Disclosed are HCFO-containing isocyanate-reactive compositions, polyurethane foam-forming compositions containing such isocyanate-reactive compositions, rigid polyurethane foams made using such polyurethane foam-forming compositions, and methods for producing such foams, including use of such foams as insulation in the construction of refrigerated storage devices. The isocyanate-reactive composition can exhibit a long shelf life, be shelf-stable, and produce a foam with good thermal insulation properties.

Described herein is a moisture-curing polyurethane hot-melt adhesive including at least 80% by weight, based on a total weight of the moisture-curing polyurethane hot-melt adhesive, of isocyanate-terminated prepolymer obtainable by mixing diisocyanate (a) with compounds having at least two isocyanate-reactive groups (b) and reacting the mixture to form the isocyanate-terminated prepolymer, where the compounds having at least two isocyanate-reactive groups (b) include at least one polylactide (b1) obtainable by reacting lactide with a linear difunctional starter molecule having 2 to 20 carbon atoms and the isocyanate content of the isocyanate-terminated prepolymer is 1 to 5% by weight. Also described herein is a process for producing such a moisture-curing polyurethane hot-melt adhesive and a method of using the moisture-curing polyurethane hot-melt adhesive in bonding of substrates.

Described herein is a cast elastomer including graphene nano platelets and a process for preparing the same.

The present invention relates to a reactive hot melt adhesive composition, a polyurethane prepolymer composition, and cured reaction product thereof having a high mechanical strength and an excellent bonding strength as well as a better reworkability. In particular, the present invention relates to a reactive hot melt adhesive composition comprising: 10% to 24% by weight of a polyisocyanate, 40% to 73% by weight of a first polyol having a number average molecular weight larger than 1,500 g/mol, 1% to 25% by weight of a (meth)acrylate polymer having a number average molecular weight of 20,000 to 80,000 g/mol, and 1% to 15% by weight of a diluent, in which the weight percentages are based on the total weight of all components of the composition.

The present invention relates to a curable photochromic composition that includes: (a) a photochromic compound; and (b) a segmented polymer that includes active hydrogen groups, at least one first segment, and at least one second segment, in which, (i) each first segment independently includes a (meth)acrylic polymer segment, and (ii) each second segment independently includes at least one of, a polycarbonate segment, a polyester segment, a polyether segment, a polyurethane segment, and combinations of two or more thereof. The curable photochromic composition further includes (c) a curing agent having reactive functional groups that are reactive with the active hydrogen groups of the segmented polymer (a), in which the curing agent includes at least one of, a polyisocyanate, a polyisothiocyanate, and an aminoplast. The present invention also relates to photochromic articles that include at least one layer formed from the curable photochromic composition of the present invention.

HCFO-containing isocyanate-reactive compositions, foam-forming compositions containing such isocyanate-reactive compositions, rigid PUR-PIR 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 includes a polyol blend, a blowing agent composition, and a tertiary amine catalyst. The polyol blend includes: (1) an aromatic polyester polyol having a functionality of 1.5 to less than 2.5 and an OH number of 150 to 360 mg KOH/g; (2) an aromatic polyester polyol having a functionality of at least 2.5 and an OH number greater than 360 mg KOH/g, which is present in an amount of at least 10% by weight, based on the total weight of the aromatic polyester polyol in the polyol blend; and (3) an amine-initiated polyether polyol having an OH number of at least 500 mg KOH/g and a functionality of 2.5 to 4. The blowing agent composition includes a hydrochlorofluoroolefin and a carbon dioxide generating chemical blowing agent.

Polymer composite materials and methods of preparation are discussed. The composite material may comprise a polyurethane foam and a plurality of inorganic particles dispersed in the polyurethane foam. The composite material may have moisture movement properties, such that (a) a sample of the composite material having a length of 48 inches has a moisture movement of less than 0.15% along the length, and/or (b) a sample having a length of 6 inches has a moisture movement of less than 0.8% along the length, when submerged in 45° C. distilled water for 14 days.

Described herein is a method for the preparation of a rigid polyisocyanate based foam, including mixing (a) polyisocyanate, (b) at least one compound having at least two hydrogen atoms reactive towards isocyanates, (c) optionally flame retardant, (d) blowing agent, (e) catalyst and (f) optionally further additives, to form a reaction mixture and reacting the reaction mixture to obtain the polyurethane based rigid foam where the compound reactive towards isocyanates (b) includes an aromatic polyetherpolyol (b2) and at least one compound selected from the group consisting of an aromatic polyesterpolyol (b1) and a polyetherpolyol (b3) different from polyether (b2). Also described herein is a rigid polyisocyanate based foam obtained from such a method and a polyol component for the production of a polyisocyanate based foam.

An embodiment of the present technology is an isocyanate-based adhesive used for a surface-treated crystalline thermoplastic resin base material, the isocyanate-based adhesive having a value represented by (JIS-A hardness)/(strength at break [MPa])×(elongation at break (%))/100 of 2.0 to 70 after being cured by being allowed to stand still under a condition at 23° C. and 50% RH for 3 days, and the crystalline thermoplastic resin base material having a value represented by (δ.sup.d/δ.sup.p+δ.sup.p) of 2.0 to 30.0. δ.sup.p=γ.sup.p−γ.sup.p0 and δ.sup.d=|γ.sup.d−γ.sup.d0|, γ.sup.p0 is a polar term of surface free energy before the surface treatment, γ.sup.p is a polar term of surface free energy after the surface treatment, γ.sup.d0 is a dispersion term of the surface free energy before the surface treatment, and γ.sup.d is a dispersion term of the surface free energy after the surface treatment.

An embodiment of the present technology is an isocyanate-based adhesive used for a surface-treated crystalline thermoplastic resin base material, the isocyanate-based adhesive having a value represented by (JIS-A hardness)/(strength at break [MPa])×(elongation at break (%))/100 of 2.0 to 70 after being cured by being allowed to stand still under a condition at 23° C. and 50% RH for 3 days, and the crystalline thermoplastic resin base material having a value represented by (δ.sup.d/δ.sup.p+δ.sup.p) of 2.0 to 30.0. δ.sup.p=γ.sup.p−γ.sup.p0 and δ.sup.d=|γ.sup.d−γ.sup.d0|, γ.sup.p0 is a polar term of surface free energy before the surface treatment, γ.sup.p is a polar term of surface free energy after the surface treatment, γ.sup.d0 is a dispersion term of the surface free energy before the surface treatment, and γ.sup.d is a dispersion term of the surface free energy after the surface treatment.