ES2835807T3 - Interpolímeros de etileno/alfa-olefina/polieno no conjugado y procesos para formar los mismos - Google Patents
Interpolímeros de etileno/alfa-olefina/polieno no conjugado y procesos para formar los mismos Download PDFInfo
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- ES2835807T3 ES2835807T3 ES12815929T ES12815929T ES2835807T3 ES 2835807 T3 ES2835807 T3 ES 2835807T3 ES 12815929 T ES12815929 T ES 12815929T ES 12815929 T ES12815929 T ES 12815929T ES 2835807 T3 ES2835807 T3 ES 2835807T3
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- hydrocarbyl
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- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 125000001118 alkylidene group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003738 black carbon Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
- XEHUIDSUOAGHBW-UHFFFAOYSA-N chromium;pentane-2,4-dione Chemical compound [Cr].CC(=O)CC(C)=O.CC(=O)CC(C)=O.CC(=O)CC(C)=O XEHUIDSUOAGHBW-UHFFFAOYSA-N 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- UVJHQYIOXKWHFD-UHFFFAOYSA-N cyclohexa-1,4-diene Chemical compound C1C=CCC=C1 UVJHQYIOXKWHFD-UHFFFAOYSA-N 0.000 description 1
- NLDGJRWPPOSWLC-UHFFFAOYSA-N deca-1,9-diene Chemical compound C=CCCCCCCC=C NLDGJRWPPOSWLC-UHFFFAOYSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 125000004983 dialkoxyalkyl group Chemical group 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 125000005044 dihydroquinolinyl group Chemical group N1(CC=CC2=CC=CC=C12)* 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000002270 exclusion chromatography Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical class OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 125000000687 hydroquinonyl group Chemical class C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 150000007527 lewis bases Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical class [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 235000011160 magnesium carbonates Nutrition 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
- 125000003518 norbornenyl group Chemical class C12(C=CC(CC1)C2)* 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003534 oscillatory effect Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 230000003938 response to stress Effects 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical class OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000001542 size-exclusion chromatography Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- HSVFKFNNMLUVEY-UHFFFAOYSA-N sulfuryl diazide Chemical compound [N-]=[N+]=NS(=O)(=O)N=[N+]=[N-] HSVFKFNNMLUVEY-UHFFFAOYSA-N 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 150000004684 trihydrates Chemical class 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- OBAJXDYVZBHCGT-UHFFFAOYSA-N tris(pentafluorophenyl)borane Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1B(C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F OBAJXDYVZBHCGT-UHFFFAOYSA-N 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
- C08F210/18—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers with non-conjugated dienes, e.g. EPT 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
- 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
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65908—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an ionising compound other than alumoxane, e.g. (C6F5)4B-X+
-
- 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
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161577720P | 2011-12-20 | 2011-12-20 | |
| US201261731891P | 2012-11-30 | 2012-11-30 | |
| PCT/US2012/070859 WO2013096573A1 (en) | 2011-12-20 | 2012-12-20 | Ethylene/alpha-olefin/nonconjugated polyene interpolymers and processes to form the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2835807T3 true ES2835807T3 (es) | 2021-06-23 |
Family
ID=47559697
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES12815929T Active ES2835807T3 (es) | 2011-12-20 | 2012-12-20 | Interpolímeros de etileno/alfa-olefina/polieno no conjugado y procesos para formar los mismos |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9422383B2 (OSRAM) |
| EP (1) | EP2794693B1 (OSRAM) |
| JP (1) | JP6189325B2 (OSRAM) |
| KR (1) | KR101989206B1 (OSRAM) |
| CN (1) | CN104169313B (OSRAM) |
| BR (1) | BR112014014855B1 (OSRAM) |
| ES (1) | ES2835807T3 (OSRAM) |
| IN (1) | IN2014CN04444A (OSRAM) |
| WO (1) | WO2013096573A1 (OSRAM) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101989206B1 (ko) | 2011-12-20 | 2019-09-24 | 다우 글로벌 테크놀로지스 엘엘씨 | 에틸렌/알파-올레핀/비공액 폴리엔 혼성중합체 및 그의 형성 방법 |
| JP5946331B2 (ja) * | 2012-06-01 | 2016-07-06 | 三井化学株式会社 | エチレン・α−オレフィン非共役ポリエン共重合体ゴムペレット |
| EP2925798B1 (en) * | 2012-11-30 | 2019-04-24 | Dow Global Technologies LLC | Ethylene/alpha-olefin/polyene based compositions |
| ES2665586T3 (es) * | 2012-12-27 | 2018-04-26 | Dow Global Technologies Llc | Sistemas catalizadores para polimerización de olefinas |
| KR102038178B1 (ko) | 2013-01-18 | 2019-10-29 | 다우 글로벌 테크놀로지스 엘엘씨 | 고분자량 폴리올레핀을 위한 중합 방법 |
| US10457765B2 (en) * | 2014-05-31 | 2019-10-29 | Bridgestone Corporation | Metallic complex catalyst, polymerization methods employing same and polymer products thereof |
| JP6763857B2 (ja) * | 2014-12-04 | 2020-09-30 | ダウ グローバル テクノロジーズ エルエルシー | エチレン系ポリマーの調製物のための五配位ビス−フェニルフェノキシ触媒 |
| MY184826A (en) | 2014-12-04 | 2021-04-24 | Dow Technology Investments Llc | Hydroformylation process |
| JP6752794B2 (ja) * | 2014-12-29 | 2020-09-09 | ダウ グローバル テクノロジーズ エルエルシー | エチレン／アルファ−オレフィンインターポリマーを形成する方法 |
| JP6718453B2 (ja) * | 2014-12-29 | 2020-07-08 | ダウ グローバル テクノロジーズ エルエルシー | 油含有エチレン系ポリマーを形成する方法 |
| KR102603126B1 (ko) * | 2015-03-31 | 2023-11-17 | 다우 글로벌 테크놀로지스 엘엘씨 | 낮은 수준의 장쇄 분지화를 갖는 고분자량 에틸렌/알파-올레핀/비-접합된 인터폴리머의 생산 방법 |
| KR102575287B1 (ko) * | 2015-05-28 | 2023-09-06 | 다우 글로벌 테크놀로지스 엘엘씨 | 에틸렌/알파-올레핀 인터폴리머를 형성하는 방법 |
| BR112018003299B1 (pt) * | 2015-09-02 | 2022-06-28 | Dow Global Technologies Llc | Composição polimérica reticulável, composição polimérica reticulada e condutor revestido |
| KR102587539B1 (ko) * | 2015-09-02 | 2023-10-12 | 다우 글로벌 테크놀로지스 엘엘씨 | 가요성 가교결합된 케이블 절연체 및 가요성 가교결합된 케이블 절연체를 제조하는 방법 |
| KR102606652B1 (ko) * | 2015-10-29 | 2023-11-28 | 다우 글로벌 테크놀로지스 엘엘씨 | 가요성 가교결합된 케이블 절연체용 가교결합성 폴리머 조성물 및 가요성 가교결합된 케이블 절연체를 제조하는 방법 |
| WO2017206009A1 (en) | 2016-05-30 | 2017-12-07 | Dow Global Technologies Llc | Ethylene/alpha-olefin/diene interpolymers compositions |
| WO2017206008A1 (en) | 2016-05-30 | 2017-12-07 | Dow Global Technologies Llc | Ethylene/alpha-olefin/diene interpolymer |
| BR122022020775B1 (pt) | 2016-06-30 | 2023-04-18 | Dow Global Technologies Llc | Processo para medir a quantidade de ramificação de cadeia longa do tipo y-pe por 1.000 carbonos totais em um interpolímero de etileno/alfa- olefina/dieno |
| WO2018005852A1 (en) | 2016-06-30 | 2018-01-04 | Dow Global Technologies Llc | Ethylene/alpha-olefin/polyene based compositions |
| WO2018013284A2 (en) | 2016-07-13 | 2018-01-18 | Exxonmobil Chemical Patents Inc. | Dual metallocene catalyst copolymer compositions |
| US11352451B2 (en) | 2016-07-13 | 2022-06-07 | Exxonmobil Chemical Patents Inc. | Dual metallocene catalyst copolymer compositions |
| JP6936303B2 (ja) | 2016-07-14 | 2021-09-15 | エクソンモービル・ケミカル・パテンツ・インク | ２元メタロセン触媒で重合されたバイモーダルのコポリマー組成物 |
| US10221260B2 (en) | 2016-07-29 | 2019-03-05 | Exxonmobil Chemical Patents Inc. | Phenolate transition metal complexes, production and use thereof |
| KR102413982B1 (ko) * | 2016-07-29 | 2022-06-30 | 다우 글로벌 테크놀로지스 엘엘씨 | 다중모드 엘라스토머 생산용 혼합 촉매 시스템 |
| WO2018022279A1 (en) | 2016-07-29 | 2018-02-01 | Exxonmobil Chemical Patents Inc. | Phenolate transition metal complexes, production and use thereof |
| WO2018119570A1 (en) * | 2016-12-26 | 2018-07-05 | Dow Global Technologies Llc | Ethylene/a-olefin/nonconjugated polyene interpolymer compositions and articles prepared from the same |
| CN110461890B (zh) * | 2017-03-31 | 2022-11-18 | 陶氏环球技术有限责任公司 | 用于烯烃聚合的双-联苯-苯氧基催化剂 |
| EP3638730B1 (en) | 2017-06-14 | 2024-05-01 | ExxonMobil Chemical Patents Inc. | Ethylene copolymer blends for cross-linking applications |
| JP7381449B2 (ja) | 2017-08-24 | 2023-11-15 | ダウ グローバル テクノロジーズ エルエルシー | エチレン／ｃ５－ｃ１０アルファ－オレフィン／ポリエチレンインターポリマー |
| EP3752560B1 (en) | 2018-02-14 | 2024-09-25 | Dow Global Technologies LLC | Ethylene/alpha-olefin interpolymer compositions with improved long term heat aging performance |
| US12006423B2 (en) | 2018-08-29 | 2024-06-11 | ExxonMobil Engineering & Technology Company | Methods of making polymer compositions with enhanced elasticity by employing VTP and HMP catalyst systems in parallel processes |
| KR102538844B1 (ko) * | 2018-12-21 | 2023-06-01 | 주식회사 엘지화학 | 방향족 비닐 화합물-비닐시안 화합물 공중합체의 제조방법 및 이를 포함하는 열가소성 수지 조성물의 제조방법 |
| EP3940009A4 (en) | 2019-03-12 | 2023-03-15 | Mitsui Chemicals, Inc. | OLEFIN-BASED RESIN, CROSSLINKER THEREOF, AND METHODS OF PRODUCTION THEREOF |
| KR102715918B1 (ko) * | 2019-03-29 | 2024-10-15 | 다우 글로벌 테크놀로지스 엘엘씨 | 열가소성 가황물을 위한 오일-증량된 펠릿 형태 에틸렌 알파-올레핀 디엔 인터폴리머 |
| US12098268B2 (en) | 2019-04-30 | 2024-09-24 | Dow Global Technologies Llc | Ethylene/propylene/nonconjugated diene interpolymer composition |
| BR112022005433A2 (pt) | 2019-09-24 | 2022-06-21 | Dow Global Technologies Llc | Composição, composição reticulada, e, artigo |
| BR112022005357A2 (pt) | 2019-09-24 | 2022-06-14 | Dow Global Technologies Llc | Composição, e, artigo |
| EP4034598A1 (en) | 2019-09-24 | 2022-08-03 | Dow Global Technologies LLC | Polymer compositions with excellent electrical and mechanical properties |
| US20230074326A1 (en) * | 2019-12-27 | 2023-03-09 | Dow Global Technologies Llc | Ethylene/Butene Multi-Block Copolymer and Process for Producing Same |
| JP2021147420A (ja) * | 2020-03-16 | 2021-09-27 | 三井化学株式会社 | オレフィン・環状オレフィン共重合体の製造方法 |
| JP7762663B2 (ja) * | 2020-03-27 | 2025-10-30 | ダウ グローバル テクノロジーズ エルエルシー | 長鎖分岐エチレン系ポリマーを生成するためのプロセス |
| US12410273B2 (en) | 2020-03-30 | 2025-09-09 | Exxonmobil Chemical Patents Inc. | Comb-block copolymers and methods thereof |
| JP2024500603A (ja) * | 2020-12-28 | 2024-01-10 | サビック エスケー ネクスレン カンパニー プライヴェート リミテッド | 金属－リガンド錯体、これを含むエチレン系重合体製造用の触媒組成物およびこれを用いたエチレン系重合体の製造方法 |
| KR20240074467A (ko) * | 2022-11-21 | 2024-05-28 | 롯데케미칼 주식회사 | 에틸렌-알파-올레핀 공중합체 제조방법 |
| WO2025117273A1 (en) | 2023-12-01 | 2025-06-05 | ExxonMobil Technology and Engineering Company | Support-bound activators, supported catalyst systems, and processes for use thereof |
Family Cites Families (14)
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|---|---|---|---|---|
| US6545088B1 (en) | 1991-12-30 | 2003-04-08 | Dow Global Technologies Inc. | Metallocene-catalyzed process for the manufacture of EP and EPDM polymers |
| US5977251A (en) | 1996-04-01 | 1999-11-02 | The Dow Chemical Company | Non-adiabatic olefin solution polymerization |
| US6680361B1 (en) * | 1998-11-02 | 2004-01-20 | Dupont Dow Elastomers Llc | Shear thinning ethylene/α-olefin interpolymers and their preparation |
| US6869904B2 (en) * | 2002-04-24 | 2005-03-22 | Symyx Technologies, Inc. | Bridged bi-aromatic ligands, catalysts, processes for polymerizing and polymers therefrom |
| WO2006020624A1 (en) | 2004-08-09 | 2006-02-23 | Dow Global Technologies Inc. | Supported bis(hydroxyarylaryloxy) catalysts for manufacture of polymers |
| WO2007136493A2 (en) | 2006-05-17 | 2007-11-29 | Dow Global Technologies Inc. | Polypropylene solution polymerization process |
| EP2212359B1 (en) | 2007-11-19 | 2013-08-28 | Dow Global Technologies LLC | Long chain branched propylene-alpha-olefin copolymers |
| US8772414B2 (en) * | 2008-09-16 | 2014-07-08 | Dow Global Technologies Llc | Polymeric compositions and foams, methods of making the same, and articles prepared from the same |
| ES2421301T3 (es) | 2009-07-01 | 2013-08-30 | Dow Global Technologies Llc | Polímero etilénico y su uso |
| WO2011002986A1 (en) | 2009-07-01 | 2011-01-06 | Dow Global Technologies Inc. | Ethylenic polymer and its use |
| CN102471551B (zh) | 2009-07-15 | 2013-09-04 | 陶氏环球技术有限责任公司 | 聚合物组合物、其制备方法、以及由该组合物制备的制品 |
| KR101865645B1 (ko) * | 2010-08-25 | 2018-06-11 | 다우 글로벌 테크놀로지스 엘엘씨 | 중합성 올레핀의 중합 방법 및 그를 위한 촉매 |
| EP2791190B1 (en) * | 2011-12-13 | 2016-07-06 | Dow Global Technologies LLC | Ethylene-propylene-diene interpolymer composition |
| KR101989206B1 (ko) | 2011-12-20 | 2019-09-24 | 다우 글로벌 테크놀로지스 엘엘씨 | 에틸렌/알파-올레핀/비공액 폴리엔 혼성중합체 및 그의 형성 방법 |
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| CN104169313B (zh) | 2016-09-21 |
| EP2794693A1 (en) | 2014-10-29 |
| BR112014014855B1 (pt) | 2022-01-11 |
| BR112014014855A2 (pt) | 2017-06-13 |
| US20150322185A1 (en) | 2015-11-12 |
| EP2794693B1 (en) | 2020-09-23 |
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