JP2000502130A - 粘着付与剤及び粘着付与剤を得る方法 - Google Patents
粘着付与剤及び粘着付与剤を得る方法Info
- Publication number
- JP2000502130A JP2000502130A JP9521468A JP52146897A JP2000502130A JP 2000502130 A JP2000502130 A JP 2000502130A JP 9521468 A JP9521468 A JP 9521468A JP 52146897 A JP52146897 A JP 52146897A JP 2000502130 A JP2000502130 A JP 2000502130A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- tackifier
- olefin
- cyclic
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 58
- 229920005989 resin Polymers 0.000 claims abstract description 102
- 239000011347 resin Substances 0.000 claims abstract description 102
- -1 cyclic olefin Chemical class 0.000 claims abstract description 89
- 239000000178 monomer Substances 0.000 claims abstract description 80
- 125000003118 aryl group Chemical group 0.000 claims abstract description 79
- 230000001070 adhesive effect Effects 0.000 claims abstract description 73
- 239000000203 mixture Substances 0.000 claims abstract description 73
- 239000000853 adhesive Substances 0.000 claims abstract description 71
- 239000004711 α-olefin Substances 0.000 claims abstract description 39
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims abstract description 37
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 31
- 239000012968 metallocene catalyst Substances 0.000 claims abstract description 16
- 238000004519 manufacturing process Methods 0.000 claims abstract description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 33
- 229920000642 polymer Polymers 0.000 claims description 31
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 30
- 239000012190 activator Substances 0.000 claims description 23
- 150000001336 alkenes Chemical class 0.000 claims description 17
- 229920001400 block copolymer Polymers 0.000 claims description 11
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- 229920001519 homopolymer Polymers 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 150000002430 hydrocarbons Chemical class 0.000 claims description 7
- 229920005604 random copolymer Polymers 0.000 claims description 6
- 150000001450 anions Chemical class 0.000 claims description 5
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims description 4
- BYPDAAZBLBEWNV-UHFFFAOYSA-N cyclopenta-2,4-dien-1-amine Chemical compound NC1C=CC=C1 BYPDAAZBLBEWNV-UHFFFAOYSA-N 0.000 claims description 3
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- 239000002954 polymerization reaction product Substances 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 abstract description 21
- 238000007334 copolymerization reaction Methods 0.000 abstract description 5
- 239000003054 catalyst Substances 0.000 description 63
- 239000003446 ligand Substances 0.000 description 43
- 238000006116 polymerization reaction Methods 0.000 description 26
- 229920005601 base polymer Polymers 0.000 description 24
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 21
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 20
- 238000012360 testing method Methods 0.000 description 20
- 239000005977 Ethylene Substances 0.000 description 19
- 150000001875 compounds Chemical class 0.000 description 19
- 239000004831 Hot glue Substances 0.000 description 16
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 16
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 125000001183 hydrocarbyl group Chemical group 0.000 description 15
- 238000010348 incorporation Methods 0.000 description 15
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- 125000000129 anionic group Chemical group 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 12
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- 150000001993 dienes Chemical class 0.000 description 11
- 239000001257 hydrogen Substances 0.000 description 11
- 229910052739 hydrogen Inorganic materials 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 10
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 10
- 239000000463 material Substances 0.000 description 9
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- 239000000654 additive Substances 0.000 description 8
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- 229910052726 zirconium Inorganic materials 0.000 description 8
- 239000013032 Hydrocarbon resin Substances 0.000 description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 7
- 229920006270 hydrocarbon resin Polymers 0.000 description 7
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 7
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000005481 NMR spectroscopy Methods 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 6
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- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 5
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- 125000004429 atom Chemical group 0.000 description 5
- 239000012876 carrier material Substances 0.000 description 5
- 239000000539 dimer Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 150000005673 monoalkenes Chemical class 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 5
- 229930015698 phenylpropene Natural products 0.000 description 5
- 238000005096 rolling process Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- 229920002799 BoPET Polymers 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 4
- 238000005227 gel permeation chromatography Methods 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 239000002655 kraft paper Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 238000012719 thermal polymerization Methods 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZOICEQJZAWJHSI-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenyl)boron Chemical compound [B]C1=C(F)C(F)=C(F)C(F)=C1F ZOICEQJZAWJHSI-UHFFFAOYSA-N 0.000 description 3
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical class C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 3
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 3
- AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 239000002841 Lewis acid Substances 0.000 description 3
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- 239000002390 adhesive tape Substances 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 150000004703 alkoxides Chemical class 0.000 description 3
- 125000005234 alkyl aluminium group Chemical group 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
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- 239000010426 asphalt Substances 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
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- 125000005842 heteroatom Chemical group 0.000 description 3
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- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
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- 229910052760 oxygen Inorganic materials 0.000 description 3
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- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 3
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- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/06—Propene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F232/00—Copolymers of cyclic compounds containing no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic ring system
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/625—Component covered by group C08F4/62 with a metal or compound covered by group C08F4/44, not provided for in a single group of groups C08F4/622 or C08F4/623
Landscapes
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56891095A | 1995-12-07 | 1995-12-07 | |
| US08/568,910 | 1995-12-07 | ||
| PCT/US1996/019480 WO1997020872A1 (en) | 1995-12-07 | 1996-12-09 | Tackifiers and a process to obtain tackifiers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000502130A true JP2000502130A (ja) | 2000-02-22 |
| JP2000502130A5 JP2000502130A5 (2) | 2004-10-28 |
Family
ID=24273262
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9521468A Pending JP2000502130A (ja) | 1995-12-07 | 1996-12-09 | 粘着付与剤及び粘着付与剤を得る方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5874512A (2) |
| EP (1) | EP0871675B1 (2) |
| JP (1) | JP2000502130A (2) |
| KR (1) | KR100441335B1 (2) |
| CN (2) | CN1109054C (2) |
| DE (1) | DE69624590T2 (2) |
| WO (1) | WO1997020872A1 (2) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2001040315A (ja) * | 1999-08-04 | 2001-02-13 | Toagosei Co Ltd | カーペットへのポリオレフィン系樹脂製パッドの接着方法 |
| JP2005239975A (ja) * | 2004-02-27 | 2005-09-08 | Maruzen Petrochem Co Ltd | 芳香族含有環状オレフィン共重合体の製造方法 |
| WO2019188447A1 (ja) * | 2018-03-30 | 2019-10-03 | 三井化学株式会社 | 光学レンズ |
| WO2021060551A1 (ja) * | 2019-09-27 | 2021-04-01 | 出光興産株式会社 | オレフィン系樹脂及びホットメルト接着剤 |
| JP2022541661A (ja) * | 2019-07-26 | 2022-09-26 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 高芳香族性を有する炭化水素ポリマー改質剤及びその使用 |
| JP2022541660A (ja) * | 2019-07-26 | 2022-09-26 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 低芳香族性を有する炭化水素ポリマー改質剤及びその使用 |
| JP2025522594A (ja) * | 2022-12-16 | 2025-07-15 | コーロン インダストリーズ インク | 粘接着付与樹脂及びその製造方法 |
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| US6632541B2 (en) * | 1998-02-10 | 2003-10-14 | Sumitomo Chemical Company, Limited | Olefin-based copolymer composition |
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| US7015276B2 (en) * | 2000-10-02 | 2006-03-21 | Sekisui Chemical Co., Ltd. | Melt-moldable thermoplastic norbornene resin composition and molded article and optical film both comprising the same |
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| US20110054117A1 (en) * | 2009-08-27 | 2011-03-03 | Hall Gregory K | Polyolefin Adhesive Compositions and Method of Making Thereof |
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| WO2018017180A1 (en) | 2016-07-21 | 2018-01-25 | Exxonmobil Chemical Patents Inc. | Rotomolded compositions, articles, and processes for making the same |
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| BR112019012767B1 (pt) * | 2016-12-29 | 2022-12-13 | Akzo Nobel Chemicals International B.V | Composição orgânica líquida espessa, composição de óleo espessa, e uso da composição de óleo espessa |
| CN107057619A (zh) * | 2017-06-07 | 2017-08-18 | 吴秀兰 | 玻璃保护膜、热塑性弹性体压敏胶及其与玻璃结合的方法 |
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-
1996
- 1996-12-09 KR KR10-1998-0704239A patent/KR100441335B1/ko not_active Expired - Fee Related
- 1996-12-09 JP JP9521468A patent/JP2000502130A/ja active Pending
- 1996-12-09 WO PCT/US1996/019480 patent/WO1997020872A1/en not_active Ceased
- 1996-12-09 EP EP96943636A patent/EP0871675B1/en not_active Expired - Lifetime
- 1996-12-09 DE DE69624590T patent/DE69624590T2/de not_active Expired - Fee Related
- 1996-12-09 CN CN96198821A patent/CN1109054C/zh not_active Expired - Fee Related
- 1996-12-09 CN CNB01137697XA patent/CN1176960C/zh not_active Expired - Fee Related
-
1997
- 1997-09-18 US US08/932,511 patent/US5874512A/en not_active Expired - Lifetime
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001040315A (ja) * | 1999-08-04 | 2001-02-13 | Toagosei Co Ltd | カーペットへのポリオレフィン系樹脂製パッドの接着方法 |
| JP2005239975A (ja) * | 2004-02-27 | 2005-09-08 | Maruzen Petrochem Co Ltd | 芳香族含有環状オレフィン共重合体の製造方法 |
| WO2019188447A1 (ja) * | 2018-03-30 | 2019-10-03 | 三井化学株式会社 | 光学レンズ |
| JPWO2019188447A1 (ja) * | 2018-03-30 | 2021-02-12 | 三井化学株式会社 | 光学レンズ |
| JP7028961B2 (ja) | 2018-03-30 | 2022-03-02 | 三井化学株式会社 | 光学レンズ |
| US12043684B2 (en) | 2018-03-30 | 2024-07-23 | Mitsui Chemicals, Inc. | Optical lens |
| JP2022541661A (ja) * | 2019-07-26 | 2022-09-26 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 高芳香族性を有する炭化水素ポリマー改質剤及びその使用 |
| JP2022541660A (ja) * | 2019-07-26 | 2022-09-26 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 低芳香族性を有する炭化水素ポリマー改質剤及びその使用 |
| JP7345048B2 (ja) | 2019-07-26 | 2023-09-14 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 低芳香族性を有する炭化水素ポリマー改質剤及びその使用 |
| JP7345049B2 (ja) | 2019-07-26 | 2023-09-14 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 高芳香族性を有する炭化水素ポリマー改質剤及びその使用 |
| WO2021060551A1 (ja) * | 2019-09-27 | 2021-04-01 | 出光興産株式会社 | オレフィン系樹脂及びホットメルト接着剤 |
| JP2025522594A (ja) * | 2022-12-16 | 2025-07-15 | コーロン インダストリーズ インク | 粘接着付与樹脂及びその製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69624590D1 (de) | 2002-12-05 |
| EP0871675B1 (en) | 2002-10-30 |
| WO1997020872A1 (en) | 1997-06-12 |
| DE69624590T2 (de) | 2003-08-14 |
| CN1203605A (zh) | 1998-12-30 |
| CN1427015A (zh) | 2003-07-02 |
| KR100441335B1 (ko) | 2004-10-25 |
| KR19990071951A (ko) | 1999-09-27 |
| US5874512A (en) | 1999-02-23 |
| EP0871675A1 (en) | 1998-10-21 |
| CN1176960C (zh) | 2004-11-24 |
| CN1109054C (zh) | 2003-05-21 |
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