Abstract:
The present invention relates to a coating composition featuring increased solids contents, which comprises at least one polyol I obtainable by subjecting at least one oligomer of the general formula I R1R2C═[═CH—R—CH═]n—CR3R4 (I) in which R=—(—CH2—)m—, in which the index m is an integer from 2 to 6, or in which X=—CH2— or an oxygen atom R1,R2,R3 and R4 independently of one another=hydrogen atoms or alkyl; and the index n=an integer from 1 to 15; to hydroformylation and reducing the resultant aldehyde-functional products I to give the polyols I, which, if desired, are subjected to partial or complete hydrogenation.
Abstract:
In the Taylor reactor, in accordance with a first alternative of the invention, the reactor housing and/or the rotor are/is equipped such that the cross section of the reaction volume initially rises from the inlet to the outlet but the rise in cross section decreases in the direction of the outlet at least over part of the length of the rotor. In accordance with a second alternative of the invention, which may also find application in addition to the first, the end face of the rotor is designed in such a way that the reaction volume opens out into the outlet in such a way that it is at least substantially free from deadspaces (FIG. 4).
Abstract:
Multicomponent coating materials, adhesives and sealing compounds comprising a (meth)acrylate (A) containing, based on (A), up to 90% by weight of hydroxyl-containing monomers in copolymerized form, of which (a1) from 20-90% by weight, based on (A), are 4-hydroxybutyl (meth)acrylate and/or 2-alkylpropane-1,3-diol mono(meth)acrylate, and (a2) from 0-40% by weight based on (A), are other hydroxyl-containing monomers; and (B) an adduct preparable from (b1) a diisocyanate, and (b2) a compound of the general formula I having an isocyanate-reactive group: wherein R1 and R2 are hydrogen or alkyl radicals, X and Y are oxygen, sulfur or >N—R6 where R6 is alkyl radical or aryl radical, R3 is alkylene radical and R4 and R5 are hydrogen, isocyanate-reactive groups or radicals R6; where R4, R5 or R6 contains an isocyanate-reactive group or R4 or R5 is an isocyanate-reactive functional group, and where R4, R5 or R6, where present, contain no isocyanate-reactive groups and the molar ratio of isocyanate groups in (b1) to the isocyanate-reactive groups in the compound I is 1.0.