Patent classifications
C08G18/6245
HIGH CREEP RECOVERY, LOW MODULUS POLYMER SYSTEMS AND METHODS OF MAKING THEM
Disclosed herein are methods of making an adhesive composition, the methods comprising providing a polyurethane acrylate and combining with a vinyl ether and co-curing the combination to form an adhesive composition, wherein after curing the adhesive composition has a modulus at −20° C. of less than about 10.0 mPa and a creep recovery of greater than about 50%. Also disclosed are the resulting adhesive compositions.
GRAFT POLYURETHANE COPOLYMER DISPERSIONS
A graft polyurethane copolymer dispersion can include dispersed polyurethane particles including a graft polyurethane copolymer. The graft polyurethane copolymer in this example includes a polyurethane backbone, a graft side-chain polymer attached to the polyurethane backbone, sulfonic acid groups, and isocyanate-generated amines. The graft side-chain polymer can include a poly(meth)acrylic moieties with C1 to C12 alkyl pendant groups, polyalkylene oxide pendant groups, or a combination thereof.
Formaldehyde free adhesive composition
A formaldehyde free adhesive composition and a plywood obtained from the adhesive composition is provided, and the plywood has a balanced performance, such as high adhesion strength, sufficient pot-life, and good workability.
Hot melt adhesive and method of forming the same
A hot melt adhesive (HMA), which is solid at room temperature, comprises the reaction product of 5 to 25% by weight of an isocyanate component having an NCO content of from about 20 to about 50% by weight, 75 to 85% by weight of a polyester, and 1 to 10% by weight of a hydroxy-polymer having an OH number of from about 40 to about 50. A method of forming the adhesive comprises the step of combining the isocyanate component, polyester, and hydroxy-polymer to form the adhesive. The adhesive can be used for various purposes, such as for forming an adhesive layer which adhesively couples surfaces together.
Polyurethane polymers cured via azido-alkyne cycloaddition at ambient or mild curing conditions
An alternative polyurethane composition is provided which comprises a reaction product of an azidated polyol and a poly(alkynyl carbamate) prepolymer reacted at a temperature of from 20° C. to 120° C., wherein the poly(alkynyl carbamate) prepolymer comprises a reaction product of a polyisocyanate and a stoichiometric equivalent of an alkynol of the formula (I),
HC≡C—R.sup.1R.sup.2—OH (I),
and wherein R.sup.1 is an electron-withdrawing group selected from the group consisting of carbonyl, ester, amide, and urethane and R.sup.2 is a linear or branched alkyl chain having from 1 to 15 carbon atoms. The inventive alternative polyurethane composition position may be used to provide adhesives, sealants, films, elastomers, castings, foams, and composites.
FORMALDEHYDE FREE ADHESIVE COMPOSITION
A formaldehyde free adhesive composition and a plywood obtained from the adhesive composition is provided, and the plywood has a balanced performance, such as high adhesion strength, sufficient pot-life, and good workability.
ADHESIVE COMPOSITION, ADHESIVE FILM, ADHESIVE OPTICAL FILTER AND DISPLAY DEVICE
The present application relates to an adhesive composition, an adhesive film, an adhesive optical filter and a display device.
Inkjet ink(s)
Inkjet inks are described herein. In an example, an inkjet ink can comprise: at least one colorant; at least one solvent comprising glycerol in an amount of from about 1 wt % to about 20 wt % based on the total weight of the inkjet ink; water; and at least one binder, wherein the binder comprises a polyurethane-based binder dispersion.
Inkjet inks
Yellow inkjet inks are disclosed. In an example, an inkjet ink composition comprises: at least one colorant comprising at least one yellow pigment; at least one solvent comprising at least one triol; water; and at least one binder. The binder comprises a polyurethane-based binder dispersion, which comprises water and a polyurethane. The polyurethane comprises: (A) a polyisocyanate, (B) a first polyol having a chain with two hydroxyl functional groups at one end of the chain and no hydroxyl groups at an opposed end of the chain, (C) a second polyol having a chain with two hydroxyl functional groups at both ends of the chain, (D) a carboxylic acid functional group with two hydroxyl functional groups, and (E) a sulfonate or sulfonic acid functional group having two amino functional groups.
POLYURETHANE POLYMERS CURED VIA AZIDO-ALKYNE CYCLOADDITION AT AMBIENT OR MILD CURING CONDITIONS
An alternative polyurethane composition is provided which comprises a reaction product of an azidated polyol and a poly(alkynyl carbamate) prepolymer reacted at a temperature of from 20° C. to 120° C., wherein the poly(alkynyl carbamate) prepolymer comprises a reaction product of a polyisocyanate and a stoichiometric equivalent of an alkynol of the formula (I),
HC≡C—R.sup.1R.sup.2—OH (I),
and wherein R.sup.1 is an electron-withdrawing group selected from the group consisting of carbonyl, ester, amide, and urethane and R.sup.2 is a linear or branched alkyl chain having from 1 to 15 carbon atoms. The inventive alternative polyurethane composition position may be used to provide adhesives, sealants, films, elastomers, castings, foams, and composites.