NO320275B1 - Katalysatorkomponent i form av en dispersjon omfattende en ionisk forbindelse og en fast addisjonspolymerisasjonskatalysator omfattende det samme - Google Patents
Katalysatorkomponent i form av en dispersjon omfattende en ionisk forbindelse og en fast addisjonspolymerisasjonskatalysator omfattende det samme Download PDFInfo
- Publication number
- NO320275B1 NO320275B1 NO19992974A NO992974A NO320275B1 NO 320275 B1 NO320275 B1 NO 320275B1 NO 19992974 A NO19992974 A NO 19992974A NO 992974 A NO992974 A NO 992974A NO 320275 B1 NO320275 B1 NO 320275B1
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- Norway
- Prior art keywords
- hydrocarbyl
- catalyst
- groups
- group
- hydrogen
- Prior art date
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- WFVLGDMOCAFNNS-UHFFFAOYSA-N n,n-di(tetradecyl)tetradecan-1-amine Chemical compound CCCCCCCCCCCCCCN(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC WFVLGDMOCAFNNS-UHFFFAOYSA-N 0.000 description 1
- IQSLPSKHVSSQOH-UHFFFAOYSA-N n,n-dibutyldecan-1-amine Chemical compound CCCCCCCCCCN(CCCC)CCCC IQSLPSKHVSSQOH-UHFFFAOYSA-N 0.000 description 1
- FTBKGTWNWSTGAY-UHFFFAOYSA-N n,n-dibutyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(CCCC)CCCC FTBKGTWNWSTGAY-UHFFFAOYSA-N 0.000 description 1
- YEVRYVXXLRUQBJ-UHFFFAOYSA-N n,n-dibutyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCN(CCCC)CCCC YEVRYVXXLRUQBJ-UHFFFAOYSA-N 0.000 description 1
- XJEPUDKDCKLTSL-UHFFFAOYSA-N n,n-didodecylaniline Chemical compound CCCCCCCCCCCCN(CCCCCCCCCCCC)C1=CC=CC=C1 XJEPUDKDCKLTSL-UHFFFAOYSA-N 0.000 description 1
- FPFTUTDQPYXFSM-UHFFFAOYSA-N n,n-didodecylcyclohexanamine Chemical compound CCCCCCCCCCCCN(CCCCCCCCCCCC)C1CCCCC1 FPFTUTDQPYXFSM-UHFFFAOYSA-N 0.000 description 1
- LYYLWJOKAQADDU-UHFFFAOYSA-N n,n-dihexadecylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCC LYYLWJOKAQADDU-UHFFFAOYSA-N 0.000 description 1
- YWWNNLPSZSEZNZ-UHFFFAOYSA-N n,n-dimethyldecan-1-amine Chemical compound CCCCCCCCCCN(C)C YWWNNLPSZSEZNZ-UHFFFAOYSA-N 0.000 description 1
- YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
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- BUHHOHWMNZQMTA-UHFFFAOYSA-N n,n-dioctadecyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCCCC BUHHOHWMNZQMTA-UHFFFAOYSA-N 0.000 description 1
- XTAZYLNFDRKIHJ-UHFFFAOYSA-N n,n-dioctyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- PEKMKFBONMBZHM-UHFFFAOYSA-N n-butyl-n-octadecyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCN(CCCC)CCCCCCCCCCCCCCCCCC PEKMKFBONMBZHM-UHFFFAOYSA-N 0.000 description 1
- ATBNMWWDBWBAHM-UHFFFAOYSA-N n-decyl-n-methyldecan-1-amine Chemical compound CCCCCCCCCCN(C)CCCCCCCCCC ATBNMWWDBWBAHM-UHFFFAOYSA-N 0.000 description 1
- GOJIVVWJAXAPGS-UHFFFAOYSA-N n-dodecyl-n-methylaniline Chemical compound CCCCCCCCCCCCN(C)C1=CC=CC=C1 GOJIVVWJAXAPGS-UHFFFAOYSA-N 0.000 description 1
- KCMTVIZYKDBFFS-UHFFFAOYSA-N n-hexadecyl-n-methylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCN(C)CCCCCCCCCCCCCCCC KCMTVIZYKDBFFS-UHFFFAOYSA-N 0.000 description 1
- KUFYUMSBZMUWAN-UHFFFAOYSA-N n-methyl-n-tetradecyltetradecan-1-amine Chemical compound CCCCCCCCCCCCCCN(C)CCCCCCCCCCCCCC KUFYUMSBZMUWAN-UHFFFAOYSA-N 0.000 description 1
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- 239000012299 nitrogen atmosphere Substances 0.000 description 1
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- ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003518 norbornenyl group Chemical class C12(C=CC(CC1)C2)* 0.000 description 1
- BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 125000002370 organoaluminium group Chemical group 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 1
- 125000002097 pentamethylcyclopentadienyl group Chemical group 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 229930015698 phenylpropene Natural products 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920000779 poly(divinylbenzene) Polymers 0.000 description 1
- 150000004291 polyenes Chemical class 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000003752 polymerase chain reaction Methods 0.000 description 1
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- 238000002459 porosimetry Methods 0.000 description 1
- 229910021426 porous silicon Inorganic materials 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
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- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
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- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229920006126 semicrystalline polymer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical class [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical class FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- ZCUFMDLYAMJYST-UHFFFAOYSA-N thorium dioxide Chemical compound O=[Th]=O ZCUFMDLYAMJYST-UHFFFAOYSA-N 0.000 description 1
- 229910003452 thorium oxide Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- BNOPYGRAXZULSM-UHFFFAOYSA-N tri(tetradecyl)phosphane Chemical compound CCCCCCCCCCCCCCP(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC BNOPYGRAXZULSM-UHFFFAOYSA-N 0.000 description 1
- ABVVEAHYODGCLZ-UHFFFAOYSA-O tridecylazanium Chemical compound CCCCCCCCCCCCC[NH3+] ABVVEAHYODGCLZ-UHFFFAOYSA-O 0.000 description 1
- MOSFSEPBWRXKJZ-UHFFFAOYSA-N tridecylphosphane Chemical compound CCCCCCCCCCCCCP MOSFSEPBWRXKJZ-UHFFFAOYSA-N 0.000 description 1
- SWZDQOUHBYYPJD-UHFFFAOYSA-N tridodecylamine Chemical compound CCCCCCCCCCCCN(CCCCCCCCCCCC)CCCCCCCCCCCC SWZDQOUHBYYPJD-UHFFFAOYSA-N 0.000 description 1
- CXKQHHJKHZXXPZ-UHFFFAOYSA-N triethylsilanylium Chemical compound CC[Si+](CC)CC CXKQHHJKHZXXPZ-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- VOYMPSZBODLRKS-UHFFFAOYSA-N trimethylsilanylium Chemical compound C[Si+](C)C VOYMPSZBODLRKS-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- RIOQSEWOXXDEQQ-UHFFFAOYSA-O triphenylphosphanium Chemical compound C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-O 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- GIIXTFIYICRGMZ-UHFFFAOYSA-N tris(2,3-dimethylphenyl)phosphane Chemical compound CC1=CC=CC(P(C=2C(=C(C)C=CC=2)C)C=2C(=C(C)C=CC=2)C)=C1C GIIXTFIYICRGMZ-UHFFFAOYSA-N 0.000 description 1
- COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 description 1
- OLFPYUPGPBITMH-UHFFFAOYSA-N tritylium Chemical compound C1=CC=CC=C1[C+](C=1C=CC=CC=1)C1=CC=CC=C1 OLFPYUPGPBITMH-UHFFFAOYSA-N 0.000 description 1
- 239000011882 ultra-fine particle Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
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- 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
- C08F4/619—Component covered by group C08F4/60 containing a transition metal-carbon bond
- C08F4/6192—Component covered by group C08F4/60 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
-
- 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
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
-
- 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
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/04—Monomers containing three or four carbon atoms
- C08F110/06—Propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- 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
- C08F4/619—Component covered by group C08F4/60 containing a transition metal-carbon bond
- C08F4/61908—Component covered by group C08F4/60 containing a transition metal-carbon bond in combination with an ionising compound other than alumoxane, e.g. (C6F5)4B-X+
-
- 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
- C08F2420/00—Metallocene catalysts
- C08F2420/02—Cp or analog bridged to a non-Cp X anionic donor
-
- 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
- C08F4/619—Component covered by group C08F4/60 containing a transition metal-carbon bond
- C08F4/61912—Component covered by group C08F4/60 containing a transition metal-carbon bond in combination with an organoaluminium compound
-
- 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
- Y10S526/943—Polymerization with metallocene catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Crystallography & Structural 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)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/768,518 US5783512A (en) | 1996-12-18 | 1996-12-18 | Catalyst component dispersion comprising an ionic compound and solid addition polymerization catalysts containing the same |
| PCT/US1997/021875 WO1998027119A1 (fr) | 1996-12-18 | 1997-12-01 | Dispersion de composants de catalyseur contenant un compose ionique et catalyseurs de polymerisation par addition solide renfermant cette dispersion |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO992974D0 NO992974D0 (no) | 1999-06-17 |
| NO992974L NO992974L (no) | 1999-08-17 |
| NO320275B1 true NO320275B1 (no) | 2005-11-21 |
Family
ID=25082729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19992974A NO320275B1 (no) | 1996-12-18 | 1999-06-17 | Katalysatorkomponent i form av en dispersjon omfattende en ionisk forbindelse og en fast addisjonspolymerisasjonskatalysator omfattende det samme |
Country Status (28)
| Country | Link |
|---|---|
| US (2) | US5783512A (fr) |
| EP (1) | EP0946601B1 (fr) |
| JP (1) | JP2001506691A (fr) |
| KR (1) | KR100520586B1 (fr) |
| CN (1) | CN1283672C (fr) |
| AR (1) | AR010791A1 (fr) |
| AT (1) | ATE224921T1 (fr) |
| AU (1) | AU726483B2 (fr) |
| BR (1) | BR9713776A (fr) |
| CA (1) | CA2271380C (fr) |
| CZ (1) | CZ298647B6 (fr) |
| DE (1) | DE69715907T2 (fr) |
| DZ (1) | DZ2378A1 (fr) |
| EG (1) | EG21570A (fr) |
| ES (1) | ES2180075T3 (fr) |
| HU (1) | HUP0000290A3 (fr) |
| ID (1) | ID22284A (fr) |
| MY (1) | MY117875A (fr) |
| NO (1) | NO320275B1 (fr) |
| NZ (1) | NZ335444A (fr) |
| PL (1) | PL334023A1 (fr) |
| PT (1) | PT946601E (fr) |
| SA (1) | SA98181018B1 (fr) |
| SK (1) | SK282300B6 (fr) |
| TR (1) | TR199901319T2 (fr) |
| TW (1) | TW460493B (fr) |
| WO (1) | WO1998027119A1 (fr) |
| ZA (1) | ZA9711325B (fr) |
Families Citing this family (170)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5384299A (en) * | 1987-01-30 | 1995-01-24 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
| US6143686A (en) * | 1994-08-03 | 2000-11-07 | Exxon Chemical Patents, Inc. | Supported ionic catalyst compositions |
| US5972823A (en) * | 1994-08-03 | 1999-10-26 | Exxon Chemical Patents Inc | Supported ionic catalyst composition |
| US6228795B1 (en) * | 1997-06-05 | 2001-05-08 | Exxon Chemical Patents, Inc. | Polymeric supported catalysts |
| KR20010032116A (ko) * | 1997-12-01 | 2001-04-16 | 보 구스타프쏜 | 수분 흡수 장치 |
| ES2237911T3 (es) * | 1998-03-04 | 2005-08-01 | Exxonmobil Chemical Patents Inc. | Aniones no coordinantes para polimerizacion de olefinas. |
| CN1240726C (zh) * | 1998-09-16 | 2006-02-08 | 陶氏环球技术公司 | 淤浆聚合法及聚合物组合物 |
| US6852811B1 (en) * | 1998-12-30 | 2005-02-08 | The Dow Chemical Company | Process for preparing a supported polymerization catalyst using reduced amounts of solvent and polymerization process |
| US6818585B2 (en) * | 1998-12-30 | 2004-11-16 | Univation Technologies, Llc | Catalyst compounds, catalyst systems thereof and their use in a polymerization process |
| PT1177225E (pt) * | 1999-05-05 | 2009-02-11 | Ineos Europe Ltd | Copolímeros de etileno e respectivos filmes |
| GB9918668D0 (en) * | 1999-08-06 | 1999-10-13 | Bp Chem Int Ltd | Polymerisation catalysts |
| WO2001046273A1 (fr) | 1999-12-20 | 2001-06-28 | Exxon Chemical Patents Inc. | Procedes relatifs a l'elaboration de resines polyolefiniques reposant sur l'utilisation de catalyseurs ioniques supportes |
| DE19962910A1 (de) * | 1999-12-23 | 2001-07-05 | Targor Gmbh | Chemische Verbindung, Verfahren zu deren Herstellung und deren Verwendung in Katalysatorsystemen zur Herstellung von Polyolefinen |
| US7041617B2 (en) | 2004-01-09 | 2006-05-09 | Chevron Phillips Chemical Company, L.P. | Catalyst compositions and polyolefins for extrusion coating applications |
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| KR20200117987A (ko) | 2017-12-29 | 2020-10-14 | 다우 글로벌 테크놀로지스 엘엘씨 | 이중 헤드 유기 알루미늄 조성물 |
| SG11202010442QA (en) * | 2018-04-26 | 2020-11-27 | Exxonmobil Chemical Patents Inc | Non-coordinating anion type activators containing cation having large alkyl groups |
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| JP2022515522A (ja) | 2018-12-28 | 2022-02-18 | ダウ グローバル テクノロジーズ エルエルシー | 不飽和ポリオレフィンを含む硬化性組成物 |
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| EP3946938B1 (fr) | 2019-03-26 | 2024-08-07 | Dow Global Technologies LLC | Films multicouches, stratifiés et articles comprenant des films multicouches |
| JP6887195B1 (ja) | 2019-10-24 | 2021-06-16 | 株式会社浅井ゲルマニウム研究所 | 新規有機ゲルマニウム化合物 |
| US11661465B2 (en) * | 2019-10-28 | 2023-05-30 | Exxonmobil Chemical Patents Inc. | Dimer selective metallocene catalysts, non-aromatic hydrocarbon soluble activators, and processes to produce poly alpha-olefin oligmers therewith |
| JP2023508013A (ja) | 2019-12-30 | 2023-02-28 | ダウ グローバル テクノロジーズ エルエルシー | アルファ－置換アクリレートを調製するためのプロセス |
| CN114929661A (zh) | 2019-12-30 | 2022-08-19 | 陶氏环球技术有限责任公司 | 用于制备α-取代的丙烯酸酯的方法 |
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| KR20230039700A (ko) | 2020-07-17 | 2023-03-21 | 다우 글로벌 테크놀로지스 엘엘씨 | 구속된 기하학 전촉매를 위한 히드로카르빌-개질된 메틸알루미녹산 공촉매 |
| JP2023547335A (ja) | 2020-10-15 | 2023-11-10 | ダウ グローバル テクノロジーズ エルエルシー | ６－アミノ－ｎ－アリールアザインドール配位子を有するオレフィン重合触媒 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2618384B2 (ja) | 1986-12-27 | 1997-06-11 | 三井石油化学工業株式会社 | オレフイン重合用固体触媒およびその製法 |
| US5064802A (en) | 1989-09-14 | 1991-11-12 | The Dow Chemical Company | Metal complex compounds |
| ES2072598T3 (es) * | 1990-01-02 | 1995-07-16 | Exxon Chemical Patents Inc | Catalizadores ionicos de metaloceno soportados para la polimerizacion de olefinas. |
| DE69222700T2 (de) * | 1991-07-11 | 1998-03-26 | Idemitsu Kosan Co | Verfahren zur Herstellung von Polymeren auf Olefinbasis und Olefin-Polymerisationskatalysatoren |
| EP0614468B1 (fr) * | 1991-11-25 | 1997-09-17 | Exxon Chemical Patents Inc. | Composition polyionique de catalyseur de metaux de transition |
| US5296433A (en) * | 1992-04-14 | 1994-03-22 | Minnesota Mining And Manufacturing Company | Tris(pentafluorophenyl)borane complexes and catalysts derived therefrom |
| JPH07509753A (ja) * | 1992-08-05 | 1995-10-26 | エクソン・ケミカル・パテンツ・インク | エチレンとｃ↓７乃至ｃ↓１↓０オレフィンの気相重合 |
| ES2167336T3 (es) * | 1992-08-05 | 2002-05-16 | Exxonmobil Chem Patents Inc | Catalizadores ionicos soportados de metal de transicion para la polimerizacion de olefinas. |
| EP0668880B1 (fr) * | 1992-10-05 | 1999-07-21 | Exxon Chemical Patents Inc. | Procede de polymerisation utilisant un systeme catalyseur a productivite amelioree |
| US5972823A (en) * | 1994-08-03 | 1999-10-26 | Exxon Chemical Patents Inc | Supported ionic catalyst composition |
| IT1272939B (it) | 1995-02-01 | 1997-07-01 | Enichem Spa | Catalizzatore metallocenico supportato per la (co)polimerizzazione delle olefine |
| DE69611554T2 (de) | 1995-02-20 | 2001-07-05 | Tosoh Corp., Shinnanyo | Katalysator für die Polymerisation von Olefinen und Verfahren zur Herstellung von Olefinpolymerisaten |
| AU712417B2 (en) * | 1995-03-10 | 1999-11-04 | Dow Chemical Company, The | Supported catalyst component, supported catalyst, preparation process, polymerization process, complex compounds, and their preparation |
| JPH09309926A (ja) * | 1996-05-17 | 1997-12-02 | Dow Chem Co:The | エチレン共重合体の製造方法 |
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1996
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- 1997-12-01 CA CA002271380A patent/CA2271380C/fr not_active Expired - Fee Related
- 1997-12-01 AU AU55120/98A patent/AU726483B2/en not_active Ceased
- 1997-12-01 KR KR10-1999-7005485A patent/KR100520586B1/ko not_active IP Right Cessation
- 1997-12-01 JP JP52773698A patent/JP2001506691A/ja active Pending
- 1997-12-01 BR BR9713776A patent/BR9713776A/pt not_active IP Right Cessation
- 1997-12-01 AT AT97951489T patent/ATE224921T1/de not_active IP Right Cessation
- 1997-12-01 US US09/297,422 patent/US6271165B1/en not_active Expired - Lifetime
- 1997-12-01 DE DE69715907T patent/DE69715907T2/de not_active Expired - Lifetime
- 1997-12-01 WO PCT/US1997/021875 patent/WO1998027119A1/fr active IP Right Grant
- 1997-12-01 ES ES97951489T patent/ES2180075T3/es not_active Expired - Lifetime
- 1997-12-01 CN CN97180691.8A patent/CN1283672C/zh not_active Expired - Fee Related
- 1997-12-01 TR TR1999/01319T patent/TR199901319T2/xx unknown
- 1997-12-01 HU HU0000290A patent/HUP0000290A3/hu unknown
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- 1997-12-01 EP EP97951489A patent/EP0946601B1/fr not_active Expired - Lifetime
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- 1997-12-16 EG EG133397A patent/EG21570A/xx active
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- 1997-12-17 TW TW086119062A patent/TW460493B/zh not_active IP Right Cessation
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- 1997-12-17 DZ DZ970228A patent/DZ2378A1/fr active
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