SG90091A1 - Process for producing epsilon-caprolactam - Google Patents
Process for producing epsilon-caprolactamInfo
- Publication number
- SG90091A1 SG90091A1 SG200000739A SG200000739A SG90091A1 SG 90091 A1 SG90091 A1 SG 90091A1 SG 200000739 A SG200000739 A SG 200000739A SG 200000739 A SG200000739 A SG 200000739A SG 90091 A1 SG90091 A1 SG 90091A1
- Authority
- SG
- Singapore
- Prior art keywords
- caprolactam
- producing epsilon
- epsilon
- producing
- Prior art date
Links
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 title 2
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J38/00—Regeneration or reactivation of catalysts, in general
- B01J38/04—Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst
- B01J38/12—Treating with free oxygen-containing gas
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D223/08—Oxygen atoms
- C07D223/10—Oxygen atoms attached in position 2
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/90—Regeneration or reactivation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D201/00—Preparation, separation, purification or stabilisation of unsubstituted lactams
- C07D201/02—Preparation of lactams
- C07D201/04—Preparation of lactams from or via oximes by Beckmann rearrangement
-
- 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
-
- 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
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11031226A JP2000229939A (ja) | 1999-02-09 | 1999-02-09 | ε−カプロラクタムの製造方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG90091A1 true SG90091A1 (en) | 2002-07-23 |
Family
ID=12325517
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG200000739A SG90091A1 (en) | 1999-02-09 | 2000-02-08 | Process for producing epsilon-caprolactam |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6265574B1 (zh) |
| EP (1) | EP1028108A1 (zh) |
| JP (1) | JP2000229939A (zh) |
| KR (1) | KR20010006615A (zh) |
| CN (1) | CN100379726C (zh) |
| SG (1) | SG90091A1 (zh) |
| TW (1) | TW593275B (zh) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002105039A (ja) * | 2000-09-29 | 2002-04-10 | Sumitomo Chem Co Ltd | シクロヘキサノンオキシムの蒸発方法とこれに使用する蒸発器、ならびにε−カプロラクタムの製造方法とその製造装置 |
| US6531595B2 (en) | 2000-09-29 | 2003-03-11 | Sumitomo Chemical Company, Limited | Method for producing ε-caprolactam and reactor for the method |
| US7022844B2 (en) | 2002-09-21 | 2006-04-04 | Honeywell International Inc. | Amide-based compounds, production, recovery, purification and uses thereof |
| US20060173205A1 (en) * | 2003-03-19 | 2006-08-03 | Yasuhisa Fukuda | Process for producing w-cyanoaldehyde compound |
| SG110097A1 (en) * | 2003-07-08 | 2005-04-28 | Sumitomo Chemical Co | Method for producing epsilon-caprolactam |
| JP4661071B2 (ja) | 2004-03-30 | 2011-03-30 | 住友化学株式会社 | ε−カプロラクタムの製造方法 |
| FR2887250B1 (fr) * | 2005-06-21 | 2009-10-02 | Arkema Sa | Procede de synthese du lauryllactame (l12) par rearrangement catalytique en phase gazeuse de la cyclododecanone oxime |
| JP2007204407A (ja) * | 2006-01-31 | 2007-08-16 | National Institute Of Advanced Industrial & Technology | 含窒素化合物の製造方法及びその装置 |
| CN101143843B (zh) * | 2006-09-14 | 2014-03-26 | 中国石油化工股份有限公司 | 一种ε-己内酰胺的制备方法 |
| CN101434569B (zh) * | 2007-11-15 | 2011-07-20 | 中国石油化工股份有限公司 | 一种由环己酮肟制备己内酰胺的方法及设备 |
| DE102008060340A1 (de) | 2008-12-03 | 2010-06-10 | Wolfgang F. Prof. Dr. Hölderich | Herstellung von Lactamen und Carbonsäureamide durch Beckmann-Umlagerung von Oximen in Gegenwart von Nb-Katalysatoren |
| ES2676918T3 (es) | 2010-03-15 | 2018-07-26 | Ube Industries, Ltd. | Método para producir un compuesto de amida |
| TWI414508B (zh) | 2011-01-17 | 2013-11-11 | China Petrochemical Dev Corp Taipei Taiwan | A catalyst composition and a method for preparing an amide using the composition |
| EP2697202B1 (en) | 2011-04-13 | 2015-07-22 | Rennovia, Inc. | Production of caprolactam from carbohydrate-containing materials |
| CN102875469B (zh) * | 2011-07-14 | 2015-01-14 | 中国石油化工股份有限公司 | 采用径向移动床反应器制备己内酰胺的方法 |
| TWI418401B (zh) | 2011-08-26 | 2013-12-11 | China Petrochemical Dev Corp Taipei Taiwan | A method for preparing a catalytic composition of amide and a method for producing amide |
| CN103648606B (zh) * | 2011-09-16 | 2016-03-09 | 住友化学株式会社 | 雾滴分离装置及反应系统 |
| CN103012263B (zh) * | 2011-09-28 | 2016-04-27 | 中国石油化工股份有限公司 | 一种己内酰胺的制备方法 |
| JP2013116434A (ja) * | 2011-12-01 | 2013-06-13 | Sumitomo Chemical Co Ltd | 反応装置 |
| JP2013141659A (ja) * | 2012-01-12 | 2013-07-22 | Sumitomo Chemical Co Ltd | 反応装置及びε−カプロラクタムの製造方法 |
| KR20140129076A (ko) | 2012-02-23 | 2014-11-06 | 레노비아 인코포레이티드 | 아디프산으로부터의 카프로락탐의 제조 |
| JP6591740B2 (ja) * | 2013-10-29 | 2019-10-16 | 中国石油化工股▲ふん▼有限公司 | 完全Si分子篩、および、その合成方法 |
| DE102015005238A1 (de) | 2015-04-24 | 2016-10-27 | Wolfgang Hölderich | Herstellung von Lactamen durch Beckmann-Umlagerung von Oximen |
| CN109503484A (zh) * | 2018-12-29 | 2019-03-22 | 清华大学 | 一种使用高沸点惰性溶剂制备己内酰胺的方法 |
| CN113831271B (zh) * | 2020-06-24 | 2023-10-31 | 中国石油化工股份有限公司 | 一种催化环己酮肟气相重排制备己内酰胺的方法 |
| CN113105362B (zh) * | 2021-04-14 | 2023-11-07 | 江苏扬农化工集团有限公司 | 一种气相法制备6-氨基己腈的装置及方法 |
| CN115337958B (zh) * | 2022-07-07 | 2023-06-16 | 郑州大学 | 一种改善成型s-1分子筛催化环己酮肟气相贝克曼重排反应活性位的方法 |
| CN115957811B (zh) * | 2023-01-12 | 2024-11-08 | 中国天辰工程有限公司 | 一种液相贝克曼重排反应催化剂的原位再生方法 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4155876A (en) * | 1976-09-15 | 1979-05-22 | Bayer Aktiengesellschaft | Catalyst regeneration of boric acid on carbon catalysts |
| US5354859A (en) * | 1991-11-27 | 1994-10-11 | Sumitomo Chemical Company Limited | ε-caprolactam |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2844880A1 (de) | 1978-10-14 | 1980-04-30 | Basf Ag | Verfahren zur herstellung von epsilon -caprolactam durch katalytische umlagerung von cyclohexanonoxim |
| US4968793A (en) * | 1989-01-26 | 1990-11-06 | Sumitomo Chemical Company, Limited | Process for producing ε-caprolactam |
| DE69000118T2 (de) * | 1989-03-08 | 1993-01-14 | Koei Chemical Co | Verfahren zur regenerierung von katalysatoren. |
| JP3301092B2 (ja) * | 1990-12-26 | 2002-07-15 | 住友化学工業株式会社 | ε−カプロラクタムの製造方法 |
| KR100287085B1 (ko) * | 1991-11-27 | 2001-04-16 | 고오사이 아끼오 | E-카프로락탐의 제조방법 |
| DE19608660A1 (de) * | 1995-05-04 | 1996-11-07 | Degussa | Verfahren zur Herstellung von epsilon-Caprolactam |
| BE1009465A3 (fr) | 1995-05-04 | 1997-04-01 | Degussa | Procede de fabrication de -caprolactame. |
-
1999
- 1999-02-09 JP JP11031226A patent/JP2000229939A/ja active Pending
-
2000
- 2000-02-01 TW TW089101675A patent/TW593275B/zh not_active IP Right Cessation
- 2000-02-08 KR KR1020000005819A patent/KR20010006615A/ko not_active Ceased
- 2000-02-08 SG SG200000739A patent/SG90091A1/en unknown
- 2000-02-08 EP EP00102152A patent/EP1028108A1/en not_active Withdrawn
- 2000-02-09 US US09/500,997 patent/US6265574B1/en not_active Expired - Lifetime
- 2000-02-09 CN CNB00104639XA patent/CN100379726C/zh not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4155876A (en) * | 1976-09-15 | 1979-05-22 | Bayer Aktiengesellschaft | Catalyst regeneration of boric acid on carbon catalysts |
| US5354859A (en) * | 1991-11-27 | 1994-10-11 | Sumitomo Chemical Company Limited | ε-caprolactam |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20010006615A (ko) | 2001-01-26 |
| US6265574B1 (en) | 2001-07-24 |
| EP1028108A1 (en) | 2000-08-16 |
| JP2000229939A (ja) | 2000-08-22 |
| CN100379726C (zh) | 2008-04-09 |
| CN1269360A (zh) | 2000-10-11 |
| TW593275B (en) | 2004-06-21 |
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