Patent classifications
C08G18/284
OXAZOLIDINEDIONE-TERMINATED PREPOLYMER
The present invention relates to a compound obtained by a process comprising the following steps: (i) Reacting at least one isocyanate containing compound, in stoichiometric excess, with a first isocyanate-reactive compound having a number average molecular weight lower than 400, resulting in the formation of at least one prepolymer, (ii) Reacting said prepolymer, in stoichiometric excess, with a second isocyanate-reactive compound having a number average molecular weight equal to or higher than 400, resulting in the formation of a modified prepolymer, (iii) Reacting said modified prepolymer with a hydroxyl-ester compound or a hydroxyl-acid compound with the formation of hydroxyl-ester terminated prepolymer or hydroxyl-acid terminated prepolymer, and Ring-closing said hydroxyl-ester terminated prepolymer or hydroxyl-acid terminated prepolymer; (iv) Formation of said compound made of oxazolidinedione-terminated prepolymer and oxazolidinedione-terminated monomer, which is soluble in said oxazolidinedione-terminated prepolymer.
OXAZOLIDINEDIONE-TERMINATED PREPOLYMER
The present invention relates to a compound obtained by a process comprising the following steps: (i) Reacting at least one isocyanate containing compound, in stoichiometric excess, with a first isocyanate-reactive compound having a number average molecular weight lower than 400, resulting in the formation of at least one prepolymer, (ii) Reacting said prepolymer, in stoichiometric excess, with a second isocyanate-reactive compound having a number average molecular weight equal to or higher than 400, resulting in the formation of a modified prepolymer, (iii) Reacting said modified prepolymer with a hydroxyl-ester compound or a hydroxyl-acid compound with the formation of hydroxyl-ester terminated prepolymer or hydroxyl-acid terminated prepolymer, and Ring-closing said hydroxyl-ester terminated prepolymer or hydroxyl-acid terminated prepolymer; (iv) Formation of said compound made of oxazolidinedione-terminated prepolymer and oxazolidinedione-terminated monomer, which is soluble in said oxazolidinedione-terminated prepolymer.
RESIN COMPOSITION FOR ADHESIVE, ADHESIVE, AND ADHESION STRUCTURE
The present invention provides a resin composition for an adhesive, being useful as a component of an adhesive having a favorable adhesion property to glass and giving favorable appearance after adhesion. The resin composition for an adhesive contains a polyhydroxyurethane resin. This polyhydroxyurethane resin contains a structural unit formed by polymerizing a compound (A) having at least two five-membered cyclic carbonate structures and a compound (B) having at least two primary amino groups, the polyurethane resin contains a urethane bond, a hydroxy group, and a secondary amino group in the structural unit. Further, this polyhydroxyurethane resin has an amine number of 1 to 50 mgKOH/g and has a hydroxyl number of 10 to 230 mgKOH/g.
RESIN COMPOSITION FOR ADHESIVE, ADHESIVE, AND ADHESION STRUCTURE
The present invention provides a resin composition for an adhesive, being useful as a component of an adhesive having a favorable adhesion property to glass and giving favorable appearance after adhesion. The resin composition for an adhesive contains a polyhydroxyurethane resin. This polyhydroxyurethane resin contains a structural unit formed by polymerizing a compound (A) having at least two five-membered cyclic carbonate structures and a compound (B) having at least two primary amino groups, the polyurethane resin contains a urethane bond, a hydroxy group, and a secondary amino group in the structural unit. Further, this polyhydroxyurethane resin has an amine number of 1 to 50 mgKOH/g and has a hydroxyl number of 10 to 230 mgKOH/g.
REACTION PRODUCTS CONTAINING URETHANE GROUPS AND UREA GROUPS
The present invention relates to reaction products containing urethane groups and urea groups, containing at least one species of general formula (I), to a method for producing said reaction products, to the use of said reaction products as wetting agents, dispersants, dispersion stabilizers, and/or adhesion promoters, and to compositions that contain the reaction products containing urethane groups and urea groups.
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URETHANE ACRYLIC HYBRID POLYMER DISPERSION WITH ROBUST DRY/WET ADHESION AND BASECOATS PREPARED THEREFROM
This invention relates to urethane acrylic hybrid polymer dispersion with robust dry/wet adhesion and the basecoats prepared therefrom for automotive applications. In this system, the polyurethane dispersion (PUD) prepolymer is based on a combination of polyols and aliphatic diisocyanates. The acrylic portion is based on (meth)acrylated monomers. A combination of this hybrid polymer dispersion and other resins having defined glass transition temperature (T.sub.g) values, organic and/or inorganic rheology modifiers, and different additives including pigment, dispersant, and defoamer are used to prepare waterborne basecoats having modified appearance and performance. The final coatings show excellent dry/wet adhesion to the primer for automotive applications.
An Amine Functional Compound Having A Urethane Group
An amine functional compound is provided comprising: i. at least one segment consisting of at least one ether unit and at least one ester unit, wherein the ether units and ester units are connected by an ether link or an ester link, and wherein the sum of the number of ether units and ester units is at least three, and wherein the ether units and ester units are arranged in random order, and ii. at least one amine group ii. selected from a tertiary amine group, a salt of a tertiary amine group and a quaternary ammonium group, and wherein each segment i. is covalently linked to the at least one amine group ii. via a linkage comprising an urethane group and another group selected from an urethane group, an urea group, a biuret group and an allophanate group.
Polyurethane adhesive layers for electro-optic assemblies
Electro-optic assemblies and related materials (e.g., adhesive) for use therein are generally provided. The electro-optic assembly comprises a hybrid adhesive layer comprising two or more adhesive materials including a polyurethane adhesive material and a polyacrylate adhesive material. The polyurethane adhesive material includes an end-capping cyclic carbonate. In some embodiments, the adhesive layer is formed by curing the two adhesive materials under two different sets of conditions, comprising two or more curing steps.
Polyurethane adhesive layers for electro-optic assemblies
Electro-optic assemblies and related materials (e.g., adhesive) for use therein are generally provided. The electro-optic assembly comprises a hybrid adhesive layer comprising two or more adhesive materials including a polyurethane adhesive material and a polyacrylate adhesive material. The polyurethane adhesive material includes an end-capping cyclic carbonate. In some embodiments, the adhesive layer is formed by curing the two adhesive materials under two different sets of conditions, comprising two or more curing steps.
Low viscosity poly(alkynyl carbamate) polymers
An alternative polyurethane composition is provided which comprises a reaction product of an azidated polyol and a poly(alkynyl carbamate) prepolymer, wherein reaction occurs at a temperature of from 20° C. to 200° C., optionally in the presence of a Cu.sup.I-containing catalyst and wherein the poly(alkynyl carbamate) prepolymer comprises a reaction product of a polyisocyanate, an alkynol, and a glycol ether, wherein from 1 mol % to 33 mol % of isocyanate groups are reacted with glycol ether and the remaining isocyanate groups are reacted with the alkynol. The inclusion of glycol ethers into the polyisocyanate chain of the poly(alkynyl carbamate) prepolymer at a level of from 1 mol % to 33 mol %, is efficient in reducing the viscosity of the composition without compromising its performance in coatings, adhesives, sealants, films, elastomers, castings, foams, and composites made with the inventive alternative polyurethane compositions.