and leaf tobacco.

In the tobacco material described herein, the tobacco material may contain a filler component. The filler component is generally a non-tobacco component, that is, a component that does not include ingredients originating from tobacco. The filler component may be a non-tobacco fibre such as wood fibre or pulp or wheat fibre. The filler component may also be an inorganic material such as chalk, perlite, vermiculite, diatomaceous earth, colloidal silica, magnesium oxide, magnesium sulphate, magnesium carbonate. The filler component may also be a non-tobacco cast material or a non-tobacco extruded material. The filler component maybe present in an amount of o to 20% by weight of the tobacco material, or in an amount of from l to io% by weight of the composition. In some embodiments, the filler component is absent. In the tobacco material described herein, the tobacco material contains an aerosol- former material. In this context, an "aerosol-former material" is an agent that promotes the generation of an aerosol. An aerosol-former material may promote the generation of an aerosol by promoting an initial vaporisation and/ or the condensation of a gas to an inhalable solid and/or liquid aerosol. In some embodiments, an aerosol-former material may improve the delivery of flavour from the aerosol generating material. In general, any suitable aerosol-former material or agents may be included in the aerosol generating material of the invention, including those described herein. Other suitable aerosol-former materials include, but are not limited to: a polyol such as sorbitol, glycerol, and glycols like propylene glycol or triethylene glycol; a non-polyol such as monohydric alcohols, high boiling point hydrocarbons, acids such as lactic acid, glycerol derivatives, esters such as diacetin, triacetin, triethylene glycol diacetate, triethyl citrate or myristates including ethyl myristate and isopropyl myristate and aliphatic carboxylic acid esters such as methyl stearate, dimethyl dodecanedioate and dimethyl tetradecanedioate. In some embodiments, the aerosol-former material may be glycerol, propylene glycol, or a mixture of glycerol and propylene glycol. Glycerol may be present in an amount of from to to 20 % by weight of the tobacco material, for example 13 to 16 % by weight of the composition, or about 14% or 15% by weight of the composition. Propylene glycol, if present, maybe present in an amount of from 0.1 to 0.3% by weight of the composition. The aerosol-former material may be included in any component, for example any tobacco component, of the tobacco material, and/ or in the filler component, if present. Alternatively or additionally the aerosol-former material may be added to the tobacco material separately. In either case, the total amount of the aerosol-former material in the tobacco material can be as defined herein.

The tobacco material can contain between 10% and 90% by weight tobacco leaf, wherein the aerosol-former material is provided in an amount of up to about 10% by weight of the leaf tobacco. To achieve an overall level of aerosol-former material between 10% and 20% by weight of the tobacco material, it has been advantageously found that this can be added in higher weight percentages to the another component of the tobacco material, such as reconstituted tobacco material.

The tobacco material described herein contains nicotine. The nicotine content is from 0.5 to 1.75% by weight of the tobacco material, and may be, for example, from 0.8 to

1.5% by weight of the tobacco material. Additionally or alternatively, the tobacco material contains between 10% and 90% by weight tobacco leaf having a nicotine content of greater than 1.5% by weight of the tobacco leaf. It has been advantageously found that using a tobacco leaf with nicotine content higher than 1.5% in combination with a lower nicotine base material, such as paper reconstituted tobacco, provides a tobacco material with an appropriate nicotine level but better sensory performance than the use of paper reconstituted tobacco alone. The tobacco leaf, for instance cut rag tobacco, can, for instance, have a nicotine content of between 1.5% and 5% by weight of the tobacco leaf.

The tobacco material described herein can contain an aerosol modifying agent, such as any of the flavours described herein. In one embodiment, the tobacco material contains menthol, forming a mentholated article. The tobacco material can comprise from 3mg to 20mg of menthol, between 5mg and i8mg or between 8mg and i6mg of menthol. In the present example, the tobacco material comprises i6mg of menthol. The tobacco material can contain between 2% and 8% by weight of menthol, between 3% and 7% by weight of menthol, or between 4% and 5.5% by weight of menthol. In one embodiment, the tobacco material includes 4.7% by weight of menthol. Such high levels of menthol loading can be achieved using a high percentage of reconstituted tobacco material, for instance greater than 50% of the tobacco material by weight. Alternatively or additionally, the use of a high volume of aerosol generating material, for instance tobacco material, can increase the level of menthol loading that can be achieved, for instance where greater than about 500 mm3₀r suitably more than about 1000 mm3 of aerosol generating material, such as tobacco material, are used. In the compositions described herein, where amounts are given in % by weight, for the avoidance of doubt this refers to a dry weight basis, unless specifically indicated to the contrary. Thus, any water that maybe present in the tobacco material, or in any component thereof, is entirely disregarded for the purposes of the determination of the weight %. The water content of the tobacco material described herein may vary and may be, for example, from 5 to 15% by weight. The water content of the tobacco material described herein may vary according to, for example, the temperature, pressure and humidity conditions at which the compositions are maintained. The water content can be determined by Karl-Fisher analysis, as known to those skilled in the art. On the other hand, for the avoidance of doubt, even when the aerosol-former material is a component that is in liquid phase, such as glycerol or propylene glycol, any component other than water is included in the weight of the tobacco material. However, when the aerosol-former material is provided in the tobacco component of the tobacco material, or in the filler component (if present) of the tobacco material, instead of or in addition to being added separately to the tobacco material, the aerosol-former material is not included in the weight of the tobacco component or filler component, but is included in the weight of the "aerosol-former material" in the weight % as defined herein. All other ingredients present in the tobacco component are included in the weight of the tobacco component, even if of non-tobacco origin (for example non tobacco fibres in the case of paper reconstituted tobacco).

In an embodiment, the tobacco material comprises the tobacco component as defined herein and the aerosol-former material as defined herein. In an embodiment, the tobacco material consists essentially of the tobacco component as defined herein and the aerosol-former material as defined herein. In an embodiment, the tobacco material consists of the tobacco component as defined herein and the aerosol-former material as defined herein.

Paper reconstituted tobacco is present in the tobacco component of the tobacco material described herein in an amount of from 10% to 100% by weight of the tobacco component. In embodiments, the paper reconstituted tobacco is present in an amount of from 10% to 80% by weight, or 20% to 70% by weight, of the tobacco component. In a further embodiment, the tobacco component consists essentially of, or consists of, paper reconstituted tobacco. In some embodiments, leaf tobacco is present in the tobacco component of the tobacco material in an amount of from at least 10% by weight of the tobacco component. For instance, leaf tobacco can be present in an amount of at least 10% by weight of the tobacco component, while the remainder of the tobacco component comprises paper reconstituted tobacco, bandcast reconstituted tobacco, or a combination of bandcast reconstituted tobacco and another form of tobacco such as tobacco granules. Paper reconstituted tobacco refers to tobacco material formed by a process in which tobacco feedstock is extracted with a solvent to afford an extract of solubles and a residue comprising fibrous material, and then the extract (usually after concentration, and optionally after further processing) is recombined with fibrous material from the residue (usually after refining of the fibrous material, and optionally with the addition of a portion of non-tobacco fibres) by deposition of the extract onto the fibrous material. The process of recombination resembles the process for making paper.

The paper reconstituted tobacco may be any type of paper reconstituted tobacco that is known in the art. In a particular embodiment, the paper reconstituted tobacco is made from a feedstock comprising one or more of tobacco strips, tobacco stems, and whole leaf tobacco. In a further embodiment, the paper reconstituted tobacco is made from a feedstock consisting of tobacco strips and/or whole leaf tobacco, and tobacco stems. However, in other embodiments, scraps, fines and winnowings can alternatively or additionally be employed in the feedstock.

The paper reconstituted tobacco for use in the tobacco material described herein may be prepared by methods which are known to those skilled in the art for preparing paper reconstituted tobacco. In some embodiments, it can be particularly advantageous to use a hollow tubular element 8 having a length of greater than about to mm, for instance between about to mm and about 30 mm or between about 12 mm and about 25 mm. It has been found that a consumer’s lips are likely to extend in some cases to about 12 mm from the mouth end of the article 1 when drawing aerosol through the article 1, and therefore a hollow tubular element 8 having a length of at least 10 mm or at least 12 mm means that most of the consumer’s lips surround this element 8. Figure 3 is a side-on cross sectional view of a further article 1’, including mouthpiece 2’ including a hollow tubular element 8. Mouthpiece 2’ is substantially the same as mouthpiece 2 described above in relation to Figure 1, except that at the downstream end 2b, the mouthpiece 2’ includes a hollow tubular element 8 formed from filamentary tow. In the present example, the tubular portion 4a, the body of material 6 and the hollow tubular element 8 are combined using the second plug wrap 9 which is wrapped around all three sections. The body of material 6 of the article 1’ of Figure 3 is similar to the body of material 6 described above in relation to Figures 1 and 2. As before, the body of material 6 is manufactured from a sheet material comprising cellulose, for example, the sheet material maybe paper. The sheet material is gathered to form the body of material 6. In the present example, the axial length Li of the body of material 6 is about 10 mm. However, a skilled person will recognise that the body of material 6 may have a different axial length Li. In some embodiments, the length Li of the body of material 6 is less than about 20 mm or less than 15 mm. In some embodiments, the length Li of the body of material 6 is less than about 10 mm. In addition, or as an alternative, the length Li of the body of material 6 may be at least about 5 mm. In some embodiments, the length Li of the body of material 6 is at least about 6 mm. In some embodiments, the length Li of the body of material 6 is from about 5 mm to about 15 mm, from about 6 mm to about 12 mm. In some embodiments, the length Li of the body of material is 6 mm, 7 mm, 8 mm, 9 mm or 10 mm.

The part of the mouthpiece which comes into contact with a consumer’s lips has usually been a paper tube, which is either hollow or surrounds a cylindrical body of filter material. Providing a hollow tubular element 8 has advantageously been found to significantly reduce the temperature of the outer surface of the mouthpiece 2’ at the downstream end 2b of the mouthpiece which comes into contact with a consumer’s mouth when the article 1’ is in use. In addition, the use of the tubular portion 4a has also been found to significantly reduce the temperature of the outer surface of the mouthpiece 2’ even upstream of the tubular portion 4a. Without wishing to be bound by theory, it is hypothesised that this is due to the tubular portion 4a channelling aerosol closer to the centre of the mouthpiece 2’, and therefore reducing the transfer of heat from the aerosol to the outer surface of the mouthpiece 2’. In addition, the body of material 6 has been found to remove moisture from aerosol generated by the aerosol generating material 3 as the aerosol passes through the body of material 6A of the mouthpiece 2, which makes the aerosol feel cooler in the user’s mouth. In the present example, the hollow tubular element 8 is formed from filamentary tow.

In alternative embodiments, the hollow tubular element may be formed using any construction as described herein for the tubular portion 4a.

The "wall thickness" of the hollow tubular element 8 corresponds to the thickness of the wall of the tube 8 in a radial direction. This may be measured in the same way as that of the tubular portion. The wall thickness is advantageously greater than 0.9 mm, and maybe 1.0 mm or greater. In some embodiments, the wall thickness is substantially constant around the entire wall of the hollow tubular element 8. However, where the wall thickness is not substantially constant, the wall thickness may be greater than 0.9 mm at any point around the hollow tubular element 8, for instance 1.0mm or greater.

The length of the hollow tubular element 8 is less than about 20 mm. In some embodiments, the length of the hollow tubular element 8 is less than about 15 mm. In some embodiments, the length of the hollow tubular element 8 is less than about 10 mm. In addition, or as an alternative, the length of the hollow tubular element 8 may be at least about 5 mm. In some embodiments, the length of the hollow tubular element 8 is at least about 6 mm. In some embodiments, the length of the hollow tubular element 8 is from about 5 mm to about 20 mm, from about 6 mm to about 10 mm, or from about 6 mm to about 8 mm. In some embodiments, the length of the hollow tubular element 8 is 6 mm, 7 mm or 8 mm. In the present example, the length of the hollow tubular element 8 is 6 mm.

The density of the hollow tubular element 8 is at least about 0.25 grams per cubic centimetre (g/cc), for instance at least about 0.3 g/cc. In some embodiments, the density of the hollow tubular element 8 is less than about 0.75 grams per cubic centimetre (g/cc), for instance less than 0.6 g/cc. In some embodiments, the density of the hollow tubular element 8 is between 0.25 g/cc and 0.75 g/cc, between 0.3 g/cc and 0.6 g/cc, or between 0.4 g/cc and 0.6 g/cc. In some embodiments, the density of the hollow tubular element 8 is about 0.5 g/ cc. These densities have been found to provide a good balance between improved firmness afforded by denser material and the lower heat transfer properties of lower density material. For the purposes of the present invention, the "density" of the hollow tubular element 8 refers to the density of the filamentary tow forming the element with any plasticiser incorporated. The density may be determined by dividing the total weight of the hollow tubular element 8 by the total volume of the hollow tubular element 8, wherein the total volume can be calculated using appropriate measurements of the hollow tubular element 8 taken, for example, using callipers. Where necessary, the appropriate dimensions maybe measured using a microscope.

The filamentary tow forming the hollow tubular element 8 may have a total denier of less than 45,000, for instance less than 42,000. This total denier has been found to allow the formation of a hollow tubular element 8 which is not too dense. In some embodiments, the total denier is at least 20,000, for instance at least 25,000. In some embodiments, the filamentary tow forming the hollow tubular element 8 has a total denier between 25,000 and 45,000, for instance between 35,000 and 45,000. In some embodiments, the cross-sectional shapes of the filaments of tow are Ύ shaped, although in other embodiments other cross-sectional shapes such as ‘X’ shaped filaments can be used.

The filamentary tow forming the hollow tubular element 8 may have a denier per filament of greater than 3. This denier per filament has been found to allow the formation of a hollow tubular element 8 which is not too dense. In some embodiments, the denier per filament is at least 4, for instance at least 5. In some embodiments, the filamentary tow forming the hollow tubular element 8 has a denier per filament between 4 and 10, for instance between 4 and 9. In one example, the filamentary tow forming the hollow tubular element 8 has an 8Y40,ooo tow formed from cellulose acetate and comprising 18% plasticiser, for instance triacetin.

The hollow tubular element 8 may have an internal diameter of greater than 3.0 mm. Smaller diameters than this can result in increasing the velocity of aerosol passing though the mouthpiece 2’ to the consumers mouth more than is desirable, such that the aerosol becomes too warm, for instance reaching temperatures greater than 40°C or greater than 45°C. In some embodiments, the hollow tubular element 8 has an internal diameter of greater than 3.1 mm, for instance greater than 3.5 mm or 3.6 mm. In one embodiment, the internal diameter of the hollow tubular element 8 is about 3.9 mm.

In some embodiments, the hollow tubular element 8 comprises from 15% to 22% by weight of plasticiser. For cellulose acetate tow, the plasticiser may be triacetin, although other plasticisers such as polyethelyne glycol (PEG) can be used. In some embodiments, the hollow tubular element 8 comprises from 16% to 20% by weight of plasticiser, for instance about 17%, about 18% or about 19% plasticiser.

In the present example, the tubular portion 4a is a first hollow tubular element, and hollow tubular element 8 is a second hollow tubular element.

In the present example, the ventilation is provided into tubular portion 4a, as described in relation to Figure 1. In alternative embodiments, the ventilation can be provided into the mouthpiece at other locations, for instance into the body of material 6 or hollow tubular element 8.

In the examples described above, the mouthpieces 2, 2’ each comprise a single body of material 6. In other examples, the mouthpiece 2, 2’ may include multiple bodies of material. The mouthpieces 2, 2’ may comprise a cavity between the bodies of material.

In some examples, the mouthpiece 2, 2’ downstream of the aerosol generating material 3 can comprise a wrapper, for instance the first or second plug wraps 7, 9, or tipping paper 5, which comprises an aerosol modifying agent as described herein or other sensate material. The aerosol modifying agent maybe disposed on an inwardly or outwardly facing surface of the mouthpiece wrapper. For instance, the aerosol modifying agent or other sensate material may be provided on an area of the wrapper, such as an outwardly facing surface of the tipping paper 5, which comes into contact with the consumer’s lips during use. By disposing the aerosol modifying agent or other sensate material on the outwardly facing surface of the mouthpiece wrapper, the aerosol modifying agent or other sensate material may be transferred to the consumer’s lips during use. Transfer of the aerosol modifying agent or other sensate material to the consumer’s lips during use of the article may modify the organoleptic properties (e.g. taste) of the aerosol generated by the aerosol generating substrate 3 or otherwise provide the consumer with an alternative sensory experience. For example, the aerosol modifying agent or other sensate material may impart flavour to the aerosol generated by the aerosol generating substrate 3. The aerosol modifying agent or other sensate material maybe at least partially soluble in water such that it is transferred to the user via the consumer’s saliva. The aerosol modifying agent or other sensate material may be one that volatilises by the heat generated by the aerosol provision system. This may facilitate transfer of the aerosol modifying agent to the aerosol generated by the aerosol generating substrate 3. A suitable sensate material may be a flavour as described herein, sucralose or a cooling agent such as menthol or similar. In some embodiments (not shown), the mouthpiece 2, 2’ may comprise an aerosol modifying agent release component, that is operable to release the aerosol-modifying agent. In some embodiments, the aerosol-modifying agent release component may be operable to selectively release the aerosol-modifying agent. As discussed above, the body of material 6 can comprise fibres having a length in the range 2 mm to 6 mm, which leads to the body of material 6 absorbing less of a certain aerosol-modifying agent when the aerosol-modifying agent is released from the aerosol-modifying agent release component.

The aerosol-modifying agent may, for example, be an additive or a sorbent. The aerosol-modifying agent may, for example, comprise one or more of a flavourant, a colourant, water, and a carbon adsorbent. The aerosol-modifying agent may, for example, be a solid, a liquid, or a gel. The aerosol-modifying agent maybe in powder, thread or granule form. The aerosol-modifying agent may be free from filtration material.

The aerosol-modifying agent release component maybe, for example, a capsule, thread or bead. In some embodiments, a plurality of aerosol-modifying agent release components are provided, and may comprise a plurality of charcoal particles loaded with aerosol-modifying agent.

In some embodiments, the aerosol-modifying agent release component comprises a thread loaded with additive. The thread may made from fibres of, for example, cellulose acetate or cotton. In some embodiments, the aerosol-modifying release component has in the range of 1 mg to 20 mg of aerosol-modifying agent, for instance in the range of 2 mg to I5mg of aerosol-modifying agent.

The aerosol-modifying agent release component, for example, a capsule, may be located in the body 6. The (or each) aerosol-modifying agent release component may be combined with the sheet material 6A, for instance, being adhered thereto, before the sheet material 6A is formed into the body 6.

In some embodiments, a non-combustible aerosol provision system is provided comprising an aerosol-modifying agent release component and a heater which, in use, is operable to heat the aerosol generating material 3 such that the aerosol generating material 3 provides an aerosol.

The aerosol-modifying agent release component may comprise a capsule. In some embodiments, the aerosol-modifying agent release component comprises first and second capsules. The first capsule is disposed in a first portion of the aerosol-modifying agent release component and the second capsule is disposed in a second portion of the aerosol-modifying agent release component downstream of the first portion. The first portion of the aerosol-modifying agent release component is heated to a first temperature during operation of the heater to generate the aerosol and the second portion is heated to a second temperature during operation of the heater to generate aerosol, wherein the second temperature is at least 4 degrees Celsius lower than the first temperature. In some embodiments, the second temperature is at least 5, 6, 7, 8, 9 or 10 degrees Celsius lower than the first temperature.

The aerosol-modifying agent release component may comprise one or more components of the article 1. In some embodiments, the first and second capsules are disposed in the body of material 6. In one embodiment, the aerosol-modifying agent release component comprises two bodies of material (not shown), wherein the first and second capsules are disposed in the first and second bodies respectively. In some embodiments, the aerosol-modifying agent release component alternatively or additionally comprises one or more tubular elements upstream and/or downstream of the body or bodies of material. The aerosol generating component may comprise the mouthpiece 2, 2’.

In some embodiments, the second capsule is spaced from the first capsule by a distance of at least 7 mm, measured as the distance between the centre of the first and second capsules. In some embodiments, the second capsule is spaced from the first capsule by a distance of at least 8 mm, 9 mm or 10 mm. It has been found that increasing the distance between the first and second capsules increases the difference between the first and second temperatures.

The first capsule comprises an aerosol modifying agent. The second capsule comprises an aerosol modifying agent which may be the same or different as the aerosol modifying agent of the first capsule. In some embodiments, a user may selectively rupture the first and second capsules by applying an external force to the aerosol modifying agent release component in order to release the aerosol modifying agent from each capsule.

The aerosol-modifying agent of the second capsule is heated to a lower temperature than the aerosol-modifying agent of the first capsule due to the difference between the first and second temperatures. The aerosol-modifying agents of the first and second capsules can be selected based on this temperature difference. For instance, the first capsule may comprise a first aerosol modifying agent that has a lower vapour pressure than a second aerosol modifying agent of the second capsule. If the capsules were both heated to the same temperature, then the higher vapour pressure of the aerosol modifying agent of the second capsule would mean that a greater amount of the second aerosol modifying agent would be volatised relative to the aerosol modifying agent of the first capsule. However, since the second capsule is heated to a lower temperature, this effect is less pronounced such that a more even amount of the aerosol modifying agents of the first and second capsules are volatised upon breaking of the first and second capsules respectively.

In some embodiments, the first and second capsules have the same aerosol-modifying profiles, meaning that both capsules contain the same type of aerosol-modifying agent and in the same amount such that if both capsules were heated to the same temperature and broken then both capsules would cause the same modification of the aerosol. However, since the first capsule is heated to a higher temperature than the second capsule, more of the aerosol-modifying agent of the first capsule will be, for example, volatised compared to the modifying agent of the second capsule and thus will cause a more pronounced modification of the aerosol than the second capsule. Therefore, despite both capsules being the same, which may make the aerosol- modifying agent release component easier and/or less expensive to manufacture, the user can decide whether to break the first capsule to cause a more pronounced modification of the aerosol, or the second capsule to cause a less pronounced modification of the aerosol, or both capsules to cause the greatest modification of the aerosol. In some embodiments, the first and second capsules both comprise first and second aerosol modifying agents. The first aerosol modifying agent has a lower vapour pressure than the second aerosol modifying agent. Thus, when the second capsule is broken, a greater proportion of the second aerosol modifying agent will be vaporised relative to the first aerosol modifying agent in comparison to when the hotter first capsule is broken during use of the system to generate aerosol. Therefore, the same capsule can be used to generate different modifications of the aerosol based on the positon of the capsule in the first or second portion of the aerosol-modifying agent release component. In some embodiments, the (or each) capsule comprises an outer shell and an inner core.

The shell of each capsule may be solid at room temperature. The shell may comprise, consist of, or essentially consist of, alginate. However, it should be recognised that in alternative embodiments the shell is formed from a different material. For example, the shell may alternatively comprise, consist of, or essentially consist of, gelatin, carageenans or pectins. The shell may comprise, consist of, or essentially consist of, one or more of alginate, gelatin, carrageenans or pectins. The shell of each additive capsule may be impermeable, or substantially impermeable, to the aerosol modifying agent agent of the core. Therefore, the shell initially prevents the agent of the core from escaping from the capsule. When the user desires to modify the aerosol, the shells of the capsules are ruptured such that the agent is released. In some embodiments (not shown), the (or each) capsule further comprises a carrier material. The carrier material may comprise, for example, gelatin.

In some embodiments, the (or each) capsule has a diameter in the range of 1 mm to 5 mm, or in the range of 2 mm to 4 mm. In some embodiments, the diameter of the (or each) capsule is about 3 mm. The (or each) capsule may be generally spherical. In other examples, other shapes and sizes of capsule can be used. The total weight of each capsule may be in the range about 5 mg to about 50 mg, or in the range of about 10 mg to about 30 mg. In some embodiments, each capsule has a weight of about 14 mg.

In some embodiments, one or more aerosol-modifying agent release components are included in the body of material 6, wherein the body of material 6 is formed from a sheet material having a basis weight of less than 40 gsm, for instance less than 35 or 30 gsm. This helps to reduce the density of the body of material 6 to compensate for the presence of the aerosol-modifying agent release component within the body 6 which may otherwise result in an increase in the firmness of the body 6.

In some embodiments, one or more aerosol-modifying agent release components are included in the body of material 6, wherein the body of material 6 is formed from a sheet material having width of less than 100 mm for instance less than 90 mm or 80 mm. This helps to reduce the density of the body of material 6 to compensate for the presence of the aerosol-modifying agent release component within the body 6 which may otherwise result in an increase in the firmness of the body 6. In some embodiments, the (or each) capsule is centred on the longitudinal axis of the mouthpiece 2.

As discussed above, the (or each) capsule may have a core-shell structure. That is, the encapsulating material or barrier material creates a shell around a core that comprises the aerosol modifying agent. The shell structure hinders migration of the aerosol modifying agent during storage of the article but allows controlled release of the aerosol modifying agent, also referred to as an aerosol modifier, during use.

In some cases, the barrier material (also referred to herein as the encapsulating material) is frangible. The (or each) capsule is crushed or otherwise fractured or broken by the user to release the encapsulated aerosol modifier. Typically, one or more of the capsules is broken immediately prior to heating being initiated but the user can select when to release the aerosol modifier of said capsule. The user can then choose to break the other capsules a later time, for example, after heating being initiated. The user may choose to break said other one of the capsules once some of the aerosol has been released from the aerosol generating material, such that the remaining aerosol generating material is modified by the aerosol modifying agent of another of the capsules. Alternatively, the user may choose to break a plurality of capsules simultaneously. The term "breakable capsule" refers to a capsule, wherein the shell can be broken by means of a pressure to release the core; more specifically the shell can be ruptured under the pressure imposed by the user's fingers when the user wants to release the core of the capsule. In some cases, the barrier material is heat resistant. That is to say, in some cases, the barrier will not rupture, melt or otherwise fail at the temperature reached at the capsule site during operation of the aerosol provision device. Illustratively, a capsule located in a mouthpiece maybe exposed to temperatures in the range of 30°C to ioo°C for example, and the barrier material may continue to retain the liquid core up to at least about 50°C to 120°C.

In other cases, the (or each) capsule releases the core composition on heating, for example by melting of the barrier material or by capsule swelling leading to rupture of the barrier material.

The total weight of each capsule may be in the range of about 1 mg to about too mg, about 5 mg to about 60 mg, about 8 mg to about 50 mg, about 10 mg to about 20 mg, or about 12 mg to about 18 mg. The total weight of the core formulation may be in the range of about 2 mg to about 90 mg, about 3 mg to about 70 mg, about 5 mg to about 25 mg, about 8 mg to about 20 mg, or about 10 mg to about 15 mg.

In some embodiments, the (or each) capsule comprises a core as described above, and a shell. The capsules may each present a crush strength from about 4.5 N to about 40 N, from about 5 N to about 30 N or from about 5 N to about 28 N (for instance about 9.8 N to about 24.5 N). The capsule burst strength of each capsule can be measured when said capsule is removed from the body of material 6 and using a force gauge to measure the force at which the capsule bursts when pressed between two flat metal plates. A suitable measurement device is the Sauter FK 50 force gauge with a flat headed attachment, which can be used to crush the capsule against a flat, hard surface having a surface similar to the attachment.

The (or each) capsule may be substantially spherical and have a diameter of at least about 0.4 mm, 0.6 mm, 0.8 mm, 1.0 mm, 2.0 mm, 2.5 mm, 2.8 mm or 3.0 mm. The diameter of the (or each) capsule maybe less than about 10.0 mm, 8.0 mm, 7.0 mm,

6.0 mm, 5.5 mm, 5.0 mm, 4.5 mm, 4.0 mm, 3.5 mm or 3.2 mm. Illustratively, the capsule diameter maybe in the range of about 0.4 mm to about 10.0 mm, about 0.8 mm to about 6.0 mm, about 2.5 mm to about 5.5 mm or about 2.8 mm to about 3.2 mm. In some cases, the (or each) capsule may have a diameter of about 3.0 mm. These sizes are particularly suitable for incorporation of the capsules into an article as described herein.

The cross-sectional area of each capsule at its largest cross sectional area is in some embodiments less than 28% of the cross sectional area of the portion of the mouthpiece 2 in which the capsule is provided, for instance less than 27% or less than 25%. For instance, for a spherical capsule having a diameter of 3.0 mm, the largest cross sectional area of the capsule is 7.07 mm². For the mouthpiece having a circumference of 21 mm as described herein, the body of material 6 has an outer circumference of 20.8 mm, and the radius of this component will be 3.31 mm, corresponding to a cross sectional area of 34.43 mm². The capsule cross sectional area is, in this example, 20.5% of the cross-sectional area of the mouthpiece 2. As another example, if a capsule had a diameter of 3.2mm, its largest cross sectional area would be 8.04 mm². In this case, the cross sectional area of the capsule would be 23.4% of the cross sectional area of the body of material 6. A capsule with a largest cross sectional area less than 28% of the cross sectional area of the portion of the mouthpiece 2 in which the capsule is provided has the advantage that the pressure drop across the mouthpiece 2 is reduced as compared to capsules with larger cross sectional areas and adequate space remains around the capsule for aerosol to pass without the body of material 6 removing significant amounts of the aerosol mass as it passes through the mouthpiece 2. In some embodiments, first and second capsules are provided, which may be the same size or different sizes.

Figure 4 is a side-on cross sectional view of a further article 1”, including mouthpiece 2”. Mouthpiece 2” is substantially the same as mouthpiece 2 described above in relation to Figures 1 and 2. A difference is that the body of material 6 of the article 1” is located upstream of the tubular portion 4a.

In the present example the tubular portion 4a and body of material 6 are combined using the second plug wrap 9 which is wrapped around both sections.

The body of material 6 of the article 1” of Figure 4 is similar to the body of material 6 described above in relation to Figures 1 to 3. As before, the body of material 6 is manufactured from a sheet material comprising cellulose, for example, the sheet material may be paper. The sheet material is gathered to form the body of material 6.

The body of material 6 is disposed at the upstream end 2a of the mouthpiece 2’. The body of material 6 is adjacent to the aerosol generating material 3. The tubular portion 4a is disposed at the downstream end 2b of the mouthpiece 2” and thus forms a cavity at the downstream end 2b. The tubular portion 4a is located downstream of the body of material 6. In the present example, the tubular portion 4a is immediately adjacent to the body of material 6. The tubular portion 4a has an axial length L2 of at least 20 mm, for instance at least 22 mm. In the present example, the axial length L2 of the tubular portion 4a is about 25 mm.

It has been found that the tube having an axial length L2 of at least 20 mm results in significant cooling of the aerosol as it passes through the tubular portion 4a. In addition, as explained previously, the cellulose containing sheet material of the body of material 6 absorbs water from the aerosol. Removing moisture from the aerosol makes the aerosol feel cooler in the user’s mouth. In some embodiments, the tubular portion 4a comprises one or more ventilation holes, which also contribute to cooling of the aerosol.

In some embodiments, the tubular portion 4a is manufactured from paper. Figure 5 is a side-on cross sectional view of a further article T”, including mouthpiece 2’”. The mouthpiece 2’” is substantially the same as mouthpiece 2 described above in relation to Figures 1 and 2. A difference is that that the mouthpiece 2’” further comprises a tubular element 20 located within the body of material 6.

In the present example, the tubular portion 4a and body of material 6 are combined using the second plug wrap 9 which is wrapped around both sections.

The body of material 6 of the article T” of Figure 5 is similar to the body of material 6 described above in relation to Figures 1 to 3. As before, the body of material 6 is manufactured from a sheet material comprising cellulose, for example, the sheet material may be paper. The sheet material is gathered to form the body of material 6.

The tubular element 20 maybe, for example, a paper or plastic tube disposed within the body of material 6. The tubular element 20 forms a cavity 21 within the body of material 6. Optionally, the tubular element 20 is located substantially radially centrally within the body of material 6.

In the present example, the cavity 21 extends to the downstream end 2b of the mouthpiece 2’”. In the present example, the axial length Li of the body of material 6 is about 10 mm. However, a skilled person will recognise that the body of material 6 may have a different axial length Li. In some embodiments, the length Li of the body of material 6 is less than about 15 mm. In some embodiments, the length Li of the body of material 6 is less than about 10 mm. In addition, or as an alternative, the length Li of the body of material 6 may be at least about 5 mm. In some embodiments, the length Li of the body of material 6 is at least about 6 mm. In some embodiments, the length Li of the body of material 6 is from about 5 mm to about 15 mm, from about 6 mm to about 12 mm, or from about 6 mm to about 12 mm. In some embodiments, the length Li of the body of material 6 is 6 mm, 7 mm, 8 mm, 9 mm or 10 mm.

In some embodiments, the tubular element 20 has an axial length L3 of at least 4 mm, for instance a length of about 5 mm.

The cavity 21 has been found to promote cooling of the aerosol. The portion 6b of the body of material 6 that surrounds the tubular element 21 has been found to effectively thermally insulate the user’s lips from the heat of the aerosol. For example, in embodiments wherein the body of material 6 is manufactured from a sheet material that is arranged into the body of material, it is thought that the multiple layers of the sheet material of the body of material 6 help to insulate the user’s lips from the heat of the aerosol. In some embodiments, there may optionally be gaps, for example, air gaps, between the layers of the sheet material that contribute to the insulating effect.

Also, the body of material 6 may be more readily biodegradable than configurations where instead a cellulose acetate tubular portion is provided at the downstream end 2b of the mouthpiece.

The body of material 6 may be manufactured from a multiple length rod 22, as shown in Figure 6, which in the present example is a four-length rod. The rod is cut at lines C- C to form individual bodies of material 6 each comprising a tubular element 20 with a corresponding cavity 21.

A non-combustible aerosol provision device is used to heat the aerosol generating material 3 of any of the articles 1, 1’, 1”, 1’” described herein. The non-combustible aerosol provision device may comprise a coil, which has been found to enable improved heat transfer to the article 1, 1’, 1”, 1’” as compared to other arrangements.

In some examples, the coil is configured to, in use, cause heating of at least one electrically-conductive heating element, so that heat energy is conductible from the at least one electrically-conductive heating element to the aerosol generating material to thereby cause heating of the aerosol generating material.

In some examples, the coil is configured to generate, in use, a varying magnetic field for penetrating at least one heating element, to thereby cause induction heating and/ or magnetic hysteresis heating of the at least one heating element. In such an arrangement, the or each heating element may be termed a “susceptor” as defined herein. A coil that is configured to generate, in use, a varying magnetic field for penetrating at least one electrically-conductive heating element, to thereby cause induction heating of the at least one electrically-conductive heating element, may be termed an “induction coil” or “inductor coil”. The device may include the heating element(s), for example electrically-conductive heating element(s), and the heating element(s) may be suitably located or locatable relative to the coil to enable such heating of the heating element(s). The heating element(s) may be in a fixed position relative to the coil. Alternatively, the at least one heating element, for example at least one electrically-conductive heating element, may be included in the article 1, i’, 1”, l’” for insertion into a heating zone of the device, wherein the article 1, i’, 1”, i’” also comprises the aerosol generating material 3 and is removable from the heating zone after use. Alternatively, both the device and such an article 1, 1’, 1”, 1’” may comprise at least one respective heating element, for example at least one electrically-conductive heating element, and the coil may be to cause heating of the heating element(s) of each of the device and the article when the article is in the heating zone.

In some examples, the coil is helical. In some examples, the coil encircles at least a part of a heating zone of the device that is configured to receive aerosol generating material. In some examples, the coil is a helical coil that encircles at least a part of the heating zone.

In some examples, the device comprises an electrically-conductive heating element that at least partially surrounds the heating zone, and the coil is a helical coil that encircles at least a part of the electrically-conductive heating element. In some examples, the electrically-conductive heating element is tubular. In some examples, the coil is an inductor coil.

In some examples, the use of a coil enables the non-combustible aerosol provision device to reach operational temperature more quickly than a non-coil aerosol provision device. For instance, the non-combustible aerosol provision device including a coil as described above can reach an operational temperature such that a first puff can be provided in less than 30 seconds from initiation of a device heating program, more preferably in less than 25 seconds. In some examples, the device can reach an operational temperature in about 20 seconds from the initiation of a device heating program.

The use of a coil as described herein in the device to cause heating of the aerosol generating material has been found to enhance the aerosol which is produced. For instance, consumers have reported that the aerosol generated by a device including a coil such as that described herein is sensorially closer to that generated in factory made cigarette (FMC) products than the aerosol produced by other non-combustible aerosol provision systems. Without wishing to be bound by theory, it is hypothesised that this is the result of the reduced time to reach the required heating temperature when the coil is used, the higher heating temperatures achievable when the coil is used and/or the fact that the coil enables such systems to simultaneously heat a relatively large volume of aerosol generating material, resulting in aerosol temperatures resembling FMC aerosol temperatures. In FMC products, the burning coal generates a hot aerosol which heats tobacco in the tobacco rod behind the coal, as the aerosol is drawn through the rod. This hot aerosol is understood to release flavour compounds from tobacco in the rod behind the burning coal. A device including a coil as described herein is thought to also be capable of heating aerosol generating material, such as tobacco material described herein, to release flavour compounds, resulting in an aerosol which has been reported to more closely resemble an FMC aerosol. Particular improvements in aerosol can be achieved through the use of a device including a coil to heat an article comprising a rod of aerosol generating material having a circumference greater than 19mm, for instance a circumference between about 19 mm and about 23 mm.

Using an aerosol provision system including a coil as described herein, for instance an induction coil which heats at least some of the aerosol generating material to at least 200°C, more preferably at least 220°C, can enable the generation of an aerosol from an aerosol generating material that has particular characteristics which are thought to more closely resemble those of an FMC product. For example, when heating an aerosol generating material, including nicotine, using an induction heater, heated to at least 250°C, for a two-second period, under an airflow of at least i.50L/m during the period, one or more of the following characteristics has been observed: at least 10 pg of nicotine is aerosolised from the aerosol generating material; the weight ratio in the generated aerosol, of aerosol-former material to nicotine is at least about 2.5:1, suitably at least 8.5:1; at least 100 pg of the aerosol-former material can be aerosolised from the aerosol generating material; the mean particle or droplet size in the generated aerosol is less than about

1000 nm; and the aerosol density is at least 0.1 pg/cc.

In some cases, at least 10 pg of nicotine, suitably at least 30 pg or 40 pg of nicotine, is aerosolised from the aerosol generating material under an airflow of at least i.50L/m during the period. In some cases, less than about 200 pg, suitably less than about 150 pg or less than about 125 pg, of nicotine is aerosolised from the aerosol generating material under an airflow of at least i.50L/m during the period.

In some cases, the aerosol contains at least 100 pg of the aerosol-former material, suitably at least 200 pg, 500 pg or 1 mg of aerosol-former material is aerosolised from the aerosol generating material under an airflow of at least i.50L/m during the period. Suitably, the aerosol-former material may comprise or consist of glycerol.

As defined herein, the term “mean particle or droplet size” refers to the mean size of the solid or liquid components of an aerosol (i.e. the components suspended in a gas). Where the aerosol contains suspended liquid droplets and suspended solid particles, the term refers to the mean size of all components together.

In some cases, the mean particle or droplet size in the generated aerosol may be less than about 900 nm, 800 nm, 700, nm 600 nm, 500nm, 450nm or 400 nm. In some cases, the mean particle or droplet size maybe more than about 25 nm, 50 nm or loonm.

In some cases, the aerosol density generated during the period is at least 0.1 pg/cc. In some cases, the aerosol density is at least 0.2 pg/cc, 0.3 pg/cc or 0.4 pg/cc. In some cases, the aerosol density is less than about 2.5 pg/cc, 2.0 pg/cc, 1.5 pg/cc or 1.0 pg/cc.

The non-combustible aerosol provision device may be arranged to heat the aerosol generating material 3 of the article 1, 1’, 1”, 1’”, to a maximum temperature of at least i6o°C. In some embodiments, the non-combustible aerosol provision device is arranged to heat the aerosol-former material 3 of the article 1, 1’, 1”, 1’”, to a maximum temperature of at least about 200°C, or at least about 220°C, at least about 240°C, or at least about 270°C, at least once during the heating process followed by the non combustible aerosol provision device.

Using an aerosol provision system including a coil as described herein, for instance an induction coil which heats at least some of the aerosol generating material to at least 200°C, or at least 220°C. In some embodiments, the temperature of the aerosol leaving the mouth end of the mouthpiece 2, 2’, 2”, 2’” is less than 50 degrees Celsius and, for instance less than 45 degrees Celsius.

Figure 7 shows an example of a non-combustible aerosol provision device 100 for generating aerosol from an aerosol generating medium/material such as the aerosol generating material 3 of any of the articles 1, T, 1”, 1’” described herein. In broad outline, the device 100 may be used to heat a replaceable article 110 comprising the aerosol generating medium, for instance the articles 1, 1’, 1”, 1’” described herein, to generate an aerosol or other inhalable medium which is inhaled by a user of the device 100. The device 100 and replaceable article 110 together form a system.

The device 100 comprises a housing 102 (in the form of an outer cover) which surrounds and houses various components of the device 100. The device 100 has an opening 104 in one end, through which the article 110 maybe inserted for heating by a heating assembly. In use, the article 110 may be fully or partially inserted into the heating assembly where it may be heated by one or more components of the heater assembly.

When the article 110 is inserted into the device too, the minimum distance between the one or more components of the heater assembly and a tubular body 4a of the article 110 may be in the range 3 mm to 10 mm, for example 3 mm, 4 mm, 5 mm, 6 mm, 7 mm, 8 mm, 9 mm or 10 mm.

The device too of this example comprises a first end member 106 which comprises a lid 108 which is moveable relative to the first end member 106 to close the opening 104 when no article 110 is in place. In Figure 8, the lid 108 is shown in an open configuration, however the lid 108 may move into a closed configuration. For example, a user may cause the lid 108 to slide in the direction of arrow “B”.

The device too may also include a user-operable control element 112, such as a button or switch, which operates the device too when pressed. For example, a user may turn on the device too by operating the switch 112.

The device too may also comprise an electrical component, such as a socket/port 114, which can receive a cable to charge a battery of the device too. For example, the socket 114 may be a charging port, such as a USB charging port. Figure 8 depicts the device 100 of Figure 7 with the outer cover 102 removed and without an article 110 present. The device 100 defines a longitudinal axis 134.

As shown in Figure 8, the first end member 106 is arranged at one end of the device 100 and a second end member 116 is arranged at an opposite end of the device 100. The first and second end members 106, 116 together at least partially define end surfaces of the device 100. For example, the bottom surface of the second end member 116 at least partially defines a bottom surface of the device 100. Edges of the outer cover 102 may also define a portion of the end surfaces. In this example, the lid 108 also defines a portion of a top surface of the device 100.

The end of the device closest to the opening 104 may be known as the proximal end (or mouth end) of the device 100 because, in use, it is closest to the mouth of the user. In use, a user inserts an article 110 into the opening 104, operates the user control 112 to begin heating the aerosol generating material and draws on the aerosol generated in the device. This causes the aerosol to flow through the device too along a flow path towards the proximal end of the device too.

The other end of the device furthest away from the opening 104 may be known as the distal end of the device too because, in use, it is the end furthest away from the mouth of the user. As a user draws on the aerosol generated in the device, the aerosol flows away from the distal end of the device too.

The device too further comprises a power source 118. The power source 118 maybe, for example, a battery, such as a rechargeable battery or a non-rechargeable battery. Examples of suitable batteries include, for example, a lithium battery (such as a lithium-ion battery), a nickel battery (such as a nickel-cadmium battery), and an alkaline battery. The battery is electrically coupled to the heating assembly to supply electrical power when required and under control of a controller (not shown) to heat the aerosol generating material. In this example, the battery is connected to a central support 120 which holds the battery 118 in place.

The device further comprises at least one electronics module 122. The electronics module 122 may comprise, for example, a printed circuit board (PCB). The PCB 122 may support at least one controller, such as a processor, and memory. The PCB 122 may also comprise one or more electrical tracks to electrically connect together various electronic components of the device 100. For example, the battery terminals maybe electrically connected to the PCB 122 so that power can be distributed throughout the device 100. The socket 114 may also be electrically coupled to the battery via the electrical tracks.

In the example device 100, the heating assembly is an inductive heating assembly and comprises various components to heat the aerosol generating material of the article 110 via an inductive heating process. Induction heating is a process of heating an electrically conducting object (such as a susceptor) by electromagnetic induction. An induction heating assembly may comprise an inductive element, for example, one or more inductor coils, and a device for passing a varying electric current, such as an alternating electric current, through the inductive element. The varying electric current in the inductive element produces a varying magnetic field. The varying magnetic field penetrates a susceptor suitably positioned with respect to the inductive element, and generates eddy currents inside the susceptor. The susceptor has electrical resistance to the eddy currents, and hence the flow of the eddy currents against this resistance causes the susceptor to be heated by Joule heating. In cases where the susceptor comprises ferromagnetic material such as iron, nickel or cobalt, heat may also be generated by magnetic hysteresis losses in the susceptor, i.e. by the varying orientation of magnetic dipoles in the magnetic material as a result of their alignment with the varying magnetic field. In inductive heating, as compared to heating by conduction for example, heat is generated inside the susceptor, allowing for rapid heating. Further, there need not be any physical contact between the inductive heater and the susceptor, allowing for enhanced freedom in construction and application.

The induction heating assembly of the example device too comprises a susceptor arrangement 132 (herein referred to as “a susceptor”), a first inductor coil 124 and a second inductor coil 126. The first and second inductor coils 124, 126 are made from an electrically conducting material. In this example, the first and second inductor coils 124, 126 are made from Litz wire/ cable which is wound in a helical fashion to provide helical inductor coils 124, 126. Litz wire comprises a plurality of individual wires which are individually insulated and are twisted together to form a single wire. Litz wires are designed to reduce the skin effect losses in a conductor. In the example device too, the first and second inductor coils 124, 126 are made from copper Litz wire which has a rectangular cross section. In other examples the Litz wire can have other shape cross sections, such as circular. The first inductor coil 124 is configured to generate a first varying magnetic field for heating a first section of the susceptor 132 and the second inductor coil 126 is configured to generate a second varying magnetic field for heating a second section of the susceptor 132. In this example, the first inductor coil 124 is adjacent to the second inductor coil 126 in a direction along the longitudinal axis 134 of the device 100 (that is, the first and second inductor coils 124, 126 to not overlap). The susceptor arrangement 132 may comprise a single susceptor, or two or more separate susceptors. Ends 130 of the first and second inductor coils 124, 126 can be connected to the PCB 122.

It will be appreciated that the first and second inductor coils 124, 126, in some examples, may have at least one characteristic different from each other. For example, the first inductor coil 124 may have at least one characteristic different from the second inductor coil 126. More specifically, in one example, the first inductor coil 124 may have a different value of inductance than the second inductor coil 126. In Figure 8, the first and second inductor coils 124, 126 are of different lengths such that the first inductor coil 124 is wound over a smaller section of the susceptor 132 than the second inductor coil 126. Thus, the first inductor coil 124 may comprise a different number of turns than the second inductor coil 126 (assuming that the spacing between individual turns is substantially the same). In yet another example, the first inductor coil 124 may be made from a different material to the second inductor coil 126. In some examples, the first and second inductor coils 124, 126 may be substantially identical.

In this example, the first inductor coil 124 and the second inductor coil 126 are wound in opposite directions. This can be useful when the inductor coils are active at different times. For example, initially, the first inductor coil 124 may be operating to heat a first section/portion of the article 110, and at a later time, the second inductor coil 126 may be operating to heat a second section/portion of the article 110. Winding the coils in opposite directions helps reduce the current induced in the inactive coil when used in conjunction with a particular type of control circuit. In Figure 8, the first inductor coil 124 is a right-hand helix and the second inductor coil 126 is a left-hand helix. However, in another embodiment, the inductor coils 124, 126 may be wound in the same direction, or the first inductor coil 124 may be a left-hand helix and the second inductor coil 126 may be a right-hand helix. The susceptor 132 of this example is hollow and therefore defines a receptacle within which aerosol generating material is received. For example, the article 110 can be inserted into the susceptor 132. In this example the susceptor 120 is tubular, with a circular cross section.

The susceptor 132 maybe made from one or more materials. Preferably the susceptor 132 comprises carbon steel having a coating of nickel or cobalt.

In some examples, the susceptor 132 may comprise at least two materials capable of being heated at two different frequencies for selective aerosolization of the at least two materials. For example, a first section of the susceptor 132 (which is heated by the first inductor coil 124) may comprise a first material, and a second section of the susceptor 132 which is heated by the second inductor coil 126 may comprise a second, different material. In another example, the first section may comprise first and second materials, where the first and second materials can be heated differently based upon operation of the first inductor coil 124. The first and second materials maybe adjacent along an axis defined by the susceptor 132, or may form different layers within the susceptor 132. Similarly, the second section may comprise third and fourth materials, where the third and fourth materials can be heated differently based upon operation of the second inductor coil 126. The third and fourth materials may be adjacent along an axis defined by the susceptor 132, or may form different layers within the susceptor 132. Third material may the same as the first material, and the fourth material may be the same as the second material, for example. Alternatively, each of the materials may be different. The susceptor may comprise carbon steel or aluminium for example.

The device too of Figure 8 further comprises an insulating member 128 which maybe generally tubular and at least partially surround the susceptor 132. The insulating member 128 may be constructed from any insulating material, such as plastic for example. In this particular example, the insulating member is constructed from polyether ether ketone (PEEK). The insulating member 128 may help insulate the various components of the device too from the heat generated in the susceptor 132.

The insulating member 128 can also fully or partially support the first and second inductor coils 124, 126. For example, as shown in Figure 9, the first and second inductor coils 124, 126 are positioned around the insulating member 128 and are in contact with a radially outward surface of the insulating member 128. In some examples the insulating member 128 does not abut the first and second inductor coils 124, 126. For example, a small gap may be present between the outer surface of the insulating member 128 and the inner surface of the first and second inductor coils 124, 126.

In a specific example, the susceptor 132, the insulating member 128, and the first and second inductor coils 124, 126 are coaxial around a central longitudinal axis of the susceptor 132. Figure 10 shows a side view of device 100 in partial cross-section. The outer cover 102 is present in this example. The rectangular cross-sectional shape of the first and second inductor coils 124, 126 is more clearly visible.

The device 100 further comprises a support 136 which engages one end of the susceptor 132 to hold the susceptor 132 in place. The support 136 is connected to the second end member 116.

The device may also comprise a second printed circuit board 138 associated within the control element 112.

The device too further comprises a second lid/cap 140 and a spring 142, arranged towards the distal end of the device too. The spring 142 allows the second lid 140 to be opened, to provide access to the susceptor 132. A user may open the second lid 140 to clean the susceptor 132 and/or the support 136.

The device too further comprises an expansion chamber 144 which extends away from a proximal end of the susceptor 132 towards the opening 104 of the device. Located at least partially within the expansion chamber 144 is a retention clip 146 to abut and hold the article 110 when received within the device too. The expansion chamber 144 is connected to the end member 106.

Figure 10 is an exploded view of the device too of Figure 9, with the outer cover 102 omitted. Figure 11A depicts a cross section of a portion of the device too of Figure 9. Figure 11B depicts a close-up of a region of Figure 11A. Figures 11A and 11B show the article 110 received within the susceptor 132, where the article 110 is dimensioned so that the outer surface of the article 110 abuts the inner surface of the susceptor 132. This ensures that the heating is most efficient. The article 110 of this example comprises aerosol generating material 110a. The aerosol generating material 110a is positioned within the susceptor 132. The article 110 may also comprise other components such as a filter, wrapping materials and/ or a cooling structure.

Figure 11B shows that the outer surface of the susceptor 132 is spaced apart from the inner surface of the inductor coils 124, 126 by a distance 150, measured in a direction perpendicular to a longitudinal axis 158 of the susceptor 132. In one particular example, the distance 150 is about 3mm to 4mm, about 3-3-5mm, or about 3.25mm.

Figure 11B further shows that the outer surface of the insulating member 128 is spaced apart from the inner surface of the inductor coils 124, 126 by a distance 152, measured in a direction perpendicular to a longitudinal axis 158 of the susceptor 132. In one particular example, the distance 152 is about 0.05mm. In another example, the distance 152 is substantially omm, such that the inductor coils 124, 126 abut and touch the insulating member 128. In one example, the susceptor 132 has a wall thickness 154 of about 0.025mm to imm, or about 0.05mm.

In one example, the susceptor 132 has a length of about 40mm to 60mm, about 40mm to 45mm, or about 44.5mm.

In one example, the insulating member 128 has a wall thickness 156 of about 0.25mm to 2mm, 0.25mm to imm, or about 0.5mm.

In use, the articles 1, T, 1”, T” described herein can be inserted into a non-combustible aerosol provision device such as the device too described with reference to Figures 7 to 11B. At least a portion of the mouthpiece 2, 2’, 2”, 2’” of the article 1, T, 1”, T” protrudes from the non-combustible aerosol provision device too and can be placed into a user’s mouth. An aerosol is produced by heating the aerosol generating material 3 using the device too. The aerosol produced by the aerosol generating material 3 passes through the mouthpiece 2 to the user’s mouth. The various embodiments described herein are presented only to assist in understanding and teaching the claimed features. These embodiments are provided as a representative sample of embodiments only, and are not exhaustive and/or exclusive. It is to be understood that advantages, embodiments, examples, functions, features, structures, and/or other aspects described herein are not to be considered limitations on the scope of the invention as defined by the claims or limitations on equivalents to the claims, and that other embodiments may be utilised and modifications may be made without departing from the scope of the claimed invention. Various embodiments of the invention may suitably comprise, consist of, or consist essentially of, appropriate combinations of the disclosed elements, components, features, parts, steps, means, etc, other than those specifically described herein. In addition, this disclosure may include other inventions not presently claimed, but which may be claimed in future.

Claims

Claims l. A component for an article for use in or as a non-combustible aerosol provision system, the component comprising: a body of material extending in a longitudinal direction, wherein the body of material comprises sheet material comprising fibres having a length in the range 2 mm to 6 mm and wherein the body of material has a density in the range between about o.i and 0.25 mg/mm3.
2. A component according to claim 1, wherein the body of material comprises crimped sheet material formed having a crimp pattern comprising a series of substantially parallel ridges and grooves, wherein the average spacing between adjacent ridges is greater than about 0.3 mm.
3. A component according to claim 1 or 2, wherein the body of material comprises crimped sheet material formed having a crimp pattern comprising a series of substantially parallel ridges and grooves, wherein the crimp amplitude is less than about 0.7 mm or between about 0.7mm and about 1.2mm. 4. A component according to any one of claims 1 to 3, wherein the average spacing between adjacent ridges is greater than about 0.
4 mm, greater than about 0.5 mm or greater than about 0.6mm.
5. A component according to any one of claims 1 to 4, wherein the body of material comprises crimped fibres having a crimp amplitude of less than about 600 pm, less than about 500 pm or less than about 400 pm.
6. A component according to any one of claims 1 to 5, wherein the body of material has a density between about 0.15 mg/mms and about 0.2 mg/ mm³, or between about 0.17 mg/mm³ and about 0.2 mg/mm³.
7. A component according to any one of claims 1 to 6, wherein the body of material has a volume of at least 100 mm3, _at least 115 mm3, _at least 150 mm3, _at l_east 200 mm3, at least 300 mm3, _at least 400 mm3, _at least 500 mm3, _at least 600 mm3, _at least 700 mm3, _at least 800 mm3, _at least 900 mm ₀r at least 1000 mm3.
8. A component according to any one of claims l to 7, wherein the body of material has a volume of at least 19 mm3 per mm of axial length of the body of material, at least 25 mm3 per mm of axial length of the body of material, or at least 30 mm3 per mm of axial length of the body of material.
9. A component according to any one of claims 1 to 8, wherein the body of material has a weight of at least 4 mg per mm of axial length of the body of material, at least 5 mg per mm of axial length of the body of material, or at least 6 mg per mm of axial length of the body of material.
10. A component according to any one of claims 1 to 9, wherein the body of material is substantially cylindrical.
11. A component according to any one of claims 1 to 10, wherein the body of material is wrapped in a plug wrap having a Wet Tensile Strength of less than lN / 15mm paper width.
12. A component according to any one of claims 1 to 11, wherein the sheet material has a basis weight of at least 20 g/m², or at least 22 g/m² or at least 24 g/m².
13. A component according to claim 12, wherein the sheet material has a basis weight of less than 50 g/m², less than 45 g/m², or less than 40 g/m².
14. A component according to any one of claims 1 to 13, wherein the sheet material has an extended width of between 120mm and 200mm, or between 150 mm and

200mm.
15. A component according to any one of claims 1 to 14, wherein the sheet material comprises paper.
16. A component according to any one of claims 1 to 14, wherein the sheet material comprises reconstituted tobacco.
17. A component according to any one of claims 1 to 16, wherein the closed pressure drop across the body of material is at least 1.0 mmH₂0 per mm of longitudinal length, or at least 1.2 mmH₂0 per mm of longitudinal length or at least 1.5 mmH₂0 per mm of longitudinal length.
18. A component according to any one of claims 1 to 17, wherein the closed pressure drop across the body of material is less than 3 mmH₂0 per mm of longitudinal length, or less than 2.8 mmH₂0 per mm of longitudinal length or less than 2.5 mmH₂0 per mm of longitudinal length.
19. A component according to any one of claims 1 to 18, wherein the body of material has an axial length of at least 4 mm, at least 5 mm, at least 6 mm, at least 7 mm, at least 8 mm, at least 9 mm, at least 10 mm or between about 6 mm and about 15 mm.
20. A component according to claim 19, wherein the body of material has an axial length of about 12 mm.
21. A component according to any one of claims 1 to 20, wherein the body of material has a circumference of at least 16 mm, at least 18 mm, or at least 20 mm.
22. A component according to any one of claims 1 to 21, further comprising an aerosol-modifying agent disposed within the body of material.
23. A component according to claim 22, further comprising an aerosol-modifying agent release component comprising the aerosol-modifying agent.
24. A component according to claim 23, wherein the aerosol-modifying agent release component comprises a capsule.
25. A component according to claim 24, wherein the capsule comprises a solid shell and a liquid core, the liquid core comprising the aerosol-modifying agent.
26. A component according to any one of claims 1 to 25, further comprising an aerosol-former material applied to the body of material.
27. A component according to claim 26, wherein the aerosol-former material comprises one or more of glycerine, glycerol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 1,3-butylene glycol, erythritol, meso-Erythritol, ethyl vanillate, ethyl laurate, a diethyl suberate, triethyl citrate, triacetin, a diacetin mixture, benzyl benzoate, benzyl phenyl acetate, tributyrin, lauryl acetate, lauric acid, myristic acid, and propylene carbonate.
28. A component according to claim 27, wherein the aerosol-former material comprises triethyl citrate or triacetin.
29. A component according to claim 27 or 28, wherein at least 0.02 mg, 0.03 mg, 0.04 mg, or 0.05 mg of aerosol-former material is applied to the body of material per 1 mm axial length of the body of material.
30. A component according to any one of claims 27 to 29, wherein 0.5 mg or less, 0.45 mg or less, 0.4 mg or less, 0.35 mg or less, or 0.3 mg or less of aerosol-former material is applied to the body of material per 1 mm axial length of the body of material.
31. A component according to any one of claims 1 to 30, comprising a tubular element located within the body of material, the tubular element comprising a cavity.
32. A component according claim 31, wherein the tubular element comprises paper.
33. A component according to any one of claims 1 to 32, wherein the component is wrapped in a wrapper having a basis weight of greater than 40 grams per m² and/or a thickness of greater than 35pm.
34. A component according to any one of claims 1 to 33, wherein the sheet material comprises fibres having an average length in the range 2 mm to 5 mm, 2 mm to 4 mm or 2 mm to 3 mm.
35. A component according to any one of claims 1 to 34, wherein the sheet material comprises a thickness of between about 50 and about too pm, or between about 60 and about 90 pm.
36. An article for use in or as a non-combustible aerosol provision system, the article comprising an aerosol generating material and a downstream portion downstream of the aerosol generating material, the downstream portion comprising a component according to any one of claims 1 to 35.
37. A non-combustible aerosol provision system comprising an article according to claim 36.
38. A non-combustible aerosol provision system according to claim 37, wherein the non-combustible aerosol provision system is an aerosol generating material heating system, optionally wherein the non-combustible aerosol provision system is a tobacco heating system.
39. A method for forming a component for an article for use in a non-combustible aerosol provision system, the method comprising forming a sheet material into a body of material, wherein the sheet material comprises fibres having a length in the range 2 mm to 6 mm and wherein the body of material has a density in the range between about 0.1 and 0.25 mg/mm3.