JPS6250453B2 - - Google Patents
Info
- Publication number
- JPS6250453B2 JPS6250453B2 JP54025349A JP2534979A JPS6250453B2 JP S6250453 B2 JPS6250453 B2 JP S6250453B2 JP 54025349 A JP54025349 A JP 54025349A JP 2534979 A JP2534979 A JP 2534979A JP S6250453 B2 JPS6250453 B2 JP S6250453B2
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- methanol
- isobutylene
- stream
- mixture
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 147
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims abstract description 80
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims abstract description 48
- 239000000203 mixture Substances 0.000 claims abstract description 32
- 239000002253 acid Substances 0.000 claims abstract description 28
- 239000002245 particle Substances 0.000 claims abstract description 27
- 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 claims abstract description 21
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 21
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 18
- 239000011541 reaction mixture Substances 0.000 claims abstract description 18
- 239000003729 cation exchange resin Substances 0.000 claims abstract description 16
- 239000007787 solid Substances 0.000 claims abstract description 16
- 239000007788 liquid Substances 0.000 claims abstract description 11
- 238000006243 chemical reaction Methods 0.000 claims description 91
- 238000011010 flushing procedure Methods 0.000 claims description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 8
- PWZFXELTLAQOKC-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide;tetrahydrate Chemical compound O.O.O.O.[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O PWZFXELTLAQOKC-UHFFFAOYSA-A 0.000 claims description 7
- 229910001701 hydrotalcite Inorganic materials 0.000 claims description 7
- 229960001545 hydrotalcite Drugs 0.000 claims description 7
- 239000003456 ion exchange resin Substances 0.000 claims description 6
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 6
- 239000011777 magnesium Substances 0.000 claims description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 239000000395 magnesium oxide Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 150000004677 hydrates Chemical class 0.000 claims description 3
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- 238000011437 continuous method Methods 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 17
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 14
- 239000007795 chemical reaction product Substances 0.000 abstract description 5
- 239000000159 acid neutralizing agent Substances 0.000 abstract 1
- 238000004064 recycling Methods 0.000 abstract 1
- 239000002994 raw material Substances 0.000 description 25
- 239000012530 fluid Substances 0.000 description 20
- 239000000126 substance Substances 0.000 description 17
- 230000002378 acidificating effect Effects 0.000 description 12
- 239000003054 catalyst Substances 0.000 description 12
- 238000006386 neutralization reaction Methods 0.000 description 10
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- -1 C 4 hydrocarbon Chemical class 0.000 description 4
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 239000003502 gasoline Substances 0.000 description 3
- 229940044654 phenolsulfonic acid Drugs 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- KOYGZROXUOTUEE-UHFFFAOYSA-N butane;but-1-ene Chemical compound CCCC.CCC=C KOYGZROXUOTUEE-UHFFFAOYSA-N 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 2
- 239000000292 calcium oxide Substances 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- 229920001429 chelating resin Polymers 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- NUMQCACRALPSHD-UHFFFAOYSA-N tert-butyl ethyl ether Chemical compound CCOC(C)(C)C NUMQCACRALPSHD-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- HNFSPSWQNZVCTB-UHFFFAOYSA-N 2-methyl-2-propan-2-yloxypropane Chemical compound CC(C)OC(C)(C)C HNFSPSWQNZVCTB-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 229940023913 cation exchange resins Drugs 0.000 description 1
- 238000006757 chemical reactions by type Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 229910003480 inorganic solid Inorganic materials 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000004230 steam cracking Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/05—Preparation of ethers by addition of compounds to unsaturated compounds
- C07C41/06—Preparation of ethers by addition of compounds to unsaturated compounds by addition of organic compounds only
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)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2534979A JPS55118431A (en) | 1979-03-05 | 1979-03-05 | Preparation of methyl t-butyl ether |
| US06/125,655 US4404409A (en) | 1979-03-05 | 1980-02-28 | Process for preparing methyl tertiary-butyl ether |
| FR8004727A FR2450799A1 (fr) | 1979-03-05 | 1980-03-03 | Procede pour preparer de maniere continue le methyl tertiobutyl ether |
| GB8007141A GB2048247B (en) | 1979-03-05 | 1980-03-03 | Process for preparing methyl tertiary-butyl ether |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2534979A JPS55118431A (en) | 1979-03-05 | 1979-03-05 | Preparation of methyl t-butyl ether |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS55118431A JPS55118431A (en) | 1980-09-11 |
| JPS6250453B2 true JPS6250453B2 (US07576130-20090818-C00114.png) | 1987-10-24 |
Family
ID=12163388
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2534979A Granted JPS55118431A (en) | 1979-03-05 | 1979-03-05 | Preparation of methyl t-butyl ether |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4404409A (US07576130-20090818-C00114.png) |
| JP (1) | JPS55118431A (US07576130-20090818-C00114.png) |
| FR (1) | FR2450799A1 (US07576130-20090818-C00114.png) |
| GB (1) | GB2048247B (US07576130-20090818-C00114.png) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6422921U (US07576130-20090818-C00114.png) * | 1987-07-31 | 1989-02-07 | ||
| JPH0271046A (ja) * | 1988-09-06 | 1990-03-09 | Rinnai Corp | 湯張り給湯システム |
| JPH02131163U (US07576130-20090818-C00114.png) * | 1989-04-06 | 1990-10-31 | ||
| JPH0389345U (US07576130-20090818-C00114.png) * | 1989-12-28 | 1991-09-11 |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1254236A (en) * | 1981-07-27 | 1989-05-16 | Donald J. Makovec | Process for the preparation of methyl tert-butyl ether |
| EP0075838A1 (en) * | 1981-09-24 | 1983-04-06 | Phillips Petroleum Company | Process for the preparation of methyl tert-butyl ether |
| DE3610190A1 (de) * | 1986-03-26 | 1987-10-01 | Blaupunkt Werke Gmbh | Verfahren und schaltungsanordnungen zur regelung des arbeitspunktes von videoendstufen |
| US5382705A (en) * | 1989-03-20 | 1995-01-17 | Mobil Oil Corporation | Production of tertiary alkyl ethers and tertiary alkyl alcohols |
| US5457243A (en) * | 1993-12-23 | 1995-10-10 | Texaco Chemical Inc. | Neutralization of crude MTBE effluent streams using solid bases |
| CN1044900C (zh) * | 1995-12-26 | 1999-09-01 | 中国石油化工总公司上海石油化工研究院 | 化工型甲基叔丁基醚制备方法 |
| US6197162B1 (en) | 1998-09-17 | 2001-03-06 | Jose M. Quiros | Liquid purifying distillation process |
| EP1492752A2 (en) * | 2002-03-14 | 2005-01-05 | Eurotecnica Development & Licensing S.p.A. | Process for the synthesis of phenol and acetone |
| CN103360221A (zh) * | 2013-07-17 | 2013-10-23 | 凯瑞化工股份有限公司 | 一种深度脱除mtbe中硫化物的方法 |
| KR102086563B1 (ko) * | 2017-01-06 | 2020-03-09 | 주식회사 엘지화학 | 메틸 3급-부틸 에테르 제조방법 |
| EP4073024A1 (en) * | 2019-12-11 | 2022-10-19 | SABIC Global Technologies B.V. | Systems and methods for mtbe production |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5569532A (en) * | 1978-11-08 | 1980-05-26 | Inst Francais Du Petrole | Manufacture of ether by reaction of olefin and alcohol |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1587866A (en) * | 1976-11-22 | 1981-04-08 | Nippon Oil Co Ltd | Methyl tert-butyl ether |
-
1979
- 1979-03-05 JP JP2534979A patent/JPS55118431A/ja active Granted
-
1980
- 1980-02-28 US US06/125,655 patent/US4404409A/en not_active Expired - Lifetime
- 1980-03-03 FR FR8004727A patent/FR2450799A1/fr active Granted
- 1980-03-03 GB GB8007141A patent/GB2048247B/en not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5569532A (en) * | 1978-11-08 | 1980-05-26 | Inst Francais Du Petrole | Manufacture of ether by reaction of olefin and alcohol |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6422921U (US07576130-20090818-C00114.png) * | 1987-07-31 | 1989-02-07 | ||
| JPH0271046A (ja) * | 1988-09-06 | 1990-03-09 | Rinnai Corp | 湯張り給湯システム |
| JPH02131163U (US07576130-20090818-C00114.png) * | 1989-04-06 | 1990-10-31 | ||
| JPH0389345U (US07576130-20090818-C00114.png) * | 1989-12-28 | 1991-09-11 |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2450799A1 (fr) | 1980-10-03 |
| GB2048247B (en) | 1983-02-16 |
| GB2048247A (en) | 1980-12-10 |
| JPS55118431A (en) | 1980-09-11 |
| US4404409A (en) | 1983-09-13 |
| FR2450799B1 (US07576130-20090818-C00114.png) | 1983-03-04 |
