C08G18/325

SELF-HEALING, SELF-CLEANING OMNIPHOBIC COMPOSITION, RELATED ARTICLES AND RELATED METHODS
20220041787 · 2022-02-10 ·

The disclosure relates to a self-healing omniphobic composition including a self-healing omniphobic polymer with a crosslinked backbone. The crosslinked backbone includes a reaction product between a polyisocyanate, a functionalized omniphobic polymer reactive therewith, a reversible polyfunctional linker including a hindered secondary amino group and/or an aromatic hydroxy group, and one or more polymeric backbone components. The crosslinked backbone includes reversible urea or reversible urethane bonds between the reversible polyfunctional linker and the polyisocyanate, which in turn provide self-healing properties to the omni-phobic composition. The self-healing omniphobic composition has favorable omniphobic properties, for example as characterized by water and/or oil contact and/or sliding angles. The omniphobic composition can be used as a coating on any of a variety of substrates to provide self-healing omniphobic properties to a surface of the substrate. Such self-healing omniphobic coatings can be scratch resistant, ink/paint resistant, and optically clear.

Self-healing, self-cleaning omniphobic composition, related articles and related methods

The disclosure relates to a self-healing omniphobic composition including a self-healing omniphobic polymer with a crosslinked backbone. The crosslinked backbone includes a reaction product between a polyisocyanate, a functionalized omniphobic polymer reactive therewith, a reversible polyfunctional linker including a hindered secondary amino group and/or an aromatic hydroxy group, and one or more polymeric backbone components. The crosslinked backbone includes reversible urea or reversible urethane bonds between the reversible polyfunctional linker and the polyisocyanate, which in turn provide self-healing properties to the omni-phobic composition. The self-healing omniphobic composition has favorable omniphobic properties, for example as characterized by water and/or oil contact and/or sliding angles. The omniphobic composition can be used as a coating on any of a variety of substrates to provide self-healing omniphobic properties to a surface of the substrate. Such self-healing omniphobic coatings can be scratch resistant, ink/paint resistant, and optically clear.

Self-healing, self-cleaning omniphobic composition, related articles and related methods

The disclosure relates to a self-healing omniphobic composition including a self-healing omniphobic polymer with a crosslinked backbone. The crosslinked backbone includes a reaction product between a polyisocyanate, a functionalized omniphobic polymer reactive therewith, a reversible polyfunctional linker including a hindered secondary amino group and/or an aromatic hydroxy group, and one or more polymeric backbone components. The crosslinked backbone includes reversible urea or reversible urethane bonds between the reversible polyfunctional linker and the polyisocyanate, which in turn provide self-healing properties to the omni-phobic composition. The self-healing omniphobic composition has favorable omniphobic properties, for example as characterized by water and/or oil contact and/or sliding angles. The omniphobic composition can be used as a coating on any of a variety of substrates to provide self-healing omniphobic properties to a surface of the substrate. Such self-healing omniphobic coatings can be scratch resistant, ink/paint resistant, and optically clear.

CURABLE RESIN COMPOSITION

Disclosed is a structural material-bonding adhesive capable of bonding materials other than iron, and maintaining the bonding ability in an environment at a high temperature and a low temperature, while maintaining performance similar to that of a structural material adhesive used as an adhesive for bonding iron materials. A curable resin composition contains an epoxy resin, blocked urethane, and an amine-based latent curing agent, wherein the blocked urethane is obtained by reacting a urethane polymer having a terminal isocyanate group with a blocking agent, the urethane polymer being obtained by reacting a polyisocyanate, a diol, and a branching agent containing at least three groups that react with an isocyanate group.

Aqueous Polyurethane Dispersions for Artificial Leather Applications
20210371698 · 2021-12-02 ·

Aqueous polyurethane dispersions are useful for making artificial leather and similar products. The dispersions contain polyurethane-urea particles dispersed in an aqueous phase. The particles are made using isophorone diisocyanate, certain cyclic amine chain extenders and certain polyol mixtures.

SOLVENT-FREE MATT POLYUREA COATING AND KIT OF PARTS FOR PRODUCING THE COATING
20220177725 · 2022-06-09 ·

The present application relates to a solvent-free matt polyurea coating which is obtained by carrying out a reaction through reacting at least following components: a) a polyisocyanate prepolymer; b) a polyether amine; c) a main chain extender, wherein the coating further comprises ground carbon fibers as a matting agent. The carbon fibers have an average fiber length greater than or equal to 50 μm and less than or equal to 150 μm, a weight fraction greater than or equal to 4.5% and less than or equal to 25%. The present application also relates to a kit of parts for producing a solvent-free matt polyurea coating.

THERMOPLASTIC POLY(URETHANE-UREA) POLYADDUCTS
20230272148 · 2023-08-31 ·

A thermoplastic poly(urethane-urea) polyadduct with sterically hindered urea groups of the following Formula (I):


—[I-M-(I—C.sub.1).sub.a—(I-M).sub.b-(I—C.sub.2).sub.c].sub.n-  (I)

I, M, C.sub.1 and C.sub.2 each representing bivalent residues linked to each other via a urethane or urea moiety. In the residues I, C.sub.1 and C.sub.2, when more than four carbon atoms are present, optionally at least one of them is substituted by a heteroatom selected from oxygen and nitrogen. Optionally at least one of the residues I, M, C.sub.1 and C.sub.2 includes one or more ester moieties. a, b and c each independently represent an integer from 0 to 10, and n is a number ≥3 representing the number of blocks in the polyadduct. Within each separate block a+c≥1, and in all blocks together at least one a≥1 and at least one c≥1.

Aqueous coating composition with soft touch upon drying

Aqueous coating compositions include dispersed polyurethane-vinyl polymer hybrid particles obtained by free-radical polymerization of at least one vinyl monomer in the presence of a polyurethane. The polyurethane and the vinyl polymer in the hybrid particles are present in a weight ratio of polyurethane to vinyl polymer ranging from 1:1 to 20:1, and the polyurethane is the reaction product of at least the following components: (a) from 5 to 40 wt. % of at least one organic difunctional isocyanate, (b) from 0.5 to 4 wt. % of an isocyanate-reactive compound containing ionic or potentially ionic water-dispersing groups having a molecular weight of from 100 to 500 g/mol, (c) from 40 to 80 wt. % of at least one diol having a molecular weight from 500 to 5000, (d) from 0 to 10 wt. % of at least one active-hydrogen chain extending compound with a functionality of at least 2 other than water, (e) from 0 to 10 wt. % of at least one diol having a molecular weight below 500 g/mol. The isocyanate and hydroxy groups on the components used are present in a respective mole ratio (NCO to OH) in the range of from 0.8:1 to 5:1.

Aqueous coating composition with soft touch upon drying

Aqueous coating compositions include dispersed polyurethane-vinyl polymer hybrid particles obtained by free-radical polymerization of at least one vinyl monomer in the presence of a polyurethane. The polyurethane and the vinyl polymer in the hybrid particles are present in a weight ratio of polyurethane to vinyl polymer ranging from 1:1 to 20:1, and the polyurethane is the reaction product of at least the following components: (a) from 5 to 40 wt. % of at least one organic difunctional isocyanate, (b) from 0.5 to 4 wt. % of an isocyanate-reactive compound containing ionic or potentially ionic water-dispersing groups having a molecular weight of from 100 to 500 g/mol, (c) from 40 to 80 wt. % of at least one diol having a molecular weight from 500 to 5000, (d) from 0 to 10 wt. % of at least one active-hydrogen chain extending compound with a functionality of at least 2 other than water, (e) from 0 to 10 wt. % of at least one diol having a molecular weight below 500 g/mol. The isocyanate and hydroxy groups on the components used are present in a respective mole ratio (NCO to OH) in the range of from 0.8:1 to 5:1.

BINDERS CONTAINING SECONDARY AMINE GROUPS, BASED ON CYCLIC ETHERS

The present invention relates to a process for producing polyaspartic ester compositions by reacting cyclic ethers bearing primary amino and/or primary aminoalkyl groups with fumaric and/or maleic esters, to the polyaspartic ester compositions thus obtainable, and to the use thereof in two-component coating compositions.