Polymer particle, polymer dispersion, method for producing said polymer dispersion, coating material produced from said polymer dispersion, and coated article
US-2015376390-A1 · Dec 31, 2015 · US
US9976047B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9976047-B2 |
| Application number | US-201414900418-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 24, 2014 |
| Priority date | Jun 25, 2013 |
| Publication date | May 22, 2018 |
| Grant date | May 22, 2018 |
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Plastisol compositions having a two-resin interpenetrating polymer network (IPN) are disclosed. The compositions begin with blocked isocyanate grafted acrylic polymer, blocked isocyanate urethane prepolymer, plasticizer, optionally pigment, and optionally thixotropic agent. When subjected to a thermal cure, the isocyanate groups on the acrylic polymer and urethane prepolymer both become unblocked and both react with the crosslinking agent to form an interpenetrating acrylic-polyurethane network. The two-resin IPN offers improved storage stability, hand-feel characteristics, and processing properties for textile printing among other uses. Preferably these plastisol compositions are essentially free of polyvinyl halides and phthalates restricted for regulatory reasons.
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What is claimed is: 1. A plastisol composition, comprising: (a) acrylic polymer; (b) urethane prepolymer; (c) plasticizer; (d) crosslinking agent; (e) optionally a thixotropic agent; and (f) optionally a pigment; wherein the crosslinking agent is multifunctional, and wherein the acrylic polymer and urethane prepolymer contain blocked isocyanate groups that become unblocked when subjected to heat and react with the crosslinking agent to form an interpenetrating acrylic-polyurethane network. 2. The plastisol composition of claim 1 , wherein the acrylic polymer is a core-shell acrylic polymer. 3. The plastisol composition of claim 2 , wherein the core-shell acrylic polymer has a glass transition temperature of between about 65° C. to about 125° C. 4. The plastisol composition of claim 1 , wherein the isocyanate content of the acrylic polymer is about 0.02% to about 10.0% by weight. 5. The plastisol composition of claim 1 , wherein the crosslinking agent is a latent amine curative. 6. The plastisol composition of claim 1 , wherein the blocked isocyanate groups of the acrylic polymer and the urethane prepolymer become unblocked when subjected to a thermal cure at temperatures of about 130° C. to about 170° C. 7. The plastisol composition of claim 1 , wherein the composition is essentially free of polyvinyl halides and restricted phthalates. 8. The plastisol composition of claim 1 , wherein the plasticizer is selected from the group consisting of dioctyl terephthalate, benzoate esters, polyadipates, citrates, alkylsulfonic acid phenyl esters, esters of 1,2-cyclohexane dicarboxylic acid, and combinations thereof. 9. The plastisol composition of claim 1 , wherein the thixotropic agent contains at least one of the following: castor oil derivative, high molecular weight polyolefin, attapulgite, montmorillonite clay, organo-clay, fumed silica, fibrated mineral, calcium sulphonate derivative, polyamide resin, polyester amide, alkyds, or oil-modified alkyd. 10. The plastisol composition of claim 1 , wherein the additional additives are selected from the group consisting of lubricants, dispersants, fillers, optical brighteners, puff matting agents, antioxidants, chemical and physical blowing agents, stabilizers, moisture scavengers, air release agents, oxidizers, reducers, surfactants, processing aids, and combinations thereof. 11. The plastisol composition of claim 1 , wherein the composition in weight percent comprises: (a) the acrylic polymer in the range of 10 to 50%; (b) the urethane prepolymer in the range of 10 to 50%; (c) the plasticizer in the range of 50 to 75%; (d) the crosslinking agent in the range 0.5 to 5%; (e) the pigment in the range of 0 to 40%; (f) the thixotropic agent in the range of 0 to 10%; and (g) an additive in the range of 0 to 40%. 12. The plastisol composition of claim 1 , wherein the ratio of the acrylic polymer resin and the urethane prepolymer to the plasticizer is in the range from about 2:1 to about 1:3. 13. The plastisol composition of claim 1 , wherein the ratio of the acrylic polymer resin to the urethane prepolymer is in the range from about 1:1 to about 4:1. 14. A method of making the plastisol composition of claim 1 , comprising the steps of: (a) blending, into a mixture, blocked isocyanate grafted acrylic polymer, plasticizer, and optionally the pigment together using a rotary mixer with jacketed cooling tub until the mixture is homogeneous; (b) de-agglomerating the mixture using a 3-roll mill, for a sufficient duration to ensure a Hegman fineness of grind value ≥4; and (c) adding crosslinking agent wherein the urethane prepolymer with blocked isocyanate functional groups is added during step (a) or step (c); and wherein optionally the thixotropic agent is added during any of the above steps to achieve the desired viscosity target. 15. The method of claim 14 , wherein the plastisol composition is cured by (d) heating the plastisol composition to unblock the isocyanate groups on the acrylic polymer and the urethane prepolymer so that the isocyanate groups will react with the crosslinking agent to form an interpenetrating acrylic-polyurethane network. 16. The method of claim 15 , wherein the plastisol composition is heated in step (d) at temperatures of about 130° C. to about 170° C. for at least about 0.5 minutes. 17. A printed textile article comprising a textile article having an image graphic printed thereon from the plastisol composition of claim 1 . 18. The printed textile article according to claim 17 , wherein the textile article is a garment and wherein the image graphic from the plastisol composition is applied by a screen-printing technique. 19. A coated article, comprising a substrate wherein the coating consists of the plastisol composition of claim 1 . 20. The coated article of claim 19 wherein the coating of the article has been applied by spin casting, slush molding, rotational molding, spray coating, or dip coating.
Processes for mixing polymers · CPC title
Polyurethanes · CPC title
esters · CPC title
containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds · CPC title
with carboxylic acids or derivatives thereof · CPC title
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