A method for reducing coefficient of friction of a laminate comprising a polyurethane adhesive is provided. The method comprises providing the polyurethane adhesive; and adhering at least two substrates with the polyurethane adhesive to form a laminate, wherein the polyurethane adhesive is formed by reacting (A) an isocyanate component comprising a prepolymer derived from the reaction of a diisocyanate, a polyethylene glycol and optionally an additional polyol; with (B) a polyol component. The method can achieve minimized COF and viscosity, while retaining other performance properties such as bond strength, heat seal strength and boil in bag resistance. A composition for preparing the adhesive, a laminate product prepared with said composition as well the method for preparing the laminate product are also provided.

Disclosed is a moisture reactive polyurethane hot melt adhesive composition that can be applied to substrates at a low coating weight even at application temperatures as low as 60 to 95° C. while retaining the advantageous high tack, green strength, cured bond strength and toughness of conventional high melting point polyurethane hot melt adhesives.

Disclosed is a moisture reactive polyurethane hot melt adhesive composition that can be applied to substrates at a low coating weight even at application temperatures as low as 60 to 95° C. while retaining the advantageous high tack, green strength, cured bond strength and toughness of conventional high melting point polyurethane hot melt adhesives.

The present invention provides a thermoplastic polyurethane (TPU) having a glass transition temperature between an ambient temperature and normal body temperature, wherein the TPU contains dicarboxyphenyl polyester structure represented by Formula 1 or 10-(2,3-dicarboxypropyl)-9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide n(DOPO-ITA) polyester structure represented by Formula 2. The present invention also provides a polyester polyol containing DOPO-ITA polyester structure represented by Formula 2, a molar percentage of the 10-(2,3-dicarboxypropyl)-9,10-dihydro-9-oxa-10-oxide polyester structure in the whole polyester polyol ranges from 30% to 70%. The present invention further provides an article thereof. ##STR00001## in Formula 1, R is C2 to C8 alkylene group or CH.sub.2CH.sub.2OCH.sub.2CH.sub.2; ##STR00002## in Formula 2, R is C2 to C8 alkylene group or CH.sub.2CH.sub.2OCH.sub.2CH.sub.2.

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.

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.

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.

The present invention relates to ether diol-derived polycarbonate diol of anhydrohexitol, a method for preparing same, polyurethane prepared from same and an adhesive comprising same and, more specifically, to polycarbonate diol, a method for preparing same, polyurethane prepared from same and an adhesive, paint and coating agent comprising same, the polycarbonate diol comprising repeating units derived from: ether diol of anhydrohexitol; carbonic diester; and random anhydrohexitol, and thus exhibiting enhanced color improving effect compared to existing polycarbonate diol and providing notably enhanced adhesion (T-peeling strength or shear strength) to polyurethane prepared by means of same.

The present invention relates to ether diol-derived polycarbonate diol of anhydrohexitol, a method for preparing same, polyurethane prepared from same and an adhesive comprising same and, more specifically, to polycarbonate diol, a method for preparing same, polyurethane prepared from same and an adhesive, paint and coating agent comprising same, the polycarbonate diol comprising repeating units derived from: ether diol of anhydrohexitol; carbonic diester; and random anhydrohexitol, and thus exhibiting enhanced color improving effect compared to existing polycarbonate diol and providing notably enhanced adhesion (T-peeling strength or shear strength) to polyurethane prepared by means of same.

A reactive PSA film that includes: (a) a polymeric film former matrix; (b) one or more reactive components; and (c) a reagent selected from an initiator, a curing agent and an activator. The component (b) is present at a mass fraction of 30%, as based on the sum of (a), (b) and (c). Further, ≥50 wt % of the polymer film former matrix is a crystallizable polymer which: (i) exhibits a crystallization enthalpy of <1 J/g in a DSC measurement on cooling at 10 K/min from at least 30K above a peak temperature of the melting peak of the matrix and ≥100° C.; and (ii) exhibits a crystallite fusion enthalpy of ≥15 mJ/mg in its pure state in a first heating curve of a DSC measurement at 10 K/min and after storage for ≥ one month from 15 to 25° C. and relative humidity from 30 to 70%.