US3861400A - Nicotine fortification of smoking products - Google Patents

Abstract

Controlled amounts of nicotine may be supplied to a tobacco product or acceptable substitute smoking composition by adding to the base small amounts of a nicotine derivative of galacturonic acid or polymannuronic acid which on pyrolysis of the composition release small amounts of nicotine into the smoke stream.

Description

United States Patent 1191 Perkins et al.

[451 Jan. 21, 1975 NICOTINE FORTIFICATION OF SMOKING PRODUCTS [75] Inventors: Paul Raymond Perkins, Portishead;

Christopher Ralph Bale, Keynsham, near Bristol, both of England [73] Assignee: Imperial Tobacco Group Limited,

London, England [22] Filed: Sept. 12, 1972 [21] Appl. No.: 288,329

[30] Foreign Application Priority Data Sept. 23, 1971 Great Britain 44370/71 [52] US. Cl ..131/2,131/17, 131/9, 424/361,131/144 [51] Int. Cl. A24b 03/14, A24b 15/04 [58] Field of Search 131/2, 17; 424/361 [56] References Cited UNITED STATES PATENTS 3,529,602 9/1970 Hind et al. 131/2 Primary Examiner-Melvin D. Rein Attorney, Agent, or Firm-Larson, Taylor and Hinds [57] ABSTRACT 7 Claims, No Drawings NICOTINE FORTIFICATION OF SMOKING PRODUCTS This invention concerns a smoking product e.g. tobacco, hand rolling tobacco, pipe tobacco, reconstituted tobacco sheet, substitute smoking materials free from tobacco, or blends and mixtures thereof and cigarettes, cigars or cigarillos containing such materials and concerns the problem of maintaining or increasing the nicotine content of the smoke whilst avoiding an undesirable level of particulate matter in the smoke from the product.

Various techniques are known for reducing particulate matter in the smoke of a smoking product. For example it is well known to filter out particulate matter but in so doing nicotine is also filtered and thus the resulting smoke from the smoking product is poorer in nicotine as well as in particulate matter.

A further example is the use of reconstituted tobacco sheet in blends for smoking products. By appropriate choice of component materials and control in the preparation and manufacture of the sheet it is possible to reduce the yield of particulate matter in the resulting smoking product. Unfortunately such sheet, prepared from mixtures of tobacco stem, tobacco lamina and/or general tobacco offals, generally contains a lower concentration of nicotine than the other tobacco grades in the blend such that a nicotine deficiency exists.

A third example is the use of synthetic and substitute smoking materials in which particulate matter is reduced considerably. As with the previous examples however the overall delivery of nicotine in the smoke is reduced in proportion to the amount of such material incorporated into the smoking product since the natural nicotine content of such smoking materials is zero.

To avoid the disadvantages of the above examples it is proposed to increase the nicotine content of a smoking product whereby, although the level of particulate matter can be reduced, the level of nicotine can be maintained or even increased. Efforts to do this in the past have been disappointing since the percentage of nicotine added to the product and subsequently appearing in the smoke has been very low. Furthermore the level of the added nicotine drops considerably with time and shelf life is poor. It is an object of the present invention to overcome such disadvantages.

According to the present invention there is provided a smoking material containing a nicotine derivative of a polyuronic acid.

Preferably the acid is a polygalacturonic or polymannuronic and the derivative is nicotine pectinate or nicotine alginate respectively.

Where nicotine pectinate is used this is formed from pectinic acid having a degree of esterification of up to 50 percent preferably 30 35 percent. Furthermore the acidity is from 1.5 to 3.5 milli equivalents per gram, preferably from 2.0 to 3.5 milli equivalents per gram (m.eq/g).

lf pectinic or alginic acids available are not of the desired acidity, they can be de-ashed or freed from inorganic materials by washing with acid, preferably with aqueous isopropanol (specific gravity 0.880) contain ing hydrochloric acid in the ratio of 1 part by volume of hydrochloric acid to parts by volume of aqueous isopropanol (specific gravity 0.880).

The base materail can be tobacco lamina. stem (mid rid), reconstituted sheet or synthetic smoking material which is tobacco free.

The product preferably contains at least 1 percent and up to 30 percent of the nicotine derivative on a dry weight basis. Preferably the smoking product contains 3 to 13 percent of the nicotine derivative on a dry weight basis.

The invention also includes a smoking product containing a material set forth above.

The invention also includes a method of making a smoking material as set forth above.

The invention is illustrated by the following two series of examples. For use in these series the following samples of nicotine alginate and nicotine pectinate were produced:

A first sample (sample 1) of nicotine pectinate was produced from citrus pectinic acid obtained from lemon peel and having a degree of esterification of 35 percent and acidity of 3.1 m.eq/g and l00gms of this acid was mixed with 30gms of water until the water was absorbed and a free-running powder was obtained. SOgms of percent pure technical grade nicotine was stirred into the powder to produce an homogeneous paste of crude nicotine pectinate. This was left 24 hours to complete the chemical reaction and the resulting product was ground to a coarse powder. One litre of ethanol was added to the powder which was filtered, washed with five ml portions of ethanol and two 50mls portions of diethyl ether and dried so that unreacted nicotine was removed. The resulting powder had a nicotine content of 25 percent. This nicotine pectinate will hereinafter be referred to as Sample 1.

A second sample hereinafter referred to as Sample 2" of nicotine pectinate was prepared from citrus pectinic acid prepared from lemon peel and having a degree of esterification of 35 percent and acidity of 2.7m.eq/g. With this pectinic acid, nicotine pectinate was prepared in exactly the same way as that set out above with reference to sample 1 but the resulting nicotine pectinate had a nicotine content of 23.8 percent.

A powder of nicotine alginate (Sample 3) was prepared using alginic acid of acidity 5.2m.eq/g supplied by British Drug Houses Ltd. of Poole, Dorset under Reference 27898 in their 1970 Catalogue. Nicotine alginate was prepared from this alginic acid in exactly the same way as samples 1 and 2 of nicotine pectinate were prepared and as described above, and the resulting nicotine alginate had a nicotine content of 31.5 percent.

A fourth sample sample 4 of nicotine pectinate was prepared in solution form but in this case technical grade nicotine 90.8 percent pure and supplied by British Drug Houses was used with lemon peel pectinic acid having a degree of esterification of 35 percent and acidity of 2.7m.eq/g. A solution of 1200 g of pectinic acid in 18.5 litres of water was prepared and 333g of nicotine added. The dissolved nicotine pectinate derivative contained 20 percent nicotine and the final solution contained 1.5 percent nicotine on a weight for weight basis.

A fifth sample sample 5 of nicotine pectinate was prepared according to the procedure of sample 4 but in this case a sugar beet pectinic acid was used having a degree of esterification of 30 percent and an acidity of 1.7m.eq/g. The resulting nicotine pectinate solution had a nicotine content of 1.5 percent on a weight for weight basis.

Sample 6 was a nicotine alginate solution made according to the method of sample 4 above but in this case the acidity of the alginic acid was 3.6m.eq/g with a negligable degree of esterification. The nicotine alginate solution had a nicotine content of 1.5 percent on a weight for weight basis.

Sample 7 was a nicotine pectinate solution prepared from the same materials as sample 4 except that litres of water was used instead of 18.5 litres. The resulting nicotine pectinate solution contained 1.8 percent nicotine on a weight for weight basis.

The first series of experiments was conducted using 9 examples, of which examples l6 involved fortification using nicotine pectinate or nicotine alginate and examples 79 were controls or standards. The second series involved 11 examples of which numbers 10l7 were fortified with nicotine alginate or nicotine pectinate and examples l820 were controls or standards.

SERIES 1: EXAMPLES l9.

EXAMPLE 1 A sheet of reconstituted tobacco was prepared in the following manner.

A mixture of 255gms of winnowings and 225gms of general offal (both oven dry weight) were soaked in 4.5 litres of tap water for one hour. The slurry was repeatedly passed through a Premier 84 colloid mill initially set to a gap of 0.01 inches between the stones. The gap was decreased by 0.003 inches after each pass until the slurry remained in a colloidal state.

gms of sample 1 nicotine pectinate were added to the tobacco slurry and mixed using a Silverson mixer. The mixture was then passed through the colloid mill set at gap zero to remove any lumps which may have formed due to coagulation.

The slurry so formed was cast onto a pre-siliconed stainless steel sheet to a wet sheet thickness of 1.2mm. The sheet was dried in air and then slightly moistened to facilitate removal from the stainless steel sheet. The tobacco sheet so prepared was tested for nicotine content, cut and plain cigarettes of mm circumference and 70mm length (commonly referred to in U.K. as class B cigarettes) were manufactured on a Hauni Baby cigarette making machine and smoked using a standard smoking machine procedure in which five equal weight cigarettes are smoked on a Filtrona CSM 14 machine to a 20mm butt using a 2 second, 35ml puff every minute. The particulate matter was collected on a Cambridge glass fibre filter and the water-free and nicotine-free particulate matter (P.M.) was measured and the nicotine delivery determined. To do this, the wet deposit on the Cambridge filter was weighed, the nicotine was determined by steam distillation followed by spectrophotometric analysis (Willits method) and water determined by gas chromotography. The resultant deposit is particulate matter (P.M.) which is water and nicotine free. The tests were repeated three months later and the results are tabulated on the accompanying Table 1.

EXAMPLE 2 A sheet of reconstituted tobacco was prepared in exactly the same way as that described above with reference to Example 1 and nicotine pectinate of sample 1 was again added but in this example 36.3gms of the nicotine pectinate were added to the same tobacco slurry.

The cast sheet was removed from the band, tested for nicotine content cut and made into plain cigarettes 25mm circumference and 70mm long which were subsequently tested by the standard method described in Example 1 for particulate matter and nicotine deliveries in the smoke. The tests were carried out soon after manufacture and three months later and the results are set out in Table 1.

EXAMPLE 3 A sheet of reconstituted tobacco was again manufactured in accordance with the details set out in Example 1 above, but in this case Sample 2 of the nicotine pectinate was added to the slurry, 21.4gms of the pectinte being used for the same amount of the tobacco slurry. Again, nicotine content of the sheet was measured. the sheet was cut, made into plain cigarettes of 25mm circumference and 70mm length and analysed by the standard method described in Example 1 for particulate matter and nicotine deliveries in the smoke both immediately after manufacture and three months later. The results are set out in Table 1.

EXAMPLE 4 EXAMPLE 5 The sheet of reconstituted tobacco described above with reference to Example 1 was again made strictly in accordance with the specification but 16.2gms of the nicotine alginate (sample 3) were added to the tobacco slurry. Again the sheet was but and made into plain cigarettes 25mm circumference and 70mm long. These were tested by the standard method described in Example l for particulate matter and nicotine deliveries in the smoke and the results are set out in Table 1.

EXAMPLE 6 The sheet of example 5 was made up but 36gms of sample 3 nicotine alginate were added and the resulting sheet cut, made into plain cigarettes 25mm circumference and 70mm long and tested by the standard method of example 1 for particulate matter and nicotine delivery in the smoke.

EXAMPLE 7 To provide one control against which one could analyse the results of storage of the samples set out above, a sample of a commercially available low tar yielding reconstituted tobacco sheet of nicotine content 0.78 percent was made into plain cigarettes 25mm circumference and 70mm length and tested by the standard method of example 1 for particulate matter and nicotine delivery in the smoke on the same dates as examples 1 to 6 were tested. This particular control sheet is recognised as being relatively stable for nicotine content and thus provided a suitable standard against which to measure the nicotine loss from the samples 1 to 6.

EXAMPLE 8 The tobacco sheet described above with reference to examples 16 was made but without any additive i.e. no nicotine pectinate or nicotine alginate, simply tobacco winnowings and offal with water The non-additive sheet so made was cast on the stainless steel band and. when removed, was cut, made into plain cigarettes 25mm circumference and 70mm long and analysed by the standard method of example 1 for particulate matter and nicotine delivery in the smoke.

EXAMPLE 9 To provide a comparison and standard by which the result set out in Table 1 can be compared, a plain cigarette 25mm circumference and 70mm long and available on the U.K. market was obtained and analysed in the same way as the other examples for particulate mat ter and nicotine delivery in the smoke and the results are set out in Table 1.

TABLE 1 Referring to Table 1 it will be noted that the amount of nicotine in the smoke in all examples 16 was appreciably higher than in any of the three control samples 7, 8 and 9. The percentage nicotine transfer (nicotine in smoke compared with nicotine in unsmoked cigarette) was better in examples 1-6 compared with examples 7 and 9. Furthermore the ratio of particulate matter (P.M.) to nicotine of example l-6, was superior to that of the control examples 7, 8 and 9 to a marked degree. The increase in value of ratio of particulate matter (P.M.) to nicotine between testings in examples 1 to 6 was not considered to be significant.

It has been found and it is indicated by results tabulated in Table 1 that, by the addition of small quantities of nicotine pectinate or nicotine alginate an appreciable retention of nicotine can be secured and transferred to the smoke whereby the nicotine content of the smoke is fortified. Furthermore it has been found that the nicotine content of the smoke is not appreciably affected by storage and thus the loss in nicotine has been found to be no greater than that from the most stable of the control examples used.

passing this through a P.U.C. mill at zero setting and then twice through a Manton-Gaulin K3 homogeniser at 3,000p.s.i.

The winnowings slurry and the offal slurry were mixed together, and 14.51bs of Sample 4 nicotine pectinate solution were added.

The nicotine fortified slurry was recycled through a P.U.C. mill to achieve thorough mixing and then cast on a Sandvik cast tobacco sheet machine. The Sandvik machine was run at 13.5 feet per minute with a 0.030

in casting gate and a 0.5m. slurry head. This produced 1 1 .251bs. of sheet.

The nicotine content of the sheet immediately after manufacture was 3.15 percent. Some of the sheet was stored for eight weeks in open containers under atmospheric conditions of 21C and 60% RH. The nicotine content after eight weeks was 3.12 percent, indicating an extremely stable situation.

The remainder of the tobacco sheet so prepared was cut and manufactured into filter tipped cigarettes on a Molins Mk 8 cigarette making machine. The cigarettes were 70mm in length and 25.3mm in circumference and had a duel myria/acetate filter. Twenty-five of the cigarettes were mechanically smoked on an lmperial Tobacco smoking machine to a butt length of 2mm longer than the filter overwrap material using a 35ml, 2 second duration puff once per minute. The smoke condensate collected on Cambridge glass fibre filter pads was analysed for particulate matter and nicotine by weighing the wet deposit on each filter, analysing the deposit for nicotine content by steam distillation (Willits method) and analysing the deposit for water content by gas chromotography. The particulate matter Table 1 Series 1 Nicotine P.M.* 1n Smoke Nicotine in Smoke Nicotine Transfer P.M.

in ((Mg/Cig.) (Mg/Cig.) 7t Nicotine Ratio TYPE Material Example 1 2.86 30.1 29.0 3.61 3.12 17.1 15.2 8.3 9.3 Example 2 3.90 32.4 30.0 5.02 4.26 17.3 14.7 6.4 7.0 Example 3 2.67 28.2 25.5 3.65 3.06 18.4 15.2 7.7 8.3 Example 4 3.93 29.7 27.1 4.91 4.42 16.8 15.6 6.1 6.1 Example 5 2.78 28.0 26.6 3.62 3.03 17.6 14.8 7.7 8.8 Example 6 4.33 25.4 25.6 5.50 4.79 17.0 14.5 4.6 5.4 Example 7 0.78 17.1 17.2 0.75 0.68 13.0 11.6 27.3 253 Example 8 1.44 27.4 1.67 15.6 16.4 Example 9 1.93 31.4 2.16 14.4 14.5

' Denotes particulate matter free from water and nicotine.

SERIES 3: EXAMPLES 10-20.

EXAMPLE 10 (P.M.) level is thus water and nicotine-free. The results obtained are set out in Table 2.

EXAMPLE 11 A sheet of reconstituted tobacco was prepared according to the method on Example 10 but 14.5lbs of Sample 5 nicotine pectinate solution was used.

The sheet so prepared had a nicotine content of 2.99 percent after making and 2.95 percent after eight weeks storage under condition of 21C and 60% RH.

Filter tipped cigarettes made to the specification outlined in Example 10 gave the results listed in Table 2 when analysed by the standa'rd methods set out in Ex ample l0.

EXAMPLE 12 A sheet of reconstituted tobacco was prepared in accordance with the method in Example 10 but l4.5lbs of solution Sample 6 nicotine alginate was substituted for the nicotine pectinate solution.

The sheet had a nicotine content of 3.00 percent after casting and 2.97 percent after eight weeks storage under conditions of 21C and 60% RH, indicating a vary stable product.

Filter tipped cigarettes manufactured and analysed according to the methods stated in Example 10 gave the results set out in Table 2.

EXAMPLE 13 The sheet of example 10 was made up as described in that example. Instead of l4.5lb of Sample 4 nicotine pectinate solution, l2lb of the sample 4 solution was added to 20lb (oven-dry weight) of sheet mixture whereby the final nicotine content of the cast sheet was 2.08 percent rather than 3.15 percent.

Again the sheet was made into cigarettes and smoked in the standard way described in example 10 and analysed according to the method of example l0. The results are listed in Table 2.

EXAMPLE 14 The sheet of example 10 was made up as described in that example, but 12lb of sample nicotine pectinate solution was added to 20lb (oven-dry weight) of the basic tobacco mixture to provide a nicotine content of 2.12 percent.

The sheet was made into cigarettes, smoked and tested as described in example 10. The results are set out in Table 2.

EXAMPLE l5 The sheet of example was again prepared but had added thereto l2lb of sample 6 nicotine alginate solution to lb (oven-dry weight) of basic tobacco mixture to provide a final nicotine content of 2.09 percent. The sheet was made into a cigarettes, smoked and analysed as described with reference to example 10.

EXAMPLE 16 Cut rolled stem (processed mid rib) was treated with nicotine pectinate to increase its nicotine content to that of commonly used tobacco lamina grades.

lb of the stem containing 12 percent moisture and 0.56 percent nicotine was placed in a polythene bin and 17%lb of sample 7 nicotine pectinate solution added in small portions. The mixture was stirred with a paddle to minimise the formation of lumps and to ensure an even application of the nicotine pectinate solution to the stem.

The mixture was allowed to stand overnight and then dried back to 15 percent moisture in a gas fired rotary drier. The material had a nicotine content of 1.64 percent.

The material was then manufactured into filter tipped cigarettes on a Molins Mk 8 cigarette making machine. The cigarettes were mm in length and 25.3mm in circumference and had a dual myria/acetate filter. They weighed 1.040g and had a pressure drop of 1 18mm of water.

The cigarettes were smoked using the standard methods previously described in Example 10 and gave the results listed in Table 2 using the analysis technique set out in Example 10.

EXAMPLE 17 The objective was to prepare a substitute smoking material in the form of a sheet such that it contained approximately 2 percent of nicotine and was completely free from any form of tobacco.

To prepare the sheet material, a solution of 35g of slow-set citrus pectin (obtained from H. P. Bulmers Ltd.) in 700 ml of water was prepared with the aid of a Silverson mixer. The slow-set citrus pectin had a degree of esterification of 63 percent and an acidity of 1.6 milli-equivalents per gramme. A second mixture was prepared by dispersing 30g calcium carbonate, 5g potassium carbonate, 5g celite (Hyflo Super Cel grade), 5g magnesium hydrogen phosphate and 2g titanium dioxide in 250ml of water. To this suspension was added 6g of citric acid.

This slurry of inorganic materials was added to the citrus pectin solution and thoroughly mixed with the Silverson stirrer. A third solution of 9g of Sample 2 nicotine pectinate in 250ml of water was then added, followed by 5g of glycerol. The resulting slurry was thoroughly mixed again, and then passed through a Premier 84 colloid mill adjusted to a running clearance of 0.003in to remove any lumps.

The slurry was cast on a continuous stainless steel band using an 1.1mm casting gate and dried using Infra Red heating lamps. The dried sheet was moistened to facilitate removal and doctored off the band.

The prepared sheet was cut at 40c.p.i. using a Hauni sample cutting machine, Model TSH V and manufactured into filter tipped cigarettes using an Eflta-Werke Privileg hand machine. These cigarettes were 83mm long, 25mm in circumference and contained 1.0g of filler material. The filler material contained 1.93 percent nicotine. The filter was a mono acetate type.

When smoked and analysed by the standard methods described in Example 10 the results listed in Table 2 were obtained EXAMPLE 18 To provide a control against which the affects of nicotine fortification can be compared, a sample of commercially available low tar yielding sheet containing 0.5 percent of nicotine was cut and manufactured into filter tipped cigarettes in the manner described in Example 10. The cigarettes were 70mm in length and 25.3mm in circumference and contained 0.70g of sheet.

When smoked under the standard conditions of Example 10 and analysed as described in Example 10, the Table 2 results were obtained.

EXAMPLE l9 To provide a standard against which the examples l0-l8 could be compared, a standard filter tip cigarette. commercially available in the United Kingdom and being of the same specification as the cigarettes referred to in Example were smoked and analysed by the standard methods set out in Example 10. The nicotine content of the filler in the cigarette was determined before smoking as 2.01 percent. The smoke analysis is given in Table 2.

EXAMPLE 20 To demonstrate the effectiveness of nicotine pectinate as a means of increasing the nicotine content of 10 stem (processed mid rib), a control sample of untreated stem containing 0.66 percent nicotine was manufactured into filter tipped cigarettes in the manner described in Example 16 and with the same physical dimensions as the cigarettes in Example 16. When smoked and analysed using the standard methods described in Example 10 the results set out in Table 2 were obtained.

The ratio of particulate matter (P.M.) to nicotine is seen to be extremely good in the Examples 1016, being far lower than in the control Examples 18 and 20 and being of the same order as the commercial cigarette Example 19 for the same initial nicotine content of approximately 2 percent (compare Examples 1315 with Example 19).

The results indicate that nicotine derivates of alginic and pectinic acids provide extremely stable nicotine fortification agents which are effective in efficiently transferring an acceptable percentage of the nicotine to the smoker. Furthermore the fortification agent is useful in fortifying not only natural lamina tobacco but also stem (mid rib), reconstituted tobacco sheet and synthetic smoking materials. Particularly with respect to the last two materials, it should be noted that best results are obtained if the pH of the material is kept below approximately 6.5.

Table 2 Series 2 Nicotine content of material Mean no. P.M.* Nicotine Filter Nicotine P.M. When After 8 of puffs in smoke in smoke Retention Transfer Nicotine TYPE made weeks per cig. (mg/cig.) (mg/cig.) Ratio Example 10 3.15 312 8.7 17.0 1.53 54.1 16.6 11.1 Example 11 2.99 2 95 8.1 14.2 1.41 54.6 18.6 10.1 Example 12 3.00 2.97 8.4 17.3 1.56 53.0 18.6 11.1 Example 13 2.08 2.06 7.0 14.2 0.98 53.7 18.5 14.5 Example 14 2.12 209 7.7 17.1 1.08 55.9 18.7 15.8 Example 15 2.09 2 06 7.6 15.8 1.14 53.0 20.3 13.9 Example 16 1.64 8.2 10.0 0.71 56.1 15.1 14.1 Example 17 1.93 8.7 12.3 1.70 29.0 17.0 7.2 Example 18 0.50 8.0 9.1 0.30 52.0 19.0 330 Example 19 2.01 11,6 21.0 1.49 47.8 21.2 14.1 Example 20 0.66 8.4 11.4 0.29 54.2 14.6 39.4

* Denotes particulate matter free from water and nicotine.

TABLE 2 Referring to Table 2 it will be noted that the additive is extremely stable. In all cases only a small loss of nicotine derivative of pectinic or alginic acid was noted in the eight weeks following application to the base tobacco material. This is far superior to previous attempts to find a stable nicotine fortification material.

Regarding the nicotine transfer figures, it will be seen that these are extremely good for all examples which were fortified. Over 16 percent of the nicotine in each starting material was transferred to the smoke and presented to the filter. It will be seen that this compares favourably with the standard or control cigarette results. Thus the commercially available cigarette tested produced a transfer figure of 21.2 percent. The test results indicate that very little reduction in this figure is to be expected even with fortified materials and blends.

It will be appreciated that the materials tested were all basic materials in Examples 10-17 i.e. no blends of materials were used. However, such blends could of course be used in any commercial use of the material.

mixture or the individual materials.

Furthermore Curie point pyrolysis followed by gas/- liquid chromotography tests on the nicotine pectinate and nicotine alginate employed'indicated that maximum yield of nicotine occurs between 500 and 550C i.e. at the temperature immediately behind the burning coal of a cigarette. It would appear from the results obtained that nicotine derivatives pectinic and alginic acids offer substantially attractive additives to tobacco products providing a nicotine agent which will fortify the nicotine content of the product whilst remaining relatively stable over a period of months and yielding the nicotine at the optimum temperature of 500 to 550C and yet being a relatively acceptable and harm less ingredient making it a most suitable and attractive additive.

Pectins, particularly those from tobacco plants, are well known as binders or sheet strengtheners in the manufacture of reconstituted tobacco sheet or synthetic smoking materials and thus the addition of nicotine pectinate has the added attraction that the pectinate so added assists in binding and strengthening reconstituted or synthetic sheet. Thus not only is the sheet fortified with nicotine but also a strengthening agent is added without the need to add additional substances as is done in reconstituted or synthetic sheet manufacture.

With the present invention there is provided a stable and effective nicotine fortification material being the nicotine derivatives of a polyuronic acid.

Although all examples have used nicotine derivatives of polygalacturonic and polymannuronic acids only, it

is considered that any polyuronic acid can be used in view of the closely similar properties of these acids. Thus nicotine derivatives of polyglucuronic acid and of polyguluronic acid would be useful nicotine fortification agents but, like all polyuronic acids other than polygalacturonic and polymannuronic they are not readily available in bulk and thus at this time are not commercially attractive. However this does not detract from their effectiveness. The examples have been limited to the two readily available and commercially attractive polyuronic acid derivatives but the invention embraces the nicotine derivatives of all polyuronic acids.

What we claim is:

l. A process for making a smoking material selected from the group consisting of tobacco, reconstituted tobacco and substitute tobacco which comprises adding 5. The process of claim 4 wherein the additive is a nicotine derivative of pectinic acid having a degree of esterification of 25-40 percent and an acidity of 1.5'to 3.5 milliequivalents per gram.

6. The process of claim 1 wherein the material is a nicotine derivative of polymannuronic acid.

7. The process of claim 6 wherein the derivative is nicotine alginate.

Claims (6)

1. 2. The process of claim 1 wherein the material is a nicotine derivative of polygalacturonic acid.
2. 3. The process of claim 2 wherein the derivative is nicotine pectinate.
3. 4. The process of claim 3 wherein the amount of dertive is 3 percent to 13 percent by weight.
4. 5. The process of claim 4 wherein the additive is a nicotine derivative of pectinic acid having a degree of esterification of 25-40 percent and an acidity of 1.5 to 3.5 milliequivalents per gram.
5. 6. The process of claim 1 wherein the material is a nicotine derivative of polymannuronic acid.
6. 7. The process of claim 6 wherein the derivative is nicotine alginate.