Abstract: Carboxyl-containing isobutene copolymers are obtainablea) by cationic polymerization of a mixture of from 1 to 99 mol % of isobutene and from 99 to 1 mol % of a 2-methylalk-1-ene at less than 20.degree. C. in the presence of a halogen-containing Lewis acid andb) subsequent grafting of the isobutene copolymer obtainable in this manner with an .alpha.,.beta.-ethylenically unsaturated carboxylic acid or carboxylic acid derivative at above 100.degree. C. and in the presence of a free radical initiator.Such carboxyl-containing isobutene copolymers are particularly suitable as adhesive raw materials or as sealing compounds.

Abstract: Carboxyl-containing isobutene copolymers are obtainablea) by cationic polymerization of a mixture of from 1 to 99 mol % of isobutene and from 99 to 1 mol % of a 2-methylalk-1-ene at less than 20.degree. C. in the presence of a halogen-containing Lewis acid andb) subsequent grafting of the isobutene copolymer obtainable in this manner with an .alpha.,.beta.-ethylenically unsaturated carboxylic acid or carboxylic acid derivative at above 100.degree. C. and in the presence of a free radical initiator.Such carboxyl-containing isobutene copolymers are particularly suitable as adhesive raw materials or as sealing compounds.

Abstract: A process for regulating the reaction in the preparation of polyisobutylene by polymerizing isobutylene at from -130.degree. to 0.degree. C. in the presence of from 0.01 to 1.0% by weight of a Friedel-Crafts catalyst, from 0.0001 to 0.1% by weight of a molecular weight regulator, and a low boiling point solvent that is inert under the reaction conditions, the percentages by weight being based in each case on isobutylene, in which the solvent that has evaporated in the polymerization is continuously removed, liquefied and recycled in the liquid state to the polymerization zone, wherein vinyl ethers are used as molecular weight regulators. The vinyl ether used in this process acts both as an accelerator and an inhibitor of the cationic polymerization.

Abstract: Hexamethylene diisocyanate and/or isomeric alkylene diisocyanates having 6 carbon atoms in the alkylene radical, preferably 2-methylpentamethylene 1,5-diisocyanate and/or 2-ethyltetramethylene 1,4-diisocyanate are prepared without the use of phosgene in a multiple-step process by means of(a) reacting hexamethylene 1,6-diamine and/or isomeric alkylene diamines having 6 carbon atoms in the alkylene radical with urea and alcohol in the presence of dialkyl carbonate and/or carbamic acid alkyl ester as well as, in some cases, catalysts to form hexamethylene 1,6-dialkylurethane and/or isomeric alkylene dialkylurethanes having 6 carbon atoms in the alkylene radical,(b) separation and return to reaction step (a) of alcohol, dialkyl carbonate, and/or carbamic acid alkyl ester from the reaction mixture(c) evaporation of the hexamethylene 1,6-dialkylurethane and/or isomeric alkylene dialkylurethanes having 6 carbon atoms in the alkylene radical,(d) cleavage of the vaporized diurethanes into hexamethylene diisocyanate an