The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Oct. 02, 2007

Filed:

Jan. 12, 2005
Applicants:

Thorsten Rische, Unna, DE;

Torsten Pohl, Köln, DE;

Jürgen Meixner, Krefeld, DE;

Uwe Klippert, Burscheid, DE;

Thomas Feller, Solingen, DE;

Inventors:

Thorsten Rische, Unna, DE;

Torsten Pohl, Köln, DE;

Jürgen Meixner, Krefeld, DE;

Uwe Klippert, Burscheid, DE;

Thomas Feller, Solingen, DE;

Assignee:

Bayer MaterialScience AG, Leverkusen, DE;

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C08K 3/00 (2006.01); C08G 18/08 (2006.01); C08G 18/28 (2006.01); C08G 18/12 (2006.01);
U.S. Cl.
CPC ...
Abstract

Coating compositions that are stable to thermal yellowing that include coating materials containing I) one or more dispersions of hydroxyl-free polyurethanes and/or polyurethane-ureas, II) one or more aqueous solutions or dispersions of ionically modified, hydroxyl-containing polyurethanes and/or polyurethane-ureas, other than the constituents of component I), and III) at least one crosslinker. The dispersions are obtained by A) preparing an NCO-containing polyurethane prepolymer by reacting polyisocyanates with polymeric polyols and/or polyamines having number-average molecular weights of 400 to 8000 g/mol, isocyanate-reactive, ionically or potentially ionically hydrophilicizing compounds and/or isocyanate-reactive nonionically hydrophilicizing compounds; B) either dissolving the prepolymer obtained from step A) in aliphatic ketones or, diluting the prepolymer solution if the preparation has already been carried out in the presence of A6) by further addition of aliphatic ketones, and C) reacting the remaining free NCO groups of the prepolymer with a chain extender component.


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