Treated porous material
US-2017355097-A1 · Dec 14, 2017 · US
US10471625B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10471625-B2 |
| Application number | US-201515537246-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 30, 2015 |
| Priority date | Dec 23, 2014 |
| Publication date | Nov 12, 2019 |
| Grant date | Nov 12, 2019 |
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A treated cellulosic material comprising a cellulosic material having a porous structure defining a plurality of pores, at least a portion of the pores containing a treating agent comprising a thermoset comprising a cured epoxy resin. The present disclosure further describes a method for preparing a treated cellulosic material comprising (a) providing a cellulosic material; and (b) a first treatment protocol comprising impregnating the cellulosic material with an aqueous dispersion, the aqueous dispersion comprising an epoxy resin and an emulsifying agent.
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What is claimed is: 1. A method for preparing a treated cellulosic material comprising: (a) providing a cellulosic material; (b) a first treatment protocol comprising impregnating the cellulosic material with an aqueous dispersion, the aqueous dispersion comprising an epoxy resin and an emulsifying agent; and (c) a second treatment protocol comprising impregnating the cellulosic material with a modifying agent, the modifying agent comprising a curing agent and/or a catalyst suitable for curing the epoxy resin. 2. The method of claim 1 , wherein the impregnation of the first treatment protocol is conducted under a pressure that is greater than or lower than ambient. 3. The method of claim 1 , wherein the epoxy resin comprises, an aromatic or aliphatic glycidyl ether, a cycloaliphatic epoxy resin, a bisphenol F epoxy resin, a novolac epoxy resin, a glycidylamine-based epoxy resin, an alicyclic epoxy resin, a linear aliphatic epoxy resin, a tetrabromobisphenol A epoxy resin, polyglycidyl ethers of polyhydric alcohols, polyglycidyl ethers of polyhydric phenols, polyglycidyl amides, polyglycidyl imides, polyglycidyl hydantoins, polyglycidyl thioethers, epoxidized fatty acids, epoxidized drying oils, epoxidized polyolefins, epoxidized di-unsaturated acid esters, epoxidized unsaturated polyesters, a bisphenol A diglycidyl ether, a bisphenol F diglycidyl ether, a resorcinol diglycidyl ether, triglycidyl ethers of para-aminophenols, reaction products of epichlorohydrin with o-cresol, phenol novolacs, or mixtures thereof. 4. The method of claim 1 , wherein the modifying agent comprises a polyfunctional alcohol, a phenol, a cycloaliphatic carboxylic acid, an aromatic amine, or an aminophenol reacted with epichlorohydrin. 5. The method of claim 1 , wherein the emulsifying agent comprises a surfactant. 6. The method of claim 5 , wherein the surfactant comprises an epoxy functional surfactant, a nonionic surfactant, an anionic surfactant or a mixture thereof.
Epoxynovolacs · CPC title
Crosslinking or vulcanising agents; including accelerators · CPC title
Lignocellulosic material, e.g. wood, straw or bagasse {(manufacture of articles made from lignocellulosic material by dry processes B27N)} · CPC title
Impregnating involving polymerisation {including use of polymer-containing impregnating agents (macromolecular compounds derived from lignocellulosic materials C08H; compositions of lignin-containing materials C08L97/02)} · CPC title
Compositions of epoxy resins; Compositions of derivatives of epoxy resins · CPC title
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