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公开(公告)号:SA1510B1
公开(公告)日:2006-11-04
申请号:SA03240323
申请日:2003-10-08
Applicant: BASF AG
Inventor: THIEL JOACHIM , HAMMON ULRIICH , BAUMANN DIETER , HEILEK JORG , SCHRODER JURGEN , -ENGEL KLAUS JOACHIM
IPC: C07C51/44
Abstract: الملخص: فىطريقةلتحضيرحمضاكريليك preparing acrylic acid،يتمتكثيفالخليطالغازىالمحتوىعلىحمضاكريليك acrylic acid الناتجمنالاكسدةالجزئيةذاتالطورالغازىالحفازةلمركب C3 اولىمنحمضالاكريليك acrylic acid،وبعدالتبريدالمباشربسائلإطفاء،تجزيئيافىعمودفصلمزودبمساحاتفاصلةداخلية،ويتصاعدداخلةبتيارجانبيمنحمضاكريليكخام crude acrylic acid،ويتمتفككاوليجوميرات oligomers حمضالاكريليك acrylic acid المتكونة،وتعريضغازالتفككالناتجالىتقويممتعاكسالاتجاهقبلاعادةتدويره.
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公开(公告)号:ES2256586T3
公开(公告)日:2006-07-16
申请号:ES02799748
申请日:2002-12-18
Applicant: BASF AG
Inventor: NESTLER GERHARD , SCHRODER JURGEN , WICKEL STEFAN
Abstract: Polímeros que forman hidrogel que absorben líquidos acuosos a base de polímeros que portan grupos ácidos, que contienen tocoferol.
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公开(公告)号:ES2216045T3
公开(公告)日:2004-10-16
申请号:ES96905803
申请日:1996-02-27
Applicant: BASF AG
Inventor: MERKLE HANS RUPERT , FRETSCHNER ERICH , SCHRODER JURGEN
IPC: C07D231/12 , C07D521/00
Abstract: PCT No. PCT/EP96/00790 Sec. 371 Date Aug. 20, 1997 Sec. 102(e) Date Aug. 20, 1997 PCT Filed Feb. 27, 1996 PCT Pub. No. WO96/27589 PCT Pub. Date Sep. 12, 1996A process for the preparation of an N-alkyl- or N-phenylalkyl-substituted pyrazole I by reacting the corresponding N-unsubstituted pyrazole II with an alcohol III of the formula R1-OH where R1 is the same alkyl or phenylalkyl group to be added to the unsubstituted nitrogen group -NH- of the pyrazole reactant. Both of the reactants, i.e. the pyrazole II and alcohol III compounds, are catalytically reacted in the liquid phase in a molar ratio of from 0.001:1 to 1:1, at temperatures of 50 DEG -400 DEG C. and under a subatmosheric pressure of from 0.8 bar up to a superatmospheric pressure of 250 bar. The catalyst required for this liquid phase reaction is selected as being at least one or more non-heterogeneous acid catalysts, their alkyl esters or their acid anhydrides.
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公开(公告)号:AU2003294002A1
公开(公告)日:2004-08-10
申请号:AU2003294002
申请日:2003-12-24
Applicant: BASF AG
Inventor: SCHRODER JURGEN , THIEL JOACHIM , DAMS ALBRECHT
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公开(公告)号:AU2003219099A1
公开(公告)日:2003-12-12
申请号:AU2003219099
申请日:2003-03-26
Applicant: BASF AG
Inventor: HOFER FRANK , HAREMZA SYLKE , WAGENBLAST GERHARD , SCHLIEPHAKE VOLKER , JAGER ULRICH , SCHRODER JURGEN , KELLER HARALD , DIELEMAN CEDRIC
IPC: C07C51/50 , C07C67/62 , C07C45/86 , C07C253/32 , C07C57/075 , C07C69/54
Abstract: The invention relates to the use of aldoximes, ketoximes which are not derived from quinones, hydroxime acid esters, and N-acyl-hydroxylamine derivatives for stabilising ethylenically unsaturated compounds containing oxygen and/or nitrogen, such as (meth)acrylic acid (esters). Co-stabilisers, such as transition metal salts, phenols, quinones, or hydroquinones, N-oxyls, aromatic amines or phenylenediamines, urea derivatives, compounds containing phosphorus, compounds containing sulphur, and sulfonamides, can be used with the above-mentioned substances. Preferably, a gas containing oxygen, such as air, is present.
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公开(公告)号:AU2003218684A1
公开(公告)日:2003-09-22
申请号:AU2003218684
申请日:2003-03-04
Applicant: BASF AG
Inventor: DIEHL VOLKER , JAGER ULRICH , SCHRODER JURGEN , MULLER-ENGEL KLAUS JOACHIM , SCHLIEPHAKE VOLKER , HAMMON ULRICH
Abstract: In process for cleaning tray columns which are used for the purposes of rectifiying liquids comprising (meth)acrylic compounds, a basic liquid is conveyed downward through the tray column and a gas is passed through the column in countercurrent to the basic liquid at an average gas phase differential pressure over all trays of at least 0.5 mbar/tray.
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公开(公告)号:CZ20013843A3
公开(公告)日:2002-02-13
申请号:CZ20013843
申请日:2000-04-27
Applicant: BASF AG
Inventor: AICHINGER HEINRICH , NESTLER GERHARD , SCHRODER JURGEN
Abstract: Free radical polymerizations immediately terminated by a process comprising the addition of an inhibitor solution which contains phenothiazine and at least 50% (w/w) N-alkylpyrrolidone to a system undergoing free radical polymerization, wherein the inhibitor solution also contains p-methoxyphenol (MEHQ).
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公开(公告)号:ID23871A
公开(公告)日:2000-05-25
申请号:ID20000704
申请日:1998-10-21
Applicant: BASF AG
Inventor: AICHINGER HEINRICH , HERBST HOLGER , NESTLER GERHARD , SCHRODER JURGEN
Abstract: Plant parts which are used for the production or processing of (meth)acrylic esters are cleaned by(a) emptying the plant parts,(b) flushing the plant parts with aqueous 5 to 50% strength by weight alkali metal hydroxide solution,(c) removing the alkali metal hydroxide solution from the plant parts,(d) if required, washing the plant parts with water and(e) if required, drying the plant parts.
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公开(公告)号:AU1230899A
公开(公告)日:1999-05-10
申请号:AU1230899
申请日:1998-10-21
Applicant: BASF AG
Inventor: AICHINGER HEINRICH , HERBST HOLGER , NESTLER GERHARD , SCHRODER JURGEN
Abstract: Plant parts which are used for the production or processing of (meth)acrylic esters are cleaned by(a) emptying the plant parts,(b) flushing the plant parts with aqueous 5 to 50% strength by weight alkali metal hydroxide solution,(c) removing the alkali metal hydroxide solution from the plant parts,(d) if required, washing the plant parts with water and(e) if required, drying the plant parts.
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公开(公告)号:NZ303185A
公开(公告)日:1999-01-28
申请号:NZ30318596
申请日:1996-02-27
Applicant: BASF AG
Inventor: MERKLE HANS RUPERT , FRETSCHNER ERICH , SCHRODER JURGEN
IPC: C07D231/12 , C07D521/00
Abstract: PCT No. PCT/EP96/00790 Sec. 371 Date Aug. 20, 1997 Sec. 102(e) Date Aug. 20, 1997 PCT Filed Feb. 27, 1996 PCT Pub. No. WO96/27589 PCT Pub. Date Sep. 12, 1996A process for the preparation of an N-alkyl- or N-phenylalkyl-substituted pyrazole I by reacting the corresponding N-unsubstituted pyrazole II with an alcohol III of the formula R1-OH where R1 is the same alkyl or phenylalkyl group to be added to the unsubstituted nitrogen group -NH- of the pyrazole reactant. Both of the reactants, i.e. the pyrazole II and alcohol III compounds, are catalytically reacted in the liquid phase in a molar ratio of from 0.001:1 to 1:1, at temperatures of 50 DEG -400 DEG C. and under a subatmosheric pressure of from 0.8 bar up to a superatmospheric pressure of 250 bar. The catalyst required for this liquid phase reaction is selected as being at least one or more non-heterogeneous acid catalysts, their alkyl esters or their acid anhydrides.
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