NL194802C - Werkwijze voor het voortbrengen van benzine. - Google Patents

Werkwijze voor het voortbrengen van benzine. Download PDF

Info

Publication number: NL194802C
Authority: NL; Netherlands
Prior art keywords: water; methanol; weight; hydrocarbons; gasoline
Prior art date: 1986-01-29

Application number

NL8700218A

Other languages

English (en)

Dutch (nl)

Other versions

NL194802B (nl

NL8700218A (nl

Original Assignee

Labofina Sa

Priority date (The priority date 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 date listed.)

1986-01-29

Filing date

1987-01-29

Publication date

2003-03-04

1987-01-29 Application filed by Labofina Sa filed Critical Labofina Sa

1987-08-17 Publication of NL8700218A publication Critical patent/NL8700218A/nl

2002-11-01 Publication of NL194802B publication Critical patent/NL194802B/xx

2003-03-04 Application granted granted Critical

2003-03-04 Publication of NL194802C publication Critical patent/NL194802C/nl

Links

238000000034 method Methods 0.000 title claims description 42
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 60
229930195733 hydrocarbon Natural products 0.000 claims description 37
150000002430 hydrocarbons Chemical class 0.000 claims description 37
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
239000000203 mixture Substances 0.000 claims description 31
238000006384 oligomerization reaction Methods 0.000 claims description 29
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 25
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical class CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 20
BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims description 20
239000003054 catalyst Substances 0.000 claims description 18
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 17
238000006266 etherification reaction Methods 0.000 claims description 15
239000002808 molecular sieve Substances 0.000 claims description 13
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims description 13
239000011148 porous material Substances 0.000 claims description 9
NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 8
239000000463 material Substances 0.000 claims description 8
150000001336 alkenes Chemical class 0.000 claims description 7
238000001035 drying Methods 0.000 claims description 7
239000000377 silicon dioxide Substances 0.000 claims description 7
150000002170 ethers Chemical class 0.000 claims description 6
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 6
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 5
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
150000001335 aliphatic alkanes Chemical class 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
239000001282 iso-butane Substances 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical class CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 3
239000002253 acid Substances 0.000 claims description 3
229920001577 copolymer Polymers 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 3
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 3
229920005989 resin Polymers 0.000 claims description 3
239000011347 resin Substances 0.000 claims description 3
230000003197 catalytic effect Effects 0.000 claims description 2
238000005342 ion exchange Methods 0.000 claims description 2
GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 claims description 2
239000001294 propane Substances 0.000 claims description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 4
229920001429 chelating resin Polymers 0.000 claims 2
YZUPZGFPHUVJKC-UHFFFAOYSA-N 1-bromo-2-methoxyethane Chemical compound COCCBr YZUPZGFPHUVJKC-UHFFFAOYSA-N 0.000 claims 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
239000004215 Carbon black (E152) Substances 0.000 description 11
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
239000000047 product Substances 0.000 description 9
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
239000010457 zeolite Substances 0.000 description 7
239000013078 crystal Substances 0.000 description 6
238000000926 separation method Methods 0.000 description 6
229910000147 aluminium phosphate Inorganic materials 0.000 description 5
239000007788 liquid Substances 0.000 description 5
235000012239 silicon dioxide Nutrition 0.000 description 5
HVZJRWJGKQPSFL-UHFFFAOYSA-N tert-Amyl methyl ether Chemical compound CCC(C)(C)OC HVZJRWJGKQPSFL-UHFFFAOYSA-N 0.000 description 5
229910021536 Zeolite Inorganic materials 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 4
238000004821 distillation Methods 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
230000002378 acidificating effect Effects 0.000 description 3
229910002026 crystalline silica Inorganic materials 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
229920002125 Sokalan® Polymers 0.000 description 2
239000000654 additive Substances 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
239000006079 antiknock agent Substances 0.000 description 2
235000013844 butane Nutrition 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000000539 dimer Substances 0.000 description 2
239000002245 particle Substances 0.000 description 2
239000012071 phase Substances 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
JFWIOFGVMQJBNT-UHFFFAOYSA-N 2-methoxy-2-methylhexane Chemical compound CCCCC(C)(C)OC JFWIOFGVMQJBNT-UHFFFAOYSA-N 0.000 description 1
WYLQOLGJMFRRLX-UHFFFAOYSA-N 2-methoxy-2-methylpentane Chemical compound CCCC(C)(C)OC WYLQOLGJMFRRLX-UHFFFAOYSA-N 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
229920002367 Polyisobutene Polymers 0.000 description 1
238000007171 acid catalysis Methods 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
238000005899 aromatization reaction Methods 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000000969 carrier Substances 0.000 description 1
238000004523 catalytic cracking Methods 0.000 description 1
238000005341 cation exchange Methods 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000012043 crude product Substances 0.000 description 1
238000010908 decantation Methods 0.000 description 1
230000007423 decrease Effects 0.000 description 1
238000010586 diagram Methods 0.000 description 1
229910003460 diamond Inorganic materials 0.000 description 1
239000010432 diamond Substances 0.000 description 1
239000000284 extract Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000013505 freshwater Substances 0.000 description 1
239000000446 fuel Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003254 gasoline additive Substances 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
238000009434 installation Methods 0.000 description 1
150000002605 large molecules Chemical class 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
238000011068 loading method Methods 0.000 description 1
229920002521 macromolecule Polymers 0.000 description 1
238000005259 measurement Methods 0.000 description 1
230000003606 oligomerizing effect Effects 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000011084 recovery Methods 0.000 description 1
150000003384 small molecules Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
238000004230 steam cracking Methods 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000013638 trimer Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
- C07C2/06—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
- C07C2/08—Catalytic processes
- C07C2/12—Catalytic processes with crystalline alumino-silicates or with catalysts comprising molecular sieves
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
- C10L1/023—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for spark ignition
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/03—Catalysts comprising molecular sieves not having base-exchange properties
- C07C2529/035—Crystalline silica polymorphs, e.g. silicalites

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Crystallography & Structural Chemistry (AREA)
Engineering & Computer Science (AREA)
General Chemical & Material Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Liquid Carbonaceous Fuels (AREA)
Catalysts (AREA)

NL8700218A 1986-01-29 1987-01-29 Werkwijze voor het voortbrengen van benzine. NL194802C (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
LU86280		1986-01-29
LU86280A LU86280A1 (fr)	1986-01-29	1986-01-29	Procede de production d'essence

Publications (3)

Publication Number	Publication Date
NL8700218A NL8700218A (nl)	1987-08-17
NL194802B NL194802B (nl)	2002-11-01
NL194802C true NL194802C (nl)	2003-03-04

Family

ID=19730629

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8700218A NL194802C (nl)	1986-01-29	1987-01-29	Werkwijze voor het voortbrengen van benzine.

Country Status (10)

Country	Link
JP (1)	JP2569319B2 (de)
BE (1)	BE1000417A4 (de)
CA (1)	CA1334105C (de)
DE (1)	DE3702630C2 (de)
ES (1)	ES2003683A6 (de)
FR (1)	FR2593513B1 (de)
GB (1)	GB2185754B (de)
IT (1)	IT1202447B (de)
LU (1)	LU86280A1 (de)
NL (1)	NL194802C (de)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8623260D0 (en) *	1986-09-26	1986-10-29	British Petroleum Co Plc	Gasoline components
US4754096A (en) *	1987-07-13	1988-06-28	Mobil Oil Corporation	Production of high viscosity index lubricating oils from lower olefins
US4788365A (en) *	1987-12-08	1988-11-29	Mobil Oil Corporation	High octane gasoline and distillates from oxygenates
US4886925A (en) *	1988-05-02	1989-12-12	Mobil Oil Corp	Olefins interconversion and etherification process
US5080691A (en) *	1990-04-04	1992-01-14	Mobil Oil Corp.	Process for the conversion of light olefins to ether-rich gasoline
ZA93594B (en) *	1992-01-30	1993-08-31	Exxon Chemical Patents Inc	Alkene oligomerisation.
US5260493A (en) *	1992-07-02	1993-11-09	Mobil Oil Corporation	Effluent treatment for ether production
US7838708B2 (en)	2001-06-20	2010-11-23	Grt, Inc.	Hydrocarbon conversion process improvements
US20050171393A1 (en)	2003-07-15	2005-08-04	Lorkovic Ivan M.	Hydrocarbon synthesis
WO2005021468A1 (en)	2003-07-15	2005-03-10	Grt, Inc.	Hydrocarbon synthesis
US20080275284A1 (en)	2004-04-16	2008-11-06	Marathon Oil Company	Process for converting gaseous alkanes to liquid hydrocarbons
US8642822B2 (en)	2004-04-16	2014-02-04	Marathon Gtf Technology, Ltd.	Processes for converting gaseous alkanes to liquid hydrocarbons using microchannel reactor
US20060100469A1 (en)	2004-04-16	2006-05-11	Waycuilis John J	Process for converting gaseous alkanes to olefins and liquid hydrocarbons
US7244867B2 (en)	2004-04-16	2007-07-17	Marathon Oil Company	Process for converting gaseous alkanes to liquid hydrocarbons
US7674941B2 (en)	2004-04-16	2010-03-09	Marathon Gtf Technology, Ltd.	Processes for converting gaseous alkanes to liquid hydrocarbons
US8173851B2 (en)	2004-04-16	2012-05-08	Marathon Gtf Technology, Ltd.	Processes for converting gaseous alkanes to liquid hydrocarbons
UA95943C2 (ru)	2006-02-03	2011-09-26	ДжиАрТи, ИНК.	Отделение легких газов от галогенов
EP1993979A4 (de)	2006-02-03	2011-07-06	Grt Inc	Kontinuierliches verfahren zur umwandlung von erdgas in flüssige kohlenwasserstoffe
EA017699B1 (ru)	2007-05-24	2013-02-28	Грт, Инк.	Зонный реактор с обратимым захватыванием и высвобождением галогеноводородов
US8282810B2 (en)	2008-06-13	2012-10-09	Marathon Gtf Technology, Ltd.	Bromine-based method and system for converting gaseous alkanes to liquid hydrocarbons using electrolysis for bromine recovery
SG192538A1 (en)	2008-07-18	2013-08-30	Grt Inc	Continuous process for converting natural gas to liquid hydrocarbons
US8198495B2 (en)	2010-03-02	2012-06-12	Marathon Gtf Technology, Ltd.	Processes and systems for the staged synthesis of alkyl bromides
US8367884B2 (en)	2010-03-02	2013-02-05	Marathon Gtf Technology, Ltd.	Processes and systems for the staged synthesis of alkyl bromides
US8815050B2 (en)	2011-03-22	2014-08-26	Marathon Gtf Technology, Ltd.	Processes and systems for drying liquid bromine
US8436220B2 (en)	2011-06-10	2013-05-07	Marathon Gtf Technology, Ltd.	Processes and systems for demethanization of brominated hydrocarbons
US8829256B2 (en)	2011-06-30	2014-09-09	Gtc Technology Us, Llc	Processes and systems for fractionation of brominated hydrocarbons in the conversion of natural gas to liquid hydrocarbons
US8802908B2 (en)	2011-10-21	2014-08-12	Marathon Gtf Technology, Ltd.	Processes and systems for separate, parallel methane and higher alkanes' bromination
US9193641B2 (en)	2011-12-16	2015-11-24	Gtc Technology Us, Llc	Processes and systems for conversion of alkyl bromides to higher molecular weight hydrocarbons in circulating catalyst reactor-regenerator systems

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2944457A1 (de) *	1979-11-03	1981-05-14	EC Erdölchemie GmbH, 5000 Köln	Verfahren zur herstellung eines gemisches, bestehend im wesentlichen aus iso-buten-oligomeren und methyl-tert.-butyl-ether, seine verwendung und treibstoffe, enthaltend ein solches gemisch
FR2477570A1 (fr) *	1980-03-10	1981-09-11	Inst Francais Du Petrole	Hydrogenation et etherification d'une coupe insaturee c5 d'hydrocarbures en vue d'en ameliorer l'indice d'octane et d'en reduire la teneur en mono-olefines
US4417088A (en) *	1981-09-25	1983-11-22	Chevron Research Company	Oligomerization of liquid olefins
DE3148109A1 (de) *	1981-12-04	1983-06-09	EC Erdölchemie GmbH, 5000 Köln	Verfahren zur herstellung von methyl-tert.-butylether (mtbe) und weitgehend von i-buten und vom methanol befreiten kohlenwasserstoff-raffinaten
FR2547830B1 (fr) *	1983-06-22	1988-04-08	Inst Francais Du Petrole	Procede de production de supercarburant par polymerisation des coupes c4
NZ209388A (en) *	1983-09-19	1987-02-20	Mobil Oil Corp	Two-stage process for converting olefinic components in feedstock to high viscosity index lubricating oils using zeolite catalyst
US4538012A (en) *	1984-02-27	1985-08-27	Chevron Research Company	Oligomerization of liquid olefin over a nickel-containing silicaceous crystalline molecular sieve
FR2565991B1 (fr) *	1984-06-18	1986-10-03	Inst Francais Du Petrole	Procede de valorisation d'essences olefiniques par etherification

1986
- 1986-01-29 LU LU86280A patent/LU86280A1/fr unknown
1987
- 1987-01-23 BE BE8700040A patent/BE1000417A4/fr not_active IP Right Cessation
- 1987-01-28 JP JP62016310A patent/JP2569319B2/ja not_active Expired - Lifetime
- 1987-01-28 ES ES8700315A patent/ES2003683A6/es not_active Expired
- 1987-01-28 CA CA000528338A patent/CA1334105C/en not_active Expired - Lifetime
- 1987-01-28 GB GB8701865A patent/GB2185754B/en not_active Expired
- 1987-01-29 FR FR878701073A patent/FR2593513B1/fr not_active Expired - Fee Related
- 1987-01-29 IT IT19199/87A patent/IT1202447B/it active
- 1987-01-29 DE DE3702630A patent/DE3702630C2/de not_active Expired - Lifetime
- 1987-01-29 NL NL8700218A patent/NL194802C/nl not_active IP Right Cessation

Also Published As

Publication number	Publication date
GB8701865D0 (en)	1987-03-04
BE1000417A4 (fr)	1988-11-29
JPS62230885A (ja)	1987-10-09
NL194802B (nl)	2002-11-01
CA1334105C (en)	1995-01-24
DE3702630C2 (de)	1997-10-09
IT8719199A0 (it)	1987-01-29
FR2593513B1 (fr)	1991-07-26
NL8700218A (nl)	1987-08-17
FR2593513A1 (fr)	1987-07-31
ES2003683A6 (es)	1988-11-01
JP2569319B2 (ja)	1997-01-08
GB2185754A (en)	1987-07-29
LU86280A1 (fr)	1987-09-03
IT1202447B (it)	1989-02-09
DE3702630A1 (de)	1987-07-30
GB2185754B (en)	1989-12-28

Legal Events

Date	Code	Title	Description
1994-03-01	BA	A request for search or an international-type search has been filed
1994-04-05	BB	A search report has been drawn up
1994-08-01	BC	A request for examination has been filed
2007-04-02	V4	Discontinued because of reaching the maximum lifetime of a patent	Effective date: 20070129

Publication	Publication Date	Title
NL194802C (nl)	2003-03-04	Werkwijze voor het voortbrengen van benzine.
EP1032550B1 (de)	2003-03-26	Verfahren zur oligomerisierung von isobuten
US6376731B1 (en)	2002-04-23	Selective olefin oligomerization
CA2346902C (en)	2010-02-09	Process for dimerizing olefinic hydrocarbon feedstock and producing a fuel component
JP2846109B2 (ja)	1999-01-13	ガソリンおよびエーテルの製造方法
US4544791A (en)	1985-10-01	Process for producing premium gasoline by polymerizing C4 cuts
CZ297855B6 (cs)	2007-04-18	Zpusob selektivní hydrogenace vysoce nenasycenýchsloucenin
US5689033A (en)	1997-11-18	Process for removal of impurities from light paraffin isomerization feedstocks
JPS6154079B2 (de)	1986-11-20
US5198590A (en)	1993-03-30	Hydrocarbon conversion
US6005150A (en)	1999-12-21	Process for the production of butene-1 from a mixture of C4 olefins
US4324938A (en)	1982-04-13	Process for upgrading C4 olefinic cuts
US5171331A (en)	1992-12-15	Process for producing gasoline
US6156947A (en)	2000-12-05	Process for the production of butene-1 from a mixture of C4 olefins
US4357147A (en)	1982-11-02	Diisopropyl ether reversion and oligomerization in isopropanol production
US4575567A (en)	1986-03-11	Adsorbent regeneration in etherification processes
US5659106A (en)	1997-08-19	Catalytic distillation process for mercaptan and olefin removal
US5210327A (en)	1993-05-11	Etherification with skeletal olefin isomerization
JP4537637B2 (ja)	2010-09-01	オレフィンのオリゴマー化
US4575566A (en)	1986-03-11	Adsorbent regeneration in etherification processes
US5399787A (en)	1995-03-21	Olefin isomerization process using etherification feed isomerization
US5792891A (en)	1998-08-11	Integrated process for the production of tame
US5276212A (en)	1994-01-04	Etherification with intermediate skeletal olefin isomerization
US5221776A (en)	1993-06-22	selective isomerization of olefinic hydrocarbons
US4761504A (en)	1988-08-02	Integrated process for high octane alkylation and etherification