CA1268878A - Removable hot melt pressure sensitive adhesive - Google Patents
Removable hot melt pressure sensitive adhesiveInfo
- Publication number
- CA1268878A CA1268878A CA000533054A CA533054A CA1268878A CA 1268878 A CA1268878 A CA 1268878A CA 000533054 A CA000533054 A CA 000533054A CA 533054 A CA533054 A CA 533054A CA 1268878 A CA1268878 A CA 1268878A
- Authority
- CA
- Canada
- Prior art keywords
- weight
- styrene
- adhesive composition
- label
- isoprene
- 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
- 239000012943 hotmelt Substances 0.000 title description 8
- 239000004820 Pressure-sensitive adhesive Substances 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims abstract description 35
- 229920005989 resin Polymers 0.000 claims abstract description 35
- 239000011347 resin Substances 0.000 claims abstract description 35
- 150000003839 salts Chemical class 0.000 claims abstract description 22
- 239000004831 Hot glue Substances 0.000 claims abstract description 20
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 11
- 239000000194 fatty acid Substances 0.000 claims abstract description 11
- 229930195729 fatty acid Natural products 0.000 claims abstract description 11
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 11
- 239000000853 adhesive Substances 0.000 claims description 35
- 230000001070 adhesive effect Effects 0.000 claims description 34
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 30
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical group CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 24
- 229920001577 copolymer Polymers 0.000 claims description 15
- 239000003963 antioxidant agent Substances 0.000 claims description 13
- 239000003921 oil Substances 0.000 claims description 13
- 239000002480 mineral oil Substances 0.000 claims description 12
- 235000010446 mineral oil Nutrition 0.000 claims description 12
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 claims description 10
- 239000004264 Petrolatum Substances 0.000 claims description 9
- 229940066842 petrolatum Drugs 0.000 claims description 9
- 235000019271 petrolatum Nutrition 0.000 claims description 9
- 230000003078 antioxidant effect Effects 0.000 claims description 8
- 229920001400 block copolymer Polymers 0.000 claims description 8
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 8
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical group [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 7
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 7
- 239000013032 Hydrocarbon resin Substances 0.000 claims description 6
- 229920006270 hydrocarbon resin Polymers 0.000 claims description 6
- 150000003505 terpenes Chemical class 0.000 claims description 6
- 235000007586 terpenes Nutrition 0.000 claims description 6
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 claims description 6
- 235000021355 Stearic acid Nutrition 0.000 claims description 4
- 235000013539 calcium stearate Nutrition 0.000 claims description 4
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 4
- 239000008117 stearic acid Substances 0.000 claims description 4
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 claims description 3
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 claims description 3
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 claims description 3
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 claims description 3
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 claims description 3
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 claims description 3
- 229930006722 beta-pinene Natural products 0.000 claims description 3
- 239000008116 calcium stearate Substances 0.000 claims description 3
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 claims description 3
- 229920006271 aliphatic hydrocarbon resin Polymers 0.000 claims 8
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 claims 4
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims 2
- 239000005642 Oleic acid Substances 0.000 claims 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 abstract description 15
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 abstract description 8
- 239000000126 substance Substances 0.000 abstract description 3
- 229920002633 Kraton (polymer) Polymers 0.000 description 16
- 230000032683 aging Effects 0.000 description 9
- 239000000758 substrate Substances 0.000 description 9
- 238000009472 formulation Methods 0.000 description 8
- 150000002989 phenols Chemical class 0.000 description 7
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- AQWSFUIGRSMCST-UHFFFAOYSA-N 3-pyridin-3-ylsulfonyl-5-(trifluoromethyl)chromen-2-one Chemical compound N1=CC(=CC=C1)S(=O)(=O)C=1C(OC2=CC=CC(=C2C=1)C(F)(F)F)=O AQWSFUIGRSMCST-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 229920013645 Europrene Polymers 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- ZEBMSMUPGIOANU-UHFFFAOYSA-N (3,5-ditert-butyl-4-hydroxyphenyl)methylphosphonic acid Chemical compound CC(C)(C)C1=CC(CP(O)(O)=O)=CC(C(C)(C)C)=C1O ZEBMSMUPGIOANU-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- OYYDSYNJXWYOBL-UHFFFAOYSA-N 2-methylbuta-1,3-diene prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=CC=C1.C=CC(C)=C.CC(=C)C1=CC=CC=C1 OYYDSYNJXWYOBL-UHFFFAOYSA-N 0.000 description 1
- JQTAVKOFIFYMKC-UHFFFAOYSA-N 2-octylsulfanylethyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCSCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 JQTAVKOFIFYMKC-UHFFFAOYSA-N 0.000 description 1
- YFHKLSPMRRWLKI-UHFFFAOYSA-N 2-tert-butyl-4-(3-tert-butyl-4-hydroxy-5-methylphenyl)sulfanyl-6-methylphenol Chemical compound CC(C)(C)C1=C(O)C(C)=CC(SC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 YFHKLSPMRRWLKI-UHFFFAOYSA-N 0.000 description 1
- ODJQKYXPKWQWNK-UHFFFAOYSA-L 3-(2-carboxylatoethylsulfanyl)propanoate Chemical class [O-]C(=O)CCSCCC([O-])=O ODJQKYXPKWQWNK-UHFFFAOYSA-L 0.000 description 1
- WPMYUUITDBHVQZ-UHFFFAOYSA-M 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=CC(CCC([O-])=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-M 0.000 description 1
- BLPODHBKBPRTPG-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]phenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C=C(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C=2)=C1 BLPODHBKBPRTPG-UHFFFAOYSA-N 0.000 description 1
- XPOLRBKMCIXLQT-UHFFFAOYSA-N 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]oxy]phenol Chemical compound CCCCCCCCSC1=NC(SCCCCCCCC)=NC(OC=2C=CC(O)=CC=2)=N1 XPOLRBKMCIXLQT-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 239000002656 Distearyl thiodipropionate Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 241000364027 Sinoe Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- ARPPLBPJWJEDIJ-UHFFFAOYSA-N aniline;methylcyclohexane Chemical compound CC1CCCCC1.NC1=CC=CC=C1 ARPPLBPJWJEDIJ-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 1
- 235000019305 distearyl thiodipropionate Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- -1 ethylene butylene Chemical group 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
- RKQOSDAEEGPRER-UHFFFAOYSA-L zinc diethyldithiocarbamate Chemical compound [Zn+2].CCN(CC)C([S-])=S.CCN(CC)C([S-])=S RKQOSDAEEGPRER-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- 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
- C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J153/02—Vinyl aromatic monomers and conjugated dienes
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesive Tapes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/852,005 US4680333A (en) | 1986-04-14 | 1986-04-14 | Removable hot melt pressure sensitive adhesive |
| US852,005 | 1986-04-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1268878A true CA1268878A (en) | 1990-05-08 |
Family
ID=25312269
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000533054A Expired - Lifetime CA1268878A (en) | 1986-04-14 | 1987-03-26 | Removable hot melt pressure sensitive adhesive |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4680333A (enExample) |
| JP (1) | JPS62243671A (enExample) |
| AU (1) | AU573124B2 (enExample) |
| CA (1) | CA1268878A (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4734447A (en) * | 1985-09-24 | 1988-03-29 | Sunstar Giken Kabushiki Kaisha | Hot-melt adhesive |
| US4948825A (en) * | 1987-06-03 | 1990-08-14 | Avery International Corporation | Curable film forming compositions |
| US4833193A (en) * | 1987-08-14 | 1989-05-23 | Sieverding David L | Novel pressure sensitive adhesives |
| US4861635A (en) * | 1987-11-06 | 1989-08-29 | Minnesota Mining And Manufacturing Company | Pressure-sensitive adhesive closure for disposable diaper |
| US5147916A (en) * | 1990-02-21 | 1992-09-15 | Dow Corning Corporation | Hot-melt silicone pressure sensitive adhesive composition and related methods and articles |
| US5162410A (en) * | 1990-04-13 | 1992-11-10 | Dow Corning Corporation | Hot-melt silicon pressure sensitive adhesives with phenyl-containing siloxane fluid additive and related methods and articles |
| FI946040A7 (fi) * | 1993-12-27 | 1995-06-28 | Shell Int Research | Irrotettava tarraliimakoostumus |
| EP0794202B2 (en) * | 1996-03-06 | 2004-03-31 | Eastman Chemical Resins, Inc. | Aliphatic petroleum-based resins and hot melt pressure sentitive adhesive containing same |
| US5741840A (en) * | 1996-07-03 | 1998-04-21 | H.B. Fuller Licensing & Financing, Inc. | Cohesively failing hot melt pressure sensitive adhesive |
| US5827591A (en) * | 1996-10-08 | 1998-10-27 | Tricor Direct, Inc. | Removable adhesive notes for an industrial setting |
| US6025071A (en) * | 1997-10-23 | 2000-02-15 | H.B.Fuller Licensing & Financing Inc. | Removable grade hot melt pressure sensitive adhesive |
| US5912295A (en) * | 1997-10-24 | 1999-06-15 | H.B. Fuller Licensing & Financing, Inc. | Low viscosity hot melt pressure sensitive adhesive which exhibits minimal staining |
| DE10016183A1 (de) * | 1999-04-13 | 2001-03-15 | Henkel Kgaa | Niedrigviskoser Schmelzklebstoff |
| JP2001234149A (ja) * | 2000-02-24 | 2001-08-28 | Sekisui Chem Co Ltd | 粘着剤組成物 |
| JP4566327B2 (ja) * | 2000-04-27 | 2010-10-20 | 株式会社クラレ | 熱可塑性重合体組成物 |
| DE10141378A1 (de) * | 2001-08-23 | 2003-04-30 | Tesa Ag | Oberflächenschutzfolie für lackierte Flächen mit einem Kleber auf Basis von hydrierten Blockcopolymeren |
| PT1530482E (pt) | 2002-07-18 | 2014-01-15 | Helix Biopharma Corp | Utilização de urease para inibição de crescimento de células cancerigenas |
| US20040045860A1 (en) * | 2002-09-05 | 2004-03-11 | Edgerly Randall L. | Packages of stacked, individually wrapped, flat disposable utensils, and methods of forming such packages |
| US20060182953A1 (en) * | 2005-02-15 | 2006-08-17 | Jensen Erick C | Mold treatment and removal apparatus and methods |
| FR2912153B1 (fr) * | 2007-02-02 | 2009-04-17 | Bostik S A Sa | Composition adhesive pour etiquette auto-adhesive decollable |
| KR101678714B1 (ko) | 2009-06-18 | 2016-11-23 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 고온 용융 감압 접착제의 제조 방법 |
| US20130090421A1 (en) * | 2011-10-05 | 2013-04-11 | Bostik, Inc. | Petrolatum Containing Hot Melt Bottle Labeling Adhesive |
| DE102015015114A1 (de) | 2015-11-21 | 2017-05-24 | Götz Thomas | Saugnapf mit einer Schnappscheibe oder Federstahlscheibe |
| EP3653682A1 (en) * | 2018-11-15 | 2020-05-20 | Bostik SA | Improved hot-melt adhesive for manufacturing disposable hygiene products |
| PT118403B (pt) | 2022-12-16 | 2025-01-07 | Colquimica Industria Nac De Colas S A | Cola termofusível lavável e seu processo de obtenção |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3932328A (en) * | 1971-11-02 | 1976-01-13 | Johnson & Johnson | Hot melt adhesive composition and tape |
| US4111874A (en) * | 1971-12-22 | 1978-09-05 | Canadian Patents And Development Limited | Transparent pressure-sensitive coatings |
| US3817887A (en) * | 1972-03-09 | 1974-06-18 | Gaf Corp | Adhesive stick comprising an alkylated n-vinylpyrrolidone polymer |
| US4046838A (en) * | 1972-09-11 | 1977-09-06 | The Goodyear Tire & Rubber Company | Adhesive compositions of a block copolymer and tackifying resin |
| JPS5153591A (en) * | 1974-11-05 | 1976-05-12 | Mitsui Petrochemical Ind | Tankasuisojushino seizohoho |
| US3970623A (en) * | 1974-11-29 | 1976-07-20 | The Goodyear Tire & Rubber Company | Adhesive composition containing a copolymer of butadiene, styrene, and acrylonitrile, plus a tackifying resin |
| US4136071A (en) * | 1976-05-18 | 1979-01-23 | Johnson & Johnson | Mixed block polymer adhesive |
| US4130603A (en) * | 1977-02-04 | 1978-12-19 | Toray Industries, Inc. | Thermoplastic linear block copolyether-polyesters as hot melt adhesives for textiles |
| US4508771A (en) * | 1979-11-19 | 1985-04-02 | Exxon Research & Engineering Co. | Extruded carpet backing with resin and elastomer components |
| US4399249A (en) * | 1980-12-24 | 1983-08-16 | Eschem Inc. | Resealable pressure sensitive adhesives and products |
| US4500021A (en) * | 1980-12-24 | 1985-02-19 | Eschem, Inc. | Resealable articles and process |
| US4351913A (en) * | 1981-02-19 | 1982-09-28 | Siecor Corporation | Filling materials for electrical and light waveguide communications cables |
| US4549920A (en) * | 1981-07-28 | 1985-10-29 | Imperial Chemical Industries, Plc | Method for impregnating filaments with thermoplastic |
| DE3138187C2 (de) * | 1981-09-25 | 1986-03-13 | Hüls AG, 4370 Marl | Textilschmelzkleber |
| US4540415A (en) * | 1982-02-12 | 1985-09-10 | Personal Products Company | Disposable diaper with a repositionable tape tab fastener |
| US4411954A (en) * | 1982-08-16 | 1983-10-25 | National Starch And Chemical Corporation | Hot melt pressure sensitive adhesive and diaper tape closures coated therewith |
| US4556151A (en) * | 1982-10-25 | 1985-12-03 | Toyo Seikan Kaisha Ltd. | Metal vessel having circumferential side seam and adhesive primer for use in production thereof |
| US4551490A (en) * | 1983-06-27 | 1985-11-05 | E. R. Squibb & Sons, Inc. | Adhesive composition resistant to biological fluids |
| US4619851A (en) * | 1983-07-21 | 1986-10-28 | Avery International Corporation | Adhesive compositions |
| US4699941A (en) * | 1985-08-12 | 1987-10-13 | National Starch And Chemical Corporation | Thermoplastic elastic adhesives |
-
1986
- 1986-04-14 US US06/852,005 patent/US4680333A/en not_active Expired - Fee Related
-
1987
- 1987-03-26 CA CA000533054A patent/CA1268878A/en not_active Expired - Lifetime
- 1987-04-09 AU AU71337/87A patent/AU573124B2/en not_active Ceased
- 1987-04-13 JP JP62088981A patent/JPS62243671A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0415269B2 (enExample) | 1992-03-17 |
| JPS62243671A (ja) | 1987-10-24 |
| US4680333A (en) | 1987-07-14 |
| AU7133787A (en) | 1987-12-10 |
| AU573124B2 (en) | 1988-05-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKLA | Lapsed |