Abstract: Modified polyaspartic acids useful as detergent and cleaner additives, as water treatment agents and as scale inhibitors in the evaporation of sugar juice are obtainable by polycondensation of(a) from 1 to 99.9 mol % of aspartic acid with(b) from 99 to 0.1 mol % of fatty acids, polybasic carboxylic acids, anhydrides of polybasic carboxylic acids, polybasic hydroxycarboxylic acids, monobasic polyhydroxycarboxylic acids, alcohols, amines, alkoxylated alcohols and amines, amino sugars, carbohydrates, sugarcarboxylic acids and/or non-proteinogenic aminocarboxylic acidsor by polymerizing monoethylenically unsaturated monomers in the presence of polyaspartic acids in the manner of a free-radically initiated graft polymerization.

Abstract: Water-soluble copolymerizates are disclosed containing carboxyl groups, and also containing the following components incorporated by polymerization: (a) 30 to 80 mol % monoethylenically unsaturated C.sub.3 -C.sub.8 carboxylic acids, anhydrides thereof and/or water-soluble salts thereof; (b) 10 to 50 mol % C.sub.2 -C.sub.8 olefines, styrene, alkyl styrene, C.sub.1 -C.sub.10 alkyl vinyl ethers and/or vinyl esters of saturated C.sub.1 -C.sub.10 monocarboxylic acids; and (c) 0.01 to 20 mol % vinyl ethers and/or allyl ethers of alkoxylated C.sub.1 -C.sub.30 alcohols. The copolymerizates in question have a K-value of at least 8 (determined after H. Fikentscher). Also disclosed are methods of producing the water-soluble copolymerizates by copolymerization of the monomers in the presence of radical-forming polymerization initiators, and the use of the polymerizates as scale inhibitors.

Abstract: Hydroxamic acids and hydroxamic acid ethers I and II ##STR1## where Z.sup.1 and Z.sup.2 are --NH --OY, --NR.sup.1 --OY or --OX, where in the case of (I) at least one of Z.sup.1 or Z.sup.2, and in the case of (II) Z.sup.1 is --NH --OY or --NR.sup.1 --OY, andR.sup.1 is C.sub.1 -C.sub.18 -alkyl,X is hydrogen, alkali metal, ammonium or substituted ammonium, andY is hydrogen, alkali metal, ammonium, substituted ammonium or C.sub.1 -C.sub.18 -alkyl, andL is a C.sub.1 -C.sub.100 linker which can also carry oxygen and nitrogen functional groups,with the exception of N,N-bis(carboxymethyl)-2-aminoacetohydroxamic acid.

Abstract: A water-soluble or water-dispersible graft copolymer obtainable by free-radical graft copolymerization of(I) at least one monoethylenically unsaturated monomer onto(II) polymers with a molecular weight of 200-5000 of monoethylenically unsaturated dicarboxylic acids or anhydrides thereofusing from 5 to 2,000 parts by weight of the monomers (I) per 100 parts by weight of grafting base, a process for preparing the graft copolymers and the use of the graft copolymers as additive to phosphate-free or reduced phosphate textile detergents, as dispersants and preventers of deposits in cleaners for hard surfaces and as water-treatment agents for reducing the deposition of scale and the separation out of water hardness in water-conveying systems.

Abstract: Process for the preparation of products of the reaction of polyaspartimides and amino acids by reaction of amino acids with polyaspartimides in aqueous medium at pH values at which at least 5% of the amino groups in the amino acids are in non-protonated form in equilibrium with the protonated form, and use of the reaction products obtainable in this way and of products of the reaction of polyaspartimides with alkanolamines or aminated C.sub.1 -C.sub.30 -fatty alcohol alkoxylates which contain as copolymerized units up to 50 mol % of ethylene oxide and/or propylene oxide per mol of fatty alcohol, as additive to detergents and cleaners, as scale inhibitor and as dispersant.

Abstract: Polycocondensates based on aspartic acid which are obtainable by condensing aspartic acid in the presence of polymers containing carboxyl groups, which contain at least 10 mol % of a monoethylenically unsaturated carboxylic acid in copolymerized form and have a molecular weight of at least 300, in the weight ratio from 1,000:1 to 2:1, processes for preparing the polycocondensates and use of the polycocondensates in the form of the free acid groups or in a form neutralized with ammonia, amines, alkali metal or alkaline earth metal bases as an additive to detergents and cleaners, as scale inhibitors or as dispersants for finely divided solids are described.

Abstract: Process for the preparation of polymers of aspartic acid by reacting (a) maleic anhydride and (b) ammonia and/or primary or secondary amines without diluent in the (a):(b) molar ratio of 1:0.1 to 1:3 to give monoamides of maleic acid, fumaric acid or their ammonium salts at up to 100.degree. C. and subsequent condensation of the reaction products, with or without compounds capable of cocondensation, at above 100.degree. C. and, where appropriate, hydrolysis of the condensates and use of the polymers as scale inhibitor, as dispersants for pigments and as additive to detergents and cleaners.

Abstract: Hair setting composition containing as film formers copolymers based on tert-butyl acrylate and/or tert-butyl methacrylate, having a K value of from 10 to 50 and obtainable by free radical polymerization ofA) from 75 to 99% by weight of tert-butyl acrylate and/or tert-butyl methacrylate,B) from 1 to 25% by weight of acrylic acid and/or methacrylic acid andC) from 0 to 10% by weight of a further free radical copolymerizable monomer,the carboxyl groups of the copolymers having been partly or wholly neutralized by amines.

Abstract: The invention relates to a curable, thickened molding material based on vinyl ester resins or vinyl ester urethane resins and containing a basic metal compound acting as thickening agent and also an acid group-containing thermoplastic vinyl polymer which is compatible with said resins.

Abstract: A curable thickened polyester resin molding compound contains from 0.1 to 20 parts by weight of a thermoplastic vinyl polymer which is compatible with the resin and contains acid groups.

Abstract: A terpolymer suitable for use as a film former in hair setting compositions is obtainable by free radical polymerization of 10%-24% by weight of N-vinylpyrrolidone, 46%-74% by weight of tert-butyl acrylate or methacrylate and 16%-30% by weight of acrylic or methacrylic acid, whose carboxyl groups may be partially or completely neutralized with an organic amine, ammonia or a basic alkali metal compound and which has a K value of from 25 to 65.

Abstract: Copolymers based on tert-butyl acrylate and/or tert-butyl methacrylate, having a K value of from 10 to 50 and obtainable by free radical polymerization ofA) from 20 to 90% by weight of tert-butyl acrylate and/or tert-butyl methacrylate,B) from 10 to 60% by weight of N-vinylpyrrolidone andC) from 0 to 30% by weight of a C.sub.1 -C.sub.20 -alkyl acrylate, a C.sub.1 -C.sub.20 -alkyl methacrylate, a C.sub.2 -C.sub.4 -hydroxyalkyl acrylate, a C.sub.2 -C.sub.4 -hydroxyalkyl methacrylate or vinyl acetate or a mixture thereof,are used as film formers in hair setting compositions and compositions for the surface protection of two- or three-dimensional structures.

Abstract: The preparation of copolymers which form clear aqueous solutions fromA) 45 to 90% by weight N-vinylpyrrolidone,B) 10 to 55% by weight of a vinyl ester andC) 0 to 10% by weight of other copolymerizable monomersby radical polymerization in an organic solvent in the presence of a radical initiator, and removal of the organic solvent and other volatiles by distillation, entails allowing the polymerization to proceed until the N-vinylpyrrolidone content in the reaction mixture is from 5 to 1% by weight of the N-vinylpyrrolidone amount employed, substantially removing the organic solvent and other volatiles by distillation, adding water to the mixture, again adding a radical initiator and leaving the aqueous solution at from 50.degree. to 100.degree. C. for from 1 to 10 hours, and then removing volatile organic constituents virtually completely by a steam distillation.