C08G18/4887

POLY(GLYCEROL SEBACATE) URETHANE FIBERS, FABRICS FORMED THEREFROM, AND METHODS OF FIBER MANUFACTURE

A manufacturing process includes combining a liquid resin with a liquid reactive cross-linking composition to form a reactive core composition. The manufacturing also includes contacting the reactive core composition with a sheath composition including a carrier polymer in a solvent. The manufacturing process further includes wet spinning the reactive core composition with the sheath composition to form a sheath-core fiber including a core including at least one continuous fiber of a reaction product of the liquid resin and liquid cross-linking composition and a sheath surrounding the core. The cross-linking composition reacts with the resin during the wet spinning. The sheath includes the carrier polymer. A continuous poly(glycerol sebacate) urethane (PGSU) fiber comprising PGSU and a continuous PGSU fiber forming system are also disclosed.

HCFO-CONTAINING ISOCYANATE-REACTIVE COMPOSITIONS, RELATED FOAM-FORMING COMPOSITIONS AND FOAMS

Disclosed are HCFO-containing isocyanate-reactive compositions that include a tertiary amine oxide catalyst. Also described are foam-forming compositions containing such isocyanate-reactive compositions, rigid foams made using such foam-forming compositions, and methods for producing such foams, including use of such foams as insulation in discontinuous foam panel applications. The isocyanate-reactive composition can exhibit a long shelf life, be shelf-stable, and produce foam with good physical properties.

POLYURETHANE OR POLYURETHANE-UREA COMPOSITIONS WITH REDUCED COLD HARDENING
20220002468 · 2022-01-06 ·

A polyurethane or polyurethane-urea composition with reduced cold hardening being the reaction product of: a) at least one block copolymer of A-B-A type with an average number molecular weight of 1000 to 5000 g/mol, and being the reaction product of a poly(alkylene oxide) diol and a cyclic lactone or ether, the poly(alkylene oxide) diol being present in the range 30-70 wt % of the block copolymer and the cyclic lactone or ether is present in the range 30-70 wt, and b) at least one diisocyanate, and associated uses of the same.

POLYOL COMPOSITIONS AND METHODS
20220002469 · 2022-01-06 ·

In one aspect, the present invention encompasses blends of polyols comprising a polycarbonate polyol and an additional polyol selected from a polyether or polyester polyol, resulting polyurethanes derived from such blends of polyols, methods of making such polyurethane compositions, and coatings and adhesives derived from such polyurethane compositions.

Aromatic polyester polyether polyurethane panels and useful materials comprising same

This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure. The disclosure provides aromatic polyester polyether polyols and compositions comprising such polyols. The disclosed aromatic polyester polyether polyols and compositions including same are the products of the transesterification reaction of polyethylene terephthalate (“PET”) and an ethoxylated triol, namely glycerin or trimethylolpropane, wherein the degree of ethoxylation is from 1 to 9 moles. At least some of the PET used to generate the aromatic polyester polyether polyols is derived from recycled PET. The disclosed aromatic polyester polyether polyols have utility in preparing polyurethane materials, for example.

AROMATIC POLYESTER POLYETHER POLYURETHANE PANELS AND USEFUL MATERIALS COMPRISING SAME

This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure. The disclosure provides aromatic polyester polyether polyols and compositions comprising such polyols. The disclosed aromatic polyester polyether polyols and compositions including same are the products of the transesterification reaction of polyethylene terephthalate (“PET”) and an ethoxylated triol, namely glycerin or trimethylolpropane, wherein the degree of ethoxylation is from 1 to 9 moles. At least some of the PET used to generate the aromatic polyester polyether polyols is derived from recycled PET. The disclosed aromatic polyester polyether polyols have utility in preparing polyurethane materials, for example.

Toughened cyanoacrylate compositions

Curable cyanoacrylate compositions are reported that comprise cyanoacrylate and a thermoplastic polyurethane (TPU) components. Such compositions are toughened cyanoacrylate compositions exhibiting long term viscosity stability when stored for prolonged periods at room temperature (25° C.). TPU components are reported having structural units in which at least one of the structural units has the formula —O—R.sup.1—O—Ar—O—R.sup.2—O—, wherein Ar is a C.sub.6-C.sub.20 aromatic group with at least one aromatic ring; R.sup.1 is a C.sub.2-C.sub.10 alkyl group; and R.sup.2 is a C.sub.2-C.sub.10 alkyl group. The thermoplastic polyurethane (TPU) component may be present in the curable cyanoacrylate composition from about 1 wt % to about 40 wt %, for example from about 2 wt % to about 30 wt %, such from about 3 wt % to about 20 wt %, suitably from about 5 wt % to about 10 wt %, based on the total weight of the composition.

Aromatic polyester polyether polyols, polyurethanes made therefrom and building materials comprising same

This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure. The disclosure provides aromatic polyester polyether polyols and compositions comprising such polyols. The disclosed aromatic polyester polyether polyols and compositions including same are the products of the transesterification reaction of polyethylene terephthalate (“PET”) and an ethoxylated triol, namely glycerin or trimethylolpropane, wherein the degree of ethoxylation is from 1 to 9 moles. At least some of the PET used to generate the aromatic polyester polyether polyols is derived from recycled PET. The disclosed aromatic polyester polyether polyols have utility in preparing polyurethane materials, for example.

Process for the preparation of polyether polyols

The invention relates to a method for producing polyether carbonate polyols, wherein (i) in a first step a polyether carbonate polyol is produced from one or more H-functional starter substances, one or more alkylene oxides, and carbon dioxide in the presence of at least one DMC catalyst, and (ii) in a second step the polyether carbonate polyol is chain-extended with a mixture of at least two different alkylene oxides in the presence of at least one DMC catalyst. The invention further relates to polyether carbonate polyols that contain a terminal mixed block of at least two alkylene oxides and to a method for producing soft polyurethane foams, wherein a polyol component containing a polyether carbonate polyol according to the invention is used.

Polyol for crosslinkable polyurethane resin composition, and crosslinkable polyurethane resin

The present invention relates to a polyol for a crosslinkable polyurethane resin composition, containing a high molecular polyol represented by the following formula (1) or (2), in which the high molecular polyol is a condensate of a polyfunctional carboxylic acid (A) with a bifunctional polyether polyol (B), the high molecular polyol has a number average molecular weight (Mn) in a range of 1,000 to 10,000, and the polyol for a crosslinkable polyurethane resin composition has a content of the high molecular polyol of 0.1 wt % to 15 wt %. ##STR00001##