NO860523L - Fremgangsmaate for fremstilling av olefiner. - Google Patents
Fremgangsmaate for fremstilling av olefiner.Info
- Publication number
- NO860523L NO860523L NO860523A NO860523A NO860523L NO 860523 L NO860523 L NO 860523L NO 860523 A NO860523 A NO 860523A NO 860523 A NO860523 A NO 860523A NO 860523 L NO860523 L NO 860523L
- Authority
- NO
- Norway
- Prior art keywords
- reactant
- olefins
- lies
- fraction
- methanol
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 72
- 238000006243 chemical reaction Methods 0.000 claims description 30
- 239000003054 catalyst Substances 0.000 claims description 24
- 229930195733 hydrocarbon Natural products 0.000 claims description 20
- 150000002430 hydrocarbons Chemical class 0.000 claims description 20
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 18
- 150000001336 alkenes Chemical class 0.000 claims description 16
- 239000000376 reactant Substances 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 12
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 12
- 239000011148 porous material Substances 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 229910052680 mordenite Inorganic materials 0.000 claims description 7
- 239000011230 binding agent Substances 0.000 claims description 3
- 239000004927 clay Substances 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000000047 product Substances 0.000 description 9
- 238000004064 recycling Methods 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000003197 catalytic 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
- 239000010457 zeolite Substances 0.000 description 4
- 229910021536 Zeolite Inorganic materials 0.000 description 3
- 229910000323 aluminium silicate Inorganic materials 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 238000004230 steam cracking Methods 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 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
- 239000004743 Polypropylene Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 235000013844 butane Nutrition 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 238000005194 fractionation 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
- 230000006872 improvement Effects 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical class CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
- C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- C07C2529/18—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type
-
- 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
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8502339A FR2577549B1 (fr) | 1985-02-15 | 1985-02-15 | Procede de conversion de methanol ou de dimethylether en olefines |
Publications (1)
Publication Number | Publication Date |
---|---|
NO860523L true NO860523L (no) | 1986-08-18 |
Family
ID=9316399
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO860523A NO860523L (no) | 1985-02-15 | 1986-02-13 | Fremgangsmaate for fremstilling av olefiner. |
Country Status (9)
Country | Link |
---|---|
AU (1) | AU586222B2 (fr) |
CA (1) | CA1252801A (fr) |
DE (1) | DE3604636C2 (fr) |
FR (1) | FR2577549B1 (fr) |
GB (1) | GB2171718B (fr) |
NL (1) | NL191648C (fr) |
NO (1) | NO860523L (fr) |
NZ (1) | NZ215131A (fr) |
ZA (1) | ZA861102B (fr) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4752651A (en) * | 1986-06-16 | 1988-06-21 | Union Carbide Corporation | Production of light olefins |
FR2633924B1 (fr) * | 1988-07-06 | 1991-01-11 | Inst Francais Du Petrole | Catalyseur a base de mordenite et son utilisation dans un procede de transformation du methanol en olefines legeres |
DE4009459A1 (de) * | 1990-03-23 | 1991-09-26 | Metallgesellschaft Ag | Verfahren zur erzeugung von niederen olefinen |
GB9024342D0 (en) * | 1990-11-08 | 1990-12-19 | British Petroleum Co Plc | Process for the preparation of branched olefins |
GB9024343D0 (en) * | 1990-11-08 | 1990-12-19 | British Petroleum Co Plc | Process for the preparation of branched olefins |
DE4405876A1 (de) * | 1994-02-23 | 1995-10-05 | Sued Chemie Ag | Katalysator- bzw. Katalysatorträger-Formkörper |
US6455749B1 (en) * | 1997-10-03 | 2002-09-24 | Exxonmobil Chemical Patents, Inc. | Method for increasing light olefin yield by conversion of a heavy hydrocarbon fraction of a product to light olefins |
US6797851B2 (en) | 2001-08-30 | 2004-09-28 | Exxonmobil Chemical Patents Inc. | Two catalyst process for making olefin |
US7084319B2 (en) * | 2003-12-05 | 2006-08-01 | Exxonmobil Chemical Patents Inc. | Catalyst fluidization in oxygenate to olefin reaction systems |
US7663012B2 (en) | 2004-06-25 | 2010-02-16 | Uop Llc | Conversion of dimethylether to propylene using moving bed technology |
US7371915B1 (en) | 2004-06-25 | 2008-05-13 | Uop Llc | Conversion of oxygenate to propylene using moving bed technology |
US7371916B1 (en) | 2004-09-16 | 2008-05-13 | Uop Llc | Conversion of an alcoholic oxygenate to propylene using moving bed technology and an etherification step |
US7405337B2 (en) | 2004-09-21 | 2008-07-29 | Uop Llc | Conversion of oxygenate to propylene with selective hydrogen treatment of heavy olefin recycle stream |
US7408092B2 (en) * | 2004-11-12 | 2008-08-05 | Uop Llc | Selective conversion of oxygenate to propylene using moving bed technology and a hydrothermally stabilized dual-function catalyst |
US7465845B2 (en) * | 2004-12-22 | 2008-12-16 | Exxonmobil Chemical Patents Inc. | Increasing ethylene and/or propylene production in an oxygenate to olefins reaction systems |
US7414167B2 (en) | 2005-01-14 | 2008-08-19 | Uop Llc | Conversion of oxygenate to propylene using moving bed technology and a separate heavy olefin interconversion step |
DE102005015923B4 (de) * | 2005-04-06 | 2014-12-04 | Air Liquide Global E&C Solutions Germany Gmbh | Verfahren zur Herstellung von C2- bis C4-Olefinen aus einem Oxygenate und Wasserdampf enthaltenden Einsatzstrom |
US7744746B2 (en) | 2006-03-31 | 2010-06-29 | Exxonmobil Research And Engineering Company | FCC catalyst stripper configuration |
EP2004776A1 (fr) | 2006-03-31 | 2008-12-24 | ExxonMobil Chemical Patents Inc. | Récupération de produits dans des réacteurs gaz-solide |
CN101130469B (zh) * | 2006-08-23 | 2011-04-13 | 中国科学院大连化学物理研究所 | 一种甲醇制取低碳烯烃过程中再生热量的回收方法 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2928922A1 (de) * | 1979-07-18 | 1981-02-12 | Hoechst Ag | Verfahren zur herstellung niederer olefine aus methanol-wasser-gemischen |
AU546815B2 (en) * | 1980-12-05 | 1985-09-19 | Commonwealth Scientific And Industrial Research Organisation | Methanol conversion to hydrocarbons with zeolites and co-catalysts |
NZ199034A (en) * | 1980-12-05 | 1984-11-09 | Ici Australia Ltd | Production of hydrocarbons from a feed containing methanol,water and a promotor passed over aluminosilicate |
DE3048084A1 (de) * | 1980-12-19 | 1982-07-15 | EC Erdölchemie GmbH, 5000 Köln | Verfahren zur herstellung von tertiaeren olefinen |
FR2519335B1 (fr) * | 1982-01-04 | 1986-05-02 | Azote & Prod Chim | Production d'hydrocarbures a partir de methanol en presence de catalyseurs du type zeolithe |
-
1985
- 1985-02-15 FR FR8502339A patent/FR2577549B1/fr not_active Expired
-
1986
- 1986-02-05 NL NL8600277A patent/NL191648C/xx not_active IP Right Cessation
- 1986-02-12 NZ NZ215131A patent/NZ215131A/en unknown
- 1986-02-13 NO NO860523A patent/NO860523L/no unknown
- 1986-02-14 GB GB08603630A patent/GB2171718B/en not_active Expired
- 1986-02-14 CA CA000501894A patent/CA1252801A/fr not_active Expired
- 1986-02-14 ZA ZA861102A patent/ZA861102B/xx unknown
- 1986-02-14 AU AU53679/86A patent/AU586222B2/en not_active Ceased
- 1986-02-14 DE DE3604636A patent/DE3604636C2/de not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
DE3604636A1 (de) | 1986-08-21 |
GB2171718A (en) | 1986-09-03 |
ZA861102B (en) | 1987-06-24 |
NZ215131A (en) | 1988-05-30 |
FR2577549B1 (fr) | 1987-03-20 |
CA1252801A (fr) | 1989-04-18 |
AU586222B2 (en) | 1989-07-06 |
GB2171718B (en) | 1988-10-12 |
GB8603630D0 (en) | 1986-03-19 |
NL8600277A (nl) | 1986-09-01 |
DE3604636C2 (de) | 1996-04-04 |
NL191648C (nl) | 1995-12-02 |
NL191648B (nl) | 1995-08-01 |
AU5367986A (en) | 1986-08-21 |
FR2577549A1 (fr) | 1986-08-22 |
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