C08G18/6625

AMINATED PHOSPHORENE-BASED FLAME-RETARDANT WATERBORNE POLYURETHANE COATING AND PREPARATION METHOD THEREOF
20230041786 · 2023-02-09 ·

This application relates to flame-retardant coatings, and more particularly to an aminated phosphorene-based flame-retardant waterborne polyurethane coating and a preparation method thereof. The aminated phosphorene-based flame-retardant waterborne polyurethane coating is prepared from a diisocyanate-terminated prepolymer, a neutralizer and an aminated phosphorene, where the diisocyanate-terminated prepolymer is prepared from polymeric diol with water-dispersible groups, aliphatic diisocyanate and carboxylic acid type hydrophilic diol under the catalysis of a catalyst for synthesizing waterborne polyurethane.

CHEMICAL RESISTANT POLYURETHANE ADHESIVE

A pressure sensitive adhesive composition includes a polyurethane polymer that includes the reaction product of a polyisocyanate component and a polyol component. The polyol component has a total solubility parameter ranging from 10 to 14 (cal/cm.sup.3).sup.1/2.

Radiation curable polyurethane resin for ink jet ink

A radiation curable polyurethane resin includes an ionic group, a polyalkylene oxide in a side chain thereof, and a (meth)acrylate or (meth)acrylamide having a hydroxyl functional group. The polyurethane resin is obtainable by reacting a polyester polyol, a polyether diol, a polyol containing an ionic group, a (meth)acrylate or (meth)acrylamide having a hydroxyl functional group, and a polyisocyanate. The polyester polyol is obtained by reacting a polycarboxylic acid and a polyol. The radiation curable polyurethane resin can be used as binder in an aqueous ink jet ink.

ADHESIVE COMPOSITION FOR TIRE CORD, TIRE CORD, AND TIRE
20220388341 · 2022-12-08 ·

This invention relates to an adhesive composition for a tire cord, a tire cord including an adhesive layer formed from the adhesive composition, and a tire including the tire cord. According to the present disclosure, an environment-friendly adhesive composition for a tire cord that can not only improve adhesive strength between tire rubber and a tire cord, but can also improve strength of a tire cord is provided.

AQUEOUS POLYURETHANE EMULSION FOR ULTRA-THIN POLYURETHANE CONDOM WITH LOW MODULUS AND HIGH STRENGTH, AND PREPARATION METHOD THEREFOR
20230029922 · 2023-02-02 ·

Provided are a waterborne polyurethane emulsion for ultra-thin polyurethane condoms having a low modulus and a high strength, and a method for preparing the emulsion, wherein the waterborne polyurethane emulsion comprises 15 to 18 parts by mass of a macromolecular diol, 4 to 6 parts by mass of a diisocyanate, 0.6 to 0.9 parts by mass of a hydrophilic chain extender, 0.4 to 0.8 parts by mass of a small-molecule chain extender, and the like. The prepared waterborne polyurethane emulsion is characterized by a low modulus, a high strength, and high resilience.

Dual cure protective display film

A display film includes a transparent polymeric substrate layer and a transparent energy dissipation layer disposed on the transparent polymeric substrate layer. The transparent energy dissipation layer includes cross-linked polyurethane and a polyacrylate polymer. The transparent energy dissipation layer has a glass transition temperature of 27 degrees Celsius or less and a Tan Delta peak value of 0.5 or greater.

Polyurethane adhesive with chemical resistant

There is provided a pressure sensitive adhesive composition comprising a polyurethane polymer that comprises the reaction product of a polyisocyanate component and a polyol component. The polyol component has a hydrophilic-lipophilic balance (HLB) less than 10. The polyurethane further comprises 0.5 to 10 wt.-% of hydrophilic polymerized units having an HLB greater than 12, such as a reaction product of a polyethylene glycol polymer. In another embodiment, the polyurethane further comprises pendent ethylenically unsaturated groups. Also described are articles such as laminating tapes and protective films as well as methods of bonding substrates with the pressure sensitive adhesive and laminating tape.

AQUEOUS POLYURETHANE DISPERSION AND TEXTILE

An aqueous polyurethane dispersion and a textile are provided. The aqueous polyurethane dispersion includes water and a bio-based polyurethane. The bio-based polyurethane includes bio-based polyester polyol, hydrophilic polyol, isocyanate, and hydrophilic compound. A weight ratio of the bio-based polyester polyol to the hydrophilic polyol is 2.7:1 to 5.3:1.

POLYURETHANE FOR COSMETIC PREPARATIONS, AND METHOD FOR PRODUCING POLYURETHANE FOR COSMETIC PREPARATIONS

This invention provides: a polyurethane for cosmetic preparations, which is obtained by reacting (A) a polyester polyol having two or more hydroxyl groups in each molecule, (B) an aliphatic diol consisting of two hydroxyl groups and an aliphatic hydrocarbon group having 3 to 8 carbon atoms, (C) a carboxyl group-containing diol which has a carboxyl group and two hydroxyl groups in the molecule and has a molecular weight of 100 to 300, (D) a diisocyanate containing at least one compound selected from the group consisting of isophorone diisocyanate, hexamethylene diisocyanate and dicyclohexylmethane-4,4′-diisocyanate, and (E) a chain extender which contains at least one compound selected from the group consisting of water, ethylene diamine and propylene diamine and which has a weight average molecular weight of 50,000 to 300,000; a production method; and a cosmetic preparation which contains this polyurethane for cosmetic preparations.

Polyurethane-based binder dispersion

A polyurethane-based binder dispersion is described. The polyurethane based binder dispersion comprises: a polyurethane, which comprises: (A) a polyisocyanate; (B) a first polyol having a chain with two hydroxyl functional groups at one end of the chain and no hydroxyl groups at an opposed end of the chain; (C) a second polyol having a chain with two hydroxyl functional groups at both ends of the chain; (D) a carboxylic acid functional group with two hydroxyl functional groups; and (E) a compound shown in formula (1): m(M+) n(X)—R—Y— (1), wherein m is 0 or 1, M is a metal, n is 2 to 10, X is an amino group, R is a C1 to C18 alkyl group, a C6 to C30 aromatic compound or a C4 to C20 aliphatic cyclic compound, and Y is SO3- or SO3H, with the proviso that when m is 0, Y is SO3H and when m is 1, Y is SO3-.