Abstract: The polyurethane material is produced from a reactive mixture comprising an isocyanate component composed of at least one isocyanate compound having at least two NCO-groups which are not directly attached to an aromatic group; isocyanate-reactive components and a catalyst component which is substantially free of lead and which comprises at least one organobismuth (III) catalyst. In order to be able to keep the emission or VOC value (Volatile Organic Compounds) of the polyurethane material below 250 ppm, preferably below 100 ppm, use is made of an organobismuth (m) and/or of an organotin (II or IV) catalyst comprising either C14-C20 carboxylate groups or C2-C20 carboxylate groups substituted with at least one isocyanate-reactive group. The catalyst component may further comprise an organozinc (11) carboxylate. The preferred catalysts are bismuth oleate, dimethyltin dioleate and zinc octoate.

Abstract: A process for the production of micro-cellular or non-cellular, light-stable elastomeric, flexible or semi-flexible polyurethane moldings which are especially suited for window encapsulation applications from a reaction mixture by the reaction injection molding process, wherein: A) an isocyanate component containing an isophorone diisocyanate (IPDI) trimer/monomer mixture having an NCO content of from 24.

Abstract: In the method according to the invention, a layer of polyurethane elastomer for obtaining a polyurethane skin (5) is produced, in a first step, against a mould surface (1). In a second step, a reaction mixture for obtaining a polyurethane foam layer (6) is applied against this polyurethane skin (5). In a third step, a suitable polyurethane or polyisocyanurate reaction mixture for obtaining a rigid synthetic carrier (8) is applied against the polyurethane foam layer (6). In this way, a synthetic trim part is obtained which is easier to recycle. This method can moreover also be performed easier.

Abstract: A method for preparing a light stable polyurethane, sprayable by means of a spray pistol, wherein use is made of an active hydrogen containing compound, wherein the functional groups consist for at least 50% of an active CH.sub.2 OH, NH and/or NH.sub.2 group, the functionality of which varies from 2 to 8 and the equivalent weight of which is comprised between 100 and 3500, together with 2 to 300 parts, per 100 parts of said compounds of a chain extender and/or a cross-linker, the functional groups of which are OH groups, at least 50% of which are primary OH groups, the equivalent weight of which is less than 100 and the functionality of which varies from 2 to 6, and with a catalytic system which comprises at least an organic lead, bismuth and/or tin (IV) compound and at least an amine initiator, having a functionality of 2 to 6, an equivalent weight lower than or equal to 200, and at least one aliphatic NH.sub.2 or NH group.

Abstract: A method for preparing a flexible polyurethane foam, wherein a polyether-polyol having an average molecular weight from 1000 to 8000 and an average functionality not larger than 4, is brought into reaction with an organic polyisocyanate in the presence of a foam stabilizer, a catalyst and blowing agent comprising methylformate, wherein a cross-linker/extender and/or amine catalyst with delayed action is added to said reaction mixture.

Abstract: A flexible highly elastical polyurethane foam having a density ranging between 25 and 150 kg/m.sup.3 and a relatively high fire resistance obtained by the reaction of an isocyanate and/or a chemically modified derivate thereof with a highly molecular reactive polyol in presence of a catalytic agent, of a cross-linker, and/or an extender, of water as blast means and of a fire retardant, characterized in that said fire retardant comprises at least one of the following components: (1) linear urea-formol oligomer mixture having the general formula NH.sub.2 --CO--NH--[CH.sub.2 --NH--CO--NH].sub.n --CH.sub.2 --NH--CO--NH.sub.

Abstract: An improved process for preparing integral skin polyurethane, wherein a reaction mixture comprising polyol, polyisocyanate the NCO groups of which are not directly bonded to an aromatic group, no more than 0.5 part by weight of water to 100 parts by weight of polyol, and a catalyst is reacted in a mould, said improvement consisting in using as catalyst a synergistic combination of at least one organic initiator, comprising at least one functional group of primary or secondary amines, with at least one organic compound of bismuth.

Abstract: A hydrophile polyurethane foam prepared from a hydrophile polyol, a polyisocyanate in which NCO groups are not directly bonded to an aromatic ring, a surface active agent, a swelling agent and a catalyst comprising:(A) at least one compound selected from the group consisting of:(1) diazabicyclo-alkenes of formula: ##STR1## (2) substituted guanidines and salts of formula: ##STR2## (3) substituted biguanidines of formula: ##STR3## (4) substituted biguanidines of formula: ##STR4## wherein the substituents can have different meanings, and (B) at least an alkali metal or alkaline earth metal salt of organic acids having a dissociation constant Ka<10.sup.-1.

Abstract: A process for preparing polyurethane with integral skin, wherein a composition comprising following ingredients: polyol, polyisocyanate, at most one part by weight of water to 100 parts by weight of polyol and catalyst, is reacted in a mould so that a polyurethane is formed, characterized in that one uses a polyisocyanate the NCO groups of which are not directly bonded to an aromatic group and, as catalyst, at least one of the following four synergistic combinations:(1) at least an amine containing the structure: ##STR1## in association with at least an alkali metal or alkaline-earth metal salt, alcoholate and/or phenolate of an acid the dissociation constant of which Ka.ltoreq.10.sup.-1, preferably Ka.ltoreq.10.sup.

Abstract: A process for preparing polyurethane foam which consists in introducing in the reaction, between a polyisocyanate and a polyol, a catalyst containing the chemical structure >N--C=N-- and also a compound selected from the group comprising metal salts of carboxylic acids having the structure ##STR1## M and metal alcoholates and/or phenolates having the structure M'OR', wherein M' represents an alkaline metal, M represents an alkaline or alkaline-earth metal, R represents hydrogen or an organic radical and R' represents an organic radical.