FI114865B - Förfarande för framställning av aluminoxaner - Google Patents
Förfarande för framställning av aluminoxaner Download PDFInfo
- Publication number
- FI114865B FI114865B FI942102A FI942102A FI114865B FI 114865 B FI114865 B FI 114865B FI 942102 A FI942102 A FI 942102A FI 942102 A FI942102 A FI 942102A FI 114865 B FI114865 B FI 114865B
- Authority
- FI
- Finland
- Prior art keywords
- aluminum
- water
- process according
- solution
- reactor
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 18
- 238000002360 preparation method Methods 0.000 title claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- 229910052782 aluminium Inorganic materials 0.000 claims description 16
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 10
- 238000002156 mixing Methods 0.000 claims description 9
- 230000003068 static effect Effects 0.000 claims description 8
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 16
- -1 aluminum oxanes Chemical class 0.000 description 8
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 7
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 238000006384 oligomerization reaction Methods 0.000 description 5
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- CPOFMOWDMVWCLF-UHFFFAOYSA-N methyl(oxo)alumane Chemical compound C[Al]=O CPOFMOWDMVWCLF-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 238000013021 overheating Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- WCFQIFDACWBNJT-UHFFFAOYSA-N $l^{1}-alumanyloxy(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]O[Al] WCFQIFDACWBNJT-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-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
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/061—Aluminium compounds with C-aluminium linkage
- C07F5/066—Aluminium compounds with C-aluminium linkage compounds with Al linked to an element other than Al, C, H or halogen (this includes Al-cyanide linkage)
- C07F5/068—Aluminium compounds with C-aluminium linkage compounds with Al linked to an element other than Al, C, H or halogen (this includes Al-cyanide linkage) preparation of alum(in)oxanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/24—Stationary reactors without moving elements inside
- B01J19/2455—Stationary reactors without moving elements inside provoking a loop type movement of the reactants
- B01J19/246—Stationary reactors without moving elements inside provoking a loop type movement of the reactants internally, i.e. the mixture circulating inside the vessel such that the upward stream is separated physically from the downward stream(s)
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/24—Stationary reactors without moving elements inside
- B01J19/2455—Stationary reactors without moving elements inside provoking a loop type movement of the reactants
- B01J19/2465—Stationary reactors without moving elements inside provoking a loop type movement of the reactants externally, i.e. the mixture leaving the vessel and subsequently re-entering it
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Claims (8)
1. Förfarande för framställning av aluminiumoxaner med den allmänna formeln R2A10[RalO]nAlR2 och/eller 5 - [-RA10-]-n+2, varvid R är en Cx-io-alkylgrupp (förgrenad eller rakkedjad), varvid grupperna R kan vara likadana el-ler olika, n är ett heltal 0 -20, genom att tillsätta vatten tili en lösning av trialkylaluminium i ett alifa-tiskt, cykloalifatiskt eller aromatiskt kolväte, kän-10 netecknat av att vattnet som erfordras för reaktionen doseras tili en statisk blandare via et blandningsmun-stycke.
1. I » > 114865
2. Förfarande enligt patentkrav 1, känneteck-nat av att som statisk blandare används en strälsling- 15 reaktor.
3. Förfarande enligt patentkrav 1, känneteck-nat av att vattnet doseras tili reaktorn i ett volym-strömningsförhällande frän 1:500 -1:40000.
4. Förfarande enligt patentkrav 1, känneteck- 2. nat av att reaktionen utförs vid en temperatur av -20 °C - +100 °C.
5. Förfarande enligt patentkrav 1, känneteck-n a t av att R är en metylgrupp.
:6. Förfarande enligt patentkrav 1, känneteck-25 nat av att molf örhällandet H20/aluminiumtrialkylföre- ,·, ; ningen är inom omrädet 0,6 - 1,2:1.
/ 7. Förfarande enligt patentkrav 1, känneteck- nat av att molf örhällandet H20/aluminiumtrialkylföre- • · ’’ 1 ningen är inom omrädet 0,65:1 -0,75:1, när man som alumi- 30 niumtrialkylförening använder trimetylaluminium. i
8. Förfarande enligt patentkrav 7, känneteck- it1 nat av att vatten doseras tili reaktorn i ett volymström-, ningsförhällande av 1:2000 - 1:20000. i 1 · T 1 • - 1 ·
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4314986A DE4314986A1 (de) | 1993-05-06 | 1993-05-06 | Verfahren zur Herstellung von Aluminoxanen |
DE4314986 | 1993-05-06 |
Publications (3)
Publication Number | Publication Date |
---|---|
FI942102A0 FI942102A0 (sv) | 1994-05-06 |
FI942102A FI942102A (sv) | 1994-11-07 |
FI114865B true FI114865B (sv) | 2005-01-14 |
Family
ID=6487323
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI942102A FI114865B (sv) | 1993-05-06 | 1994-05-06 | Förfarande för framställning av aluminoxaner |
Country Status (7)
Country | Link |
---|---|
US (1) | US5403942A (sv) |
EP (1) | EP0623624B1 (sv) |
JP (1) | JP3764495B2 (sv) |
CA (1) | CA2112918C (sv) |
DE (2) | DE4314986A1 (sv) |
FI (1) | FI114865B (sv) |
NO (1) | NO306817B1 (sv) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE59500269D1 (de) * | 1995-09-13 | 1997-07-03 | Witco Gmbh | Verfahren zur Herstellung von Metallocen-Katalysatorsystemen auf inerten Trägermaterialien unter Verwendung von Gasphasenreaktoren |
CN1048977C (zh) * | 1995-11-15 | 2000-02-02 | 中国石油化工总公司 | 制备低碳α-烯烃的方法 |
ES2179899T3 (es) * | 1996-03-19 | 2003-02-01 | Crompton Gmbh | Formulaciones homogeneas de compuestos organicos metalicos, sensibles a la oxidacion, en parafinas, y procedimiento para su preparacion. |
US5606087A (en) * | 1996-04-19 | 1997-02-25 | Albemarle Corporation | Process for making aluminoxanes |
EP0906319B2 (en) * | 1996-04-19 | 2006-12-06 | Albemarle Corporation | Process for making aluminoxanes |
US5663394A (en) * | 1996-07-15 | 1997-09-02 | Albemarle Corporation | High yield aluminoxane synthesis process |
US5599964A (en) * | 1996-04-19 | 1997-02-04 | Albemarle Corporation | Continuous process for preparing hydrocarbylaluminoxanes |
CN1044648C (zh) * | 1997-05-22 | 1999-08-11 | 南开大学 | 共沉淀还原扩散法制备钕铁硼永磁合金 |
CA2412488C (en) * | 2001-12-11 | 2009-09-08 | Crompton Gmbh | Process for preparing partial hydrolysates of organometallic compounds or transition metal catalysts immobilized on inert support materials |
DE102008041652A1 (de) * | 2008-08-28 | 2010-03-04 | Evonik Oxeno Gmbh | Vorrichtung und Verfahren für die kontinuierliche Umsetzung einer Flüssigkeit mit einem Gas |
SG11201506224UA (en) | 2013-02-08 | 2015-09-29 | Mitsui Chemicals Inc | Solid polyaluminoxane composition, olefin polymerization catalyst, olefin polymer production method and solid polyaluminoxane composition production method |
CN111454285B (zh) * | 2019-01-18 | 2023-04-07 | 中国石油天然气股份有限公司 | 铝氧烷的制备方法 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3242099A (en) * | 1964-03-27 | 1966-03-22 | Union Carbide Corp | Olefin polymerization catalysts |
DE2516284C3 (de) * | 1975-04-14 | 1978-04-13 | Burdosa, Herwig Burgert, 6301 Roedgen | Schlaufenreaktor |
DE3127133A1 (de) * | 1981-07-09 | 1983-01-27 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von polyolefinen und deren copolymerisaten |
DE3240383A1 (de) * | 1982-11-02 | 1984-05-03 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung von oligomeren aluminoxanen |
US4730072A (en) * | 1986-08-15 | 1988-03-08 | Shell Oil Company | Process for preparing aluminoxanes |
US4772736A (en) * | 1987-11-23 | 1988-09-20 | Union Carbide Corporation | Process for the preparation of aluminoxanes |
US4908463A (en) * | 1988-12-05 | 1990-03-13 | Ethyl Corporation | Aluminoxane process |
US4968827A (en) * | 1989-06-06 | 1990-11-06 | Ethyl Corporation | Alkylaluminoxane process |
US4924018A (en) * | 1989-06-26 | 1990-05-08 | Ethyl Corporation | Alkylaluminoxane process |
US5041585A (en) * | 1990-06-08 | 1991-08-20 | Texas Alkyls, Inc. | Preparation of aluminoxanes |
-
1993
- 1993-05-06 DE DE4314986A patent/DE4314986A1/de not_active Withdrawn
- 1993-11-11 EP EP93118245A patent/EP0623624B1/de not_active Expired - Lifetime
- 1993-11-11 DE DE59308892T patent/DE59308892D1/de not_active Expired - Lifetime
-
1994
- 1994-01-06 CA CA002112918A patent/CA2112918C/en not_active Expired - Lifetime
- 1994-03-16 US US08/213,948 patent/US5403942A/en not_active Expired - Lifetime
- 1994-05-02 JP JP09356494A patent/JP3764495B2/ja not_active Expired - Lifetime
- 1994-05-05 NO NO941659A patent/NO306817B1/no not_active IP Right Cessation
- 1994-05-06 FI FI942102A patent/FI114865B/sv not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
NO941659L (no) | 1994-11-07 |
DE59308892D1 (de) | 1998-09-24 |
EP0623624B1 (de) | 1998-08-19 |
FI942102A0 (sv) | 1994-05-06 |
EP0623624A1 (de) | 1994-11-09 |
CA2112918C (en) | 1997-10-21 |
NO306817B1 (no) | 1999-12-27 |
JP3764495B2 (ja) | 2006-04-05 |
CA2112918A1 (en) | 1994-11-07 |
US5403942A (en) | 1995-04-04 |
JPH06329680A (ja) | 1994-11-29 |
NO941659D0 (no) | 1994-05-05 |
DE4314986A1 (de) | 1994-11-10 |
FI942102A (sv) | 1994-11-07 |
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Legal Events
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FG | Patent granted |
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MM | Patent lapsed |