Abstract

ABSTRACT A precise determination of the temperatures and enthalpies of thermally induced various phases of n-alkanes, especially those having the molecular weights in the petroleum wax range, have been done by using a differential scanning calorimeter (DSC). These phase transitional parameters are shown to be dependent on the rate of heating/cooling, particularly on the faster rates. Also, the parameters measured during heating cycle (melting) differ from those obtained during the cooling cycle (crystallization). The typical shape of the solid-solid transition curve in the DSC thermograms(cooling cycle) of even n-alkanes readily distinguishes these from the odd n-alkanes, which is greately influenced by the increase in the carbon numbers in the chain (n-C34 and beyond) and the purity of the sample.High molecular weight n-alkanes also showed instability in the structures at the phase transitions The formation of solid solutions of n-alkanes have been studied by measuring phase transitional parameters and studying nature of the DSC thermograms of various binary and multicomponent mixtures of n-tetracosane (n-C24) with other n-alkanes. It is observed that the immiscibility between two n-alkanes of the binary mixture begins when chain-length difference between them is more than four carbon atoms. In between the two extremes of solid solution and eutectic formations, there also existed the partial miscibility of two n-alkanes, particularly at high temperatures The DSC thermograms of multicomponent n-alkane mixtures and Fischer-Tropsch waxes revealed that perfect solid solution is formed when the involved n-alkanes have carbon number very close to each other or the carbon number distribution is in a narrow range with smaller chain n-alkanes dominating.

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