FI75845B - Katalytkomponenter foer polymeringskatalyter av alfaolefiner och foerfarande foer deras framstaellning. - Google Patents
Katalytkomponenter foer polymeringskatalyter av alfaolefiner och foerfarande foer deras framstaellning. Download PDFInfo
- Publication number
- FI75845B FI75845B FI861389A FI861389A FI75845B FI 75845 B FI75845 B FI 75845B FI 861389 A FI861389 A FI 861389A FI 861389 A FI861389 A FI 861389A FI 75845 B FI75845 B FI 75845B
- Authority
- FI
- Finland
- Prior art keywords
- component
- magnesium
- compound
- solution
- electron donor
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 51
- 230000003197 catalytic effect Effects 0.000 title claims description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 59
- 239000011777 magnesium Substances 0.000 claims abstract description 42
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 32
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 26
- 239000007787 solid Substances 0.000 claims abstract description 21
- 239000010936 titanium Substances 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000001035 drying Methods 0.000 claims abstract description 16
- -1 titanium halogen compound Chemical class 0.000 claims abstract description 16
- 150000002681 magnesium compounds Chemical class 0.000 claims abstract description 15
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 15
- 238000010533 azeotropic distillation Methods 0.000 claims abstract description 11
- 239000004711 α-olefin Substances 0.000 claims abstract description 11
- 239000002685 polymerization catalyst Substances 0.000 claims abstract description 8
- 230000001376 precipitating effect Effects 0.000 claims abstract 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims description 6
- 239000002002 slurry Substances 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- 238000001556 precipitation Methods 0.000 claims description 2
- 239000011949 solid catalyst Substances 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000002899 organoaluminium compounds Chemical class 0.000 abstract 1
- 230000000737 periodic effect Effects 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 15
- 238000006116 polymerization reaction Methods 0.000 description 12
- 230000000694 effects Effects 0.000 description 10
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 9
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 9
- 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 8
- 239000000460 chlorine Substances 0.000 description 7
- 238000004821 distillation Methods 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 235000010755 mineral Nutrition 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 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
- 239000007858 starting material Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 229910001873 dinitrogen Inorganic materials 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052599 brucite Inorganic materials 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- 235000014380 magnesium carbonate Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000002901 organomagnesium compounds Chemical class 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910017639 MgSi Inorganic materials 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000007860 aryl ester derivatives Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- LJWBIAMZBJWAOW-UHFFFAOYSA-N benzhydryloxysilane Chemical compound C=1C=CC=CC=1C(O[SiH3])C1=CC=CC=C1 LJWBIAMZBJWAOW-UHFFFAOYSA-N 0.000 description 1
- WXBLLCUINBKULX-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1.OC(=O)C1=CC=CC=C1 WXBLLCUINBKULX-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000012535 impurity 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
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 239000011654 magnesium acetate Substances 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- 229940031958 magnesium carbonate hydroxide Drugs 0.000 description 1
- 235000011147 magnesium chloride Nutrition 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 229910001607 magnesium mineral Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- GMDNUWQNDQDBNQ-UHFFFAOYSA-L magnesium;diformate Chemical compound [Mg+2].[O-]C=O.[O-]C=O GMDNUWQNDQDBNQ-UHFFFAOYSA-L 0.000 description 1
- XDKQUSKHRIUJEO-UHFFFAOYSA-N magnesium;ethanolate Chemical compound [Mg+2].CC[O-].CC[O-] XDKQUSKHRIUJEO-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- WNJYXPXGUGOGBO-UHFFFAOYSA-N magnesium;propan-1-olate Chemical compound CCCO[Mg]OCCC WNJYXPXGUGOGBO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 150000003609 titanium compounds Chemical class 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
- 238000005406 washing 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Catalysts (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Claims (10)
1 Patentkrav
1. Katalytkomponent för sadana polymerisationskatalyter för alfaole-finer, vilka bestar av en organoaluminiumförening, en yttre elektron- 5 donor samt en fast katalytkomponent som innehaller magnesium, som er-hallits under det att en fasta bärämneskomponent som innehaller magnesium reagerat med en titanhalogenförening, kännetecknad därav, att nämnda katalytkomponent bildats genom att bringa en fast bärämneskomponent, som framställts 10 a) genom upplösning eller suspendering av en magnesiumförening i etanol eller vatten b) genom införing av en väsentligen stökiömetrisk mängd saltsyra i 15 lösningen c) genom torkning av magneslumkomponentens etanollösnlng genom stegvis azeotrop-destillering, och 20 d) genom utfällning av den fasta bärnämneskomponenten ur etanollösningen; att reagera med en titanhalogenförenlng i närvaro av en inre elektron-donor eller utan elektrondonor. 25
2. Katalytkomponent enligt patentkrav 1, kännetecknad därav, att magnesiumföreningen är vald ur gruppen MgfCH^COO)^, Mg(CHOO)2, Mg(O-CO-C^H^), Mg(C2H5COO)2 och deras kristallvattensalter samt bland-ningar av ovannämnda. 30
3. Katalytkomponent enligt nagot av föregaende patentkrav, kännetecknad därav, att bärämneskomponenten är utfälld efter azeotrop-destilleringstorkningen genom tillsättning av organisk kolvätelösning.
4. Katalytkomponent enligt patentkrav 3, kännetecknad därav, att nämnda kolväte är heptan. 13 75845 1 5. Förfarande for framställnlng av katalytkomponenter för sädana polyme- risatlonskatalyter för alfaolefiner, vilka bestir av en organoalumlnlum-förening, en yttre elektrondonor saint en fast katalytkomponent son inne-haller magnesium, som erhalllts under det att en fast bärämneskompo-5 nenten som innehiller magnesium reagerat med en titanhalogenförenlng, kännetecknad därav, att nämnda katalytkomponent bildas genom att bringa en fast bärämneskomponent, som framställts a) genom upplösning eller suspendering av en magnesiumförenlng i 10 etanol eller vatten b) genom införing av en väeentligen stökiömetrisk mängd saltsyra i lösningen 15 c) genom torkning av magnesiumkomponentens etanollösning genom stegvis azeotrop-destillering, ooh d) genom utfällning av den fasta bärnämneskomponenten ur etanollös-ningen; 20 att reagera med en titanhalogenförenlng i närvaro av en inre elektrondonor eller utan elektrondonor.
6. Förfarande enllgt patentkrav 5, kännetecknat därav, 25 att magneslumföreningen är vald ur gruppen Mg(CH^COO^, MgiCHOO)^, Mg(0-C0-C,.Hc), Mg(CLH_C00)0 och deras krietallvattensalter samt bland- O J Z J L ningar av ovannämnda.
7. Förfarande enllgt patentkrav 5 eller 6, kännetecknat 30 därav, att bärämneskomponenten är utfälld efter azeotropdestillerings- torknlngen genom tillsättning av organisk kolvätelösnlng.
8. Förfarande enligt patentkrav 7, kännetecknat därav, att man som nämnda kolväte använder heptan. 35
9. Förfarande enligt nigot av patentkraven 5-8, kännetecknat därav, att 1-15 azeotropdestilleringsserier utförs i samband med tork-
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI861389A FI75845C (sv) | 1986-04-01 | 1986-04-01 | Katalytkomponenter för polymeringskatalyter av alfaolefiner och förfar ande för deras framställning |
| NO871300A NO167152C (no) | 1986-04-01 | 1987-03-27 | Fremgangsmaate for fremstilling av en katalysatorkomponentfor alfa-olefin-polymerisasjonskatalysatorer og anvendelse av komponenten. |
| DK160387A DK160387A (da) | 1986-04-01 | 1987-03-30 | Katalysatorkomponent og fremgangsmaade til fremstilling deraf |
| EP87302809A EP0240322B1 (en) | 1986-04-01 | 1987-03-31 | Catalyst components for alpha olephine-polymerizing catalysts and procedure for manufacturing same |
| DE8787302809T DE3762865D1 (de) | 1986-04-01 | 1987-03-31 | Katalysatorbestandteile fuer alpha-olefinpolymerisation und verfahren zur herstellung derselben. |
| ES87302809T ES2016104B3 (es) | 1986-04-01 | 1987-03-31 | Componentes catalizadores para catalizadores de polimerizacion de alfa-olefinas y procedimiento para la fabricacion de los mismos. |
| AT87302809T ATE53042T1 (de) | 1986-04-01 | 1987-03-31 | Katalysatorbestandteile fuer alphaolefinpolymerisation und verfahren zur herstellung derselben. |
| US07/034,169 US4780441A (en) | 1986-04-01 | 1987-04-01 | Catalyst component for alpha olefine-polymerizing catalysts and procedure for manufacturing the same |
| CA000533587A CA1305468C (en) | 1986-04-01 | 1987-04-01 | Catalyst components for alpha olephine-polymerizing catalysts and procedure for manufacturing same |
| BE8700333A BE1000128A3 (fr) | 1986-04-01 | 1987-04-01 | Composants de catalyseurs pour catalyseurs de polymerisation d'alpha-olefines, et procede pour les fabriquer. |
| JP62080865A JPS62265311A (ja) | 1986-04-01 | 1987-04-01 | α−オレフイン重合触媒の触媒成分および、その製法 |
| CN87103194A CN1006983B (zh) | 1986-04-01 | 1987-04-01 | α-烯烃聚合催化剂中的催化成分及其制造方法 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI861389 | 1986-04-01 | ||
| FI861389A FI75845C (sv) | 1986-04-01 | 1986-04-01 | Katalytkomponenter för polymeringskatalyter av alfaolefiner och förfar ande för deras framställning |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI861389A0 FI861389A0 (fi) | 1986-04-01 |
| FI861389A FI861389A (fi) | 1987-10-02 |
| FI75845B true FI75845B (fi) | 1988-04-29 |
| FI75845C FI75845C (sv) | 1988-08-08 |
Family
ID=8522390
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI861389A FI75845C (sv) | 1986-04-01 | 1986-04-01 | Katalytkomponenter för polymeringskatalyter av alfaolefiner och förfar ande för deras framställning |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4780441A (sv) |
| EP (1) | EP0240322B1 (sv) |
| JP (1) | JPS62265311A (sv) |
| CN (1) | CN1006983B (sv) |
| AT (1) | ATE53042T1 (sv) |
| BE (1) | BE1000128A3 (sv) |
| CA (1) | CA1305468C (sv) |
| DE (1) | DE3762865D1 (sv) |
| DK (1) | DK160387A (sv) |
| ES (1) | ES2016104B3 (sv) |
| FI (1) | FI75845C (sv) |
| NO (1) | NO167152C (sv) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ZA884614B (en) * | 1987-06-29 | 1989-03-29 | Shell Oil Co | Method for crystallizing magnesium chloride for use in a catalyst composition |
| US4874737A (en) * | 1988-09-06 | 1989-10-17 | Shell Oil Company | Silicate-modified magnesium alkoxide polymerization catalysts |
| US4876230A (en) * | 1988-09-06 | 1989-10-24 | Shell Oil Company | Magnesium alkoxide polymerization catalyst by boiling in organic solvents |
| US4959336A (en) * | 1989-04-07 | 1990-09-25 | Shell Oil Company | Silicate-modified magnesium ethoxide polymerization catalysts |
| CN104558273B (zh) * | 2013-10-09 | 2016-09-21 | 中国石油化工股份有限公司 | 用于烯烃聚合的催化剂组分及其制备方法和用于烯烃聚合的催化剂以及烯烃聚合方法 |
| CN104558271B (zh) * | 2013-10-09 | 2016-09-21 | 中国石油化工股份有限公司 | 一种烯烃聚合催化剂载体及其制备方法 |
| CN104558272B (zh) * | 2013-10-09 | 2016-09-21 | 中国石油化工股份有限公司 | 一种烯烃聚合催化剂载体及其制备方法 |
| CN108102014B (zh) * | 2018-01-09 | 2020-10-27 | 为信（深圳）材料科技有限公司 | 一种球形烷氧基镁颗粒的组份及制备方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL162664B (nl) * | 1969-06-20 | 1980-01-15 | Montedison Spa | Werkwijze om een katalysator te bereiden voor de poly- merisatie van alkenen-1. |
| US3953414A (en) * | 1972-09-13 | 1976-04-27 | Montecatini Edison S.P.A., | Catalysts for the polymerization of olefins to spherically shaped polymers |
| US4107415A (en) * | 1972-09-26 | 1978-08-15 | Montecatini Edison S.P.A. | Process for the stereospecific polymerization of alpha-olefins |
| IT1054410B (it) * | 1975-11-21 | 1981-11-10 | Mitsui Petrochemical Ind | Catalizzatori per la polimerizzazione delle alfa olefine |
| US4487845A (en) * | 1980-05-09 | 1984-12-11 | Stauffer Chemical Company | Method of enhancing stereospecificity of a catalyst system |
| IT1136627B (it) * | 1981-05-21 | 1986-09-03 | Euteco Impianti Spa | Catalizzatore supportato per la polimerizzazione di etilene |
| IT1195953B (it) * | 1982-09-10 | 1988-11-03 | Montedison Spa | Componenti e catalizzatori per la polimerizzazione di olefine |
| US4532313A (en) * | 1982-10-13 | 1985-07-30 | Himont Incorporated | Method for preparing an improved catalyst support, Ziegler-Natta catalyst utilizing said support and polymerization of 1-olefins utilizing said catalyst |
-
1986
- 1986-04-01 FI FI861389A patent/FI75845C/sv not_active IP Right Cessation
-
1987
- 1987-03-27 NO NO871300A patent/NO167152C/no unknown
- 1987-03-30 DK DK160387A patent/DK160387A/da not_active Application Discontinuation
- 1987-03-31 AT AT87302809T patent/ATE53042T1/de not_active IP Right Cessation
- 1987-03-31 ES ES87302809T patent/ES2016104B3/es not_active Expired - Lifetime
- 1987-03-31 EP EP87302809A patent/EP0240322B1/en not_active Expired - Lifetime
- 1987-03-31 DE DE8787302809T patent/DE3762865D1/de not_active Expired - Fee Related
- 1987-04-01 CA CA000533587A patent/CA1305468C/en not_active Expired - Fee Related
- 1987-04-01 CN CN87103194A patent/CN1006983B/zh not_active Expired
- 1987-04-01 US US07/034,169 patent/US4780441A/en not_active Expired - Fee Related
- 1987-04-01 JP JP62080865A patent/JPS62265311A/ja active Pending
- 1987-04-01 BE BE8700333A patent/BE1000128A3/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CA1305468C (en) | 1992-07-21 |
| NO167152C (no) | 1991-10-09 |
| ES2016104B3 (es) | 1990-10-16 |
| CN1006983B (zh) | 1990-02-28 |
| BE1000128A3 (fr) | 1988-04-12 |
| NO871300L (no) | 1987-10-02 |
| FI861389A (fi) | 1987-10-02 |
| EP0240322B1 (en) | 1990-05-23 |
| NO167152B (no) | 1991-07-01 |
| DK160387D0 (da) | 1987-03-30 |
| DE3762865D1 (de) | 1990-06-28 |
| NO871300D0 (no) | 1987-03-27 |
| EP0240322A2 (en) | 1987-10-07 |
| FI75845C (sv) | 1988-08-08 |
| EP0240322A3 (en) | 1987-10-28 |
| ATE53042T1 (de) | 1990-06-15 |
| US4780441A (en) | 1988-10-25 |
| JPS62265311A (ja) | 1987-11-18 |
| DK160387A (da) | 1987-10-02 |
| CN87103194A (zh) | 1987-12-09 |
| FI861389A0 (fi) | 1986-04-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed | ||
| MM | Patent lapsed |
Owner name: NESTE OY |