CA2154497A1 - Production technique for blocks of hot melt adhesives - Google Patents
Production technique for blocks of hot melt adhesivesInfo
- Publication number
- CA2154497A1 CA2154497A1 CA002154497A CA2154497A CA2154497A1 CA 2154497 A1 CA2154497 A1 CA 2154497A1 CA 002154497 A CA002154497 A CA 002154497A CA 2154497 A CA2154497 A CA 2154497A CA 2154497 A1 CA2154497 A1 CA 2154497A1
- Authority
- CA
- Canada
- Prior art keywords
- film
- adhesive
- hot melt
- molten
- cavity
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 30
- 239000004831 Hot glue Substances 0.000 title claims abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 47
- 230000001070 adhesive effect Effects 0.000 claims abstract description 46
- 239000000853 adhesive Substances 0.000 claims abstract description 45
- 238000002844 melting Methods 0.000 claims abstract description 12
- 230000008018 melting Effects 0.000 claims abstract description 11
- 239000007788 liquid Substances 0.000 claims abstract description 7
- 238000004806 packaging method and process Methods 0.000 claims abstract description 7
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 14
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 13
- 239000011248 coating agent Substances 0.000 claims description 12
- 238000000576 coating method Methods 0.000 claims description 12
- 239000002985 plastic film Substances 0.000 claims description 11
- 229920006255 plastic film Polymers 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 9
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims description 5
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 5
- 239000001913 cellulose Substances 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 229920000881 Modified starch Polymers 0.000 claims description 2
- 239000004368 Modified starch Substances 0.000 claims description 2
- 238000004090 dissolution Methods 0.000 claims description 2
- 238000003475 lamination Methods 0.000 claims description 2
- 235000019426 modified starch Nutrition 0.000 claims description 2
- 239000012943 hotmelt Substances 0.000 description 15
- -1 polyethylene Polymers 0.000 description 10
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 10
- 238000001816 cooling Methods 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 238000005507 spraying Methods 0.000 description 7
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- 239000001993 wax Substances 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 230000000903 blocking effect Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical class C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 239000002826 coolant Substances 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 239000002195 soluble material Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- MFYSYFVPBJMHGN-UHFFFAOYSA-N Cortisone Natural products O=C1CCC2(C)C3C(=O)CC(C)(C(CC4)(O)C(=O)CO)C4C3CCC2=C1 MFYSYFVPBJMHGN-UHFFFAOYSA-N 0.000 description 1
- VVNCNSJFMMFHPL-VKHMYHEASA-N D-penicillamine Chemical compound CC(C)(S)[C@@H](N)C(O)=O VVNCNSJFMMFHPL-VKHMYHEASA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000286209 Phasianidae Species 0.000 description 1
- YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- QYMGIIIPAFAFRX-UHFFFAOYSA-N butyl prop-2-enoate;ethene Chemical compound C=C.CCCCOC(=O)C=C QYMGIIIPAFAFRX-UHFFFAOYSA-N 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229940075911 depen Drugs 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- QHZOMAXECYYXGP-UHFFFAOYSA-N ethene;prop-2-enoic acid Chemical compound C=C.OC(=O)C=C QHZOMAXECYYXGP-UHFFFAOYSA-N 0.000 description 1
- 229920006226 ethylene-acrylic acid Polymers 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B63/00—Auxiliary devices, not otherwise provided for, for operating on articles or materials to be packaged
- B65B63/08—Auxiliary devices, not otherwise provided for, for operating on articles or materials to be packaged for heating or cooling articles or materials to facilitate packaging
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D65/00—Wrappers or flexible covers; Packaging materials of special type or form
- B65D65/38—Packaging materials of special type or form
- B65D65/46—Applications of disintegrable, dissolvable or edible materials
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Packaging Of Annular Or Rod-Shaped Articles, Wearing Apparel, Cassettes, Or The Like (AREA)
- Package Closures (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Making Paper Articles (AREA)
- Wrappers (AREA)
Abstract
In a process for the packaging of molten hot melt adhesive in a film cavity wherein the adhesive is filled into the cavity at a temperature above the melting point of the film and wherein the film cavity is in direct contact with a liquid or gaseous heat sink the improvement which comprises using as the film a heat sealable film at least a portion of which is water soluble.
Description
- 2154~7 This invention relates to a method for packaging hot melt adhesives compositions and to the resulting packaged adhesive compositions.
Hot melt adhesives which are generally applied while in the molten or liquid state are solid at room te",pe,dlure. Typically, these adhesives are provided in the form of blocks; however, because of the nature of these n,dle(ials there are p,.~l-. "s asso~ ed with handling and packaging them. The solid adhesive blocks not only stick or adhere to hands or mechan'~-' handling devices and to each other, but they also pick up dirt and other contaminants. Additionally, certain a~r' ~ ' -ns require high tack fommulations which result in blocks that will deform or cold flow unless suppo, led during shipment.
The need and advanldges for providing tackless or non-blocking hot melt adhesives are appar~:nt and various ways of acco"lpl ~'ning this have been developed.
Japanese Patent 48-103635 published Dece",t,er 26, 1973, cl: ~vloses a granular adhesive which is tacky at room tt:---pe-dture and coated or enveloped with a non-tacky hot ,.,o't~ ' 'o material that is the same type or is miscible or mixable with it.
French Patent 2,544,654 published October 26, 1984, ~lisclQses forrning a ~d~,kless hot melt by adding molten hot melt to a mold containing a preformed support layer having a transfer film thereon which is co"",dl;ble with the hot melt.
U.S. Patent Nos. 4,748,796 issued June 12, 1988, and 4,755,245 issued July 5, 1988, disclose fomming a protective coating for an adhesive material by ele~t,usldlically coating a mo!d or cavity with a powder screen and then pouring hot melt into the mold.
215 4~97 French Patent 2,601,616 published October 22, 1988, ~ oses forming blocks of hot melt pressure sensitive adhesives by casting the pressure sensitive adhesive into molds plt:co~led by spraying with a film of non self-sticking hot melt material thereby forming a fusible non-tacky veil around the pressure sensitive block.
5In German Patent 22 48 046 the hot melt adhesive is squeeze-cut into pillow-shaped pieces;
the pieces 5''hsequently cooled and s-' ' qe~
Still other patents teach coating or wrapping the formed hot melt block with various types of plastic films. Thus, German patents DE 31 38 222 and 32 34 065 disclose coating the circumference of elongdled hot melt portions with a thin polyolefin film. German patent 36 25 358 to Hausdorf teaches 10wrapping the solid hot melt block in a thellllopl~lic, especially copolyamide film with a melting point of 120C to 150C, while EP app' ~ 'icn 0 469 564 and WO 94/01330, both to Rouyer et al. Ilis~loses v"i~p: ,g the solidified hot melt in a plastic or biodegl_de ''- polymeric packaging material.
All the latter methods have provided some degree of improvement in the pack~g ng and handling of hot melt adhesives however they have suffered by virtue of either the need to unwrap or otherwise 15u"pachdge the hot melt or, in the cases of coated hot melts which are added directly to the melting pots, by virtue of the contamination resulting from the build up over time of large quantities of the pa-,hdyi"g ",d~e~;als in the melt pot and app"~ equipment.
In order to overcome the disadvallt~ges inherent in the methods of the prior art, U.S. Patent 5,401,455, issued March 28, 1995, d;,~,loses the finding that when the hot melt adhesive is poured in 20its molten state into a mold or cavity lined with plastic pa '~_ ,9 film and then allowed to solidify, the adhesive is fused to some extent into the film, resulting in a non-blocking adhesive pachage which will melt faster in the melt pot and will not cause a sub~ idl build-up of undesi-~' 'e plastic residue even after extended periods of time.
Since the melting point of the plastic film should be compa,~' 'e to, and p~:r~rably lower than, 25the melting point of the hot melt adl ,esivc in order to provide for s~ ory melting in the melt pot which does not have a source of agitation, it is necessary that the lined mold be in direct contact with a heat 21S~97 sink so as to remove excess heat from the film as quickly as possible and thereby prevent melting, buming or charring of the plastic film wrap.
An improvement on that method is described in U.S. Patent 5,373,682, issued December 20, 1994. According to that e" b" ' ~e~l, the molten adhesive is directly pumped or poured into a cy; ~lical plastic-tube, the cylindrical tube being in di-ect contact with the heat sin~ The resultant adhesive pa~,hdge is thus provided in a readily handleable cartridge form which may be produced in a continuous line ope,dlion and which a~ 'i'icnally plossesses all the ad~,a"t~ges ofthe easily p,uc s s ~'e non-blocking adhesive package of the parent a~ n.
While the methods desc~ ed in the cope~ " ~9 ~r~ ~ 'iOl~ have proved useful for packaging and re-melting of most hot melt adhesive formulations, there remain some:,, ' "- 15, for eAdlll, 'e for non-pressure sensitive adhesives, where ~ FP'-l9 during storage and shipping is unnecess~-y. There are also other eFF'ic "^ns where even sma~l amounts of unmelted film may create pr~bl? ,~s in the melt tank.
lt is ll,e,~ desirable in a limited number of ~"~ inns to provide hot melt adhesive po,li~ns in the convenient size and shape produced by the p,~cesses of the copending ap~ n but without any extemal pacl~ _ ,9 film.
Accor~ , to an aspect of the present invention, a process for the p~ ~ng of molten hot melt a&esive in a film cavity is provided wherein the a&esive is filled into the cavity at a lule above the m~ltir~ point of the film and ~.,.e~ the plastic film cavity is in direct contact with a liquid or gaseous heat sink the ~prvv~melll which co~ .. ;~,s using.as the film, a heat sealable film at least a portion of wllich is water soluble.
According to an embodiment of the invention the water soluble portion of the film co~ .ses polyvinyl alcohol, modified starch or cellulose. Accol~ding to an embodiment of the invention the entire surface of the film co..~l.. ;~; polyvinyl alcohol.
- Accol~ g to a~ ,l embodiment of the present invention the cavity cG.~ es a cylindrical tube of the heat sealable film. In a pIc~;llcd embodiment molten hot melt a&esive is filled into the cavity at a molten viscosity of l,OOO cps. to 200,000 cps.
~_ 215~497 , .
We have now found that when a heat s- '-' 'o film, at least a portion of which is water soluble, is utilized as the film, the molten adhesive can be effectively pa-,hdged using the procedures described previously. The water soluble film or portion thereof will then be slowly d;ssolved in a water bath, after which the resultant adhesive mass will be fully s.,''J'fied and may be packaged directly or may be s~hsequently coated with anti-stick ",dlerial~ using III~UIods conventional in the art The method of the present invention is ada~t ''e to the pac~ 9 of virtually any type of hot melt adhesive co"lposiuon. As eAdll, 'es the method disclosed herein may be used to pachage hot melt adhesives p~pal~d from polymers and copolymers of synthetic resins, rubbers, polyethylene, poly~n~ pjlene, polyurethane, acrylics, vinyl acetate, ethylene vinyl acetate and polyvinyl alcohol. More specific ~Adlll, 'S include hot melt adhesives pl~:pal~d from the r ":.~i.ly.
3a 2 1 ~ 7 a. rubber polymers such as block copolymers of monovinyl a,u",dtic hydrocarbons and conjugateddiene,e.g.,styrene-butadiene, styrene-but-" ne-styrene, styrene-isoprene-styrene, styrene-ethylene-butylene-styrene and styrene-ethylene propylene-styrene;
b. ethylene-vinyl acetate poly~,,ela~ other ethylene esters and copolymers, e.g., ethylene 5 ",etl,ac~ylate, ethylene n-butyl acrylate and ethylene acrylic acid;
c. polyolefins such as polyethylene and poly~,,u~,ylene;
d. polyvinyl acetate and random copolymers thereof;
e. polyacrylates;
f. polyamides;
9. polyesters;
h. polyvinyl alcohols and copolymers thereof;
i. polyurethanes;
j. polystyrenes;
k. polyepu~ides;
I. graft copoly",e,a of vinyl n,ono"~,(s) and polyalkylene ox'lde polymers; and m. ''hydecontainingresinssuchasphenol-aldehyde,urea-aldehyde,IIIeICA~ c~'~ehyde and the like.
Most often such adl,esives are formulated with tackifying resins in order to improve adhesion and introduce tack into the adl.cs.-e. Such resin indude, among other ",dt~rials, (a) natural and ",~ d 20 resins, (b) polyterpene resins, (c) phen~ ",o lified hyd~uca~l on resins, (d) coumarone-indene resins, (e) aliphatic and 'dl~llldtiC p~t,.' ~ ~n l"rd~-)cd,bon resins, (f) phthdldtt: esters and (g) hyd~gendled hydlu~,d,l,ons, I.~d~ugendled rosins and hydlugel,dled rosin esters.
Desi, ''- opffonal iny,~ r,ts include diluents, e.g., liquid polybutene orpolypropylene, pet,-' ~urn waxes such as paraffn and microcrystalline waxes, polyethylene greases, I"rd,ugend~ed animal, fish and 25 vegetable fats, mineral oil and synthetic waxes as well as hyd,ucd,~on oils such as napl~U, ~n~ or pd,drri".~ mineral oils.
'-. 215~g7 Other optional additives may include stabilizers alllioxiddlll:~ co!ard"l:, and fillers. The selection of components and amounts as well as the prepa,dlion thereof are well known in the art and described in the literature.
The heat s,e- - e water soluble film into which the molten adhesive is poured may be any film which will ~ , its integrity during filling but will suhsequently dissolve in water. Suitable materials include polyvinyl alcohol n,odi~ied sld~d~es cellulose films and the like. Polyvinyl alcohol hlms are the most preferred Rather than using the water soluble material as the entire hlm substrate in accordance with an alternative embodiment of the invention it is p~s- 'E that the film include a non-water soluble portion with the water soluble portion serving only as the vehicle to effect dissolution and separdtion of the film from the adhesive mass during the water cooling. In the case of hlms which comprise more than one material it is only necessary that the portion of the film which will provide the longitudinal lapped seal around the adhesive mass during the filling ope,dtion be heat see It may also be desi, e in the case of pressure sensitive adhesives to use a co",posite water soluble film la" Idted to a non-soluble coating the latter remaining on the adhesive mass and providing a cori",dtil)le tackless coating after d . ~ ution of the water soluble film. For eAdlllr ~ pressure sensitive masses may be so pachaged by using a lamination of an ethylene vinyl acetate coating on the polyvinyl alcohol film.
The tl, k.,ess of the film utilked generally varies between about 0.1 mil to 5 mil pl~ldbly 0.5 mil to 4 mil. The tl, k.,ess of the particular film also varies depending upon the te",perdlure at which the molten adhesive is pumped or poured into the plastic film cylinder. The particular viscosity at which the adl,e:,;ve can be introduced into the plastic film cylinder will vary depen~ ,9 on a variety of factors induding the pumping capacity of the pump the strength of then plastic film and the like. Visco~i~ies in the range of 1 000 to 200 000 cps pr~f~.dbly 2 000 to 100 000 may be utilized. I IuJ elcr we have found that the most p,t:fer~ed viscosity of the adhesive which is to be pa l~aged in accordance with the invention is b~tv een 10 000 and 50 000 cps. It will be l~coylli~ed that the l~",pe,dture at which an adhesive ~r"pos;tion will exhibit this viscosity range will vary from one adhesive to another. In the case of adhesives which obtain their viscosity within the tenlpe,dlure range of 110 to 130C, film thicknesses of about 1.25 mil are preferred; while for adhesives which exhibit this viscosity at temperatures of 130 to 150C, films of about 1.5 mil are plt:f~ d.
The heat sink may colllplise any means which will effectively and rapidly remove o~ absorb the 5 excess heat from the entire surface of the film which is in contad with the molten hot melt adhesive colll~.osition so as to prevent the lelll~eldlure of the film from exceeding its melting point even though the molten hot melt adhesive temperature is higher than the film melting temperature. Suitable heat sinks are provided by spraying the surface of the cylindrical plastic tube with cooled water or other ~rligel~lll means such as chilled glycol, liquid or g~seous nitrogen, colllpl~:ssed carbon dioxide or the like. The spraying may be accomr' hed, for exdr,l, 'e, using a series of spray nozzles aimed at the mandrel or a water or cooling ring or series of rings may be positioned around the mandrel so as to provide a curtain or ca~cade of water or r~:rliger~lll around the entire circumference of the cylinder.
As ~liscussed above, the molten adhesive is generally poured or pumped into the film cylinder at a tel I Ipera~ure at which the molten adhesive exhibits a viscosity of 1,000 to 200,000, pr~re, ~tly 10,000 to 50,000 cps. This lellq~er~lure will generally vary from about 110 to about 150C depending upon the particular adllesive. Since the adhesive is pumped or poured continuously through the mandrel into the film cylinder, it is possible to void and then cut the continuous filled tube into individual callridges at virtually any desired length. In general, the individual cal ll idges are produced in a variety of sizes ranging from about three inches to 18 inches in length and varying in weight, depending upon length, from about 20 0.5 to five pounds.
After filling, the adhesive cdll~idges, either individually orin a connected series, are further cooled in a water bath to ambient t~lllpelal-Jre so as to dissolve the film and solidify the adhesive. Depending upon the water soluble material used in the film, the film may begin to sepdldt~ from the adhesive and dissolve within about fifteen minutes after being placed in the water bath in which case any residual film 25 remaining after cooling can be removed by placing the adhesive cdlllidge in water of about 60C prior to bulk packaging. Some films may not be soluble in the cold water bath and, in such cases, when -- ` 215~497 removal of the plastic film is desired the s ' ~ ed packages are submerged in room temperature of slightly heated water until ~iss~ tion of the film occurs. In either case any residual amounts of film which remain may be readîly removed by passing the pa._hdges through a series of rotating brushes or using other scrubbing me.;l,ani;",ls. In the e",bodil"enl wherein the film co",prises a non-water soluble 5 component the It:fll_ ,9 film may be readily removed from the chilled water bath and may if desired be recycled. This emba 'i ~e~l has the additional advantage in that less of the water soluble polymer is present in the water bath thus pr~!an~' ,g the useful life thereof and producing less dissolved matter in the water when it is d:~rosed of. The pa- l~ges are then dried either under ambient condilions or using hot air knives or the like.
In the case of non-pressure sensitive adhesives the resultant ii~dividually packaged hot melt adhesive cd,llidges can be stored handled and used directly. In the case of pressure sensitive adhesives the s 'i~'i'ied adhesive ca,llidge may be treated with an anti-stick agent such for eAc",l~'e as by dipping or spraying with molten wax or other non-tacky cor"pdlible coating.
The resultant hot melt adhesive ~,l,idge may be pa._kaged in a conbiner to reduce its exposure 15 to the env;.on",enl moisture or other contaminants. The container or other v~"~pp ,gs would then be removed by conventional procedures prior to utilkation of the hot melt adhesive.
A prer~"ed e",L~ ' "ent of the method of the invention described herein is illustrated in Figure 1. In the Figure the water soluble film (1) is passed through a series of idler rollers (2) which smoothes the film and controls the tension across the web. The film is then ll"~aded into a film folder (3) which 20 folds the film and forms a lap seal around a one to four inch d;d",~ler fill pipe or mandrel (4). The lap seal is sealed with hot air (5) induction sealing or ultrasonic welding and then may be further sprayed with cooling air to set the seal.
After the seal has set the tubular film is carried along the exterior of the fill pipe p~rerdbly using a series of spreader rings (6) film guide(s) (7) and drive wheels (8) until it reaches the end of the fill 25 pipe at which point the molten hot melt adhesive pumped from a remote holding container through the mandrel enters the cylindrical tube (9). If desired in order to maintain the desired molten viscosity the 2151~97 .
hll pipe may be insulated or jacketed as with double walls and filled with inlet and outlet ports (10) through which heated water, steam or mixtures thereof may be circulated, so as to prevent premature cooling of the molten adhesive in the mandrel and melting of the plastic film on the mandrel. The double wall construction also ~ s con~r'~' ~ deaning and purging of the mandrel after the filling operation is completed.
During filling, the tubular package is in contact with cooling water (11) or other refrigerant medium. This water contact may be acco,l, ' hed using a series of water 3ets positioned around the circumference of the cylind-ical tube. Altematively, a water or cooling ring (12) or series of water or cooling rings may be positioned around the mandrel. It will be recognized that while the term "spraying with coolant" is utilked herein, the invention also cort~"lpldles carrying out the entire filling opeldlion in a cooled env;.onllælll as in the pl~:sence of liquid nitrogen.
Suhsequently, the adhesive filled tube is passed through voider rolls (13) which crimp or pinch the continuous filled cylinder into smaller cd,(,idge sked seyllæn(s and which are set so as to assure the proper Cdl Uidge length. Spraying with coolant is continued through additional spray nozles (14) until the pa-,hage is sufficiently cooled so that the pa~ ged adhesive forms a self-seal formed at the voided porbons. The cdlt,idge pa~ ges may then be cut at the voided area using conventional means, e.g., "e.,han - ' scissor (15), laser cutter, water jet or a heated knife or wire and subsequently cooled to room telllpe.d(ure in a water bath. Altematively, the voided but uncut call,idge segments, still attached in serial form may be cooled and cut Uleredrl~r.
As cliscussed above, the film may be dissolved in the cooling water bath itself or may be subsequently dissolved in a sepaldle water bath prior to final pa-,h~ 9.
~ 215~497 ` While the invention has been specifically described with respect to the continuous hlling of adhesive cartridges claimed in U.S.-ar~ n Serial No. 07/993,890, it is equally adapt ''e to the method described in pending f~rP'~ n Serial No. 07/883,994, wherein a mold, preferably a mesh screen mold, is lined with the water soluble film and the molten adhesive poured therein all the while ,l ,la;" ,9 the mold in contact with a heat sink.
In accordance with the latter embodiment, the mold into which the the""oplaalic film is placed and into which the molten adhesive is to be poured may comprise any rigid, self-supporting material The molds are generally forrned from rigid plastic, e.g., acrylonitrile/butadiene/styrene polymers or polypropylene orfrom metallic s(Jbslldles. Since it is desirable to keep the film in direct contact with the water bath after filling, the use of pe,tu,dled or otherwise apertured molds is desired. A particularly preferred mold is formed from steel mesh. The size of the mold varies according to the size of the desired hot melt adhesive block. In general each mold is app,uxi",dl~ly 3" x 3" x 11" in di",ension and often a series of molds are formed from one contiguous plastic m -'lulosic or metal sheet.
Fur~er details of the pl~,f~l~d çmbotlimP.nt~ of the invention are ;llustrated in the follo~nng F,Y~mples. The Exarnples are p~so~ d for the ~ ose of illusl~ation of the invention and are not intPn-lP, i to be l;...;l;~ of the invention as defined in the appended claims.
A conve~ltiohal pressure sensitilc hot melt adhesive co",position suitable for dispcs.''e ar F ' - 'i~ ns was p~ ~:pared using a ta ,hilied and pl ~ ; ed blend of ethylene vinyl acetate copobmer and wax.
A continuous supported cylindrical tube was formed by vnat~,~ ,g a plastic film co~prising a 1.2 mil p olyvinyl alcohol film around a 1.5 inch d;d",t:ler insulated mandrel or fill pipe. After the lap seam was formed, it was sealed using hot air and then set by spraying with ambient l~llq)eldlure air.
The molten hot melt adhesive, at a viscosity of 10,û00-15,000 cps. (120-130C) was pumped therein through a nozle while the entire surface of the film was sprayed with chilled water (5-1 0C). The filled tubes were voided at lengths of 6 inches and then cut to form individual cartridges. The resultant ca,l,idges were allowed to cool in a chilled water bath until they had co"., '~t ~y s 3 '~e~l The resultant cd,l-idges were lldllat~ d to a hot water bath (about 65C.) where the film was dii,solved and the blocks then removed, dried and packed in dp~JIuplidle shipping co"l~ 1e,a.
., The procedure of Example 1 was repeated to package a pressure sensitive hot melt adhesive composition suitable for can/bottle labelling app'i~ ns.
After transfer to the hot water bath, the film was d;ssolved, the adhesive removed, dried and then 5 passed to a tank COIlbdi~ 9 a molten COlllr ~ !e wax material. The block was dipped into the tank, the surplus material allowed to run off, dried and packed to the shipping container. The outer coating thus fommed a non-tacky wax coating co"lF "' !e with the adhesive.
The procedure of Example I may also be repeated using film which consi~ts of low density 10 polyethylene film with a strip of polyvinyl alcohol film adhered to one side wherein the polyvinyl alcohol strip co",prises about 20% of the surface area of the film. After, ~;~ sn'ution of the polyvinyl alcohol portion of the film, the remaining low density polyethylene may be readily peeled off the caill idge.
Testing of the resultant ca,l,i~ges indicates that the adhesive properties of the adhesive blocks are ~"drr~l~d by the filling and pac~ "9 process. Similar results would also be obtained when 15 packaging other hot melt adhesive forrnulations.
Although prGrG~ d embo~ x of the invention have been described herein, it w~ll be lm-l.orstood by those skilled in the art that variations, modifications, and equ;valents may be made thereto wi~ ul departing from the sp~r~t of the invention or the scope of the appended claims.
Hot melt adhesives which are generally applied while in the molten or liquid state are solid at room te",pe,dlure. Typically, these adhesives are provided in the form of blocks; however, because of the nature of these n,dle(ials there are p,.~l-. "s asso~ ed with handling and packaging them. The solid adhesive blocks not only stick or adhere to hands or mechan'~-' handling devices and to each other, but they also pick up dirt and other contaminants. Additionally, certain a~r' ~ ' -ns require high tack fommulations which result in blocks that will deform or cold flow unless suppo, led during shipment.
The need and advanldges for providing tackless or non-blocking hot melt adhesives are appar~:nt and various ways of acco"lpl ~'ning this have been developed.
Japanese Patent 48-103635 published Dece",t,er 26, 1973, cl: ~vloses a granular adhesive which is tacky at room tt:---pe-dture and coated or enveloped with a non-tacky hot ,.,o't~ ' 'o material that is the same type or is miscible or mixable with it.
French Patent 2,544,654 published October 26, 1984, ~lisclQses forrning a ~d~,kless hot melt by adding molten hot melt to a mold containing a preformed support layer having a transfer film thereon which is co"",dl;ble with the hot melt.
U.S. Patent Nos. 4,748,796 issued June 12, 1988, and 4,755,245 issued July 5, 1988, disclose fomming a protective coating for an adhesive material by ele~t,usldlically coating a mo!d or cavity with a powder screen and then pouring hot melt into the mold.
215 4~97 French Patent 2,601,616 published October 22, 1988, ~ oses forming blocks of hot melt pressure sensitive adhesives by casting the pressure sensitive adhesive into molds plt:co~led by spraying with a film of non self-sticking hot melt material thereby forming a fusible non-tacky veil around the pressure sensitive block.
5In German Patent 22 48 046 the hot melt adhesive is squeeze-cut into pillow-shaped pieces;
the pieces 5''hsequently cooled and s-' ' qe~
Still other patents teach coating or wrapping the formed hot melt block with various types of plastic films. Thus, German patents DE 31 38 222 and 32 34 065 disclose coating the circumference of elongdled hot melt portions with a thin polyolefin film. German patent 36 25 358 to Hausdorf teaches 10wrapping the solid hot melt block in a thellllopl~lic, especially copolyamide film with a melting point of 120C to 150C, while EP app' ~ 'icn 0 469 564 and WO 94/01330, both to Rouyer et al. Ilis~loses v"i~p: ,g the solidified hot melt in a plastic or biodegl_de ''- polymeric packaging material.
All the latter methods have provided some degree of improvement in the pack~g ng and handling of hot melt adhesives however they have suffered by virtue of either the need to unwrap or otherwise 15u"pachdge the hot melt or, in the cases of coated hot melts which are added directly to the melting pots, by virtue of the contamination resulting from the build up over time of large quantities of the pa-,hdyi"g ",d~e~;als in the melt pot and app"~ equipment.
In order to overcome the disadvallt~ges inherent in the methods of the prior art, U.S. Patent 5,401,455, issued March 28, 1995, d;,~,loses the finding that when the hot melt adhesive is poured in 20its molten state into a mold or cavity lined with plastic pa '~_ ,9 film and then allowed to solidify, the adhesive is fused to some extent into the film, resulting in a non-blocking adhesive pachage which will melt faster in the melt pot and will not cause a sub~ idl build-up of undesi-~' 'e plastic residue even after extended periods of time.
Since the melting point of the plastic film should be compa,~' 'e to, and p~:r~rably lower than, 25the melting point of the hot melt adl ,esivc in order to provide for s~ ory melting in the melt pot which does not have a source of agitation, it is necessary that the lined mold be in direct contact with a heat 21S~97 sink so as to remove excess heat from the film as quickly as possible and thereby prevent melting, buming or charring of the plastic film wrap.
An improvement on that method is described in U.S. Patent 5,373,682, issued December 20, 1994. According to that e" b" ' ~e~l, the molten adhesive is directly pumped or poured into a cy; ~lical plastic-tube, the cylindrical tube being in di-ect contact with the heat sin~ The resultant adhesive pa~,hdge is thus provided in a readily handleable cartridge form which may be produced in a continuous line ope,dlion and which a~ 'i'icnally plossesses all the ad~,a"t~ges ofthe easily p,uc s s ~'e non-blocking adhesive package of the parent a~ n.
While the methods desc~ ed in the cope~ " ~9 ~r~ ~ 'iOl~ have proved useful for packaging and re-melting of most hot melt adhesive formulations, there remain some:,, ' "- 15, for eAdlll, 'e for non-pressure sensitive adhesives, where ~ FP'-l9 during storage and shipping is unnecess~-y. There are also other eFF'ic "^ns where even sma~l amounts of unmelted film may create pr~bl? ,~s in the melt tank.
lt is ll,e,~ desirable in a limited number of ~"~ inns to provide hot melt adhesive po,li~ns in the convenient size and shape produced by the p,~cesses of the copending ap~ n but without any extemal pacl~ _ ,9 film.
Accor~ , to an aspect of the present invention, a process for the p~ ~ng of molten hot melt a&esive in a film cavity is provided wherein the a&esive is filled into the cavity at a lule above the m~ltir~ point of the film and ~.,.e~ the plastic film cavity is in direct contact with a liquid or gaseous heat sink the ~prvv~melll which co~ .. ;~,s using.as the film, a heat sealable film at least a portion of wllich is water soluble.
According to an embodiment of the invention the water soluble portion of the film co~ .ses polyvinyl alcohol, modified starch or cellulose. Accol~ding to an embodiment of the invention the entire surface of the film co..~l.. ;~; polyvinyl alcohol.
- Accol~ g to a~ ,l embodiment of the present invention the cavity cG.~ es a cylindrical tube of the heat sealable film. In a pIc~;llcd embodiment molten hot melt a&esive is filled into the cavity at a molten viscosity of l,OOO cps. to 200,000 cps.
~_ 215~497 , .
We have now found that when a heat s- '-' 'o film, at least a portion of which is water soluble, is utilized as the film, the molten adhesive can be effectively pa-,hdged using the procedures described previously. The water soluble film or portion thereof will then be slowly d;ssolved in a water bath, after which the resultant adhesive mass will be fully s.,''J'fied and may be packaged directly or may be s~hsequently coated with anti-stick ",dlerial~ using III~UIods conventional in the art The method of the present invention is ada~t ''e to the pac~ 9 of virtually any type of hot melt adhesive co"lposiuon. As eAdll, 'es the method disclosed herein may be used to pachage hot melt adhesives p~pal~d from polymers and copolymers of synthetic resins, rubbers, polyethylene, poly~n~ pjlene, polyurethane, acrylics, vinyl acetate, ethylene vinyl acetate and polyvinyl alcohol. More specific ~Adlll, 'S include hot melt adhesives pl~:pal~d from the r ":.~i.ly.
3a 2 1 ~ 7 a. rubber polymers such as block copolymers of monovinyl a,u",dtic hydrocarbons and conjugateddiene,e.g.,styrene-butadiene, styrene-but-" ne-styrene, styrene-isoprene-styrene, styrene-ethylene-butylene-styrene and styrene-ethylene propylene-styrene;
b. ethylene-vinyl acetate poly~,,ela~ other ethylene esters and copolymers, e.g., ethylene 5 ",etl,ac~ylate, ethylene n-butyl acrylate and ethylene acrylic acid;
c. polyolefins such as polyethylene and poly~,,u~,ylene;
d. polyvinyl acetate and random copolymers thereof;
e. polyacrylates;
f. polyamides;
9. polyesters;
h. polyvinyl alcohols and copolymers thereof;
i. polyurethanes;
j. polystyrenes;
k. polyepu~ides;
I. graft copoly",e,a of vinyl n,ono"~,(s) and polyalkylene ox'lde polymers; and m. ''hydecontainingresinssuchasphenol-aldehyde,urea-aldehyde,IIIeICA~ c~'~ehyde and the like.
Most often such adl,esives are formulated with tackifying resins in order to improve adhesion and introduce tack into the adl.cs.-e. Such resin indude, among other ",dt~rials, (a) natural and ",~ d 20 resins, (b) polyterpene resins, (c) phen~ ",o lified hyd~uca~l on resins, (d) coumarone-indene resins, (e) aliphatic and 'dl~llldtiC p~t,.' ~ ~n l"rd~-)cd,bon resins, (f) phthdldtt: esters and (g) hyd~gendled hydlu~,d,l,ons, I.~d~ugendled rosins and hydlugel,dled rosin esters.
Desi, ''- opffonal iny,~ r,ts include diluents, e.g., liquid polybutene orpolypropylene, pet,-' ~urn waxes such as paraffn and microcrystalline waxes, polyethylene greases, I"rd,ugend~ed animal, fish and 25 vegetable fats, mineral oil and synthetic waxes as well as hyd,ucd,~on oils such as napl~U, ~n~ or pd,drri".~ mineral oils.
'-. 215~g7 Other optional additives may include stabilizers alllioxiddlll:~ co!ard"l:, and fillers. The selection of components and amounts as well as the prepa,dlion thereof are well known in the art and described in the literature.
The heat s,e- - e water soluble film into which the molten adhesive is poured may be any film which will ~ , its integrity during filling but will suhsequently dissolve in water. Suitable materials include polyvinyl alcohol n,odi~ied sld~d~es cellulose films and the like. Polyvinyl alcohol hlms are the most preferred Rather than using the water soluble material as the entire hlm substrate in accordance with an alternative embodiment of the invention it is p~s- 'E that the film include a non-water soluble portion with the water soluble portion serving only as the vehicle to effect dissolution and separdtion of the film from the adhesive mass during the water cooling. In the case of hlms which comprise more than one material it is only necessary that the portion of the film which will provide the longitudinal lapped seal around the adhesive mass during the filling ope,dtion be heat see It may also be desi, e in the case of pressure sensitive adhesives to use a co",posite water soluble film la" Idted to a non-soluble coating the latter remaining on the adhesive mass and providing a cori",dtil)le tackless coating after d . ~ ution of the water soluble film. For eAdlllr ~ pressure sensitive masses may be so pachaged by using a lamination of an ethylene vinyl acetate coating on the polyvinyl alcohol film.
The tl, k.,ess of the film utilked generally varies between about 0.1 mil to 5 mil pl~ldbly 0.5 mil to 4 mil. The tl, k.,ess of the particular film also varies depending upon the te",perdlure at which the molten adhesive is pumped or poured into the plastic film cylinder. The particular viscosity at which the adl,e:,;ve can be introduced into the plastic film cylinder will vary depen~ ,9 on a variety of factors induding the pumping capacity of the pump the strength of then plastic film and the like. Visco~i~ies in the range of 1 000 to 200 000 cps pr~f~.dbly 2 000 to 100 000 may be utilized. I IuJ elcr we have found that the most p,t:fer~ed viscosity of the adhesive which is to be pa l~aged in accordance with the invention is b~tv een 10 000 and 50 000 cps. It will be l~coylli~ed that the l~",pe,dture at which an adhesive ~r"pos;tion will exhibit this viscosity range will vary from one adhesive to another. In the case of adhesives which obtain their viscosity within the tenlpe,dlure range of 110 to 130C, film thicknesses of about 1.25 mil are preferred; while for adhesives which exhibit this viscosity at temperatures of 130 to 150C, films of about 1.5 mil are plt:f~ d.
The heat sink may colllplise any means which will effectively and rapidly remove o~ absorb the 5 excess heat from the entire surface of the film which is in contad with the molten hot melt adhesive colll~.osition so as to prevent the lelll~eldlure of the film from exceeding its melting point even though the molten hot melt adhesive temperature is higher than the film melting temperature. Suitable heat sinks are provided by spraying the surface of the cylindrical plastic tube with cooled water or other ~rligel~lll means such as chilled glycol, liquid or g~seous nitrogen, colllpl~:ssed carbon dioxide or the like. The spraying may be accomr' hed, for exdr,l, 'e, using a series of spray nozzles aimed at the mandrel or a water or cooling ring or series of rings may be positioned around the mandrel so as to provide a curtain or ca~cade of water or r~:rliger~lll around the entire circumference of the cylinder.
As ~liscussed above, the molten adhesive is generally poured or pumped into the film cylinder at a tel I Ipera~ure at which the molten adhesive exhibits a viscosity of 1,000 to 200,000, pr~re, ~tly 10,000 to 50,000 cps. This lellq~er~lure will generally vary from about 110 to about 150C depending upon the particular adllesive. Since the adhesive is pumped or poured continuously through the mandrel into the film cylinder, it is possible to void and then cut the continuous filled tube into individual callridges at virtually any desired length. In general, the individual cal ll idges are produced in a variety of sizes ranging from about three inches to 18 inches in length and varying in weight, depending upon length, from about 20 0.5 to five pounds.
After filling, the adhesive cdll~idges, either individually orin a connected series, are further cooled in a water bath to ambient t~lllpelal-Jre so as to dissolve the film and solidify the adhesive. Depending upon the water soluble material used in the film, the film may begin to sepdldt~ from the adhesive and dissolve within about fifteen minutes after being placed in the water bath in which case any residual film 25 remaining after cooling can be removed by placing the adhesive cdlllidge in water of about 60C prior to bulk packaging. Some films may not be soluble in the cold water bath and, in such cases, when -- ` 215~497 removal of the plastic film is desired the s ' ~ ed packages are submerged in room temperature of slightly heated water until ~iss~ tion of the film occurs. In either case any residual amounts of film which remain may be readîly removed by passing the pa._hdges through a series of rotating brushes or using other scrubbing me.;l,ani;",ls. In the e",bodil"enl wherein the film co",prises a non-water soluble 5 component the It:fll_ ,9 film may be readily removed from the chilled water bath and may if desired be recycled. This emba 'i ~e~l has the additional advantage in that less of the water soluble polymer is present in the water bath thus pr~!an~' ,g the useful life thereof and producing less dissolved matter in the water when it is d:~rosed of. The pa- l~ges are then dried either under ambient condilions or using hot air knives or the like.
In the case of non-pressure sensitive adhesives the resultant ii~dividually packaged hot melt adhesive cd,llidges can be stored handled and used directly. In the case of pressure sensitive adhesives the s 'i~'i'ied adhesive ca,llidge may be treated with an anti-stick agent such for eAc",l~'e as by dipping or spraying with molten wax or other non-tacky cor"pdlible coating.
The resultant hot melt adhesive ~,l,idge may be pa._kaged in a conbiner to reduce its exposure 15 to the env;.on",enl moisture or other contaminants. The container or other v~"~pp ,gs would then be removed by conventional procedures prior to utilkation of the hot melt adhesive.
A prer~"ed e",L~ ' "ent of the method of the invention described herein is illustrated in Figure 1. In the Figure the water soluble film (1) is passed through a series of idler rollers (2) which smoothes the film and controls the tension across the web. The film is then ll"~aded into a film folder (3) which 20 folds the film and forms a lap seal around a one to four inch d;d",~ler fill pipe or mandrel (4). The lap seal is sealed with hot air (5) induction sealing or ultrasonic welding and then may be further sprayed with cooling air to set the seal.
After the seal has set the tubular film is carried along the exterior of the fill pipe p~rerdbly using a series of spreader rings (6) film guide(s) (7) and drive wheels (8) until it reaches the end of the fill 25 pipe at which point the molten hot melt adhesive pumped from a remote holding container through the mandrel enters the cylindrical tube (9). If desired in order to maintain the desired molten viscosity the 2151~97 .
hll pipe may be insulated or jacketed as with double walls and filled with inlet and outlet ports (10) through which heated water, steam or mixtures thereof may be circulated, so as to prevent premature cooling of the molten adhesive in the mandrel and melting of the plastic film on the mandrel. The double wall construction also ~ s con~r'~' ~ deaning and purging of the mandrel after the filling operation is completed.
During filling, the tubular package is in contact with cooling water (11) or other refrigerant medium. This water contact may be acco,l, ' hed using a series of water 3ets positioned around the circumference of the cylind-ical tube. Altematively, a water or cooling ring (12) or series of water or cooling rings may be positioned around the mandrel. It will be recognized that while the term "spraying with coolant" is utilked herein, the invention also cort~"lpldles carrying out the entire filling opeldlion in a cooled env;.onllælll as in the pl~:sence of liquid nitrogen.
Suhsequently, the adhesive filled tube is passed through voider rolls (13) which crimp or pinch the continuous filled cylinder into smaller cd,(,idge sked seyllæn(s and which are set so as to assure the proper Cdl Uidge length. Spraying with coolant is continued through additional spray nozles (14) until the pa-,hage is sufficiently cooled so that the pa~ ged adhesive forms a self-seal formed at the voided porbons. The cdlt,idge pa~ ges may then be cut at the voided area using conventional means, e.g., "e.,han - ' scissor (15), laser cutter, water jet or a heated knife or wire and subsequently cooled to room telllpe.d(ure in a water bath. Altematively, the voided but uncut call,idge segments, still attached in serial form may be cooled and cut Uleredrl~r.
As cliscussed above, the film may be dissolved in the cooling water bath itself or may be subsequently dissolved in a sepaldle water bath prior to final pa-,h~ 9.
~ 215~497 ` While the invention has been specifically described with respect to the continuous hlling of adhesive cartridges claimed in U.S.-ar~ n Serial No. 07/993,890, it is equally adapt ''e to the method described in pending f~rP'~ n Serial No. 07/883,994, wherein a mold, preferably a mesh screen mold, is lined with the water soluble film and the molten adhesive poured therein all the while ,l ,la;" ,9 the mold in contact with a heat sink.
In accordance with the latter embodiment, the mold into which the the""oplaalic film is placed and into which the molten adhesive is to be poured may comprise any rigid, self-supporting material The molds are generally forrned from rigid plastic, e.g., acrylonitrile/butadiene/styrene polymers or polypropylene orfrom metallic s(Jbslldles. Since it is desirable to keep the film in direct contact with the water bath after filling, the use of pe,tu,dled or otherwise apertured molds is desired. A particularly preferred mold is formed from steel mesh. The size of the mold varies according to the size of the desired hot melt adhesive block. In general each mold is app,uxi",dl~ly 3" x 3" x 11" in di",ension and often a series of molds are formed from one contiguous plastic m -'lulosic or metal sheet.
Fur~er details of the pl~,f~l~d çmbotlimP.nt~ of the invention are ;llustrated in the follo~nng F,Y~mples. The Exarnples are p~so~ d for the ~ ose of illusl~ation of the invention and are not intPn-lP, i to be l;...;l;~ of the invention as defined in the appended claims.
A conve~ltiohal pressure sensitilc hot melt adhesive co",position suitable for dispcs.''e ar F ' - 'i~ ns was p~ ~:pared using a ta ,hilied and pl ~ ; ed blend of ethylene vinyl acetate copobmer and wax.
A continuous supported cylindrical tube was formed by vnat~,~ ,g a plastic film co~prising a 1.2 mil p olyvinyl alcohol film around a 1.5 inch d;d",t:ler insulated mandrel or fill pipe. After the lap seam was formed, it was sealed using hot air and then set by spraying with ambient l~llq)eldlure air.
The molten hot melt adhesive, at a viscosity of 10,û00-15,000 cps. (120-130C) was pumped therein through a nozle while the entire surface of the film was sprayed with chilled water (5-1 0C). The filled tubes were voided at lengths of 6 inches and then cut to form individual cartridges. The resultant ca,l,idges were allowed to cool in a chilled water bath until they had co"., '~t ~y s 3 '~e~l The resultant cd,l-idges were lldllat~ d to a hot water bath (about 65C.) where the film was dii,solved and the blocks then removed, dried and packed in dp~JIuplidle shipping co"l~ 1e,a.
., The procedure of Example 1 was repeated to package a pressure sensitive hot melt adhesive composition suitable for can/bottle labelling app'i~ ns.
After transfer to the hot water bath, the film was d;ssolved, the adhesive removed, dried and then 5 passed to a tank COIlbdi~ 9 a molten COlllr ~ !e wax material. The block was dipped into the tank, the surplus material allowed to run off, dried and packed to the shipping container. The outer coating thus fommed a non-tacky wax coating co"lF "' !e with the adhesive.
The procedure of Example I may also be repeated using film which consi~ts of low density 10 polyethylene film with a strip of polyvinyl alcohol film adhered to one side wherein the polyvinyl alcohol strip co",prises about 20% of the surface area of the film. After, ~;~ sn'ution of the polyvinyl alcohol portion of the film, the remaining low density polyethylene may be readily peeled off the caill idge.
Testing of the resultant ca,l,i~ges indicates that the adhesive properties of the adhesive blocks are ~"drr~l~d by the filling and pac~ "9 process. Similar results would also be obtained when 15 packaging other hot melt adhesive forrnulations.
Although prGrG~ d embo~ x of the invention have been described herein, it w~ll be lm-l.orstood by those skilled in the art that variations, modifications, and equ;valents may be made thereto wi~ ul departing from the sp~r~t of the invention or the scope of the appended claims.
Claims (13)
1. In a process for the packaging of molten hot melt adhesive in a film cavity wherein the adhesive is filled into the cavity at a temperature above the melting point of the film and wherein the plastic film cavity is in direct contact with a liquid or gaseous heat sink the improvement which comprises using as the film a heat sealable film at least a portion of which is water soluble.
2. The process of Claim 1 wherein the water soluble portion of the film comprises polyvinyl alcohol modified starch or cellulose.
3. The process of Claim 2 wherein the water soluble portion of the film comprises polyvinyl alcohol.
4. The process of Claim 1 wherein the entire surface of the film comprises polyvinyl alcohol.
5. The process of Claim 1 wherein the film comprises a lamination of a water soluble film laminated to a non-soluble coating.
6. The process of Claim 5 wherein the film comprises an ethylene vinyl acetate coating on a polyvinyl alcohol film.
7. The process of Claim 1 wherein the cavity comprises a cylindrical tube of the heat sealable film.
8. The process of Claim 1 wherein the molten hot melt adhesive is filled into the cavity at a molten viscosity of 1 000 cps. to 200 000 cps.
9. The process of Claim 1 wherein the film is present in an amount of 0.2 to 1.0% by weight of the adhesive mass.
10. The process of Claim 1 wherein the hot melt adhesive is non-pressure sensitive.
11. The process of Claim 1 wherein the hot melt adhesive is pressure sensitive and wherein the adhesive mass, after dissolution and removal of the water soluble film is coated with a compatible non-tacky coating material.
12. The process of Claim 1 wherein the molten adhesive is poured into the film cylinder at a temperature of 110-130°C. and wherein the thickness of the film is 1.25 mil.
13. The process of Claim 1 wherein the molten adhesive is poured into the film cylinder at a temperature of 130-150°C and wherein the thickness of the film is 1.5 mil.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US28959694A | 1994-08-12 | 1994-08-12 | |
US08/289,596 | 1994-08-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2154497A1 true CA2154497A1 (en) | 1996-02-13 |
Family
ID=23112229
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002154497A Abandoned CA2154497A1 (en) | 1994-08-12 | 1995-08-10 | Production technique for blocks of hot melt adhesives |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0699586A1 (en) |
JP (1) | JPH0892531A (en) |
KR (1) | KR960007132A (en) |
AU (1) | AU672555B2 (en) |
CA (1) | CA2154497A1 (en) |
NO (1) | NO952682L (en) |
TW (1) | TW298582B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19720705A1 (en) * | 1997-05-16 | 1998-11-19 | Basf Ag | Method and device for producing pressure sensitive adhesive tapes |
DE19913034A1 (en) * | 1998-05-13 | 1999-11-18 | Henkel Kgaa | Packaging of hot-melt adhesive |
DE10054836C2 (en) * | 2000-11-04 | 2002-11-07 | Vermee Frans Gmbh | Device for cooling packaging |
GB2410209B (en) * | 2002-01-26 | 2005-12-14 | Aquasol Ltd | Improvements in or relating to devices |
US7350644B2 (en) * | 2002-10-21 | 2008-04-01 | National Starch And Chemical Investment Holding Corporation | Multi-layer film packaging of hot melt adhesive |
DE102018219353A1 (en) * | 2018-11-13 | 2020-05-14 | Tesa Se | Packed viscoelastic polymer mass |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
LU62159A1 (en) * | 1970-11-30 | 1971-11-09 | ||
JPS48103635A (en) | 1972-04-12 | 1973-12-26 | ||
MX151028A (en) * | 1978-11-17 | 1984-09-11 | Unilever Nv | IMPROVEMENTS IN INSOLUBLE BAG BUT PERMEABLE TO WATER THAT HAS A DISPERSIBLE PROTECTIVE LAYER OR SOLUBLE IN WATER, WHICH CONTAINS A PARTICULATE DETERGENT COMPOSITION |
DE3138222C1 (en) | 1981-09-25 | 1983-05-19 | Dr. Rudolf Schieber Chemische Fabrik GmbH & Co KG, 7085 Bopfingen | Release means for producing strands of hot-melt adhesive |
DE3234065A1 (en) | 1981-09-25 | 1983-04-14 | Dr. Rudolf Schieber Chemische Fabrik GmbH & Co KG, 7085 Bopfingen | Process for treating pressure-sensitive hot melt plastics produced in mixing units |
SE454168B (en) * | 1982-09-27 | 1988-04-11 | Tetra Pak Ab | SET AND DEVICE FOR DOSING OF FILLED GOODS IN THE MANUFACTURE OF PACKAGING CONTAINERS |
FR2541930B1 (en) | 1983-03-01 | 1985-07-26 | Ceresines Belix Ste Nle Raffin | PROCESS FOR PACKAGING IN BLOCK OR PROFILE FORM OF A PERMANENT ADHESIVE COMPOSITION, INSTALLATION FOR AND PACKAGING OBTAINED BY IMPLEMENTING THIS PROCESS |
FR2541966B1 (en) | 1983-03-01 | 1986-05-16 | Ceresines Belix Ste Nle Raffin | PACKAGING PROCESS IN A HONEYCOMB TRAY OF A PERMANENT ADHESIVE COMPOSITION, INSTALLATION FOR AND PACKAGING OBTAINED BY THE IMPLEMENTATION OF THIS PROCESS |
FR2544654B1 (en) | 1983-04-21 | 1985-11-22 | Keller Dorian Papiers | PROCESS AND MEANS FOR PACKAGING A SOLID OR PASTY PRODUCT HAVING A STICKY POWER AND NEW PRODUCT OBTAINED |
GB8607934D0 (en) * | 1986-04-01 | 1986-05-08 | Ball A C | Packaging |
FR2601616B1 (en) | 1986-07-21 | 1989-06-02 | Ceca Sa | NEW PROCESS FOR OBTAINING SELF-ADHESIVE BLOCKS WITH NON-ADHESIVE SURFACE. |
DE3625358A1 (en) | 1986-07-26 | 1988-02-04 | H & H Hausdorf Ohg | Process for processing of viscous compositions, for example hot-melt adhesives |
RU2096277C1 (en) | 1990-08-01 | 1997-11-20 | Х.Б.Фуллер Лайсенсинг энд Файнэнсинг Инк. | Glueing composition packing method (versions) and packed glueing composition (versions) |
AU639855B2 (en) * | 1991-06-11 | 1993-08-05 | Orihiro Co., Ltd. | Vertical type forming, filling and closing machine for flexible package |
BR9306378A (en) | 1992-05-18 | 1998-09-01 | Nat Starch Chem Invest | Process for packaging hot melt adhesive compositions and non-blocking hot melt adhesive |
US5373682A (en) | 1992-05-18 | 1994-12-20 | National Starch And Chemical Investment Holding Corporation | Method for tackless packaging of hot melt adhesives |
ES2106358T3 (en) | 1992-07-06 | 1997-11-01 | Fuller H B Licensing Financ | A METHOD FOR PACKAGING AN ADHESIVE COMPOSITION AND THE COMPOSITION OF PACKAGING MATERIAL. |
DE670765T1 (en) * | 1992-12-09 | 1996-01-18 | National Starch And Chemical Investment Holding Corp., Wilmington, Del. | PACKAGING METHOD OF MELTABLE ADHESIVES. |
JP2741564B2 (en) * | 1993-01-25 | 1998-04-22 | アイセロ化学 株式会社 | Composite film bag for packaging |
-
1995
- 1995-06-16 AU AU21740/95A patent/AU672555B2/en not_active Ceased
- 1995-07-06 NO NO952682A patent/NO952682L/en unknown
- 1995-08-09 KR KR1019950024493A patent/KR960007132A/en not_active Application Discontinuation
- 1995-08-09 TW TW084108306A patent/TW298582B/zh active
- 1995-08-10 CA CA002154497A patent/CA2154497A1/en not_active Abandoned
- 1995-08-10 EP EP95110096A patent/EP0699586A1/en not_active Withdrawn
- 1995-08-14 JP JP7207066A patent/JPH0892531A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
EP0699586A1 (en) | 1996-03-06 |
NO952682D0 (en) | 1995-07-06 |
KR960007132A (en) | 1996-03-22 |
AU2174095A (en) | 1996-04-18 |
TW298582B (en) | 1997-02-21 |
AU672555B2 (en) | 1996-10-03 |
NO952682L (en) | 1996-02-13 |
JPH0892531A (en) | 1996-04-09 |
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