SA516371206B1 - جزيئات المحفز الأولي وعملية بلمرة البوليمرات المشتركة الصدمية - Google Patents
جزيئات المحفز الأولي وعملية بلمرة البوليمرات المشتركة الصدمية Download PDFInfo
- Publication number
- SA516371206B1 SA516371206B1 SA516371206A SA516371206A SA516371206B1 SA 516371206 B1 SA516371206 B1 SA 516371206B1 SA 516371206 A SA516371206 A SA 516371206A SA 516371206 A SA516371206 A SA 516371206A SA 516371206 B1 SA516371206 B1 SA 516371206B1
- Authority
- SA
- Saudi Arabia
- Prior art keywords
- propylene
- copolymer
- phenylene
- particles
- polymerization
- Prior art date
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- 238000006116 polymerization reaction Methods 0.000 title claims abstract description 76
- 229920001577 copolymer Polymers 0.000 title claims abstract description 75
- 239000002245 particle Substances 0.000 title claims abstract description 56
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 80
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 79
- -1 phenylene aromatic diester Chemical class 0.000 claims abstract description 65
- 229920000642 polymer Polymers 0.000 claims abstract description 63
- 239000000203 mixture Substances 0.000 claims abstract description 61
- 239000003054 catalyst Substances 0.000 claims abstract description 56
- 230000002140 halogenating effect Effects 0.000 claims abstract description 13
- 239000002243 precursor Substances 0.000 claims abstract description 10
- 239000012041 precatalyst Substances 0.000 claims description 42
- 239000000178 monomer Substances 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 34
- 239000010936 titanium Substances 0.000 claims description 32
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- 150000001875 compounds Chemical class 0.000 claims description 28
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- 230000015572 biosynthetic process Effects 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 150000001336 alkenes Chemical group 0.000 claims description 16
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 16
- 238000005658 halogenation reaction Methods 0.000 claims description 15
- 125000004429 atom Chemical group 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 14
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- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- 238000012360 testing method Methods 0.000 claims description 11
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
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- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- UBZYKBZMAMTNKW-UHFFFAOYSA-J titanium tetrabromide Chemical group Br[Ti](Br)(Br)Br UBZYKBZMAMTNKW-UHFFFAOYSA-J 0.000 claims description 3
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- QLCPUVSLEIUUEM-UHFFFAOYSA-G tetrachlorotitanium trichlorotitanium Chemical compound Cl[Ti](Cl)(Cl)[Ti](Cl)(Cl)(Cl)Cl QLCPUVSLEIUUEM-UHFFFAOYSA-G 0.000 claims description 2
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- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 claims 1
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- 238000009825 accumulation Methods 0.000 description 4
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- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- NHYFIJRXGOQNFS-UHFFFAOYSA-N dimethoxy-bis(2-methylpropyl)silane Chemical compound CC(C)C[Si](OC)(CC(C)C)OC NHYFIJRXGOQNFS-UHFFFAOYSA-N 0.000 description 4
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- JOTOPCOJPUYXPE-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1.ClC1=CC=CC=C1 JOTOPCOJPUYXPE-UHFFFAOYSA-N 0.000 description 1
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- 230000005494 condensation Effects 0.000 description 1
- 229940092125 creon Drugs 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- YRMPTIHEUZLTDO-UHFFFAOYSA-N cyclopentyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C1CCCC1 YRMPTIHEUZLTDO-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- ZVMRWPHIZSSUKP-UHFFFAOYSA-N dicyclohexyl(dimethoxy)silane Chemical compound C1CCCCC1[Si](OC)(OC)C1CCCCC1 ZVMRWPHIZSSUKP-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- AHUXYBVKTIBBJW-UHFFFAOYSA-N dimethoxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](OC)(OC)C1=CC=CC=C1 AHUXYBVKTIBBJW-UHFFFAOYSA-N 0.000 description 1
- JVUVKQDVTIIMOD-UHFFFAOYSA-N dimethoxy(dipropyl)silane Chemical compound CCC[Si](OC)(OC)CCC JVUVKQDVTIIMOD-UHFFFAOYSA-N 0.000 description 1
- HVEBTMFRWKOCGF-UHFFFAOYSA-N dimethoxy(propan-2-yl)silane Chemical compound CO[SiH](OC)C(C)C HVEBTMFRWKOCGF-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- DKQVJMREABFYNT-UHFFFAOYSA-N ethene Chemical group C=C.C=C DKQVJMREABFYNT-UHFFFAOYSA-N 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 125000005343 heterocyclic alkyl group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000000592 heterocycloalkyl group Chemical group 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 238000011090 industrial biotechnology method and process Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 229940107604 lutein esters Drugs 0.000 description 1
- 150000002658 luteins Chemical class 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical compound CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 1
- 229940095102 methyl benzoate Drugs 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229920006029 tetra-polymer Polymers 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 description 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- LGROXJWYRXANBB-UHFFFAOYSA-N trimethoxy(propan-2-yl)silane Chemical compound CO[Si](OC)(OC)C(C)C LGROXJWYRXANBB-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 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
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/06—Propene
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/001—Multistage polymerisation processes characterised by a change in reactor conditions 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
- 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
- C08F4/647—Catalysts containing a specific non-metal or metal-free compound
- C08F4/649—Catalysts containing a specific non-metal or metal-free compound organic
- C08F4/6493—Catalysts containing a specific non-metal or metal-free compound organic containing halogen
-
- 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
- C08F4/65—Pretreating the metal or compound covered by group C08F4/64 before the final contacting with the metal or compound covered by group C08F4/44
- C08F4/651—Pretreating with non-metals or metal-free compounds
-
- 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
- C08F2410/06—Catalyst characterized by its size
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361909461P | 2013-11-27 | 2013-11-27 | |
| PCT/US2014/067703 WO2015081254A1 (en) | 2013-11-27 | 2014-11-26 | Procatalyst particles and polymerization process for impact copolymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SA516371206B1 true SA516371206B1 (ar) | 2019-07-31 |
Family
ID=53199650
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SA516371206A SA516371206B1 (ar) | 2013-11-27 | 2016-05-26 | جزيئات المحفز الأولي وعملية بلمرة البوليمرات المشتركة الصدمية |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US10059784B2 (https=) |
| EP (1) | EP3074435B1 (https=) |
| JP (2) | JP6573885B2 (https=) |
| KR (1) | KR102205993B1 (https=) |
| CN (2) | CN105764936B (https=) |
| BR (1) | BR112016012033B1 (https=) |
| ES (1) | ES2901954T3 (https=) |
| PL (1) | PL3074435T3 (https=) |
| RU (1) | RU2709203C1 (https=) |
| SA (1) | SA516371206B1 (https=) |
| WO (1) | WO2015081254A1 (https=) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105764936B (zh) * | 2013-11-27 | 2018-05-11 | 格雷斯公司 | 主催化剂颗粒及抗冲共聚物的聚合方法 |
| KR102763007B1 (ko) | 2016-08-30 | 2025-02-04 | 더블유.알. 그레이스 앤드 컴파니 -씨오엔엔. | 저회분 함량의 폴리올레핀들 및 그 제조방법 |
| WO2018167305A1 (en) * | 2017-03-17 | 2018-09-20 | Sabic Global Technologies B.V. | Process for preparing a procatalyst for polymerization of olefins |
| WO2019094216A1 (en) * | 2017-11-13 | 2019-05-16 | W.R. Grace & Co.-Conn. | Catalyst components for propylene polymerization |
| WO2019094347A1 (en) * | 2017-11-13 | 2019-05-16 | W.R. Grace & Co.-Conn. | Catalyst components for propylene polymerization |
| KR20230091125A (ko) * | 2020-10-23 | 2023-06-22 | 더블유.알. 그레이스 앤드 캄파니-콘. | Voc 함량이 감소한 충격 저항성 폴리프로필렌 중합체 조성물 |
| EP4359448A1 (en) | 2021-06-25 | 2024-05-01 | Braskem, S.A. | Propylene preliminary polymerization |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4882380A (en) | 1987-07-07 | 1989-11-21 | Union Carbide Chemicals And Plastics Company Inc. | Process for the production of impact polypropylene copolymers |
| JPH0693061A (ja) * | 1992-09-16 | 1994-04-05 | Sumitomo Chem Co Ltd | ポリプロピレンブロック共重合体及びそのフィルム |
| US5885924A (en) | 1995-06-07 | 1999-03-23 | W. R. Grace & Co.-Conn. | Halogenated supports and supported activators |
| FI981718L (fi) | 1998-08-07 | 2000-02-08 | Borealis As | Katalysaattorikomponentti, joka käsittää magnesiumia, titaania, halogeenia ja elektrodonorin, sen valmistus ja käyttö |
| FI981717A7 (fi) * | 1998-08-07 | 2000-02-08 | Borealis As | Katalysaattorikomponentti, joka käsittää magnesiumia, titaania, halogeenia ja elektronidonorin, sen valmistus ja käyttö |
| US6825146B2 (en) | 2001-05-29 | 2004-11-30 | Union Carbide Chemicals & Plastics Technology Corporation | Olefin polymerization catalyst compositions and method of preparation |
| EP1668044B1 (en) | 2003-09-23 | 2014-05-07 | W.R. Grace & CO. - CONN. | Self limiting catalyst composition with dicarboxylic acid ester internal donor and propylene polymerization process |
| US8788826B1 (en) | 2008-06-06 | 2014-07-22 | Marvell International Ltd. | Method and apparatus for dynamically allocating a mobile network prefix to a mobile terminal |
| EP2315790B1 (en) * | 2008-08-21 | 2018-04-25 | W.R. Grace & CO. - CONN. | High melt flow propylene impact copolymer and method |
| US8604118B2 (en) * | 2008-12-26 | 2013-12-10 | Dow Global Technologies Llc | Antifoulant for impact copolymers and method |
| PL2373702T3 (pl) * | 2008-12-31 | 2018-07-31 | W.R. Grace & Co.-Conn. | Kompozycja prekatalizatora z wewnętrznym donorem w postaci podstawionego aromatycznego diestru 1,2-fenylenowego oraz sposób |
| JP5731988B2 (ja) * | 2008-12-31 | 2015-06-10 | ダブリュー・アール・グレイス・アンド・カンパニー−コネチカット | プロピレン系ポリマー、物品およびその製造プロセス |
| JP5448702B2 (ja) * | 2009-10-14 | 2014-03-19 | 日本ポリプロ株式会社 | プロピレン系ブロック共重合体の製造方法 |
| US20120157645A1 (en) | 2010-12-21 | 2012-06-21 | Linfeng Chen | Procatalyst Composition with Alkoxypropyl Ester Internal Electron Donor and Polymer From Same |
| JP2014500384A (ja) * | 2010-12-21 | 2014-01-09 | ダウ グローバル テクノロジーズ エルエルシー | アルコキシアルキルエステル内部電子供与体を有するプロ触媒組成物の製造方法および製品 |
| US20120157295A1 (en) * | 2010-12-21 | 2012-06-21 | Linfeng Chen | Process for Producing Procatalyst Composition with Alkoxyalkyl Ester Internal Electron Donor and Product |
| MX2013007356A (es) * | 2010-12-21 | 2014-01-23 | Dow Global Technologies Llc | Proceso para producir polimeros basados en propileno con alto indice de fluidez y productos preparados a partir de los mismos. |
| US9133286B2 (en) * | 2011-08-30 | 2015-09-15 | W. R. Grace & Co.-Conn | Production of substituted phenylene dibenzoate internal electron donor and procatalyst with same |
| CN105764936B (zh) | 2013-11-27 | 2018-05-11 | 格雷斯公司 | 主催化剂颗粒及抗冲共聚物的聚合方法 |
-
2014
- 2014-11-26 CN CN201480064998.XA patent/CN105764936B/zh active Active
- 2014-11-26 US US15/036,365 patent/US10059784B2/en active Active
- 2014-11-26 RU RU2016125244A patent/RU2709203C1/ru active
- 2014-11-26 BR BR112016012033-7A patent/BR112016012033B1/pt active IP Right Grant
- 2014-11-26 EP EP14865185.4A patent/EP3074435B1/en active Active
- 2014-11-26 CN CN201810337337.XA patent/CN108503734B/zh active Active
- 2014-11-26 JP JP2016534668A patent/JP6573885B2/ja active Active
- 2014-11-26 KR KR1020167016790A patent/KR102205993B1/ko active Active
- 2014-11-26 WO PCT/US2014/067703 patent/WO2015081254A1/en not_active Ceased
- 2014-11-26 ES ES14865185T patent/ES2901954T3/es active Active
- 2014-11-26 PL PL14865185T patent/PL3074435T3/pl unknown
-
2016
- 2016-05-26 SA SA516371206A patent/SA516371206B1/ar unknown
-
2018
- 2018-06-27 US US16/019,693 patent/US20180305479A1/en not_active Abandoned
-
2019
- 2019-02-07 JP JP2019020934A patent/JP6869276B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| EP3074435B1 (en) | 2021-11-10 |
| JP6573885B2 (ja) | 2019-09-11 |
| EP3074435A4 (en) | 2017-06-28 |
| WO2015081254A1 (en) | 2015-06-04 |
| JP6869276B2 (ja) | 2021-05-12 |
| CN105764936B (zh) | 2018-05-11 |
| US10059784B2 (en) | 2018-08-28 |
| JP2019131811A (ja) | 2019-08-08 |
| BR112016012033B1 (pt) | 2021-02-09 |
| PL3074435T3 (pl) | 2022-01-24 |
| RU2016125244A (ru) | 2018-01-09 |
| KR20160091952A (ko) | 2016-08-03 |
| CN105764936A (zh) | 2016-07-13 |
| KR102205993B1 (ko) | 2021-01-21 |
| CN108503734A (zh) | 2018-09-07 |
| US20180305479A1 (en) | 2018-10-25 |
| RU2709203C1 (ru) | 2019-12-17 |
| EP3074435A1 (en) | 2016-10-05 |
| CN108503734B (zh) | 2021-09-03 |
| ES2901954T3 (es) | 2022-03-24 |
| JP2016538396A (ja) | 2016-12-08 |
| US20160297906A1 (en) | 2016-10-13 |
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