NO300276B1 - Etylenkopolymerer og fremgangsmåte for fremstilling av slike - Google Patents
Etylenkopolymerer og fremgangsmåte for fremstilling av slike Download PDFInfo
- Publication number
- NO300276B1 NO300276B1 NO930940A NO930940A NO300276B1 NO 300276 B1 NO300276 B1 NO 300276B1 NO 930940 A NO930940 A NO 930940A NO 930940 A NO930940 A NO 930940A NO 300276 B1 NO300276 B1 NO 300276B1
- Authority
- NO
- Norway
- Prior art keywords
- olefin
- copolymer
- carbon atoms
- propylene
- reactor
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 35
- 230000008569 process Effects 0.000 title claims description 9
- 229920001038 ethylene copolymer Polymers 0.000 title claims description 6
- 238000002360 preparation method Methods 0.000 title description 3
- 239000003054 catalyst Substances 0.000 claims description 45
- 239000004711 α-olefin Substances 0.000 claims description 41
- 239000000203 mixture Substances 0.000 claims description 34
- -1 alkyl radical Chemical group 0.000 claims description 31
- 229920000642 polymer Polymers 0.000 claims description 31
- 239000007789 gas Substances 0.000 claims description 28
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 27
- 125000004432 carbon atom Chemical group C* 0.000 claims description 25
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 25
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 22
- 229920001577 copolymer Polymers 0.000 claims description 22
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 16
- 239000005977 Ethylene Substances 0.000 claims description 16
- 238000006116 polymerization reaction Methods 0.000 claims description 14
- 239000007787 solid Substances 0.000 claims description 14
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 13
- 239000000178 monomer Substances 0.000 claims description 13
- 239000008096 xylene Substances 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 12
- 239000001294 propane Substances 0.000 claims description 12
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 239000002245 particle Substances 0.000 claims description 11
- 239000011949 solid catalyst Substances 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 239000011777 magnesium Substances 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 229910052749 magnesium Inorganic materials 0.000 claims description 7
- 229920005606 polypropylene copolymer Polymers 0.000 claims description 7
- 239000010936 titanium Substances 0.000 claims description 6
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 4
- 230000000707 stereoselective effect Effects 0.000 claims description 4
- 150000001336 alkenes Chemical class 0.000 claims description 3
- 150000005840 aryl radicals Chemical class 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 2
- 229920005684 linear copolymer Polymers 0.000 claims description 2
- 229910000077 silane Inorganic materials 0.000 claims description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 12
- 239000004707 linear low-density polyethylene Substances 0.000 description 12
- 239000012071 phase Substances 0.000 description 10
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 5
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 5
- 229910003074 TiCl4 Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 150000003609 titanium compounds Chemical class 0.000 description 5
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 4
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229920002959 polymer blend Polymers 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 235000005911 diet Nutrition 0.000 description 2
- 230000037213 diet Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000012685 gas phase polymerization Methods 0.000 description 2
- 238000010574 gas phase reaction Methods 0.000 description 2
- 238000005469 granulation Methods 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 2
- JQCXWCOOWVGKMT-UHFFFAOYSA-N phthalic acid diheptyl ester Natural products CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- OUPPKRIDJAMCCA-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2,3-dimethylbutane Chemical compound COCC(C)(C(C)C)COC OUPPKRIDJAMCCA-UHFFFAOYSA-N 0.000 description 1
- ROSQVPGTZCDBOC-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2,4-dimethylpentane Chemical compound COCC(C)(COC)CC(C)C ROSQVPGTZCDBOC-UHFFFAOYSA-N 0.000 description 1
- HEWZVZIVELJPQZ-UHFFFAOYSA-N 2,2-dimethoxypropane Chemical compound COC(C)(C)OC HEWZVZIVELJPQZ-UHFFFAOYSA-N 0.000 description 1
- PVWCLOAAEFMTLH-UHFFFAOYSA-N 4,4-bis(methoxymethyl)-2,6-dimethylheptane Chemical compound COCC(COC)(CC(C)C)CC(C)C PVWCLOAAEFMTLH-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- QCZVIXQXGWIBHR-UHFFFAOYSA-N ClC(CCCO[Ti])(Cl)Cl Chemical compound ClC(CCCO[Ti])(Cl)Cl QCZVIXQXGWIBHR-UHFFFAOYSA-N 0.000 description 1
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 description 1
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 238000002083 X-ray spectrum Methods 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000007860 aryl ester derivatives Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- SJJCABYOVIHNPZ-UHFFFAOYSA-N cyclohexyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C1CCCCC1 SJJCABYOVIHNPZ-UHFFFAOYSA-N 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 239000003085 diluting agent Substances 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
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005243 fluidization Methods 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000003944 halohydrins Chemical class 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000001282 iso-butane Substances 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
- 150000002576 ketones Chemical class 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- BKXVGDZNDSIUAI-UHFFFAOYSA-N methoxy(triphenyl)silane Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(OC)C1=CC=CC=C1 BKXVGDZNDSIUAI-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000012495 reaction gas Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- NETBVGNWMHLXRP-UHFFFAOYSA-N tert-butyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C(C)(C)C NETBVGNWMHLXRP-UHFFFAOYSA-N 0.000 description 1
- ZLMGMVJGEULFPP-UHFFFAOYSA-J titanium(4+) trichloride phenoxide Chemical compound Cl[Ti](Cl)(Cl)OC1=CC=CC=C1 ZLMGMVJGEULFPP-UHFFFAOYSA-J 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 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
- 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
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
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)
- 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 |
|---|---|---|---|
| ITMI912142A IT1250731B (it) | 1991-07-31 | 1991-07-31 | Procedimento per la preparazione di polietilene lineare a bassa densita' |
| PCT/EP1992/001731 WO1993003078A1 (en) | 1991-07-31 | 1992-07-30 | Process for the preparation of linear low density polyethylene |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO930940D0 NO930940D0 (no) | 1993-03-16 |
| NO930940L NO930940L (no) | 1993-03-16 |
| NO300276B1 true NO300276B1 (no) | 1997-05-05 |
Family
ID=11360481
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO930940A NO300276B1 (no) | 1991-07-31 | 1993-03-16 | Etylenkopolymerer og fremgangsmåte for fremstilling av slike |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US5387749A (es) |
| EP (2) | EP0551485B2 (es) |
| JP (1) | JP3239184B2 (es) |
| KR (1) | KR100229255B1 (es) |
| CN (2) | CN1040986C (es) |
| AR (1) | AR246749A1 (es) |
| AT (1) | ATE130015T1 (es) |
| AU (1) | AU663884B2 (es) |
| BR (1) | BR9205312A (es) |
| CA (1) | CA2092921A1 (es) |
| DE (1) | DE69205960T3 (es) |
| DK (1) | DK0551485T4 (es) |
| ES (1) | ES2079881T5 (es) |
| FI (1) | FI108647B (es) |
| GR (2) | GR3018043T3 (es) |
| IL (1) | IL102667A (es) |
| IT (1) | IT1250731B (es) |
| MX (1) | MX9204447A (es) |
| MY (1) | MY108479A (es) |
| NO (1) | NO300276B1 (es) |
| RU (1) | RU2120448C1 (es) |
| TW (1) | TW297026B (es) |
| WO (1) | WO1993003078A1 (es) |
| ZA (1) | ZA925664B (es) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6025448A (en) | 1989-08-31 | 2000-02-15 | The Dow Chemical Company | Gas phase polymerization of olefins |
| US6538080B1 (en) | 1990-07-03 | 2003-03-25 | Bp Chemicals Limited | Gas phase polymerization of olefins |
| ATE163946T1 (de) * | 1992-06-18 | 1998-03-15 | Montell Technology Company Bv | Verfahren und apparat für gasphase-polymerisation von olefinen |
| IT1269194B (it) * | 1994-01-21 | 1997-03-21 | Spherilene Srl | Composizioni polimeriche ad elevata processabilita' basate su lldpe |
| US5455303A (en) | 1994-06-20 | 1995-10-03 | Montell North America Inc. | Linear low density polyethylene based compositions with improved optics |
| US5589539A (en) * | 1994-11-23 | 1996-12-31 | Union Carbide Chemicals & Plastics Technology Corporation | Process for preparing an in situ polyethylene blend |
| CN1285624C (zh) * | 1994-12-16 | 2006-11-22 | 三菱化学株式会社 | 乙烯聚合物 |
| EP0677624A3 (de) * | 1995-06-07 | 1996-11-13 | Sarna Patent & Lizenz Ag | Kunststoffdichtungsbahnen. |
| IT1276121B1 (it) * | 1995-11-14 | 1997-10-24 | Montell Technology Company Bv | Film multistrato estensibili |
| IT1276120B1 (it) * | 1995-11-14 | 1997-10-24 | Montell Technology Company Bv | Film multistrato estensibili basati su lldpe |
| IT1281198B1 (it) | 1995-12-18 | 1998-02-17 | Montell Technology Company Bv | Film termoretraibili basati su composizioni poliolefiniche comprendenti un copolimero lineare dell'etilene con alfa-olefine |
| IT1277095B1 (it) * | 1995-12-18 | 1997-11-04 | Montell Technology Company Bv | Film termoretraibili multistrato |
| DE19604520A1 (de) * | 1996-02-08 | 1997-08-14 | Buna Sow Leuna Olefinverb Gmbh | Polyethylenblend |
| US5744551A (en) * | 1997-03-28 | 1998-04-28 | Union Carbide Chemicals & Plastics Technology Corporation | High strength polyethylene film |
| IT1292138B1 (it) * | 1997-06-12 | 1999-01-25 | Montell Technology Company Bv | Film multistrato estensibili |
| CA2294237A1 (en) | 1998-05-06 | 1999-11-11 | Montell Technology Company B.V. | Polyolefin compositions and films obtained therefrom |
| ITMI981548A1 (it) * | 1998-07-07 | 2000-01-07 | Montell Tecnology Company Bv | Scomposizioni polietileniche aventi elevate proprieta' ottiche e meccaniche e migliorata lavorabilita' allo stato fuso |
| ITMI981547A1 (it) | 1998-07-07 | 2000-01-07 | Montell Technology Company Bv | Composizioni polietileniche aventi elevate proprieta' meccaniche e migliorata lavorabilita'allo stato fuso |
| IL141358A0 (en) | 1999-06-18 | 2002-03-10 | Basell Technology Co Bv | Catalyst components for the polymerization of olefins and catalysts obtained therefrom |
| DE60033315D1 (de) | 1999-09-10 | 2007-03-22 | Basell Poliolefine Srl | Katalysator für die polymerisation von olefinen |
| KR100572915B1 (ko) * | 1999-11-30 | 2006-04-24 | 삼성토탈 주식회사 | 압출코팅용 폴리프로필렌 수지 조성물 |
| JP2004522849A (ja) | 2001-03-15 | 2004-07-29 | バセル ポリオレフィン イタリア エス．ピー．エー． | エチレンの（共）重合方法 |
| DE60232745D1 (de) | 2001-06-26 | 2009-08-06 | Basell Poliolefine Srl | Verfahren zur Herstellung von Katalysator-Komponenten für die Olefinpolymerisation |
| MY136330A (en) | 2001-12-12 | 2008-09-30 | Basell Poliolefine Spa | Process for the polymerization of olefins |
| US7208436B2 (en) | 2002-06-13 | 2007-04-24 | Basell Poliolenfine Italia S.R.L. | Catalyst components for the polymerization of olefins |
| TR200400209T1 (tr) | 2002-06-13 | 2005-04-21 | Basell Poliolefine Italia S.P.A | Etilen kopolimerlerini hazırlamak için işlem |
| JP2006510751A (ja) | 2002-12-18 | 2006-03-30 | バセル ポリオレフィン イタリア エス．アール．エル． | オレフィン重合用触媒成分 |
| TW200504093A (en) * | 2003-05-12 | 2005-02-01 | Dow Global Technologies Inc | Polymer composition and process to manufacture high molecular weight-high density polyethylene and film therefrom |
| KR101167538B1 (ko) | 2003-05-29 | 2012-07-20 | 바셀 폴리올레핀 이탈리아 에스.알.엘 | 촉매 성분의 제조 방법 및 그로부터 수득된 성분들 |
| BRPI0611460A2 (pt) * | 2005-03-30 | 2010-09-08 | Basell Poliolefine Srl | componentes catalìticos para a polimerização de olefinas |
| RU2007139935A (ru) | 2005-03-30 | 2009-05-10 | Базелль Полиолефин Италия С.Р.Л. (It) | Каталитические компоненты для полимеризации олефинов |
| JP2008534724A (ja) | 2005-03-30 | 2008-08-28 | バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ | 結晶性エチレン（コ）ポリマーの製造法 |
| WO2008061662A1 (en) * | 2006-11-21 | 2008-05-29 | Basell Poliolefine Italia S.R.L. | Catalyst component for the polymerization of olefins |
| WO2008077770A1 (en) | 2006-12-22 | 2008-07-03 | Basell Poliolefine Italia S.R.L. | Catalyst components for the polymerization of olefins and catalysts therefrom obtained |
| WO2010020575A1 (en) | 2008-08-20 | 2010-02-25 | Basell Poliolefine Italia S.R.L. | Catalyst components for the polymerization of olefins and catalysts therefrom obtained |
| EP2443158A1 (en) | 2009-06-18 | 2012-04-25 | Basell Poliolefine Italia S.r.l. | Catalyst components for the polymerization of olefins and catalysts therefrom obtained |
| BR112013004167B1 (pt) | 2010-08-24 | 2020-02-04 | Basell Poliolefine Italia Srl | componente catalisador sólido, processo para sua preparação e catalisador para a polimerização de olefinas |
| US10138310B2 (en) | 2010-08-24 | 2018-11-27 | Equistar Chemicals, Lp | Preparation of LLDPE resins and films having low gels |
| CN103442808A (zh) | 2011-04-01 | 2013-12-11 | 巴塞尔聚烯烃意大利有限责任公司 | 用于烯烃聚合的催化剂组分和由其得到的催化剂 |
| EP2518090A1 (en) | 2011-04-28 | 2012-10-31 | Basell Poliolefine Italia S.r.l. | Catalyst components for the polymerization of olefins and catalysts therefrom obtained |
| BR112017018424B1 (pt) * | 2015-03-25 | 2021-11-03 | Basell Polyolefine Gmbh | Processo contínuo para a preparação de homopolímeros de etileno ou copolímeros de etileno |
| US11021555B2 (en) | 2016-07-15 | 2021-06-01 | Basell Poliolefine Italia S.R.L. | Catalyst for the polymerization of olefins |
| EP3555150B1 (en) | 2016-12-19 | 2023-10-25 | Basell Poliolefine Italia S.r.l. | Catalyst components for the polymerization of olefins and catalysts therefrom obtained |
| FI4061858T3 (fi) | 2019-11-20 | 2024-01-26 | Basell Poliolefine Italia Srl | Menetelmä katalyyttikomponentin valmistamiseksi ja siitä saatuja komponentteja |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1141093A (en) * | 1979-05-17 | 1983-02-08 | Brian L. Goodall | Olefin polymerization catalyst compositions and a process for the polymerization of olefins employing such compositions |
| JPS6024805B2 (ja) * | 1979-09-05 | 1985-06-14 | 日石三菱株式会社 | 共重合体の製法 |
| JPS5767612A (en) * | 1980-10-15 | 1982-04-24 | Mitsui Petrochem Ind Ltd | Preparation of ethylene copolymer |
| DE3230516C3 (de) * | 1981-08-20 | 2000-09-14 | Mitsubishi Petrochemical Co | Verfahren zur Herstellung eines Vernetzungsprodukts |
| IT1206128B (it) * | 1984-07-30 | 1989-04-14 | Himont Inc | Composizioni polipropileniche resistenti all'urto aventi migliorata resistenza allo sbiancamento. |
| US4567155A (en) * | 1984-09-24 | 1986-01-28 | Standard Oil Company (Indiana) | Olefin polymerization catalyst system producing polymer with low active chloride |
| FR2603291B1 (fr) * | 1986-09-02 | 1992-10-16 | Bp Chimie Sa | Composition a base de polyethylene de basse densite lineaire, destinee a la fabrication de film |
| DE3827565A1 (de) * | 1988-08-13 | 1990-02-15 | Basf Ag | Verfahren zum herstellen von propylen-ethylen-polymerisaten vom typ der sogenannten "schlagzaehmodifizierten polypropylene" |
| US5149738A (en) * | 1988-11-16 | 1992-09-22 | Union Carbide Chemicals & Plastics Technology Corporation | Process for the in situ blending of polymers |
| US4946816A (en) * | 1989-08-21 | 1990-08-07 | Amoco Corporation | Morphology-controlled olefin polymerization catalyst |
| US5166268A (en) * | 1990-04-12 | 1992-11-24 | Union Carbide Chemicals & Plastics Technology Corporation | Process for cold forming propylene copolymers |
-
1991
- 1991-07-31 IT ITMI912142A patent/IT1250731B/it active IP Right Grant
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1992
- 1992-07-27 MY MYPI92001337A patent/MY108479A/en unknown
- 1992-07-28 IL IL10266792A patent/IL102667A/en not_active IP Right Cessation
- 1992-07-28 ZA ZA925664A patent/ZA925664B/xx unknown
- 1992-07-30 EP EP92916690A patent/EP0551485B2/en not_active Expired - Lifetime
- 1992-07-30 MX MX9204447A patent/MX9204447A/es not_active IP Right Cessation
- 1992-07-30 US US08/030,053 patent/US5387749A/en not_active Expired - Lifetime
- 1992-07-30 BR BR9205312A patent/BR9205312A/pt not_active IP Right Cessation
- 1992-07-30 CA CA002092921A patent/CA2092921A1/en not_active Abandoned
- 1992-07-30 WO PCT/EP1992/001731 patent/WO1993003078A1/en active IP Right Grant
- 1992-07-30 AT AT92916690T patent/ATE130015T1/de not_active IP Right Cessation
- 1992-07-30 AR AR92322850A patent/AR246749A1/es active
- 1992-07-30 EP EP92113006A patent/EP0525767A1/en active Pending
- 1992-07-30 RU RU93005129/04A patent/RU2120448C1/ru not_active IP Right Cessation
- 1992-07-30 JP JP50325893A patent/JP3239184B2/ja not_active Expired - Fee Related
- 1992-07-30 AU AU23792/92A patent/AU663884B2/en not_active Ceased
- 1992-07-30 ES ES92916690T patent/ES2079881T5/es not_active Expired - Lifetime
- 1992-07-30 DE DE69205960T patent/DE69205960T3/de not_active Expired - Lifetime
- 1992-07-30 DK DK92916690T patent/DK0551485T4/da active
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1993
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- 1993-03-29 FI FI931406A patent/FI108647B/fi not_active IP Right Cessation
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1995
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