C08G18/815

METHOD FOR PRODUCING POLYURETHANE, EPOXY CARBOXYLATE COMPOSITION, POLYURETHANE, AND POLYURETHANE RESIN COMPOSITION
20210221938 · 2021-07-22 · ·

A method for producing a polyurethane according to the present invention including: a first step wherein an epoxy carboxylate compound (X) is obtained by reacting (a) an epoxy compound that includes a halogen atom content of 10 ppm by mass or less, while having only two epoxy groups and no hydroxyl group in each molecule, (b) an unsaturated aliphatic monocarboxylic acid that has an ethylenic unsaturated group in each molecule, while having no aromatic ring, and (c) an aromatic monocarboxylic acid that has no ethylenic unsaturated group in each molecule; and a second step wherein the epoxy carboxylate compound (X) obtained in the first step is reacted with a diisocyanate compound (Y).

UV-curable inkjet inks

The present disclosure is drawn to UV-curable inkjet inks, fluid sets, and printing systems. An example UV-curable inkjet ink can include water, a photo-initiator, from 8 wt % to 25 wt % organic co-solvent, and from 2 wt % to 20 wt % of a polyurethane. The polyurethane can include a polymer strand including a polymer backbone having two ends terminating at first and second capping units. The polymer backbone can be formed of polymerized monomers including a diisocyanate and a reactive diol selected from an acrylate-containing diol or a methacrylate-containing diol. The first capping unit can include an acrylate-containing monoalcohol, a methacrylate-containing monoalcohol, an allyl-containing monoalcohol, an allyl-containing monoamine, a styrene-containing monoalcohol, an acrylamide-containing monoalcohol, or a methacrylamide-containing monoalcohol reacted with an isocyanate group of the diisocyanate. The second capping unit can include 3-(cyclohexylamino)-1-propanesulfonic acid or 2-(cyclohexylamino)ethanesulfonic acid reacted with an isocyanate group of the diisocyanate.

Reactive polyurethane dispersions

The present disclosure is drawn to a reactive polyurethane dispersion including a polymer strand having a polymer backbone that has two ends terminating at a first capping unit and a second capping unit. The polymer backbone can include polymerized monomers including a reactive diol and a diisocyanate. The reactive diol can be an acrylate-containing diol, a methacrylate-containing diol, a styrene-containing diol, or combination thereof. The first capping unit can be a styrene-containing monoalcohol reacted with an isocyanate group of the diisocyanate. The second capping unit can be an ionic stabilizing group.

Reactive polyurethane dispersions

The present disclosure is drawn to reactive polyurethane dispersions. In one example, a reactive polyurethane dispersion can include a polymer strand having a polymer backbone that has two ends terminating at a first capping unit and a second capping unit. The polymer backbone can include polymerized monomers including a reactive diol and a diisocyanate. The reactive diol can be an acrylate-containing diol, a methacrylate-containing diol, an acrylamide-containing diol, a methacrylamide-containing diol, or combination thereof. The first capping unit can be an acrylamide-containing monoalcohol or methacrylamide-containing monoalcohol reacted with an isocyanate group of the diisocyanate. The second capping unit can be an ionic stabilizing group.

Reactive polyurethane dispersions

The present disclosure is drawn to a reactive polyurethane dispersion including a polymer strand having a polymer backbone that has two ends terminating at a first capping unit and a second capping unit. The polymer backbone can include polymerized monomers including a reactive diol and a blend of two or more diisocyanates. The reactive diol can be an acrylate-containing diol, a methacrylate-containing diol, or combination thereof. The first capping unit can be an acrylate-containing monoalcohol or methacrylate-containing monoalcohol reacted with an isocyanate group of the diisocyanates. The second capping unit can be an ionic stabilizing group. The polymer backbone can be devoid of ionic stabilizing groups.

Low VOC polymers with release properties
10889736 · 2021-01-12 · ·

A polymer that can be used as a release coating or a release agent in an LAB, either of which can be provided in VOC-free form and which exhibits excellent release even after aging under high humidity, includes mer that contain pendent groups that include carbamate functionalities.

Reactive polyurethane dispersions

The present disclosure is drawn to a reactive polyurethane dispersion including a polymer strand having a polymer backbone that has two ends terminating at a first capping unit and a second capping unit. The polymer backbone can include polymerized monomers including a reactive diol and a diisocyanate. The reactive diol can be an acrylate-containing diol, a methacrylate-containing diol, an allyl-containing diol, or combination thereof. The first capping unit can be an allyl-containing monoalcohol reacted with an isocyanate group of the diisocyanate. The second capping unit can be an ionic stabilizing group.

UV-CURABLE INKJET INKS

The present disclosure is drawn to UV-curable inkjet inks, fluid sets, and printing systems. An example UV-curable inkjet ink can include water, a photo-initiator, from 8 wt % to 25 wt % organic co-solvent, and from 2 wt % to 20 wt % of a polyurethane. The polyurethane can include a polymer strand including a polymer backbone having two ends terminating at first and second capping units. The polymer backbone can be formed of polymerized monomers including a diisocyanate and a reactive diol selected from an acrylate-containing diol or a methacrylate-containing diol. The first capping unit can include an acrylate-containing monoalcohol, a methacrylate-containing monoalcohol, an allyl-containing monoalcohol, an allyl-containing monoamine, a styrene-containing monoalcohol, an acrylamide-containing monoalcohol, or a methacrylamide-containing monoalcohol reacted with an isocyanate group of the diisocyanate. The second capping unit can include 3-(cyclohexylamino)-1-propanesulfonic acid or 2-(cyclohexylamino)ethanesulfonic acid reacted with an isocyanate group of the diisocyanate.

OPTICAL ADHESIVE FOR GLASS AND POLYCARBONATE
20200095487 · 2020-03-26 · ·

Disclosed are UV curable adhesive compositions and methods to adhere polycarbonate substrates containing UV absorbers to glass for use in ophthalmic lenses.

CURABLE COMPOSITION FOR USE IN A HIGH TEMPERATURE LITHOGRAPHY-BASED PHOTOPOLYMERIZATION PROCESS AND METHOD OF PRODUCING CROSSLINKED POLYMERS THEREFROM

Provided herein are curable compositions for use in a high temperature lithography-based photopolymerization process, a method of producing crosslinked polymers using said curable compositions, crosslinked polymers thus produced, and orthodontic appliances comprising the crosslinked polymers.