A mathematical model for analysis of sequentially coupled crystallization–melting differential scanning calorimetry peaks and the use of the model for assessing the crystallization resistance of tellurite glasses

Abstract

Differential scanning calorimetry (DSC) characterization of tellurite glasses doped with lanthanum oxide, which improves their crystallization resistance, has revealed a phase transformation specific to such glasses, in which partial crystallization of a sample is followed by melting of the crystals formed. The experimentally observed dependence of the decrease of crystallization–melting peaks across a series of disperse samples of (TeO2)0.72(WO3)0.24(La2O3)0.04 glass with increasing particle size upon extrapolation to the size of a bulk sample has been used to assess the crystallization resistance of tellurite glasses for optical applications. The assessment technique comprises DSC characterization of particle-size-classified glass samples and the use of a mathematical model for obtaining the degree of crystallization as a function of temperature and time, α(T, t) through analysis of nonisothermal DSC peaks representing a partial glass crystallization process passing into melting. The crystallization resistance of glass is estimated by extrapolating the maximum α values as a function of particle size to a preform size. Tested for (TeO2)0.72(WO3)0.24(La2O3)0.04 glass, the technique offers the possibility of selecting preforms for producing fibers from compositionally new, chemically pure tellurite glasses at a given phase purity level.