NL8204735A - Werkwijze voor het afscheiden van zeer zuiver buteen-1 of een buteen-1/isobuteen-mengsel uit een fractie van koolwaterstoffen met 4 koolstofatomen. - Google Patents
Werkwijze voor het afscheiden van zeer zuiver buteen-1 of een buteen-1/isobuteen-mengsel uit een fractie van koolwaterstoffen met 4 koolstofatomen. Download PDFInfo
- Publication number
- NL8204735A NL8204735A NL8204735A NL8204735A NL8204735A NL 8204735 A NL8204735 A NL 8204735A NL 8204735 A NL8204735 A NL 8204735A NL 8204735 A NL8204735 A NL 8204735A NL 8204735 A NL8204735 A NL 8204735A
- Authority
- NL
- Netherlands
- Prior art keywords
- butene
- distillation column
- column
- fraction
- isobutene
- Prior art date
Links
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 title claims description 75
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 title claims description 60
- 239000000203 mixture Substances 0.000 title claims description 34
- 238000000034 method Methods 0.000 title claims description 12
- -1 CARBON HYDROGEN Chemical class 0.000 title description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title 1
- 229910052799 carbon Inorganic materials 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 title 1
- 239000001257 hydrogen Substances 0.000 title 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 45
- 238000004821 distillation Methods 0.000 claims description 42
- 229930195733 hydrocarbon Natural products 0.000 claims description 27
- 150000002430 hydrocarbons Chemical class 0.000 claims description 25
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 22
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical class CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 21
- 239000002798 polar solvent Substances 0.000 claims description 20
- 238000000895 extractive distillation Methods 0.000 claims description 19
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 18
- 238000009835 boiling Methods 0.000 claims description 12
- 239000001282 iso-butane Substances 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 8
- AQEFLFZSWDEAIP-UHFFFAOYSA-N di-tert-butyl ether Chemical compound CC(C)(C)OC(C)(C)C AQEFLFZSWDEAIP-UHFFFAOYSA-N 0.000 claims description 8
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 7
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 claims description 5
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 4
- 235000013844 butane Nutrition 0.000 claims 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 33
- 239000004215 Carbon black (E152) Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- KOYGZROXUOTUEE-UHFFFAOYSA-N butane;but-1-ene Chemical compound CCCC.CCC=C KOYGZROXUOTUEE-UHFFFAOYSA-N 0.000 description 10
- 235000013847 iso-butane Nutrition 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- 238000006266 etherification reaction Methods 0.000 description 7
- 238000010992 reflux Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 230000002378 acidificating effect Effects 0.000 description 4
- QNRMTGGDHLBXQZ-UHFFFAOYSA-N buta-1,2-diene Chemical compound CC=C=C QNRMTGGDHLBXQZ-UHFFFAOYSA-N 0.000 description 4
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 4
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- WFYPICNXBKQZGB-UHFFFAOYSA-N butenyne Chemical compound C=CC#C WFYPICNXBKQZGB-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 239000003456 ion exchange resin Substances 0.000 description 3
- 229920003303 ion-exchange polymer Polymers 0.000 description 3
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- KDKYADYSIPSCCQ-UHFFFAOYSA-N but-1-yne Chemical compound CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 235000010288 sodium nitrite Nutrition 0.000 description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- OOWFYDWAMOKVSF-UHFFFAOYSA-N 3-methoxypropanenitrile Chemical compound COCCC#N OOWFYDWAMOKVSF-UHFFFAOYSA-N 0.000 description 1
- JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 description 1
- 102100039339 Atrial natriuretic peptide receptor 1 Human genes 0.000 description 1
- SAJVFNKRQKPAFM-UHFFFAOYSA-N C=CCC.C=CCC.CCCC.CCCC Chemical compound C=CCC.C=CCC.CCCC.CCCC SAJVFNKRQKPAFM-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 101000961044 Homo sapiens Atrial natriuretic peptide receptor 1 Proteins 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- IAQRGUVFOMOMEM-ARJAWSKDSA-N cis-but-2-ene Chemical compound C\C=C/C IAQRGUVFOMOMEM-ARJAWSKDSA-N 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229940113088 dimethylacetamide Drugs 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002193 fatty amides Chemical class 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- LCEDQNDDFOCWGG-UHFFFAOYSA-N morpholine-4-carbaldehyde Chemical compound O=CN1CCOCC1 LCEDQNDDFOCWGG-UHFFFAOYSA-N 0.000 description 1
- JSOQIZDOEIKRLY-UHFFFAOYSA-N n-propylnitrous amide Chemical compound CCCNN=O JSOQIZDOEIKRLY-UHFFFAOYSA-N 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000004230 steam cracking Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 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
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- 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
- C10G21/00—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
- C10G21/06—Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents characterised by the solvent used
- C10G21/12—Organic compounds only
- C10G21/20—Nitrogen-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/04—Purification; Separation; Use of additives by distillation
- C07C7/05—Purification; Separation; Use of additives by distillation with the aid of auxiliary compounds
- C07C7/08—Purification; Separation; Use of additives by distillation with the aid of auxiliary compounds by extractive distillation
-
- C—CHEMISTRY; METALLURGY
- 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
- C10G7/00—Distillation of hydrocarbon oils
- C10G7/08—Azeotropic or extractive distillation
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Water Supply & Treatment (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP828882 | 1982-01-22 | ||
| JP57008288A JPS58126820A (ja) | 1982-01-22 | 1982-01-22 | Ｃ↓４炭化水素留分より高純度ブテン−１又はブテン−１／イソブテン混合物の分離方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8204735A true NL8204735A (nl) | 1983-08-16 |
Family
ID=11688982
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8204735A NL8204735A (nl) | 1982-01-22 | 1982-12-07 | Werkwijze voor het afscheiden van zeer zuiver buteen-1 of een buteen-1/isobuteen-mengsel uit een fractie van koolwaterstoffen met 4 koolstofatomen. |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4556461A (OSRAM) |
| JP (1) | JPS58126820A (OSRAM) |
| HU (1) | HU199368B (OSRAM) |
| IT (1) | IT1159826B (OSRAM) |
| NL (1) | NL8204735A (OSRAM) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4558168A (en) * | 1985-06-19 | 1985-12-10 | Air Products And Chemicals, Inc. | Production of high purity butene-1 from an n-butane feedstock |
| FR2673178B1 (fr) * | 1991-02-26 | 1994-02-11 | Institut Francais Petrole | Procede de separation de butanes et de butenes par distillation extractive. |
| FR2674245B1 (fr) * | 1991-03-20 | 1994-05-27 | Inst Francais Du Petrole | Procede de separation de butenes et de butanes par distillation extractive. |
| DE69219624T2 (de) * | 1991-12-20 | 1997-09-11 | Exxon Chemical Patents Inc | Verfahren zur entfernung von grünöl aus kohlenwasserstoffenbeschickungen |
| US5276246A (en) * | 1991-12-23 | 1994-01-04 | Uop | Process for separating normal olefins from non-normal olefins |
| US5446231A (en) * | 1994-01-24 | 1995-08-29 | Chemical Research & Licensing Company | Method for removing contaminants from hydrocarbon streams |
| US5569788A (en) * | 1995-03-20 | 1996-10-29 | Uop | Process for removal of impurities from etherification feedstocks |
| US5763715A (en) * | 1996-10-08 | 1998-06-09 | Stone & Webster Engineering Corp. | Butadiene removal system for ethylene plants with front end hydrogenation systems |
| JP4863186B2 (ja) * | 2005-02-09 | 2012-01-25 | Ｊｘ日鉱日石エネルギー株式会社 | オレフィン重合体の製造方法 |
| RU2338735C1 (ru) * | 2007-04-20 | 2008-11-20 | Открытое акционерное общество Научно-исследовательский институт "Ярсинтез" (ОАО НИИ "Ярсинтез") | Способ выделения изобутилена полимеризационной чистоты |
| KR100836707B1 (ko) * | 2007-04-25 | 2008-06-10 | 한국에너지기술연구원 | 올레핀/파라핀 혼합가스에서 고순도 부텐-1 분리 기술 |
| JP5343041B2 (ja) * | 2010-06-18 | 2013-11-13 | Ｊｘ日鉱日石エネルギー株式会社 | オレフィン重合体の製造方法 |
| CN102452889B (zh) * | 2010-10-22 | 2014-07-09 | 中国石油化工股份有限公司 | 一种采用二甲基甲酰胺及其混合物抽提丁二烯的方法 |
| KR101303403B1 (ko) * | 2011-06-30 | 2013-09-05 | 주식회사 엘지화학 | 병렬 반응기를 이용한 1,3-부타디엔의 제조방법 |
| CN104812725B (zh) | 2012-11-07 | 2016-10-19 | 鲁姆斯科技公司 | 选择性烯烃提取 |
| US11952333B2 (en) | 2019-09-13 | 2024-04-09 | Sabic Global Technologies B.V. | Integrated systems and methods for producing 1,3-butadiene via extractive distillation, distillation, and/or selective hydrogenation |
| JP2024506792A (ja) * | 2021-01-27 | 2024-02-15 | エボニック オクセノ ゲーエムベーハー ウント コー． カーゲー | Ｃ４炭化水素流からブテンを除去し、その後のｎ／ｉｓｏ分離を行うためのエネルギー効率の高い方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2911452A (en) * | 1956-06-22 | 1959-11-03 | Universal Oil Prod Co | Process for separating butylenes from butanes |
| US3121124A (en) * | 1959-05-04 | 1964-02-11 | Sinclair Research Inc | Tertiary olefin separation via etherification |
| US3232849A (en) * | 1961-10-27 | 1966-02-01 | Phillips Petroleum Co | Butene and butadiene purification by plural stage distillation |
| US3232850A (en) * | 1961-10-27 | 1966-02-01 | Phillips Petroleum Co | Butene and butadiene purification by plural stage distillation |
| US3170000A (en) * | 1962-10-24 | 1965-02-16 | Sinclair Research Inc | Tertiary olefin separation via etherification with small surface area catalysts |
| DE1916255C3 (de) * | 1969-03-29 | 1979-04-05 | Krupp-Koppers Gmbh, 4300 Essen | Verfahren zur Trennung von Kohlenwasserstoffgemischen, die Paraffine, Monoolefine, Diolefine sowie gegebenenfalls geringe Mengen stärker ungesättigte Kohlenwasserstoffe enthalten |
| US3772158A (en) * | 1971-03-29 | 1973-11-13 | Shell Oil Co | Butadiene recovery process |
| DE2908426A1 (de) * | 1979-03-05 | 1980-09-25 | Basf Ag | Verfahren zur gewinnung von isobuten aus isobuten enthaltenden c tief 4 -kohlenwasserstoffgemischen |
| DE2965767D1 (en) * | 1979-03-21 | 1983-07-28 | Davy Mckee London | Process for the production of a sulphur-free butene-1 rich stream |
| US4269668A (en) * | 1980-05-19 | 1981-05-26 | The B. F. Goodrich Company | Extractive distillation of C-4 hydrocarbons using modified alkoxynitrile solvent |
| US4356339A (en) * | 1980-12-15 | 1982-10-26 | Nippon Oil Company, Limited | Process for isolating and recovering butene-1 of high purity |
| JPS5892625A (ja) * | 1981-11-27 | 1983-06-02 | Nippon Zeon Co Ltd | Ｃ↓４炭化水素留分より高純度ブテン−１又はブテン−１／イソブテン混合物の分離方法 |
-
1982
- 1982-01-22 JP JP57008288A patent/JPS58126820A/ja active Granted
- 1982-12-01 US US06/445,974 patent/US4556461A/en not_active Expired - Lifetime
- 1982-12-07 NL NL8204735A patent/NL8204735A/nl active Search and Examination
- 1982-12-10 HU HU824000A patent/HU199368B/hu not_active IP Right Cessation
-
1983
- 1983-01-11 IT IT19057/83A patent/IT1159826B/it active
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58126820A (ja) | 1983-07-28 |
| IT8319057A0 (it) | 1983-01-11 |
| HU199368B (en) | 1990-02-28 |
| IT1159826B (it) | 1987-03-04 |
| US4556461A (en) | 1985-12-03 |
| JPS6332337B2 (OSRAM) | 1988-06-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4556461A (en) | Process for separating highly pure butene-1 or butene-1/isobutene mixture from C4 hydrocarbon fraction | |
| NL8204591A (nl) | Werkwijze voor het afscheiden van zeer zuiver buteen-1 of een buteen-1/isobuteenmengsel uit een fractie van koolwaterstoffen met 4 koolstofatomen. | |
| CN102712555A (zh) | 丁二烯生产方法 | |
| US20170253540A1 (en) | Method and apparatus for producing hydrocarbons | |
| SE448086B (sv) | Forfarande for framstellning av metyl-t-butyleter | |
| JP4589317B2 (ja) | 粗製ｃ４カットの分離方法 | |
| US5908964A (en) | Process for preparing alkyl ethers and mixtures thereof | |
| EP0079679B1 (en) | Process for separating highly pure butene-1 and butene-2 | |
| EP0643679B1 (en) | Process for the removal of green oil from a hydrocarbon stream | |
| US5510566A (en) | Regenerant recycle process for oxygenate removal | |
| CN103958647A (zh) | 提供气态经纯化的c4粗馏分作为进料流用于使用选择性溶剂的萃取蒸馏工艺的方法 | |
| US5399787A (en) | Olefin isomerization process using etherification feed isomerization | |
| US11891358B2 (en) | Process and apparatus for preparing purified styrene composition from styrene containing feedstock | |
| RU2005710C1 (ru) | Способ выделения третичных олефинов c1-c4 | |
| US3004083A (en) | Hydrocarbon separation | |
| US20140378726A1 (en) | Catalytic conversion processes using ionic liquids | |
| CN101108793A (zh) | 在反应器中的最佳温控下制备烷基叔丁基醚的方法 | |
| US2426821A (en) | Azeotropic distillation of five carbon diolefins in the presence of methyl formate | |
| RU2686693C2 (ru) | Удаление ароматических примесей из потока алкенов при помощи кислотного катализатора, такого как кислотная ионная жидкость | |
| RU2005709C1 (ru) | Способ выделения третичных олефинов c4-c5 | |
| SA06270421B1 (ar) | عملية لفصل هيدروكربونات c5 موجودة بتيارات تحتوي بشكل سائد على منتجات c4 تستخدم في إنتاج مركبات هيدروكربونية عالية الاوكتان بالديمرة الإنتقائية للايزوبيوتين | |
| JPS5865227A (ja) | Ｃ↓４炭化水素留分よりの高純度ブテン−１及びブテン−２の分離精製方法 | |
| US20160332957A1 (en) | Process and apparatus for purifying a hydrocarbon stream comprising linear alpha-olefins (lao) from amines | |
| FR2497193A1 (fr) | Procede et appareillage pour la production de vinyltoluene | |
| BE605030A (OSRAM) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A85 | Still pending on 85-01-01 | ||
| BA | A request for search or an international-type search has been filed | ||
| BB | A search report has been drawn up | ||
| BC | A request for examination has been filed | ||
| BN | A decision not to publish the application has become irrevocable |