Abstract: Process for producing coatings or moldings by radiation curing, which involves using high-energy light to irradiate radiation-curable compositions containing 1-100% by weight, based on the total amount of free-radically or cationically polymerizable compounds, of compounds A) containing at least one cationically polymerizable 2,3-dihydrofuran structure.

Abstract: Described are aqueous, radiation-curable coating compositions comprising:a) from 5.0 to 90.0% by weight of at least one water-dispersible polymer P comprising at least one .alpha.,.beta.-ethylenically unsaturated, radiation-polymerizable double bond,b) from 0.1 to 90% by weight of at least one radiation-curable compound S which is different from P and which is soluble in water or is dilutable with at least 10% by weight of water, based on the overall weight of the coating composition, and which comprises at least one .alpha.,.beta.-ethylenically unsaturated, radiation-polymerizable double bond,c) from 0 to 20% by weight of a photoinitiator,d) from 0 to 60% by weight of a filler,e) from 0 to 20% by weight of further additives,f) water to 100% by weight and their use.

Abstract: Radiation-curable compositions based on radiation-curable, free-radically polymerizable compounds comprise .alpha.-olefins having more than 8 carbon atoms.

Abstract: Urethane(meth)acrylates are obtainable bya) reacting polyether(meth)acrylates or polyester(meth)acrylates, which may also have at least one free hydroxyl group, with primary or secondary amino compounds which have at least one hydroxyl group, so that from 0.5 to 60 mol % of the (meth)acrylate groups are present in the form of Michael adducts with the amino compounds, andb) subsequently reacting the product obtained in a) with isocyanates.

Abstract: A process for the preparation of a radiation-curable acrylate composition, wherein to compounds A containing at least 2 acrylic groups there are added benzophenone derivatives which are not copolymerizable by free-radical copolymerization and which contain at least one primary or secondary amino group or a hydroxyl group or a mercapto group.

Abstract: A process for preparing (meth)acrylic esters by esterifying (meth)acrylic acid with monohydric or polyhydric alcohols comprises adding to the reaction mixture still comprising (meth)acrylic acid corresponding to an acid number of at least 5 mg of KOH per 1 g of reaction mixture at least one amino compound having at least one primary, secondary or tertiary amino group.

Abstract: Radiation-curable compositions of reduced oxygen sensitivity comprisea) radiation-curable, free-radically polymerizable compounds, andb) capped amino compounds which are surface-active in compounds a) and on irradiation with high-energy light liberate amino compounds having primary, secondary or primary and secondary amino groups, the overall number of hydrogen atoms bonded in the amino groups (amine hydrogens) being at least 2.

Abstract: A process for coating or printing substrates with a coating or printing composition comprises applying a polymerizable material containing liquid-crystalline, polymerizable monomers which carryat least two polymerizable groups for coating andat least one polymerizable group for printing,to the substrate, and subsequently carrying out the polymerization, where the coating composition or the printing composition comprisesa.sub.1) a chiral liquid-crystalline monomer andb) a polymeric binder and/or monomeric compounds which can be converted into the polymeric binder by polymerization, or, in the case of emulsion coatings and printing inks, a dispersion auxiliary d),or the coating composition or the printing composition comprisesa.sub.

Abstract: Radiation-curable (meth)acrylates obtainable by reacting compounds of the formula ##STR1## in which R is C.sub.1 -C.sub.4 -alkyl, aryl or R.sup.1 and R.sup.1 is ##STR2## in which R.sup.2 to R.sup.6 independently of one another are H, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, OH, phenyl, SH, SCH.sub.3, SC.sub.2 H.sub.5, F, Cl, Br, CN, COOH, COO--(C.sub.1 -C.sub.17 -alkyl), COO--(C.sub.5 -C.sub.10 -aryl), CF.sub.3, N(alkyl).sub.2, N(alkyl)(aryl), N(aryl).sub.2, N.sup..sym. (alkyl).sub.3 A.sup..crclbar., N.sup..sym. H(alkyl).sub.2 A.sup..crclbar., A.sup..crclbar. is the anion of an acid, and alkyl or aryl, unless indicated otherwise, is C.sub.1 -C.sub.10 -alkyl or C.sub.5 -C.sub.10 -aryl, respectively, and at least one but not more than 3 of R.sup.2 to R.sup.6 are ##STR3## with hydroxy(meth)acrylates containing at least 1 free hydroxyl group and at least 2 (meth)acrylic groups in the molecule.

Abstract: Urethane(meth)acrylates are obtainable bya) reacting polyether(meth)acrylates or polyester(meth)acrylates, which may also have at least one free hydroxyl group, with primary or secondary amino compounds which have at least one hydroxyl group, so that from 0.5 to 60 mol % of the (meth)acrylate groups are present in the form of Michael adducts with the amino compounds, andb) subsequently reacting the product obtained in a) with isocyanates.

Abstract: Radiation-curable compositions comprisinga) compounds having at least two carbon-carbon double bonds with which it is possible for primary or secondary amino groups to form adducts in the form of a Michael-analogous addition reaction (referred to in short below as activated double bonds)b) capped amino compounds which on irradiation with high-energy light liberate amino compounds having primary, secondary or primary and secondary amino groups, the overall number of hydrogen atoms bonded in the amino groups (amine hydrogen atoms) being at least 2.

Abstract: Radiation-curable acrylates are prepared by a process in which the hydroxy compound is reacted with acrylic acid or methacrylic acid in a first stage and, in a second stage, the reaction product of the first stage is reacted with an epoxide compound in the presence of, as a catalyst, a quaternary ammonium or phosphonium compound of the general formula ##STR1## where X.sup.- is an opposite ion and R.sup.1 to R.sup.4 independently of one another are each C.sub.1 -C.sub.18 -alkyl which may be substituted by one or two phenyl groups or are each C.sub.6 -C.sub.12 -aryl which may be substituted by one or two C.sub.1 -C.sub.6 -alkyl groups.

Abstract: Radiation-curable acrylates are prepared by a process in which, in a 1st stage, a hydroxy compound is reacted with acrylic acid or methacrylic acid and, in or before a 2nd stage, the reaction product of the 1st stage is then reacted with an epoxy compound and compounds having one or more primary or secondary amino groups are added in the 2nd stage and the reaction in the 2nd stage is continued, after the addition of these compounds, until the acid number of the reaction mixture has decreased by at least 3 mg KOH/g of reaction mixture from the time of the addition of these compounds.

Abstract: Radiation-curable binders which are obtained by reactingA) an amine/formaldehyde condensate having a molar ratio of formaldehyde to amino groups of from 1:1 to 2:1 withB) one or more esters, having a free hydroxyl group, of acrylic acid or of methacrylic acid with polyalcohols which contain from two to four alcoholic hydroxyl groups, from 0.1 to 0.3 hydroxyl equivalent of component B) being used per methylol equivalent of component A),in the presence of a strong acid are suitable for use in coating materials.

Abstract: Radiation-curable urethane acrylate compounds containing amine and urea groups and based on di- or polyisocyanates, hydroxy compounds and amines contain secondary or tertiary amino groups which are bonded to isocyanate via hydroxyl groups and are obtainable by an addition reaction of primary or secondary amines with hydroxyacrylates.

Abstract: Aqueous dispersions containA) from 20 to 90% by weight of a dispersed polymer having a glass transition temperature above 30.degree. C. andB) from 10 to 80% by weight of a tri-, tetra-, penta-or hexa(meth)acrylate of an alkoxylated, trivalent to hexavalent alcohol having a mean degree of alkoxylation of the hydroxyl groups of the alcohol, defined as the quotient of the number of alkoxy groups to the number of hydroxyl groups, ie. the functionality of the alcohol prior to the alkoxylation, of at least 0.5,the stated weights being based on the sum of A) and B).

Abstract: In disc brakes, disturbing noises, such as whistling or squealing, occurring during braking operations can be prevented if the brake shoe, to be pressed against a brake disc by a pressure member, for example a hydraulically actuated piston, is taken along in the circumferential direction of the latter as soon as the brake shoe comes into contact with the brake disc, and is laid against bearing faces of a brake anchor plate. Accordingly, the pressure member is provided, on its end face facing the brake shoe, a pressing element which projects beyond the end face, is transversely movable to a limited extent and returns automatically to its initial position again, and which is arranged in the pressure member so as to be axially displaceable counter to a return force which, in the event of mutual contact between the pressing element and brake shoe, is lower than the pressing force of the pressure member.

Abstract: Polyurethane vinyl ethers are obtainable by reactingA) 1 NCO equivalent of one or more isocyanurate-containing polyisocyanates withB) 0.01-1.0 OH equivalent of one or more monohydroxyvinyl ethers andC) 0-0.99 equivalent of functional groups of further compounds, which groups are reactive with OCN.

Abstract: A reaction product useful for preparing radiation-sensitive materials, in particular materials whose solubility in water or aqueous alkali increases on irradiation, contains urea and urethane groups and also carboxyl groups and is obtained by reaction ofi) an ethylenically monounsaturated or polyunsaturated mono- or polyalcohol withii) a di- or polyisocyanate,iii) at least one amino compound andiv) at least one anhydride of an at least dibasic carboxylic acid,the number of NCO and anhydride groups in ii) and iv) being equal to or less than the number of groups in i) and iii) which are reactive therewith.

Abstract: Radiation-curable catalysts are obtainable by reactingA) 1 equivalent of a dihydric to hexahydric oxyalkylated C.sub.2 -C.sub.10 -alcohol withB) from 0.05 to 1 equivalent of a dibasic to tetrabasic C.sub.3 -C.sub.36 -carboxylic acid or its anhydride andC) from 0.1 to 1.5 equivalents of acrylic acid and/or methacrylic acidand reacting the excess carboxyl groups with an equivalent amount of epoxide compound, and are used in radiation-curable coating materials.