Patent classifications
C09D175/12
Biobased highly functional oligomers and thermosets therefrom
The invention relates to a polyfunctional bio-based oligomer which is the reaction product of a) at least one epoxidized sucrose fatty acid ester resin; b) at least one ethylenically unsaturated acid selected from methacrylic acid, acrylic acid, crotonic acid, and mixtures thereof; c) at least one acid anhydride selected from acetic acid anhydride, acrylic acid anhydride, methacrylic acid anhydride, crotonic acid anhydride, and mixtures thereof; d) optionally, at least one catalyst; and e) optionally, at least one inhibitor. In a polyfunctional bio-based oligomer of the invention, the ratio of ethylenically unsaturated acid to acid anhydride ranges from 90:1 to 1:90; at least one epoxide group of the at least one epoxidized sucrose fatty acid ester resin is esterified by at least one ethylenically unsaturated acid; and at least one epoxide group of the at least one epoxidized sucrose fatty acid ester resin is esterified by at least one acid anhydride. Other embodiments of the invention relate to methods of making the polyfunctional bio-based oligomers of the invention and to curable coating compositions containing them.
Non-Isocyanate Polyurethane Inks for 3D Printing
In one aspect, inks for use with a 3D printer are described herein. In some embodiments, an ink described herein comprises a cyclic carbonate monomer and an amine monomer. Further, in some instances, an ink described herein also comprises an ethylenically unsaturated monomer such as a (meth)acrylate. Additionally, an ink described herein, in some cases, further comprises a colorant, such as a molecular dye, a particulate inorganic pigment, or a particulate organic colorant. An ink described herein may also comprise one or more additives selected from the group consisting of inhibitors, stabilizing agents, photoinitiators, and photosensitizers.
Non-Isocyanate Polyurethane Inks for 3D Printing
In one aspect, inks for use with a 3D printer are described herein. In some embodiments, an ink described herein comprises a cyclic carbonate monomer and an amine monomer. Further, in some instances, an ink described herein also comprises an ethylenically unsaturated monomer such as a (meth)acrylate. Additionally, an ink described herein, in some cases, further comprises a colorant, such as a molecular dye, a particulate inorganic pigment, or a particulate organic colorant. An ink described herein may also comprise one or more additives selected from the group consisting of inhibitors, stabilizing agents, photoinitiators, and photosensitizers.
POLYURETHANE UREA WATER DISPERSION, MATTE COATING MATERIAL, AND SURFACE TREATMENT AGENT
The present invention relates to a polyurethane urea water dispersion that is a reaction product of a polyol component containing a polymer polyol (A), a polysiloxane compound (S) having at least one active hydrogen-containing group, a compound (B) having at least one active hydrogen and a hydrophilic group in a molecule thereof, and a dihydric alcohol (C); a polyisocyanate (D); and a polyamine (E) having two primary amino groups and at least one secondary amino group, wherein the polyurethane urea water dispersion has an acid value of 1 to 16 mgKOH/g as expressed in terms of a solid component.
POLYURETHANE UREA WATER DISPERSION, MATTE COATING MATERIAL, AND SURFACE TREATMENT AGENT
The present invention relates to a polyurethane urea water dispersion that is a reaction product of a polyol component containing a polymer polyol (A), a polysiloxane compound (S) having at least one active hydrogen-containing group, a compound (B) having at least one active hydrogen and a hydrophilic group in a molecule thereof, and a dihydric alcohol (C); a polyisocyanate (D); and a polyamine (E) having two primary amino groups and at least one secondary amino group, wherein the polyurethane urea water dispersion has an acid value of 1 to 16 mgKOH/g as expressed in terms of a solid component.
SELF-HEALING LAMINATE COMPOSITION, RELATED ARTICLES AND RELATED METHODS
The disclosure relates to a self-healing laminate composition. The composition includes a first, self-healing layer with a self-healing polymer and a second, mechanical layer adjacent to the first layer. The second layer includes any desired polymer, for example a crosslinked polymer, a thermoplastic polymer, or a functional thermoset polymer. Self-healing polymers with dynamic covalent bonds are suitable, for example those with dynamic urea bonds and/or dynamic urethane bonds. A self-healing polymer that is damaged can undergo autonomous repair when separated surfaces re-contact each other due to the soft nature of the self-healing polymer, whereupon reversible bonds can reform to rejoin and repair the damaged self-healing polymer. When the self-healing laminate according to the disclosure is damaged, the self-healing mechanism of the first layer can cause the repair of both layers. The self-healing laminate composition can be used as a coating on any of a variety of substrates to provide self-healing properties to a surface
SELF-HEALING LAMINATE COMPOSITION, RELATED ARTICLES AND RELATED METHODS
The disclosure relates to a self-healing laminate composition. The composition includes a first, self-healing layer with a self-healing polymer and a second, mechanical layer adjacent to the first layer. The second layer includes any desired polymer, for example a crosslinked polymer, a thermoplastic polymer, or a functional thermoset polymer. Self-healing polymers with dynamic covalent bonds are suitable, for example those with dynamic urea bonds and/or dynamic urethane bonds. A self-healing polymer that is damaged can undergo autonomous repair when separated surfaces re-contact each other due to the soft nature of the self-healing polymer, whereupon reversible bonds can reform to rejoin and repair the damaged self-healing polymer. When the self-healing laminate according to the disclosure is damaged, the self-healing mechanism of the first layer can cause the repair of both layers. The self-healing laminate composition can be used as a coating on any of a variety of substrates to provide self-healing properties to a surface
Coated proppant and methods of making and use thereof
Methods for producing proppants with a fluorinated polyurethane proppant coating are provided. The methods include coating the proppant particles with a strengthening agent, a strengthening agent, and a resin to produce proppants with fluorinated polyurethane proppant coating. Additionally, a proppant comprising a proppant particle and a fluorinated polyurethane proppant coating is provided. The fluorinated polyurethane proppant coating includes a strengthening agent, a strengthening agent, and a resin. The fluorinated polyurethane proppant coating coats the proppant particle. Additionally, a method for increasing a rate of hydrocarbon production from a subsurface formation through the use of the proppants is provided.
Coated proppant and methods of making and use thereof
Methods for producing proppants with a fluorinated polyurethane proppant coating are provided. The methods include coating the proppant particles with a strengthening agent, a strengthening agent, and a resin to produce proppants with fluorinated polyurethane proppant coating. Additionally, a proppant comprising a proppant particle and a fluorinated polyurethane proppant coating is provided. The fluorinated polyurethane proppant coating includes a strengthening agent, a strengthening agent, and a resin. The fluorinated polyurethane proppant coating coats the proppant particle. Additionally, a method for increasing a rate of hydrocarbon production from a subsurface formation through the use of the proppants is provided.
Composition for production of coatings having an antimicrobial property
A curable composition, for production of coatings with an antimicrobial property, contains at least one film-forming polymer, at least one up-conversion phosphor, optionally at least one additive, and optionally at least one curing agent. The phosphor is selected from the idealized general formula (1), Lu.sub.3-a-b-nLn.sub.b(Mg.sub.1-zCa.sub.z).sub.aLi.sub.n(Al.sub.1-u-vGa.sub.uSc.sub.v).sub.5-a-2n(Si.sub.1-d-eZr.sub.dHf.sub.e).sub.a+2nO.sub.12, where a=0-1, 1≥b>0, d=0-1, e=0-1, n=0-1, z=0-1, u=0-1, v=0-1; with u+v≤1 and d+e≤1; Ln=praseodymium (Pr), gadolinium (Gd), erbium (Er), neodymium (Nd), or yttrium (Y); Lu=lutetium; and Li=lithium.