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公开(公告)号:ES2169418T3
公开(公告)日:2002-07-01
申请号:ES97940102
申请日:1997-08-21
Applicant: BASF AG
Inventor: LUYKEN HERMANN , VOIT GUIDO , BASSLER PETER , REHFINGER ALWIN , FISCHER ROLF
IPC: B01J27/187 , C07B61/00 , C07C209/48 , C07C209/84 , C07C211/12 , C07C253/30 , C07C253/34 , C07C255/24
Abstract: A process for coproduction of 6-aminocapronitrile and hexamethylenediamine starting from adiponitrile comprises(1) partially hydrogenating adiponitrile in the presence of a catalyst to obtain a mixture comprising 6-aminocapronitrile, hexamethylenediamine and adiponitrile,(2) removing 6-aminocapronitrile and hexamethylenediamine from the mixture,(3) adding to the portion comprising essentially adiponitrile from 0.01 to 10% by weight of an acid, based on adiponitrile, or an acidic ion exchanger and removing the adiponitrile from the mixture, and(4) recycling the adiponitrile into step (1).
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公开(公告)号:BR0014456A
公开(公告)日:2002-06-11
申请号:BR0014456
申请日:2000-09-15
Applicant: BASF AG
Inventor: OHLBACH FRANK , FISCHER ROLF , LUYKEN HERMANN , MELDER JOHANN-PETER , MERGER MARTIN , ANSMANN ANDREAS , BASSLER PETER
IPC: B01J23/745 , B01J37/18 , C07B61/00 , C07C209/48 , C07C211/12 , C07C231/06 , C07C237/06
Abstract: Passivated iron useful as catalytically active component after activation is activated by hydrogen at elevated temperature and elevated pressure in the presence of a nitrile.
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公开(公告)号:SK282367B6
公开(公告)日:2002-01-07
申请号:SK10698
申请日:1996-07-26
Applicant: BASF AG
Inventor: SIGWART CHRISTOPH , FISCHER ROLF , ELLER KARSTEN , BECKER RAINER , PLITZKO KLAUS-DIETER , HEILEN GERD
Abstract: PCT No. PCT/EP96/03297 Sec. 371 Date Jan. 22, 1998 Sec. 102(e) Date Jan. 22, 1998 PCT Filed Jul. 26, 1996 PCT Pub. No. WO97/05188 PCT Pub. Date Feb. 13, 1997In a process for the preparation of copolymers of tetrahydrofuran and but-2-yne-1,4-diol by catalytic polymerization of tetrahydrofuran, the polymerization is carried out over a heterogeneous acidic catalyst which has acid centers of acidity pKa
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公开(公告)号:DE10028950A1
公开(公告)日:2001-12-20
申请号:DE10028950
申请日:2000-06-16
Applicant: BASF AG
Inventor: OHLBACH FRANK , ANSMANN ANDREAS , FISCHER ROLF , MELDER JOHANN-PETER
IPC: C07B61/00 , C07D201/08 , C07D223/10 , C07D233/10
Abstract: Caprolactam is produced from a cyanovaleric acid derivative (I) by: (a) catalytically hydrogenating (I) or a mixture containing (I) with H2 in the presence of ammonia and optionally also a liquid diluent; (b) separating-off H2 and the catalyst; and (c) catalytically converting the mixture obtained to caprolactam optionally in the presence of a liquid diluent. Caprolactam is produced from a cyanovaleric acid derivative of formula (I) by: (a) catalytically hydrogenating (I) or a mixture containing (I) with H2 in the presence of ammonia and optionally also a liquid diluent; (b) separating-off H2 and the catalyst; and (c) catalytically converting the mixture obtained to caprolactam optionally in the presence of a liquid diluent. NC-(CH2)5-CO-R (I) R = a carbonamide, carboxylic acid or carboxylic acid ester group.
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公开(公告)号:DE10027328A1
公开(公告)日:2001-12-06
申请号:DE10027328
申请日:2000-06-05
Applicant: BASF AG
Inventor: LUYKEN HERMANN , OHLBACH FRANK , MAIXNER STEFAN , FISCHER ROLF , MELDER JOHANN-PETER , BASLER PETER , ANSMANN ANDREAS
IPC: C01C1/10 , C07D201/08 , C07D201/16 , C07D223/10
Abstract: Distillative separation of ammonia (NH3) from solutions (I) containing a lactam and NH3 is carried out at an absolute pressure less than 10 bar in still (a).
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公开(公告)号:DE10021193A1
公开(公告)日:2001-11-08
申请号:DE10021193
申请日:2000-05-03
Applicant: BASF AG
Inventor: OHLBACH FRANK , ANSMANN ANDREAS , BASLER PETER , FISCHER ROLF , LUYKEN HERMANN , MAIXNER STEFAN , MELDER JOHANN-PETER
IPC: C07D223/10 , C07B61/00 , C07D201/08 , C07D207/263 , C07D211/76 , C07D225/02 , C07D207/267 , C07D227/02
Abstract: The invention relates to a method for producing cyclic lactams of the formula (II), wherein n and m may each represent 0, 1, 2, 3, 4, 5, 6, 7, 8 and 9 and the sum of n + m is at least 3, preferably at least 4, R and R represent C1-C6 alkyl, C5-C7 cycloalkyl or C6-C12 aryl groups, by reacting a compound of the formula (I), wherein R , R , m and n have the meaning indicated above, and R represents nitrile groups, carboxylic acid amide groups and carboxylic acid groups, with water vapor in the gaseous phase. The inventive method is further characterized in that a) the compound (I) is reacted with water vapor in the gaseous phase, adding an organic diluent (III) before or after the reaction, which diluent has a miscibility gap under certain quantitative, pressure and temperature conditions, said reaction resulting in a mixture (IV) that contains a lactam (II), b) adjusting the mixture (IV) before or after the removal of ammonia to quantitative, pressure and temperature conditions under which the diluent (III) and water are present in a liquid form and have a miscibility gap, and obtaining a two-phase system consisting of a phase (V) that has a higher proportion of diluent (III) than water, and a phase (VI) that has a higher proportion of water than diluent (III), c) separating phase (V) from phase (VI) and, d) removing from phase (V) the diluent (III) and optionally by-products selected from the group of the low-boilers, high-boilers and unreacted compound (I), and obtaining a lactam (II).
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公开(公告)号:DE10021192A1
公开(公告)日:2001-11-08
申请号:DE10021192
申请日:2000-05-03
Applicant: BASF AG
Inventor: BASLER PETER , BAUMANN DIETER , FISCHER ROLF , FUCHS EBERHARD , MELDER JOHANN-PETER , OHLBACH FRANK
IPC: C07D223/12 , C07D201/08 , C07D223/10
Abstract: The invention relates to a method for producing caprolactam, which is characterized by a) reacting, in the presence of a catalyst, a mixture (I) that contains 6-aminocapronitrile and water in the gaseous phase to give a mixture (II) that contains caprolactam, ammonia, water, high-boiling and low-boiling substances, subsequently b) removing the ammonia from mixture (II), thereby producing a mixture (III) that contains caprolactam, water, high-boiling and low-boiling substances, c) removing the water from mixture (III), thereby producing a mixture (IV) that contains caprolactam, high-boiling and low-boiling substances, and finally d) obtaining by crystallization a caprolactam-containing solid substance (V) from mixture (IV), the weight percentage of caprolactam in the solid substance (V) being higher than in mixture (IV).
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公开(公告)号:DE59607693D1
公开(公告)日:2001-10-18
申请号:DE59607693
申请日:1996-12-11
Applicant: BASF AG
Inventor: FISCHER ROLF , KRATZ DETLEF , PINKOS ROLF , SCHAEFER MARTIN , HOEHN ARTHUR
IPC: C07D303/04 , B01J31/24 , C07B61/00 , C07C29/132 , C07C29/17 , C07C31/20 , C07D303/22
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公开(公告)号:DE10014646A1
公开(公告)日:2001-09-27
申请号:DE10014646
申请日:2000-03-24
Applicant: BASF AG
Inventor: FISCHER ROLF , PINKOS ROLF , SCHUNK STEFAN , WULFF-DOERING JOACHIM
IPC: B01J21/18 , B01J23/36 , B01J23/656 , B01J23/889 , C07B61/00 , C07C29/136 , C07C29/149 , C07C31/20 , C07C31/27 , C07C31/133
Abstract: A catalyst (I) comprises 0.01-50 wt.% rhenium and 0-20 wt.% of an additional metal comprising Zn, Cu, Ag, Au, Ni, Fe, Cr or V on an oxidatively pretreated activated carbon support. An independent claim is included for production of alcohols by catalytic hydrogenation of carbonyl compounds by means of a catalyst (I).
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公开(公告)号:SK281653B6
公开(公告)日:2001-06-11
申请号:SK38397
申请日:1995-09-21
Applicant: BASF AG
Inventor: BECKER RAINER , SIGWART CHRISTOPH , HESSE MICHAEL , FISCHER ROLF , ELLER KARSTEN , HEILEN GERD , PLITZKO KLAUS-DIETER
Abstract: PCT No. PCT/EP95/03651 Sec. 371 Date Mar. 10, 1997 Sec. 102(e) Date Mar. 10, 1997 PCT Filed Sep. 21, 1995 PCT Pub. No. WO96/09335 PCT Pub. Date Mar. 28, 1996A process for the preparation of polytetrahydrofuran or polytetrahydrofuran monoesters of C1-C10 monocarboxylic acids by the polymerization of tetrahydrofuran over a heterogeneous catalyst in the presence of one of the telogens water, 1,4-butanediol or polytetrahydrofuran having a molecular weight of from 200 to 700 dalton or a C1-C10 monocarboxylic acid or mixtures of these telogens, wherein a supported catalyst is used as catalyst, which contains a catalytically active amount of an oxygen-containing tungsten or molybdenum compound or mixtures of these compounds on an oxidic support material and which was calcined at temperatures ranging from 500 DEG to 1000 DEG C. following the application of the precursor compounds of said oxygen-containing molybdenum and/or tungsten compounds to the support material precursor.
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