Abstract: A process for preparing stabilized olefin polymers which have a low cold heptane extractables content by polymerization of olefins with Ziegler or Phillips catalysts, wherein the polymer is, immediately after leaving the polymerization reactor, brought into contact with an involatile phenol derivative.

Abstract: Aqueous polymer emulsions whose polymer component essentially consists ofA) from 15 to 50% by weight of copolymer A ofI from 25 to 98.5% by weight of a C.sub.1 -C.sub.20 -alkyl acrylate or methacrylate or a mixture of these esters,II from 0 to 60% by weight of a monomer I or a vinylaromatic,III from 1.

Abstract: A synthetic resin which carries basic nitrogen groups and is water-dilutable by protonation with acid is obtainable by reacting(A) an epoxy resin having an average molecular weight M.sub.n of from 300 to 6,000 and on average from 1.5 to 3.0 epoxy groups per molecule with(B) a ketimine of a primary amine additionally containing one or more urethane groups and optionally also with(C) a diketimine of a diprimary amine containing no urethane groups and optionally also with(D) a secondary amine which may contain a tertiary amino group also, a ketimine of a primary monoamine and/or a ketimine of a primary/tertiary diamine.

Abstract: A synthetic resin which carries basic nitrogen groups and is water-dilutable by protonation with acid is obtainable by reacting(A) an epoxy resin having an average molecular weight M.sub.n of from 300 to 6,000 and on average from 1.5 to 3.0 epoxy groups per molecule with(B) a ketimine of a primary amine additionally containing one or more urethane groups and optionally also with(C) a diketimine of a diprimary amine containing no urethane groups and optionally also with(D) a secondary amine which may contain a tertiary amino group also, a ketimine of a primary monoamine and/or a ketimine of a primary/tertiary diamine.

Abstract: A synthetic resin which carries basic nitrogen groups and is water-dilutable by protonation with an acid, containing(A) a chain-extended, amine-modified epoxy resin obtainable by reacting(a.sub.1) an epoxy resin having an average molecular weight M.sub.n of from 300 to 6,000 and on average from 1.5 to 3.0 epoxy groups per molecule with(a.sub.2) a diketimine of a diprimary diamine, which diprimary diamine contains no further groups reactive with epoxy groups under mild conditions and(B) an amino-modified epoxy resin obtainable by reactingb.sub.1) an epoxy resin having an average molecular weight M.sub.n of from 800 to 6,000 and on average from 1.5 to 3.0 epoxy groups per molecule with(b.sub.2) a secondary amine or a secondary-tertiary diamine, a ketimine of a primary monoamine or a ketimine of a primary/tertiary diamine or a mixture of these (b.sub.2) components, with the proviso that (A) and (B) are different.

Abstract: A synthetic resin which carries basic nitrogen groups and is water-dilutable by protonation with acid is obtainable by reacting(A) an epoxy resin having an average molecular weight M.sub.n of from 200 to 6,000 and on average from 1.5 to 3.0 epoxy groups per molecule with(B) a ketimine of a primary amine additionally containing one or more urethane groups and optionally also with(C) a diketimine of a diprimary amine containing no urethane groups and optionally also with(D) a secondary amine which may contain a tertiary amimo group also, a ketimine of a primary monoamine and/or a ketimine of a primary/tertiary diamine.

Abstract: Aqueous polymer dispersions which have a long shelf life are obtainable by dispersing a mixture of 15-50% by weight of a copolymer (A) of(I) 1.5-15% by weight of copolymerizable compounds of 3 to 10 carbon atoms which contain a carboxyl or carboxylic anhydride group,(II) 30-98.5% by weight of C.sub.1 -C.sub.20 -alkyl acrylates or methacrylates,(III) 0-60% by weight of vinylaromatics,(IV) 0-20% by weight of copolymerizable carbonyl compounds and(V) 0-20% by weight of further copolymerizable organic compounds not stated under (I) to (IV) and50-85% by weight of a copolymer (B) of40-100% by weight of the monomers (II) and0-60% by weight of the monomers (III) to (V),with the proviso that the copolymers (A) and (B) together contain, as components, up to 65% by weight of alkyl (meth)acrylates (II) whose homopolymers have glass transition temperatures of less than 0.degree. C.

Abstract: Aqueous polymer dispersions which have a long shelf life are obtainable by dispersing a mixture of from 15 to 70% by weight of a copolymer (A) of(I) from 1.5 to 15% by weight of copolymerizable compounds of 3 to 10 carbon atoms which contain a carboxyl or carboxylic anhydride group,(II) from 65 to 98.5% by weight of C.sub.1 -C.sub.20 -alkyl acrylates or methacrylates,(III) from 0 to 20% by weight of vinylaromatics,(IV) from 0 to 20% by weight of copolymerizable carbonyl compounds and(V) from 0 to 10% by weight of further copolymerizable organic compounds not stated under (I) to (IV), and from 30to 85% by weight of a copolymer (B) of from 60 to 100% by weight of the monomers (II) and from 0 to 40% by weight of the monomers (III) to (V), with the proviso that the copolymers (A) and (B) together contain, as components, more than 65% by weight of alkyl (meth)acrylates (II) whose homopolymers have glass transition temperatures of less than 0.degree. C.

Abstract: A process for the preparation of stable dispersions of finely divided polyisocyanates, and the preparation of heat-crosslinkable isocyanate systems.Stable dispersions of finely divided polyisocyanates in a liquid which may or may not contain surfactants, protective colloids and other assistants are obtained by a method in which polyisocyanates are treated with a stabilizer in the presence of absence of the liquid, and the dispersions prepared from these are finely dispersed and/or milled under the action of high shear forces, if necessary with the addition of further stabilizer.These dispersions are useful as crosslinking agents, particularly for the preparation of heat-cross-linkable isocyanate systems.

Abstract: A binder which is water-dilutable on protonation with acid and obtainable by a reaction of(A) an epoxy resin having an average molecular weight of from 300 to 6,000 and on average from 1.5 to 3.0 epoxide groups per molecule and(B) from 20 to 30 mol %, based on the amount of epoxide groups present in epoxy resin (A), of one or more secondary amine and/or alkanolamine of up to 40 carbon atomsand subsequent reaction with(C) a copolymer which is based on butadiene and acrylonitrile and contains primary and/or secondary amino groups, the amount of (C) being so dimensioned that the number of primary and secondary amino groups corresponds to from 1 to 50 mol % of the epoxide groups present in the epoxy resin (A), and also(D) with one or more primary and/or secondary amine to convert any epoxide groups still present, is usedin particular for cathodic electrocoating.

Abstract: Condensates based on substituted ureas, their reaction products with di- and/or polyisocyanates, derivatives of di- and/or polycarboxylic acids or p-substituted phenols and/or their methylol derivatives, their preparation and their use. These condensates each contain two or more cyclic urea units and can be prepared either by reacting primary di- or polyamines with ureas and reacting the product with predominantly CH-acidic aldehydes or by reacting primary amines with isocyanates and reacting the product with predominantly CH-acidic aldehydes in the presence of an acidic catalyst. The said condensates and their reaction products are useful for the preparation of heat-curable coating materials and of binders for cathodic electrocoating.

Abstract: Epoxy resin materials essentially contain(A) an epoxy resin having a mean molecular weight of from 300 to 6,000 and on average from 1.5 to 3.0 epoxy groups in the molecule and(B) a polyacrylate resin obtainable by polymerization of essentially(b.sub.1) from 30 to 95% by weight of esters of acrylic acid and/or methacrylic acid and/or ethylacrylic acid with C.sub.1 -C.sub.20 -alcohols in the presence of(b.sub.2) from 5 to 70% by weight of carboxyl-containing copolymers having a mean molecular weight of from 500 to 20,000, obtainable by bulk or solution polymerizationand are used for heat-curable finishes, adhesive bonds and coatings.

Abstract: Nonaqueous polymer dispersions are obtainable by polymerization of esters (A) of acrylic acid and/or methacrylic acid and/or ethylacrylic acid with C.sub.1 -C.sub.20 -alcohols in an organic solvent or a mixture of organic solvents in which the polymers formed are insoluble, and in the presence of copolymers (B) having a molecular weight of from 500 to 20,000 and obtainable by bulk or solution polymerization of monoolefinically unsaturated monomers at from 180.degree. to 400.degree. C. and from 1 to 200 bar, and the said dispersions are used for the production of finishes, coating materials and adhesives.

Abstract: Polymeric compositions which undergo crosslinking after drying at room temperature or elevated temperatures and are dissolved or dispersed in water are prepared by reacting polymeric organic compounds containing carbonyl and carboxyl groups with polyhydrazides in the presence of monoketones or monoaldehydes and are dissolved or dispersed in water by partially or completely neutralizing the carboxyl groups.They are useful as crosslinking agents and as binders for coatings on sheet-like substrates.

Abstract: Binders contain(A) copolymers of(a) from 5 to 70% by weight of monoesters of acrylic acid and/or methacrylic with dihydric to hexahydric C.sub.2 -C.sub.18 -alcohols,(b) from 0.1 to 80% by weight of esters or amides of acrylic acid and/or methacrylic acid with monofunctional C.sub.2 -C.sub.20 -alcohols or -amines which have an open-chain and/or cyclic urea group in the ester or amide radical,(c) from 1 to 60% by weight of esters of acrylic acid and/or methacrylic acid with monofunctional C.sub.1 -C.sub.20 -alcohols and(d) from 0 to 60% by weight of other comonomers, and(B) polyisocyanates, some or all of whose isocyanate groups may be blocked with CH--, NH--- or OH--acidic blocking agents and which have an isocyanate functionality of from 2.5 to 6.These binders are employed for the preparation of polyurethane finishes, which are used to produce coatings.

Abstract: Binders which are rendered water-dilutable by protonation with an acid, a process for their preparation and their use.These binders are obtainable by reacting a(A) Reaction product of a(a) carboxyl-containing component, consisting of a(a1) carboxyl-containing butadiene/acrylonitrile copolymer having a molecular weight of from 500 to 8,000, if necessary as a mixture with(a2) a dicarboxylic acid which differs from (a1) and, if appropriate,(a3) a monocarboxylic acid and(b) a diprimary and/or primary/secondary amine, with the proviso that from 0.7 to 5 moles of the said amine are used per mole of carboxyl groups of component (a),with one or more(B) epoxy resins having a mean molecular weight from 300 to 6,000 and containing on average from 1.5 to 3.0 epoxide groups per molecule and, if required,(C) an aliphatic or cycloaliphatic secondary amine.In combination with a crosslinking agent, they are useful as coating materials, in particular for cathodic electrocoating.

Abstract: Crosslinkable polymeric compositions which are dissolved or dispersed in an organic solvent, a process for their preparation and their use.These polymeric compositions which undergo crosslinking at room temperature or elevated temperatures after drying are obtained by reacting polymeric organic compounds containing carbonyl groups with polyhydrazides in the presence of monoketones or monoaldehydes.They are useful as crosslinking agents for polyepoxide compounds.

Abstract: Binders for cathodic electrocoating which are based on polyadducts/polycondensates which carry basic nitrogen groups and are rendered water-dilutable by protonation with an acid, and one or more crosslinkng agents for these polyadducts/polycondensates, and their use.These binders essentially consist of a mixture of(A) from 50 to 90% by weight of a polyadduct/polycondensate which carries basic nitrogen groups and is obtainable by reacting(a) an adduct of a secondary amine and a polyepoxide compound, the adduct still containing free epoxide groups, with(b) a condensate which contains primary amino groups and is obtained from a primary diamine of not less than 4 carbon atoms and one or more mono- and/or dicarboxylic acids, one or more primary amino groups of the condensate (b) being used per free epoxide group of the adduct (a), and(B) from 10 to 50% by weight of a crosslinking agent which does not react with component (A) at room temperature but reacts with the latter at elevated temperatures with crosslinking.

Abstract: A synthetic resin which contains quaternary ammonium groups, and its preparation.The water-dilutable synthetic resin which contains quaternary ammonium groups and furthermore contains one or more basic secondary and/or tertiary amino groups per quaternary ammonium group is an adduct of(A) a quaternary ammonium salt which is obtained by reacting(a) an organic compound containing two or more basic amino groups per molecule, one of which is a primary group and is protected as a ketimine by prior reaction with a ketone, and the remaining groups are tertiary groups, with(b) an organic or inorganic acid and(c) a monoepoxide compound, and, if necessary, then eliminating the ketone hydrolytically,(B) a resin which contains on average from 1.5 to 3.0 epoxide groups per molecule, and, if required,(C) one or more monofunctional organic compounds whose functional group is capable of undergoing an addition reaction with an epoxide.

Abstract: Cathodic coating agents which are rendered water-dilutable by the addition of an acid, contain binder systems possessing basic nitrogen groups and may or may not contain pigments, dyes, fillers, solvents, antioxidants, other surface coating assistants and/or additional crosslinking components, the binder system containing sulfonate and/or phosphonate groups or the esters of these groups in an amount of from 0.05 to 3% by weight, and the preparation of such products.The novel coating agents are useful for the cathodic electrocoating of electrically conductive substrates.