Abstract:
New compounds containing isocyanatophenoxy groups, corresponding to ##STR1## wherein R.sup.1 denotes a residue of a n-valent polyhydroxyl compound having a molecular weight of about 92-6000, R.sup.2 denotes hydrogen or methyl group and n denotes an integer of from 3 to 8 were found to be suitable as hardeners in the preparation of adhesives.
Abstract:
A process for the solventless preparation of ethylenically unsaturated polyurethanes. The process includes preparing a prepolymer from an isocyanate-containing component A) and an isocyanate-reactive component B) in a batch reaction, and reacting the prepolymer with a further component C) in a second, continuous reaction to provide a polyurethane, where at least one of the components A, B and C have ethylenically unsaturated groups.
Abstract:
Compounds containing ester groups and tertiary amino groups and optionally hydroxyl groups are made by reacting optionally hydroxyfunctional acetoacetic acid esters of monofunctional or polyfunctional alcohols (particularly polyfunctional polyether polyols) with primary/tertiary polyamines (particularly diamines). These compounds are useful as optionally incorporable catalysts for the isocyanate addition reaction in the production of polyurethane foams by the isocyanate polyaddition process.
Abstract:
The present invention is directed to a process for preparing amine terminated compounds by reacting a polyfunctional acetoacetic acid ester with either ammonia or an organic compound which contains one or more primary amino groups in the presence of a solvent and an acidic catalyst selected from the group consisting of (i) boron trifuloride etherate and (ii) organic acids having pKa values of from 0.1 to 0.8 with the proviso that if the primary amino group containing compound contains no aromatically bound amino groups, the pKa of said organic acid is from 0.1 to less than 0.7.
Abstract:
The present invention relates to a process for the phosgenation of amines in the gas phase, in which a specific type of heat exchanger is used for vaporizing the amines.
Abstract:
A process for the preparation of carboxylic acids which contain ether groups by the catalytically accelerated addition of alcoholic hydroxyl groups from mono- or polyhydric alcohols to tertiary-alkyl esters of .alpha.,.beta.-unsaturated carboxylic acids, and followed with acid hydrolysis of the tertiary-alkyl .beta.-ethercarboxylate obtained as intermediates in this way.
Abstract:
Disclosed herein is a process for the preparation of a reaction injection molded elastomer comprising injecting a reaction mixture into a closed mold via a RIM machine, with the ratio of components being such that the isocyanate index is from about 70 to about 130, said reaction mixture comprising (a) an organic di- and/or polyisocyanate, (b) an amine terminated chain extender, and (c) a compound which is derived from the reaction of a polyfunctional acetoacetic acid ester and an aliphatic amine having amino groups of different reactivity.
Abstract:
The present invention relates to a stabilized composition containing a polyol/melamine and an effective stabilizing amount of an amine terminated polyether.
Abstract:
The present invention is directed to a novel solvent-free process for preparing amine terminated compounds by reacting a polyfunctional acetoacetic acid ester with either ammonia or an organic compound which contains one or more primary amino groups in the presence of an acidic catalyst selected from the group consisting of (i) boron trifluoride etherate and (ii) organic acids having pKa values of from 0.1 to 0.8.
Abstract:
N,N-disubstituted monourethanes and oligourethanes are produced by reacting (a) N-aliphatically and/or N-cycloaliphatically and/or N-araliphatically substituted monourethanes and/or oligourethanes with an alkylating agent in the presence of a solid alkali metal hydroxide. No solvent need by employed but if a solvent is used, that solvent should be an aprotic organic solvent. The alkali metal hydroxide must be used in an equivalent amount. A phase transfer catalyst may optionally be employed. The N,N-disubstituted urethanes obtained by this process are useful in the production of dyes, pharmaceutical products and thermostable synthetic materials.