DE2029992A1 - - Google Patents
Info
- Publication number
- DE2029992A1 DE2029992A1 DE19702029992 DE2029992A DE2029992A1 DE 2029992 A1 DE2029992 A1 DE 2029992A1 DE 19702029992 DE19702029992 DE 19702029992 DE 2029992 A DE2029992 A DE 2029992A DE 2029992 A1 DE2029992 A1 DE 2029992A1
- Authority
- DE
- Germany
- Prior art keywords
- compound
- titanium
- magnesium halide
- electron donor
- catalysts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- -1 magnesium halide Chemical class 0.000 claims description 56
- 239000010936 titanium Substances 0.000 claims description 55
- 150000001875 compounds Chemical class 0.000 claims description 38
- 229920000642 polymer Polymers 0.000 claims description 31
- 239000011777 magnesium Substances 0.000 claims description 27
- 229910052749 magnesium Inorganic materials 0.000 claims description 27
- 239000003054 catalyst Substances 0.000 claims description 25
- 238000006116 polymerization reaction Methods 0.000 claims description 22
- 229910052719 titanium Inorganic materials 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 20
- 150000003609 titanium compounds Chemical class 0.000 claims description 19
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 15
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 12
- 239000005977 Ethylene Substances 0.000 claims description 12
- 150000002902 organometallic compounds Chemical class 0.000 claims description 11
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 9
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 8
- 230000000737 periodic effect Effects 0.000 claims description 8
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 claims description 7
- 150000004678 hydrides Chemical class 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 150000002739 metals Chemical class 0.000 claims description 7
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- 238000010586 diagram Methods 0.000 claims description 5
- 238000001228 spectrum Methods 0.000 claims description 5
- 229930192474 thiophene Natural products 0.000 claims description 5
- 238000000227 grinding Methods 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 230000004913 activation Effects 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims description 3
- 239000002685 polymerization catalyst Substances 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 239000002841 Lewis acid Substances 0.000 claims description 2
- 239000002879 Lewis base Substances 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 229910052787 antimony Inorganic materials 0.000 claims description 2
- 229910052785 arsenic Inorganic materials 0.000 claims description 2
- 238000000354 decomposition reaction Methods 0.000 claims description 2
- 150000001993 dienes Chemical class 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 150000007527 lewis bases Chemical class 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 238000005979 thermal decomposition reaction Methods 0.000 claims description 2
- 239000004711 α-olefin Substances 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 239000000047 product Substances 0.000 claims 2
- XIEQDDLBXUOZOD-UHFFFAOYSA-N 2,3,4a,6,7,8a-hexahydro-[1,4]dioxino[2,3-b][1,4]dioxine Chemical compound O1CCOC2OCCOC21 XIEQDDLBXUOZOD-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 239000013078 crystal Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 239000004698 Polyethylene Substances 0.000 description 23
- 229920000573 polyethylene Polymers 0.000 description 23
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 10
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 150000004820 halides Chemical class 0.000 description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000000379 polymerizing effect Effects 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 239000008139 complexing agent Substances 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910001629 magnesium chloride Inorganic materials 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- KCXZNSGUUQJJTR-UHFFFAOYSA-N Di-n-hexyl phthalate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC KCXZNSGUUQJJTR-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 229910001623 magnesium bromide Inorganic materials 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- UATJOMSPNYCXIX-UHFFFAOYSA-N Trinitrobenzene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 UATJOMSPNYCXIX-UHFFFAOYSA-N 0.000 description 1
- 238000002083 X-ray spectrum Methods 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical class [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- OTCKOJUMXQWKQG-UHFFFAOYSA-L magnesium bromide Chemical compound [Mg+2].[Br-].[Br-] OTCKOJUMXQWKQG-UHFFFAOYSA-L 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- DLRJIFUOBPOJNS-UHFFFAOYSA-N phenetole Chemical compound CCOC1=CC=CC=C1 DLRJIFUOBPOJNS-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- OUULRIDHGPHMNQ-UHFFFAOYSA-N stibane Chemical class [SbH3] OUULRIDHGPHMNQ-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- 150000003682 vanadium compounds Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- C08F4/02—Carriers therefor
- C08F4/022—Magnesium halide as support anhydrous or hydrated or complexed by means of a Lewis base for Ziegler-type catalysts
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/906—Comminution of transition metal containing catalyst
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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT1846269 | 1969-06-20 | ||
| IT1882369 | 1969-06-27 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2029992A1 true DE2029992A1 (en, 2012) | 1970-12-23 |
| DE2029992B2 DE2029992B2 (de) | 1974-08-15 |
| DE2029992C3 DE2029992C3 (de) | 1975-04-17 |
Family
ID=26326998
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2029992A Expired DE2029992C3 (de) | 1969-06-20 | 1970-06-18 | Verfahren zur Herstellung von Polymerisationskatalysatoren |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US4544717A (en, 2012) |
| JP (1) | JPS5819334B1 (en, 2012) |
| AT (1) | AT302648B (en, 2012) |
| BE (1) | BE752252A (en, 2012) |
| CS (1) | CS153084B2 (en, 2012) |
| DE (1) | DE2029992C3 (en, 2012) |
| DK (1) | DK130744B (en, 2012) |
| ES (1) | ES380918A1 (en, 2012) |
| FR (1) | FR2052706A5 (en, 2012) |
| GB (1) | GB1310547A (en, 2012) |
| IL (1) | IL34739A (en, 2012) |
| NL (1) | NL162664B (en, 2012) |
| PL (1) | PL80715B1 (en, 2012) |
| RO (1) | RO62731A (en, 2012) |
| SE (1) | SE417611B (en, 2012) |
| SU (1) | SU414770A3 (en, 2012) |
| YU (1) | YU36189B (en, 2012) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2230752A1 (de) * | 1971-06-25 | 1972-12-28 | Montedison Spa | Verfahren zur stereoregulären Polymerisation von alpha-Olefinen |
| DE2347577A1 (de) * | 1972-09-26 | 1974-05-02 | Montedison Spa | Verfahren zur stereospezifischen polymerisation von alpha-olefinen |
| DE2515211A1 (de) * | 1974-04-08 | 1975-10-16 | Mitsubishi Chem Ind | Katalysator zur polymerisation von olefinen |
| FR2697526A1 (fr) * | 1992-10-30 | 1994-05-06 | Bp Chemicals Snc | Procédé de préparation d'un catalyseur de type Ziegler-Natta pour la polymérisation des oléfines. |
| US5539067A (en) * | 1980-08-13 | 1996-07-23 | Montedison S.P.A. | Components and catalysts for the polymerization of olefins |
| US6777508B1 (en) | 1980-08-13 | 2004-08-17 | Basell Poliolefine Italia S.P.A. | Catalysts for the polymerization of olefins |
Families Citing this family (101)
| 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. |
| NL7113778A (en, 2012) * | 1970-10-13 | 1972-04-17 | ||
| NL7114641A (en, 2012) * | 1970-10-29 | 1972-05-03 | ||
| CH543546A (fr) | 1971-03-23 | 1973-10-31 | Solvay | Système catalytique de polymérisation des alpha-oléfines |
| US4187196A (en) | 1971-06-25 | 1980-02-05 | Montedison S.P.A. | Process for the stereoregular polymerization of alpha-olefins |
| US4107414A (en) | 1971-06-25 | 1978-08-15 | Montecatini Edison S.P.A. | Process for the stereoregular polymerization of alpha olefins |
| US4226963A (en) | 1971-06-25 | 1980-10-07 | Montedison S.P.A. | Process for the stereoregular polymerization of alpha-olephins |
| US4107413A (en) | 1971-06-25 | 1978-08-15 | Montedison S.P.A. | Process for the stereoregular polymerization of alpha olefins |
| US4156063A (en) | 1971-06-25 | 1979-05-22 | Montecanti Edison, S.p.A. | Process for the stereoregular polymerization of alpha olefins |
| IT1005486B (it) | 1974-02-15 | 1976-08-20 | Montedison Spa | Gomme termoplastiche e processo per la loro preparazione |
| US4174429A (en) * | 1975-03-28 | 1979-11-13 | Montedison S.P.A. | Process for polymerizing olefins |
| JPS5242584A (en) | 1975-10-02 | 1977-04-02 | Nippon Oil Co Ltd | Process for producing polyolefine |
| IT1054410B (it) * | 1975-11-21 | 1981-11-10 | Mitsui Petrochemical Ind | Catalizzatori per la polimerizzazione delle alfa olefine |
| JPS5952643B2 (ja) * | 1977-01-27 | 1984-12-20 | 三井化学株式会社 | エチレン共重合体 |
| CA1125733A (en) * | 1978-03-27 | 1982-06-15 | Arthur W. Langer, Jr. | T.sub.nmr' in3-n xx cocatalysts |
| CA1142161A (en) * | 1978-03-29 | 1983-03-01 | Exxon Research And Engineering Company | Trialkyl aluminum cocatalyst |
| CA1144300A (en) * | 1978-11-20 | 1983-04-05 | Allen Noshay | Preparation of low density ethylene copolymers in fluid bed reactor |
| US4243552A (en) | 1978-12-11 | 1981-01-06 | Phillips Petroleum Company | Polymerization catalyst and process |
| JPS5923561B2 (ja) * | 1979-02-06 | 1984-06-02 | 三井化学株式会社 | オレフインの重合方法 |
| US4224182A (en) * | 1979-03-07 | 1980-09-23 | Exxon Research & Engineering Co. | Novel hindered alkyl aluminum amide cocatalysts |
| US4308369A (en) * | 1979-09-28 | 1981-12-29 | The Dow Chemical Company | High efficiency catalyst for polymerizing olefins |
| US4482687A (en) * | 1979-10-26 | 1984-11-13 | Union Carbide Corporation | Preparation of low-density ethylene copolymers in fluid bed reactor |
| JPS58125706A (ja) * | 1982-01-22 | 1983-07-26 | Mitsubishi Petrochem Co Ltd | エチレンの重合法 |
| US5064795A (en) * | 1982-08-27 | 1991-11-12 | Phillips Petroleum Company | Polymerization of olefins |
| JPS58189189A (ja) * | 1982-09-20 | 1983-11-04 | Mitsubishi Chem Ind Ltd | 塩化マグネシウム・テトラビドロフラン錯体のテトラヒドロフラン溶液の製造方法 |
| US4866022A (en) * | 1984-03-23 | 1989-09-12 | Amoco Corporation | Olefin polymerization catalyst |
| US4988656A (en) * | 1984-03-23 | 1991-01-29 | Amoco Corporation | Olefin polymerization catalyst |
| FI75844C (fi) * | 1986-04-01 | 1988-08-08 | Neste Oy | Katalytkomponenter foer polymeringskatalyter av alfaolefiner och foerfarande foer deras framstaellning. |
| FI75841C (fi) * | 1986-04-01 | 1988-08-08 | Neste Oy | Katalytkomponenter foer polymeringskatalyter av alfaolefiner och foerfarande foer deras framstaellning. |
| FI75842C (fi) * | 1986-04-01 | 1988-08-08 | Neste Oy | Katalytkomponenter foer polymeringskatalyter av alfaolefiner och foerfarande foer deras framstaellning. |
| FI75845C (fi) * | 1986-04-01 | 1988-08-08 | Neste Oy | Katalytkomponenter foer polymeringskatalyter av alfaolefiner och foerfarande foer deras framstaellning. |
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-
1970
- 1970-06-15 NL NL7008708.A patent/NL162664B/xx not_active Application Discontinuation
- 1970-06-16 SE SE7008315A patent/SE417611B/sv unknown
- 1970-06-16 DK DK309870AA patent/DK130744B/da not_active IP Right Cessation
- 1970-06-17 IL IL34739A patent/IL34739A/xx unknown
- 1970-06-17 YU YU1539/70A patent/YU36189B/xx unknown
- 1970-06-17 FR FR7022249A patent/FR2052706A5/fr not_active Expired
- 1970-06-17 PL PL1970141392A patent/PL80715B1/pl unknown
- 1970-06-17 GB GB2930170A patent/GB1310547A/en not_active Expired
- 1970-06-17 SU SU1444973A patent/SU414770A3/ru active
- 1970-06-18 JP JP45052439A patent/JPS5819334B1/ja active Granted
- 1970-06-18 DE DE2029992A patent/DE2029992C3/de not_active Expired
- 1970-06-19 BE BE752252D patent/BE752252A/xx not_active IP Right Cessation
- 1970-06-19 AT AT552370A patent/AT302648B/de not_active IP Right Cessation
- 1970-06-19 ES ES380918A patent/ES380918A1/es not_active Expired
- 1970-06-19 CS CS432070A patent/CS153084B2/cs unknown
- 1970-06-20 RO RO7000063695A patent/RO62731A/ro unknown
-
1980
- 1980-05-22 US US06/152,531 patent/US4544717A/en not_active Expired - Lifetime
-
1985
- 1985-07-30 US US06/760,539 patent/US4636486A/en not_active Expired - Lifetime
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2230752A1 (de) * | 1971-06-25 | 1972-12-28 | Montedison Spa | Verfahren zur stereoregulären Polymerisation von alpha-Olefinen |
| DE2230728A1 (de) * | 1971-06-25 | 1972-12-28 | Montedison Spa | Verfahren zur stereoregulären Polymerisation von alpha-Olefinen |
| DE2230672A1 (de) * | 1971-06-25 | 1972-12-28 | Montedison Spa | Verfahren zur stereoregulären Polymerisation von alpha-Olefinen |
| DE2347577A1 (de) * | 1972-09-26 | 1974-05-02 | Montedison Spa | Verfahren zur stereospezifischen polymerisation von alpha-olefinen |
| DE2515211A1 (de) * | 1974-04-08 | 1975-10-16 | Mitsubishi Chem Ind | Katalysator zur polymerisation von olefinen |
| US5539067A (en) * | 1980-08-13 | 1996-07-23 | Montedison S.P.A. | Components and catalysts for the polymerization of olefins |
| US6194342B1 (en) | 1980-08-13 | 2001-02-27 | Montell Technology Company Bv | Components and catalysts for the polymerization of olefins |
| US6515085B1 (en) | 1980-08-13 | 2003-02-04 | Basell Poliolefine Italia S.P.A. | Components and catalysts for the polymerization of olefins |
| US6777508B1 (en) | 1980-08-13 | 2004-08-17 | Basell Poliolefine Italia S.P.A. | Catalysts for the polymerization of olefins |
| FR2697526A1 (fr) * | 1992-10-30 | 1994-05-06 | Bp Chemicals Snc | Procédé de préparation d'un catalyseur de type Ziegler-Natta pour la polymérisation des oléfines. |
Also Published As
| Publication number | Publication date |
|---|---|
| US4544717A (en) | 1985-10-01 |
| ES380918A1 (es) | 1973-04-01 |
| DE2029992C3 (de) | 1975-04-17 |
| NL7008708A (en, 2012) | 1970-12-22 |
| CS153084B2 (en, 2012) | 1974-02-22 |
| RO62731A (fr) | 1978-03-15 |
| IL34739A (en) | 1973-10-25 |
| AT302648B (de) | 1972-10-25 |
| JPS5819334B1 (en, 2012) | 1983-04-18 |
| PL80715B1 (en, 2012) | 1975-08-30 |
| IL34739A0 (en) | 1970-08-19 |
| DK130744C (en, 2012) | 1975-09-08 |
| FR2052706A5 (en, 2012) | 1971-04-09 |
| NL162664B (nl) | 1980-01-15 |
| GB1310547A (en) | 1973-03-21 |
| DE2029992B2 (de) | 1974-08-15 |
| DK130744B (da) | 1975-04-07 |
| YU36189B (en) | 1982-02-25 |
| YU153970A (en) | 1981-06-30 |
| BE752252A (fr) | 1970-12-21 |
| US4636486A (en) | 1987-01-13 |
| SU414770A3 (ru) | 1974-02-05 |
| SE417611B (sv) | 1981-03-30 |
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Legal Events
| Date | Code | Title | Description |
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| C3 | Grant after two publication steps (3rd publication) | ||
| E77 | Valid patent as to the heymanns-index 1977 |