US20040250516A1 - Foamed adhesive and applications thereof - Google Patents
Foamed adhesive and applications thereof Download PDFInfo
- Publication number
- US20040250516A1 US20040250516A1 US10/462,183 US46218303A US2004250516A1 US 20040250516 A1 US20040250516 A1 US 20040250516A1 US 46218303 A US46218303 A US 46218303A US 2004250516 A1 US2004250516 A1 US 2004250516A1
- Authority
- US
- United States
- Prior art keywords
- adhesive
- bag
- container
- foamed
- heat
- 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
- 239000000853 adhesive Substances 0.000 title claims abstract description 105
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 105
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 238000000034 method Methods 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 239000000839 emulsion Substances 0.000 claims description 12
- 238000004806 packaging method and process Methods 0.000 claims description 11
- 239000004615 ingredient Substances 0.000 claims description 10
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 7
- 241000482268 Zea mays subsp. mays Species 0.000 claims description 7
- 229920001169 thermoplastic Polymers 0.000 claims description 6
- 239000004416 thermosoftening plastic Substances 0.000 claims description 6
- 238000011049 filling Methods 0.000 claims description 4
- 239000011118 polyvinyl acetate Substances 0.000 claims description 3
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 3
- 239000011347 resin Substances 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims description 3
- 239000005022 packaging material Substances 0.000 abstract description 6
- 239000000758 substrate Substances 0.000 description 41
- 239000000178 monomer Substances 0.000 description 18
- 239000000123 paper Substances 0.000 description 14
- 239000000203 mixture Substances 0.000 description 13
- 229920001577 copolymer Polymers 0.000 description 12
- 239000000835 fiber Substances 0.000 description 12
- 235000013305 food Nutrition 0.000 description 11
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 10
- 239000005038 ethylene vinyl acetate Substances 0.000 description 8
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000000945 filler Substances 0.000 description 7
- 239000006260 foam Substances 0.000 description 7
- 229920001519 homopolymer Polymers 0.000 description 7
- -1 2-ethylhexylacrylate Chemical class 0.000 description 6
- 229920006243 acrylic copolymer Polymers 0.000 description 6
- 239000011324 bead Substances 0.000 description 6
- 239000006229 carbon black Substances 0.000 description 6
- 238000010411 cooking Methods 0.000 description 6
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 6
- 239000011087 paperboard Substances 0.000 description 5
- 229920000058 polyacrylate Polymers 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 125000005250 alkyl acrylate group Chemical group 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- 239000003755 preservative agent Substances 0.000 description 4
- 230000007420 reactivation Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000004831 Hot glue Substances 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 239000011101 paper laminate Substances 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- NXQMCAOPTPLPRL-UHFFFAOYSA-N 2-(2-benzoyloxyethoxy)ethyl benzoate Chemical group C=1C=CC=CC=1C(=O)OCCOCCOC(=O)C1=CC=CC=C1 NXQMCAOPTPLPRL-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- AEPWOCLBLLCOGZ-UHFFFAOYSA-N 2-cyanoethyl prop-2-enoate Chemical class C=CC(=O)OCCC#N AEPWOCLBLLCOGZ-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- QFOHBWFCKVYLES-UHFFFAOYSA-N Butylparaben Chemical compound CCCCOC(=O)C1=CC=C(O)C=C1 QFOHBWFCKVYLES-UHFFFAOYSA-N 0.000 description 1
- 101150015280 Cel gene Proteins 0.000 description 1
- 241000557626 Corvus corax Species 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Chemical class 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 235000015496 breakfast cereal Nutrition 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000004673 fluoride salts Chemical class 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000013611 frozen food Nutrition 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 239000011084 greaseproof paper Substances 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 150000005165 hydroxybenzoic acids Chemical class 0.000 description 1
- 238000007641 inkjet printing Methods 0.000 description 1
- 239000002650 laminated plastic Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical class CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- YRDNVESFWXDNSI-UHFFFAOYSA-N n-(2,4,4-trimethylpentan-2-yl)prop-2-enamide Chemical compound CC(C)(C)CC(C)(C)NC(=O)C=C YRDNVESFWXDNSI-UHFFFAOYSA-N 0.000 description 1
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
- RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 description 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000011049 pearl Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000004714 phosphonium salts Chemical group 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 238000004826 seaming Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- PZTAGFCBNDBBFZ-UHFFFAOYSA-N tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCCC1CO PZTAGFCBNDBBFZ-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000013024 troubleshooting Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
- C09J5/08—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers using foamed adhesives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B31—MAKING ARTICLES OF PAPER, CARDBOARD OR MATERIAL WORKED IN A MANNER ANALOGOUS TO PAPER; WORKING PAPER, CARDBOARD OR MATERIAL WORKED IN A MANNER ANALOGOUS TO PAPER
- B31B—MAKING CONTAINERS OF PAPER, CARDBOARD OR MATERIAL WORKED IN A MANNER ANALOGOUS TO PAPER
- B31B70/00—Making flexible containers, e.g. envelopes or bags
- B31B70/60—Uniting opposed surfaces or edges; Taping
- B31B70/62—Uniting opposed surfaces or edges; Taping by adhesives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L31/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers
- C08L31/06—Homopolymers or copolymers of esters of polycarboxylic acids
- C08L31/08—Homopolymers or copolymers of esters of polycarboxylic acids of phthalic acid
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2431/00—Presence of polyvinyl acetate
Definitions
- the invention relates to improvements in packaging materials, more specifically to packaging materials comprising foamed adhesives.
- the adhesives find use in useful in bag closing, laminating, susceptor patch attachment and seaming applications, and are particularly well suited for use in pre-applied application including heat seal applications.
- Water-based and hot melt adhesives are commonly used to manufacture packaging materials, including bags having heat sealable seams and closures.
- adhesive is applied in a liquid or molten state and allowed to dry.
- Application of adhesive is generally applied by the packaging converter, thereby allowing the packager to avoid adhesive related issues such as adhesive selection, processing, trouble shooting, inventory and maintenance of adhesive application equipment. The packager then fills the package, reactivates the adhesive and seals the bag.
- aqueous liquid adhesives are safer, easier to handle and less expensive then hot melt adhesives
- water-based adhesives have a number of disadvantages associated with their use.
- Water-based liquid adhesives require significant drying times, require long set times, and the water contained within them tends to swell the substrates surfaces that come in contact with the adhesive, leading to warpage, wrinkling, curling or bending of the substrate. Problems such as warping increases the costs associated with packaging defects due to unacceptable appearance and the like.
- the invention provides a water-based adhesive that can be applied to a substrate and later reactivated in order to bond the substrate to a second substrate.
- the adhesive finds use in packaging applications, in particular reactivatable heat seal applications, more preferable seam and bag ending heal seal applications.
- the adhesive is foamed prior to application to the substrate, such as a bag ending or the like, and allowed to dry.
- One aspect of the invention is directed to a packaging container having preapplied to at least a portion thereof a reactivatable adhesive, wherein the reactivatable adhesive was applied to the container in the form of a foamed water-based adhesive.
- the packaging container is a bag, more preferable a bag having a top or bottom ending comprising the adhesive.
- the packaging container is a bag adapted to package microwave popcorn.
- any water-based adhesive that can be foamed can be used in the practice of the invention as long as the dried adhesive is thermoplastic.
- water-based adhesives that can be used in the practice of the invention are adhesives comprising polyvinylacetate homopolymers and ethylene/vinyl acetate copolymers.
- the adhesives are foamed prior to application to the substrate surface. Foam levels of from about 10% to a 60% per volume, more preferably 20 to 45% by volume, even more preferable 20% to about 30% by volume are preferred.
- Another aspect of the invention is directed to a method of packaging items such as food and consumer goods, and packaged items.
- goods that can be packaged include food, pharmaceuticals, cosmetics, breakfast cereals, beverage containers, bakery items, dry foods (e.g., dog food), produce, household products, paper products, soaps and detergents, candy, popcorn, wet food, frozen food, diapers, light bulbs and the like.
- a particular preferred embodiment comprises packaged microwavable popcorn wherein the heat seal is used at both ends of the bag and on the side seam.
- Adhesives are formulated for complete hold and fiber tear on the bottom heat seal and side seal and proper “venting” and non-destructive fiber tear on the top.
- the invention involves the use of foamed water-based adhesive useful in the manufacture of packaging materials including but not limited to bags that are heat sealable, e.g., heat sealable bag closures.
- heat seal as this term is used and understood in the hot melt adhesive art means that a seal is made through the use of heat.
- the seal will typically be made upon the application of an external source of heat.
- an external source of heat As a more specific example of heat sealing, as may be used in the practice of the invention, a first substrate having an adhesive preapplied thereon is brought in contact with a second substrate to the bonded to the first substrate. An external source of heat, and typically pressure, is then applied, whereby the adhesive is reactivated, thereby bonding the first substrate to the second substrate. Both the first and the second substrate may desirable be pre-coated with the adhesive.
- Adhesives used in accordance with the invention comprise synthetic and/or natural ingredients. When modified and mechanically agitated with air, these adhesives form highly stable, consistent foams that can be applied to a substrate and dried. Following drying the dried adhesive is thermoplastic and may be reactivated by an external energy source. Typical sources of heat for reactivation of the adhesive include but are not limited to heated platens or bars, infrared, forced hot air, flame and the like.
- the substrates to be sealed together with the adhesive of the invention will generally be subjected to heat (140-350° F.) and pressure (40 to 100 psi) for a period of from about 0.2 to about 3.0 seconds.
- the adhesives of the invention may also be formulated to reactivate upon exposure to short durations of radiant energy.
- the aqueous adhesive to be foamed contains an energy-absorbing ingredient.
- Energy absorbing ingredients for use in the practice of the invention will typically have an absorption in the range of from about 400 nm to about 100,000 nM, more preferably from about 700 nm to about 10,000 nm, even more preferably from about 750 nm to about 5000 nm.
- Energy-absorbing ingredients include those dyes, pigments, fillers, polymers and resins or other ingredients that are capable of absorbing energy and provide an optimal balance of absorption, reflection, transmission and conduction.
- Pigments and dyes are particularly preferred energy absorbing ingredients, and near infrared absorbing dyes and pigments being particularly preferred.
- Preferred energy-absorbing ingredients for use in the practice of the invention are broad band near IR absorbers such as Epolight 1125 (Epolene, Inc), SDA6248 (H.W. Sands Corp.), SDA2072 (H.W. Sands Corp.) and carbon black.
- Carbon black can be purchased from Cabot under trade name of Monarch, Regal, Black Pearl, and Elftex, or Degussa (FW series), or from Columbian Chemical Company (Raven Series). Carbon black can be manufactured by different methods such as the furnace black method, the gas (channel) black method, and the lamp black method.
- Adhesive may be coated to either or both surfaces of a substrate to be bonded. Following activation, the substrates are brought together for bonding. If the substrate is transparent or translucent to the energy used for reactivation, the adhesive formula may be sandwiched between substrates first, and then NIR energy can be applied to initiate cure.
- Foamable adhesives can also be formulated for reactivation using ultrasonic energy.
- Preferred adhesives will reactive upon exposure to ultrasonic energy having a frequency of from about 15 kilohertz to about 40 kilohertz.
- Substrates to be bonded are brought together with the adhesive sandwiched there between and pressed against an ultrasonic horn with booster.
- Benefits of using the foamed adhesive of the invention include improved economics and performance, such as reduced penetration into substrates, reduced moisture and faster set times. It has been discovered that adding air bubbles to the adhesive significantly reduces moisture content. Faster drying times and a substantial reduction in incidence of warping and/or wrinkling encountered in prior art methods are possible when bags are prepared in accordance with the invention.
- Water-based adhesives that can be foamed and pre-applied to e.g., a bag ending, for later reactivation and closure include, but are not limited to, synthetic resins, natural rubbers, etc that are thermoplastic in the dried state.
- the adhesives of the invention can be formulated as an emulsion or a solution.
- Adhesives comprising single homopolymer or copolymer emulsions as well as blends of two or more homopolymers or copolymers are contemplated for use in the practice of the invention.
- Vinyl acetate containing emulsions include vinyl acetate homopolymers, emulsions comprising vinyl acetate copolymers such as ethylene vinyl acetate, and various mixtures thereof. Mixtures of vinyl acetate containing emulsions and vinyl acetate copolymer containing emulsions may be used. Included are ethylene vinyl acetate, copolymers of vinyl acetate and other acrylates such as 2-ethylhexylacrylate, and vinyl acetate homopolymers. Emulsions comprising a vinyl acetate polymer and/or copolymer and an acrylic copolymer may also be used in the practice of the invention.
- the foamable adhesives of the invention may also comprise, in addition the vinyl acetate containing component, an acrylic copolymer containing component.
- Typical acrylic copolymers useful in the practice of the invention comprise acrylic monomers such as the C 1 -C 12 esters of acrylic or methacrylic acid a well as ethylenically unsaturated monomers containing functional groups.
- Nonlimiting examples of acrylic copolymers include methyl methacrylate/butyl acrylate/2,2-hydoxyethylhexyl acrylate copolymers and methyl methacrylate/ethyl acrylate/2,2-hydoxyethylhexyl acrylate copolymers and the like. Both high and low molecular weight acrylic polymers are contemplated for use.
- the acrylic polymer is formed of acrylate monomers. Both high and low Tg alkyl acrylates may be used. Low transition temperature monomers are those having a Tg of less than about 0° C. Included are alkyl acrylates that have up to about 18 carbon atoms in the alkyl group, preferably from about 4 to about 10 carbon atoms in the alkyl group. Such alkyl acrylates include butyl acrylate, amyl acrylate, hexyl acrylate, 2-ethylhexyl acrylate, isooctyl acrylate, decyl acrylate, dodecyl acrylates, isomers thereof, and combinations thereof. A preferred alkyl acrylate for use in the practice of the invention is butyl acrylate.
- the monomer system making up the acrylic copolymer may be solely based on low Tg alkyl acrylate ester monomers, inclusion of high Tg monomers and/or functional comonomers, in particular carboxy-containing functional monomers, and/or, even more preferably, hydroxy-containing functional monomers is preferred.
- High Tg monomer components which may be present, and in some embodiments are preferably present, include methyl acrylate, ethyl acrylate, isobutyl methacrylate, vinyl acetate, styrene-butadiene copolymers and/or styrene-acrylate copolymers.
- the high Tg monomers may be present in a total amount of up to about 50% by weight, preferably from about 5 to about 50% by weight, even more preferably from about 10 to about 40% by weight, based on total weight of the hybrid polymer.
- the acrylic polymer may also comprise one or more functional monomers.
- Carboxy functional monomers may be present in the polymer in an amount of up to about 7% by weight, more typically from about 1 to about 5% by weight, based on the total weight of the monomers.
- Useful carboxylic acids preferably contain from about 3 to about 5 carbon atoms and include, among others, acrylic acid, methacrylic acid, itaconic acid, and the like. Acrylic acid, methacrylic acid and mixtures thereof are preferred.
- the acrylic copolymer may comprises hydroxy functional monomers such as hydroxyalkyl (meth)acrylate esters, and acrylic polymers used to form the backbone of the invention are preferably acrylic ester/hydroxy (meth)alkyl ester copolymers.
- hydroxy functional monomers include hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxyethyl methacrylate and hydroxypropyl methacrylate. Hydroxy functional monomers are generally used in an amount of from about 1 to about 10%, preferably from about 3 to about 7%.
- comonomers can be used to modify the Tg of the acrylic polymer or to further enhance adhesion to various surfaces.
- Such comonomers include styrene, N-vinyl pyrrolidone, N-vinyl caprolactam, N-alkyl (meth)acrylamides such as t-octyl acrylamide, cyanoethylacrylates, diacetoneacrylamide, N-vinyl acetamide, N-vinyl formamide, glycidyl methacrylate and allyl glycidyl ether.
- additives include, but are not limited to, plasticizers, acids, waxes, synthetic resins, tackifiers, defoamers, preservatives, bases such as sodium hydroxide, fillers, dyes, pigments, UV indicators, crosslinkers and other additives commonly used in the art.
- the adhesive may also contain a surface-active agent.
- surface-active agents include anionic, cationic, amphoteric, or nonionic surfactants, or mixtures thereof.
- Suitable anionic surfactants include, alkyl sulfonates, alkylaryl sulfonates, alkyl sulfates, sulfates of hydroxylalkanols, alkyl and alkylaryl disulfonates, sulfonated fatty acids, sulfates and phosphates of polyethoxylated alkanols and alkylphenols, and esters of sulfosuccinic acid.
- Suitable cationic surfactants include, alkyl quaternary ammonium salts, and alkyl quaternary phosphonium salts.
- Suitable non-ionic surfactants include the addition products of 5 to 50 moles of ethylene oxide adducted to straight-chain and branched-chain alkanols having 6 to 22 carbon atoms, alkylphenols, higher fatty acids, higher fatty acid amines, primary or secondary higher alkyl amines, and block copolymers of propylene oxide with ethylene oxide, and mixtures thereof.
- the surface active agent will typically be added in amounts up to about 20% by weight, based on the foamable composition as a whole. More usually from amounts of from about 0.05 to about 20% by weight, and preferably at from 0.2 to 2% by weight.
- Suitable fillers are those fillers known in the art as adhesives fillers and include polysaccharides, calcium carbonate, clay, mica, nut shell flours, silica, talc and wood flour.
- a clay filler may typically be used to prepare adhesives for use in the practice of the invention. The addition of a filler allows for foam generated to remain consistent and stable for several hours.
- Preservatives for use herein include those conventionally used in aqueous adhesives such as benzoates, amides and fluorides such as sodium fluoride. Also included are the hydroxybenzoic acid esters such as p-hydroxybenzoic acid methyl ester or p-hydroxybenzoic butyl ester.
- commercially available preservatives which may be used in the practice of the invention include KATHON LXE sold by Rohm & Haas Company and Nipacide OBS sold by Clariant. The preservative will generally be included in amounts of from 0.05% to about 0.2% by weight.
- Preferred adhesives are foamable adhesives comprising from about 80 to about 100% by weight of a polymer emulsion comprising a vinyl acetate homopolymer or ethylene-vinyl acetate copolymer.
- the foamable adhesive composition of the invention is foamed by the addition of energy, by means known in the art such as, but not limited to, by mechanical and/or chemical means. Air or other gases are added to the foamable adhesive composition along with the addition of said energy to produce a stable, consistent foamed adhesive. Preferably air is used to produce the foamed adhesive.
- the adhesive foam may be produced by mechanical means such as mechanical stirring or agitation, introduction of gases or by chemical means.
- the amount of air dispersed in the adhesive can vary depending on the particular formulation, but will generally be from about 10% (by volume) up to about 50% (by volume) or greater.
- the foamed adhesive of the invention is particularly well suited for use in the preparation of bags having a closable end and an opposite closed or open end. Alternatively, both ends of the bag may be closable. Both flat tube style bags and bags having gussets may be manufactured in accordance with the invention. Also encompassed are block bottom and satchel bottom bags. Bags of the invention may constitute a secondary package (sealed bag within a cereal box) or be the primary package such as a popcorn bag. The containers of the invention can be used for filling, storing, shipping and cooking food, such as popcorn.
- the packaging material of the invention is typically a paper product.
- Paper products are defined herein as any article of manufacture, at least a portion of which comprises paper.
- the paper product may be made totally of paper or partially of paper.
- the invention encompasses paper products made of either single or multiple layers, e.g., a paper laminate, plastic/paper laminate.
- a preferred packaging bag useful for filling, storing, shipping and cooking popcorn comprises The bag comprises front and back panels and inwardly extending first and second gusseted side panels.
- the front and back panels and the first and second gusseted side panels each have an exterior surface and an interior surface collectively defining an interior cooking region, a top end and a bottom end.
- each of the front and back panel means and the first and second gusseted side panel means of the bag means comprises an inner ply of substantially grease proof paper material and an outer ply of paper material.
- the bottom ends will typically be operably configured to form a substantially sealed bottom region through adhesive attachment.
- the adhesively attached bottom ends are then further crimped and attached by adhesive to a portion of the exterior surface of one of the front and back panel means to further secure the substantially sealed bottom region.
- Each of the top ends of the front and back panel means and the first and second gusseted side panel means are operably sealable to one another after filling and prior to cooking, and then releasable from each other after cooking, by bag closure means. Accordingly, the bag closure means form a substantially sealed top region after the food is operably positioned within the interior region, which may be re-opened for exposure to the food after cooking.
- the bag closure means comprises adhesive that is are operably positioned adjacent to the top end of the interior surfaces of the front and back panel means and the corresponding adjacent portions of the first and second flaps of the first and second gusseted side panel means.
- the bag closure means are releasable after the food has been fully cooked within the interior region of the bag means.
- a thin layer of a water-based foamed adhesive is applied and allowed to dry, thereby forming a thin layer of a thermoplastic adhesive.
- the thermoplastic adhesive is then activated by heat sealing after the bag is filled.
- Bags of the invention may also comprises a heat enhancement means comprising a heat absorbing susceptor member which is operably attached to a least a portion of the front panel adjacent the food in the interior region of the bag.
- the heat enhancement means may be positioned between the inner and outer plies of paper material or, may be directly exposed to the food without the intervening ply.
- the foamed adhesive of the invention may be used to seal, either directly or by heat seal means any side seams, the top and bottom ends, to laminate bag plies and/or for attachment of a heat enhancement means.
- the adhesive formulations of the invention may be pre-applied in a continuous or discontinuous, e.g., as evenly spaced beads or dots, manner depending on surface area and coating weight desired. Particular patterns may be used to optimize substrate/adhesive contact. Depending on the adhesive, the bead size, thickness, distance apart and pattern will vary.
- the adhesive may be pre-applied to the substrate by any method known in the art, and include, without limitation roll coating, painting, dry-brushing, dip coating spraying, slot-coating, swirl spraying, printing (e.g., ink jet printing), flexographic, extrusion, atomized spraying, gravure (pattern wheel transfer), electrostatic, vapor deposition, fiberization and/or screen printing.
- the method of pre-application to the substrate is not critical to the practice of the invention.
- An adhesive comprising 100.0% by weight of an ethylene/vinyl acetate copolymer (81% vinyl acetate, 19% ethylene) was prepared and mechanically foamed at a 20-30% by volume foam level.
- the foamed adhesive was used to coat the surface of a paper substrate and allowed to dry. A second paper substrate was brought in contact with the dried adhesive and subjected to heat (300° F.) and pressure (70 psi) for 0.4 seconds.
- An adhesive comprising 99.8% of a polyvinyl acetate homopolymer and 0.2% by weight of a defoamer combination comprising 0.1% Hodag Antifoam PX-653, supplied by Celgene Chemical Co. and 0.1% Foamaster V, supplied by Cognis Corp., was prepared and mechanically foamed at a 20-30% by volume foam level.
- the foamed adhesive was used to coat the surface of a paper substrate and allowed to dry. A second paper substrate was brought in contact with the dried adhesive and subjected to heat (300° F.) and pressure (70 psi) for 0.4 seconds.
- An EVA based waterborne emulsion comprising 88 EVA Emulsion (Dur-o-set E-200, Vinamul), 7.5 Diethylene/Dipropylene Glycol Dibenzoate Plasticizer, 4 Water and 0.5 Carbon Black (Plack Pearls 4750, Cabot) was prepared by pre-dispersing carbon black in the plasticizer using a rotor-stator. The EVA emulsion and water was added using moderate speed axial paddle stirring. Following mechanically foaming of the adhesive at a 20-30% by volume foam level, the adhesive was applied and then was dried to the surface of a tack free film. The adhesive layer was later reactivated by exposure to a NIR energy source for a time sufficient to achieve melting of the adhesive material. The substrates were quickly mated together. 24 hours following bonding the substrates were pulled apart and resulting bond force and the percent fiber tear recorded. Good bond strength and 100 fiber tear is observed with both paperboard and plastic substrates.
- An ethylene vinyl acetate based adhesive available from National Starch and Chemical Company (Product No. 40-1103) was foamed and used to precoat a substrate.
- This adhesive contains about 88 wt % EVA base resin, 8 wt % plasticizer, 0.2 wt % surfactant and water.
- Adhesive in a bead shape form and a coat weight of 1.5 g/m was cast onto paperboard substrates 2 inches long, 1 inch wide and 2 mm thick. After 24 hours, a second substrate was placed upon the adhesive bead present on the paperboard substrate. Second substrates tested were paperboard and plastic. The substrate layers with the reactivatable adhesive layer sandwiched in the middle thereof was pressed into an ultrasonic horn with booster and ultrasonic energy 20 kHz was applied for 5 seconds. 24 hours following ultrasonic bonding the substrates were pulled apart and resulting bond force, adhesive bead flatness and the percent fiber tear recorded. Good bond strength, almost total bead flatness and 100 fiber tear is observed with both paperboard and the plastic substrates.
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Abstract
Description
- The invention relates to improvements in packaging materials, more specifically to packaging materials comprising foamed adhesives. The adhesives find use in useful in bag closing, laminating, susceptor patch attachment and seaming applications, and are particularly well suited for use in pre-applied application including heat seal applications.
- Water-based and hot melt adhesives are commonly used to manufacture packaging materials, including bags having heat sealable seams and closures. In conventional heat sealable bag endings, adhesive is applied in a liquid or molten state and allowed to dry. Application of adhesive is generally applied by the packaging converter, thereby allowing the packager to avoid adhesive related issues such as adhesive selection, processing, trouble shooting, inventory and maintenance of adhesive application equipment. The packager then fills the package, reactivates the adhesive and seals the bag.
- While aqueous liquid adhesives are safer, easier to handle and less expensive then hot melt adhesives, water-based adhesives have a number of disadvantages associated with their use. Water-based liquid adhesives require significant drying times, require long set times, and the water contained within them tends to swell the substrates surfaces that come in contact with the adhesive, leading to warpage, wrinkling, curling or bending of the substrate. Problems such as warping increases the costs associated with packaging defects due to unacceptable appearance and the like.
- A need exists in the art for adhesives that are safe, effective and provide a substantial saving in terms of cost and reduction in packaging defects. The invention fulfills this need.
- The invention provides a water-based adhesive that can be applied to a substrate and later reactivated in order to bond the substrate to a second substrate. The adhesive finds use in packaging applications, in particular reactivatable heat seal applications, more preferable seam and bag ending heal seal applications. The adhesive is foamed prior to application to the substrate, such as a bag ending or the like, and allowed to dry.
- One aspect of the invention is directed to a packaging container having preapplied to at least a portion thereof a reactivatable adhesive, wherein the reactivatable adhesive was applied to the container in the form of a foamed water-based adhesive. In one embodiment, the packaging container is a bag, more preferable a bag having a top or bottom ending comprising the adhesive. In one particularly preferred embodiment, the packaging container is a bag adapted to package microwave popcorn.
- Any water-based adhesive that can be foamed can be used in the practice of the invention as long as the dried adhesive is thermoplastic. Examples of water-based adhesives that can be used in the practice of the invention are adhesives comprising polyvinylacetate homopolymers and ethylene/vinyl acetate copolymers. The adhesives are foamed prior to application to the substrate surface. Foam levels of from about 10% to a 60% per volume, more preferably 20 to 45% by volume, even more preferable 20% to about 30% by volume are preferred.
- Another aspect of the invention is directed to a method of packaging items such as food and consumer goods, and packaged items. Examples of goods that can be packaged include food, pharmaceuticals, cosmetics, breakfast cereals, beverage containers, bakery items, dry foods (e.g., dog food), produce, household products, paper products, soaps and detergents, candy, popcorn, wet food, frozen food, diapers, light bulbs and the like. A particular preferred embodiment comprises packaged microwavable popcorn wherein the heat seal is used at both ends of the bag and on the side seam. Adhesives are formulated for complete hold and fiber tear on the bottom heat seal and side seal and proper “venting” and non-destructive fiber tear on the top.
- The invention involves the use of foamed water-based adhesive useful in the manufacture of packaging materials including but not limited to bags that are heat sealable, e.g., heat sealable bag closures. The term “heat seal” as this term is used and understood in the hot melt adhesive art means that a seal is made through the use of heat.
- The seal will typically be made upon the application of an external source of heat. As a more specific example of heat sealing, as may be used in the practice of the invention, a first substrate having an adhesive preapplied thereon is brought in contact with a second substrate to the bonded to the first substrate. An external source of heat, and typically pressure, is then applied, whereby the adhesive is reactivated, thereby bonding the first substrate to the second substrate. Both the first and the second substrate may desirable be pre-coated with the adhesive.
- Adhesives used in accordance with the invention comprise synthetic and/or natural ingredients. When modified and mechanically agitated with air, these adhesives form highly stable, consistent foams that can be applied to a substrate and dried. Following drying the dried adhesive is thermoplastic and may be reactivated by an external energy source. Typical sources of heat for reactivation of the adhesive include but are not limited to heated platens or bars, infrared, forced hot air, flame and the like. The substrates to be sealed together with the adhesive of the invention will generally be subjected to heat (140-350° F.) and pressure (40 to 100 psi) for a period of from about 0.2 to about 3.0 seconds.
- The adhesives of the invention may also be formulated to reactivate upon exposure to short durations of radiant energy. In this embodiment, the aqueous adhesive to be foamed contains an energy-absorbing ingredient. Energy absorbing ingredients for use in the practice of the invention will typically have an absorption in the range of from about 400 nm to about 100,000 nM, more preferably from about 700 nm to about 10,000 nm, even more preferably from about 750 nm to about 5000 nm. Energy-absorbing ingredients include those dyes, pigments, fillers, polymers and resins or other ingredients that are capable of absorbing energy and provide an optimal balance of absorption, reflection, transmission and conduction. Pigments and dyes are particularly preferred energy absorbing ingredients, and near infrared absorbing dyes and pigments being particularly preferred. Preferred energy-absorbing ingredients for use in the practice of the invention are broad band near IR absorbers such as Epolight 1125 (Epolene, Inc), SDA6248 (H.W. Sands Corp.), SDA2072 (H.W. Sands Corp.) and carbon black. Carbon black can be purchased from Cabot under trade name of Monarch, Regal, Black Pearl, and Elftex, or Degussa (FW series), or from Columbian Chemical Company (Raven Series). Carbon black can be manufactured by different methods such as the furnace black method, the gas (channel) black method, and the lamp black method. The key parameters affecting the radian energy absorption of carbon black prepared by these various methods are average primary particle size, surface chemistry and aggregate structure. Adhesive may be coated to either or both surfaces of a substrate to be bonded. Following activation, the substrates are brought together for bonding. If the substrate is transparent or translucent to the energy used for reactivation, the adhesive formula may be sandwiched between substrates first, and then NIR energy can be applied to initiate cure.
- Foamable adhesives can also be formulated for reactivation using ultrasonic energy. Preferred adhesives will reactive upon exposure to ultrasonic energy having a frequency of from about 15 kilohertz to about 40 kilohertz. Substrates to be bonded are brought together with the adhesive sandwiched there between and pressed against an ultrasonic horn with booster.
- Benefits of using the foamed adhesive of the invention include improved economics and performance, such as reduced penetration into substrates, reduced moisture and faster set times. It has been discovered that adding air bubbles to the adhesive significantly reduces moisture content. Faster drying times and a substantial reduction in incidence of warping and/or wrinkling encountered in prior art methods are possible when bags are prepared in accordance with the invention.
- Water-based adhesives that can be foamed and pre-applied to e.g., a bag ending, for later reactivation and closure include, but are not limited to, synthetic resins, natural rubbers, etc that are thermoplastic in the dried state.
- The adhesives of the invention can be formulated as an emulsion or a solution. Adhesives comprising single homopolymer or copolymer emulsions as well as blends of two or more homopolymers or copolymers are contemplated for use in the practice of the invention.
- Vinyl acetate containing emulsions include vinyl acetate homopolymers, emulsions comprising vinyl acetate copolymers such as ethylene vinyl acetate, and various mixtures thereof. Mixtures of vinyl acetate containing emulsions and vinyl acetate copolymer containing emulsions may be used. Included are ethylene vinyl acetate, copolymers of vinyl acetate and other acrylates such as 2-ethylhexylacrylate, and vinyl acetate homopolymers. Emulsions comprising a vinyl acetate polymer and/or copolymer and an acrylic copolymer may also be used in the practice of the invention.
- The foamable adhesives of the invention may also comprise, in addition the vinyl acetate containing component, an acrylic copolymer containing component. Typical acrylic copolymers useful in the practice of the invention comprise acrylic monomers such as the C 1-C12 esters of acrylic or methacrylic acid a well as ethylenically unsaturated monomers containing functional groups. Nonlimiting examples of acrylic copolymers include methyl methacrylate/butyl acrylate/2,2-hydoxyethylhexyl acrylate copolymers and methyl methacrylate/ethyl acrylate/2,2-hydoxyethylhexyl acrylate copolymers and the like. Both high and low molecular weight acrylic polymers are contemplated for use.
- The acrylic polymer is formed of acrylate monomers. Both high and low Tg alkyl acrylates may be used. Low transition temperature monomers are those having a Tg of less than about 0° C. Included are alkyl acrylates that have up to about 18 carbon atoms in the alkyl group, preferably from about 4 to about 10 carbon atoms in the alkyl group. Such alkyl acrylates include butyl acrylate, amyl acrylate, hexyl acrylate, 2-ethylhexyl acrylate, isooctyl acrylate, decyl acrylate, dodecyl acrylates, isomers thereof, and combinations thereof. A preferred alkyl acrylate for use in the practice of the invention is butyl acrylate.
- While the monomer system making up the acrylic copolymer may be solely based on low Tg alkyl acrylate ester monomers, inclusion of high Tg monomers and/or functional comonomers, in particular carboxy-containing functional monomers, and/or, even more preferably, hydroxy-containing functional monomers is preferred.
- High Tg monomer components which may be present, and in some embodiments are preferably present, include methyl acrylate, ethyl acrylate, isobutyl methacrylate, vinyl acetate, styrene-butadiene copolymers and/or styrene-acrylate copolymers. The high Tg monomers may be present in a total amount of up to about 50% by weight, preferably from about 5 to about 50% by weight, even more preferably from about 10 to about 40% by weight, based on total weight of the hybrid polymer.
- The acrylic polymer may also comprise one or more functional monomers. Preferred are carboxy and/or hydroxy functional monomers. Carboxy functional monomers may be present in the polymer in an amount of up to about 7% by weight, more typically from about 1 to about 5% by weight, based on the total weight of the monomers. Useful carboxylic acids preferably contain from about 3 to about 5 carbon atoms and include, among others, acrylic acid, methacrylic acid, itaconic acid, and the like. Acrylic acid, methacrylic acid and mixtures thereof are preferred.
- The acrylic copolymer may comprises hydroxy functional monomers such as hydroxyalkyl (meth)acrylate esters, and acrylic polymers used to form the backbone of the invention are preferably acrylic ester/hydroxy (meth)alkyl ester copolymers. Specific examples of hydroxy functional monomers include hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxyethyl methacrylate and hydroxypropyl methacrylate. Hydroxy functional monomers are generally used in an amount of from about 1 to about 10%, preferably from about 3 to about 7%.
- Other comonomers can be used to modify the Tg of the acrylic polymer or to further enhance adhesion to various surfaces. Such comonomers include styrene, N-vinyl pyrrolidone, N-vinyl caprolactam, N-alkyl (meth)acrylamides such as t-octyl acrylamide, cyanoethylacrylates, diacetoneacrylamide, N-vinyl acetamide, N-vinyl formamide, glycidyl methacrylate and allyl glycidyl ether.
- Other components typical of adhesive compositions may be added to the foamable compositions. Said additives include, but are not limited to, plasticizers, acids, waxes, synthetic resins, tackifiers, defoamers, preservatives, bases such as sodium hydroxide, fillers, dyes, pigments, UV indicators, crosslinkers and other additives commonly used in the art.
- The adhesive may also contain a surface-active agent. Examples of surface-active agents include anionic, cationic, amphoteric, or nonionic surfactants, or mixtures thereof. Suitable anionic surfactants include, alkyl sulfonates, alkylaryl sulfonates, alkyl sulfates, sulfates of hydroxylalkanols, alkyl and alkylaryl disulfonates, sulfonated fatty acids, sulfates and phosphates of polyethoxylated alkanols and alkylphenols, and esters of sulfosuccinic acid. Suitable cationic surfactants include, alkyl quaternary ammonium salts, and alkyl quaternary phosphonium salts. Suitable non-ionic surfactants include the addition products of 5 to 50 moles of ethylene oxide adducted to straight-chain and branched-chain alkanols having 6 to 22 carbon atoms, alkylphenols, higher fatty acids, higher fatty acid amines, primary or secondary higher alkyl amines, and block copolymers of propylene oxide with ethylene oxide, and mixtures thereof. When used, the surface active agent will typically be added in amounts up to about 20% by weight, based on the foamable composition as a whole. More usually from amounts of from about 0.05 to about 20% by weight, and preferably at from 0.2 to 2% by weight.
- Suitable fillers are those fillers known in the art as adhesives fillers and include polysaccharides, calcium carbonate, clay, mica, nut shell flours, silica, talc and wood flour. A clay filler may typically be used to prepare adhesives for use in the practice of the invention. The addition of a filler allows for foam generated to remain consistent and stable for several hours.
- Preservatives for use herein include those conventionally used in aqueous adhesives such as benzoates, amides and fluorides such as sodium fluoride. Also included are the hydroxybenzoic acid esters such as p-hydroxybenzoic acid methyl ester or p-hydroxybenzoic butyl ester. Commercially available preservatives which may be used in the practice of the invention include KATHON LXE sold by Rohm & Haas Company and Nipacide OBS sold by Clariant. The preservative will generally be included in amounts of from 0.05% to about 0.2% by weight.
- Preferred adhesives are foamable adhesives comprising from about 80 to about 100% by weight of a polymer emulsion comprising a vinyl acetate homopolymer or ethylene-vinyl acetate copolymer.
- The foamable adhesive composition of the invention is foamed by the addition of energy, by means known in the art such as, but not limited to, by mechanical and/or chemical means. Air or other gases are added to the foamable adhesive composition along with the addition of said energy to produce a stable, consistent foamed adhesive. Preferably air is used to produce the foamed adhesive. The adhesive foam may be produced by mechanical means such as mechanical stirring or agitation, introduction of gases or by chemical means.
- The amount of air dispersed in the adhesive can vary depending on the particular formulation, but will generally be from about 10% (by volume) up to about 50% (by volume) or greater.
- The foamed adhesive of the invention is particularly well suited for use in the preparation of bags having a closable end and an opposite closed or open end. Alternatively, both ends of the bag may be closable. Both flat tube style bags and bags having gussets may be manufactured in accordance with the invention. Also encompassed are block bottom and satchel bottom bags. Bags of the invention may constitute a secondary package (sealed bag within a cereal box) or be the primary package such as a popcorn bag. The containers of the invention can be used for filling, storing, shipping and cooking food, such as popcorn.
- The packaging material of the invention is typically a paper product. Paper products are defined herein as any article of manufacture, at least a portion of which comprises paper. The paper product may be made totally of paper or partially of paper. The invention encompasses paper products made of either single or multiple layers, e.g., a paper laminate, plastic/paper laminate.
- A preferred packaging bag useful for filling, storing, shipping and cooking popcorn. In one embodiment, the bag comprises The bag comprises front and back panels and inwardly extending first and second gusseted side panels. The front and back panels and the first and second gusseted side panels each have an exterior surface and an interior surface collectively defining an interior cooking region, a top end and a bottom end. In the preferred embodiment of the invention, each of the front and back panel means and the first and second gusseted side panel means of the bag means comprises an inner ply of substantially grease proof paper material and an outer ply of paper material.
- The bottom ends will typically be operably configured to form a substantially sealed bottom region through adhesive attachment. In one such embodiment, the adhesively attached bottom ends are then further crimped and attached by adhesive to a portion of the exterior surface of one of the front and back panel means to further secure the substantially sealed bottom region.
- Each of the top ends of the front and back panel means and the first and second gusseted side panel means are operably sealable to one another after filling and prior to cooking, and then releasable from each other after cooking, by bag closure means. Accordingly, the bag closure means form a substantially sealed top region after the food is operably positioned within the interior region, which may be re-opened for exposure to the food after cooking.
- In the practice of the invention, the bag closure means comprises adhesive that is are operably positioned adjacent to the top end of the interior surfaces of the front and back panel means and the corresponding adjacent portions of the first and second flaps of the first and second gusseted side panel means. The bag closure means are releasable after the food has been fully cooked within the interior region of the bag means. Typically, a thin layer of a water-based foamed adhesive is applied and allowed to dry, thereby forming a thin layer of a thermoplastic adhesive. The thermoplastic adhesive is then activated by heat sealing after the bag is filled.
- Bags of the invention may also comprises a heat enhancement means comprising a heat absorbing susceptor member which is operably attached to a least a portion of the front panel adjacent the food in the interior region of the bag. The heat enhancement means may be positioned between the inner and outer plies of paper material or, may be directly exposed to the food without the intervening ply.
- The foamed adhesive of the invention may be used to seal, either directly or by heat seal means any side seams, the top and bottom ends, to laminate bag plies and/or for attachment of a heat enhancement means.
- The adhesive formulations of the invention may be pre-applied in a continuous or discontinuous, e.g., as evenly spaced beads or dots, manner depending on surface area and coating weight desired. Particular patterns may be used to optimize substrate/adhesive contact. Depending on the adhesive, the bead size, thickness, distance apart and pattern will vary. The adhesive may be pre-applied to the substrate by any method known in the art, and include, without limitation roll coating, painting, dry-brushing, dip coating spraying, slot-coating, swirl spraying, printing (e.g., ink jet printing), flexographic, extrusion, atomized spraying, gravure (pattern wheel transfer), electrostatic, vapor deposition, fiberization and/or screen printing. The method of pre-application to the substrate is not critical to the practice of the invention.
- The invention is further illustrated by the following non-limiting examples.
- An adhesive comprising 100.0% by weight of an ethylene/vinyl acetate copolymer (81% vinyl acetate, 19% ethylene) was prepared and mechanically foamed at a 20-30% by volume foam level.
- The foamed adhesive was used to coat the surface of a paper substrate and allowed to dry. A second paper substrate was brought in contact with the dried adhesive and subjected to heat (300° F.) and pressure (70 psi) for 0.4 seconds.
- Heat sealability, bond strength and fiber tear was tested. 100% fiber tear was observed. Substrate coated with the dry adhesive was stored for 6 months and again tested for heat sealability, bond strength and fiber tear. Aging studies showed no loss of reactivatability.
- An adhesive comprising 99.8% of a polyvinyl acetate homopolymer and 0.2% by weight of a defoamer combination comprising 0.1% Hodag Antifoam PX-653, supplied by Celgene Chemical Co. and 0.1% Foamaster V, supplied by Cognis Corp., was prepared and mechanically foamed at a 20-30% by volume foam level.
- The foamed adhesive was used to coat the surface of a paper substrate and allowed to dry. A second paper substrate was brought in contact with the dried adhesive and subjected to heat (300° F.) and pressure (70 psi) for 0.4 seconds.
- Heat sealability, bond strength and fiber tear was tested. 100% fiber tear was observed. Substrate coated with the dry adhesive was stored for 6 months and again tested for heat sealability, bond strength and fiber tear. Aging studies showed no loss of reactivatability.
- An EVA based waterborne emulsion comprising 88 EVA Emulsion (Dur-o-set E-200, Vinamul), 7.5 Diethylene/Dipropylene Glycol Dibenzoate Plasticizer, 4 Water and 0.5 Carbon Black (Plack Pearls 4750, Cabot) was prepared by pre-dispersing carbon black in the plasticizer using a rotor-stator. The EVA emulsion and water was added using moderate speed axial paddle stirring. Following mechanically foaming of the adhesive at a 20-30% by volume foam level, the adhesive was applied and then was dried to the surface of a tack free film. The adhesive layer was later reactivated by exposure to a NIR energy source for a time sufficient to achieve melting of the adhesive material. The substrates were quickly mated together. 24 hours following bonding the substrates were pulled apart and resulting bond force and the percent fiber tear recorded. Good bond strength and 100 fiber tear is observed with both paperboard and plastic substrates.
- An ethylene vinyl acetate based adhesive available from National Starch and Chemical Company (Product No. 40-1103) was foamed and used to precoat a substrate. This adhesive contains about 88 wt % EVA base resin, 8 wt % plasticizer, 0.2 wt % surfactant and water.
- Adhesive in a bead shape form and a coat weight of 1.5 g/m was cast onto paperboard substrates 2 inches long, 1 inch wide and 2 mm thick. After 24 hours, a second substrate was placed upon the adhesive bead present on the paperboard substrate. Second substrates tested were paperboard and plastic. The substrate layers with the reactivatable adhesive layer sandwiched in the middle thereof was pressed into an ultrasonic horn with booster and ultrasonic energy 20 kHz was applied for 5 seconds. 24 hours following ultrasonic bonding the substrates were pulled apart and resulting bond force, adhesive bead flatness and the percent fiber tear recorded. Good bond strength, almost total bead flatness and 100 fiber tear is observed with both paperboard and the plastic substrates.
- Many modifications and variations of this invention can be made without departing from its spirit and scope, as will be apparent to those skilled in the art. The specific embodiments described herein are offered by way of example only, and the invention is to be limited only by the terms of the appended claims, along with the full scope of equivalents to which such claims are entitled.
Claims (17)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/462,183 US20040250516A1 (en) | 2003-06-16 | 2003-06-16 | Foamed adhesive and applications thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/462,183 US20040250516A1 (en) | 2003-06-16 | 2003-06-16 | Foamed adhesive and applications thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20040250516A1 true US20040250516A1 (en) | 2004-12-16 |
Family
ID=33511414
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/462,183 Abandoned US20040250516A1 (en) | 2003-06-16 | 2003-06-16 | Foamed adhesive and applications thereof |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US20040250516A1 (en) |
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| US20060117728A1 (en) * | 2004-12-07 | 2006-06-08 | National Starch And Chemical Investment Holding Corporation | Method of preparing filters |
| US20100266834A1 (en) * | 2007-12-05 | 2010-10-21 | Szilagyi Otto | Process and Apparatus to Foam a Water-Base Adhesive |
| US20110064926A1 (en) * | 2008-05-15 | 2011-03-17 | Meadwestvaco Corporation | Combined boards without corrugated medium having enhanced surface properties |
| US20110161301A1 (en) * | 2009-12-14 | 2011-06-30 | Ian Pratt | Methods and systems for optimizing a process of archiving at least one block of a virtual disk image |
| WO2014116395A1 (en) * | 2013-01-24 | 2014-07-31 | Henkel Ltd. | Foamable hot melt adhesive compositions and use thereof |
| EP2653514A3 (en) * | 2012-04-20 | 2017-05-17 | Jowat AG | Joining and/or gluing method and products produced according to this method |
| EP2653513A3 (en) * | 2012-04-20 | 2017-05-17 | Jowat AG | Gluing method and products produced according to this method |
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| US20060117728A1 (en) * | 2004-12-07 | 2006-06-08 | National Starch And Chemical Investment Holding Corporation | Method of preparing filters |
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| US20110161301A1 (en) * | 2009-12-14 | 2011-06-30 | Ian Pratt | Methods and systems for optimizing a process of archiving at least one block of a virtual disk image |
| EP2653514A3 (en) * | 2012-04-20 | 2017-05-17 | Jowat AG | Joining and/or gluing method and products produced according to this method |
| EP2653513A3 (en) * | 2012-04-20 | 2017-05-17 | Jowat AG | Gluing method and products produced according to this method |
| WO2014116395A1 (en) * | 2013-01-24 | 2014-07-31 | Henkel Ltd. | Foamable hot melt adhesive compositions and use thereof |
| US10336920B2 (en) | 2013-01-24 | 2019-07-02 | Henkel Ag & Co. Kgaa | Foamable hot melt adhesive compositions and use thereof |
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