Lanny D. Venham - Oakdale PA, US Myron W. Shaffer - New Cumberland WV, US Karsten Danielmeier - Bethel Park PA, US Karen M. Henderson - Coraopolis PA, US
Assignee:
Bayer MaterialScience LLC - Pittsburgh PA
International Classification:
C07D203/12
US Classification:
548962, 524430
Abstract:
The invention relates to a process for reducing the monomeric aziridine content in a polyaziridine forming reaction mixture by adding to the polyaziridine forming reaction mixture an excess of a carbodiimide scavenger wherein the excess is based on the equivalent ratio of scavenger to monomeric aziridine, and to a product obtained by this process and to a coating composition containing the product obtained by the process.
Lanny D. Venham - Oakdale PA, US Kyli Martin - Bridgeville PA, US Richard R. Roesler - Wexford PA, US Myron W. Shaffer - New Cumberland WV, US Michael K. Jeffries - Follansbee WV, US
A composition that includes isocyanate group containing compounds that include on average i) a NCO functionality less than or equal to 3. 5; and ii) from 1. 5 to 8 percent by weight, based on the isocyanate containing compound, of allophanate groups; and which is substantially free of uretdione groups. The composition can be used in two component elastomeric coating compositions that include a component A the above-described composition and a component B that includes a compound containing one or more functional groups that are reactive with isocyanate groups. The elastomeric coating compositions can be used to coat substrates.
Biuretized Isocyanates And Blocked Biuretized Isocyanates
Richard Roesler - Wexford PA, US Yuliya Berezkin - Pittsburgh PA, US Carol Kinney - Eighty Four PA, US Kyli Martin - Bridgeville PA, US Myron Shaffer - New Cumberland WV, US
International Classification:
C08G 18/00
US Classification:
528044000
Abstract:
The present invention is directed to a biuret group-containing polyisocyanate composition having an isocyanate functionality of at least 4 prepared by a process comprising reacting a polyisocyanate adduct which a) is prepared from an aliphatic and/or cycloaliphatic diisocyanate; b) has an average isocyanate functionality of at least 2.5, and c) contains isocyanurate groups, with a secondary monoamine at an isocyanate to amine equivalent ratio of from about 4:1 to about 14:1 to incorporate biuret groups into said polyisocyanate. The invention is also directed to a blocked biuret group-containing polyisocyanate composition which is prepared by reacting the biuret-containing polyisocyanate with a blocking agent.
Richard Roesler - Wexford PA, US Yuliya Berezkin - Pittsburgh PA, US Carol Kinney - Eighty Four PA, US Kyli Martin - Bridgeville PA, US Myron Shaffer - New Cumberland WV, US Poli Yu - Jinqiao, CN Dorota Greszta-Franz - Erkrath, DE Reinhard Halpaap - Odenthal, DE Joachim Petzoldt - Monheim, DE
International Classification:
C08G 18/00
US Classification:
528044000
Abstract:
The present invention is directed to blocked biuret group-containing polyisocyanate compositions, wherein the blocking agent is selected from the group consisting of di-C-C-alkyl and/or alkoxyalkyl malonates and acetoacetic acid C-C-alkyl and/or alkoxyalkyl esters.
David Zielinski - Wexford PA, US Myron Shaffer - New Cumberland WV, US Michael Jeffries - Follansbee WV, US
International Classification:
C08G 18/00
US Classification:
528044000
Abstract:
A composition that includes isocyanate group containing compounds that include on average i) a NCO functionality less than or equal to 3.5; and ii) from 1.5 to 8 percent by weight, based on the isocyanate containing compound, of allophanate groups; and which is substantially free of uretdione groups. The composition can be used in two component elastomeric coating compositions that include a component A the above-described composition and a component B that includes a compound containing one or more functional groups that are reactive with isocyanate groups. The elastomeric coating compositions can be used to coat substrates.
Carol Kinney - Eighty Four PA, US Charles Gambino - McDonald PA, US Michael Dvorchak - Monroeville PA, US Myron Shaffer - New Cumberland WV, US
International Classification:
C08G 18/00
US Classification:
528044000
Abstract:
The present invention relates to low viscosity, ethylenically-unsaturated polyurethanes which are substantially free from isocyanate groups, are liquid at 25 C., have a total content of ethylenically unsaturated groups (calculated as C═C, MW 24) of 1 to 12% by weight and contain the reaction product of A) 4-isocyanatomethyl-1,8-octamethylene diisocyanate (NTI) with B) a hydroxyl component comprising i) 5 to 100 hydroxyl equivalent % of one or more hydroxy functional lactone ester (meth)acrylates having a number average molecular weight of about 200 to 1000, ii) up to 95 hydroxyl equivalent % of a monohydroxy-functional, ethylenically unsaturated compound other than B-i), and iii) up to 20 hydroxyl equivalent % of a saturated hydroxyl compound or an unsaturated hydroxyl compound other than B-i) or B-ii), wherein i) the hydroxyl equivalent %'s of components B-i), B-ii) and B-iii) add up to 100%, based on the total weights of components B-i), B-ii) and B-iii) and ii) the NCO:OH equivalent ratio of component A) to component B) is 1.10:1 to 1:1.10. The present invention also relates to a one-component coating composition containing these ethylenically unsaturated polyurethanes.
Article Having Photochromic Properties And Process For Its Manufacture
A process for making an article molded of polymeric material, the article featuring photochromic properties is disclosed. To at least a portion of the surface of an article, molded of a composition that contains at least one transparent thermoplastic polymer or a transparent thermosetting composition there is applied a curable weatherable polyurethane coating. At least a portion of the coating is after curing brought into contact with a material system that contains (i) water, (ii) at least one carrier conforming to wherein Ris a radical selected from the group consisting of linear or branched C-Calkyl, benzyl, benzoyl and phenyl, Ris Ror H, n is 2, 3 or 4, and m is 1 to 35; (iii) a photochromic compound and (iv) a diol, under conditions calculated to bring about diffusion of said compound into the cured coating.