Renewable Bio-Based (Meth)Acrylated Monomers as Vinyl Ester Cross-Linkers

US2016222149A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016222149-A1
Application numberUS-201615130165-A
CountryUS
Kind codeA1
Filing dateApr 15, 2016
Priority dateAug 10, 2011
Publication dateAug 4, 2016
Grant date

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Abstract

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Anhydrosugar-based monomers prepared from isosorbide, isomannide, and isoidide and resin systems containing these anhydrosugar-based monomers that are partially to fully bio-based, which may produce materials having properties that meet or exceed the properties of similar petroleum derived vinyl ester resins.

First claim

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1 . A polymerizable monomer selected from the group consisting of: 2 . A polymerizable monomer as claimed in claim 1 , wherein the monomer is: 3 . A polymerizable monomer as claimed in claim 1 , wherein the monomer is: 4 .- 9 . (canceled) 10 . A polymerizable monomer as claimed in claim 1 , wherein the monomer is: 11 . A polymerizable monomer as claimed in claim 1 , wherein the monomer is: 12 - 30 . (canceled) 31 . A method for producing a polymerizable monomer comprising the step of acylating one or more hydroxyl groups of an anhydrosugar using acrylic anhydride or methacrylic anhydride and a base catalyst in an aprotic solvent, wherein the anhydrosugar is selected from the group consisting of: isosorbide, isomannide, and isoidide. 32 . The method of claim 31 , wherein the one or more hydroxyl groups of the anhydrosugar are acylated using methacrylic anhydride and the base catalyst in the aprotic solvent. 33 . A copolymer formed by curing a curable composition comprising at least one monomer selected from the group consisting of the polymerizable monomers of claim 1 using a free-radical initiator. 34 . The copolymer of claim 33 , wherein the curable composition comprises at least one vinyl ester resin monomer and/or at least one unsaturated polyester monomer. 35 . The copolymer of claim 34 , wherein the curable composition further comprises at least one reactive diluent. 36 . The copolymer of claim 34 , wherein the curable composition comprises 1-99% by weight of at least one monomer selected from the group consisting of the polymerizable monomers of claim 1 , 1 - 70 % by weight of vinyl ester resin monomer and/or unsaturated polyester monomer and 0-60% by weight of at least one reactive diluent. 37 . The copolymer of claim 34 , wherein the curable composition comprises 5-95% by weight of at least one monomer selected from the group consisting of the polymerizable monomers of claim 1 , 10 - 55 % by weight of vinyl ester resin monomer and/or unsaturated polyester monomer and 0-50% by weight of at least one reactive diluent. 38 . The copolymer of claim 35 , wherein the composition comprises 15-90% by weight of at least one monomer selected from the group consisting of the polymerizable monomers of claim 1 , 10 - 55 % by weight of vinyl ester resin monomer and/or unsaturated polyester monomer and 5-45% by weight of at least one reactive diluent. 39 . The copolymer of claim 34 , comprising a vinyl ester resin monomer selected from the group consisting of (meth)acrylated glycidyl ethers of bisphenols, (meth)acrylated ethoxylated bisphenols and novolac vinyl esters. 40 . The copolymer of claim 34 , comprising a vinyl ester monomer selected from the group consisting of: bisphenol A, hexafluorobisphenol A, bisphenol E, bisphenol F, tetramethyl bisphenol E, tetramethyl bisphenol F, bisphenol M, bisphenol C, bisphenol P and bisphenol Z. 41 . The copolymer of claim 40 , wherein the curable composition further comprises a reactive diluent selected from the group consisting of: styrene, 2-hydroxymethacrylate, methyl methacrylate, methyl acrylate, furfuryl methacrylate, methacyrlated lauric acid and methacrylated fatty acids. 42 . The copolymer of claim 41 , wherein the monomer of claim 1 is selected from a monomer of the formula 2 and a monomer of the formula 2a. 43 . The copolymer of claim 34 , wherein the curable composition comprises an unsaturated polyester monomer made from one or more of the following components: phthalic acid, terephtalic acid, m-phthalic acid, suberic acid, adipic acid, succinic acid, maleic acid, fumaric acid, butylene glycol, propylene glycol, and ethylene glycol. 44 . The copolymer of claim 43 , wherein the curable composition further comprises a reactive diluent selected from the group consisting of: styrene, 2-hydroxymethacrylate, methyl methacrylate, methyl acrylate, furfuryl methacrylate, methacyrlated lauric acid and methacrylated fatty acids. 45 . The copolymer of claim 44 , wherein the monomer of claim 1 is selected from a monomer of the formula 2 and a monomer of the formula 2a.

Assignees

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Classifications

  • and containing two or more oxygen atoms · CPC title

  • Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen (cyclic esters of polyfunctional acids C08F118/00; cyclic anhydrides of unsaturated acids C08F120/00, C08F122/00) · CPC title

  • Ortho-condensed systems · CPC title

  • Esters containing oxygen in addition to the carboxy oxygen · CPC title

  • Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen (cyclic esters of polyfunctional acids C08F218/00; cyclic anhydrides of unsaturated acids C08F220/00, C08F222/00) · CPC title

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What does patent US2016222149A1 cover?
Anhydrosugar-based monomers prepared from isosorbide, isomannide, and isoidide and resin systems containing these anhydrosugar-based monomers that are partially to fully bio-based, which may produce materials having properties that meet or exceed the properties of similar petroleum derived vinyl ester resins.
Who is the assignee on this patent?
Univ Drexel, Us Gov As Represented By The Secretary Of The Army
What technology area does this patent fall under?
Primary CPC classification C08F222/20. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Aug 04 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).