NO309771B1 - Fremgangsmåte for fremstilling av en Ziegler-Natta- katalysator, fremgangsmåte for kopolymerisasjon av olefiner samt fremgangsmåte for fremstilling av etylenpolymerer eller - kopolymerer - Google Patents
Fremgangsmåte for fremstilling av en Ziegler-Natta- katalysator, fremgangsmåte for kopolymerisasjon av olefiner samt fremgangsmåte for fremstilling av etylenpolymerer eller - kopolymerer Download PDFInfo
- Publication number
- NO309771B1 NO309771B1 NO962064A NO962064A NO309771B1 NO 309771 B1 NO309771 B1 NO 309771B1 NO 962064 A NO962064 A NO 962064A NO 962064 A NO962064 A NO 962064A NO 309771 B1 NO309771 B1 NO 309771B1
- Authority
- NO
- Norway
- Prior art keywords
- compound
- contact
- placing
- product
- catalyst
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 45
- 150000001336 alkenes Chemical class 0.000 title claims abstract description 8
- 229920000573 polyethylene Polymers 0.000 title claims description 8
- 229920001038 ethylene copolymer Polymers 0.000 title claims description 4
- 238000002360 preparation method Methods 0.000 title abstract description 8
- 238000007334 copolymerization reaction Methods 0.000 title description 7
- 239000011954 Ziegler–Natta catalyst Substances 0.000 title 1
- 239000003054 catalyst Substances 0.000 claims abstract description 30
- 150000003609 titanium compounds Chemical class 0.000 claims abstract description 20
- 150000002896 organic halogen compounds Chemical class 0.000 claims abstract description 9
- 239000007787 solid Substances 0.000 claims abstract description 8
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 42
- 239000000047 product Substances 0.000 claims description 35
- 150000004796 dialkyl magnesium compounds Chemical class 0.000 claims description 21
- 239000007789 gas Substances 0.000 claims description 18
- 229930195733 hydrocarbon Natural products 0.000 claims description 18
- 150000002430 hydrocarbons Chemical class 0.000 claims description 18
- 239000004215 Carbon black (E152) Substances 0.000 claims description 17
- 239000007788 liquid Substances 0.000 claims description 16
- 238000004519 manufacturing process Methods 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 150000003377 silicon compounds Chemical class 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000012265 solid product Substances 0.000 claims description 7
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 239000000725 suspension Substances 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 150000002902 organometallic compounds Chemical class 0.000 claims description 3
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 230000000737 periodic effect Effects 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 abstract description 8
- 229920000642 polymer Polymers 0.000 abstract description 7
- 150000002899 organoaluminium compounds Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 24
- 239000010936 titanium Substances 0.000 description 17
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 14
- 229910052719 titanium Inorganic materials 0.000 description 14
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 13
- -1 alkyl aluminum compound Chemical class 0.000 description 13
- 229910052749 magnesium Inorganic materials 0.000 description 13
- 239000011777 magnesium Substances 0.000 description 13
- 239000000843 powder Substances 0.000 description 13
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 10
- 239000005977 Ethylene Substances 0.000 description 10
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 9
- 229910052782 aluminium Inorganic materials 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 8
- 239000000155 melt Substances 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- 235000012239 silicon dioxide Nutrition 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 6
- 230000003197 catalytic effect Effects 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 6
- 239000010419 fine particle Substances 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 230000006641 stabilisation Effects 0.000 description 5
- 238000011105 stabilization Methods 0.000 description 5
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000002366 halogen compounds Chemical class 0.000 description 4
- 239000012299 nitrogen atmosphere Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 3
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- NDQXKKFRNOPRDW-UHFFFAOYSA-N 1,1,1-triethoxyethane Chemical compound CCOC(C)(OCC)OCC NDQXKKFRNOPRDW-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical class Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- 238000012685 gas phase polymerization Methods 0.000 description 2
- 238000005658 halogenation reaction Methods 0.000 description 2
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- KJJBSBKRXUVBMX-UHFFFAOYSA-N magnesium;butane Chemical compound [Mg+2].CCC[CH2-].CCC[CH2-] KJJBSBKRXUVBMX-UHFFFAOYSA-N 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 150000003961 organosilicon compounds Chemical class 0.000 description 2
- 150000002905 orthoesters Chemical class 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000011949 solid catalyst Substances 0.000 description 2
- NBRKLOOSMBRFMH-UHFFFAOYSA-N tert-butyl chloride Chemical compound CC(C)(C)Cl NBRKLOOSMBRFMH-UHFFFAOYSA-N 0.000 description 2
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical group CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005234 alkyl aluminium group Chemical group 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000012320 chlorinating reagent Substances 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 239000003426 co-catalyst Substances 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- UFCXHBIETZKGHB-UHFFFAOYSA-N dichloro(diethoxy)silane Chemical compound CCO[Si](Cl)(Cl)OCC UFCXHBIETZKGHB-UHFFFAOYSA-N 0.000 description 1
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005243 fluidization Methods 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 235000011147 magnesium chloride Nutrition 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910000096 monohydride Inorganic materials 0.000 description 1
- SNMVRZFUUCLYTO-UHFFFAOYSA-N n-propyl chloride Chemical group CCCCl SNMVRZFUUCLYTO-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000002901 organomagnesium compounds Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 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
- 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
- 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
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)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9506392A FR2734570B1 (fr) | 1995-05-22 | 1995-05-22 | Procede de preparation d'un catalyseur de type ziegler-natta |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO962064D0 NO962064D0 (no) | 1996-05-21 |
| NO962064L NO962064L (no) | 1996-11-25 |
| NO309771B1 true NO309771B1 (no) | 2001-03-26 |
Family
ID=9479487
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO962064A NO309771B1 (no) | 1995-05-22 | 1996-05-21 | Fremgangsmåte for fremstilling av en Ziegler-Natta- katalysator, fremgangsmåte for kopolymerisasjon av olefiner samt fremgangsmåte for fremstilling av etylenpolymerer eller - kopolymerer |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP0744416B1 (de) |
| KR (1) | KR100425564B1 (de) |
| CN (1) | CN1095849C (de) |
| AT (1) | ATE169307T1 (de) |
| CA (1) | CA2176994C (de) |
| DE (1) | DE69600487T2 (de) |
| ES (1) | ES2119546T3 (de) |
| FR (1) | FR2734570B1 (de) |
| GR (1) | GR3027594T3 (de) |
| MY (1) | MY113243A (de) |
| NO (1) | NO309771B1 (de) |
| TW (1) | TW387907B (de) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2746672B1 (fr) | 1996-04-02 | 1998-04-24 | Atochem Elf Sa | Composante catalytique et son utilisation en polymerisation des olefines |
| US6046126A (en) * | 1998-05-12 | 2000-04-04 | Kelly; Mark | Titanium process for making catalyst |
| US6140264A (en) * | 1998-05-12 | 2000-10-31 | Nova Chemicals Ltd. | Split aluminum addition process for making catalyst |
| US6825293B1 (en) * | 2001-08-20 | 2004-11-30 | Nova Chemicals (International) S.A. | Polymer control through co-catalyst |
| DE10163075A1 (de) * | 2001-12-20 | 2003-07-10 | Basell Polyolefine Gmbh | Katalysatorsysteme von Typ der Ziegler-Natta-Katalysatoren und ein Verfahren zu deren Herstellung |
| US7335250B2 (en) | 2004-02-06 | 2008-02-26 | Ivoclar Vivadent Ag | Dental composites based on X-ray-opaque mixed oxides prepared by flame spraying |
| US7211535B2 (en) | 2004-10-29 | 2007-05-01 | Nova Chemicals Corporation | Enhanced polyolefin catalyst |
| EP2003151A1 (de) | 2007-06-15 | 2008-12-17 | Nova Chemicals Corporation | Verbesserte Wasserstoffempfindlichkeit mittels Katalysatormodifizierung |
| RU2636660C2 (ru) | 2012-04-19 | 2017-11-27 | Инеос Юроуп Аг | Катализатор, предназначенный для полимеризации олефинов, способ его получения и применение |
| US10640584B2 (en) | 2015-12-30 | 2020-05-05 | Sabic Global Technologies B.V. | Process for making a solid catalyst component for ethylene polymerization and co-polymerization |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54123594A (en) * | 1978-03-17 | 1979-09-25 | Asahi Chem Ind Co Ltd | Olefin polymerization catalyst |
| JPS58189206A (ja) * | 1982-04-30 | 1983-11-04 | Chisso Corp | α−オレフイン重合用触媒成分 |
| FR2546522B1 (fr) * | 1983-05-25 | 1985-07-26 | Ato Chimie | Procede de preparation d'une composante de metal de transition pour un systeme catalytique de polymerisation d'olefines |
| DE3620060A1 (de) * | 1986-06-14 | 1987-12-17 | Hoechst Ag | Verfahren zur herstellung eines polyolefins |
| US4711865A (en) * | 1986-12-18 | 1987-12-08 | Exxon Chemical Patents Inc. | Olefin polymerization catalysts, production and use |
| FR2706467B1 (fr) * | 1992-10-26 | 1995-09-15 | Bp Chemicals Snc | Procédé de préparation d'un catalyseur de type Ziegler-Natta et utilisation. |
| BE1008494A3 (nl) * | 1994-07-01 | 1996-05-07 | Dsm Nv | Katalysatorsysteem voor de polymerisatie van etheen. |
-
1995
- 1995-05-22 FR FR9506392A patent/FR2734570B1/fr not_active Expired - Fee Related
-
1996
- 1996-05-13 AT AT96303304T patent/ATE169307T1/de active
- 1996-05-13 EP EP96303304A patent/EP0744416B1/de not_active Expired - Lifetime
- 1996-05-13 ES ES96303304T patent/ES2119546T3/es not_active Expired - Lifetime
- 1996-05-13 DE DE69600487T patent/DE69600487T2/de not_active Expired - Lifetime
- 1996-05-21 NO NO962064A patent/NO309771B1/no unknown
- 1996-05-21 TW TW085105987A patent/TW387907B/zh not_active IP Right Cessation
- 1996-05-21 CA CA002176994A patent/CA2176994C/en not_active Expired - Fee Related
- 1996-05-21 KR KR1019960017264A patent/KR100425564B1/ko not_active IP Right Cessation
- 1996-05-22 CN CN96108958A patent/CN1095849C/zh not_active Expired - Lifetime
- 1996-05-22 MY MYPI96001910A patent/MY113243A/en unknown
-
1998
- 1998-08-06 GR GR980401579T patent/GR3027594T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE69600487D1 (de) | 1998-09-10 |
| MY113243A (en) | 2001-12-31 |
| ES2119546T3 (es) | 1998-10-01 |
| TW387907B (en) | 2000-04-21 |
| GR3027594T3 (en) | 1998-11-30 |
| EP0744416B1 (de) | 1998-08-05 |
| FR2734570A1 (fr) | 1996-11-29 |
| NO962064L (no) | 1996-11-25 |
| CA2176994C (en) | 2007-09-18 |
| EP0744416A1 (de) | 1996-11-27 |
| ATE169307T1 (de) | 1998-08-15 |
| CN1143085A (zh) | 1997-02-19 |
| CN1095849C (zh) | 2002-12-11 |
| FR2734570B1 (fr) | 1997-07-04 |
| KR100425564B1 (ko) | 2004-07-07 |
| DE69600487T2 (de) | 1998-12-03 |
| KR960041203A (ko) | 1996-12-19 |
| NO962064D0 (no) | 1996-05-21 |
| CA2176994A1 (en) | 1996-11-23 |
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