KR910016654A - 디메틸나프탈렌의 제조방법 - Google Patents
디메틸나프탈렌의 제조방법 Download PDFInfo
- Publication number
- KR910016654A KR910016654A KR1019910003935A KR910003935A KR910016654A KR 910016654 A KR910016654 A KR 910016654A KR 1019910003935 A KR1019910003935 A KR 1019910003935A KR 910003935 A KR910003935 A KR 910003935A KR 910016654 A KR910016654 A KR 910016654A
- Authority
- KR
- South Korea
- Prior art keywords
- zsm
- zeolite
- kpa
- pressures
- temperatures
- Prior art date
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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
- C07C15/20—Polycyclic condensed hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/20—Polycyclic condensed hydrocarbons
- C07C15/24—Polycyclic condensed hydrocarbons containing two rings
-
- 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
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/373—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen with simultaneous isomerisation
- C07C5/393—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen with simultaneous isomerisation with cyclisation to an aromatic six-membered ring, e.g. dehydrogenation of n-hexane to benzene
- C07C5/41—Catalytic processes
-
- 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
- C07C2529/08—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y
-
- 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
-
- 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
- C07C2529/65—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the ferrierite type, e.g. types ZSM-21, ZSM-35 or ZSM-38
-
- 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
- C07C2529/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups C07C2529/08 - C07C2529/65
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- a) 알킬화 가능 방향족 화합물과 C5올레핀이 함유된 공급액을 컨스트레인트 인덱스가 5 이하이 합성 결정성 제올라이트로 이루어진 알킬화촉매 조성물과 접촉해 알킬레이트를 제조하고, B)알킬레이트를 탈수소고리화 촉매와 접촉해 디메틸나프탈렌이 함유된 생성물을 제조하는 단계로 이루어진 디메틸나프탈렌의 제조방법.
- 제1항에서, 알킬화촉매 조성물중 결정성 제올라이트의 컨스트레인트 인덱스가 3 이하인 방법.
- 제1항에서, 결정성 제올라이트가 ZSM - 4, ZSM - 12, ZSM - 20, ZSM - 35, ZSM - 48, ZSM - 50, MCM - 22, TMA 오프레타이트, 모데나이트, 크리노프티로라이트, 제올라이트 Y 그리고 제올라이트 베타중에서 선택된 방법.
- 제1항에서, 소성 형태인 결정성 제올라이트의X - 선 회절패턴이 명세서중 표 A에 나타난 평면간 d-거리를 지니는 방법.
- 제1항 - 4항중 어느 하나에서, 공급액중 알킬화 가능 방향족이 톨루엔인 방법.
- 제1항 - 5항중 어느 하나에서, C5올레핀이 1 - 펜텐인 방법.
- 제1항에서, 알킬화 조건이 온도가 -20 -480℃ (0-900°F)이고 압력이 20 -25250 KPa (0.2-250 기압)인 방법.
- 제1항에서, 알킬화 조건이 온도가 -10-260℃(50-500°F)이고 압력이 100-2525KPa(1-25기압)인 방법.
- 제1항 - 8항중의 어느 하나에서, 탈수소고리화 촉매가 제올라이트 L인 방법.
- 제1항 - 9항중 어느 하나에서, 탈수소고리화 조건이 온도가 260-815℃(500-1500°F)이고 압력이 100 - 7000KPa (0 - 1000psig)인 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US494,255 | 1990-03-15 | ||
US07/494,255 US5043501A (en) | 1990-03-15 | 1990-03-15 | Process for preparing dimethylnaphthalene |
Publications (1)
Publication Number | Publication Date |
---|---|
KR910016654A true KR910016654A (ko) | 1991-11-05 |
Family
ID=23963725
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019910003935A KR910016654A (ko) | 1990-03-15 | 1991-03-12 | 디메틸나프탈렌의 제조방법 |
Country Status (7)
Country | Link |
---|---|
US (1) | US5043501A (ko) |
EP (1) | EP0447069B1 (ko) |
JP (1) | JP2898770B2 (ko) |
KR (1) | KR910016654A (ko) |
AU (1) | AU631483B2 (ko) |
CA (1) | CA2036827A1 (ko) |
DE (1) | DE69109526T2 (ko) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5236575A (en) * | 1991-06-19 | 1993-08-17 | Mobil Oil Corp. | Synthetic porous crystalline mcm-49, its synthesis and use |
DE4126533A1 (de) * | 1991-08-10 | 1993-02-11 | Ver Glaswerke Gmbh | Verfahren zum kontaktieren von elektrisch heizbaren glasscheiben mit transparenten heizwiderstandsschichten |
AU658937B2 (en) * | 1991-11-19 | 1995-05-04 | Mobil Oil Corporation | Hydrocarbon upgrading process |
JP3175744B2 (ja) * | 1992-02-03 | 2001-06-11 | 三菱瓦斯化学株式会社 | ジメチルナフタレンの製造方法 |
US5362697A (en) * | 1993-04-26 | 1994-11-08 | Mobil Oil Corp. | Synthetic layered MCM-56, its synthesis and use |
EP0703887A1 (en) * | 1993-06-16 | 1996-04-03 | Mobil Oil Corporation | Liquid phase ethylbenzene synthesis |
US5329059A (en) * | 1993-07-06 | 1994-07-12 | Mobil Oil Corp. | Alkylaromatic disproportionation |
US5900520A (en) * | 1995-01-23 | 1999-05-04 | Mobil Oil Corporation | Aromatics alkylation |
US6057487A (en) * | 1997-12-30 | 2000-05-02 | Chevron Chemical Company | Method for producing 2,6-DMN from mixed dimethylnaphthalenes by crystallization, adsorption and isomerization |
US5955641A (en) * | 1998-03-16 | 1999-09-21 | Chevron Chemical Company Llc | Method of making dimethylnaphthalenes |
IT1300061B1 (it) * | 1998-04-17 | 2000-04-19 | Eniricerche S P A Ora Enitecno | Processo per preparare 2,6-dimetilnaftalene |
US6313362B1 (en) | 1998-12-17 | 2001-11-06 | Exxonmobil Corporation | Aromatic alkylation process |
US7837861B2 (en) * | 2006-10-18 | 2010-11-23 | Exxonmobil Research & Engineering Co. | Process for benzene reduction and sulfur removal from FCC naphthas |
CN103797091B (zh) | 2011-08-19 | 2016-07-06 | 巴杰许可有限责任公司 | 降低汽油的苯含量的方法 |
CN104447179A (zh) * | 2013-09-24 | 2015-03-25 | 中国石油化工股份有限公司 | 利用戊醇生产2,6-二甲基萘的方法 |
CN104447180A (zh) * | 2013-09-24 | 2015-03-25 | 中国石油化工股份有限公司 | 利用费托反应产物中的戊烯生产2,6-二甲基萘的方法 |
CN109847791A (zh) * | 2017-11-30 | 2019-06-07 | 中国科学院大连化学物理研究所 | 一种催化剂、其制备方法及在丁烯歧化反应中的应用 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3775496A (en) * | 1972-08-09 | 1973-11-27 | Sun Research Development | Preparation of 2,6-dimethylnaphthalene and 2,7-dimethylnaphthalene |
GB1448136A (en) * | 1972-12-25 | 1976-09-02 | Mitsui Petrochemical Ind | Process for preparing dimethyl naphthalenes |
DE3117135A1 (de) * | 1981-04-30 | 1982-11-18 | Bayer Ag, 5090 Leverkusen | Kristallines alumosilicat, verfahren zu dessen herstellung sowie dessen verwendung zur katalytischen umwandlung von methanol und/oder dimethylether in kohlenwasserstoffe |
GB2133032B (en) * | 1983-01-07 | 1986-09-24 | Coalite Group Plc | Preparation of dimethylnaphthalenes |
DE3334084A1 (de) * | 1983-09-21 | 1985-04-18 | Hoechst Ag, 6230 Frankfurt | Verfahren zur alkylierung von naphthalin oder alkylnaphthalinen |
AU3595984A (en) * | 1984-01-04 | 1985-07-11 | Mobil Oil Corp. | Para-diisopropylbenzene and hydroquinone from cumene |
US4623632A (en) * | 1984-11-05 | 1986-11-18 | Uop Inc. | Catalytic composite for conversion of hydrocarbons and the method of preparation and use thereof |
US4735929A (en) * | 1985-09-03 | 1988-04-05 | Uop Inc. | Catalytic composition for the isomerization of paraffinic hydrocarbons |
US4826667A (en) * | 1986-01-29 | 1989-05-02 | Chevron Research Company | Zeolite SSZ-25 |
NZ218939A (en) * | 1986-01-29 | 1989-11-28 | Chevron Res | Zeolite ssz-25; mole ratio of sio 2 or geo 2 to other framework oxides greater than 20 to 1 |
US4954325A (en) * | 1986-07-29 | 1990-09-04 | Mobil Oil Corp. | Composition of synthetic porous crystalline material, its synthesis and use |
DE3703291A1 (de) * | 1987-02-04 | 1988-08-18 | Ruetgerswerke Ag | Verfahren zur herstellung von 2,6-dialkylnaphthalin |
IT1205681B (it) * | 1987-05-26 | 1989-03-31 | Eniricerche Spa | Materiale sintetico cristallino poroso contenente ossidi di silicio e boro |
US4891458A (en) * | 1987-12-17 | 1990-01-02 | Innes Robert A | Liquid phase alkylation or transalkylation process using zeolite beta |
US5008479A (en) * | 1988-09-27 | 1991-04-16 | Mitsubishi Gas Chemical Company, Inc. | Process for production of 2,6-dimethylnaphthalene |
-
1990
- 1990-03-15 US US07/494,255 patent/US5043501A/en not_active Expired - Fee Related
-
1991
- 1991-02-20 AU AU71251/91A patent/AU631483B2/en not_active Ceased
- 1991-02-21 CA CA002036827A patent/CA2036827A1/en not_active Abandoned
- 1991-02-28 EP EP91301664A patent/EP0447069B1/en not_active Expired - Lifetime
- 1991-02-28 DE DE69109526T patent/DE69109526T2/de not_active Expired - Fee Related
- 1991-03-12 KR KR1019910003935A patent/KR910016654A/ko active IP Right Grant
- 1991-03-14 JP JP3049902A patent/JP2898770B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
AU631483B2 (en) | 1992-11-26 |
JPH04217634A (ja) | 1992-08-07 |
EP0447069B1 (en) | 1995-05-10 |
CA2036827A1 (en) | 1991-09-16 |
EP0447069A2 (en) | 1991-09-18 |
US5043501A (en) | 1991-08-27 |
DE69109526D1 (de) | 1995-06-14 |
EP0447069A3 (en) | 1991-11-27 |
AU7125191A (en) | 1991-09-19 |
JP2898770B2 (ja) | 1999-06-02 |
DE69109526T2 (de) | 1995-09-14 |
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