KR920001786B1 - 알킬벤젠의 제조방법 - Google Patents
알킬벤젠의 제조방법 Download PDFInfo
- Publication number
- KR920001786B1 KR920001786B1 KR1019900700029A KR900700029A KR920001786B1 KR 920001786 B1 KR920001786 B1 KR 920001786B1 KR 1019900700029 A KR1019900700029 A KR 1019900700029A KR 900700029 A KR900700029 A KR 900700029A KR 920001786 B1 KR920001786 B1 KR 920001786B1
- Authority
- KR
- South Korea
- Prior art keywords
- benzene
- alkylation
- alkylator
- column
- transalkylation
- 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
- 238000000034 method Methods 0.000 title claims description 40
- 150000004996 alkyl benzenes Chemical class 0.000 title claims description 15
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 312
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 claims description 76
- 238000005804 alkylation reaction Methods 0.000 claims description 54
- 230000029936 alkylation Effects 0.000 claims description 51
- 238000010555 transalkylation reaction Methods 0.000 claims description 43
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 claims description 42
- 238000006243 chemical reaction Methods 0.000 claims description 36
- 239000003054 catalyst Substances 0.000 claims description 32
- 150000001336 alkenes Chemical class 0.000 claims description 20
- LGXAANYJEHLUEM-UHFFFAOYSA-N 1,2,3-tri(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC(C(C)C)=C1C(C)C LGXAANYJEHLUEM-UHFFFAOYSA-N 0.000 claims description 18
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 15
- BUZMJVBOGDBMGI-UHFFFAOYSA-N 1-phenylpropylbenzene Chemical compound C=1C=CC=CC=1C(CC)C1=CC=CC=C1 BUZMJVBOGDBMGI-UHFFFAOYSA-N 0.000 claims description 14
- 229910021536 Zeolite Inorganic materials 0.000 claims description 14
- 239000010457 zeolite Substances 0.000 claims description 14
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 13
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 13
- 238000004821 distillation Methods 0.000 claims description 10
- 239000000047 product Substances 0.000 claims description 9
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 7
- 238000011084 recovery Methods 0.000 claims description 7
- -1 diphenyl alkane Chemical class 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 235000010290 biphenyl Nutrition 0.000 claims description 5
- 239000004305 biphenyl Substances 0.000 claims description 5
- 239000006227 byproduct Substances 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 5
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 5
- 150000001555 benzenes Chemical class 0.000 claims description 3
- 238000000926 separation method Methods 0.000 claims description 2
- 230000002152 alkylating effect Effects 0.000 claims 1
- JRXXLCKWQFKACW-UHFFFAOYSA-N biphenylacetylene Chemical group C1=CC=CC=C1C#CC1=CC=CC=C1 JRXXLCKWQFKACW-UHFFFAOYSA-N 0.000 claims 1
- WUXSWGVAYSJTJS-UHFFFAOYSA-N pentacyclo[4.2.0.02,5.03,8.04,7]oct-1-ene Chemical compound C12C3C4=C1C1C2C3C14 WUXSWGVAYSJTJS-UHFFFAOYSA-N 0.000 claims 1
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 66
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 22
- 238000010586 diagram Methods 0.000 description 12
- 239000001294 propane Substances 0.000 description 11
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- 239000005977 Ethylene Substances 0.000 description 6
- BSZXAFXFTLXUFV-UHFFFAOYSA-N 1-phenylethylbenzene Chemical compound C=1C=CC=CC=1C(C)C1=CC=CC=C1 BSZXAFXFTLXUFV-UHFFFAOYSA-N 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 3
- VIDOPANCAUPXNH-UHFFFAOYSA-N 1,2,3-triethylbenzene Chemical compound CCC1=CC=CC(CC)=C1CC VIDOPANCAUPXNH-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- FEWANSQOXSIFOK-UHFFFAOYSA-N 1,2,3,4-tetraethylbenzene Chemical compound CCC1=CC=C(CC)C(CC)=C1CC FEWANSQOXSIFOK-UHFFFAOYSA-N 0.000 description 1
- KKIGDGWHHNXWNM-UHFFFAOYSA-N 1,2,3-tripropylbenzene Chemical compound CCCC1=CC=CC(CCC)=C1CCC KKIGDGWHHNXWNM-UHFFFAOYSA-N 0.000 description 1
- KCMUPXHVDCXAHS-UHFFFAOYSA-N 1,2-diethylbenzene;ethylbenzene Chemical compound CCC1=CC=CC=C1.CCC1=CC=CC=C1CC KCMUPXHVDCXAHS-UHFFFAOYSA-N 0.000 description 1
- MILSYCKGLDDVLM-UHFFFAOYSA-N 2-phenylpropan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)C1=CC=CC=C1 MILSYCKGLDDVLM-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- UNYSKUBLZGJSLV-UHFFFAOYSA-L calcium;1,3,5,2,4,6$l^{2}-trioxadisilaluminane 2,4-dioxide;dihydroxide;hexahydrate Chemical compound O.O.O.O.O.O.[OH-].[OH-].[Ca+2].O=[Si]1O[Al]O[Si](=O)O1.O=[Si]1O[Al]O[Si](=O)O1 UNYSKUBLZGJSLV-UHFFFAOYSA-L 0.000 description 1
- 229910052676 chabazite Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/02—Monocyclic hydrocarbons
- C07C15/085—Isopropylbenzene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/02—Monocyclic hydrocarbons
-
- 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
- C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
- C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
- C07C2/66—Catalytic processes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C4/00—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms
-
- 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
-
- 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
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19135188A | 1988-05-09 | 1988-05-09 | |
| US191,351 | 1988-05-09 | ||
| PCT/US1989/001610 WO1989010910A1 (en) | 1988-05-09 | 1989-04-17 | Manufacture of alkylbenzenes |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR900701697A KR900701697A (ko) | 1990-12-04 |
| KR920001786B1 true KR920001786B1 (ko) | 1992-03-02 |
Family
ID=22705125
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019900700029A Expired KR920001786B1 (ko) | 1988-05-09 | 1989-04-17 | 알킬벤젠의 제조방법 |
Country Status (13)
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR9107311A (pt) * | 1991-06-21 | 1995-04-25 | Dow Chemical Co | Processo para alquilar benzeno ou benzeno substituído. |
| US6060632A (en) * | 1996-07-19 | 2000-05-09 | Asahi Kasei Kogyo Kabushiki Kaisha | Process for producing ethylbenzene |
| CN1055912C (zh) * | 1997-11-13 | 2000-08-30 | 中国石油化工总公司 | 烷基苯的生产工艺 |
| US7074978B2 (en) * | 2003-02-25 | 2006-07-11 | Abb Lummus Global Inc. | Process for the production of alkylbenzene |
| US7238843B2 (en) * | 2003-02-28 | 2007-07-03 | Abb Lummus Global, Inc. | Process for the production of alkylaromatics |
| US6964935B2 (en) | 2004-03-12 | 2005-11-15 | Chevron Oronite Company Llc. | Mordenite zeolite alkylation catalysts |
| US7692054B2 (en) * | 2006-10-30 | 2010-04-06 | Uop Llc | Process and apparatus for alkylation of aromatic compound with aliphatic mono-olefin compound of 8 to 18 carbon atoms |
| US7642389B2 (en) * | 2007-02-12 | 2010-01-05 | Uop Llc | Energy integrated processes including alkylation and transalkylation for making detergent range alkylbenzenes |
| US7652182B2 (en) * | 2007-02-12 | 2010-01-26 | Uop Llc | Energy integrated processes including alkylation and transalkylation for making detergent range alkylbenzenes |
| TWI367878B (en) | 2008-01-09 | 2012-07-11 | Uop Llc | Process for separating diisopropylbenzene (dipb) and triisopropylbenzene (tipb) from a feed comprising dipb, tipb, and polyalkylate heavies |
| BRPI0822024B1 (pt) * | 2008-01-09 | 2017-06-20 | Uop Llc | A process for separating diisopropylbenzene and triisopropylbenzene |
| US9150469B2 (en) * | 2009-05-18 | 2015-10-06 | Uop Llc | Aromatic alkylation process with reduced byproduct formation |
| US8350111B2 (en) * | 2010-10-12 | 2013-01-08 | Uop Llc | Method for producing cumene |
| CN102464565B (zh) * | 2010-11-17 | 2014-08-13 | 中国石油化工股份有限公司 | 由苯和丙烯生产异丙苯的方法 |
| CN102464564B (zh) * | 2010-11-17 | 2015-05-13 | 中国石油化工股份有限公司 | 生产异丙苯的方法 |
| WO2012065365A1 (zh) | 2010-11-17 | 2012-05-24 | 中国石油化工股份有限公司 | 异丙苯的生产方法 |
| CN112250538B (zh) * | 2020-11-13 | 2023-01-13 | 万华化学集团股份有限公司 | 一种异丙苯精制工艺流程 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3109037A (en) * | 1960-06-06 | 1963-10-29 | Exxon Research Engineering Co | Synthesis of isopropyl benzene |
| US3751504A (en) * | 1972-05-12 | 1973-08-07 | Mobil Oil Corp | Vapor-phase alkylation in presence of crystalline aluminosilicate catalyst with separate transalkylation |
| IT1127296B (it) * | 1979-12-19 | 1986-05-21 | Euteco Impianti Spa | Procedimento perfezionato per la produzione di cumene |
| IT1127297B (it) * | 1979-12-19 | 1986-05-21 | Euteco Impianti Spa | Procedimento per la produzione di cumene |
-
1989
- 1989-04-17 WO PCT/US1989/001610 patent/WO1989010910A1/en active IP Right Grant
- 1989-04-17 KR KR1019900700029A patent/KR920001786B1/ko not_active Expired
- 1989-04-17 EP EP89904993A patent/EP0424393B1/en not_active Expired - Lifetime
- 1989-04-17 JP JP1504815A patent/JP2663302B2/ja not_active Expired - Lifetime
- 1989-04-17 BR BR898907423A patent/BR8907423A/pt unknown
- 1989-04-17 DE DE68923795T patent/DE68923795T2/de not_active Expired - Lifetime
- 1989-04-19 IN IN300/CAL/89A patent/IN172055B/en unknown
- 1989-05-04 MX MX015915A patent/MX172351B/es unknown
- 1989-05-08 CA CA000599017A patent/CA1321404C/en not_active Expired - Lifetime
- 1989-05-09 ES ES8901589A patent/ES2013187A6/es not_active Expired - Lifetime
- 1989-05-09 CN CN89103069A patent/CN1019007B/zh not_active Expired
- 1989-05-09 AR AR89313873A patent/AR246940A1/es active
-
1990
- 1990-11-08 FI FI905537A patent/FI92480C/fi not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CN1037699A (zh) | 1989-12-06 |
| EP0424393A1 (en) | 1991-05-02 |
| DE68923795D1 (de) | 1995-09-14 |
| KR900701697A (ko) | 1990-12-04 |
| BR8907423A (pt) | 1991-05-14 |
| ES2013187A6 (es) | 1990-04-16 |
| JP2663302B2 (ja) | 1997-10-15 |
| JPH04502451A (ja) | 1992-05-07 |
| DE68923795T2 (de) | 1996-03-28 |
| FI92480B (fi) | 1994-08-15 |
| CA1321404C (en) | 1993-08-17 |
| FI905537A0 (fi) | 1990-11-08 |
| MX172351B (es) | 1993-12-14 |
| EP0424393B1 (en) | 1995-08-09 |
| AR246940A1 (es) | 1994-10-31 |
| IN172055B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-03-27 |
| FI92480C (fi) | 1994-11-25 |
| WO1989010910A1 (en) | 1989-11-16 |
| CN1019007B (zh) | 1992-11-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
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| PG1501 | Laying open of application | ||
| G160 | Decision to publish patent application | ||
| PG1605 | Publication of application before grant of patent |
Comment text: Decision on Publication of Application Patent event code: PG16051S01I Patent event date: 19910128 |
|
| E701 | Decision to grant or registration of patent right | ||
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