PREPARATION OF DIMETHYL BUTANEDICARBOXYLATES

    公开(公告)号:CA1126754A

    公开(公告)日:1982-06-29

    申请号:CA333752

    申请日:1979-08-14

    Applicant: BASF AG

    Abstract: O.Z. 0050/033380 In a process for the preparation of dimethyl butanedicarboxylates, whereina) butadiene or a hydrocarbon mixture containing butadiene is reacted with carbon monoxide and methanol in the presence of a tertiary nitrogen base and a cobalt carbonyl catalyst at from 80 to 150.degree.C under superatmospheric pressure,b) the greater part of the tertiary nitrogen base and any excess hydrocarbons are removed andc) the methyl pentenoate thus obtained is reacted with carbon monoxide and methanol, in the presence of a cobalt carbonyl catalyst and the residual amount of tertiary nitrogen base, at from 140 to 200.degree.C under superatmospheric pressure, to give the dimethyl butanedicarboxylate, the improvement that the reaction mixture obtained in stagea) after reaction of the butadiene is cooled until it separates into two phases, and a part-stream of from 20 to 80% by volume of the lower phase is recycled to stage a).

    DEVICE FOR PRODUCING CRYSTALS
    15.
    发明专利

    公开(公告)号:PL358987A1

    公开(公告)日:2004-08-23

    申请号:PL35898701

    申请日:2001-05-21

    Applicant: BASF AG

    Abstract: An apparatus and a process for crystallizing substances from solutions or dispersions containing these substances, in a crystallizer containing a classifying zone ( 3 ), comprise a) an inner and an outer circulation system ( 1; 2 ), the inner circulation system ( 1 ) being present in the crystallizer, the inlet of the outer circulation system ( 2 ) being connected to the inner circulation system ( 1 ) via the classifying zone ( 3 ), the outer circulation system, being present outside the crystallizer, the outlet of the outer circulation system ( 2 ) being connected to the inner circulation system ( 1 ) of the crystallizer, and a means for dissolving crystals being arranged in the outer circulation system ( 2 ), before its outlet, b) an inflow ( 4 ) for solution and/or dispersion, which inflow is present on the crystallizer or on the outer circulation system, and c) an outflow ( 5 ) for dispersions, which outflow is arranged on the crystallizer or on the outer circulation system. The novel apparatus has the special feature that a line ( 8 ) connecting the outer and inner circulation systems ( 1; 2 ) to one another and intended for transporting (recycling) dispersion and/or a line ( 8 ) for transporting (recycling) dispersion are additionally present, in which both its entrance and its exit are connected to the inner circulation system ( 1 ).

    Device for producing crystals
    16.
    发明专利

    公开(公告)号:SK16782002A3

    公开(公告)日:2003-05-02

    申请号:SK16782002

    申请日:2001-05-21

    Applicant: BASF AG

    Abstract: An apparatus and a process for crystallizing substances from solutions or dispersions containing these substances, in a crystallizer containing a classifying zone ( 3 ), comprise a) an inner and an outer circulation system ( 1; 2 ), the inner circulation system ( 1 ) being present in the crystallizer, the inlet of the outer circulation system ( 2 ) being connected to the inner circulation system ( 1 ) via the classifying zone ( 3 ), the outer circulation system, being present outside the crystallizer, the outlet of the outer circulation system ( 2 ) being connected to the inner circulation system ( 1 ) of the crystallizer, and a means for dissolving crystals being arranged in the outer circulation system ( 2 ), before its outlet, b) an inflow ( 4 ) for solution and/or dispersion, which inflow is present on the crystallizer or on the outer circulation system, and c) an outflow ( 5 ) for dispersions, which outflow is arranged on the crystallizer or on the outer circulation system. The novel apparatus has the special feature that a line ( 8 ) connecting the outer and inner circulation systems ( 1; 2 ) to one another and intended for transporting (recycling) dispersion and/or a line ( 8 ) for transporting (recycling) dispersion are additionally present, in which both its entrance and its exit are connected to the inner circulation system ( 1 ).

    METHOD OF MANUFACTURING A HYDROGENATION CATALYST

    公开(公告)号:CA2250745A1

    公开(公告)日:1997-10-16

    申请号:CA2250745

    申请日:1997-04-01

    Applicant: BASF AG

    Abstract: The invention concerns the manufacture of a hydrogenation catalyst by the reduction of platinum from an oxidation state of not less than two with a reducing agent in an aqueous medium in the presence of a carbon-containing support following partial poisoning, the method using a compound of general formula (I) in which X, Y and Z, which may be the same or different, are hydrogen, C1-C18 alkyl, C5-C10 cycloalkyl, halogen, hydroxyl, C1-C6 alkoxy orNR'R'', whereby R, R' and R'', which may by the same or different, are hydrogen, C1-C18 alkyl or C5-C10 cycloalkyl. The invention also concerns a hydrogenation catalyst manufactured by this method, its use in the production of hydroxylammonium salts, a method of producing hydroxylammonium salts and a method of regenerating platinum-based hydrogenation catalysts of this kind.

    MANUFACTURE OF BUTANEDICARBOXYLIC ACID ESTERS

    公开(公告)号:CA1113491A

    公开(公告)日:1981-12-01

    申请号:CA298297

    申请日:1978-03-03

    Applicant: BASF AG

    Abstract: A process for the manufacture of butanedicarboxylic acid esters, whereina) an aqueous cobalt salt solution is treated, at from 50 to 200.degree.C and under a pressure of from 50 to 500 bars, with excess carbon monoxide and hydrogen in the presence of active charcoal laden with cobalt carbonyl,b) the resulting aqueous solution of cobalt carbonyl hydride is extracted with butadiene or with a hydrocarbon mixture containing butadiene and the aqueous phase is separated off,c) the butadiene, or butadiene-hydrocarbon mixture, containing cobalt carbonyl hydride, cobalt carbonyl and butenyl-cobalt tricarbonyl is reacted with carbon monoxide and an excess of an alkanol of 1 to 4 carbon atoms in the presence of from 0.5 to 2 moles, per mole of butadiene, of a tertiary nitrogen base having a pKa of from 3 to 11, at from 80 to 150.degree.C under a pressure of from 300 to 2,000 bars, andd) the resulting reaction mixture is freed from the tertiary nitrogen base contained therein, except for from 0.1 to 0.3 mole per mole of pentenoic acid ester, and from excess hydrocarbons, the pentenoic acid ester remaining in the reaction mixture is reacted with carbon monoxide and an excess of an alkanol of 1 to 4 carbon atoms at from 140 to 200.degree.C and under pressures of from 100 to 400 bars in the presence of the amounts of cobalt carbonyl and tertiary nitrogen base contained in the reaction mixture, and excess alkanol and free nitrogen base are then distilled off, ande) the reaction mixture which remains, and which contains cobalt catalyst, the butanedicarboxylic acid ester and by-products is treated with an oxidizing agent in an aqueous acid medium and the mixture is separated into an organic phase, from which the butanedicarboxylic acid ester is isolated by distillation, and into an aqueous phase containing cobalt salts. Butanedicarboxylic acid esters may be used for the manufacture of adipic acid and of nylons.

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