NO324730B1 - Fremgangsmate for omdannelse av et oksygenatramateriale til olefiner. - Google Patents

Fremgangsmate for omdannelse av et oksygenatramateriale til olefiner. Download PDF

Info

Publication number: NO324730B1
Authority: NO; Norway
Prior art keywords: sapo; temperature; whsv; tcnms; stated
Prior art date: 1996-12-31

Application number

NO19993229A

Other languages

English (en)

Norwegian (no)

Other versions

NO993229L (no

NO993229D0 (no

Inventor

Hsiang-Ning Sun

Stephen N Vaughn

Jr David R Lumgair

Original Assignee

Exxonmobil Chem Patents Inc

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.)

1996-12-31

Filing date

1999-06-29

Publication date

2007-12-03

1999-06-29 Application filed by Exxonmobil Chem Patents Inc filed Critical Exxonmobil Chem Patents Inc

1999-06-29 Publication of NO993229D0 publication Critical patent/NO993229D0/no

1999-08-31 Publication of NO993229L publication Critical patent/NO993229L/no

2007-12-03 Publication of NO324730B1 publication Critical patent/NO324730B1/no

Links

238000000034 method Methods 0.000 title claims description 40
150000001336 alkenes Chemical class 0.000 title claims description 32
239000000463 material Substances 0.000 title description 3
IVAOQJNBYYIDSI-UHFFFAOYSA-N [O].[Na] Chemical compound [O].[Na] IVAOQJNBYYIDSI-UHFFFAOYSA-N 0.000 title 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 49
239000003054 catalyst Substances 0.000 claims description 35
238000006243 chemical reaction Methods 0.000 claims description 24
239000000203 mixture Substances 0.000 claims description 15
125000004432 carbon atom Chemical group C* 0.000 claims description 6
239000002994 raw material Substances 0.000 claims description 6
-1 aliphatic alcohols Chemical class 0.000 claims description 5
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 2
125000001931 aliphatic group Chemical group 0.000 claims description 2
150000001412 amines Chemical class 0.000 claims description 2
150000001728 carbonyl compounds Chemical class 0.000 claims description 2
150000002170 ethers Chemical class 0.000 claims description 2
150000004820 halides Chemical class 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
150000003568 thioethers Chemical class 0.000 claims description 2
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 33
150000001875 compounds Chemical class 0.000 description 16
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 12
239000005977 Ethylene Substances 0.000 description 12
239000000047 product Substances 0.000 description 12
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 11
229920006395 saturated elastomer Polymers 0.000 description 9
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
239000003085 diluting agent Substances 0.000 description 7
239000011148 porous material Substances 0.000 description 7
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
238000004519 manufacturing process Methods 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
239000006227 byproduct Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
229910001868 water Inorganic materials 0.000 description 5
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
239000010779 crude oil Substances 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
239000001569 carbon dioxide Substances 0.000 description 3
229910002092 carbon dioxide Inorganic materials 0.000 description 3
229910002091 carbon monoxide Inorganic materials 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000007789 gas Substances 0.000 description 3
239000011368 organic material Substances 0.000 description 3
230000008929 regeneration Effects 0.000 description 3
238000011069 regeneration method Methods 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
239000003575 carbonaceous material Substances 0.000 description 2
230000003197 catalytic effect Effects 0.000 description 2
LJSQFQKUNVCTIA-UHFFFAOYSA-N diethyl sulfide Chemical compound CCSCC LJSQFQKUNVCTIA-UHFFFAOYSA-N 0.000 description 2
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 2
238000005243 fluidization Methods 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000003701 inert diluent Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
239000010453 quartz Substances 0.000 description 2
238000011084 recovery Methods 0.000 description 2
238000000926 separation method Methods 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
229910000619 316 stainless steel Inorganic materials 0.000 description 1
229910000975 Carbon steel Inorganic materials 0.000 description 1
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 description 1
229910021536 Zeolite Inorganic materials 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
238000009835 boiling Methods 0.000 description 1
238000001354 calcination Methods 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000010962 carbon steel Substances 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
238000004523 catalytic cracking Methods 0.000 description 1
HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
239000003245 coal Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000005336 cracking Methods 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
229960003750 ethyl chloride Drugs 0.000 description 1
238000000855 fermentation Methods 0.000 description 1
230000004151 fermentation Effects 0.000 description 1
238000011049 filling Methods 0.000 description 1
239000000446 fuel Substances 0.000 description 1
239000011491 glass wool Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
229910052734 helium Inorganic materials 0.000 description 1
239000001307 helium Substances 0.000 description 1
SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000003345 natural gas Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
238000005457 optimization Methods 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000012071 phase Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000010454 slate Substances 0.000 description 1
229910001256 stainless steel alloy Inorganic materials 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000004230 steam cracking Methods 0.000 description 1
150000003463 sulfur Chemical class 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000012808 vapor phase Substances 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000010457 zeolite Substances 0.000 description 1

Classifications

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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
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- C07C1/207—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms from carbonyl compounds
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- C07—ORGANIC CHEMISTRY
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- C—CHEMISTRY; METALLURGY
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- C—CHEMISTRY; METALLURGY
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/40—Ethylene production

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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Oil, Petroleum & Natural Gas (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Crystallography & Structural Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Contacts (AREA)
Oxygen, Ozone, And Oxides In General (AREA)
Catalysts (AREA)

NO19993229A 1996-12-31 1999-06-29 Fremgangsmate for omdannelse av et oksygenatramateriale til olefiner. NO324730B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US3411596P	1996-12-31	1996-12-31
PCT/US1997/023887 WO1998029363A1 (en)	1996-12-31	1997-12-31	Use of short contact time in oxygenate conversion

Publications (3)

Publication Number	Publication Date
NO993229D0 NO993229D0 (no)	1999-06-29
NO993229L NO993229L (no)	1999-08-31
NO324730B1 true NO324730B1 (no)	2007-12-03

Family

ID=21874400

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO19993229A NO324730B1 (no)	1996-12-31	1999-06-29	Fremgangsmate for omdannelse av et oksygenatramateriale til olefiner.

Country Status (19)

Country	Link
US (1)	US5952538A (de)
EP (1)	EP0960085B1 (de)
JP (1)	JP2001507698A (de)
KR (1)	KR100518055B1 (de)
CN (1)	CN1133608C (de)
AR (1)	AR010865A1 (de)
AT (1)	ATE210621T1 (de)
AU (1)	AU731024B2 (de)
BR (1)	BR9713665A (de)
CA (1)	CA2274662C (de)
DE (1)	DE69709175T2 (de)
ES (1)	ES2169883T3 (de)
ID (1)	ID22538A (de)
MY (1)	MY129420A (de)
NO (1)	NO324730B1 (de)
SA (1)	SA98181084B1 (de)
TW (1)	TW444002B (de)
WO (1)	WO1998029363A1 (de)
ZA (1)	ZA9711648B (de)

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1997
- 1997-06-23 US US08/880,962 patent/US5952538A/en not_active Expired - Lifetime
- 1997-12-17 TW TW086119110A patent/TW444002B/zh not_active IP Right Cessation
- 1997-12-29 MY MYPI97006389A patent/MY129420A/en unknown
- 1997-12-29 AR ARP970106219A patent/AR010865A1/es unknown
- 1997-12-29 ZA ZA9711648A patent/ZA9711648B/xx unknown
- 1997-12-31 AU AU56207/98A patent/AU731024B2/en not_active Expired
- 1997-12-31 BR BR9713665-4A patent/BR9713665A/pt not_active Application Discontinuation
- 1997-12-31 CA CA002274662A patent/CA2274662C/en not_active Expired - Fee Related
- 1997-12-31 ID IDW990595A patent/ID22538A/id unknown
- 1997-12-31 WO PCT/US1997/023887 patent/WO1998029363A1/en not_active Ceased
- 1997-12-31 ES ES97952642T patent/ES2169883T3/es not_active Expired - Lifetime
- 1997-12-31 CN CNB971811024A patent/CN1133608C/zh not_active Expired - Lifetime
- 1997-12-31 EP EP97952642A patent/EP0960085B1/de not_active Expired - Lifetime
- 1997-12-31 JP JP53021398A patent/JP2001507698A/ja not_active Ceased
- 1997-12-31 AT AT97952642T patent/ATE210621T1/de not_active IP Right Cessation
- 1997-12-31 DE DE69709175T patent/DE69709175T2/de not_active Expired - Lifetime
- 1997-12-31 KR KR10-1999-7005884A patent/KR100518055B1/ko not_active Expired - Fee Related
1998
- 1998-04-14 SA SA98181084A patent/SA98181084B1/ar unknown
1999
- 1999-06-29 NO NO19993229A patent/NO324730B1/no unknown

Also Published As

Publication number	Publication date
ID22538A (id)	1999-11-04
US5952538A (en)	1999-09-14
DE69709175T2 (de)	2002-08-14
CA2274662C (en)	2007-06-19
NO993229L (no)	1999-08-31
ATE210621T1 (de)	2001-12-15
MY129420A (en)	2007-03-30
JP2001507698A (ja)	2001-06-12
NO993229D0 (no)	1999-06-29
AU5620798A (en)	1998-07-31
KR100518055B1 (ko)	2005-09-28
CN1241990A (zh)	2000-01-19
ES2169883T3 (es)	2002-07-16
BR9713665A (pt)	2000-04-04
AR010865A1 (es)	2000-07-12
EP0960085A1 (de)	1999-12-01
ZA9711648B (en)	1998-12-07
CA2274662A1 (en)	1998-07-09
TW444002B (en)	2001-07-01
DE69709175D1 (de)	2002-01-24
KR20000062374A (ko)	2000-10-25
SA98181084B1 (ar)	2006-05-20
CN1133608C (zh)	2004-01-07
WO1998029363A1 (en)	1998-07-09
EP0960085B1 (de)	2001-12-12
AU731024B2 (en)	2001-03-22

Publication	Publication Date	Title
AU731024B2 (en)	2001-03-22	Use of short contact time in oxygenate conversion
US5817906A (en)	1998-10-06	Process for producing light olefins using reaction with distillation as an intermediate step
CA2136625C (en)	1999-05-04	Use of acid extracted molecular sieve catalysts in oxygenate conversion
EP0642485B1 (de)	1996-08-14	Verfahren zur herstellung von hochreinen olefinen
US6137022A (en)	2000-10-24	Process for increasing the selectivity of a reaction to convert oxygenates to olefins
US6051746A (en)	2000-04-18	Oxygenate conversions using modified small pore molecular sieve catalysts
RU2165955C2 (ru)	2001-04-27	Трехстадийный способ получения легких олефинов из метана и/или этана
US5932512A (en)	1999-08-03	Fluorination of synthesized molecular sieve catalysts for increased selectivity to ethylene during conversion of oxygenates to olefins
NO321269B1 (no)	2006-04-10	Fremgangsmate for selektiv konvertering av oksygenater til etylen og propylen som er katalysert av en molekylsiktkatalysatorer
EP0876313A1 (de)	1998-11-11	Verwendung und übergangsmetallen enthaltende molekularsieben als katalysatoren bei der umsetzung von säueerstoffverbindungen
NO323919B1 (no)	2007-07-23	Fremgangsmate for fremstilling av et olefinprodukt.
SG172742A1 (en)	2011-07-28	Production of light olefins
AU776126B2 (en)	2004-08-26	Catalyst pretreatment in an oxygenate to olefins reaction system
CN101500707B (zh)	2014-03-12	轻质烯烃的制备
MXPA99006017A (en)	2000-01-21	Use of short contact time in oxygenate conversion
AU726688B2 (en)	2000-11-16	Oxygenate conversions using modified small pore molecular sieve catalysts