Synthesis and Physico-Chemical Properties of Polycyanurates of 2-(N,N-Diphenylhydrazino)4,6-Dichloro-s-Triazine with Various Aromatic Diols

Abstract

Various polycynaurates were synhesised by stirred interfacial polycondensation of 2-(N.N-diphenynhydrazino)-4,6-dichloro-s-triaziae (DPHDCT) with each of the aromatic diols: bisphenol-A (BPA); bisphenol-C (BPC); bisphenol-S (BPS); phenolphthalein (Ph); catechol; resorcinol; 1,5and 2.7-dihydroxynaphthalene (DHN-1,5 and DHN-2,7) and 1,8-dihydroxyanthraquinone (DHA-1,8). Interfacial polycondensation of DPHDCT with BPA was investigated in detail in order to select optimum reaction conditions. The yield of polycyanurates varies from 6 I% to 79%. The polycyanurates are soluble in chlorinated solvents such as chloroform, dichloroethane. dichloromethane and chlorobenzene. The reduced viscosity for polycyanurates, determined with a 1 g disolution in chloroform at 25 + 3°C was found to be in the range 0.50-0.68 dl g. All the polycyanurates were characterized by IR spectra. The densities of the polycyanurates, determined using the suspension method at 25 3°C, range between 1.196 and 1.330 g cm. The overall reactivity of diols, based on reduced viscosity values, was found to decrease in the following order: PCBPA> PCPh> PCBPC> PCR>PCDHN-2,7 > PCDHN-I,5 > PCC > PCDHA-1.8 > PCBPS. The thermal stability of polycyanurates, derived from various temperature characteristics, was found to decrease in the following order: PCBPA> PCBPS> PCBPC > PCC PCR> PCDHN-2,7 PCDHN-.l 5 > PCDHA-1,8 > PCPh.

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