C08G18/12

MODIFIED LIGNIN PRODUCTS FOR RIGID FOAMS
20230025729 · 2023-01-26 ·

Modified lignin products, processes for making them, and their use to produce rigid polyurethane or polyisocyanurate foams are disclosed. The processes comprise heating a lignin source with a nitrogen source and a starved concentration of a C.sub.1-C.sub.5 aldehyde to give a reaction mixture comprising a Mannich condensation product, neutralizing the reaction mixture, and isolating the modified lignin product. The process is performed at a mass ratio of lignin source to nitrogen source within the range of 1:1 to 1:5 and at a molar ratio of nitrogen source to C.sub.1-C.sub.5 aldehyde within the range of 3.5:1 to 1:1. Polyol blends and performance additives that contain the modified lignin products are described. Rigid foams that process well and incorporate up to 60 wt.%, based on the amount of polyol component, of the modified lignin contribute to excellent flame retardancy and low-temperature R-value performance.

Silylated polyurethanes and methods for preparing thereof

The invention relates to a silylated polyurethane obtainable by reacting: d) at least one polyol having a number average molecular weight of from 1000 to 50,000 g/mol; e) at least one polyisocyanate, preferably diisocyanate; and f) at least one tertiary hydroxyl functional alkoxysilane of the general formula (I) ##STR00001##
wherein R.sup.1 is selected from the group consisting of hydrogen and a linear or branched, substituted or unsubstituted hydrocarbon residue having 1 to 20 carbon atoms; R.sup.2 and R.sup.3 are same or different and are, independent from one another, selected from a linear or branched, substituted or unsubstituted hydrocarbon residue having 1 to 20 carbon atoms; R.sup.4 is selected from a linear or branched, substituted or unsubstituted hydrocarbon residue having 1 to 20 carbon atoms; R.sup.5 is selected from a linear or branched, substituted or unsubstituted hydrocarbon residue having 1 to 20 carbon atoms; R.sup.6 and R.sup.7 are same or different and are, independent from one another, selected from a linear or branched, substituted or unsubstituted hydrocarbon residue having 1 to 20 carbon atoms; and n is 1, 2 or 3, a method for preparing thereof, a curable composition comprising the thereby obtained silylated polyurethane, and its use.

Silylated polyurethanes and methods for preparing thereof

The invention relates to a silylated polyurethane obtainable by reacting: d) at least one polyol having a number average molecular weight of from 1000 to 50,000 g/mol; e) at least one polyisocyanate, preferably diisocyanate; and f) at least one tertiary hydroxyl functional alkoxysilane of the general formula (I) ##STR00001##
wherein R.sup.1 is selected from the group consisting of hydrogen and a linear or branched, substituted or unsubstituted hydrocarbon residue having 1 to 20 carbon atoms; R.sup.2 and R.sup.3 are same or different and are, independent from one another, selected from a linear or branched, substituted or unsubstituted hydrocarbon residue having 1 to 20 carbon atoms; R.sup.4 is selected from a linear or branched, substituted or unsubstituted hydrocarbon residue having 1 to 20 carbon atoms; R.sup.5 is selected from a linear or branched, substituted or unsubstituted hydrocarbon residue having 1 to 20 carbon atoms; R.sup.6 and R.sup.7 are same or different and are, independent from one another, selected from a linear or branched, substituted or unsubstituted hydrocarbon residue having 1 to 20 carbon atoms; and n is 1, 2 or 3, a method for preparing thereof, a curable composition comprising the thereby obtained silylated polyurethane, and its use.

Optical adhesive and optical laminates and lenses formed with same

The present invention pertains to polyurethane-urea based optical adhesives for formation of optical film laminates, optically functional film laminates, and ophthalmic or eyeglass lenses employing the same and methods for producing the same.

Optical adhesive and optical laminates and lenses formed with same

The present invention pertains to polyurethane-urea based optical adhesives for formation of optical film laminates, optically functional film laminates, and ophthalmic or eyeglass lenses employing the same and methods for producing the same.

Optical adhesive and optical laminates and lenses formed with same

The present invention pertains to polyurethane-urea based optical adhesives for formation of optical film laminates, optically functional film laminates, and ophthalmic or eyeglass lenses employing the same and methods for producing the same.

Urethane adhesive composition
11560501 · 2023-01-24 · ·

The present invention is to provide a urethane adhesive composition which exhibits excellent heat-resistant adhesion after storage to resin. The present invention relates to a urethane adhesive composition including: a urethane prepolymer having an isocyanate group; an isocyanurate compound having an isocyanurate ring; a terpene compound having active hydrogen; and a vinyl silane coupling agent represented by Formula (A) below: (where in Formula (A), R.sup.1 and R.sup.3 each independently represent a monovalent hydrocarbon group, R.sup.2 represents a (n+1) valent hydrocarbon group, Vi represents —CH═CH.sub.2, m1 is from 1 to 3, m2 is from 1 to 3, m3 is from 0 to 2, m1+m2+m3 is 4, and n is 1 or greater). ##STR00001##

Urethane adhesive composition
11560501 · 2023-01-24 · ·

The present invention is to provide a urethane adhesive composition which exhibits excellent heat-resistant adhesion after storage to resin. The present invention relates to a urethane adhesive composition including: a urethane prepolymer having an isocyanate group; an isocyanurate compound having an isocyanurate ring; a terpene compound having active hydrogen; and a vinyl silane coupling agent represented by Formula (A) below: (where in Formula (A), R.sup.1 and R.sup.3 each independently represent a monovalent hydrocarbon group, R.sup.2 represents a (n+1) valent hydrocarbon group, Vi represents —CH═CH.sub.2, m1 is from 1 to 3, m2 is from 1 to 3, m3 is from 0 to 2, m1+m2+m3 is 4, and n is 1 or greater). ##STR00001##

Urethane adhesive composition
11560501 · 2023-01-24 · ·

The present invention is to provide a urethane adhesive composition which exhibits excellent heat-resistant adhesion after storage to resin. The present invention relates to a urethane adhesive composition including: a urethane prepolymer having an isocyanate group; an isocyanurate compound having an isocyanurate ring; a terpene compound having active hydrogen; and a vinyl silane coupling agent represented by Formula (A) below: (where in Formula (A), R.sup.1 and R.sup.3 each independently represent a monovalent hydrocarbon group, R.sup.2 represents a (n+1) valent hydrocarbon group, Vi represents —CH═CH.sub.2, m1 is from 1 to 3, m2 is from 1 to 3, m3 is from 0 to 2, m1+m2+m3 is 4, and n is 1 or greater). ##STR00001##

Two-component solventless adhesive compositions

Two-component solventless polyurethane adhesive compositions comprising an isocyanate component and an isocyanate-reactive are disclosed, the compositions comprising an isocyanate component comprising an isocyanate-terminated prepolymer and an isocyanate-reactive component comprising a hydroxy-terminated polyurethane resin, a polyether polyol, a phosphate ester adhesion promoter, and, optionally, a bio-based polyol. Methods for forming laminate structures are also disclosed, the methods comprising forming an adhesive composition by mixing an isocyanate adhesive component comprising an isocyanate-terminated prepolymer and an isocyanate-reactive adhesive component comprising a hydroxy-terminated polyurethane resin, a polyether polyol, a phosphate ester adhesion promoter, and optionally, a bio-based polyol, applying the adhesive composition to a surface of a first substrate, and bringing a surface of a second substrate into contact with the adhesive composition on the surface of the first substrate, thereby forming the laminate structure. Laminate structures are also disclosed.