22.
    发明专利
    未知

    公开(公告)号:DE19849527A1

    公开(公告)日:2000-05-04

    申请号:DE19849527

    申请日:1998-10-27

    Applicant: BASF AG

    Inventor: OTT CHRISTIAN

    Abstract: The invention relates to a method of epoxidizing olefins with percarboxylic acid in a reaction mixture consisting of an aqueous phase and an organic phase. According to said method, the percarboxylic acid in the aqueous phase is formed in situ from hydrogen peroxide and a carboxylic acid or a carboxylic acid anhydride and the olefins in the organic phase are dissolved in an organic solvent. The epoxidation is carried out in several steps. Each step is carried out with a fresh aqueous phase each and after each step the aqueous phase is removed.

    24.
    发明专利
    未知

    公开(公告)号:AT300563T

    公开(公告)日:2005-08-15

    申请号:AT01938098

    申请日:2001-04-10

    Applicant: BASF AG

    Abstract: Multifunctional polymers containing polymerized units of (a) alpha-Acyloxyacrylonitrile, alpha-haloacrylic acid, alpha-acyloxyacrylic ester and/or alpha-hydroxyacrylic acid, (b) monoethylenically unsaturated carboxylic acids, (c) vinyl esters of saturated aliphatic monocarboxylic acids and/or vinyl alcohol and optionally (d) other monoethylenically unsaturated monomers copolymerizable with said monomers (a) to (c) and optionally (e) crosslinkers containing at least two ethylenically unsaturated double bonds and having a K value of at least 7 (determined after H. Fikentscher in acetone at 25° C. and a polymer concentration of 1% by weight), processes for preparing multifunctional polymers by copolymerizing monomer mixtures of (a) alpha-acyloxyacrylonitrile, alpha-haloacrylic acid and/or alpha-acyloxyacrylic ester, (b) monoethylenically unsaturated carboxylic acids, (c) vinyl esters of saturated aliphatic monocarboxylic acids and optionally (d) other monoethylenically unsaturated monomers copolymerizable with said monomers (a) to (c) and optionally (e) crosslinkers containing at least two ethylenically unsaturated double bonds in the presence of polymerization initiators that form free radicals and partially or completely hydrolyzing the polymerized monomer units (a) and (c) in the copolymers thus obtainable and use of the multifunctional polymers in laundry detergents and cleaners, to bind polyvalent metal ions, as a stabilizer in textile bleaching and the bleaching of pulp for papermaking.

    Production of vicinal diols by oxidation of olefins with peracid, formed in-situ comprises addition of saponification agent and distillation in presence of azeotropic organic solvent

    公开(公告)号:DE19929196A1

    公开(公告)日:2000-12-28

    申请号:DE19929196

    申请日:1999-06-25

    Applicant: BASF AG

    Inventor: OTT CHRISTIAN

    Abstract: A process for the production of vicinal diols by oxidation of olefins with a peracid, formed in-situ from hydrogen peroxide and formic acid and/or acetic acid comprises addition of a saponification agent, optionally separation of the precipitated solid and distillation of the mixture in the presence of an organic solvent that forms an azeotrope. A process for the production of vicinal diols by oxidation of olefins with a peracid, formed in-situ from hydrogen peroxide and formic acid and/or acetic acid comprises: (A) mixing formic acid and/or acetic acid and hydrogen peroxide with olefins in a reactor to allow the olefins to react with the resulting peracid in the absence of additional organic solvent, to form a product mixture comprising a diol containing product phase (A1) and optionally a further aqueous formic acid and/or acetic acid containing phase (A2); (B) addition, optionally after separation of (A2) from (A1), of an organic solvent that forms a ternary azeotrope with water and formic acid and/or acetic acid; and distillation of the mixture to remove solvent, formic acid and/or acetic acid and water; (C) addition of a saponification agent; (D) optionally separation of the precipitated solid; and (E) distillation of the mixture in the presence of an organic solvent that forms an azeotrope with water in order to remove water from the mixture.

    Use of new or known amino-, hydroxy-substituted fatty acid or derivative

    公开(公告)号:DE19607642A1

    公开(公告)日:1997-09-04

    申请号:DE19607642

    申请日:1996-02-29

    Applicant: BASF AG

    Abstract: The following compounds are new. A1-CO-OR4 (Ia); A4-CO-NR12R13 (XV); G-CO-NR16R17 (XXI); A3-CO-R8 (VIIIa); and alkoxylated fatty acid derivatives (VII) obtained by reacting a fatty acid derivative of formula A2-CO-R5 (VIII) with 3-15 equivalents alkylene oxide (XXX) per equivalent of group (ix) in (VIII). (XXX) is ethylene oxide, propylene oxide or butylene oxide. Also claimed are 1) use of fatty acids derivatives of formula A1-CO-R1 (I) as surfactants in compositions for cleaning fat-soiled non-textile materials; 2) epoxidised fatty acid amides of formula B3-CO-NR121R13 (XVII) as intermediates for surfactants; 3) mixtures of fatty acids derivatives of formula A41-CO-NR16R17 (XVIII) and E-CO-NR16R17 (XIX) in weight ratio 99:1-1:99; and 4) washing and cleaning compositions containing (VII), (VIIIa) or (XXI), and other additives. A1 = 8-24C unbranched aliphatic group containing one or more groups of formula -CH(NR2R3)-CH(OH)- (ii); A2 = 8-24C unbranched aliphatic group containing one or more groups of formula -CH(NR6R7)-CH(OH)- (ix); A3 = 8-24C unbranched aliphatic group containing one or more groups of formula -CH(NR9R10)-CH(OH)- (ix); A4 = 8-24C unbranched aliphatic group containing one or more groups of formula -CH(NR14R15)-CH(OH)- (xvi); B3 = 8-24C unbranched aliphatic group carrying one or more epoxy groups; A41 = 8-24C unbranched aliphatic group containing one or more groups of formula -CH(NR121R141)-CH(OH)- (ii); E = 8-24C unbranched aliphatic group containing one or more groups of formula -CH(OR18)-CH(OH)- (xx); G = 8-24C unbranched aliphatic group containing one or more groups of formula -CH(OR19)-CH(OH)- (xxi); R1 = N(R2)R3, OH or its alkali or ammonium salt, 1-4C alkoxy, or a residue of a mono-, di- or tri-glyceride, (where the two latter residues may be from natural fatty acids or the same or different A1 residues); R2 = 2-40C hydrophilic group; R3 = H, 1-4C alkyl or R2; R4 = H or alkali or ammonium cation; R5 = N(R6)R7, OH or its alkali or ammonium salt, 1-4C alkoxy, or a residue of a mono-, di- or tri-glyceride, (where the two latter residues may be from natural fatty acids or the same or different A2 residues); R6, R7 = H, 1-6C alkyl, or 1-14 C alkyl (substituted by OH, NH2 and/or CONH2 and/or interrupted by non-adjacent O, NH or N(1-4C)alkyl, and/or COOH or SO3H, or their alkali- or ammonium-salts); R8 = N(R6)R7, OH or its alkali or ammonium salt, 1-4C alkoxy, or a residue of a mono-, di- or tri-glyceride, (where the two latter residues may be from natural fatty acids or the same or different A3 residues); R9 = 1-6C alkyl (optionally substituted by OH, NH2 and/or CONH2 and/or interrupted by non-adjacent NH, and substituted by one SO3H or at least one COOH, or their alkali- or ammonium-salts); R10 = H, or a group as for R9; R12 = hydroxy- and/or amino- substituted 2-40C hydrophilic group; R13 = H, 1-4C alkyl or as for R12; R14 = 1-14C alkyl carrying COOH and/or SO3H groups as free acids and/or as alkali or ammonium salts, and optionally interrupted by non-adjacent O, NH and/or N-(1-4C)alkyl groups; R15 = H, 1-6C alkyl or as for R14; R121, R17 = as for R12 or R14; R141, R17 = H, 1-6C alkyl or as for R12; R18 = 1-4C alkyl; R19 = H or 1-4C alkyl.

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