JPH06504994A - アルコールの製造方法 - Google Patents
アルコールの製造方法Info
- Publication number
- JPH06504994A JPH06504994A JP4503521A JP50352192A JPH06504994A JP H06504994 A JPH06504994 A JP H06504994A JP 4503521 A JP4503521 A JP 4503521A JP 50352192 A JP50352192 A JP 50352192A JP H06504994 A JPH06504994 A JP H06504994A
- Authority
- JP
- Japan
- Prior art keywords
- butene
- olefin
- alcohol
- raw material
- catalyst
- 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.)
- Pending
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims description 15
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 39
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 39
- 150000001336 alkenes Chemical class 0.000 claims description 34
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 29
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 28
- 239000003054 catalyst Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 26
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 24
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 16
- 239000002994 raw material Substances 0.000 claims description 15
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 14
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 11
- 230000000694 effects Effects 0.000 claims description 9
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- 238000005984 hydrogenation reaction Methods 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 6
- 238000006384 oligomerization reaction Methods 0.000 claims description 6
- 239000001273 butane Substances 0.000 claims description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 230000032050 esterification Effects 0.000 claims description 2
- 238000005886 esterification reaction Methods 0.000 claims description 2
- 229920001519 homopolymer Polymers 0.000 claims description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical group CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims 2
- 238000006772 olefination reaction Methods 0.000 claims 1
- 230000003606 oligomerizing effect Effects 0.000 claims 1
- 239000001294 propane Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 30
- 239000000047 product Substances 0.000 description 17
- 238000006116 polymerization reaction Methods 0.000 description 10
- -1 tetraethyl lead Butene Chemical compound 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 7
- 239000004014 plasticizer Substances 0.000 description 7
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 description 4
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 3
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910052776 Thorium Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 238000007037 hydroformylation reaction Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 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
- 238000007254 oxidation reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229910001392 phosphorus oxide Inorganic materials 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical class [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/16—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxo-reaction combined with reduction
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9102513.0 | 1991-02-06 | ||
| GB919102513A GB9102513D0 (en) | 1991-02-06 | 1991-02-06 | Hydrocarbon production |
| PCT/EP1992/000245 WO1992013818A1 (en) | 1991-02-06 | 1992-02-04 | Alcohol production |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH06504994A true JPH06504994A (ja) | 1994-06-09 |
Family
ID=10689613
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4503521A Pending JPH06504994A (ja) | 1991-02-06 | 1992-02-04 | アルコールの製造方法 |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0570411B1 (https=) |
| JP (1) | JPH06504994A (https=) |
| KR (1) | KR930703225A (https=) |
| AT (1) | ATE142190T1 (https=) |
| AU (1) | AU661987B2 (https=) |
| BR (1) | BR9205595A (https=) |
| CA (1) | CA2103587C (https=) |
| CZ (1) | CZ162093A3 (https=) |
| DE (1) | DE69213435T2 (https=) |
| GB (1) | GB9102513D0 (https=) |
| HU (1) | HUT64936A (https=) |
| MY (1) | MY110784A (https=) |
| RU (1) | RU2094420C1 (https=) |
| SG (1) | SG43211A1 (https=) |
| SK (1) | SK84293A3 (https=) |
| TW (1) | TW213446B (https=) |
| WO (1) | WO1992013818A1 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000248017A (ja) * | 1999-02-26 | 2000-09-12 | Oxeno Olefinchemie Gmbh | ブテンオリゴマーからビニルエステルを製造する方法、コモノマーおよび可塑剤としてのその使用 |
| JP2003523967A (ja) * | 2000-01-27 | 2003-08-12 | ビーエーエスエフ アクチェンゲゼルシャフト | Ｃ９−アルコールの製造方法およびｃ９−アルコールおよびｃ１０−アルコールの組み合わせた製造方法 |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4221472A1 (de) * | 1992-06-30 | 1994-01-05 | Hoechst Ag | Gemische isomerer Decylalkohole, daraus erhältliche Phthalsäureester und ihre Verwendung als Weichmacher |
| DE19906518A1 (de) | 1999-02-17 | 2000-08-31 | Oxeno Olefinchemie Gmbh | Verfahren zur Fraktionierung von Dibuten |
| BR9917230A (pt) * | 1999-04-21 | 2002-01-08 | Basf Ag | Mistura de diésteres de nonanol isomérico de um ácido dicarboxìlico, e, uso da mesma |
| DK1113034T3 (da) * | 1999-12-23 | 2001-11-19 | Basf Ag | Med isomere nonanoler termineret polyester, fremgangsmåde til dens fremstilling og dens anvendelse som blødgører |
| DE10135906A1 (de) | 2001-07-24 | 2003-02-06 | Oxeno Olefinchemie Gmbh | Verfahren zur Hydroformylierung von höheren Olefinen mit Kobaltverbindungen als Katalysator |
| CN1882521B (zh) * | 2003-10-15 | 2010-06-09 | 国际壳牌研究有限公司 | 使用来自氢化单元和脱氢异构化单元的组合工艺物流制备支化脂族醇的方法 |
| DE102004033410A1 (de) * | 2004-02-14 | 2005-09-01 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Olefinen mit 8 bis 12 Kohlenstoffatomen |
| DE102004029732A1 (de) | 2004-06-21 | 2006-01-19 | Basf Ag | Hilfsmittel enthaltend Cyclohexanpolycarbonsäurederivate |
| ATE404515T1 (de) | 2004-08-04 | 2008-08-15 | Exxonmobil Chem Patents Inc | Mischungen von c8-c10-alkoholen und davon abgeleitete weichmacher |
| DE102004059293A1 (de) | 2004-12-09 | 2006-06-14 | Oxeno Olefinchemie Gmbh | Verfahren zur Hydroformylierung von Olefinen |
| DE102004059292A1 (de) | 2004-12-09 | 2006-06-14 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Alkoholen aus Olefinen durch Hydroformylierung und Hydrierung |
| TWI260798B (en) | 2005-05-02 | 2006-08-21 | Ind Tech Res Inst | Highly heat-dissipating light-emitting diode |
| DE102005021075A1 (de) | 2005-05-06 | 2006-11-09 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Carbonsäureestern |
| DE102008007080A1 (de) | 2008-01-31 | 2009-08-06 | Evonik Oxeno Gmbh | Verfahren zur Herstellung von C9-Alkohol aus C8-Olefinen |
| US20110232825A1 (en) | 2008-12-05 | 2011-09-29 | Basf Se | Cyclohexane polycarboxylic acid derivatives as plasticizers for adhesives and sealants |
| EP2379482B1 (de) | 2008-12-16 | 2015-08-26 | Basf Se | Herstellung von carbonsäureestern unter strippen mit alkohol-dampf |
| CN102256923B (zh) | 2008-12-16 | 2013-12-04 | 巴斯夫欧洲公司 | 制备羧酸酯的方法 |
| DE102009029284A1 (de) | 2009-09-08 | 2011-03-10 | Evonik Oxeno Gmbh | Verfahren zur Oligomerisierung von Olefinen |
| US20120220678A1 (en) | 2009-11-03 | 2012-08-30 | Christof Mehler | Thermoplastic compositions having improved flowability |
| ES2522843T3 (es) | 2010-06-01 | 2014-11-18 | Basf Se | Procedimiento para la preparación de composiciones de polímero de estireno expandibles |
| EP2649160B1 (en) | 2010-12-07 | 2022-03-16 | ExxonMobil Chemical Patents Inc. | Processes utilizing solvent extraction |
| US9776937B2 (en) | 2011-07-25 | 2017-10-03 | Exxonmobil Chemical Patents Inc. | Integrated nitrile poison adsorption and desorption system |
| US9505685B2 (en) | 2011-07-25 | 2016-11-29 | Exxonmobil Chemical Patents Inc. | Olefin oligomerization process |
| US9550705B2 (en) | 2011-07-25 | 2017-01-24 | Exxonmobill Chemical Patents Inc. | Olefin oligomerization process |
| WO2013013884A2 (en) | 2011-07-25 | 2013-01-31 | Exxonmobil Chemical Patents Inc. | Process for nitrile removal from hydrocarbon feeds |
| US9573861B2 (en) | 2011-07-25 | 2017-02-21 | Exxonmobil Chemical Patents Inc. | Olefin oligomerization process |
| EP2716623A1 (de) | 2012-10-05 | 2014-04-09 | Basf Se | Verfahren zur Herstellung von Cyclohexanpolycarbonsäure-Derivaten mit geringem Nebenproduktanteil |
| DE102014200072A1 (de) | 2014-01-08 | 2015-07-09 | Evonik Industries Ag | Dimerisierung von Olefinen |
| PL3174845T3 (pl) | 2014-08-01 | 2020-11-16 | Basf Se | Sposób obróbki surowego estru, który zawiera produkt hydrolizy katalizatora estryfikacji w postaci zawieszonych cząstek |
| ZA201801183B (en) | 2017-02-27 | 2019-01-30 | Evonik Degussa Gmbh | Selective oligomerization of olefins |
| WO2020173818A1 (de) | 2019-02-25 | 2020-09-03 | Basf Se | Verfahren zur aufarbeitung von benzolpolycarbonsäureestern und deren verwendung zur herstellung von cyclohexanpolycarbonsäureestern |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB477128A (en) * | 1936-10-16 | 1937-12-22 | Universal Oil Prod Co | Process for the manufacture of hydrocarbons suitable for use in motor fuel blends |
| IT1074653B (it) * | 1977-01-11 | 1985-04-20 | Euteco Spa | Procedimento per la produzione di olefine |
| US4123471A (en) * | 1977-07-26 | 1978-10-31 | Natale Bertolini | Olefin production process |
| JPS5847410B2 (ja) * | 1977-12-23 | 1983-10-22 | 日産化学工業株式会社 | 可塑剤組成物 |
| US4229586A (en) * | 1979-06-07 | 1980-10-21 | Uop Inc. | Process for production of motor fuel and phthalate esters or acyclic alcohols |
| US4675463A (en) * | 1986-02-05 | 1987-06-23 | Exxon Chemical Patents Inc. | Process for reducing fouling in higher olefin plants |
| DE3889936T2 (de) * | 1987-02-09 | 1995-01-26 | Mitsubishi Chem Ind | Alkoholgemisch für Plastifiziermittel. |
-
1991
- 1991-02-06 GB GB919102513A patent/GB9102513D0/en active Pending
-
1992
- 1992-01-31 MY MYPI92000169A patent/MY110784A/en unknown
- 1992-02-01 TW TW081100797A patent/TW213446B/zh active
- 1992-02-04 DE DE69213435T patent/DE69213435T2/de not_active Expired - Fee Related
- 1992-02-04 AT AT92903627T patent/ATE142190T1/de not_active IP Right Cessation
- 1992-02-04 BR BR9205595A patent/BR9205595A/pt not_active Application Discontinuation
- 1992-02-04 RU RU9293051536A patent/RU2094420C1/ru active
- 1992-02-04 WO PCT/EP1992/000245 patent/WO1992013818A1/en not_active Ceased
- 1992-02-04 CZ CS931620A patent/CZ162093A3/cs unknown
- 1992-02-04 SK SK842-93A patent/SK84293A3/sk unknown
- 1992-02-04 SG SG1996005601A patent/SG43211A1/en unknown
- 1992-02-04 CA CA002103587A patent/CA2103587C/en not_active Expired - Fee Related
- 1992-02-04 EP EP92903627A patent/EP0570411B1/en not_active Expired - Lifetime
- 1992-02-04 HU HU9302272A patent/HUT64936A/hu unknown
- 1992-02-04 JP JP4503521A patent/JPH06504994A/ja active Pending
- 1992-02-04 KR KR1019930702326A patent/KR930703225A/ko not_active Ceased
- 1992-02-04 AU AU11842/92A patent/AU661987B2/en not_active Ceased
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000248017A (ja) * | 1999-02-26 | 2000-09-12 | Oxeno Olefinchemie Gmbh | ブテンオリゴマーからビニルエステルを製造する方法、コモノマーおよび可塑剤としてのその使用 |
| JP2003523967A (ja) * | 2000-01-27 | 2003-08-12 | ビーエーエスエフ アクチェンゲゼルシャフト | Ｃ９−アルコールの製造方法およびｃ９−アルコールおよびｃ１０−アルコールの組み合わせた製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| MY110784A (en) | 1999-04-30 |
| AU661987B2 (en) | 1995-08-17 |
| CA2103587C (en) | 2003-09-16 |
| SK84293A3 (en) | 1994-04-06 |
| KR930703225A (ko) | 1993-11-29 |
| EP0570411B1 (en) | 1996-09-04 |
| WO1992013818A1 (en) | 1992-08-20 |
| DE69213435D1 (de) | 1996-10-10 |
| BR9205595A (pt) | 1994-05-03 |
| RU2094420C1 (ru) | 1997-10-27 |
| EP0570411A1 (en) | 1993-11-24 |
| TW213446B (https=) | 1993-09-21 |
| SG43211A1 (en) | 1997-10-17 |
| HUT64936A (en) | 1994-03-28 |
| HU9302272D0 (en) | 1993-11-29 |
| ATE142190T1 (de) | 1996-09-15 |
| GB9102513D0 (en) | 1991-03-27 |
| DE69213435T2 (de) | 1997-02-13 |
| AU1184292A (en) | 1992-09-07 |
| CA2103587A1 (en) | 1992-08-07 |
| CZ162093A3 (en) | 1994-02-16 |
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