C08G18/4261

Alkoxylated bio-oil polyol compositions

Methods are provided for producing bio-oil polyols, alkoxylating bio-oil polyols to provide polyols, and for employing the alkoxylated bio-oil polyols for making polymers or copolymers of polyesters or polyurethanes.

Moisture-Curable Hot-Melt Adhesive Agent
20200095471 · 2020-03-26 ·

Objective:

To provide a moisture-curable hot-melt adhesive agent having excellent balance of initial adhesive strength, adhesive strength after curing and heat resistance and the like, and a layered product bonded with the moisture-curable hot-melt adhesive agent.

Means for solving the problem: A moisture-curable hot-melt adhesive agent comprising an urethane prepolymer having an isocyanate group at the end (A), a styrene based block copolymer (B), and a tackifying resin (C), wherein the styrene based block copolymer (B) comprises a styrene based block copolymer having 10 to 35% by weight of a styrene content (B1) and a styrene based block copolymer having 40 to 70% by weight of a styrene content (B2).

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.

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.

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.

PUR/PIR RIGID FOAMS MADE OF POLYADDITION OLIGOESTERS
20180334530 · 2018-11-22 ·

The invention relates to a method for producing PUR/PIR rigid foam materials, having the steps of reacting at least one polyester polyol (a), which can be obtained by reacting a. I.) at least one cyclic carboxylic acid anhydride; a.2.) at least one low-molecular dial with a molecular mass of 62 to 450 Da; and a.3.) at least one alkylene oxide; by esterifying the components a.I.) and a.2.) and subsequently oxalkylating the resulting carboxylic acid half-ester using component a.3.); wherein at least the oxalkylation is carried out using a.4.) at least one amine catalyst in which (the) nitrogen atom(s) is/are part of an aromatic ring system, with (b) at least one polyisocyanate-containing component, (c) at least one propellant, (d) at least one or more catalysts, (e) optionally at one flameproofing agent and/or other auxiliary agents, and (f) optionally at least one additional compound with at least two groups which are reactive towards isocyanates and which differ from polyester polyol (a). The invention also relates to a PUR/PIR rigid foam material which can be obtained using a method according to the invention, to a composite element comprising the PUR/PIR rigid foam material according to the invention, at least one cover layer selected from concrete, wood, press board, aluminum, copper, steel, stainless steel, paper, non-wovens, and plastic, and multilayer composites or a combination thereof. The invention also relates to the use of the PUR/PIR rigid foam materials according to the invention or the composite element according to the invention for heat damping.

QUICK-DRYING, ENERGY-ELASTIC, SCRATCH-RESISTANT AND STABLE COATING COMPOUNDS

The present invention relates to fast-drying, hard-elastic, scratch-resistant, and robust two-component polyurethane coating compositions, to their use, and to coating methods. Synthesis components in the coating compositions comprise polyisocyanate, hydroxyl-containing poly(meth)acrylate polyol, and certain branched polyester polyols, obtainable by polycondensation of hexahydrophthalic anhydride, trimethylolpropane, and optionally further components.

Bioresorbable microparticles

Polyurethane microparticles are derived from structural units comprising poly(alkylene oxide) moieties, caprolactone moieties and urethane moieties. The microparticles may include an active agent and have a particle size from 0.1 to 100 microns. Microparticles for injection have a particle size of 15 to 80 microns; for use as a aerosol 1 to 3 microns; and for intraocular use 0.02 to 2 microns. Dispersivity is in the range 1 to 3.

Insulation moulding and method for its manufacture

A cavity between inner and outer walls of an open-box-shaped mold is filled with a polyurethane reaction mixture, containing an isocyanate and an emulsion of an isocyanate-reactive composition with three polyols and a blowing agent, which is cured to a polyurethane containing polymer. The inner and outer wall are a fixed distance from one another and each wall comprises a bottom and sides. The mixture is fed through an inlet in the bottom of the outer wall. Before filling the cavity, the mold is turned downwards so that the mixture foams upwards, filling the cavity. The three polyols are polyether polyol obtained by adding an epoxy to carbohydrates or difunctional or higher-functional alcohols; polyether polyol obtained by adding an epoxy to an aromatic amine; and polyester polyether polyol obtained by adding an epoxy to the esterification product of an aromatic dicarboxylic acid derivative and a difunctional or higher-functional alcohol.

Process for preparing polyoxyalkylene polyester polyols
12227614 · 2025-02-18 · ·

The present invention relates to a process for preparing polyoxyalkylene polyester polyols by reacting a starter compound having Zerewitinoff-active H atoms, a cyclic dicarboxylic acid anhydride and a fatty acid ester with an alkylene oxide in the presence of a basic catalyst. The invention further relates to polyoxyalkylene polyester polyols resulting from the method and to a preparation method for polyurethanes by reaction of the polyoxyalkylene polyester polyols according to the invention.