RU2007134419A - ФУНКЦИОНАЛИЗИРОВАННЫЕ КОМПОЗИЦИИ ИНТЕРПОЛИМЕРОВ ЭТЛЕНА/α-ОЛЕФИНА - Google Patents
ФУНКЦИОНАЛИЗИРОВАННЫЕ КОМПОЗИЦИИ ИНТЕРПОЛИМЕРОВ ЭТЛЕНА/α-ОЛЕФИНА Download PDFInfo
- Publication number
- RU2007134419A RU2007134419A RU2007134419/04A RU2007134419A RU2007134419A RU 2007134419 A RU2007134419 A RU 2007134419A RU 2007134419/04 A RU2007134419/04 A RU 2007134419/04A RU 2007134419 A RU2007134419 A RU 2007134419A RU 2007134419 A RU2007134419 A RU 2007134419A
- Authority
- RU
- Russia
- Prior art keywords
- interpolymer
- ethylene
- olefin
- composition
- composition according
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims 48
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 30
- 239000005977 Ethylene Substances 0.000 claims 30
- 239000004711 α-olefin Substances 0.000 claims 20
- 150000001336 alkenes Chemical class 0.000 claims 18
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 18
- 150000001875 compounds Chemical class 0.000 claims 14
- 229910000077 silane Inorganic materials 0.000 claims 12
- 229920000642 polymer Polymers 0.000 claims 9
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 8
- 229920000098 polyolefin Polymers 0.000 claims 7
- -1 tetrahydride male Chemical compound 0.000 claims 7
- 239000007795 chemical reaction product Substances 0.000 claims 5
- 125000005842 heteroatom Chemical group 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 239000000155 melt Substances 0.000 claims 3
- 230000008018 melting Effects 0.000 claims 3
- 238000002844 melting Methods 0.000 claims 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 2
- 238000005698 Diels-Alder reaction Methods 0.000 claims 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- 125000004423 acyloxy group Chemical group 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
- 238000005194 fractionation Methods 0.000 claims 2
- 239000003999 initiator Substances 0.000 claims 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims 2
- 150000002978 peroxides Chemical class 0.000 claims 2
- 239000000047 product Substances 0.000 claims 2
- HSVFKFNNMLUVEY-UHFFFAOYSA-N sulfuryl diazide Chemical compound [N-]=[N+]=NS(=O)(=O)N=[N+]=[N-] HSVFKFNNMLUVEY-UHFFFAOYSA-N 0.000 claims 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 2
- KNDQHSIWLOJIGP-UMRXKNAASA-N (3ar,4s,7r,7as)-rel-3a,4,7,7a-tetrahydro-4,7-methanoisobenzofuran-1,3-dione Chemical compound O=C1OC(=O)[C@@H]2[C@H]1[C@]1([H])C=C[C@@]2([H])C1 KNDQHSIWLOJIGP-UMRXKNAASA-N 0.000 claims 1
- CISIJYCKDJSTMX-UHFFFAOYSA-N 2,2-dichloroethenylbenzene Chemical compound ClC(Cl)=CC1=CC=CC=C1 CISIJYCKDJSTMX-UHFFFAOYSA-N 0.000 claims 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims 1
- CUEJHYHGUMAGBP-UHFFFAOYSA-N 2-[2-(1h-indol-5-yl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1C1=CC=C(NC=C2)C2=C1 CUEJHYHGUMAGBP-UHFFFAOYSA-N 0.000 claims 1
- LPIQIQPLUVLISR-UHFFFAOYSA-N 2-prop-1-en-2-yl-4,5-dihydro-1,3-oxazole Chemical compound CC(=C)C1=NCCO1 LPIQIQPLUVLISR-UHFFFAOYSA-N 0.000 claims 1
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 claims 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 1
- 239000004743 Polypropylene Substances 0.000 claims 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 claims 1
- 229940018557 citraconic acid Drugs 0.000 claims 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims 1
- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 claims 1
- BLKQQTCUGZJWLN-QXMHVHEDSA-N dicyclohexyl (z)-but-2-enedioate Chemical compound C1CCCCC1OC(=O)\C=C/C(=O)OC1CCCCC1 BLKQQTCUGZJWLN-QXMHVHEDSA-N 0.000 claims 1
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 claims 1
- XHSDDKAGJYJAQM-ULDVOPSXSA-N dioctadecyl (e)-but-2-enedioate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCCCCCCCCCC XHSDDKAGJYJAQM-ULDVOPSXSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000001530 fumaric acid Substances 0.000 claims 1
- 230000004927 fusion Effects 0.000 claims 1
- 230000009477 glass transition Effects 0.000 claims 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims 1
- 150000004678 hydrides Chemical class 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 150000003949 imides Chemical class 0.000 claims 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 1
- 239000011976 maleic acid Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims 1
- 229920001155 polypropylene Polymers 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 238000011084 recovery Methods 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- JIYNFFGKZCOPKN-UHFFFAOYSA-N sbb061129 Chemical compound O=C1OC(=O)C2C1C1C=C(C)C2C1 JIYNFFGKZCOPKN-UHFFFAOYSA-N 0.000 claims 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims 1
- 229940014800 succinic anhydride Drugs 0.000 claims 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 claims 1
- 239000005050 vinyl trichlorosilane Substances 0.000 claims 1
Classifications
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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
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
- C08F297/083—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins the monomers being ethylene or propylene
- C08F297/086—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins the monomers being ethylene or propylene the block polymer contains at least three blocks
-
- 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
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
-
- 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
- C08F287/00—Macromolecular compounds obtained by polymerising monomers on to block polymers
-
- 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
- C08F295/00—Macromolecular compounds obtained by polymerisation using successively different catalyst types without deactivating the intermediate polymer
-
- 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
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
- C08F297/083—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins the monomers being ethylene or propylene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms
- C08L23/0815—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms with aliphatic 1-olefins containing one carbon-to-carbon double bond
-
- 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
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/01—Additive used together with the catalyst, excluding compounds containing Al or B
-
- 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
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/21—Rubbery or elastomeric properties
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Graft Or Block Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2005/008917 WO2005090427A2 (en) | 2004-03-17 | 2005-03-17 | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation |
| USPCT/US2005/008917 | 2005-03-17 | ||
| US71818405P | 2005-09-16 | 2005-09-16 | |
| US60/718,184 | 2005-09-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2007134419A true RU2007134419A (ru) | 2009-01-20 |
Family
ID=36847629
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2007134419/04A RU2007134419A (ru) | 2005-03-17 | 2006-03-15 | ФУНКЦИОНАЛИЗИРОВАННЫЕ КОМПОЗИЦИИ ИНТЕРПОЛИМЕРОВ ЭТЛЕНА/α-ОЛЕФИНА |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP1858937B1 (enExample) |
| JP (2) | JP5231986B2 (enExample) |
| KR (1) | KR101399699B1 (enExample) |
| AR (1) | AR055043A1 (enExample) |
| AU (1) | AU2006227475A1 (enExample) |
| BR (1) | BRPI0609829B1 (enExample) |
| CA (1) | CA2601344A1 (enExample) |
| MX (1) | MX2007011313A (enExample) |
| RU (1) | RU2007134419A (enExample) |
| SG (1) | SG160417A1 (enExample) |
| TW (1) | TWI388576B (enExample) |
| WO (1) | WO2006102016A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2650960C2 (ru) * | 2012-09-14 | 2018-04-18 | ХЕНКЕЛЬ АйПи ЭНД ХОЛДИНГ ГМБХ | Адгезионные композиции и их применение |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US7786216B2 (en) * | 2005-03-17 | 2010-08-31 | Dow Global Technologies Inc. | Oil based blends of interpolymers of ethylene/α-olefins |
| AR064670A1 (es) * | 2006-12-21 | 2009-04-15 | Dow Global Technologies Inc | Polimeros de olefina funcionalizados, composiciones y articulos preparados a partir de ellas y metodos para prepararlos |
| AU2010275394B2 (en) | 2009-07-24 | 2015-06-18 | Bostik, Inc. | Hot melt adhesive based on olefin block copolymers |
| BR112012001942B1 (pt) * | 2009-07-29 | 2019-10-22 | Dow Global Technologies Llc | agente de permuta de cadeia multifuncional, processo para preparar um agente de permuta de cadeia multifuncional, processo para preparar uma composição multifuncional, composição multifuncional, processo para preparar um agente de permuta de cadeia multifuncional contendo poli-radical poliolefina, poliolefina telequélica, processo para preparar uma poliolefina com funcionalidade terminal e separador de bateria |
| US8674027B2 (en) * | 2009-09-18 | 2014-03-18 | Dow Global Technologies Llc | Powdered thermoplastic polyolefin elastomer composition for slush molding processes |
| SG178597A1 (en) * | 2009-09-21 | 2012-04-27 | Saint Gobain Performance Plast | Method of forming an article from non-melt processible polymers and articles formed thereby |
| BR112013024365A8 (pt) | 2011-03-24 | 2018-02-06 | Henkel US IP LLC | Adesivo para laminação de filme extensível |
| CN103842438B (zh) | 2011-09-30 | 2016-01-20 | 陶氏环球技术有限责任公司 | 聚碳酸酯和聚丙烯的热塑性阻燃组合物 |
| WO2013090396A1 (en) | 2011-12-14 | 2013-06-20 | Dow Global Technologies Llc | Functionalized block composite and crystalline block composite compositions |
| CN108384033B (zh) * | 2012-02-03 | 2021-11-12 | 陶氏环球技术有限责任公司 | 包括含硅烷乙烯互聚物配方的膜和包括其的电子设备模块 |
| KR102090071B1 (ko) | 2012-06-29 | 2020-03-17 | 다우 글로벌 테크놀로지스 엘엘씨 | 올레핀 블록 공중합체를 가진 얼룩 저항성 물품 및 방법 |
| JP5711713B2 (ja) * | 2012-10-01 | 2015-05-07 | 住友電気工業株式会社 | 多層熱回復物品 |
| MX2015004606A (es) | 2012-10-09 | 2017-04-04 | Avery Dennison Corp | Adhesivos y metodos relacionados. |
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| JP5651161B2 (ja) | 2012-12-20 | 2015-01-07 | 住友電気工業株式会社 | 多層熱回復物品、ワイヤスプライス及びワイヤハーネス |
| JP6443634B2 (ja) | 2013-01-24 | 2018-12-26 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェンＨｅｎｋｅｌ ＡＧ ＆ Ｃｏ． ＫＧａＡ | 発泡性ホットメルト接着剤組成物およびその使用 |
| CN105143277B (zh) | 2013-03-20 | 2017-11-17 | Byk化学公司 | 用于制造功能化热塑弹性体的方法 |
| KR102354070B1 (ko) * | 2013-12-30 | 2022-01-24 | 다우 글로벌 테크놀로지스 엘엘씨 | 작용화된, 저점도 에틸렌계 중합체의 제조 방법 |
| MX2016017343A (es) | 2014-07-03 | 2017-05-12 | Bostik Inc | Adhesivos termofusibles sin mancha que fallan cohesivamente. |
| JP6782164B2 (ja) * | 2014-10-08 | 2020-11-11 | 古河電気工業株式会社 | 架橋樹脂成形体及び架橋性樹脂組成物とそれらの製造方法、シランマスターバッチ、並びに、成形品 |
| ES2992760T3 (en) | 2015-02-05 | 2024-12-17 | Avery Dennison Corp | Label assemblies for adverse environments |
| US20180127564A1 (en) * | 2015-06-24 | 2018-05-10 | Dow Global Technologies Llc | Filled polymer-based compositions with low viscosity, good mechanical properties and adhesion |
| US10526511B2 (en) | 2016-12-22 | 2020-01-07 | Avery Dennison Corporation | Convertible pressure sensitive adhesives comprising urethane (meth)acrylate oligomers |
| AR111452A1 (es) | 2017-04-07 | 2019-07-17 | Henkel IP & Holding GmbH | Adhesivos termoplásticos de alto rendimiento y sus usos |
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- 2006-03-15 KR KR1020077021234A patent/KR101399699B1/ko not_active Expired - Lifetime
- 2006-03-15 RU RU2007134419/04A patent/RU2007134419A/ru not_active Application Discontinuation
- 2006-03-15 TW TW095108759A patent/TWI388576B/zh not_active IP Right Cessation
- 2006-03-15 JP JP2008502067A patent/JP5231986B2/ja not_active Expired - Lifetime
- 2006-03-15 BR BRPI0609829-0A patent/BRPI0609829B1/pt active IP Right Grant
- 2006-03-15 CA CA002601344A patent/CA2601344A1/en not_active Abandoned
- 2006-03-15 AU AU2006227475A patent/AU2006227475A1/en not_active Abandoned
- 2006-03-15 AR ARP060100999A patent/AR055043A1/es unknown
- 2006-03-15 WO PCT/US2006/009591 patent/WO2006102016A2/en not_active Ceased
- 2006-03-15 MX MX2007011313A patent/MX2007011313A/es unknown
- 2006-03-15 SG SG201001862-0A patent/SG160417A1/en unknown
- 2006-03-15 EP EP06748414.7A patent/EP1858937B1/en not_active Expired - Lifetime
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2012
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2650960C2 (ru) * | 2012-09-14 | 2018-04-18 | ХЕНКЕЛЬ АйПи ЭНД ХОЛДИНГ ГМБХ | Адгезионные композиции и их применение |
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0609829B1 (pt) | 2017-08-01 |
| JP5231986B2 (ja) | 2013-07-10 |
| SG160417A1 (en) | 2010-04-29 |
| MX2007011313A (es) | 2007-10-08 |
| JP2012251165A (ja) | 2012-12-20 |
| JP5860367B2 (ja) | 2016-02-16 |
| CA2601344A1 (en) | 2006-09-28 |
| EP1858937B1 (en) | 2019-09-25 |
| AU2006227475A1 (en) | 2006-09-28 |
| TW200700441A (en) | 2007-01-01 |
| TWI388576B (zh) | 2013-03-11 |
| BRPI0609829A2 (pt) | 2010-04-27 |
| KR20080006541A (ko) | 2008-01-16 |
| JP2008533285A (ja) | 2008-08-21 |
| EP1858937A2 (en) | 2007-11-28 |
| WO2006102016A2 (en) | 2006-09-28 |
| WO2006102016A3 (en) | 2007-08-16 |
| KR101399699B1 (ko) | 2014-05-27 |
| AR055043A1 (es) | 2007-08-01 |
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