Chemische Werke Huels Aktiengesellschaft

Chemische Werke Huls Aktiengesellschaft

Chemische Werke Huels, Aktiengellschaft

Wolfgang Zaar

Gunther Maahs

Konrad Rombusch

Manfred Schroeder

Peter Hanssle

In the isomerization of isolated double bonds to conjugated double bonds in optionally substituted cyclooctadienes, the isomerization catalyst comprises: (a) a transition metal compound of the formula Me(OR.sup.1).sub.4, wherein Me is Ti, Zr, or Hf, and R.sup.1 is C.sub.1-4 alkyl, and (b) an organoaluminum compound of the general formula AlR.sup.2.sub.3-n X.sub.n, wherein R.sup.2 is C.sub.1-4 alkyl, n is 0, 1, 2, or a fraction between 1 and 2, and X is halogen or, if n is 1, also hydrogen; the molar ratio of (a):(b) being in the range from 0.1 to 1:1, the catalyst having prolonged activity and the isomerization being conducted at a temperature of 50.degree.-200.degree. C.

Isomerization of isolated double bonds to conjugated double bonds in

A process for preparing a copolymer by copolymerizing ethylene and at least one other 1-monoolefin and, optionally, and unconjugated diene in the presence of a mixed catalyst of (1) a compound of a metal of main Groups I-III of the periodic table having at least one hydrogen atom or an alkyl or aryl group bound to the metal atom, and (2) a compound of a metal of Subgroups IV-VI of the periodic table, comprises performing the copolymerization in the presence of an amount effective as an activator of a 2, 3,4,4-tetrachloro-2-butenoic acid ester of the fromula

Preparation of copolymers of ethylene with at least one other

The process for making cyclododecatriene(1,5,9)-enes by catalytically trimerizing butadiene using a catalyst from a titanium halide and an alkylaluminum halide in the presence of hydrocarbons or halogenated hydrocarbons is improved by carrying out the reaction in the presence of dibenzyenes having the general formula ##STR1## where R.sub.1 through R.sub.6 represent hydrogen atoms, halogen atoms, alkyl groups, aralkyl groups, cycloalkyl groups, or aryl groups, the dibenzylbenzenes being used in at least equimolar amounts with respect to the titanium compound.

1,5,9-Cyclododecatriene from butadiene trimerization using

Ethylene and at least one other 1-monoolefin monomer, alone or in admixture with a non-conjugated hydrocarbon diene monomer, are copolymerized in the presence of organic chlorine compound-activated Ziegler-Natta catalyst, wherein the organic chlorine compound is a hydrocarbon or a halohydrocarbon ester of up to 15 carbon atoms of 2,3,4,4-tetrachloro-3-butenoic acid.

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Marl, Germany

Wolfgang Zaar