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公开(公告)号:DE19740112A1
公开(公告)日:1999-03-18
申请号:DE19740112
申请日:1997-09-12
Applicant: BASF AG
Inventor: PAPKALLA THOMAS DR , LUX JUERGEN ALFRED DR , EBEL KLAUS DR
Abstract: In the production of polycarboxylic acids (I), crosslinked polysaccharides (II) are used for oxidation with gaseous nitrogen dioxide/dinitrogen tetroxide in a fluidized bed at 30-150 deg C, in which at least some of the hydroxyl groups of (II) are converted to carboxyl groups and then optionally (partly) neutralized.
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公开(公告)号:DE19641483A1
公开(公告)日:1998-04-16
申请号:DE19641483
申请日:1996-10-09
Applicant: BASF AG
Inventor: EIERMANN MATTHIAS DR , PAPKALLA THOMAS DR
IPC: C07C309/04 , C07C303/14
Abstract: Process to manufacture methane sulfonic acid by irradiation of a mixture containing acetic acid, sulphur dioxide and oxygen with light. Accumulated irradiation density of light in 240-320 nm range on light entrance surface in reaction mixture is on average 0.05 to 50 nMol quantum/cm h.
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公开(公告)号:ES2105049T3
公开(公告)日:1997-10-16
申请号:ES93118478
申请日:1993-11-16
Applicant: BASF AG
Inventor: BAUR KARL GERHARD DR , PAPKALLA THOMAS DR , KANNE ULRICH DR , STOPS PETER
IPC: C02F1/58 , C02F1/72 , C02F11/08 , C02F101/16 , C02F101/30
Abstract: Oxidation of ammonium ions and organic carbon in ammonium-ion-containing and organic carbon-containing waste waters (effluents) by nitric acid at 100 to 350@C, in that the molar ratio of organic carbon to ammonium nitrogen is established at a range of 0.3:1 to 4:1 by addition of organic carbon or ammonium nitrogen. In a preferred embodiment which is reproduced by way of example in the figure, the waste water, which can be enriched, depending on the TOC content, with organic carbon, is transported via the feedline (1), possibly from an intermediate tank (2), by a pump (3) through a heat exchanger (4) in which it is preheated to, for example, 270@C. The preheated waste water is then heated by direct feed of 100 bar high-pressure steam via feedline (5) or by indirect heating to 290@C. After establishing the nitric acid concentration necessary for the ammonium degradation, e.g. via a feedline (6) in the waste water at 290@C, this is conveyed through a reactor (7) without back-mixing (e.g. a tubular reactor having internals and which is clad with titanium). After a residence time of, for example, 5 to 10 min, the reaction solution is cooled in counter-current with the feed and is depressurised in a separator (8). The waste water is removed via a line (9), via an intermediate tank (10) and a heat exchanger (11).
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公开(公告)号:DE19503327A1
公开(公告)日:1996-08-08
申请号:DE19503327
申请日:1995-02-02
Applicant: BASF AG
Inventor: EBEL KLAUS DR , EIERMANN MATTHIAS DR , PAPKALLA THOMAS DR
IPC: C07C67/333 , C07C69/738
Abstract: Prepn. of 5-oxo-6-heptenoic acid alkyl esters of formula (I) comprises: (a) reaction of 5-acetyl-2-norbornene (VI) with a dialkylcarbonate of formula (VII), in the presence of a base, to give a 3-(2-norbornen-5-yl)-3-oxopropionic acid alkyl ester of formula (II); (b) reaction of (II) with an unsatd. cpd. of formula (III) in the presence of a base, and hydrolysis to give a 5-(2-norbornen-5-yl)-5- oxopentanoic acid of formula (IV); (c) esterification to a 5-(2-norbornen-5-yl)-5- oxopentanoic acid ester of formula (V); and (d) thermal cleavage of this cpd. at 300-700 degrees C to give (I). Q = H (in (IV)) or R (in (V)); X, Y = H or Me; R = 1-8C alkyl; R = 1-4C alkyl; Z = CN or CO2R ; R = 1-4C alkyl;
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公开(公告)号:DE4239487A1
公开(公告)日:1994-05-26
申请号:DE4239487
申请日:1992-11-25
Applicant: BASF AG
Inventor: BAUR KARL GERHARD DR , PAPKALLA THOMAS DR , KANNE ULRICH DR , STOPS PETER
IPC: C02F1/58 , C02F1/72 , C02F11/08 , C02F101/16 , C02F101/30 , C02F1/02
Abstract: Oxidation of ammonium ions and organic carbon in ammonium-ion-containing and organic carbon-containing waste waters (effluents) by nitric acid at 100 to 350@C, in that the molar ratio of organic carbon to ammonium nitrogen is established at a range of 0.3:1 to 4:1 by addition of organic carbon or ammonium nitrogen. In a preferred embodiment which is reproduced by way of example in the figure, the waste water, which can be enriched, depending on the TOC content, with organic carbon, is transported via the feedline (1), possibly from an intermediate tank (2), by a pump (3) through a heat exchanger (4) in which it is preheated to, for example, 270@C. The preheated waste water is then heated by direct feed of 100 bar high-pressure steam via feedline (5) or by indirect heating to 290@C. After establishing the nitric acid concentration necessary for the ammonium degradation, e.g. via a feedline (6) in the waste water at 290@C, this is conveyed through a reactor (7) without back-mixing (e.g. a tubular reactor having internals and which is clad with titanium). After a residence time of, for example, 5 to 10 min, the reaction solution is cooled in counter-current with the feed and is depressurised in a separator (8). The waste water is removed via a line (9), via an intermediate tank (10) and a heat exchanger (11).
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公开(公告)号:DE59910556D1
公开(公告)日:2004-10-28
申请号:DE59910556
申请日:1999-04-06
Applicant: BASF AG
Inventor: PAPKALLA THOMAS DR , BAUR KARL GERHARD DR , LANGENSIEPEN HANS-WERNER DR , MACKENROTH WOLFGANG PROF DR
IPC: A62D3/40 , A62D101/26 , A62D101/28 , C02F1/02 , C02F1/58
Abstract: PROBLEM TO BE SOLVED: To decompose different aromatic nitro compounds in waste water as many as possible in a single process when decomposing nitro compounds in the waste water and a mixture of more than two these compounds, by using at least one aromatic nitro compound not having a hydroxyl group in its aromatic ring. SOLUTION: Waste water is thermally decomposed in a pressure vessel under such a condition that temperature is 150-350 deg.C, favorably 250-320 deg.C, pressure is 10-300 bars, favorably 40-250 bars, and the pH of the waste water is 7-14, favorably 10-13. The temperature of the waste water is adjusted so that nitroaromatic compounds with low solubility do not form an organic phase. The amount of the nitro compound with low solubility in water is adjusted according to the temperature of the waste water preferably of 40-80 deg.C. Thereby, the aromatic nitro compounds having no hydroxyl group and the nitro hydroxy aromatic compounds in the waste water can be decomposed at the same time in a single process.
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公开(公告)号:DE4443528A1
公开(公告)日:1996-06-13
申请号:DE4443528
申请日:1994-12-07
Applicant: BASF AG
Inventor: BAUR KARL GERHARD DR , PAPKALLA THOMAS DR
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公开(公告)号:DE59200035D1
公开(公告)日:1994-02-03
申请号:DE59200035
申请日:1992-02-27
Applicant: BASF AG
Inventor: BAUR KARL GERHARD DR , DOCKNER TONI DR , KANNE ULRICH DR , PAPKALLA THOMAS DR
Abstract: A process for breaking down aromatic nitro compounds in waste waters from plants for the production of nitrobenzene by treatment with nitric acid is carried out at from 180 DEG to 350 DEG C. and under a pressure of from 40 to 250 bar.
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公开(公告)号:DE59307258D1
公开(公告)日:1997-10-09
申请号:DE59307258
申请日:1993-11-16
Applicant: BASF AG
Inventor: BAUR KARL GERHARD DR , PAPKALLA THOMAS DR , KANNE ULRICH DR , STOPS PETER
IPC: C02F1/58 , C02F1/72 , C02F11/08 , C02F101/16 , C02F101/30
Abstract: Oxidation of ammonium ions and organic carbon in ammonium-ion-containing and organic carbon-containing waste waters (effluents) by nitric acid at 100 to 350@C, in that the molar ratio of organic carbon to ammonium nitrogen is established at a range of 0.3:1 to 4:1 by addition of organic carbon or ammonium nitrogen. In a preferred embodiment which is reproduced by way of example in the figure, the waste water, which can be enriched, depending on the TOC content, with organic carbon, is transported via the feedline (1), possibly from an intermediate tank (2), by a pump (3) through a heat exchanger (4) in which it is preheated to, for example, 270@C. The preheated waste water is then heated by direct feed of 100 bar high-pressure steam via feedline (5) or by indirect heating to 290@C. After establishing the nitric acid concentration necessary for the ammonium degradation, e.g. via a feedline (6) in the waste water at 290@C, this is conveyed through a reactor (7) without back-mixing (e.g. a tubular reactor having internals and which is clad with titanium). After a residence time of, for example, 5 to 10 min, the reaction solution is cooled in counter-current with the feed and is depressurised in a separator (8). The waste water is removed via a line (9), via an intermediate tank (10) and a heat exchanger (11).
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公开(公告)号:AT157636T
公开(公告)日:1997-09-15
申请号:AT93118478
申请日:1993-11-16
Applicant: BASF AG
Inventor: BAUR KARL GERHARD DR , PAPKALLA THOMAS DR , KANNE ULRICH DR , STOPS PETER
IPC: C02F1/58 , C02F1/72 , C02F11/08 , C02F101/16 , C02F101/30
Abstract: Oxidation of ammonium ions and organic carbon in ammonium-ion-containing and organic carbon-containing waste waters (effluents) by nitric acid at 100 to 350@C, in that the molar ratio of organic carbon to ammonium nitrogen is established at a range of 0.3:1 to 4:1 by addition of organic carbon or ammonium nitrogen. In a preferred embodiment which is reproduced by way of example in the figure, the waste water, which can be enriched, depending on the TOC content, with organic carbon, is transported via the feedline (1), possibly from an intermediate tank (2), by a pump (3) through a heat exchanger (4) in which it is preheated to, for example, 270@C. The preheated waste water is then heated by direct feed of 100 bar high-pressure steam via feedline (5) or by indirect heating to 290@C. After establishing the nitric acid concentration necessary for the ammonium degradation, e.g. via a feedline (6) in the waste water at 290@C, this is conveyed through a reactor (7) without back-mixing (e.g. a tubular reactor having internals and which is clad with titanium). After a residence time of, for example, 5 to 10 min, the reaction solution is cooled in counter-current with the feed and is depressurised in a separator (8). The waste water is removed via a line (9), via an intermediate tank (10) and a heat exchanger (11).
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