Abstract:
The present invention relates to a lamination printing ink comprising an aqueous polyurethane dispersion binder, pigments, an aqueous carrier and optional additives, wherein the polyurethane is made of polyisocyanates, specific polyesterdiols, polytetrahydrofuran diol, monohydroxy-poly(alkylene oxide), diamino acid compound, polyamine compound and optionally one or more low molecular weight polyols.
Abstract:
Die Erfindung betrifft neue wasseremulgierbare Isocyanate, ein Verfahren zur Herstellung von wasseremulgierbaren Isocyanaten und deren Verwendung.
Abstract:
Die vorliegende Erfindung betrifft Polyurethandispersionen mit verbesserter Chemikalienbeständigkeit, deren Verwendung und Verfahren zu deren Herstellung.
Abstract:
Die Erfindung betrifft neue wasseremulgierbare Isocyanate, ein Verfahren zur Herstellung von wasseremulgierbaren Isocyanaten und deren Verwendung.
Abstract:
A process for purifying a polycarbodiimide comprising (a) providing a mixture comprising a polycarbodiimide and a carbodiimidization catalyst; (b) separating carbodiimidization catalyst from the polycarbodiimide by subjecting the mixture according to (a) to a first distillation, (c) adding an entrainer to the first bottom product obtained from (b) to obtain a mixture; (d) further separating carbodiimidization catalyst from the polycarbodiimide by subjecting the mixture obtained from (c) to a second distillation.
Abstract:
The present invention relates to aqueous binder compositions which are based on aqueous multistage polymer dispersions, to the uses of such binder compositions, and to coating compositions comprising them. The aqueous binder composition comprises: a) a polymer P in the form of an aqueous multistage polymer dispersion of dispersed polymer particles, where the polymer particles comprise a first polymer having a glass transition temperature of at least 30°C and being made of ethylenically unsaturated monomers M-A, and a second polymer having a glass transition temperature of not more than 20°C and being made of ethylenically unsaturated monomers M-B, where the ethylenically unsaturated monomers M-A and M-B together comprise: i. 85% to 99.45% by weight, preferably 87.5% to 97% by weight and in particular 90% to 95.5% by weight, based in each case on the total amount of monomers M-A + M-B, of at least one neutral, monoethylenically unsaturated monomer M1 having a solubility in water of at most 50 g/l at 25°C and 1 bar; ii. 0.5% to 10% by weight, preferably 1 % to 7.5% by weight and in particular 1.5% to 6.5% by weight, based in each case on the total amount of monomers M-A + M-B, of at least one neutral, monoethylenically unsaturated monomer M2 having a solubility in water of at least 100 g/l at 25°C and 1 bar; iii. 0.05 to 0.5% by weight, preferably 0.15% to 0.5% by weight and in particular 0.3% to 0.5% by weight, based in each case on the total amount of monomers M-A + M-B, of one or more monoethylenically unsaturated monomers M3 having an acidic group; and iv. optionally from 0 to 5% by weight and in particular from 0 to 4.5% by weight, based in each case on the total amount of monomers M-A + M-B, of one or more monomers M4 having at least two non-conjugated ethylenically unsaturated double bonds; and b) at least one carbodiimide having at least two carbodiimide moieties, which are bound to an aliphatic carbon atom.
Abstract:
Verwendung von substituierten Diharnstoffen, Polyharnstoffen, Bisurethanen oder Polyurethanen der Formel R 1 X-CO-NR 3 R 4 , worin X für R 2 N oder O steht und R 1 bis R 4 unabhängig voneinander Wasserstoff, Alkylreste, Alkenylreste, Cycloalkylreste, Arylreste oder Arylalkylreste bedeuten, wobei mindestens eine Variablen einen Rest mit mindestens 4 Kohlenstoffatomen bezeichnen muss und wobei die Harnstoff- bzw. Urethan-Funktionalität über Brückenglieder vervielfachte vorliegen muss, zur Verbesserung der Gebrauchseigenschaften von mineralischen und synthetischen nichtwässrigen Industrieflüssigkeiten.
Abstract:
Wässrige Polyurethandispersion, enthaltend ein Alkanolamin der Formel (I), wobei R 1 und R 2 für eine C1 bis C4 Alkylgruppe es gehen zur Neutralisation nur tertiäre Amine, R 3 für ein Wasserstoffatomatom oder eine C1 bis C4 Alkylgruppe und R 4 und R 5 unabhängig voneinander für eine C1 bis C4 Alkylgruppe stehen.
Abstract:
Mikrokapseln, dadurch gekennzeichnet, dass die Kapselwand aus einem organischen Polymer (kurz Kapselwand-Polymer) gebildet wird und die Mikrokapseln im Kern Verbindungen mit Carbodiimidgruppen (kurz Carbodiimid-Verbindung) enthalten.
Abstract:
A process for producing a polycarbodiimide, comprising polymerizing a diisocyanate in the presence of a carbodiimidization catalyst in a reaction vessel in liquid phase at a temperature in the range of from 20 to 250 °C, at a pressure in the range of from 20 to 800 mbar and in the presence of at least one inert gas, wherein the at least one inert gas is introduced into the liquid phase in the reaction vessel with a flow rate in the range of from 0.1 x/h to 100 x/h, x being the volume of the reaction vessel.