Terpolymer resins (8-HQDF) were synthesized by the condensation of 8-hydroxyquinoline (8-HQ) and dithiooxamide (D) with formaldehyde (F) in the presence of acid catalyst and using varied molar ratios of reacting monomers. Terpolymer resins compositions have been determined on the basis of their elemental analysis and the number average molecular weights of these resins were determined by conductometric titration in non-aqueous medium. Viscometric measurements in dimethyl formamide (DMF) have been carried out with a view to ascertain the characteristic functions and constants. The UV-visible, FTIR, and proton nuclear magnetic resonance (H þ NMR) spectra were studied to elucidate the structure.
Terpolymer (p-CDF) has been prepared by using the monomer p-cresol, dithiooxanude and formaldehyde in 1:1:2 molar proportions. The structure of p-CDF terpolymer has been elucidated on the basis of elemental analysis and various physicochemical technique like UV-visible, FTIR, 1 H NMR and TG analysis. Detailed thermal degradation curve is discussed which shows four steps decomposition. The activation energy (Ea) and thermal stability calculated by using the Sharp Wentworth, Frceman-Carroll methods. Thermodynamics parameters such as entropy change (∆S), apparent entropy change (S*) and frequency factor (z) have also been evaluated on the basis of the data of Freeman-Carroll method. The order of reaction (n) is found to be 1.05.
Terpolymer resins o-APDF have been prepared by the condensation and dithio oxamide with formaldehyde in the presence of acid catalyst and using varied molar ration of reacting monomers. The electrical conductivity terpolymer were measured over a wide range of temperature in their pellets from. From the electrical conductivity of this polymer activation energy of electrical conduction have been evaluated and values lies in the range. 1.18 x 10 -4 to 6.88 x 10 -4 ev. The terpolymer at room temperature have an electric conductivity in the range 1.69 x 10 -7 to 1.17 x 10 -8 Siemen.
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