ZA200400953B - Process for producing branched olefins from linear olefin/paraffin feed. - Google Patents
Process for producing branched olefins from linear olefin/paraffin feed. Download PDFInfo
- Publication number
- ZA200400953B ZA200400953B ZA200400953A ZA200400953A ZA200400953B ZA 200400953 B ZA200400953 B ZA 200400953B ZA 200400953 A ZA200400953 A ZA 200400953A ZA 200400953 A ZA200400953 A ZA 200400953A ZA 200400953 B ZA200400953 B ZA 200400953B
- Authority
- ZA
- South Africa
- Prior art keywords
- olefins
- feed
- linear
- isomerisation
- stage
- Prior art date
Links
- 150000001336 alkenes Chemical class 0.000 title claims description 93
- 238000000034 method Methods 0.000 title claims description 43
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims description 42
- 239000012188 paraffin wax Substances 0.000 title claims description 17
- 238000006317 isomerization reaction Methods 0.000 claims description 52
- 239000003054 catalyst Substances 0.000 claims description 32
- 238000006356 dehydrogenation reaction Methods 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 21
- 238000000926 separation method Methods 0.000 claims description 20
- 239000003599 detergent Substances 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 230000029936 alkylation Effects 0.000 claims description 6
- 238000005804 alkylation reaction Methods 0.000 claims description 6
- 238000007037 hydroformylation reaction Methods 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 230000003197 catalytic effect Effects 0.000 claims description 4
- 150000001993 dienes Chemical class 0.000 claims description 4
- 239000012535 impurity Substances 0.000 claims description 3
- 239000010687 lubricating oil Substances 0.000 claims description 3
- 150000005673 monoalkenes Chemical class 0.000 claims description 3
- 238000007710 freezing Methods 0.000 claims description 2
- 230000008014 freezing Effects 0.000 claims description 2
- 239000000047 product Substances 0.000 description 23
- 239000010457 zeolite Substances 0.000 description 12
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 10
- 229910001657 ferrierite group Inorganic materials 0.000 description 8
- 229910021536 Zeolite Inorganic materials 0.000 description 7
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 239000003921 oil Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 4
- 239000003463 adsorbent Substances 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 239000011491 glass wool Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 229910021641 deionized water Inorganic materials 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002808 molecular sieve Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 3
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 3
- 229910010271 silicon carbide Inorganic materials 0.000 description 3
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 3
- 238000006277 sulfonation reaction Methods 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 238000007046 ethoxylation reaction Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 description 2
- 229910052809 inorganic oxide Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- GGQQNYXPYWCUHG-RMTFUQJTSA-N (3e,6e)-deca-3,6-diene Chemical compound CCC\C=C\C\C=C\CC GGQQNYXPYWCUHG-RMTFUQJTSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- VXAUWWUXCIMFIM-UHFFFAOYSA-M aluminum;oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Al+3] VXAUWWUXCIMFIM-UHFFFAOYSA-M 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- AQBOUNVXZQRXNP-UHFFFAOYSA-L azane;dichloropalladium Chemical compound N.N.N.N.Cl[Pd]Cl AQBOUNVXZQRXNP-UHFFFAOYSA-L 0.000 description 1
- 229910001680 bayerite Inorganic materials 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 229910052663 cancrinite Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052878 cordierite Inorganic materials 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000005342 ion exchange Methods 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
- 239000003350 kerosene Substances 0.000 description 1
- 229910001711 laumontite Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 229910052680 mordenite Inorganic materials 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052678 stilbite Inorganic materials 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/23—Rearrangement of carbon-to-carbon unsaturated bonds
- C07C5/25—Migration of carbon-to-carbon double bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/02—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof
- C07C303/04—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups
- C07C303/06—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups by reaction with sulfuric acid or sulfur trioxide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C11/00—Aliphatic unsaturated hydrocarbons
- C07C11/02—Alkenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/02—Monocyclic hydrocarbons
- C07C15/107—Monocyclic hydrocarbons having saturated side-chain containing at least six carbon atoms, e.g. detergent alkylates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/27—Rearrangement of carbon atoms in the hydrocarbon skeleton
- C07C5/2767—Changing the number of side-chains
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01306995 | 2001-08-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200400953B true ZA200400953B (en) | 2004-10-18 |
Family
ID=8182198
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200400953A ZA200400953B (en) | 2001-08-17 | 2004-02-05 | Process for producing branched olefins from linear olefin/paraffin feed. |
Country Status (14)
Country | Link |
---|---|
US (3) | US7157613B2 (pt) |
EP (1) | EP1421048A1 (pt) |
JP (1) | JP4263599B2 (pt) |
KR (1) | KR100905809B1 (pt) |
CN (1) | CN100447115C (pt) |
AR (1) | AR035467A1 (pt) |
AU (1) | AU2002340811B2 (pt) |
BR (1) | BR0211897B1 (pt) |
MX (1) | MXPA04001319A (pt) |
MY (1) | MY140827A (pt) |
NZ (1) | NZ530984A (pt) |
RU (1) | RU2294915C2 (pt) |
WO (1) | WO2003016249A1 (pt) |
ZA (1) | ZA200400953B (pt) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ530984A (en) | 2001-08-17 | 2005-07-29 | Shell Int Research | Process for producing branched olefins from linear olefin / paraffin feed |
US6815570B1 (en) * | 2002-05-07 | 2004-11-09 | Uop Llc | Shaped catalysts for transalkylation of aromatics for enhanced xylenes production |
US8207380B2 (en) | 2007-04-27 | 2012-06-26 | Chevron Oronite LLC | Alkylated hydroxyaromatic compound substantially free of endocrine disruptive chemicals and method of making the same |
US8193111B2 (en) * | 2009-07-24 | 2012-06-05 | Uop Llc | Process or system for desorbing an adsorbent bed |
US8486877B2 (en) | 2009-11-18 | 2013-07-16 | Chevron Oronite Company Llc | Alkylated hydroxyaromatic compound substantially free of endocrine disruptive chemicals |
US20110118517A1 (en) * | 2009-11-19 | 2011-05-19 | Uop Llc | Manufacturing Process for Branched and Linear Alkylated Benzene as Precursor for Enhanced Oil Recovery Surfactant |
EP2186783A3 (en) * | 2010-01-27 | 2010-09-01 | Shell Internationale Research Maatschappij B.V. | Process for the preparation of olefins |
CN109126779B (zh) * | 2018-08-03 | 2020-11-20 | 北京化工大学 | 一种小分子多碳直链烯烃烷烃化及异构化可控制备方法 |
CN110639426A (zh) * | 2019-10-10 | 2020-01-03 | 太原理工大学 | 一种支链烷基磺酸盐表面活性剂及其制备工艺 |
TW202124340A (zh) * | 2019-10-18 | 2021-07-01 | 日商出光興產股份有限公司 | 丙烯低聚物之製造方法 |
CN114075452B (zh) * | 2020-08-14 | 2023-06-09 | 国家能源投资集团有限责任公司 | 直链烯烃的异构化方法 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US556959A (en) * | 1896-03-24 | Means for attaching and detaching electric lamps | ||
US3169987A (en) * | 1960-12-30 | 1965-02-16 | Universal Oil Prod Co | Alkaryl sulfonate production via n-olefin isomerization |
US3830870A (en) * | 1973-03-05 | 1974-08-20 | Dow Chemical Co | Method of isomerizing butene-1 to butene-2 |
DE3427979A1 (de) * | 1984-07-28 | 1986-01-30 | Basf Ag, 6700 Ludwigshafen | Verfahren zur gewinnung von 2-butenen aus 1-buten und gegebenenfalls 2-butene enthaltenden c(pfeil abwaerts)4(pfeil abwaerts)-kohlenwasserstoffgemischen |
US4773622A (en) * | 1987-07-07 | 1988-09-27 | Graphics 3, Inc. | Self-erecting display device |
US5516959A (en) * | 1991-09-16 | 1996-05-14 | Mobil Oil Corporation | Highly selective n-olefin isomerization process using ZSM-35 |
US5849960A (en) * | 1996-11-26 | 1998-12-15 | Shell Oil Company | Highly branched primary alcohol compositions, and biodegradable detergents made therefrom |
US6111158A (en) * | 1999-03-04 | 2000-08-29 | Uop Llc | Process for producing arylalkanes at alkylation conditions using a zeolite having a NES zeolite structure type |
US6187981B1 (en) * | 1999-07-19 | 2001-02-13 | Uop Llc | Process for producing arylalkanes and arylalkane sulfonates, compositions produced therefrom, and uses thereof |
NZ530984A (en) | 2001-08-17 | 2005-07-29 | Shell Int Research | Process for producing branched olefins from linear olefin / paraffin feed |
-
2002
- 2002-08-07 NZ NZ530984A patent/NZ530984A/en unknown
- 2002-08-07 CN CNB028161149A patent/CN100447115C/zh not_active Expired - Fee Related
- 2002-08-07 KR KR1020047002307A patent/KR100905809B1/ko not_active IP Right Cessation
- 2002-08-07 JP JP2003521178A patent/JP4263599B2/ja not_active Expired - Fee Related
- 2002-08-07 EP EP02774506A patent/EP1421048A1/en not_active Withdrawn
- 2002-08-07 MX MXPA04001319A patent/MXPA04001319A/es active IP Right Grant
- 2002-08-07 RU RU2004107796/04A patent/RU2294915C2/ru not_active IP Right Cessation
- 2002-08-07 BR BRPI0211897-1A patent/BR0211897B1/pt not_active IP Right Cessation
- 2002-08-07 WO PCT/EP2002/008884 patent/WO2003016249A1/en active IP Right Grant
- 2002-08-07 AU AU2002340811A patent/AU2002340811B2/en not_active Ceased
- 2002-08-14 US US10/218,732 patent/US7157613B2/en not_active Expired - Fee Related
- 2002-08-15 MY MYPI20023019A patent/MY140827A/en unknown
- 2002-08-16 AR ARP020103100A patent/AR035467A1/es not_active Application Discontinuation
-
2004
- 2004-02-05 ZA ZA200400953A patent/ZA200400953B/en unknown
-
2006
- 2006-09-28 US US11/540,529 patent/US7414161B2/en not_active Expired - Fee Related
-
2008
- 2008-06-06 US US12/134,811 patent/US7560605B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP1421048A1 (en) | 2004-05-26 |
US7157613B2 (en) | 2007-01-02 |
US20080242748A1 (en) | 2008-10-02 |
US20030097030A1 (en) | 2003-05-22 |
RU2004107796A (ru) | 2005-10-10 |
JP4263599B2 (ja) | 2009-05-13 |
RU2294915C2 (ru) | 2007-03-10 |
CN100447115C (zh) | 2008-12-31 |
BR0211897A (pt) | 2004-09-21 |
AU2002340811B2 (en) | 2006-10-19 |
US7560605B2 (en) | 2009-07-14 |
BR0211897B1 (pt) | 2012-12-25 |
KR20040032923A (ko) | 2004-04-17 |
US20070021628A1 (en) | 2007-01-25 |
JP2005500376A (ja) | 2005-01-06 |
MXPA04001319A (es) | 2004-05-20 |
WO2003016249A1 (en) | 2003-02-27 |
MY140827A (en) | 2010-01-29 |
AR035467A1 (es) | 2004-05-26 |
NZ530984A (en) | 2005-07-29 |
US7414161B2 (en) | 2008-08-19 |
CN1543448A (zh) | 2004-11-03 |
KR100905809B1 (ko) | 2009-07-02 |
WO2003016249A8 (en) | 2004-03-18 |
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