AU6334800A - Hot melt pressure sensitive adhesives based on compatibilized blends of elastomers - Google Patents
Hot melt pressure sensitive adhesives based on compatibilized blends of elastomers Download PDFInfo
- Publication number
- AU6334800A AU6334800A AU63348/00A AU6334800A AU6334800A AU 6334800 A AU6334800 A AU 6334800A AU 63348/00 A AU63348/00 A AU 63348/00A AU 6334800 A AU6334800 A AU 6334800A AU 6334800 A AU6334800 A AU 6334800A
- Authority
- AU
- Australia
- Prior art keywords
- styrene
- hot melt
- pressure sensitive
- compatible
- sensitive adhesive
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000004820 Pressure-sensitive adhesive Substances 0.000 title claims description 30
- 239000012943 hotmelt Substances 0.000 title claims description 30
- 239000000203 mixture Substances 0.000 title claims description 29
- 229920001971 elastomer Polymers 0.000 title description 4
- 239000000806 elastomer Substances 0.000 title description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 68
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 30
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 30
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 claims description 30
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 28
- 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 claims description 28
- 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 claims description 28
- 229920005989 resin Polymers 0.000 claims description 20
- 239000011347 resin Substances 0.000 claims description 20
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 18
- -1 glycerol ester Chemical class 0.000 claims description 13
- 239000000155 melt Substances 0.000 claims description 12
- 239000003921 oil Substances 0.000 claims description 12
- 229920000428 triblock copolymer Polymers 0.000 claims description 10
- 239000001993 wax Substances 0.000 claims description 10
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 238000002844 melting Methods 0.000 claims description 6
- 230000008018 melting Effects 0.000 claims description 6
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 239000003784 tall oil Substances 0.000 claims description 4
- 239000002023 wood Substances 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- 229920006271 aliphatic hydrocarbon resin Polymers 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000004200 microcrystalline wax Substances 0.000 claims description 2
- 235000019808 microcrystalline wax Nutrition 0.000 claims description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 229920006380 polyphenylene oxide Polymers 0.000 claims description 2
- VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 description 24
- FACXGONDLDSNOE-UHFFFAOYSA-N buta-1,3-diene;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 FACXGONDLDSNOE-UHFFFAOYSA-N 0.000 description 24
- 239000000853 adhesive Substances 0.000 description 17
- 230000001070 adhesive effect Effects 0.000 description 17
- 229920000642 polymer Polymers 0.000 description 12
- 238000012360 testing method Methods 0.000 description 10
- 229920001400 block copolymer Polymers 0.000 description 9
- 239000003963 antioxidant agent Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 229910001220 stainless steel Inorganic materials 0.000 description 7
- 239000010935 stainless steel Substances 0.000 description 7
- 229920002799 BoPET Polymers 0.000 description 6
- 229920002633 Kraton (polymer) Polymers 0.000 description 6
- 239000005041 Mylar™ Substances 0.000 description 6
- 150000002989 phenols Chemical class 0.000 description 6
- 239000004831 Hot glue Substances 0.000 description 5
- 229920001195 polyisoprene Polymers 0.000 description 5
- ROGIWVXWXZRRMZ-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1 ROGIWVXWXZRRMZ-UHFFFAOYSA-N 0.000 description 4
- 239000005062 Polybutadiene Substances 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000003750 conditioning effect Effects 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 229920002857 polybutadiene Polymers 0.000 description 4
- VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 3
- 102100023444 Centromere protein K Human genes 0.000 description 3
- 101000907931 Homo sapiens Centromere protein K Proteins 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 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 3
- 230000032683 aging Effects 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000011115 styrene butadiene Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000000518 rheometry Methods 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- CZNRFEXEPBITDS-UHFFFAOYSA-N 2,5-bis(2-methylbutan-2-yl)benzene-1,4-diol Chemical compound CCC(C)(C)C1=CC(O)=C(C(C)(C)CC)C=C1O CZNRFEXEPBITDS-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
- SAJFQHPVIYPPEY-UHFFFAOYSA-N 2,6-ditert-butyl-4-(dioctadecoxyphosphorylmethyl)phenol Chemical compound CCCCCCCCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCCCCCCCC)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SAJFQHPVIYPPEY-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
- YMWUHNXJHDCNPP-UHFFFAOYSA-N 3,5-ditert-butyl-2-octadecylbenzene-1,4-diol Chemical compound CCCCCCCCCCCCCCCCCCC1=C(O)C=C(C(C)(C)C)C(O)=C1C(C)(C)C YMWUHNXJHDCNPP-UHFFFAOYSA-N 0.000 description 1
- VKMJNFBOHLMRMS-UHFFFAOYSA-N C(CCCCCCCCCCC)C(CC(=O)O)SCCC(=O)O.C(CCCCCCCCCCC)C(CC(=O)O)SCCC(=O)O.C(CCCCCCCCCCC)C(CC(=O)O)SCCC(=O)O.C(CCCCCCCCCCC)C(CC(=O)O)SCCC(=O)O.OCC(CO)(CO)CO Chemical compound C(CCCCCCCCCCC)C(CC(=O)O)SCCC(=O)O.C(CCCCCCCCCCC)C(CC(=O)O)SCCC(=O)O.C(CCCCCCCCCCC)C(CC(=O)O)SCCC(=O)O.C(CCCCCCCCCCC)C(CC(=O)O)SCCC(=O)O.OCC(CO)(CO)CO VKMJNFBOHLMRMS-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 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
- 239000003508 Dilauryl thiodipropionate Substances 0.000 description 1
- 239000002656 Distearyl thiodipropionate Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- ULFUTCYGWMQVIO-PCVRPHSVSA-N [(6s,8r,9s,10r,13s,14s,17r)-17-acetyl-6,10,13-trimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1h-cyclopenta[a]phenanthren-17-yl] acetate;[(8r,9s,13s,14s,17s)-3-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] pentano Chemical compound C1CC2=CC(O)=CC=C2[C@@H]2[C@@H]1[C@@H]1CC[C@H](OC(=O)CCCC)[C@@]1(C)CC2.C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 ULFUTCYGWMQVIO-PCVRPHSVSA-N 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 230000003679 aging effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 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
- 239000010775 animal oil Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 235000019304 dilauryl thiodipropionate Nutrition 0.000 description 1
- 235000019305 distearyl thiodipropionate Nutrition 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- HWYHZTIRURJOHG-UHFFFAOYSA-N luminol Chemical compound O=C1NNC(=O)C2=C1C(N)=CC=C2 HWYHZTIRURJOHG-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent 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
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- MGMXGCZJYUCMGY-UHFFFAOYSA-N tris(4-nonylphenyl) phosphite Chemical compound C1=CC(CCCCCCCCC)=CC=C1OP(OC=1C=CC(CCCCCCCCC)=CC=1)OC1=CC=C(CCCCCCCCC)C=C1 MGMXGCZJYUCMGY-UHFFFAOYSA-N 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- 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
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/02—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
-
- 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
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
- C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/387—Block-copolymers
-
- 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
-
- 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
- C08L2666/24—Graft or block copolymers according to groups C08L51/00, C08L53/00 or C08L55/02; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L93/00—Compositions of natural resins; Compositions of derivatives thereof
- C08L93/04—Rosin
-
- 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
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/334—Applications of adhesives in processes or use of adhesives in the form of films or foils as a label
-
- 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
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/302—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier the adhesive being pressure-sensitive, i.e. tacky at temperatures inferior to 30°C
-
- 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
- C09J2453/00—Presence of block copolymer
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)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/326,856 US6162859A (en) | 1999-06-07 | 1999-06-07 | Hot melt pressure sensitive adhesives based on compatibilized blends of elastomers |
| US09326856 | 1999-06-07 | ||
| PCT/US2000/015605 WO2000075257A1 (en) | 1999-06-07 | 2000-06-07 | Hot melt pressure sensitive adhesives based on compatibilized blends of elastomers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU6334800A true AU6334800A (en) | 2000-12-28 |
Family
ID=23274020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU63348/00A Abandoned AU6334800A (en) | 1999-06-07 | 2000-06-07 | Hot melt pressure sensitive adhesives based on compatibilized blends of elastomers |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6162859A (OSRAM) |
| EP (1) | EP1105440A1 (OSRAM) |
| JP (1) | JP5079957B2 (OSRAM) |
| AU (1) | AU6334800A (OSRAM) |
| CA (1) | CA2339820A1 (OSRAM) |
| WO (1) | WO2000075257A1 (OSRAM) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6379791B1 (en) | 2000-02-08 | 2002-04-30 | 3M Innovative Properties Company | Compatibilized pressure-sensitive adhesives |
| US20050013996A1 (en) * | 2002-03-08 | 2005-01-20 | Hatfield Stephen F. | Hot melt pressure sensitive adhesives for disposable articles |
| US7795336B2 (en) * | 2002-10-18 | 2010-09-14 | Henkel Ag & Co. Kgaa | Low application temperature hot melt adhesive |
| US7081498B2 (en) * | 2003-04-10 | 2006-07-25 | Morgan Adhesives Company | Pressure-sensitive adhesive compositions and constructions |
| US7442739B1 (en) | 2003-11-12 | 2008-10-28 | Henkel Corporation | Hot melt pressure sensitive adhesives |
| US7648771B2 (en) | 2003-12-31 | 2010-01-19 | Kimberly-Clark Worldwide, Inc. | Thermal stabilization and processing behavior of block copolymer compositions by blending, applications thereof, and methods of making same |
| US8377027B2 (en) | 2005-04-29 | 2013-02-19 | Kimberly-Clark Worldwide, Inc. | Waist elastic members for use in absorbent articles |
| US8163824B2 (en) | 2006-10-02 | 2012-04-24 | Bostik, Inc. | High styrene SBS hot melt adhesive |
| US20080081858A1 (en) * | 2006-10-02 | 2008-04-03 | Genta Okazaki | High styrene SBS hot melt adhesive |
| DE102006054936A1 (de) * | 2006-11-22 | 2008-05-29 | Hella Kgaa Hueck & Co. | Temperaturinduziertes Klebschweißverfahren und Klebschweißzusatzstoff zum Verbinden von thermodynamisch unverträglichen Kunststoffen |
| EP2094803A4 (en) | 2006-12-07 | 2010-01-20 | 3M Innovative Properties Co | MIXTURES OF BLOCK COPOLYMER ADHESIVES AND ACRYLIC ADHESIVES |
| FR2912153B1 (fr) * | 2007-02-02 | 2009-04-17 | Bostik S A Sa | Composition adhesive pour etiquette auto-adhesive decollable |
| US8829105B2 (en) | 2012-01-18 | 2014-09-09 | Eastman Chemical Company | Low molecular weight polystyrene resin and methods of making and using the same |
| CN103849105A (zh) * | 2014-01-15 | 2014-06-11 | 洛阳骏腾能源科技有限公司 | 一种耐温安全的高分子防漏胶 |
| CN103849101A (zh) * | 2014-01-15 | 2014-06-11 | 洛阳骏腾能源科技有限公司 | 一种用于轮胎的高分子弹性材料 |
| CN103849108A (zh) * | 2014-01-15 | 2014-06-11 | 洛阳骏腾能源科技有限公司 | 一种具有自补功能的高分子防漏材料 |
| CN103849106A (zh) * | 2014-01-15 | 2014-06-11 | 洛阳骏腾能源科技有限公司 | 一种喷涂于轮胎内壁的高分子弹性材料 |
| CN103849104A (zh) * | 2014-01-15 | 2014-06-11 | 洛阳骏腾能源科技有限公司 | 一种高分子自密封轮胎补漏材料 |
| CN103865222A (zh) * | 2014-01-23 | 2014-06-18 | 青岛喜乐途商贸有限公司 | 一种新型轮胎防漏密补材料 |
| KR20170052579A (ko) | 2014-09-09 | 2017-05-12 | 에이치. 비. 풀러, 컴퍼니 | 탄성 핫 멜트 접착제 조성물 및 그로 제조된 탄성 복합재 |
| EP3234057B1 (en) | 2014-12-17 | 2020-10-21 | H. B. Fuller Company | Hot melt adhesive composition for bonding packs of plastic containers |
| PL3234058T3 (pl) | 2014-12-17 | 2021-05-17 | H. B. Fuller Company | Opakowanie metalowych pojemników |
| KR102492432B1 (ko) | 2015-03-16 | 2023-01-26 | 에이치. 비. 풀러, 컴퍼니 | 도포 온도가 낮은 핫 멜트 접착제 조성물 |
| JP7005349B2 (ja) * | 2015-03-16 | 2022-01-21 | エイチ．ビー．フラー カンパニー | 弾性接着剤組成物及びそれを用いて作製される弾性複合材料 |
| JP6672919B2 (ja) * | 2016-03-17 | 2020-03-25 | 日立化成株式会社 | 粘着組成物および粘着テープ |
| EP3333236B1 (de) * | 2016-12-09 | 2021-03-31 | tesa SE | Haftklebestreifen |
| EP3333235B1 (de) | 2016-12-09 | 2023-06-07 | tesa SE | Haftklebestreifen |
| KR102545319B1 (ko) * | 2017-02-20 | 2023-06-21 | 보스틱, 인크. | 고온 용융 접착제를 위한 스티렌계 재료 |
| EP3650500B1 (en) * | 2017-08-07 | 2022-08-17 | Asahi Chemical Synthetic Co., Ltd. | Hot-melt composition and sealing material |
| KR102397831B1 (ko) | 2017-12-27 | 2022-05-12 | 주식회사 엘지화학 | 핫 멜트 접착제 조성물 |
| EP3894503A4 (en) * | 2018-12-14 | 2022-08-17 | 3M Innovative Properties Company | ADHESIVE ARTICLES AND PROCESSES |
| JP7289502B2 (ja) * | 2019-01-28 | 2023-06-12 | 旭化学合成株式会社 | ホットメルト組成物およびシール材 |
| NL2025746B1 (en) * | 2020-06-03 | 2022-03-04 | Univ Delft Tech | Rejuvenator for Recycling of polymer Modified Asphalt Concrete Pavement |
| WO2022130081A1 (en) | 2020-12-16 | 2022-06-23 | Savare' I.C. S.R.L. | Self-adhesive hot-melt formulations with improved characteristics and high stability of adhesive properties on long times |
| CN115216258B (zh) * | 2022-05-13 | 2023-06-20 | 嘉好(太仓)新材料股份有限公司 | 一种耐低温纸尿裤生产用结构胶及其制备方法 |
| CN115919810B (zh) * | 2022-12-29 | 2025-10-28 | 佛山南宝高盛高新材料有限公司 | 一种新型黑膏药基质热熔压敏胶及其制备方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4080348A (en) * | 1976-05-18 | 1978-03-21 | Johnson & Johnson | Tacky adhesive |
| US4125665A (en) * | 1977-08-29 | 1978-11-14 | Johnson & Johnson | Container sealing tape |
| JPS5682863A (en) * | 1979-12-12 | 1981-07-06 | Furukawa Electric Co Ltd:The | Hot-melt type adhesive composition |
| US4419494A (en) * | 1982-03-16 | 1983-12-06 | National Starch And Chemical Corporation | Heat resistant hot melt adhesives |
| JPS61192743A (ja) * | 1985-02-21 | 1986-08-27 | Mitsubishi Petrochem Co Ltd | オレフイン系樹脂用プライマ−組成物 |
| JPH0686586B2 (ja) * | 1985-04-05 | 1994-11-02 | 日東電工株式会社 | 感圧性接着剤組成物 |
| DE69131448T2 (de) * | 1990-03-14 | 1999-11-04 | Avery Dennison Corp., Pasadena | Druckempfindliche klebemittel auf der grundlage von vorzugsweise klebriggemachten nichtmischbaren elastomeren |
| US5290842A (en) * | 1991-09-03 | 1994-03-01 | Avery Dennison Corporation | Pressure-sensitive adhesives based on preferentially tackified immiscible elastomers |
| US5705551A (en) * | 1991-12-06 | 1998-01-06 | Avery Dennison Corporation | Elastomeric pressure-sensitive adhesive compositions exhibiting good cutting performance |
| ES2139969T3 (es) * | 1996-03-06 | 2000-02-16 | Hercules Inc | Resinas alifaticas basadas en petroleo, metodo para controlar su punto de ablandamiento y peso molecular y adhesivo sensible a la presion fundida caliente que las contiene. |
| US6172156B1 (en) * | 1996-07-03 | 2001-01-09 | H. B. Fuller Licensing & Financing, Inc. | Cohesively failing hot melt pressure sensitive adhesive |
-
1999
- 1999-06-07 US US09/326,856 patent/US6162859A/en not_active Expired - Lifetime
-
2000
- 2000-06-07 JP JP2001502528A patent/JP5079957B2/ja not_active Expired - Lifetime
- 2000-06-07 EP EP00950214A patent/EP1105440A1/en not_active Withdrawn
- 2000-06-07 WO PCT/US2000/015605 patent/WO2000075257A1/en not_active Ceased
- 2000-06-07 CA CA002339820A patent/CA2339820A1/en not_active Abandoned
- 2000-06-07 AU AU63348/00A patent/AU6334800A/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP1105440A1 (en) | 2001-06-13 |
| JP5079957B2 (ja) | 2012-11-21 |
| US6162859A (en) | 2000-12-19 |
| JP2003501546A (ja) | 2003-01-14 |
| CA2339820A1 (en) | 2000-12-14 |
| WO2000075257A1 (en) | 2000-12-14 |
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