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filingDate 2009-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b776b0879b6ef80c36746abd05766689
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publicationDate 2013-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2402222-T3
titleOfInvention Production of a solid epoxy resin
abstract An improved process for the preparation of an improved process for the preparation of a glycidyl ether, a process comprising submitting glycidyl ether, a process comprising submitting a reaction mixture, a reaction mixture containing a reaction mixture, a reaction mixture comprising a compound containing contains aromatic hydroxyl comprises a compound that contains aromatic hydroxyls, an epihalohydrin, water and an inoatic hydroxide, an epihalohydrin, water and an inorganic hydroxide that is at least one of organic metal hydroxide that is at least one of alkali metal hydroxide or an alkaline earth metal hydroxide , to alkaline or an alkaline earth metal hydroxide, under conditions sufficient to produce a resin under conditions sufficient to produce a glycidyl ether resin, which is a solid at room temperature and glycidyl ether, which is a solid at room temperature, the compound containing it being present. present the compound containing aromatic hydroxyls and the epihalohydrin in one r aromatic hydroxyls and the epihalohydrin in a molar equivalent ratio between moles (a molar equivalent equation between moles (one molar equivalent) of epihalohydrin and molar hydroxylic moieties) of epihalohydrin and hydroxylic moieties of the compound containing the aromatic hydroxy compound containing aromatic hydroxyls that falls within a range of 0.5: 1 to 1: 1, and s that falls within a range of 0.5: 1 to 1: 1, and laepihalohydrin and the hydroxide being present being epihalohydrin and alkali metal hydroxide or alkali metal alkaline metal hydroxide or alkaline earth metal hydroxide in a molar ratio of hydroxide to earth in a molar ratio of hydroxide to epihalohydrin that falls within a range of 0 epihalohydrin that falls within a range 0.2: 1 to 2: 1, wherein the enhancement comprises adding u, 2: 1 to 2: 1, wherein the enhancement comprises adding u n reaction solvent to the reaction mixture, n reaction solvent to the reaction mixture, the reaction solvent being at least one alcohol, the reaction solvent being at least one alcohol-ether comprising both an ether residue and an ether comprising both a ether residue as alcohol residue alcohol residue
priorityDate 2008-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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