CA2556466C - Cohesive coating for snack food packaging - Google Patents
Cohesive coating for snack food packaging Download PDFInfo
- Publication number
- CA2556466C CA2556466C CA 2556466 CA2556466A CA2556466C CA 2556466 C CA2556466 C CA 2556466C CA 2556466 CA2556466 CA 2556466 CA 2556466 A CA2556466 A CA 2556466A CA 2556466 C CA2556466 C CA 2556466C
- Authority
- CA
- Canada
- Prior art keywords
- weight
- cohesive
- cohesive coating
- coating
- substrate
- 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.)
- Expired - Lifetime
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 70
- 239000011248 coating agent Substances 0.000 title claims abstract description 62
- 235000013305 food Nutrition 0.000 title claims abstract description 15
- 238000004806 packaging method and process Methods 0.000 title abstract description 14
- 235000011888 snacks Nutrition 0.000 title abstract description 7
- 239000000839 emulsion Substances 0.000 claims abstract description 56
- 239000000758 substrate Substances 0.000 claims abstract description 55
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 52
- 238000004132 cross linking Methods 0.000 claims abstract description 51
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 33
- 229920006173 natural rubber latex Polymers 0.000 claims abstract description 31
- 239000004094 surface-active agent Substances 0.000 claims abstract description 29
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 20
- 239000002981 blocking agent Substances 0.000 claims abstract description 17
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 16
- 239000004615 ingredient Substances 0.000 claims abstract description 15
- 239000000945 filler Substances 0.000 claims abstract description 8
- 230000003750 conditioning effect Effects 0.000 claims abstract description 5
- 239000000463 material Substances 0.000 claims description 17
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 11
- -1 glycol ester Chemical class 0.000 claims description 9
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 239000011888 foil Substances 0.000 claims description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- 229920001909 styrene-acrylic polymer Polymers 0.000 claims description 6
- 239000000908 ammonium hydroxide Substances 0.000 claims description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 5
- 239000004927 clay Substances 0.000 claims description 4
- 229910021485 fumed silica Inorganic materials 0.000 claims description 4
- 239000002480 mineral oil Substances 0.000 claims description 4
- 235000010446 mineral oil Nutrition 0.000 claims description 4
- 239000004743 Polypropylene Substances 0.000 claims description 3
- 239000005021 flexible packaging material Substances 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 229920006267 polyester film Polymers 0.000 claims description 3
- 229920005862 polyol Polymers 0.000 claims description 3
- 150000003077 polyols Chemical class 0.000 claims description 3
- 229920001155 polypropylene Polymers 0.000 claims description 3
- 229920001296 polysiloxane Polymers 0.000 claims description 3
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 229910052570 clay Inorganic materials 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 229920000098 polyolefin Polymers 0.000 claims description 2
- 238000003825 pressing Methods 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims 1
- 229920006262 high density polyethylene film Polymers 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 57
- 239000000203 mixture Substances 0.000 abstract description 29
- 229910021529 ammonia Inorganic materials 0.000 abstract description 28
- 230000000903 blocking effect Effects 0.000 abstract description 4
- 230000002829 reductive effect Effects 0.000 abstract description 3
- 230000001070 adhesive effect Effects 0.000 description 28
- 239000000853 adhesive Substances 0.000 description 27
- 229920000126 latex Polymers 0.000 description 21
- 239000004816 latex Substances 0.000 description 21
- 239000000047 product Substances 0.000 description 11
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 9
- 229920001971 elastomer Polymers 0.000 description 9
- 238000009459 flexible packaging Methods 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- 229920006397 acrylic thermoplastic Polymers 0.000 description 7
- 239000005022 packaging material Substances 0.000 description 7
- 239000000123 paper Substances 0.000 description 7
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 7
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 7
- 239000004971 Cross linker Substances 0.000 description 6
- 244000043261 Hevea brasiliensis Species 0.000 description 6
- 239000005060 rubber Substances 0.000 description 6
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- 239000000654 additive Substances 0.000 description 5
- 229920003052 natural elastomer Polymers 0.000 description 5
- 229920001194 natural rubber Polymers 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 4
- 229920002799 BoPET Polymers 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 3
- 235000009508 confectionery Nutrition 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 239000000976 ink Substances 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000004005 microsphere Substances 0.000 description 3
- 239000011087 paperboard Substances 0.000 description 3
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- 238000012545 processing Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- 229920013646 Hycar Polymers 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 150000003973 alkyl amines Chemical class 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 2
- 229960002447 thiram Drugs 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- LXOFYPKXCSULTL-UHFFFAOYSA-N 2,4,7,9-tetramethyldec-5-yne-4,7-diol Chemical compound CC(C)CC(C)(O)C#CC(C)(O)CC(C)C LXOFYPKXCSULTL-UHFFFAOYSA-N 0.000 description 1
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 1
- JYCQQPHGFMYQCF-UHFFFAOYSA-N 4-tert-Octylphenol monoethoxylate Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCO)C=C1 JYCQQPHGFMYQCF-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- FPVVYTCTZKCSOJ-UHFFFAOYSA-N Ethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 1
- 229920005928 JONCRYL® 77 Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 108010064851 Plant Proteins Proteins 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- NKSOSPOXQKNIKJ-CLFAGFIQSA-N Polyoxyethylene dioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCOC(=O)CCCCCCC\C=C/CCCCCCCC NKSOSPOXQKNIKJ-CLFAGFIQSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- 241000274582 Pycnanthus angolensis Species 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 239000004147 Sorbitan trioleate Substances 0.000 description 1
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 238000007754 air knife coating Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000010428 baryte Substances 0.000 description 1
- 229910052601 baryte Inorganic materials 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
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- 239000012530 fluid Substances 0.000 description 1
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- 150000002314 glycerols Chemical class 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
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- 230000000977 initiatory effect Effects 0.000 description 1
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000012939 laminating adhesive Substances 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
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- 239000002245 particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 235000021118 plant-derived protein Nutrition 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920003009 polyurethane dispersion Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000007763 reverse roll coating Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- BTJYKXPSPBJJDQ-UHFFFAOYSA-M sodium;1,4-bis(4-methylpentan-2-yloxy)-1,4-dioxobutane-2-sulfonate Chemical compound [Na+].CC(C)CC(C)OC(=O)CC(S([O-])(=O)=O)C(=O)OC(C)CC(C)C BTJYKXPSPBJJDQ-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
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- 239000008399 tap water Substances 0.000 description 1
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- 238000010998 test method Methods 0.000 description 1
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- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- 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
- B65D75/00—Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes or webs of flexible sheet material, e.g. in folded wrappers
- B65D75/52—Details
- B65D75/58—Opening or contents-removing devices added or incorporated during package manufacture
- B65D75/5855—Peelable seals
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D107/00—Coating compositions based on natural rubber
- C09D107/02—Latex
-
- 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
- C09J133/00—Adhesives based on 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09J133/08—Homopolymers or copolymers of acrylic acid esters
-
- 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
- B65D75/00—Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes or webs of flexible sheet material, e.g. in folded wrappers
- B65D75/04—Articles or materials wholly enclosed in single sheets or wrapper blanks
- B65D75/20—Articles or materials wholly enclosed in single sheets or wrapper blanks in sheets or blanks doubled around contents and having their opposed free margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding
-
- 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
- B65D75/00—Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes or webs of flexible sheet material, e.g. in folded wrappers
- B65D75/28—Articles or materials wholly enclosed in composite wrappers, i.e. wrappers formed by associating or interconnecting two or more sheets or blanks
- B65D75/30—Articles or materials enclosed between two opposed sheets or blanks having their margins united, e.g. by pressure-sensitive adhesive, crimping, heat-sealing, or welding
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
- C08L2666/08—Homopolymers or copolymers according to C08L7/00 - C08L21/00; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/08—Homopolymers or copolymers of acrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
- C08L7/02—Latex
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2813—Heat or solvent activated or sealable
- Y10T428/2817—Heat sealable
- Y10T428/2826—Synthetic resin or polymer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2852—Adhesive compositions
- Y10T428/2857—Adhesive compositions including metal or compound thereof or natural rubber
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2852—Adhesive compositions
- Y10T428/2878—Adhesive compositions including addition polymer from unsaturated monomer
- Y10T428/2891—Adhesive compositions including addition polymer from unsaturated monomer including addition polymer from alpha-beta unsaturated carboxylic acid [e.g., acrylic acid, methacrylic acid, etc.] Or derivative thereof
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31826—Of natural rubber
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31935—Ester, halide or nitrile of addition polymer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Wrappers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
- General Preparation And Processing Of Foods (AREA)
Abstract
A water based, cold seal, cohesive coating for bonding one or more substrates together to form a flexible package to contain an article, especially useful for snack food packaging. The cohesive coating includes about 25% to about 90% by weight of a natural rubber latex emulsion, about 10% to about 75% by weight of a non-self-crosslinking acrylic emulsion, about 0.01% to about 10% by weight water, and one or more ingredient selected from an anti-foam agent, ammonia, a surfactant, an anti-blocking agent, an inert filler, and a conditioning agent, so that in combination the components total 100% by weight of the composition. The use of a non-self-crosslinking acrylic emulsion provides an improved cold seal cohesive that may be employed with current high temperature converting systems and provides improved adhesion to substrates, enhanced cohesion to itself, reduced blocking and avoids seal deadening.
Description
COHESIVE COATING FOR SNACK FOOD PACKAGING
BACKGROUND OF THE INVENTION
The present invention relates to a water based, cold seal, cohesive coating for flexible packaging systems, and more particularly to a water based, cold seal, cohesive coating containing a non-self-crosslinking acrylic emulsion for use in food packaging and especially snack food packaging.
A cold seal adhesive, also referred to as a cohesive coating, is a type of pressure sensitive adhesive which possesses the ability to form a strong bond to itself when pressure is applied and also to form a bond with the flexible substrate on which it is applied. Cohesive coatings are thus pressure respondent, i.e.
the introduction of mechanical energy is all that is required to initiate seal formation.
Cold seal adhesives also preferably lack adhesion to the surfaces such as plastic films and overprint varnishes which are on the opposite face of these flexible substrates so that such flexible substrates or webs coated with the cold seal adhesive may be stored in roll form without blocking, i.e. without sticking together.
Cohesive coatings are used in a variety of different types of applications, but are particularly desirable for use as sealants in packaging for snack food such as candies, chocolates, ice cream and the like which are sensitive to heat thus rendering undesirable the use of heat sealable adhesives to seal such packages.
Typical cold seal adhesives have been formulated by combining a natural rubber elastomer, particularly a latex, with other ingredients such as stabilizers, antioxidants, and the like. Natural rubber elastomers exhibit most of the desirable cold seal properties noted above. Typically, these natural rubber elastomers where blended together with an acrylic emulsion. The acrylic emulsion provides advantageous properties to the natural rubber latex to enable the latex to adequately bond to flexible packaging substrates that may be covered with various types of inks, primers, release modifiers, slip agents and the like. Unfortunately, acrylic emulsions used in the past had heat reactive sites in the polymer chain which allow crosslinking of the polymer at temperatures ranging from above about 127 C
(260 F). Crosslinking results in an improvement of some physical properties and in better water and solvent resistance, but also makes the acrylic more brittle so that its adhesive properties are reduced. In the past, the heat reactive functionality of such acrylic emulsions was not important since there was no way for the crosslinking to be initiated, i.e. processing temperatures of the flexible packaging substrates were well below the critical temperature of 127 C (260 F), and there were no known chemical initiators in the packaging materials per se. Thus, the acrylic emulsion was adapted for use in cohesive or cold seal coatings for flexible food packaging systems.
In more recent years, however, new inks such as acrylic based and polyurethane based inks have been introduced for use on flexible packaging substrates. Also, the substrates themselves are typically laminations of various types of films bonded together with new laminating adhesives such as water based polyurethane dispersions (PUD's) and acrylics to form the substrate lamination.
Further, the substrate itself is being manufactured from new films with multiple co-extrusion layers such as high barrier resins, high surface energy resins and low temperature sealing resins for the purpose of promoting adhesion of cold seal or cohesive coatings to the surface of the substrates. In addition, new processing equipment has been developed to speed the rate of converting raw materials to the flexible end product packaging assembly. New "extreme dryers" are being used to superheat and compress oven air that is used to dry flexible packaging coatings, and for example these extreme dryers run at 135 C (275 F) at 2.1 kg/cm2 (30 psi).
Unfortunately, running at such temperatures results in being 15 degrees higher than the critical temperature of 127 C (260 F) mentioned above for initiating crosslinking. As a result, the acrylic latex used in the past crosslinked with the result that although it became tougher, it also decreased its cohesiveness resulting in what is commonly referred to in the art as "seal deadening." Seal deadening of a flexible package results in failure of the seal which is unacceptable to manufacturers and consumers. As a result, it was desirable to develop a water based cohesive which could be utilized with flexible packaging systems that are manufactured by current techniques so that such systems do not result in cohesive failure.
SUMMARY OF THE INVENTION
The present invention provides a water based, cold seal, cohesive coating containing a natural rubber latex emulsion together with a non-self-crosslinking acrylic emulsion for flexible packaging systems, preferably food packaging systems, and most preferably snack food packaging systems. The cold seal cohesive coating is applied to selected areas of a substrate in the form of a flexible sheet of material, and provides satisfactory adhesion to the surface of the substrate and also provides the ability to form a strong bond to itself when pressure is applied to seal the package. The cold seal cohesive coating thus provides improved adhesion to meet the desired goal of providing at least 118.11g/cm (300g/inch) minimum bond strengths, offers enhanced cohesion to itself, offers resistance to seal deadening or degradation, and acceptable blocking strength so that it can be conveniently wound up on a reel for storage purposes.
In order to accomplish the above, the cold seal cohesive coating of the present invention is comprised of about 25% to about 90% by weight of a natural rubber latex emulsion, about 10% to about 75% by weight of a non-self-crosslinking acrylic emulsion, about 0.01% to about 10% by weight water, and one or more ingredients selected from an anti-foam agent, ammonia, a surfactant, an anti-blocking agent, an inert filler, and a conditioning agent, so that in combination the components total 100% by weight of the cohesive coating. Preferably, the cohesive coating of the present invention includes about 50% to about 90% by weight of the natural rubber latex emulsion and about 10% to about 50% by weight of the non-self-crosslinking acrylic emulsion in a blend with water and one or more of the other ingredients described above. In one particularly preferred composition the cohesive coating includes about 60% to about 80% by weight of -the natural rubber latex emulsion, about 20% to about 40% by weight of the non-self-crosslinking acrylic emulsion, about 0.01 % to about 5% by weight water, and about 0.01% to about 5% by weight of each of the anti-foam agent, ammonia, the surfactant, and the anti-blocking agent. Most preferably, the cohesive coating composition contains about 65% to about 70% by weight of the natural rubber latex emulsion, about 25% to about 35% by weight of the non-self-crosslinking acrylic emulsion, about 0.01% to about 3% by weight water, and about 0.01 % to about 5%
by weight of each of the anti-foam agent, the ammonia, the surfactant, and the anti-blocking agent.
The exact proportions of natural rubber latex emulsion and non-self-crosslinking acrylic emulsion are dependent on the commercial end use. For example, low pressure sealing which occurs at about 162.5kpa (20lbs./in.2) would require a higher proportion of latex emulsion whereas higher pressure sealing as for example at about 650kpa (80lbs./in2) would require a lower proportion of latex.
The cold seal cohesive coating of the present invention may be advaritageously applied to selected areas of the substrate by conventional means, e.g_ gravure, reverse roll coating, flexo, Meyer rod or air knife coating. In addition, the cold seal cohesive coating of the present invention may then also be advantageously dried by conventional means, e.g. in an oven, at temperatures above 127 C (260 F), if desired, without detrimentally affecting the seals of the package.
In another aspect of the invention, there is provided a flexible packaging assembly for containing a food article. The flexible packaging assembly includes a substrate in the form of a flexible sheet of material having opposite longitudinal edges, and a water based, cold seal cohesive coating disposed on at least one of the longitudinal edges. The cohesive coating is comprised of the ingredients listed above.
In yet another aspect of the invention, the present invention provides a method for making a flexible package comprising the steps of applying a cold seal, cohesive coating containing the ingredients listed above to opposite longitudinal edges of a substrate in the form of a flexible sheet of material, contacting the cold seal cohesive coating applied along one longitudinal edge of the substrate with the cold seal cohesive coating applied on the opposite longitudinal edge of the substrate, and applying pressure to seal the cold seal cohesive coatings to one another and thus bond the two opposite longitudinal edges of the substrate together.
The cold seal cohesive coating may also be applied transversely across the substrate so that when the longitudinal edges of the substrate are brought together, the coating at the end of each individual package is also brought together into intimate contact so that when pressure is applied, it will cause the cold seal cohesive coating to cohere and thus provide an end seal for the package.
It should also be noted that the method of forming a flexible package can also be utilized with two separate substrates. In such case, the cold seal cohesive coating applied to the longitudinal edges and the transverse ends of each substrate are brought into contact with each other so that when pressure is applied, the cold seal cohesive coatings on the two substrates are caused to cohere and thus bond the two substrates together to form a package.
BRIEF DESCRIPTION OF THE DRAWINGS
In the drawings:
Fig. 1 is a plan view of an unassembled cold seal package utilizing a single flexible substrate and having the cohesive coating of the present invention applied thereon;
Fig. 2 is a cross-sectional view of the single flexible substrate of Fig. 1 formed into an assembled cold seal package in accordance with the present invention; and Fig. 3 is a cross-sectional view of an alternate embodiment of an assembled cold seal package utilizing two separate substrates.
BACKGROUND OF THE INVENTION
The present invention relates to a water based, cold seal, cohesive coating for flexible packaging systems, and more particularly to a water based, cold seal, cohesive coating containing a non-self-crosslinking acrylic emulsion for use in food packaging and especially snack food packaging.
A cold seal adhesive, also referred to as a cohesive coating, is a type of pressure sensitive adhesive which possesses the ability to form a strong bond to itself when pressure is applied and also to form a bond with the flexible substrate on which it is applied. Cohesive coatings are thus pressure respondent, i.e.
the introduction of mechanical energy is all that is required to initiate seal formation.
Cold seal adhesives also preferably lack adhesion to the surfaces such as plastic films and overprint varnishes which are on the opposite face of these flexible substrates so that such flexible substrates or webs coated with the cold seal adhesive may be stored in roll form without blocking, i.e. without sticking together.
Cohesive coatings are used in a variety of different types of applications, but are particularly desirable for use as sealants in packaging for snack food such as candies, chocolates, ice cream and the like which are sensitive to heat thus rendering undesirable the use of heat sealable adhesives to seal such packages.
Typical cold seal adhesives have been formulated by combining a natural rubber elastomer, particularly a latex, with other ingredients such as stabilizers, antioxidants, and the like. Natural rubber elastomers exhibit most of the desirable cold seal properties noted above. Typically, these natural rubber elastomers where blended together with an acrylic emulsion. The acrylic emulsion provides advantageous properties to the natural rubber latex to enable the latex to adequately bond to flexible packaging substrates that may be covered with various types of inks, primers, release modifiers, slip agents and the like. Unfortunately, acrylic emulsions used in the past had heat reactive sites in the polymer chain which allow crosslinking of the polymer at temperatures ranging from above about 127 C
(260 F). Crosslinking results in an improvement of some physical properties and in better water and solvent resistance, but also makes the acrylic more brittle so that its adhesive properties are reduced. In the past, the heat reactive functionality of such acrylic emulsions was not important since there was no way for the crosslinking to be initiated, i.e. processing temperatures of the flexible packaging substrates were well below the critical temperature of 127 C (260 F), and there were no known chemical initiators in the packaging materials per se. Thus, the acrylic emulsion was adapted for use in cohesive or cold seal coatings for flexible food packaging systems.
In more recent years, however, new inks such as acrylic based and polyurethane based inks have been introduced for use on flexible packaging substrates. Also, the substrates themselves are typically laminations of various types of films bonded together with new laminating adhesives such as water based polyurethane dispersions (PUD's) and acrylics to form the substrate lamination.
Further, the substrate itself is being manufactured from new films with multiple co-extrusion layers such as high barrier resins, high surface energy resins and low temperature sealing resins for the purpose of promoting adhesion of cold seal or cohesive coatings to the surface of the substrates. In addition, new processing equipment has been developed to speed the rate of converting raw materials to the flexible end product packaging assembly. New "extreme dryers" are being used to superheat and compress oven air that is used to dry flexible packaging coatings, and for example these extreme dryers run at 135 C (275 F) at 2.1 kg/cm2 (30 psi).
Unfortunately, running at such temperatures results in being 15 degrees higher than the critical temperature of 127 C (260 F) mentioned above for initiating crosslinking. As a result, the acrylic latex used in the past crosslinked with the result that although it became tougher, it also decreased its cohesiveness resulting in what is commonly referred to in the art as "seal deadening." Seal deadening of a flexible package results in failure of the seal which is unacceptable to manufacturers and consumers. As a result, it was desirable to develop a water based cohesive which could be utilized with flexible packaging systems that are manufactured by current techniques so that such systems do not result in cohesive failure.
SUMMARY OF THE INVENTION
The present invention provides a water based, cold seal, cohesive coating containing a natural rubber latex emulsion together with a non-self-crosslinking acrylic emulsion for flexible packaging systems, preferably food packaging systems, and most preferably snack food packaging systems. The cold seal cohesive coating is applied to selected areas of a substrate in the form of a flexible sheet of material, and provides satisfactory adhesion to the surface of the substrate and also provides the ability to form a strong bond to itself when pressure is applied to seal the package. The cold seal cohesive coating thus provides improved adhesion to meet the desired goal of providing at least 118.11g/cm (300g/inch) minimum bond strengths, offers enhanced cohesion to itself, offers resistance to seal deadening or degradation, and acceptable blocking strength so that it can be conveniently wound up on a reel for storage purposes.
In order to accomplish the above, the cold seal cohesive coating of the present invention is comprised of about 25% to about 90% by weight of a natural rubber latex emulsion, about 10% to about 75% by weight of a non-self-crosslinking acrylic emulsion, about 0.01% to about 10% by weight water, and one or more ingredients selected from an anti-foam agent, ammonia, a surfactant, an anti-blocking agent, an inert filler, and a conditioning agent, so that in combination the components total 100% by weight of the cohesive coating. Preferably, the cohesive coating of the present invention includes about 50% to about 90% by weight of the natural rubber latex emulsion and about 10% to about 50% by weight of the non-self-crosslinking acrylic emulsion in a blend with water and one or more of the other ingredients described above. In one particularly preferred composition the cohesive coating includes about 60% to about 80% by weight of -the natural rubber latex emulsion, about 20% to about 40% by weight of the non-self-crosslinking acrylic emulsion, about 0.01 % to about 5% by weight water, and about 0.01% to about 5% by weight of each of the anti-foam agent, ammonia, the surfactant, and the anti-blocking agent. Most preferably, the cohesive coating composition contains about 65% to about 70% by weight of the natural rubber latex emulsion, about 25% to about 35% by weight of the non-self-crosslinking acrylic emulsion, about 0.01% to about 3% by weight water, and about 0.01 % to about 5%
by weight of each of the anti-foam agent, the ammonia, the surfactant, and the anti-blocking agent.
The exact proportions of natural rubber latex emulsion and non-self-crosslinking acrylic emulsion are dependent on the commercial end use. For example, low pressure sealing which occurs at about 162.5kpa (20lbs./in.2) would require a higher proportion of latex emulsion whereas higher pressure sealing as for example at about 650kpa (80lbs./in2) would require a lower proportion of latex.
The cold seal cohesive coating of the present invention may be advaritageously applied to selected areas of the substrate by conventional means, e.g_ gravure, reverse roll coating, flexo, Meyer rod or air knife coating. In addition, the cold seal cohesive coating of the present invention may then also be advantageously dried by conventional means, e.g. in an oven, at temperatures above 127 C (260 F), if desired, without detrimentally affecting the seals of the package.
In another aspect of the invention, there is provided a flexible packaging assembly for containing a food article. The flexible packaging assembly includes a substrate in the form of a flexible sheet of material having opposite longitudinal edges, and a water based, cold seal cohesive coating disposed on at least one of the longitudinal edges. The cohesive coating is comprised of the ingredients listed above.
In yet another aspect of the invention, the present invention provides a method for making a flexible package comprising the steps of applying a cold seal, cohesive coating containing the ingredients listed above to opposite longitudinal edges of a substrate in the form of a flexible sheet of material, contacting the cold seal cohesive coating applied along one longitudinal edge of the substrate with the cold seal cohesive coating applied on the opposite longitudinal edge of the substrate, and applying pressure to seal the cold seal cohesive coatings to one another and thus bond the two opposite longitudinal edges of the substrate together.
The cold seal cohesive coating may also be applied transversely across the substrate so that when the longitudinal edges of the substrate are brought together, the coating at the end of each individual package is also brought together into intimate contact so that when pressure is applied, it will cause the cold seal cohesive coating to cohere and thus provide an end seal for the package.
It should also be noted that the method of forming a flexible package can also be utilized with two separate substrates. In such case, the cold seal cohesive coating applied to the longitudinal edges and the transverse ends of each substrate are brought into contact with each other so that when pressure is applied, the cold seal cohesive coatings on the two substrates are caused to cohere and thus bond the two substrates together to form a package.
BRIEF DESCRIPTION OF THE DRAWINGS
In the drawings:
Fig. 1 is a plan view of an unassembled cold seal package utilizing a single flexible substrate and having the cohesive coating of the present invention applied thereon;
Fig. 2 is a cross-sectional view of the single flexible substrate of Fig. 1 formed into an assembled cold seal package in accordance with the present invention; and Fig. 3 is a cross-sectional view of an alternate embodiment of an assembled cold seal package utilizing two separate substrates.
DETAILED DESCRIPTION OF THE INVENTION
The present invention relates to a water based cold seal adhesive flexible packaging material which utilizes a cohesive coating containing natural latex and a non-self-crosslinking acrylic to provide a bond between one or more substrates when sealed. The packaging material can be utilized to wrap various types of products, such as food products like candy and other snack food to provide a flexible package to contain the product. Although food products are the preferred articles wrapped by the present cold seal adhesive system, the present disclosure is not limited to such packages, but instead may be utilized with other forms of packaging for containing both comestible as well as non-comestible products.
Referring to Fig. 1, the creation of a package typically begins with the production of a continuous sheet or web of wrapping material 2. The continuous web of material 2 is generally in the form of a thin, flexible film, and as is conventional, proceeds generally horizontally downstream to multi-station printing presses where artwork and text in one or more colors is applied to its exterior surface 4 (see Fig. 2), and adhesive in applied to its interior surface 6 in either a predetermined pattern or overall coverage. The adhesive pattern typically will be rectangular defined by a pair of longitudinal strips 8 and 10 along opposite edges of the web and a transverse strip 12 extending between the two longitudinal strips 8, 10. The distance between the transverse strips of adhesive define the length of the particular package, and is indicated by transverse dashed line 14. The adhesive layer is typically applied to the interior surface of the web after the application of the artwork and text on the exterior of the web by Gravure roll application, or by any other conventional means, so that the layer of adhesive has a thickness of about 0.05 to about 1.0 mil and may consist of either a multitude of separate spots or dots or a solid continuous layer. Also, it is typical for a protective surface, such as an overprint varnish or a release film, to be applied over the artwork and text to protect the artwork and text from smudging, and to control the coefficient of friction of the exterior surface of the web. As is conventional, the adhesive is applied in lengthwise and widthwise strips in appropriate selected surface areas of the web to form a rectangular configuration so that after insertion of the article 16 (Fig. 2) to be wrapped, the web 2 may be folded, as shown best in Fig. 2, so that the longitudinal and transverse strips 8, 10, 12 of adhesive register with one another and become aligned so that upon the application of pressure, the web 2 forms the shape, size and volume of the package desired.
As noted above, the web 2 itself is generally preferred to be formed as a thin, flexible material to function as a substrate for the materials to be applied. The web 2 itself may be made of a plastic film material such as polyethylene, polypropylene, polyester, polyolefins, polystyrene, nylon, polycarbonates, cellophane, ethylenevinyl acetates, ethylenevinyl alcohols, polyvinyl alcohols, polyvinyl chloride, alphaolefins, polyvinyl butyrate, cellulose acetate, butyrate or cellulose acetate propionate or metalized versions of any of the aforementioned films. Alternately, depending upon the article to be packaged, the web 2 may be made of a metalized foil such as aluminum foil, or the metalized foil may be laminated to the web. Another alternative, is for one or more webs to be formed of paper and paper products, including paperboard such as containerboard, which includes corrugating medium and linerboard used to make corrugated paper, and boxboard used to make folding cartons. In addition, paper products such as publication grade paper or bleached or unbleached kraft paper, or recycled paper may also be utilized. The above paper products may also be clay-coated to enhance printing of the artwork and text.
In the packaging of food products, it is desirable to provide a peelable but non-resealable closure system (hereinafter referred to as a PNR system). In order to provide a peelable but non-resealable closure for the packaging material, the present invention provides a water based cold seal cohesive system containing natural rubber latex and a non-self-crosslinking acrylic. The system is comprised of a cohesive coating applied to one or more substrates or webs. Regardless of what is being packaged, it should be noted that in one form the packaging material may be comprised of a single substrate or web 2 and composed of the same substrate material. However, as shown best in Fig. 3, the packaging material may be separate substrates 20, 22 and each may be composed of a different material depending upon the particular packaging desired and article 18 to be wrapped, and each substrate 20, 22 may contain a cohesive coating 24, 26 respectively, as described above. In any event, the cohesive coatings 24 and 26 must have sufficient affinity for each other so that when a sealing pressure appropriate for the marketplace, typically 5 to 20 pounds per linear inch for low pressure packaging and 60 to 100 pounds per linear inch for confectionery, is applied thereto, the cohesive bonds to itself to form a closure for the packaging material and thus contain or wrap the article 18 inside.
However, for a PNR system, it is essential that the cohesive has more affinity for itself than it does for the substrate on which it is applied. It is also essential that the cohesive does not destroy, pull fibers, or if the web is laminated, de-laminate the web substrate when the package is opened. This necessarily implies that it is essential that the cohesive has more affinity for bonding to itself than the cohesive has for bonding to the substrate on which it is applied.
This is typically measured by percent transfer of the cohesive when peeling in a T-peel configuration. The adhesive, when peeled, must not be resealable to the web or substrate from which it transferred.
Thus, the bond formed when the packaging material is closed must be stronger than the bond between the cohesive and the web resulting in the transfer of the cohesive when the substrates are peeled apart, i.e. the package is opened by a user, to thereby provide a non-resealable package.
In all PNR systems, the acceptable mode of failure is determined by the market in which the cold seal cohesive will be sold. Modes of failure include but are not restricted to, cohesive failure, cohesive split, adhesive failure, film or paper destruct, etc.
The present invention relates to a water based cold seal adhesive flexible packaging material which utilizes a cohesive coating containing natural latex and a non-self-crosslinking acrylic to provide a bond between one or more substrates when sealed. The packaging material can be utilized to wrap various types of products, such as food products like candy and other snack food to provide a flexible package to contain the product. Although food products are the preferred articles wrapped by the present cold seal adhesive system, the present disclosure is not limited to such packages, but instead may be utilized with other forms of packaging for containing both comestible as well as non-comestible products.
Referring to Fig. 1, the creation of a package typically begins with the production of a continuous sheet or web of wrapping material 2. The continuous web of material 2 is generally in the form of a thin, flexible film, and as is conventional, proceeds generally horizontally downstream to multi-station printing presses where artwork and text in one or more colors is applied to its exterior surface 4 (see Fig. 2), and adhesive in applied to its interior surface 6 in either a predetermined pattern or overall coverage. The adhesive pattern typically will be rectangular defined by a pair of longitudinal strips 8 and 10 along opposite edges of the web and a transverse strip 12 extending between the two longitudinal strips 8, 10. The distance between the transverse strips of adhesive define the length of the particular package, and is indicated by transverse dashed line 14. The adhesive layer is typically applied to the interior surface of the web after the application of the artwork and text on the exterior of the web by Gravure roll application, or by any other conventional means, so that the layer of adhesive has a thickness of about 0.05 to about 1.0 mil and may consist of either a multitude of separate spots or dots or a solid continuous layer. Also, it is typical for a protective surface, such as an overprint varnish or a release film, to be applied over the artwork and text to protect the artwork and text from smudging, and to control the coefficient of friction of the exterior surface of the web. As is conventional, the adhesive is applied in lengthwise and widthwise strips in appropriate selected surface areas of the web to form a rectangular configuration so that after insertion of the article 16 (Fig. 2) to be wrapped, the web 2 may be folded, as shown best in Fig. 2, so that the longitudinal and transverse strips 8, 10, 12 of adhesive register with one another and become aligned so that upon the application of pressure, the web 2 forms the shape, size and volume of the package desired.
As noted above, the web 2 itself is generally preferred to be formed as a thin, flexible material to function as a substrate for the materials to be applied. The web 2 itself may be made of a plastic film material such as polyethylene, polypropylene, polyester, polyolefins, polystyrene, nylon, polycarbonates, cellophane, ethylenevinyl acetates, ethylenevinyl alcohols, polyvinyl alcohols, polyvinyl chloride, alphaolefins, polyvinyl butyrate, cellulose acetate, butyrate or cellulose acetate propionate or metalized versions of any of the aforementioned films. Alternately, depending upon the article to be packaged, the web 2 may be made of a metalized foil such as aluminum foil, or the metalized foil may be laminated to the web. Another alternative, is for one or more webs to be formed of paper and paper products, including paperboard such as containerboard, which includes corrugating medium and linerboard used to make corrugated paper, and boxboard used to make folding cartons. In addition, paper products such as publication grade paper or bleached or unbleached kraft paper, or recycled paper may also be utilized. The above paper products may also be clay-coated to enhance printing of the artwork and text.
In the packaging of food products, it is desirable to provide a peelable but non-resealable closure system (hereinafter referred to as a PNR system). In order to provide a peelable but non-resealable closure for the packaging material, the present invention provides a water based cold seal cohesive system containing natural rubber latex and a non-self-crosslinking acrylic. The system is comprised of a cohesive coating applied to one or more substrates or webs. Regardless of what is being packaged, it should be noted that in one form the packaging material may be comprised of a single substrate or web 2 and composed of the same substrate material. However, as shown best in Fig. 3, the packaging material may be separate substrates 20, 22 and each may be composed of a different material depending upon the particular packaging desired and article 18 to be wrapped, and each substrate 20, 22 may contain a cohesive coating 24, 26 respectively, as described above. In any event, the cohesive coatings 24 and 26 must have sufficient affinity for each other so that when a sealing pressure appropriate for the marketplace, typically 5 to 20 pounds per linear inch for low pressure packaging and 60 to 100 pounds per linear inch for confectionery, is applied thereto, the cohesive bonds to itself to form a closure for the packaging material and thus contain or wrap the article 18 inside.
However, for a PNR system, it is essential that the cohesive has more affinity for itself than it does for the substrate on which it is applied. It is also essential that the cohesive does not destroy, pull fibers, or if the web is laminated, de-laminate the web substrate when the package is opened. This necessarily implies that it is essential that the cohesive has more affinity for bonding to itself than the cohesive has for bonding to the substrate on which it is applied.
This is typically measured by percent transfer of the cohesive when peeling in a T-peel configuration. The adhesive, when peeled, must not be resealable to the web or substrate from which it transferred.
Thus, the bond formed when the packaging material is closed must be stronger than the bond between the cohesive and the web resulting in the transfer of the cohesive when the substrates are peeled apart, i.e. the package is opened by a user, to thereby provide a non-resealable package.
In all PNR systems, the acceptable mode of failure is determined by the market in which the cold seal cohesive will be sold. Modes of failure include but are not restricted to, cohesive failure, cohesive split, adhesive failure, film or paper destruct, etc.
It is important to note that the cold seal cohesive utilized in the present system contains natural rubber. As used herein, the term "natural rubber"
includes all materials made from or containing natural latex. The term "natural latex"
as used herein is defined as a milky fluid that consists of extremely small particles of rubber obtained from plants, principally from the H. brasiliensis (rubber) tree dispersed in an aqueous medium. It contains a variety of naturally occurring substances, including cis-1, 4-polyisoprene in a colloidal suspension and plant proteins.
The water based cold seal cohesive coating for bonding one or more substrates together to form a flexible package material to contain an article in accordance with the present invention comprises a cohesive coating containing the following components: about 25% to about 90% by weight of a natural rubber latex emulsion, about 10% to about 75% by weight of a non-self-crosslinking acrylic emulsion, about 0.0 1% to about 10% by weight water, and one or more ingredient selected from an anti-foam agent, ammonia, a surfactant, an anti-blocking agent, an inert filler, and a conditioning agent, so that in combination the components total 100% by weight of the cohesive coating. Preferably, the cohesive coating of the present invention includes about 50% to about 90% by weight of the natural rubber latex emulsion and about 10% to about 50% by weight of the non-self-crosslinking acrylic emulsion in a blend with water and one or more of the other ingredients described above. In one particularly preferred composition, the cohesive coating composition comprises about 60% to about 80% by weight of the natural rubber latex emulsion, about 20% to about 40% by weight of the non-self-crosslinking acrylic emulsion, about 0.01% to about 5% by weight water, about 0.01% to about 5% by weight of the anti-foam agent, about 0.01% to about 5% by weight of ammonia, about 0.01% to about 5% by weight of the surfactant, and about 0.01% to about 5% by weight of the anti-blocking agent. The most preferred composition for the cohesive coating comprises about 65% to about 70% by weight of the natural rubber latex emulsion, about 25% to about 35% by weight of the non-self-crosslinking acrylic emulsion, about 0.01% to about 3% by weight water, about 0.01% to about 1% by weight of the anti-foam agent, about 0.01% to about 1% by weight of ammonia, about 0.01% to about 1% by weight of the surfactant, and about 0.01% to about 1% by weight of the anti-blocking agent. It has been determined that one particularly desirable cohesive coating composition comprises about 68% by weight of the natural rubber latex emulsion, about 30% by weight of the non-self-crosslinking acrylic emulsion, about 1.2% by weight water, about 0.4% by weight of the anti-foam agent, about 0.2% by weight of ammonia, about 0.1 % by weight of the surfactant, and about 0.1 % by weight of the anti-blocking agent.
The natural rubber latex utilized in the composition of the present invention may be standard grade natural latex, high ammonia natural latex, low ammonia natural latex, double centrifuged latex, and/or high dry rubber content latex.
The preferred natural rubber latex is of the high ammonia type. Typically, high ammonia natural latex is centrifuged natural latex preserved with ammonia only or by formaldehyde followed by ammonia. The ammonia (alkalinity) content of high ammonia latex is not less than 0.6% on latex percent, as per ISO-2004 ('88E) and ASTM D1076-88. Low ammonia latex is typically a centrifuged natural latex preserved with low ammonia and other preservatives. The ammonia content of low ammonia latex does not exceed 0.29% on latex percent as per the above cited ISO
and ASTM Standards. Typically, low ammonia latex is preserved with 0.2%
ammonia together with a suitable combination of zinc oxide (ZnO) and tetramethylthiuramdisulphide (TMTD) of not more than 0.1% in total, based on latex weight. Double centrifuged latex is a highly purified latex concentrate prepared by recentrifuging the first centrifuged latex which has been suitably diluted. As a result, the non-rubber constituents of latex are further reduced. High dry rubber content (65-67%) latex is prepared by centrifugation, and provides an alternative to the above latex emulsions because it dries faster.
includes all materials made from or containing natural latex. The term "natural latex"
as used herein is defined as a milky fluid that consists of extremely small particles of rubber obtained from plants, principally from the H. brasiliensis (rubber) tree dispersed in an aqueous medium. It contains a variety of naturally occurring substances, including cis-1, 4-polyisoprene in a colloidal suspension and plant proteins.
The water based cold seal cohesive coating for bonding one or more substrates together to form a flexible package material to contain an article in accordance with the present invention comprises a cohesive coating containing the following components: about 25% to about 90% by weight of a natural rubber latex emulsion, about 10% to about 75% by weight of a non-self-crosslinking acrylic emulsion, about 0.0 1% to about 10% by weight water, and one or more ingredient selected from an anti-foam agent, ammonia, a surfactant, an anti-blocking agent, an inert filler, and a conditioning agent, so that in combination the components total 100% by weight of the cohesive coating. Preferably, the cohesive coating of the present invention includes about 50% to about 90% by weight of the natural rubber latex emulsion and about 10% to about 50% by weight of the non-self-crosslinking acrylic emulsion in a blend with water and one or more of the other ingredients described above. In one particularly preferred composition, the cohesive coating composition comprises about 60% to about 80% by weight of the natural rubber latex emulsion, about 20% to about 40% by weight of the non-self-crosslinking acrylic emulsion, about 0.01% to about 5% by weight water, about 0.01% to about 5% by weight of the anti-foam agent, about 0.01% to about 5% by weight of ammonia, about 0.01% to about 5% by weight of the surfactant, and about 0.01% to about 5% by weight of the anti-blocking agent. The most preferred composition for the cohesive coating comprises about 65% to about 70% by weight of the natural rubber latex emulsion, about 25% to about 35% by weight of the non-self-crosslinking acrylic emulsion, about 0.01% to about 3% by weight water, about 0.01% to about 1% by weight of the anti-foam agent, about 0.01% to about 1% by weight of ammonia, about 0.01% to about 1% by weight of the surfactant, and about 0.01% to about 1% by weight of the anti-blocking agent. It has been determined that one particularly desirable cohesive coating composition comprises about 68% by weight of the natural rubber latex emulsion, about 30% by weight of the non-self-crosslinking acrylic emulsion, about 1.2% by weight water, about 0.4% by weight of the anti-foam agent, about 0.2% by weight of ammonia, about 0.1 % by weight of the surfactant, and about 0.1 % by weight of the anti-blocking agent.
The natural rubber latex utilized in the composition of the present invention may be standard grade natural latex, high ammonia natural latex, low ammonia natural latex, double centrifuged latex, and/or high dry rubber content latex.
The preferred natural rubber latex is of the high ammonia type. Typically, high ammonia natural latex is centrifuged natural latex preserved with ammonia only or by formaldehyde followed by ammonia. The ammonia (alkalinity) content of high ammonia latex is not less than 0.6% on latex percent, as per ISO-2004 ('88E) and ASTM D1076-88. Low ammonia latex is typically a centrifuged natural latex preserved with low ammonia and other preservatives. The ammonia content of low ammonia latex does not exceed 0.29% on latex percent as per the above cited ISO
and ASTM Standards. Typically, low ammonia latex is preserved with 0.2%
ammonia together with a suitable combination of zinc oxide (ZnO) and tetramethylthiuramdisulphide (TMTD) of not more than 0.1% in total, based on latex weight. Double centrifuged latex is a highly purified latex concentrate prepared by recentrifuging the first centrifuged latex which has been suitably diluted. As a result, the non-rubber constituents of latex are further reduced. High dry rubber content (65-67%) latex is prepared by centrifugation, and provides an alternative to the above latex emulsions because it dries faster.
A particularly preferred natural rubber latex for use in the present cohesive composition is a high ammonia natural rubber latex available under the trade-mark "UNITEX" from Guthrie Latex, Inc. Another suitable high ammonia natural rubber latex emulsion is available under the trade-mark Revertex from Centrotrade Rubber J SA, Inc.
The cohesive composition of the present invention also includes a non-self-crosslinking acrylic emulsion. It is essential that the acrylic emulsion does not contain any self-crosslinking functionality. The acrylic emulsion may contain from about 45% to about 60% solids, with about 48% to about 56% solids preferred.
The non-self-crosslinking acrylic emulsions may be selected from various types, such as styrene/acrylic, nitrile/acrylic and all-acrylic (i.e. 100% acrylic emulsion).
Non-self-crosslinking emulsions are available under the trade-marks Hycar 26548 (a styrene acrylic emulsion), Joncryl 77 (a styrene acrylic emulsion), or Eastarez 1040 (a styrene acrylic emulsion), from Noveon, Johnson Polymer, or Eastman Chemical Products, respectively, and may be employed herein. However, the preferred non-self crosslinking acrylic emulsion is a styrene acrylic emulsion which contains from about 20% to about 40% styrene. The preferred styrene-acrylic emulsion is that available under the trade-mark Eastarez 4000 available from Eastman Chemical Products. The use of a non-self-crosslinking acrylic emulsion provides water resistance, film clarity, alkali resistance, and pigment binding strength. In addition, since it contains no self crosslinking functionalities, it can be used with the high temperature converting processes currently used in the industry and in particular above 127 C (260 F) without resulting in seal deadening of the packaged product.
The water utilized in the present cohesive composition may be local tap water, distilled water or deionized water. The only requirement is that the water utilized not contain any substantial degree of impurities and/or dissolved components that would not be compatible with the other formulating ingredients utilized in the present cohesive composition.
The cohesive composition of the present invention also includes a non-self-crosslinking acrylic emulsion. It is essential that the acrylic emulsion does not contain any self-crosslinking functionality. The acrylic emulsion may contain from about 45% to about 60% solids, with about 48% to about 56% solids preferred.
The non-self-crosslinking acrylic emulsions may be selected from various types, such as styrene/acrylic, nitrile/acrylic and all-acrylic (i.e. 100% acrylic emulsion).
Non-self-crosslinking emulsions are available under the trade-marks Hycar 26548 (a styrene acrylic emulsion), Joncryl 77 (a styrene acrylic emulsion), or Eastarez 1040 (a styrene acrylic emulsion), from Noveon, Johnson Polymer, or Eastman Chemical Products, respectively, and may be employed herein. However, the preferred non-self crosslinking acrylic emulsion is a styrene acrylic emulsion which contains from about 20% to about 40% styrene. The preferred styrene-acrylic emulsion is that available under the trade-mark Eastarez 4000 available from Eastman Chemical Products. The use of a non-self-crosslinking acrylic emulsion provides water resistance, film clarity, alkali resistance, and pigment binding strength. In addition, since it contains no self crosslinking functionalities, it can be used with the high temperature converting processes currently used in the industry and in particular above 127 C (260 F) without resulting in seal deadening of the packaged product.
The water utilized in the present cohesive composition may be local tap water, distilled water or deionized water. The only requirement is that the water utilized not contain any substantial degree of impurities and/or dissolved components that would not be compatible with the other formulating ingredients utilized in the present cohesive composition.
The ammonia which may be utilized in the cohesive composition is preferably in the form of ammonia hydroxide containing from about 20% to about 40% ammonia. However, the source of ammonia that can be utilized in the cohesive coating of the present invention may also be concentrated ammonia itself, or may be available as aqueous ammonia, ammonium hydroxide 29.4%, or ammonium hydroxide BE. Ammonia hydroxide available under the trade-n park 26 DE from Hydrite Chemical Company has been found to be a preferred ingredient.
Anti-foam agents such as an emulsified silicone, a mineral oil based product and/or a glycol ester/polyol may be added to the cohesive coating to prevent foaming during application. Typical anti-foam agents include an emulsified silicone available under the trade-mark Dow Antifoam AF from Dow Coming, a mineral oil based blend available under the trade-mark Ultra Deefo 2001 from Ultra Additives, Inc. and a mineral oil available under the trade-mark Rhodoline 675 from Rhodia, Inc. A particularly preferred anti-foam agent is a glycol ester/polyol available under the trade-mark Rhodoline 999 from Rhodia, Inc.
Anti-blocking agents such as clays, calcium carbonate and/or fumed silica may be added to the cohesive coating to prevent blocking of the coating to the exterior side of the flexible material and which is not coated with the cohesive.
These anti-blocking agents thus aid in preventing the cohesive coating from adhering to that exterior surface when the material is rolled up on a reel for storage.
Typical anti-blocking agents include a clay available under the trade designation ASP600 from Fleming Co., a fumed silica available under the trade-mark Lo-Vel from PPG Industries, and a calcium carbonate available under the trade-mark Atomite from Harry Holland. A particularly preferred anti-blocking agent is a fumed silica available under the trade-mark Lo-Vel 29 available from PPG Industries.
Anti-foam agents such as an emulsified silicone, a mineral oil based product and/or a glycol ester/polyol may be added to the cohesive coating to prevent foaming during application. Typical anti-foam agents include an emulsified silicone available under the trade-mark Dow Antifoam AF from Dow Coming, a mineral oil based blend available under the trade-mark Ultra Deefo 2001 from Ultra Additives, Inc. and a mineral oil available under the trade-mark Rhodoline 675 from Rhodia, Inc. A particularly preferred anti-foam agent is a glycol ester/polyol available under the trade-mark Rhodoline 999 from Rhodia, Inc.
Anti-blocking agents such as clays, calcium carbonate and/or fumed silica may be added to the cohesive coating to prevent blocking of the coating to the exterior side of the flexible material and which is not coated with the cohesive.
These anti-blocking agents thus aid in preventing the cohesive coating from adhering to that exterior surface when the material is rolled up on a reel for storage.
Typical anti-blocking agents include a clay available under the trade designation ASP600 from Fleming Co., a fumed silica available under the trade-mark Lo-Vel from PPG Industries, and a calcium carbonate available under the trade-mark Atomite from Harry Holland. A particularly preferred anti-blocking agent is a fumed silica available under the trade-mark Lo-Vel 29 available from PPG Industries.
The surfactant can be optionally present in the cohesive composition of the present invention in order to make the adhesive more hydrophilic. The surfactant has a hydrophile-lipophile balance (HLB) number of preferably less than 15.
The I LB of a surfactant is an expression of its hydrophile-lipophile balance, i.e. the balance of the size and strength of the hydrophilic (water-loving or polar) and the lipophilic (oil-loving or non-polar) groups of the surfactant. All surfactants consist of a molecule that combines both hydrophilic and lipophilic groups.
The surfactant must be reasonably compatible with the other raw materials used in the cohesive so that it does not adversely affect the construction and performance of the adhesive. On the other hand, the surfactant must "bloom" to the surface of the adhesive so as to make the adhesive more hydrophilic. Thus, a delicate balance of compatibility must be maintained. The surfactant also must be sufficiently stable and non-volatile to allow processing in manufacturing and application equipment without effect on the cohesive.
As used herein, the term "surfactant" or "surface-active agent" refers to any compound that reduces surface tension when dissolved in water or water solutions, or which reduces interfacial tension between two liquids, or between a liquid and a solid. The surfactant may be selected from both nonionic and anionic types of surfactants. Examples of suitable surfactants include, but are not limited to, the following:
(1) Fatty acid esters such as glycerol esters, PEG esters, and sorbitan esters, including ethylene glycol distearate, ethylene glycol monostrearate, glycerol mono and/or dioleate, PEG dioleate, PEG monolaurate, sorbitan monolaurate, sorbitan trioleate, etc. These surfactants are available from ICI, Rhone-Poulenc, and other sources.
(2) Nonionic ethoxylates such as alkylphenol ethoxylates, alcohol ethoxylates, alkylamine ethoxylates, etc., including octylphenol ethoxylate, nonylphenol ethoxylate, alkylamine ethoxylates, etc. These surfactants are available from Rhone-Poulenc, Union Carbide, and other sources.
The I LB of a surfactant is an expression of its hydrophile-lipophile balance, i.e. the balance of the size and strength of the hydrophilic (water-loving or polar) and the lipophilic (oil-loving or non-polar) groups of the surfactant. All surfactants consist of a molecule that combines both hydrophilic and lipophilic groups.
The surfactant must be reasonably compatible with the other raw materials used in the cohesive so that it does not adversely affect the construction and performance of the adhesive. On the other hand, the surfactant must "bloom" to the surface of the adhesive so as to make the adhesive more hydrophilic. Thus, a delicate balance of compatibility must be maintained. The surfactant also must be sufficiently stable and non-volatile to allow processing in manufacturing and application equipment without effect on the cohesive.
As used herein, the term "surfactant" or "surface-active agent" refers to any compound that reduces surface tension when dissolved in water or water solutions, or which reduces interfacial tension between two liquids, or between a liquid and a solid. The surfactant may be selected from both nonionic and anionic types of surfactants. Examples of suitable surfactants include, but are not limited to, the following:
(1) Fatty acid esters such as glycerol esters, PEG esters, and sorbitan esters, including ethylene glycol distearate, ethylene glycol monostrearate, glycerol mono and/or dioleate, PEG dioleate, PEG monolaurate, sorbitan monolaurate, sorbitan trioleate, etc. These surfactants are available from ICI, Rhone-Poulenc, and other sources.
(2) Nonionic ethoxylates such as alkylphenol ethoxylates, alcohol ethoxylates, alkylamine ethoxylates, etc., including octylphenol ethoxylate, nonylphenol ethoxylate, alkylamine ethoxylates, etc. These surfactants are available from Rhone-Poulenc, Union Carbide, and other sources.
(3) Nonionic surfactants such as 2,4,7,9-tetramethyl-5-decyn-4,7-diol available from Air Products.
(4) Ethylene oxide/Propylene oxide copolymers which are available from Union Carbide, BASF, etc. It should be noted that these and other surfactants can be blended if necessary to produce the best blend of hydrophilic performance properties.
TM
Aerosol MA80I is a sulfosuccinate anionic surfactant available from Cytec Industries which has been found to be a preferred surfactant for use in the present cohesive composition.
The cohesive composition useful in the present invention may be formulated using any of the techniques known in the art. A representative example of the prior art procedure involves placing the ingredients one by one into a stainless steel mixing vessel, while providing enough agitation to ensure proper and effective mixing of the ingredients. After all the ingredients have been added, the adhesive batch is adjusted to meet its critical physical parameters.
Optional conditioning additives may. be incorporated into the cohesive composition in order to- modify particular physical properties. These additives may include colorants, such as titanium dioxide, sequestrants, deionized water, preservatives, biocides, stabilizers, anti-cling agents, pH adjusters, and other commonly known and used additives. As noted above, each of such additives can be present in amounts ranging from 0% to about 5% by weight.
Fillers may also optionally be incorporated into the adhesive composition in amounts ranging from about 0% to 5% by weight, preferably 0% to 3% by weight.
These are inert in the formulation, and are typically added to increase the bulk of the composition. Also, depending upon the substance employed, a filler may function as an anti-blocking agent. Fillers may include alumina, hydrated alumina (A1203-3H20), a silicate such as magnesium silicate, aluminum silicate, sodium silicate, potassium silicate and the like, mica, calcium carbonate (CaCO3) and silica. Other commonly employed fillers such as talc, clay, wollastonite, feldspar, glass microspheres, ceramic microspheres, thermoplastic microspheres, baryte and wood flour may also be used as long as they do not materially alter the function of the remaining ingredients in'the formulation.
EXAMPLES
The following data was obtained by comparing bond strength performance using a self-crosslinkng styrene/acrylic (Hycar 26288) to a non-self-crosslinking styrene/acrylic (Eastarez 4000) in cohesive formulations.
Test Method and Sample Preparation:
Test Equipment Instron Model 1122 Material Tester with Model 5500 Electronics Instron Test Equipment Setting - Crosshead Speed 30.5 cm/minute (12 inches/minute) TMI SupersealerTM - Sealing conditions 5.63 kg/cm2 (80 psi/) 0.5 second dwell/serrated jaws.
Test Environment - Temperature 22.2 C (72 F)/Humidity 48%
Sample Size - 2.54 cm by 10.16 cm (1 inch by 4 inches) Cohesive Coat Weight - approximately 1.5 kg (3.3 lb)/ream Cohesive samples for bond strength testing were prepared using a number 7-wire wound rod drawing down cohesive on 20.32 cm by 27.94 cm (8 inches by 11 inches) film substrate then dried at 82 C (180 F) for 30 seconds in a convection oven. Samples were then allowed to cool to ambient temperature. 2.54 cm by 10.16 cm (1 inch by 4 inch) samples were cut from lab draw down, sealed using TM[
SupersealerTM then within 60 seconds of sealing tested for bond strength on the Instron Tester. Bond strength data was then recorded in grams/inch units.
(4) Ethylene oxide/Propylene oxide copolymers which are available from Union Carbide, BASF, etc. It should be noted that these and other surfactants can be blended if necessary to produce the best blend of hydrophilic performance properties.
TM
Aerosol MA80I is a sulfosuccinate anionic surfactant available from Cytec Industries which has been found to be a preferred surfactant for use in the present cohesive composition.
The cohesive composition useful in the present invention may be formulated using any of the techniques known in the art. A representative example of the prior art procedure involves placing the ingredients one by one into a stainless steel mixing vessel, while providing enough agitation to ensure proper and effective mixing of the ingredients. After all the ingredients have been added, the adhesive batch is adjusted to meet its critical physical parameters.
Optional conditioning additives may. be incorporated into the cohesive composition in order to- modify particular physical properties. These additives may include colorants, such as titanium dioxide, sequestrants, deionized water, preservatives, biocides, stabilizers, anti-cling agents, pH adjusters, and other commonly known and used additives. As noted above, each of such additives can be present in amounts ranging from 0% to about 5% by weight.
Fillers may also optionally be incorporated into the adhesive composition in amounts ranging from about 0% to 5% by weight, preferably 0% to 3% by weight.
These are inert in the formulation, and are typically added to increase the bulk of the composition. Also, depending upon the substance employed, a filler may function as an anti-blocking agent. Fillers may include alumina, hydrated alumina (A1203-3H20), a silicate such as magnesium silicate, aluminum silicate, sodium silicate, potassium silicate and the like, mica, calcium carbonate (CaCO3) and silica. Other commonly employed fillers such as talc, clay, wollastonite, feldspar, glass microspheres, ceramic microspheres, thermoplastic microspheres, baryte and wood flour may also be used as long as they do not materially alter the function of the remaining ingredients in'the formulation.
EXAMPLES
The following data was obtained by comparing bond strength performance using a self-crosslinkng styrene/acrylic (Hycar 26288) to a non-self-crosslinking styrene/acrylic (Eastarez 4000) in cohesive formulations.
Test Method and Sample Preparation:
Test Equipment Instron Model 1122 Material Tester with Model 5500 Electronics Instron Test Equipment Setting - Crosshead Speed 30.5 cm/minute (12 inches/minute) TMI SupersealerTM - Sealing conditions 5.63 kg/cm2 (80 psi/) 0.5 second dwell/serrated jaws.
Test Environment - Temperature 22.2 C (72 F)/Humidity 48%
Sample Size - 2.54 cm by 10.16 cm (1 inch by 4 inches) Cohesive Coat Weight - approximately 1.5 kg (3.3 lb)/ream Cohesive samples for bond strength testing were prepared using a number 7-wire wound rod drawing down cohesive on 20.32 cm by 27.94 cm (8 inches by 11 inches) film substrate then dried at 82 C (180 F) for 30 seconds in a convection oven. Samples were then allowed to cool to ambient temperature. 2.54 cm by 10.16 cm (1 inch by 4 inch) samples were cut from lab draw down, sealed using TM[
SupersealerTM then within 60 seconds of sealing tested for bond strength on the Instron Tester. Bond strength data was then recorded in grams/inch units.
In the following Examples, the abbreviation "NRL" refers to "natural rubber latex."
Most preferred formula using non-self-crosslinking acrylics vs. standard cohesive formulations using self-crosslinking acrylics on polypropylene film.
Results are an average of three data points.
Minimum Cohesive Samples on OPP film Bond Strength Mode of Failure C2881 (most preferred formula) (69% 449g adhesive failure/non-NRL/3 1 % Non-self-crosslinking acrylic) resealable C 1099B (Standard w/self crosslinker) 324g cohesive failure/resealable C 13 80-01 (Standard w/self crosslinker) 314g cohesive failure/resealable Preferred formula range using non self-crosslinking acrylics vs. standard cohesive formulation using a self-crosslinking acrylic on primed polyester film.
Results are an average of three data points.
Minimum Cohesive Samples on primed PET film Bond Strength Mode of Failure C1772 (preferred range 75% NRL/25% 686g adhesive failure/non-Non self-crosslinking acrylic) resealable C2942 (preferred range 80% NRL/20% 915g adhesive failure/non-Non self-crosslinking acrylic resealable C1380-01 (Standard w/self crosslinker) 180g cohesive failure/resealable Preferred formula range using non self-crosslinking acrylics vs. standard cohesive formulation using a self-crosslinking acrylic on polyester film.
Results are an average of three data points.
Cohesive Samples on primed PET film Minimum Bond Strength Mode of Failure C 1704 (preferred range 65% NRL/35% 547g adhesive failure/non-Non self-crosslinking acrylic resealable C1380-01 (Standard w/self crosslinker) 455g cohesive failure/resealable Preferred formula range using non self-crosslinking acrylics vs. standard cohesive formulation using a self-crosslinking acrylic on primed foil film.
Results are an average of three data points.
Cohesive Samples on primed PET film Minimum Bond Strength Mode of Failure C2942 (preferred range 80% NRL/20% 660g adhesive failure/non-Non self-crosslinking acrylic resealable C 1099 (Standard w/self crosslinker) 220g cohesive failure/resealable Most preferred formulation using non self-crosslinking acrylics vs. standard cohesive formulation using a self crosslinking acrylic on OPP film. Results are an average of three data points and are from a customer's test trial roll.
Cohesive Samples on primed foil film Minimum Bond Strength Mode of Failure C2881 (most preferred formula) (69% 371g adhesive failure/non-NRL/3 1% Non-self-crosslinking acrylic) resealable C 1099 (Standard w/self crosslinker) 217g cohesive failure/resealable In summary, it can be seen from the above data that in each case the use of a non-self-crosslinking acrylic resulted in higher bond strength than the use of a self-crosslinking acrylic.
Most preferred formula using non-self-crosslinking acrylics vs. standard cohesive formulations using self-crosslinking acrylics on polypropylene film.
Results are an average of three data points.
Minimum Cohesive Samples on OPP film Bond Strength Mode of Failure C2881 (most preferred formula) (69% 449g adhesive failure/non-NRL/3 1 % Non-self-crosslinking acrylic) resealable C 1099B (Standard w/self crosslinker) 324g cohesive failure/resealable C 13 80-01 (Standard w/self crosslinker) 314g cohesive failure/resealable Preferred formula range using non self-crosslinking acrylics vs. standard cohesive formulation using a self-crosslinking acrylic on primed polyester film.
Results are an average of three data points.
Minimum Cohesive Samples on primed PET film Bond Strength Mode of Failure C1772 (preferred range 75% NRL/25% 686g adhesive failure/non-Non self-crosslinking acrylic) resealable C2942 (preferred range 80% NRL/20% 915g adhesive failure/non-Non self-crosslinking acrylic resealable C1380-01 (Standard w/self crosslinker) 180g cohesive failure/resealable Preferred formula range using non self-crosslinking acrylics vs. standard cohesive formulation using a self-crosslinking acrylic on polyester film.
Results are an average of three data points.
Cohesive Samples on primed PET film Minimum Bond Strength Mode of Failure C 1704 (preferred range 65% NRL/35% 547g adhesive failure/non-Non self-crosslinking acrylic resealable C1380-01 (Standard w/self crosslinker) 455g cohesive failure/resealable Preferred formula range using non self-crosslinking acrylics vs. standard cohesive formulation using a self-crosslinking acrylic on primed foil film.
Results are an average of three data points.
Cohesive Samples on primed PET film Minimum Bond Strength Mode of Failure C2942 (preferred range 80% NRL/20% 660g adhesive failure/non-Non self-crosslinking acrylic resealable C 1099 (Standard w/self crosslinker) 220g cohesive failure/resealable Most preferred formulation using non self-crosslinking acrylics vs. standard cohesive formulation using a self crosslinking acrylic on OPP film. Results are an average of three data points and are from a customer's test trial roll.
Cohesive Samples on primed foil film Minimum Bond Strength Mode of Failure C2881 (most preferred formula) (69% 371g adhesive failure/non-NRL/3 1% Non-self-crosslinking acrylic) resealable C 1099 (Standard w/self crosslinker) 217g cohesive failure/resealable In summary, it can be seen from the above data that in each case the use of a non-self-crosslinking acrylic resulted in higher bond strength than the use of a self-crosslinking acrylic.
Claims (17)
1. A water based cold seal cohesive coating for bonding one or more substrates together to form a flexible package to contain an article, said cohesive coating comprised of the following components:
25% to 90% by weight of a natural rubber latex emulsion;
10% to 75% by weight of a non-self-crosslinking acrylic emulsion;
0.01 % to 10% by weight water; and one or more ingredients in the form of an anti-foam agent, ammonium hydroxide, a surfactant, an anti-blocking agent, an inert filler, or a conditioning agent;
so that in combination the components total 100% by weight of said cohesive coating and wherein the cohesive coating forms a peelable and non-resealable closure for a flexible package, said closure having a cohesive strength of at least about 118.11 g/cm after being dried on a substrate for said package at a temperature of at least 127 C.
25% to 90% by weight of a natural rubber latex emulsion;
10% to 75% by weight of a non-self-crosslinking acrylic emulsion;
0.01 % to 10% by weight water; and one or more ingredients in the form of an anti-foam agent, ammonium hydroxide, a surfactant, an anti-blocking agent, an inert filler, or a conditioning agent;
so that in combination the components total 100% by weight of said cohesive coating and wherein the cohesive coating forms a peelable and non-resealable closure for a flexible package, said closure having a cohesive strength of at least about 118.11 g/cm after being dried on a substrate for said package at a temperature of at least 127 C.
2. The cohesive coating of claim 1, comprising:
50% to 90% by weight of the natural rubber latex emulsion; and 10% to 50% by weight of the non-self-crosslinking acrylic emulsion.
50% to 90% by weight of the natural rubber latex emulsion; and 10% to 50% by weight of the non-self-crosslinking acrylic emulsion.
3. The cohesive coating of claim 1, comprising:
60% to 80% by weight of the natural rubber latex emulsion; and 20% to 40% by weight of the non-self-crosslinking acrylic emulsion.
60% to 80% by weight of the natural rubber latex emulsion; and 20% to 40% by weight of the non-self-crosslinking acrylic emulsion.
4. The cohesive coating of claim 1, comprising the following components:
about 68% by weight of the natural rubber latex emulsion;
about 30% by weight of the non-self-crosslinking acrylic emulsion;
about 1.2% by weight water;
about 0.4% by weight of an anti-foam agent;
about 0.2% by weight of ammonium hydroxide;
about 0.1 % by weight of a surfactant; and about 0.1% by weight of an anti-blocking agent.
about 68% by weight of the natural rubber latex emulsion;
about 30% by weight of the non-self-crosslinking acrylic emulsion;
about 1.2% by weight water;
about 0.4% by weight of an anti-foam agent;
about 0.2% by weight of ammonium hydroxide;
about 0.1 % by weight of a surfactant; and about 0.1% by weight of an anti-blocking agent.
5. The cohesive coating of any one of claims 1 to 4, wherein said anti-foam agent is an emulsified silicone, a mineral oil based product or a glycol ester/polyol.
6. The cohesive coating of any one of claims 1 to 5, wherein said surfactant is a ftty acid ester, a non-ionic ethoxylate or an anionic sulfosuccinate.
7. The cohesive coating of any one of claims 1 to 6, wherein said anti-blocking agent is fumed silica, clay or calcium carbonate.
8. The cohesive coating of any one of claims 1 to 7, wherein said coating contains 0.01%
to 5% by weight of the anti-foam agent.
to 5% by weight of the anti-foam agent.
9. The cohesive coating of any one of claims 1 to 8, wherein said coating contains 0.01%
to 5% by weight of ammonium hydroxide.
to 5% by weight of ammonium hydroxide.
10. The cohesive coating of any one of claims 1 to 9, wherein said coating contains 0.01%
to 5% by weight of the surfactant.
to 5% by weight of the surfactant.
11. The cohesive coating of any one of claims 1 to 10, wherein said coating contains 0.01% to 5% by weight of the anti-blocking agent.
12. The cohesive coating of any one of claims 1 to 11, wherein said non-self-crosslinking acrylic emulsion is styrene acrylic, nitrile acrylic or all-acrylic.
13. A flexible packaging material for containing a food article, comprising:
a substrate in the form of a flexible sheet of material having opposite longitudinal edges; and a water based cold seal cohesive coating as claimed in any one of claims I to disposed on at least one of said longitudinal edges.
a substrate in the form of a flexible sheet of material having opposite longitudinal edges; and a water based cold seal cohesive coating as claimed in any one of claims I to disposed on at least one of said longitudinal edges.
14. The flexible packaging material of claim 13, wherein said substrate is a polyester film, a high density polyethylene film, a polypropylene film, a foil, a primed foil or a primed polyolefin film.
15. A method of making a cold seal flexible package comprising the steps of.
applying a cold seal cohesive coating in accordance with any one of claims 1 to 12 to selected areas of one side of a substrate in the form of a flexible sheet of material;
forming said substrate into a package; and applying pressure to said selected areas to seal said package.
applying a cold seal cohesive coating in accordance with any one of claims 1 to 12 to selected areas of one side of a substrate in the form of a flexible sheet of material;
forming said substrate into a package; and applying pressure to said selected areas to seal said package.
16. The method of claim 15, wherein the step of forming said substrate into a package comprises folding said substrate so that the cohesive coating on different portions of said selected areas of said substrate contact each other.
17. The method of claim 15 or 16, wherein the step of forming said substrate into a package comprises contacting different portions of said selected areas of the cohesive coating on said substrate with a separate substrate.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/780,524 | 2004-02-17 | ||
| US10/780,524 US7235294B2 (en) | 2004-02-17 | 2004-02-17 | Cohesive coating for snack food packaging |
| PCT/US2005/004233 WO2005080519A1 (en) | 2004-02-17 | 2005-02-11 | Cohesive coating for snack food packaging |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2556466A1 CA2556466A1 (en) | 2005-09-01 |
| CA2556466C true CA2556466C (en) | 2012-07-10 |
Family
ID=34838619
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2556466 Expired - Lifetime CA2556466C (en) | 2004-02-17 | 2005-02-11 | Cohesive coating for snack food packaging |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US7235294B2 (en) |
| EP (1) | EP1725627B1 (en) |
| JP (1) | JP5248018B2 (en) |
| CN (2) | CN1946824A (en) |
| AT (1) | ATE409734T1 (en) |
| AU (1) | AU2005214330B2 (en) |
| BR (1) | BRPI0507770B1 (en) |
| CA (1) | CA2556466C (en) |
| DE (1) | DE602005010057D1 (en) |
| ES (1) | ES2315846T3 (en) |
| MX (1) | MXPA06009639A (en) |
| WO (1) | WO2005080519A1 (en) |
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| US7576149B2 (en) * | 2006-05-31 | 2009-08-18 | Xerox Corporation | Varnish |
| EP2086757A1 (en) * | 2006-12-01 | 2009-08-12 | Akzo Nobel N.V. | Packaging laminate |
| DE202006020454U1 (en) | 2006-12-29 | 2008-08-07 | Kraft Foods R & D, Inc. Zweigniederlassung München | Resealable packaging |
| US8616372B2 (en) * | 2007-10-17 | 2013-12-31 | Quality Packaging, Inc. | Recyclable blister pack and process of making |
| US7681732B2 (en) | 2008-01-11 | 2010-03-23 | Cryovac, Inc. | Laminated lidstock |
| US20090078590A1 (en) | 2008-01-21 | 2009-03-26 | Smith Dennis R | Ultrasecure card package |
| CN101225286B (en) * | 2008-01-31 | 2010-06-02 | 常州市塑料彩印有限公司 | Self-sticky cold-seal adhesive and preparation method thereof |
| DE102008062368A1 (en) * | 2008-12-17 | 2010-06-24 | Tesa Se | Pressure-sensitive adhesives based on natural rubber and polyacrylates |
| CN102355876B (en) * | 2009-03-24 | 2014-05-14 | 琳得科株式会社 | Package material for adhesive bandage and packaged adhesive bandage |
| PH12012501694A1 (en) | 2010-02-26 | 2012-11-05 | Intercontinental Great Brands Llc | Reclosable package using low tack adhesive |
| JP5496810B2 (en) * | 2010-07-29 | 2014-05-21 | ヘンケルジャパン株式会社 | Adhesive for packaging bags |
| CN102120922B (en) * | 2010-10-11 | 2014-06-04 | 上海晶华粘胶制品发展有限公司 | Adhesive for high-temperature-resistant masking tape and high-temperature-resistant masking tape |
| US9365003B1 (en) | 2013-03-15 | 2016-06-14 | Bryce Corporation | Extrusion lamination with registered cold seal adhesive |
| US11167898B2 (en) | 2014-03-12 | 2021-11-09 | Bemis Company, Inc. | Packaging film with product-release coating |
| WO2016014052A1 (en) | 2014-07-23 | 2016-01-28 | Bemis Company, Inc. | Pell-open package |
| CN105349065A (en) * | 2015-12-04 | 2016-02-24 | 重庆江北工农化工有限责任公司 | Emulsion adhesive |
| JP2017138180A (en) * | 2016-02-03 | 2017-08-10 | デュプロ精工株式会社 | Folding and bonding device, bonding state detection method, and folding and bonding method |
| US11077637B2 (en) | 2016-09-30 | 2021-08-03 | Pregis Innovative Packaging Llc | Connective protective packaging |
| FI128604B (en) * | 2017-10-11 | 2020-08-31 | Build Care Oy | PROCEDURE FOR THE PRODUCTION OF ELASTIC COATINGS AND ELASTIC COATINGS |
| DE102020114211A1 (en) | 2020-05-27 | 2021-12-02 | Sprick Gmbh Bielefelder Papier- Und Wellpappenwerke & Co. | Packaging material web, packaging bag, packaging material cutting and manufacturing process |
| CN111933376A (en) * | 2020-06-29 | 2020-11-13 | 洛阳中赫非晶科技有限公司 | Formula for ferrite magnetic core |
| JP7676954B2 (en) * | 2021-05-25 | 2025-05-15 | Dic株式会社 | Pressure-sensitive adhesive composition, laminate having pressure-sensitive adhesive layer of pressure-sensitive adhesive composition, and resealable packaging material using said laminate |
| CN114179458A (en) * | 2021-11-30 | 2022-03-15 | 河南墨道石墨烯科技有限公司 | Graphene-based heating cloth for far infrared underwear, and preparation method and application thereof |
| CN114626810B (en) * | 2022-03-09 | 2025-07-29 | 前锦网络信息技术(上海)有限公司 | False recruitment identification method and system |
| DE102022113441A1 (en) | 2022-05-27 | 2023-11-30 | Sprick Gmbh Bielefelder Papier- Und Wellpappenwerke & Co. | Packaging material sheet and packaging bag |
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| GB1052953A (en) * | 1962-05-25 | 1966-12-30 | Bx Plastics Ltd | Sealing process |
| GB1067568A (en) * | 1963-05-10 | 1967-05-03 | Bx Plastics Ltd | Adhesive compositions |
| US4804573A (en) * | 1986-05-05 | 1989-02-14 | Mccarthy Brian A | Packaging materials |
| GB9109576D0 (en) * | 1991-05-02 | 1991-06-26 | United Biscuits Ltd | Improvements in and relating to wrapping food products |
| CA2220774A1 (en) * | 1995-06-02 | 1996-12-05 | Dennis Emmett Mcgee | Heat sealable film |
| JP2000515568A (en) * | 1997-06-17 | 2000-11-21 | モービル・オイル・コーポレーション | Cold sealable bonding polymer |
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-
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- 2004-02-17 US US10/780,524 patent/US7235294B2/en not_active Expired - Lifetime
-
2005
- 2005-02-11 DE DE200560010057 patent/DE602005010057D1/en not_active Expired - Lifetime
- 2005-02-11 JP JP2006554133A patent/JP5248018B2/en not_active Expired - Lifetime
- 2005-02-11 MX MXPA06009639A patent/MXPA06009639A/en active IP Right Grant
- 2005-02-11 CN CNA2005800116100A patent/CN1946824A/en active Pending
- 2005-02-11 ES ES05713278T patent/ES2315846T3/en not_active Expired - Lifetime
- 2005-02-11 EP EP20050713278 patent/EP1725627B1/en not_active Expired - Lifetime
- 2005-02-11 AU AU2005214330A patent/AU2005214330B2/en not_active Expired
- 2005-02-11 WO PCT/US2005/004233 patent/WO2005080519A1/en not_active Ceased
- 2005-02-11 CN CN201410174358.6A patent/CN103923580B/en not_active Expired - Lifetime
- 2005-02-11 AT AT05713278T patent/ATE409734T1/en not_active IP Right Cessation
- 2005-02-11 BR BRPI0507770-2A patent/BRPI0507770B1/en active IP Right Grant
- 2005-02-11 CA CA 2556466 patent/CA2556466C/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AU2005214330A1 (en) | 2005-09-01 |
| EP1725627B1 (en) | 2008-10-01 |
| US20050181205A1 (en) | 2005-08-18 |
| CN103923580A (en) | 2014-07-16 |
| BRPI0507770A (en) | 2007-07-10 |
| CA2556466A1 (en) | 2005-09-01 |
| MXPA06009639A (en) | 2007-01-25 |
| ATE409734T1 (en) | 2008-10-15 |
| DE602005010057D1 (en) | 2008-11-13 |
| AU2005214330B2 (en) | 2011-08-04 |
| US7235294B2 (en) | 2007-06-26 |
| BRPI0507770B1 (en) | 2019-04-24 |
| JP5248018B2 (en) | 2013-07-31 |
| JP2007525579A (en) | 2007-09-06 |
| EP1725627A1 (en) | 2006-11-29 |
| CN103923580B (en) | 2017-01-11 |
| ES2315846T3 (en) | 2009-04-01 |
| WO2005080519A1 (en) | 2005-09-01 |
| CN1946824A (en) | 2007-04-11 |
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