C08G18/485

PROCESSES FOR MAKING MOLDED FLEXIBLE FOAMS AND FLEXIBLE FOAMS PRODUCED THEREBY
20220235168 · 2022-07-28 ·

A process for making a molded flexible foam. The processes includes: (a) depositing a foam-forming reaction mixture onto a surface of a mold cavity, and (b) allowing the foam-forming reaction mixture to react in the mold cavity. The foam-forming reaction mixture includes: (1) a polyisocyanate present in an amount of less than 45% by weight, based on the total weight of the reaction mixture; (2) an isocyanate-reactive composition; (3) a blowing agent; and (4) a catalyst. The isocyanate-reactive composition includes: (i) at least 50% by weight, based on the total weight of polyol in the isocyanate-reactive composition, of a polyether polyol having a functionality of greater than 2, an oxyethylene content of 0 to 50% by weight, based on the total weight of the polyether polyol, more than 50 mol % of primary OH groups and an OH number of 8 to 112 mg KOH/g; and (ii) a component comprising: (A) an amine-initiated polyether polyol (II), wherein amine-initiated polyether polyol (II) has an OH number of at least 500 mg KOH/g and a functionality of 2.5 to 4, and wherein amine-initiated polyether polyol (II) is present in an amount of greater than 0 and no more than 10% by weight, based on the total weight of polyol in the isocyanate-reactive composition; (B) a CO.sub.2-producing carbamic acid which is present in an amount of greater than 0 and no more than 10% by weight, based on the total weight of polyol in the isocyanate-reactive composition; or (C) both (A) and (B).

PROCESSES FOR MAKING MOLDED FLEXIBLE FOAMS AND FLEXIBLE FOAMS PRODUCED THEREBY
20220234262 · 2022-07-28 ·

Processes for making a molded flexible foam. The processes include: (a) depositing a foam-forming reaction mixture onto a surface of a mold cavity, and (b) allowing the foam-forming reaction mixture to react in the mold cavity. The foam-forming reaction mixture comprises: (1) a polyisocyanate present in an amount of less than 45% by weight, based on the total weight of the foam-forming reaction mixture; (2) an isocyanate-reactive composition comprising at least 50% by weight, based on the total weight of polyol in the isocyanate-reactive composition, of a polyether polyol having a functionality of greater than 2, an oxyethylene content of 0 to 50% by weight, based on the total weight of the polyether polyol, more than 50 mol % of primary OH groups, and an OH number of 8 to 112 mg KOH/g; (3) a blowing agent comprising water present in an amount of at least 0.5% by weight, based on the total weight of the foam-forming reaction mixture; and (4) a tin-free metallic catalyst composition comprising a bismuth-based catalyst and a zinc-based catalyst.

ACCELERATE CURE POLYURETHANE ADHESIVE COMPOSITION

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.

COATING OF WIRES WITH CATALYTICALLY CROSSLINKED BLOCKED POLYISOCYANATES
20210388153 · 2021-12-16 ·

The present invention relates to the coating of wires with coatings which are obtained by crosslinking blocked polyisocyanates. The coatings are characterized in that they are substantially free of urethane groups and the crosslinking of the monomers is predominantly effected by isocyanurate groups.

BROMINATED FLAME RETARDANTS AND POLYURETHANES CONTAINING THE SAME

The disclosure includes brominated alkenyl alcohols, their use as a flame retardant in polyurethane and polyurethane foams, and polyurethanes containing the brominated alkenyl alcohols. Compositions, methods, and processes are disclosed. The brominated alkenyl alcohols used as flame retardants in polyurethanes can be generally described by Formula (I), the scope of which is disclosed herein.

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Water-resistive coating composition

A weather-resistive coating composition comprises from 21 to 25 weight percent of aromatic isocyanate with a functionality of at least 2.0, from 28 to 32 weight percent of polyol, from 4 to 8 weight percent of a diol having a molecular weight in the range of from 80 to 200, from 38 to 42 weight percent of filler having a particle size of no greater than 400 micrometers, and from 0.01 to 0.03 weight percent of a catalyst, wherein the coating composition has a water vapor permeability of at least 16 grains per m.sup.2 per 1 hour per 3.4 kPa of mercury, and the coating composition is a component of a building wall or roofing structure.

POLYCARBODIIMIDE COMPOSITION, PRODUCING METHOD OF POLYCARBODIIMIDE COMPOSITION, AQUEOUS DISPERSION COMPOSITION, SOLUTION COMPOSITION, RESIN COMPOSITION, RESIN CURED PRODUCT, AND CARBODIIMIDE CROSS-LINKING AGENT FOR FIBER TREATMENT

A polycarbodiimide composition is obtained by subjecting a reaction product of a straight-chain aliphatic diisocyanate and alcohols to carbodiimidization, and the alcohols include a polyol and a monool; in the alcohols, a mole ratio (hydroxyl group derived from polyol/hydroxyl group derived from monool) of the amount of hydroxyl groups derived from the polyol to the amount of hydroxyl groups derived from the monool is below 2.0; and a carbodiimide equivalent of the polycarbodiimide composition is 300 g/mol or more and below 550 g/mol.

Polyol component and use thereof for the production of rigid polyurethane foams
20220204715 · 2022-06-30 · ·

A polyol component P) contains at least two different polyether polyols A) and C), and at least one polyether ester polyol D). A process can be used for producing rigid polyurethane foams using the polyol component P), and the rigid polyurethane foams produced therefrom are useful.

Adhesive Selection Method, Adhesion Complex, and Production Method for Adhesion Complex
20220207213 · 2022-06-30 ·

In an adhesive selection method, test data is acquired by subjecting an adhesion complex, obtained by integrally bonding one material and an other material that are heterogeneous using an adhesive, to a shear test, in which a tensile shear load is applied to the adhesion complex in a direction that causes shear deformation in the adhesive, until adhesive failure takes place. Based on the test data, a plurality of two- or three-dimensional FEM analysis models of the adhesion complex with varied adhesives are constructed. On each of the analysis models, a simulation is performed in which a tensile shear load is applied. Based on the stresses and locations of the stresses generated in each of the analysis models in the course of the, the adhesive for binding one member made of the one material and the other member made of the other material is selected from among the adhesives.

Polymer suitable as a thickener

The invention relates to polymer comprising structural units according to formula (I), R.sup.1—X—(C═O)—NH—R.sup.2—NH—(C═O)—O—POA-R.sup.3—(O—POA-R.sup.4).sub.n wherein R.sup.1 represents an organic group terminated by a hydrocarbyl group having 6 to 50 carbon atoms, X represents O or N—R.sup.5, wherein R.sup.5 represents a hydrogen atom or a hydrocarbyl group having 1 to 30 carbon atoms, R.sup.2 represents a hydrocarbyl group comprising an aromatic group and having 6 to 40 carbon atoms, POA represents a polyoxyalkylene group, R.sup.3 represents an organic group having 2 to 40 carbon atoms, n is an integer from 1 to 6, R.sup.4 is independently selected from —(C═O)—NH—R.sup.2—NH—(C═O)—NH—R.sup.1, —R.sup.6, wherein R.sup.6 represents a hydrogen atom or an aliphatic or aromatic group having 1 to 24 carbon atoms, and wherein the polymer has an average of at least 1.8 end groups R.sup.1 per molecule, a number average molecular weight in the range of 2000 to 100000 Daltons, and a polydispersity in the range of 1.0 to 5.0, wherein the quotient of the polydispersity divided by (n+1) is less than 1.0.