16 research outputs found

    Curing of epoxy resins by complex based on monoamide of phosphonic acid and ammonium chloride

    No full text
    Reaction of epoxy-diane resin with complex based on monoamide of phosphonic acid and ammonium chloride (MODAF) is studied. It is established that the MODAF equivalent in the reaction with epoxy resin is equal to 1/5 of its molecular weight. Epoxy resin is cured via the reactions of both monoamide and ammonium chloride. The dependence of the epoxide and hydroxyl groups has a stepped character over time, which is probably due to the existence of certain threshold concentrations of the curing coefficients. The investigated reaction is a new example of macroscopic coherence manifestation. © 2010 Pleiades Publishing, Ltd

    Curing of epoxy resins by complex based on monoamide of phosphonic acid and ammonium chloride

    No full text
    Reaction of epoxy-diane resin with complex based on monoamide of phosphonic acid and ammonium chloride (MODAF) is studied. It is established that the MODAF equivalent in the reaction with epoxy resin is equal to 1/5 of its molecular weight. Epoxy resin is cured via the reactions of both monoamide and ammonium chloride. The dependence of the epoxide and hydroxyl groups has a stepped character over time, which is probably due to the existence of certain threshold concentrations of the curing coefficients. The investigated reaction is a new example of macroscopic coherence manifestation. © 2010 Pleiades Publishing, Ltd

    Determination of hydroxyl groups in epoxy resins by potentiometric titration using a reaction with maleic anhydride

    No full text
    A reaction of maleic anhydride with epoxy-dian resins in methyl ethyl ketene was investigated. It was shown by potentiometric titration that the resulting maleic esters are stable to hydrolysis in acid and weakly acid organic solutions. This reaction can be used for the quantitative determination of hydroxyl groups in epoxy resins. Epoxy groups do not interfere with the formation of maleic esters under the conditions of determination. The optimal reaction conditions were found. The reaction kinetic was investigated, the reaction rate constants were determined at various temperatures, and the activation energy was found. The value of the activation energy indicates that the reaction is characterized by a low potential barrier. © 2001 MAIK "Nauka/Interperiodica"
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