Provided are ink-receptive coating compositions including: (a) an aqueous anionic polyurethane dispersion; and (b) an aqueous solution of a nonionic polyurethane. Methods of coating substrates, and of printing, including providing and/or coating the composition onto a substrate are also provided.

A method for setting conditions for use of a polymerization catalyst includes a step of acquiring a physical property value derived from remaining functional groups after maintaining a temperature of a composition including a polymerization-reactive compound and a predetermined amount of a polymerization catalyst, a step of calculating a remaining functional group ratio from the physical property value, a step of calculating a reaction rate constant based on a reaction rate equation from the remaining functional group ratio, a step of calculating an activation energy and a frequency factor from the reaction rate constant using an Arrhenius plot, a step of determining whether or not the activation energy satisfies a predetermined condition for the polymerization catalyst, an step of setting an approximation equation from the frequency factor, and a step of setting an addition range with respect to the polymerization-reactive compound.

The present disclosure belongs to the technical field of polymer materials, and in particular relates to a chain extender and a preparation method and application thereof, a recyclable thermosetting polyurethane and a preparation method thereof. The present disclosure provides a chain extender whose chemical formula is shown in formula I. The chain extender provided by the present disclosure contains two types of dynamic covalent bonds, and the total number of dynamic covalent bonds is 4. The thermosetting polyurethane prepared by the provided chain extender has better hot-pressing repair efficiency. The results of the examples show that under the same hot-pressing conditions, the repair efficiency of the thermosetting polyurethane prepared by the 4,4′-dithiodianiline chain extender is 59%. The repair efficiency of thermosetting polyurethane is 97%, which is significantly improved.

Provided is a polycarbonate polyol used as a raw material of a polyurethane that yields a polyurethane solution having good storage stability and exhibits excellent flexibility and solvent resistance. This polycarbonate polyol is a polycarbonate diol that includes structural units represented by the following Formulae (A) and (B), wherein, R.sup.1 and R.sup.2 each independently represent an alkyl group having 1 to 4 carbon atoms and, in this range of the number of carbon atoms, optionally have an oxygen atom, a sulfur atom, a nitrogen atom, a halogen atom, or a substituent containing these atoms; and R.sup.3 represents a linear aliphatic hydrocarbon having 3 or 4 carbon atoms. This polycarbonate diol has a molecular weight of 500 to 5,000, and the value of the following Formula (I) is 0.3 to 20.0: (Content ratio of branched-chain moiety in polymer)/(Content ratio of carbonate group in polymer)×100(%) (I). ##STR00001##

A method of three-dimensional stereolithography printing a thiourethane polymer part using the vat resin. Adding a resin to a vat of a three-dimensional stereolithography printer, the resin a liquid mixture including: a first type of monomer including two or more thiol functional groups, a second type of monomer including two or more isocyanate functional groups, a photolatent base, an anionic step-growth polymerization reaction inhibitor and a light absorber. The photolatent base is decomposable upon exposure to a light to form a non-nucleophillic base catalyst having a pKa greater than 7. The anionic step-growth polymerization reaction inhibitor has an acidic group configured to form an acid-base pair with the non-nucleophillic base. The light absorber has an absorbance in the liquid mixture that is greater than an absorbance of the photolatent base at a wavelength of the light used for the exposure.

Articles are provided including at least one polyurethane prepared from: (a) about 1 equivalent of at least one polyisocyanate; (b) about 0.005 to about 0.35 equivalent of at least one polycaprolactone polyol; (c) about 0.01 to about 1.0 equivalent of at least one polyol selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 1,2-ethanediol, propanediol, butanediol, pentanediol, hexanediol, heptanediol, octanediol, nonanediol, decanediol, dodecane diol, octadecanediol, cyclopentanediol, 1,4-cyclohexanediol, cyclohexanedimethanol, 1,4-benzenedimethanol, xylene glycol, hydroxybenzyl alcohol, dihydroxytoluene, bis(2-hydroxyethyl) terephthalate, 1,4-bis(hydroxyethyl)piperazine, N,N′,bis(2-hydroxyethyl)oxamide and mixtures thereof; and (d) about 0.01 to about 0.5 equivalent of at least one polyol selected from the group consisting of glycerol, tetramethylolmethane, trimethylolethane, trimethylolpropane, erythritol, pentaerythritol, dipentaerythritol, tripentaerythritol, sorbitan, and mixtures thereof, each based upon the about 1 equivalent of the at least one polyisocyanate, wherein the article has a Gardner Impact strength of at least about 400 in-lb according to ASTM D-5420-04.

The present invention relates to an asphalt composition comprising a thermosetting reactive compound.

The present invention relates to a multi-aziridine compound having: a) at least 2 of the following structural units (A) whereby R.sub.1 is H; R.sub.2 and R.sub.4 are independently chosen from H, a linear group containing from 1 to 8 carbon atoms and optionally containing one or more heteroatoms, a branched or cyclic group containing from 3 to 8 carbon atoms and optionally containing one or more heteroatoms, phenyl, benzyl, or pyridinyl; R.sub.3 is chosen from a linear group containing from 1 to 8 carbon atoms and optionally containing one or more heteroatoms, a branched or cyclic group containing from 3 to 8 carbon atoms and optionally containing one or more heteroatoms, phenyl, benzyl, or pyridinyl; or R.sub.2 and R.sub.3 (in case R.sub.2 is different than H) may be part of the same cyclic group containing from 3 to 8 carbon atoms; R′ and R″ are independently H or an aliphatic hydrocarbon group containing from 1 to 12 carbon atoms; and b) a molecular weight of at least 600 Daltons, wherein the molecular weight is determined using MALDI-TOF mass spectrometry according to the description.

Provided herein is a method of producing a polyurethane foam. The method includes dispersing turbostratic graphene in a polymerization solution. The polymerization solution includes a first component for polymerization into a polymer. The method includes adding a second component for polymerizing with the first component to chemically convert the polymerization solution into a polyurethane foam. Provided herein is also a polyurethane foam which includes a turbostratic graphene and a polymer formed from the polymerization of a polyol with an isocyanate. Provided herein is also a turbostratic graphene dispersion which includes a turbostratic graphene and a solvent for dispersing the turbostratic graphene.

The present invention relates to a composition comprising a mixture of a first and a second hydrophobically modified alkylene oxide polymer, wherein the first hydrophobically modified alkylene oxide polymer is endcapped with at least one first hydrophobic group functionalized with a secondary amine or a salt thereof, or a tertiary amine or a salt thereof;

and wherein the second hydrophobically modified alkylene oxide polymer is endcapped with at least one second hydrophobic group, structure I:

##STR00001##

where R.sup.1, R.sup.2, m, and n are as defined herein. The present invention also relates to a method for preparing the composition. The composition of the present invention provides an associative thickener with an excellent balance of as-is viscosity and temperature stability over a wide temperature range.