Patent classifications
C08G18/798
Anti-smudge and anti-graffiti compositions
Polyurethane-based and epoxy-based coating compositions are described that provide coatings and adhesives that are clear, amphiphobic and durable. Both water and hexadecane readily slide off these surfaces without leaving a residue. Coatings with thicknesses ranging from about 10 nm to about 10 μm exhibited excellent transmittance properties. Such films exhibited durability against abrasion, ink-resistance, anti-graffiti, anti-fingerprint, and strong adhesion to glass surfaces. The coatings are applicable to electronic devices, fabrics, glass, etc. to prepare optically clear, stain-resistant, and smudge-resistant surfaces.
Polyurethane article and methods of making the same
Articles are provided including at least one polyurethane prepared from: (a) about 1 equivalent of at least one polyisocyanate; (b) about 0.005 to about 0.35 equivalent of at least one polycaprolactone polyol; (c) about 0.01 to about 1.0 equivalent of at least one polyol selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 1,2-ethanediol, propanediol, butanediol, pentanediol, hexanediol, heptanediol, octanediol, nonanediol, decanediol, dodecane diol, octadecanediol, cyclopentanediol, 1,4-cyclohexanediol, cyclohexanedimethanol, 1,4-benzenedimethanol, xylene glycol, hydroxybenzyl alcohol, dihydroxytoluene, bis(2-hydroxyethyl) terephthalate, 1,4-bis(hydroxyethyl)piperazine, N,N′,bis(2-hydroxyethyl)oxamide and mixtures thereof; and (d) about 0.01 to about 0.5 equivalent of at least one polyol selected from the group consisting of glycerol, tetramethylolmethane, trimethylolethane, trimethylolpropane, erythritol, pentaerythritol, dipentaerythritol, tripentaerythritol, sorbitan, and mixtures thereof, each based upon the about 1 equivalent of the at least one polyisocyanate, wherein the article has a Gardner Impact strength of at least about 400 in-lb according to ASTM D-5420-04.
MULTI-AZIRIDINE COMPOUND
The present invention relates to a multi-aziridine compound having: a) at least 2 of the following structural units (A) whereby R.sub.1 is H; R.sub.2 and R.sub.4 are independently chosen from H, a linear group containing from 1 to 8 carbon atoms and optionally containing one or more heteroatoms, a branched or cyclic group containing from 3 to 8 carbon atoms and optionally containing one or more heteroatoms, phenyl, benzyl, or pyridinyl; R.sub.3 is chosen from a linear group containing from 1 to 8 carbon atoms and optionally containing one or more heteroatoms, a branched or cyclic group containing from 3 to 8 carbon atoms and optionally containing one or more heteroatoms, phenyl, benzyl, or pyridinyl; or R.sub.2 and R.sub.3 (in case R.sub.2 is different than H) may be part of the same cyclic group containing from 3 to 8 carbon atoms; R′ and R″ are independently H or an aliphatic hydrocarbon group containing from 1 to 12 carbon atoms; and b) a molecular weight of at least 600 Daltons, wherein the molecular weight is determined using MALDI-TOF mass spectrometry according to the description.
Single-component polysiloxane non-skid / non-slip coatings
Disclosed is a composition having: an organosilane polymer, a polyamide polymer; and an abrasive aggregate. The organosilane is made by: reacting an amino-functional alkoxysilane with one or more polyisocyanates to form one or more adducts having an unreacted isocyanate group; and reacting the adducts with one or more polyfunctional amino- and/or hydroxyl compounds so that the polymer contains no unreacted isocyanate groups. The polyfunctional amino- and/or hydroxyl compound has a cycloaliphatic group or an aromatic group. The composition can be used to make a single-component polysiloxane non-skid/non-slip coating that is applied by rolling, spraying, or troweling and cures with atmospheric moisture.
METHOD FOR PRODUCING ISOCYANURATES FROM URETDIONES
The invention relates to a process of preparing allophanate- and/or thioallophanate group-containing compounds comprising the following steps: reacting A) at least one component having at least one uretdione group with B) at least one component having at least one hydroxyl and/or thiol group, in the presence C) of at least one catalyst, containing a structural element of the general formulae (I) and/or (II), wherein R1, R2, R3, R4, R5 and R6 independently of each other represent the same or different radicals meaning saturated or unsaturated, linear or branched, aliphatic, cycloaliphatic, araliphatic or aromatic organic radicals with 1 to 18 carbon atoms that are substituted or unsubstituted and/or have heteroatoms in the chain, the radicals being capable of forming, even when combined with each other and optionally together with an additional heteroatom, rings with 3 to 8 carbon atoms that can optionally be further substituted, wherein R3, R4, R5 and R6 independently of each other also can represent hydrogen, and R7 represents hydrogen or a carboxylate anion (COO—), the at least one component A) having at least one uretdione group being polyaddition compounds A2) that can be obtained by reacting isocyanate-functional uretdione groups A1) with alcohols and/or amines that have a free isocyanate group content of less than 5 wt. % in their solvent-free form.
PROCESS FOR PREPARING ISOCYANATE-BASED STABLE DISPERSIONS COMPRISING DERIVATIZED POLYSACCHARIDES
The invention relates to a process for preparing a derivatized polysaccharide and stable isocyanate-based dispersions comprising derivatized polysaccharide.
USE OF SPECIFIC OPEN-CHAIN ETHER ISOCYANATES
The invention relates to the use of at least one open-chain, optionally branched, ether isocyanate having an NCO functionality≥1, wherein 2 or 3 carbon atoms are present between at least one NCO group and at least one ether-oxygen atom, optionally in the presence of other reactants such as alcohols, amines, water, CO.sub.2, or of other reactants having an NCO functionality≥1, optionally in the presence of at least one catalyst, to increase the reaction speed and/or to reduce the optionally required catalyst amount during isocyanate modification. The invention further relates to a process for modifying isocyanates, to the modified isocyanates as such and to a two-component system or one-component system and to the moldings, coatings and composite parts obtainable therefrom.
Thermally activatable latently reactive adhesive film
The invention relates to a thermally activatable reactive adhesive film comprising a carrier film made of thermoplastic polyurethane, which is coated on at least one side with a latently reactive, thermally activatable adhesive compound.
Method for forming multilayer coating film
Provided is a method for forming a multilayer coating film, the method being capable of forming a multilayer coating film having excellent chipping resistance, adhesion, and finished appearance. The method for forming a coating film uses a 3-coat and 1-bake system in which a three-layered multilayer coating film obtained by sequentially applying a first coloring paint (X), a second coloring paint (Y), and a clear coating paint (Z) onto an object to be coated is heated and cured at the same time, wherein the first coloring paint (X) and the second coloring paint (Y) contain a hydroxyl group-containing resin, and the clear coating paint (Z) contains a hydroxyl group-containing acrylic resin (a) and an aliphatic triisocyanate compound (b1) having a molecular weight within a specific range.
TWO-COMPONENT COATING SYSTEM
The present invention relates to a two-component coating system comprising a first component and a second component each of which is separate and distinct from each other, wherein the first component comprises a carboxylic acid functional polymer dissolved and/or dispersed in an aqueous medium, and the second component comprises a multi-aziridine compound having: a) from 2 to 6 of the following structural units (A): b) whereby m is an integer from 1 to 8; and o R′ and R″ are both H b) one or more linking chains wherein each one of these linking chains links two of the structural units A; c) one or more connecting groups whereby each one of the connecting groups connects two of the structural units A; and d) a molecular weight in the range from 840 Daltons to 5000 Daltons, wherein the molecular weight is measured using MALDI-TOF mass spectrometry.
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