RU2298017C2 - Статистический сополимер пропилена, способ его получения, изделия из сополимера - Google Patents
Статистический сополимер пропилена, способ его получения, изделия из сополимера Download PDFInfo
- Publication number
- RU2298017C2 RU2298017C2 RU2004102045/04A RU2004102045A RU2298017C2 RU 2298017 C2 RU2298017 C2 RU 2298017C2 RU 2004102045/04 A RU2004102045/04 A RU 2004102045/04A RU 2004102045 A RU2004102045 A RU 2004102045A RU 2298017 C2 RU2298017 C2 RU 2298017C2
- Authority
- RU
- Russia
- Prior art keywords
- comonomer
- reactor
- ethylene
- propylene
- copolymer
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 74
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 title claims abstract description 61
- 229920001577 copolymer Polymers 0.000 title claims abstract description 56
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 title claims abstract description 40
- 229920005604 random copolymer Polymers 0.000 title claims abstract description 16
- 238000002360 preparation method Methods 0.000 title abstract description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 62
- 239000005977 Ethylene Substances 0.000 claims abstract description 60
- 229920000642 polymer Polymers 0.000 claims abstract description 59
- 238000009826 distribution Methods 0.000 claims abstract description 37
- 239000003054 catalyst Substances 0.000 claims abstract description 23
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 16
- 238000006243 chemical reaction Methods 0.000 claims abstract description 15
- 239000000725 suspension Substances 0.000 claims abstract description 14
- 239000004711 α-olefin Substances 0.000 claims abstract description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 10
- 238000001746 injection moulding Methods 0.000 claims abstract description 7
- 239000000835 fiber Substances 0.000 claims abstract description 6
- 238000010828 elution Methods 0.000 claims description 17
- 239000002002 slurry Substances 0.000 claims description 16
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 11
- 238000000071 blow moulding Methods 0.000 claims description 11
- 239000008096 xylene Substances 0.000 claims description 11
- 238000002844 melting Methods 0.000 claims description 10
- 230000008018 melting Effects 0.000 claims description 10
- 230000002902 bimodal effect Effects 0.000 claims description 6
- 229920006301 statistical copolymer Polymers 0.000 claims description 5
- 238000007334 copolymerization reaction Methods 0.000 claims description 3
- 229920006254 polymer film Polymers 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 8
- 239000000178 monomer Substances 0.000 abstract description 5
- 230000000694 effects Effects 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract description 2
- 238000000465 moulding Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 description 43
- 239000007789 gas Substances 0.000 description 21
- -1 polypropylene units Polymers 0.000 description 14
- 239000004743 Polypropylene Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- 229920001155 polypropylene Polymers 0.000 description 9
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 229920001038 ethylene copolymer Polymers 0.000 description 6
- 239000000654 additive Substances 0.000 description 4
- 238000005336 cracking Methods 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- JWCYDYZLEAQGJJ-UHFFFAOYSA-N dicyclopentyl(dimethoxy)silane Chemical group C1CCCC1[Si](OC)(OC)C1CCCC1 JWCYDYZLEAQGJJ-UHFFFAOYSA-N 0.000 description 3
- 238000005194 fractionation Methods 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 238000009827 uniform distribution Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 235000013539 calcium stearate Nutrition 0.000 description 2
- 239000008116 calcium stearate Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- YWEWWNPYDDHZDI-JJKKTNRVSA-N (1r)-1-[(4r,4ar,8as)-2,6-bis(3,4-dimethylphenyl)-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical compound C1=C(C)C(C)=CC=C1C1O[C@H]2[C@@H]([C@H](O)CO)OC(C=3C=C(C)C(C)=CC=3)O[C@H]2CO1 YWEWWNPYDDHZDI-JJKKTNRVSA-N 0.000 description 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 239000011954 Ziegler–Natta catalyst Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000005234 alkyl aluminium group Chemical group 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 1
- 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 1
- VHPUZTHRFWIGAW-UHFFFAOYSA-N dimethoxy-di(propan-2-yl)silane Chemical compound CO[Si](OC)(C(C)C)C(C)C VHPUZTHRFWIGAW-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- OANIYCQMEVXZCJ-UHFFFAOYSA-N ditert-butyl(dimethoxy)silane Chemical compound CO[Si](OC)(C(C)(C)C)C(C)(C)C OANIYCQMEVXZCJ-UHFFFAOYSA-N 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 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
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- FATBGEAMYMYZAF-UHFFFAOYSA-N oleicacidamide-heptaglycolether Natural products CCCCCCCCC=CCCCCCCCC(N)=O FATBGEAMYMYZAF-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000003756 stirring Methods 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
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
Images
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
- 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only 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
- 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
- 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
- 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
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)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01115471A EP1270628B1 (en) | 2001-06-27 | 2001-06-27 | Propylene random copolymer and process for the production thereof |
| EP01115471.3 | 2001-06-27 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2004102045A RU2004102045A (ru) | 2005-04-10 |
| RU2298017C2 true RU2298017C2 (ru) | 2007-04-27 |
Family
ID=8177837
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2004102045/04A RU2298017C2 (ru) | 2001-06-27 | 2002-06-26 | Статистический сополимер пропилена, способ его получения, изделия из сополимера |
Country Status (13)
| Country | Link |
|---|---|
| US (3) | US7470756B2 (enExample) |
| EP (3) | EP1270628B1 (enExample) |
| JP (1) | JP4217155B2 (enExample) |
| KR (1) | KR100869164B1 (enExample) |
| CN (1) | CN100386354C (enExample) |
| AT (3) | ATE278723T1 (enExample) |
| CZ (1) | CZ20033535A3 (enExample) |
| DE (3) | DE60106219T2 (enExample) |
| ES (2) | ES2273300T3 (enExample) |
| PL (1) | PL202978B1 (enExample) |
| PT (2) | PT1580207E (enExample) |
| RU (1) | RU2298017C2 (enExample) |
| WO (1) | WO2003002625A1 (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2518065C2 (ru) * | 2008-12-31 | 2014-06-10 | ДАУ ГЛОБАЛ ТЕКНОЛОДЖИЗ ЭлЭлСи | Композиции и изделия из статистического сополимера пропилена и способ их получения |
| US9790300B2 (en) | 2013-05-22 | 2017-10-17 | Borealis Ag | Propylene copolymer for thin-wall packaging |
| RU177792U1 (ru) * | 2014-10-15 | 2018-03-13 | Пайплайф Чех с.р.о | Трубка на основе термопластичного композитного материала |
| RU2648675C2 (ru) * | 2013-05-22 | 2018-03-28 | Бореалис Аг | Полипропилен для применения в пленках |
| RU2800648C2 (ru) * | 2018-10-26 | 2023-07-25 | В.Р.Грейс Энд Ко.-Конн. | Композиция статистического сополимера полипропилена для труб холодного и горячего водоснабжения |
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60129939T2 (de) * | 2001-06-27 | 2008-05-15 | Borealis Technology Oy | Verfahren zur Herstellung einer Polymerfolie die ein statistisches Propylencopolymer enthält |
| US7579408B2 (en) | 2004-03-17 | 2009-08-25 | Dow Global Technologies Inc. | Thermoplastic vulcanizate comprising interpolymers of ethylene/α-olefins |
| US7622529B2 (en) | 2004-03-17 | 2009-11-24 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/alpha-olefin with improved compatibility |
| US7714071B2 (en) | 2004-03-17 | 2010-05-11 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/α-olefins and flexible molded articles made therefrom |
| US7671106B2 (en) | 2004-03-17 | 2010-03-02 | Dow Global Technologies Inc. | Cap liners, closures and gaskets from multi-block polymers |
| US7863379B2 (en) | 2004-03-17 | 2011-01-04 | Dow Global Technologies Inc. | Impact modification of thermoplastics with ethylene/alpha-olefin interpolymers |
| US7514517B2 (en) | 2004-03-17 | 2009-04-07 | Dow Global Technologies Inc. | Anti-blocking compositions comprising interpolymers of ethylene/α-olefins |
| US7671131B2 (en) | 2004-03-17 | 2010-03-02 | Dow Global Technologies Inc. | Interpolymers of ethylene/α-olefins blends and profiles and gaskets made therefrom |
| DE602005009648D1 (de) * | 2005-01-14 | 2008-10-23 | Borealis Polymers Oy | Heterophasische Polymerzusammensetzung und Verfahren zu ihrer Herstellung |
| WO2006095762A1 (ja) * | 2005-03-08 | 2006-09-14 | Du Pont/Mitsui Polychemicals Co. Ltd. | 太陽電池封止材 |
| ZA200707883B (en) * | 2005-03-17 | 2008-12-31 | Dow Global Technologies Inc | Thermoplastic vulcanizate comprising interpolymers ethylene/alpha-olefins |
| CA2601233A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | Anti-blocking compositions comprising interpolymers of ethylene/alpha-olefins |
| CN101175778B (zh) | 2005-05-12 | 2011-12-07 | 巴塞尔聚烯烃意大利有限责任公司 | 丙烯-乙烯共聚物和它们的制备方法 |
| EP1801157B1 (en) * | 2005-12-22 | 2010-09-22 | Borealis Technology Oy | Polypropylene composition comprising a propylene copolymer component |
| US7977435B2 (en) * | 2006-07-12 | 2011-07-12 | Lin Chon-Yie | Propylene polymer compositions and processes for making the same |
| BRPI0713834B1 (pt) * | 2006-07-28 | 2018-12-26 | Basell Poliolefine Italia Srl | polímeros de propileno |
| EP1980577A1 (en) * | 2007-04-10 | 2008-10-15 | Borealis Technology OY | Pipes comprising ß-nucleated propylene copolymers |
| ES2354383T5 (es) * | 2007-08-10 | 2021-06-21 | Borealis Tech Oy | Artículo que comprende una composición de polipropileno |
| PL2072587T3 (pl) * | 2007-12-20 | 2020-11-02 | Borealis Technology Oy | Powlekane rury o ulepszonych właściwościach mechanicznych w wysokich temperaturach i sposób ich wytwarzania |
| WO2010034515A1 (en) | 2008-09-29 | 2010-04-01 | Borealis Ag | Polyolefin composition |
| EP2174965B1 (en) * | 2008-10-08 | 2013-05-29 | Borealis AG | Preparation of propylene copolymer with dynamically operated reactor |
| CN102203179B (zh) * | 2008-10-27 | 2013-09-11 | 北欧化工公司 | 具有高刚度和透明度的挤出吹塑成型瓶子 |
| EP2350186B1 (en) | 2008-10-27 | 2013-02-20 | Borealis AG | Extrusion blown molded bottles with high stiffness and transparency |
| CN102224173B (zh) * | 2008-11-21 | 2013-11-06 | 北欧化工公司 | 用于改进无规聚丙烯粉末流动性的方法 |
| EP2199650A1 (en) * | 2008-12-19 | 2010-06-23 | Borealis AG | Layer for pipes made of multimodal polyethylene composition |
| KR101060012B1 (ko) * | 2009-06-02 | 2011-08-29 | 주식회사 효성 | 폴리프로필렌 랜덤 공중합체의 제조방법 |
| EP2338930A1 (en) | 2009-12-23 | 2011-06-29 | Borealis AG | Blownfilm grade showing superior stiffness, transparency and processing behaviour |
| EP2338931A1 (en) | 2009-12-23 | 2011-06-29 | Borealis AG | Blown grade showing superior stiffness, transparency and processing behaviour |
| EP2386604B1 (en) * | 2010-04-20 | 2018-11-28 | Borealis AG | Polypropylene bottles |
| PL2561016T3 (pl) | 2010-04-21 | 2015-10-30 | Borealis Ag | Kompozycja kopolimeru propylenowo-1-heksenowego o niskiej temperaturze zgrzewania |
| EP2380926B1 (en) | 2010-04-26 | 2017-06-21 | Borealis AG | Masterbatch for improving stiffness and transparency of a random propylene copolymer |
| CN102453181A (zh) * | 2010-10-29 | 2012-05-16 | 中国石油化工股份有限公司 | 一种丙烯乙烯无规共聚物 |
| CN102453186B (zh) * | 2010-10-29 | 2016-04-27 | 中国石油化工股份有限公司 | 一种丙烯乙烯无规共聚物的制备方法 |
| CN102453179A (zh) * | 2010-10-29 | 2012-05-16 | 中国石油化工股份有限公司 | 一种丙烯无规共聚物 |
| EP2487203B2 (en) | 2011-02-14 | 2020-11-25 | Borealis AG | Sealing propylene copolymer |
| CA2830286C (en) | 2011-03-18 | 2020-03-10 | Ineos Manufacturing Belgium Nv | Propylene-ethylene random copolymer |
| EP2736930B1 (en) * | 2011-07-28 | 2016-04-06 | W.R. Grace & Co.-Conn. | Propylene/ethylene copolymer film for heat seal |
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