Reaction path in formation of Ti1−xWxC solid solution by combustion synthesis

Abstract

Ti1−xWxC solid solution powders have been prepared by combustion synthesis in two reaction modes of self-propagating high-temperature synthesis (SHS) and thermal explosion (TE). The reaction mechanism in combustion synthesis is investigated and the effects of processing parameters are discussed. Two reaction paths are proposed for the formation of the Ti1−xWxC solid solution. In path 1, Ti1−xWxC crystals are directly precipitated from Ti-W-C melt, and in path 2 the Ti1−xWxC phase is formed by solid-state reaction between TiC and WC. The availability of the two reaction paths depends on the x value and reaction temperature. For smaller x values and higher temperatures, the reaction path 1 dominates and almost full conversion is achieved. For larger x values and lower temperatures, however, path 2 becomes dominant. In path 2, the rate-limiting step is the formation of WC by slow diffusion-controlled solid-state reaction between W and C, which is unable to be completed during the short reaction period and results in the presence of W2C and unreacted W in the products. The reaction between W and C cannot be improved by the addition of excessive C, but can be promoted by using carbon black instead of graphite powder as C source or carrying out the synthesis in a high-pressure N2 atmosphere instead of vacuum. In the fast combustion reaction with high heating/cooling rates, a non-equilibrium state is likely to be created because the mass transfer and energy exchange are limited. The non-equilibrium condition has a strong influence on the reaction kinetics, where the decomposition of W2C is avoided, a localized compositional heterogeneity is caused, and ultrafine grains on a submicron scale are obtained in the products.