Chemische Werke Huls Aktiengesellschaft

Veba-chemie Aktiengesellschaft

Huels Aktiengesellschaft

Chemische Werke Huels Aktiengesellschaft

Huls Aktiengesellschaft

Studiengesellschaft Aktiengesellschaft

Veba-chemie Atkiengesellschaft

Chemische Werke

Chemische Werke Huls Aktiengesellshcaft

Josef Disteldorf

Werner Hubel

Elmar Wolf

Werner Flakus

Horst Schnurbusch

Rainer Gras

Karl Schmitt

Werner Huebel

Hans-Jurgen Haage

Peter Kirchner

Hans-Werner Michalczak

Manfred Zur Hausen

Gerd Bohmholdt

Klaus Rindtorff

Gunter Kriebel

Karl Schmitz

Werner Nagengast

Felix Schmitt

Hubert Libera

Johannes Reiffer

Lothar Broschinski

Horst-Wolfram Borsdorff

Flexi Schmitt

Gunter Hasser

Monoblocked diisocyanates which contain little free and diblocked diisocyanate are obtained by a process which involves adding 1 mole of a blocking agent to a diisocyanate which is present in excess and subsequently removing the excess diisocyanate by thin film evaporation. The compounds produced are useful for the production of cataphoresis resins.

Process for the production of monoblocked diisocyanates

A circulation process for the production of (cyclo)aliphatic diisocyanates, in which the biscarbamate is produced from diamines, by-products from the thermal cracking, urea, and alcohol in the presence of N-unsubstituted carbamates and dialkyl carbonates, and with separation of NH.sub.3 ; the subsequent cracking of the biscarbamate is carried out in the liquid phase without solvent; the diisocyanate and alcohol are condensed; the diisocyanate is subjected to a purifying distillation; and a portion of the cracking reaction mixture is discharged with the by-products formed and recycled to the biscarbamate production step after prior reaction with the crude alcohol formed, effectively utilizes the by-products formed in the cracking step and is an industrially practical and economical process.

Circulation process for the production of aliphatic and cycloaliphatic

A stabilizer system for stabilization of polyolefins against light, heat, and oxidative degradation, comprising:

Stabilizer system for polyolefins comprised of monocarboxylic acid

A process for the preparation of a uretedione, comprising the steps of:

Process for the preparation of (cyclo)aliphatic uretediones

Cis-2,6-dimethylmorpholine is manufactured by catalytic isomerization of trans-2,6-dimethylmorpholine. A previously hydrogen-activated copper chromite catalyst is used for catalytic isomerization of the trans-2,6-dimethylmorpholine. The catalyst preferably also contains barium oxide and/or manganese dioxide. The process is carried out at 180.degree.-300.degree. C. and 1-500 bar absolute. The inexpensive novel catalyst enables conversions which are better than those with known methods.

Method of manufacturing cis-2,6-dimethylmorpholine

A polyurethane coating composition comprising:

Heat- and oxidation-resistant polyurethane coatings

Isocyanate-uretdiones having the formula: ##STR1## wherein the R groups are identical or different and are hydrocarbon groups having the formulas: ##STR2## and n is an integral or fractional number from 1 to 5. Production of the isocyanate-uretdiones, which can be dissociated by heat up to an extent of greater than 70%, is accomplished through dimerization of aliphatic diisocyanates having the formula: ##STR3## with a phosphine catalyst having the formula:

Isocyanate-uretdiones and a method for their production

A method for preparing an aqueous polyurethane dispersion, comprising (a) preparing a prepolymer with free NCO groups by reacting an aliphatic or cycloaliphatic polyisocyanate with a polyol, and an anionic compound; (b) dispersing said prepolymer in water; (c) reacting said water-dispersed prepolymer with a diamino hydrazide of the formula: ##STR1## wherein R is an alkylene group of 2 to 15 carbon atoms or a cycloalkylene or arylene group of 6 to 15 carbon atoms as a chain lengthening agent; (d) reacting the prepolymer of step (c) in said dispersion with formaldehyde to effect crosslinking.

Cold-crosslinking polyurethane dispersions, manufacture and use of the

This invention relates to a process for the production of organic isocyanates by the continous hot phosgenation of amines, whereby the solids are retained in the reactor by an appropriate separator and the isocyanate formed during the reaction is constantly removed from the reactor. Preferably the amount of solids of the suspension in the reactor is set so that the amount of the isocyanate taken off per unit of time reaches a maximum.

Process for continuous hot phosgenation of amines

A process for producing polyalkylpiperidylamines of the formula (I): ##STR1## wherein R.sub.1 is hydrogen or a C.sub.1 -C.sub.12 alkylradical; R.sub.2 and R.sub.3 are each C.sub.1 -C.sub.5 alkylradicals or R.sub.2 and R.sub.3, taken together, are --(CH)--.sub.a or --CH.sub.2 --NR.sub.1 --C(R.sub.5,R.sub.6)--CH.sub.2 --; R.sub.4 is a C.sub.2 -C.sub.18 alkylene radical, which is unsubstituted or substituted by C.sub.1 -C.sub.3 alkyl; a C.sub.5 -C.sub.12 cycloalkylene radical, which is unsubstituted or is methyl-substituted; a cycloalkylene radical of the formula ##STR2## where the cyclohexyl rings are unsubstituted or are methyl-substituted; or groups of the formula --(CH.sub.2).sub.k --X--[CH.sub.2).sub.m --X]--.sub.n (CH.sub.2).sub.p --, where X is --O--, --NH--, --NR.sub.5 and R.sub.5 and R.sub.6 are each a C.sub.1 -C.sub.5 alkyl radical and a is 4 or 5, k is 2 or 3, n is 0-3 and p is 2 or 3; which process involves reductively alkylating an alkylated 4-aminopiperidine of the formula (II): ##STR3## with a difunctional alcohol of the formula HO--R.sub.4 --OH, wherein R.sub.1 and R.sub.4 have the above definitions.

Process for the production of polyalkylpiperidylamines

Moisture-hardening varnishes which have an isocyanate resin base of adducts of a mixture of diisocyanates, wherein the diisocyanate mixture has 88 to 99% by weight of 2-methyl-1,5-diisocyanatopentane and 12 to 1% by weight of 2-ethyl-1,4-diisocyanatobutane. These varnishes exhibit excellent thermal and oxidative stability and have excellent storage stability. They also exhibit excellent compatibility with solvents, pigments and other auxiliary materials.

Moisture-hardening varnishes with an isocyanate resin base

A mixture of substances suitable as a powder varnish or a binder for powder varnishes containing an isocyanate component with partially or totally blocked isocyanate groups, and a polyhydroxyl component, wherein mixed trimers or mixtures of individual trimers are used as the isocyanate component from a mixture of 2-methyl-1,5-diisocyanato-pentane (MPDI) and 2-ethyl-1,4-diisocyanatobutane (EBDI) in the amounts of 88 to 99% by weight of (MPDI) and about 12 to 1% by weight of (EBDI), in combination with 3-isocyanato-3,5,5-trimethylcyclohexylioscyanate (IPDI) or mixed urethane adducts obtained from the reaction of the (MPDI/EBDI) mixture in combination with (IPDI) with diols, triols or a mixture thereof.

Mixture of substances suitable for use as a powder varnish or binder for

One-component baking enamels of polyesters, which contain hydroxyl groups, and a polyisocyanate component, wherein the polyisocyanate component is a totally or partially blocked adduct or adducts of a mixture of 2-methyl-1,5-diisocyanatopentane (I) and 2-ethyl-1,5-diisocyanatobutane (II) according to the formulas (I) and (II): ##STR1## wherein the mixture of diisocyanates contains 88 to 99% by weight of totally or partially blocked (I) and about 12 to 1% by weight of totally or partially blocked (II). The enamel films exhibit excellent flexibility and weather resistance and can be coated on metal, glass and plastic.

One-component baking enamels

A method for producing a polyaddition product of isophorone diisocyanate and diols which comprises, reacting a uretidione group-containing dimer of isophoronediisocyanate, which is decomposable by heat into 98% isophorone diisocyanate, with a diol, wherein the ratio of NCO to OH groups is such that the final polyaddition product has free terminal NCO groups, or free terminal OH groups.

Polyaddition products containing uretidione groups and process for their

A process for producing a substantially isocyanurate-free uretidione dimer of isophorone diisocyanate, which is more than 98% decomposable by heat to isophorone diisocyanate, which comprises dimerizing isophorone diisocyanate, optionally in an inert organic solvent, in the presence of a catalyst of the formula X.sub.m P(NR.sub.2).sub.3-m wherein m=0, 1, 2; X=Cl OR of R wherein R is selected from the group consisting of the same or different aklyl radical, aralkyl radical, cycloalkyl radical, substituted cycloalkyl radical and radicals wherein two or more of the aforementioned radicals form a hererocyclic ring together with the nitrogen atom; at temperatures of 0.degree.-80.degree. C., isolating the resulting 1,3-diazacyclobutane-2,4-dione, after 5-70% conversion, without previous inactivation of the catalyst, from the reaction mixture as the residue of a thin film distillation and isolating the catalyst and monomer as the distillate.

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Herne, Germany

Josef Disteldorf