A fire-retardant polyurethane foam mattress and a method of manufacture thereof are provided. The mattress comprises a polyurethane foam prepared from a composition comprising at least a polyol, an organic polyisocyanate and a fire retardant and is provided with an outer layer encapsulating the polyurethane foam, the outer layer comprising a waterproof membrane of silicone rubber. A fire-resistant barrier layer is disposed substantially between the waterproof membrane and the polyurethane foam.

A reaction system for forming a polyurethane foam includes an isocyanate component that has at least one isocyanate and an isocyanate-reactive component that is a mixture formed by adding at least a polyol component, an additive component, and a preformed aqueous polymer dispersion. The mixture includes, based on the total weight of the mixture, from 50.0 wt % to 99.8 wt % of a polyol component including at least one polyether polyol, from 0.1 wt % to 50.0 wt % of an additive component including at least one catalyst, and from 0.1 wt % to 6.0 wt % of a preformed aqueous polymer dispersion. The preformed aqueous polymer dispersion has a solids content from 10 wt % to 80 wt %, based on the total weight of the preformed aqueous polymer dispersion, and is one of an aqueous acid polymer dispersion or an aqueous acid modified polyolefin polymer dispersion in which the polyolefin is derived from at least one C.sub.2 to C.sub.20 alpha-olefin.

The invention relates to a method for producing seals made of polyurethane, in which (a) aliphatic polyisocyanate, (b) compounds containing at least two isocyanate-reactive groups, (c) catalysts, (d) antioxidants and/or light stabilizers, and, optionally, (e) blowing agents, and (f) auxiliary agents and/or additives are mixed to form a reaction mixture, and the reaction mixture is allowed to complete the reaction to form polyurethane. The seal made of polyurethane has a Shore A hardness of less than 90 and a density of at least 850 g/L. The polymeric compounds having groups reactive toward isocyanate include b1) polyetherols having a functionality of 2 to 4 and a hydroxyl number of 20 to 100 mg KOH/g, b2) hydrophobic polyols having an OH number of less than 180 mg KOH/g and a functionality of greater than 2 to 3, and b3) chain extenders.

The invention relates to reaction mixtures having a high ratio of isocyanate groups to isocyanate-reactive groups, which reaction mixtures mostly cure through the formation of isocyanurate groups, and to the use of such reaction mixtures for producing semifinished materials.

The present invention discloses a 3-aryl-benzofuranone compound in which R.sub.1-R.sub.6, in the formula are mutually independent H or C.sub.1-C.sub.20 alkyls, and R.sub.7 is C.sub.7-C.sub.20 alkyl or C.sub.7-C.sub.20 mixed alkyl. The present invention also discloses a composition of 3-aryl-benzofuranone compound and the preparation method. The 3-aryl-benzofuranone compound and the composition thereof has the superiority in application due to the characteristics of less proneness to volatilize, less proneness to be extracted, higher resistance to migration and less proneness to bloom and precipitate on the surface of organic materials, and with a wide range of application, it is effective during the application.

A rigid polyurethane foam which is a polymerization product of a composition including a concentrated acid hydrolytic lignin, a polyol, and an isocyanate, and a method of preparing the rigid polyurethane foam.

Disclosed is an adhesive system and method of use thereof wherein the adhesive composition comprises a moisture curable adhesive comprised of an isocyanate terminated prepolymer and a cure accelerator having two curatives components having different cure kinetics. The cure accelerator is comprised of an isocyanate reactive compound comprising a primary, secondary or tertiary amino group, or a primary thiol group having faster curing kinetics resulting an increase in bead stability within the first minutes and a polyol selected from a diol and/or triol with slower curing kinetics allowing for sufficient open time and yet a fast strength build up. The preferred method of application of the adhesive system is via a 1K application gun.

Described herein is a process for producing polyurethane foams having a density of 30 g/dm.sup.3 to 70 g/dm.sup.3, in which (a) aromatic polyisocyanate is mixed with (b) polymeric compounds having isocyanate-reactive groups, (c) optionally chain extender and/or crosslinking agent, (d) catalyst, (e) blowing agent including water, (f) 0.1% to 5% by weight of lactam, and (g) optionally additives, at an isocyanate index of 50 to 95 to form a reaction mixture, and the reaction mixture is converted to the polyurethane foam, wherein the catalyst includes metal catalyst and amine catalyst, and the amine catalyst has tertiary nitrogen atoms and the content of tertiary nitrogen atoms in the amine catalyst is from 0.0001 to 0.003 mol/100 g of foam. Also described herein is a polyurethane foam and a method of using such a flexible polyurethane foam for the production of cushions, seat cushions, or mattresses.

The present invention relates to a process for producing a polyurethane elastomer, a polyurethane elastomer produced by the process, and the use of the polyurethane elastomer in a glass encapsulation/elastic gasket or the like. The process mainly includes adding a hindered amine light stabilizer to the isocyanate-containing component A. Its reaction with the organotin catalyst in the isocyanate reactive component (i.e. component B), which may cause a loss of the catalytic performance of the catalyst, is avoided. The curing speed of the polyurethane elastomer is increased, thereby the production efficiency is improved and costs are reduced.

A composition and a material prepared from the composition are provided. The composition includes 50-99 parts by weight of a polyether polyol and 1-50 parts by weight of a compound having a structure represented by Formula (I)

##STR00001##

wherein R.sup.1 is C.sub.1-6 independent alkylene group; R.sup.2 is

##STR00002##

R.sup.3 is independently C.sub.1-6 alkylene group; i≥1; j≥0; k=0, 1, or 2; R.sup.4 is C.sub.1-24 alkyl group when k=1, or 2, or R.sup.4 is C.sub.6-24 alkyl group when k is 0; and B is independently

##STR00003##