C08G18/8166

SKIN CONTACT ADHESIVE AND METHODS FOR ITS PREPARATION AND USE

A crosslinkable composition is useful for preparing a skin contact adhesive or a coating on a substrate. The crosslinkable composition includes (A) a polyurethane-polyorganosiloxane copolymer and (B) a curing catalyst. The skin contact adhesive prepared by crosslinking the crosslinkable composition is useful in applications such as adhesives for medical tapes, adhesives for wound dressings, adhesives for prosthetics, ostomy appliance adhesives, adhesives for medical monitoring appliances, adhesives for scar therapy treatments, adhesives for cosmetic patches, and transdermal drug delivery systems.

NETWORK POLYMERS AND METHODS OF MAKING AND USING SAME

The present invention relates to covalent adaptable networks (CANs) having exchangeable crosslinks that are able to undergo repeated covalent bond reshuffling through photo-activation at ambient temperatures. The invention provides covalent adaptable network forming compositions as well as methods of forming, remolding and recycling the CANs of the invention.

POLYURETHANE-POLYORGANOSILOXANE COPOLYMER AND METHOD FOR ITS PREPARATION
20210230423 · 2021-07-29 ·

A polyurethane—polyorganosiloxane copolymer and methods for its preparation are disclosed. The copolymer has polyfunctional end groups, which render it crosslinkable by multiple crosslinking reactions.

PERSONAL CARE COMPOSITIONS INCLUDING A POLYURETHANE - POLYORGANOSILOXANE COPOLYMER
20210177726 · 2021-06-17 ·

A polyurethane-polyorganosiloxane copolymer is useful as a film forming agent in personal care compositions, such as hair care compositions and skin care compositions.

Silicone urethane urea copolymer and preparation and use thereof
11041042 · 2021-06-22 · ·

A silicone urethane urea copolymer and methods for preparation and use of the copolymer are disclosed. The copolymer is crosslinkable. The copolymer is useful in various applications, including personal care compositions, such as hair care compositions and skin care compositions and in health care compositions such as skin contact adhesive compositions and transdermal drug delivery systems.

Liquid crystal aligning agent containing crosslinking agent and polymer that has site having isocyanate group and/or blocked isocyanate group and site having photoreactivity, liquid crystal alignment film, and liquid crystal display element

Provided is a liquid crystal display element that can be baked at a low temperature when forming a liquid crystal alignment film capable of imparting an alignment regulating property and a pretilt angle developing property via a photoalignment method. Further provided is a liquid crystal display element in which the liquid crystal pretilt angles are highly stable, and display burn-in hardly occurs even due to long usage. Further provided are a vertical liquid crystal alignment film to be used in the liquid crystal display element, and a liquid crystal aligning agent with which it is possible to provide the vertical liquid crystal alignment film. A liquid crystal aligning agent of the present invention contains: component (A), which is a polymer including (A-1) a site having an isocyanate group and/or a blocked isocyanate group and (A-2) a site having photoreactivity; component (B), which is a compound having, in a molecule, at least two functional groups of at least one type selected from the group consisting of an amino group and a hydroxyl group; and an organic solvent.

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.

NOVEL OLIGOMER OR POLYMER AND COMPOSITION COMPRISING THE SAME
20210070919 · 2021-03-11 ·

Disclosed is an oligomer or polymer obtained by reacting at least one monomeric, oligomeric or polymeric isocyanate having two or more isocyanate groups with 2-hydroxy-3-butenoic acid and/or at least one alkyl ester of 2-hydroxy-3-butenoic acid. A composition comprising a said oligomer or polymer is also disclosed.

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 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.