C08G18/2865

Ice-Shedding and Smudge-Repellant Coating
20230056474 · 2023-02-23 ·

A coating that is able to shed accumulated material (such as ice) that includes a crosslinkable copolymer with hydrogen bonding moieties and liquid-like side chains, and an oil (or other non-aqueous liquid) that is compatible with the side-chains and that resides in the crosslinked coating and on the surface of the coating together with the side-chains that are on the external surface. Methods may use the coating for de-icing, shedding of marine organisms, and smudge-repellency.

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.

ONE-PART POLYURETHANE SEALANT FOR LOW TEMPERATURE APPLICATIONS
20220356295 · 2022-11-10 · ·

An one-part polyurethane composition, including: A) 15-75 wt.-% of at least one isocyanate-functional polyurethane polymer; B) 5-30 wt.-% of at least one organic thixotropy agent; C) 2-25 wt.-% of at least one plasticizer having viscosity of less than 500 mPa s, measured at 0° C. with cone-plate viscosimeter, shear rate 10 s.sup.−1, cone angle 1°, spindle 25-2, and cone tip-plate distance of 0.05 mm; D) 0-15 wt.-% of at least one solvent; E) 0-50 wt.-% of at least one filler; F) at least one catalyst for curing of polyurethane compositions; wherein isocyanate-functional polyurethane polymer has NCO content in range of 0.8%-2.5% by weight and is obtained from reaction of methylene diphenyl diisocyanate (MDI) and polyol in NCO/OH ratio of at least 3/1 and subsequent removal of non-reacted MDI; and polyol has viscosity, measured according to ASTM D4878-15 at 25° C., of less than 2000 mPa s; and isocyanate-functional polyurethane polymer has remaining content of MDI of at most 0.5% by weight.

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.

SOLVENT-BASED PRETREATMENT AGENT HAVING IMPROVED ADHESION TO RESIDUAL ADHESIVE BEADS
20220348793 · 2022-11-03 · ·

A pretreatment composition for adhesive bonds, including i) between 10 and 30 parts by weight of at least one polyurethane polymer PU containing isocyanate groups, obtained from the reaction of at least one poly(meth)acrylate polyol P and at least one polyisocyanate Il, with the proviso that the poly(meth)acrylate polyol P has an OH number of at least 35 and the polyurethane polymer PU has an NCO content of between 2.0% and 25.0% by weight, based on the polyurethane polymer PU; ii) 0.1 to 10 parts by weight of at least one organosilane OS; iii) 0 to 10 parts by weight of at least one further polyisocyanate I2; iv) 60 to 90 parts by weight of a solvent L; v) 0 to 15 parts by weight of an industrial carbon black; vi) 0 to 10 parts by weight of a fumed hydrophobic silica.

End-capped polyisobutylene polyurethane

A polymeric material includes a polyisobutylene-polyurethane block copolymer. The polyisobutylene-polyurethane block copolymer includes soft segments, hard segments, and end groups. The soft segments include a polyisobutylene diol residue. The hard segments include a diisocyanate residue. The end groups are bonded by urea bonds to a portion of the diisocyanate residue. The end groups include a residue of a mono-functional amine.

End-capped polyisobutylene polyurethane

A polymeric material includes a polyisobutylene-polyurethane block copolymer. The polyisobutylene-polyurethane block copolymer includes soft segments, hard segments, and end groups. The soft segments include a polyisobutylene diol residue. The hard segments include a diisocyanate residue. The end groups are bonded by urea bonds to a portion of the diisocyanate residue. The end groups include a residue of a mono-functional amine.

Polymers, coating compositions containing such polymers, and anti-fingerprint coatings formed therefrom

A substrate at least partially coated with an anti-fingerprint coating is prepared from a coating composition that includes: (a) an organic solvent; and (b) an alkoxysilane functional polymer having at least one ester linkage, at least one urethane linkage, and at least one alkoxysilane functional group. Further, the polymer is prepared from components including: (i) an active hydrogen functional compound having a hydroxyl group, amino group, thiol group, or a combination thereof; (ii) an intramolecular cyclic ester; and (iii) an isocyanate functional compound. The active hydrogen functional compound (i), the isocyanate functional compound (iii), or both (i) and (iii) have one or more alkoxysilane functional groups. Alkoxysilane functional polymers and coating compositions containing the same are also included.

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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URETHANE PREPOLYMER, ADHESIVE, MULTILAYER BODY AND SYNTHETIC LEATHER

The present invention relates to a urethane prepolymer having an isocyanate group, a viscosity at 100° C. of 30 to 600 dPa.Math.s, and a thermal softening temperature after moisture curing of 75 to 155° C.