CZ162093A3 - Process for preparing alcohols - Google Patents
Process for preparing alcohols Download PDFInfo
- Publication number
- CZ162093A3 CZ162093A3 CS931620A CS162093A CZ162093A3 CZ 162093 A3 CZ162093 A3 CZ 162093A3 CS 931620 A CS931620 A CS 931620A CS 162093 A CS162093 A CS 162093A CZ 162093 A3 CZ162093 A3 CZ 162093A3
- Authority
- CZ
- Czechia
- Prior art keywords
- butene
- process according
- catalyst
- olefin
- fraction
- Prior art date
Links
- 150000001298 alcohols Chemical class 0.000 title description 6
- 238000004519 manufacturing process Methods 0.000 title description 6
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims abstract description 48
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims abstract description 44
- 238000006243 chemical reaction Methods 0.000 claims abstract description 38
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims abstract description 13
- 230000003197 catalytic effect Effects 0.000 claims abstract description 5
- 239000003054 catalyst Substances 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 31
- 150000001336 alkenes Chemical class 0.000 claims description 30
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 28
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 27
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 24
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 18
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 13
- 239000007787 solid Substances 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 230000000694 effects Effects 0.000 claims description 9
- 238000005984 hydrogenation reaction Methods 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 6
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 6
- 238000006384 oligomerization reaction Methods 0.000 claims description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical group CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 2
- 229920001519 homopolymer Polymers 0.000 claims description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 2
- 239000001294 propane Substances 0.000 claims description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims 2
- 239000001273 butane Substances 0.000 claims 1
- 230000000447 dimerizing effect Effects 0.000 claims 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims 1
- 238000006471 dimerization reaction Methods 0.000 abstract description 6
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 abstract description 6
- 239000000047 product Substances 0.000 description 25
- 239000004014 plasticizer Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 5
- -1 nonyl alcohols Chemical class 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000007423 decrease Effects 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
- 239000005909 Kieselgur Substances 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-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
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 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
- 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
- 238000004821 distillation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000006385 ozonation reaction Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical class CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical class CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 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
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-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
- 238000005299 abrasion Methods 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000003158 alcohol group Chemical group 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
- 238000009835 boiling Methods 0.000 description 1
- 235000013844 butane Nutrition 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
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 125000005442 diisocyanate group Chemical group 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
- 235000011180 diphosphates Nutrition 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000007037 hydroformylation reaction Methods 0.000 description 1
- 239000012535 impurity 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
- 235000010755 mineral Nutrition 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
- DUUPDCPVCHSTFF-UHFFFAOYSA-N nonane Chemical compound [CH2]CCCCCCCC DUUPDCPVCHSTFF-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
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 230000002035 prolonged effect Effects 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
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- ZCUFMDLYAMJYST-UHFFFAOYSA-N thorium dioxide Chemical compound O=[Th]=O ZCUFMDLYAMJYST-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc 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 (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| 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 |
|---|---|
| CZ162093A3 true CZ162093A3 (en) | 1994-02-16 |
Family
ID=10689613
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS931620A CZ162093A3 (en) | 1991-02-06 | 1992-02-04 | Process for preparing alcohols |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0570411B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JPH06504994A (cg-RX-API-DMAC10.html) |
| KR (1) | KR930703225A (cg-RX-API-DMAC10.html) |
| AT (1) | ATE142190T1 (cg-RX-API-DMAC10.html) |
| AU (1) | AU661987B2 (cg-RX-API-DMAC10.html) |
| BR (1) | BR9205595A (cg-RX-API-DMAC10.html) |
| CA (1) | CA2103587C (cg-RX-API-DMAC10.html) |
| CZ (1) | CZ162093A3 (cg-RX-API-DMAC10.html) |
| DE (1) | DE69213435T2 (cg-RX-API-DMAC10.html) |
| GB (1) | GB9102513D0 (cg-RX-API-DMAC10.html) |
| HU (1) | HUT64936A (cg-RX-API-DMAC10.html) |
| MY (1) | MY110784A (cg-RX-API-DMAC10.html) |
| RU (1) | RU2094420C1 (cg-RX-API-DMAC10.html) |
| SG (1) | SG43211A1 (cg-RX-API-DMAC10.html) |
| SK (1) | SK84293A3 (cg-RX-API-DMAC10.html) |
| TW (1) | TW213446B (cg-RX-API-DMAC10.html) |
| WO (1) | WO1992013818A1 (cg-RX-API-DMAC10.html) |
Families Citing this family (33)
| 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 |
| DE19908320A1 (de) * | 1999-02-26 | 2000-08-31 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Vinylestern aus Butenoligomeren |
| WO2000063151A1 (de) * | 1999-04-21 | 2000-10-26 | Basf Aktiengesellschaft | Gemisch von diestern der adipin- oder phthalsäure mit isomeren nonanolen |
| ATE205509T1 (de) * | 1999-12-23 | 2001-09-15 | Basf Ag | Mit isomeren nonanolen abgeschlossene polyester, verfahren zu ihrer herstellung und ihre verwendung als weichmacher |
| DE10003482A1 (de) * | 2000-01-27 | 2001-08-02 | Basf Ag | Verfahren zur Herstellung von C9-Alkoholen und Verfahren zur integrierten Herstellung von C9-Alkoholen und C10-Alkoholen |
| DE10135906A1 (de) | 2001-07-24 | 2003-02-06 | Oxeno Olefinchemie Gmbh | Verfahren zur Hydroformylierung von höheren Olefinen mit Kobaltverbindungen als Katalysator |
| EP1680388A1 (en) * | 2003-10-15 | 2006-07-19 | Shell International Research Maatschappij B.V. | Preparation of branched aliphatic alcohols using combined process streams from a hydrogenation unit and a dehydrogenation-isomerization unit |
| 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 |
| CN1993309B (zh) | 2004-08-04 | 2010-11-10 | 埃克森美孚化学专利公司 | C8-c10醇的混合物以及衍生的增塑剂和表面活性剂 |
| DE102004059292A1 (de) | 2004-12-09 | 2006-06-14 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Alkoholen aus Olefinen durch Hydroformylierung und Hydrierung |
| DE102004059293A1 (de) | 2004-12-09 | 2006-06-14 | Oxeno Olefinchemie Gmbh | Verfahren zur Hydroformylierung von Olefinen |
| 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 |
| KR101757936B1 (ko) | 2008-12-16 | 2017-07-13 | 바스프 에스이 | 카르복실산 에스테르의 제조 방법 |
| EP2379482B1 (de) | 2008-12-16 | 2015-08-26 | Basf Se | Herstellung von carbonsäureestern unter strippen mit alkohol-dampf |
| 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 |
| PT2576674E (pt) | 2010-06-01 | 2014-10-09 | Basf Se | Método para a produção de composições de polímero de estireno expansíveis |
| US9643902B2 (en) | 2010-12-07 | 2017-05-09 | Exxonmobil Chemical Patents Inc. | Processes utilizing solvent extraction |
| US9428427B2 (en) | 2011-07-25 | 2016-08-30 | Exxonmobil Chemical Patents Inc. | Process for nitrile removal from hydrocarbon feeds |
| WO2013013885A2 (en) | 2011-07-25 | 2013-01-31 | 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 |
| WO2013013887A2 (en) | 2011-07-25 | 2013-01-31 | Exxonmobil Chemical Patents Inc. | Olefin oligomerization process |
| US9550705B2 (en) | 2011-07-25 | 2017-01-24 | Exxonmobill 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 |
| US9932292B2 (en) | 2014-08-01 | 2018-04-03 | Basf Se | Process for workup of a crude ester comprising esterification catalyst hydrolysis product in suspended particulate form |
| ZA201801183B (en) | 2017-02-27 | 2019-01-30 | Evonik Degussa Gmbh | Selective oligomerization of olefins |
| PL3931175T3 (pl) | 2019-02-25 | 2024-07-29 | Basf Se | Sposób przetwarzania estrów kwasu benzenopolikarboksylowego i ich zastosowanie do wytwarzania estrów kwasu cykloheksanopolikarboksylowego |
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 CA CA002103587A patent/CA2103587C/en not_active Expired - Fee Related
- 1992-02-04 CZ CS931620A patent/CZ162093A3/cs unknown
- 1992-02-04 JP JP4503521A patent/JPH06504994A/ja active Pending
- 1992-02-04 RU RU9293051536A patent/RU2094420C1/ru active
- 1992-02-04 EP EP92903627A patent/EP0570411B1/en not_active Expired - Lifetime
- 1992-02-04 BR BR9205595A patent/BR9205595A/pt not_active Application Discontinuation
- 1992-02-04 AU AU11842/92A patent/AU661987B2/en not_active Ceased
- 1992-02-04 WO PCT/EP1992/000245 patent/WO1992013818A1/en not_active Ceased
- 1992-02-04 SK SK842-93A patent/SK84293A3/sk unknown
- 1992-02-04 SG SG1996005601A patent/SG43211A1/en unknown
- 1992-02-04 HU HU9302272A patent/HUT64936A/hu unknown
- 1992-02-04 KR KR1019930702326A patent/KR930703225A/ko not_active Ceased
- 1992-02-04 AT AT92903627T patent/ATE142190T1/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE69213435T2 (de) | 1997-02-13 |
| MY110784A (en) | 1999-04-30 |
| AU1184292A (en) | 1992-09-07 |
| EP0570411A1 (en) | 1993-11-24 |
| SK84293A3 (en) | 1994-04-06 |
| DE69213435D1 (de) | 1996-10-10 |
| RU2094420C1 (ru) | 1997-10-27 |
| CA2103587A1 (en) | 1992-08-07 |
| ATE142190T1 (de) | 1996-09-15 |
| SG43211A1 (en) | 1997-10-17 |
| JPH06504994A (ja) | 1994-06-09 |
| KR930703225A (ko) | 1993-11-29 |
| EP0570411B1 (en) | 1996-09-04 |
| BR9205595A (pt) | 1994-05-03 |
| WO1992013818A1 (en) | 1992-08-20 |
| HUT64936A (en) | 1994-03-28 |
| CA2103587C (en) | 2003-09-16 |
| TW213446B (cg-RX-API-DMAC10.html) | 1993-09-21 |
| GB9102513D0 (en) | 1991-03-27 |
| HU9302272D0 (en) | 1993-11-29 |
| AU661987B2 (en) | 1995-08-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2103587C (en) | Alcohol production | |
| EP1993981B1 (en) | Oligomerization of isobutene-containing feedstocks | |
| US9260355B2 (en) | Production of propylene via simultaneous dehydration and skeletal isomerisation of isobutanol on acid catalysts followed by metathesis | |
| US7112711B2 (en) | Alkene oligomerization process | |
| EA008481B1 (ru) | Олигомеризация олефинов | |
| JP2011042799A (ja) | オリゴマー化反応の生成物の分岐度を制御する方法 | |
| AU685472B2 (en) | Process for reducing the degree of branching of branched olefins | |
| KR100902694B1 (ko) | 개선된 연성의 에스테르를 제공하는 α,α-분지 알칸카르복시산의 합성을 위한 제조방법 | |
| CA2211306A1 (en) | Process for preparing butene oligomers from field butanes | |
| WO2012084950A1 (en) | Production of fuel additives via simultaneous dehydration and skeletal isomerisation of isobutanol on acid catalysts followed by etherification | |
| KR102758359B1 (ko) | 감소된 올레핀 함량을 갖는 스트림을 사용한 올레핀의 올리고머화 방법 | |
| JP2021031495A (ja) | 最適化された蒸留によるオレフィンのオリゴマー化のプロセス | |
| KR20200131761A (ko) | 올리고머화되는 탄화수소 스트림에서 올리고머 함량을 조절하는 올레핀의 올리고머화 방법 | |
| WO2004035530A2 (de) | Verfahren zur herstellung von alkylarylsulfonaten |