KR910011715A - 벤젠 또는 치환된 벤젠을 알킬화시키거나 알킬화 벤젠을 트랜스알킬화시키는 방법 및 이를 위한 촉매 조성물 - Google Patents
벤젠 또는 치환된 벤젠을 알킬화시키거나 알킬화 벤젠을 트랜스알킬화시키는 방법 및 이를 위한 촉매 조성물 Download PDFInfo
- Publication number
- KR910011715A KR910011715A KR1019900021123A KR900021123A KR910011715A KR 910011715 A KR910011715 A KR 910011715A KR 1019900021123 A KR1019900021123 A KR 1019900021123A KR 900021123 A KR900021123 A KR 900021123A KR 910011715 A KR910011715 A KR 910011715A
- Authority
- KR
- South Korea
- Prior art keywords
- benzene
- catalyst
- silica
- crystal structure
- ray diffraction
- Prior art date
Links
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 title claims 28
- 239000003054 catalyst Substances 0.000 title claims 14
- 238000000034 method Methods 0.000 title claims 12
- 150000001555 benzenes Chemical class 0.000 title claims 10
- 230000002152 alkylating effect Effects 0.000 title claims 3
- 239000000203 mixture Substances 0.000 title claims 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 26
- 239000000377 silicon dioxide Substances 0.000 claims 13
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 7
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims 6
- 239000011230 binding agent Substances 0.000 claims 6
- 239000013078 crystal Substances 0.000 claims 6
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 claims 6
- 238000002441 X-ray diffraction Methods 0.000 claims 5
- 229910021536 Zeolite Inorganic materials 0.000 claims 5
- 230000002378 acidificating effect Effects 0.000 claims 5
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 5
- 229910052680 mordenite Inorganic materials 0.000 claims 5
- 239000010457 zeolite Substances 0.000 claims 5
- 238000006243 chemical reaction Methods 0.000 claims 4
- 230000029936 alkylation Effects 0.000 claims 3
- 238000005804 alkylation reaction Methods 0.000 claims 3
- 238000010555 transalkylation reaction Methods 0.000 claims 3
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 claims 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 2
- 229940100198 alkylating agent Drugs 0.000 claims 2
- 239000002168 alkylating agent Substances 0.000 claims 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 2
- 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 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000002131 composite material Substances 0.000 claims 1
- 230000009849 deactivation Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/68—Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton
-
- 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
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
- C07C37/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms by addition reactions, i.e. reactions involving at least one carbon-to-carbon unsaturated bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
- C07C6/08—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond
- C07C6/12—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond of exclusively hydrocarbons containing a six-membered aromatic ring
- C07C6/126—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond of exclusively hydrocarbons containing a six-membered aromatic ring of more than one hydrocarbon
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- C07C2521/08—Silica
-
- 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
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
-
- 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)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Heat Treatment Of Sheet Steel (AREA)
- Separation Of Gases By Adsorption (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (12)
- 벤젠 또는 치환된 벤젠을 실리카/알루미나 몰비가 30 : 1이상이고 X-선 회절법에 의해 대칭수가 1 이상인 것으로 측정되는 결정구조를 갖는 산성 모오데나이트 제올라이트 및 내부 실리카 결합제를 포함하는 촉매의 존재하에 알킬화 벤젠 또는 알킬화 치환된 벤젠이 생성되고 촉매는 필수적으로 사용한지 500시간 이상후에 탈환성화를 나타내지 않도록 하는 반응조건하에서 탄소수 2 내지 18의 알킬화제를 접촉시킴을 특징으로 하여, 벤젠 또는 치환된 벤젠을 알킬화시키거나, 알킬화 벤젠을 트랜스알킬화시키는 방법.
- 제1항에 있어서, 알킬화제가 프로필렌 또는 에틸렌인 방법.
- 제1항에 있어서, 촉매의 실리카/알루미나 몰비가 40 : 1 내지 300 : 1인 방법.
- 제1항에 있어서, 온도가 100 내지 250℃범위인 방법.
- 벤젠과 디알킬화 벤젠의 혼합물을 실리카/알루미나 몰비가 30 : 1 이상이고 X-선 회절법에 의해 대칭수가 1이상인 것으로 측정되는 결정구조를 갖는 산성 모오데나이트 제올라이트 및 내부 실리카 결합제를 포함하는 촉매의 존재하에 필수적으로 무색 알킬화 벤젠이 생성되고 촉매는 필수적으로 사용한지 500시간 이상후에 탈활성화를 나타내지 않도록 하는 반응조건하에서 접촉시킴을 특징으로 하여 트랜스알킬화시킴으로써 큐멘 및 에틸벤젠을 포함하는 알킬화 벤젠을 제조하는 방법.
- 제5항에 있어서, 촉매의 실리카/알루미나 몰비가 40 : 1 내지 300 : 1인 방법.
- 제5항에 있어서, 촉매 복합체가 내부 실리카 결합체인 방법.
- 제5항에 있어서, 온도가 100 내지 250℃ 범위인 방법.
- 벤젠과 디이소프로필벤젠 및 프로필렌을 실리카/알루미나 몰비가 30 : 1 이상이고 X-선 회절법에 의해 대칭지수가 1이상인 것으로 측정되는 결정구조를 갖는 산성 모오데나이트 제올라이트 및 내부 실리카 결합제를 포함하는 촉매의 존재하에 필수적으로 무색 큐멘이 생성되고 촉매는 사용한지 500시간 이상후에 탈활성화되지 않도록 하는 반응조건하에서 접촉시킴을 특징으로 하여 알킬화/트랜스알킬화시킴으로써, 큐멘을 제조하는 방법.
- 벤젠과 디에틸벤젠 및 에틸렌을 실리카/알루미나 몰비가 30 : 1 이상이고 X-선 회절법에 의해 대칭지수가 1 이상인 것으로 측정되는 결정구조를 갖는 산성 모오데나이트 제올라이트 및 내부 실리카 결합제를 포함하는 촉매의 존재하에 필수적으로 무색 에틸벤젠이 생성되고 촉매는 사용한지 500시간 이상후에 탈활성화 되지 않도록 하는 반응조건하에서 접촉시킴을 특징으로 하여, 알킬화/트랜스알킬화시킴으로써, 에틸벤젠을 제조하는 방법.
- 제1항에 있어서, 치환된 벤젠이 페놀 또는 아닐린인 방법.
- 실리카/알루미나 몰비가 30 : 1 이상이고, X-선 회절법에 의해 대칭지수가 1이상인 것으로 측정되는 결정구조를 갖는 산성 모오데나이트 제올라이트와 불활성 실리카 결합제를 포함함을 특징으로 하는 촉매 조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US45567789A | 1989-12-22 | 1989-12-22 | |
US455677 | 1989-12-22 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR910011715A true KR910011715A (ko) | 1991-08-07 |
KR100206050B1 KR100206050B1 (ko) | 1999-07-01 |
Family
ID=23809811
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900021123A KR100206050B1 (ko) | 1989-12-22 | 1990-12-20 | 벤젠 또는 치환된 벤젠을 알킬화시키거나 알킬화 벤젠을 트랜스알킬화시키는 방법 |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP0433932B1 (ko) |
JP (1) | JPH06239771A (ko) |
KR (1) | KR100206050B1 (ko) |
CN (1) | CN1031989C (ko) |
AT (1) | ATE137483T1 (ko) |
AU (1) | AU651565B2 (ko) |
CA (1) | CA2033021C (ko) |
DE (1) | DE69026802T2 (ko) |
ES (1) | ES2085878T3 (ko) |
FI (1) | FI906369A (ko) |
IL (1) | IL96758A0 (ko) |
NO (1) | NO175249C (ko) |
NZ (1) | NZ236508A (ko) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2121776T3 (es) * | 1991-03-21 | 1998-12-16 | Solutia Europ Nv Sa | Procedimiento catalitico mejorado para la alquilacion selectiva de hidrocarburos aromaticos. |
BR9107311A (pt) * | 1991-06-21 | 1995-04-25 | Dow Chemical Co | Processo para alquilar benzeno ou benzeno substituído. |
EP0528096B1 (en) * | 1991-08-21 | 1998-05-27 | Solutia Europe N.V./S.A. | Catalytic process for the selective alkylation of polycyclic aromatic compounds |
US5756873A (en) * | 1992-08-05 | 1998-05-26 | Exxon Chemical Patents Inc. | Design for aromatics alkylation |
CN1055876C (zh) * | 1996-01-25 | 2000-08-30 | 中国石油化工总公司 | 用于制备烷基苯的烷基化催化剂 |
US5955642A (en) * | 1996-10-30 | 1999-09-21 | Fina Technology, Inc. | Gas phase alkylation-liquid transalkylation process |
FR2761905B1 (fr) * | 1997-04-09 | 1999-05-14 | Inst Francais Du Petrole | Catalyseur a base de mordenite desaluminee contenant au moins un metal des groupes vi, vii et viii, et son utilisation en dismutation et/ou transalkylation d'hydrocarbures aromatiques |
FR2761904B1 (fr) * | 1997-04-09 | 1999-05-14 | Inst Francais Du Petrole | Catalyseur a base de mordenite desaluminee et son utilisation en dismutation et/ou transalkylation d'hydrocarbures aromatiques |
CN100532506C (zh) * | 2001-11-16 | 2009-08-26 | 弗纳技术股份有限公司 | 载于二氧化硅上的烷基化催化剂 |
US6964935B2 (en) | 2004-03-12 | 2005-11-15 | Chevron Oronite Company Llc. | Mordenite zeolite alkylation catalysts |
CN102909052B (zh) * | 2011-08-01 | 2014-12-10 | 中国石油化工股份有限公司 | 含丝光沸石的催化剂及其制备方法和应用 |
BR102014002154A2 (pt) * | 2014-01-28 | 2015-10-27 | Whirlpool Sa | processo de produção de composto alquilaromático, processo de transalquilação de polialquilaromáticos para produção seletiva de composto monoalquilaromático, e, processo de alquilação e transalquilação de compostos aromáticos e/ou poliaromáticos |
CN108530246B (zh) * | 2017-03-03 | 2021-03-30 | 中国石油化工股份有限公司 | 苯和丙烯生产正丙苯的方法 |
CN114426451A (zh) * | 2020-09-24 | 2022-05-03 | 中国石油化工股份有限公司 | 一种多取代异丙苯烷基转移制备异丙苯的方法及其所得异丙苯 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2112223B2 (de) * | 1970-03-16 | 1973-12-20 | Universal Oil Products Co., Des Plaines, Ill. (V.St.A.) | Verfahren zur Herstellung von synthetischem Mordenit und dessen Verwendung |
US3849340A (en) * | 1971-11-10 | 1974-11-19 | Universal Oil Prod Co | Hydrocarbon conversion catalyst |
US4301317A (en) * | 1979-11-20 | 1981-11-17 | Mobil Oil Corporation | Preparation of 2-phenylalkanes |
US4735929A (en) * | 1985-09-03 | 1988-04-05 | Uop Inc. | Catalytic composition for the isomerization of paraffinic hydrocarbons |
US4891448A (en) * | 1987-11-23 | 1990-01-02 | The Dow Chemical Company | Alkylation of polycyclic aromatic compounds to alkylates enriched in the para-substituted isomers |
FR2638157B1 (fr) * | 1988-10-26 | 1991-04-19 | Inst Francais Du Petrole | Procede de production d'alkylbenzenes utilisant un catalyseur a base de mordenite modifiee |
-
1990
- 1990-12-14 JP JP2402255A patent/JPH06239771A/ja active Pending
- 1990-12-17 DE DE69026802T patent/DE69026802T2/de not_active Expired - Fee Related
- 1990-12-17 AT AT90124342T patent/ATE137483T1/de active
- 1990-12-17 EP EP90124342A patent/EP0433932B1/en not_active Expired - Lifetime
- 1990-12-17 ES ES90124342T patent/ES2085878T3/es not_active Expired - Lifetime
- 1990-12-18 NZ NZ236508A patent/NZ236508A/en unknown
- 1990-12-20 KR KR1019900021123A patent/KR100206050B1/ko not_active IP Right Cessation
- 1990-12-21 FI FI906369A patent/FI906369A/fi not_active IP Right Cessation
- 1990-12-21 CN CN90106037A patent/CN1031989C/zh not_active Expired - Fee Related
- 1990-12-21 AU AU68437/90A patent/AU651565B2/en not_active Ceased
- 1990-12-21 CA CA002033021A patent/CA2033021C/en not_active Expired - Fee Related
- 1990-12-21 IL IL96758A patent/IL96758A0/xx unknown
- 1990-12-21 NO NO905568A patent/NO175249C/no unknown
Also Published As
Publication number | Publication date |
---|---|
NO175249B (no) | 1994-06-13 |
FI906369A0 (fi) | 1990-12-21 |
CA2033021A1 (en) | 1991-06-23 |
JPH06239771A (ja) | 1994-08-30 |
FI906369A (fi) | 1991-06-23 |
CN1052655A (zh) | 1991-07-03 |
ATE137483T1 (de) | 1996-05-15 |
AU651565B2 (en) | 1994-07-28 |
NO905568D0 (no) | 1990-12-21 |
NO905568L (no) | 1991-06-24 |
AU6843790A (en) | 1991-06-27 |
EP0433932A1 (en) | 1991-06-26 |
CN1031989C (zh) | 1996-06-12 |
DE69026802D1 (de) | 1996-06-05 |
ES2085878T3 (es) | 1996-06-16 |
NO175249C (no) | 1994-09-21 |
CA2033021C (en) | 2001-05-01 |
DE69026802T2 (de) | 1996-11-21 |
KR100206050B1 (ko) | 1999-07-01 |
IL96758A0 (en) | 1991-09-16 |
EP0433932B1 (en) | 1996-05-01 |
NZ236508A (en) | 1992-05-26 |
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