Watson Deborah E, Martin Steve W
Department of Materials Science and Engineering , Iowa State University , Ames , Iowa 50010-2300 , United States.
J Phys Chem B. 2018 Nov 21;122(46):10637-10646. doi: 10.1021/acs.jpcb.8b08603. Epub 2018 Nov 8.
The glass-transition temperature, T, and molar volume, V̅, are two physical properties known to exhibit the mixed glass former effect (MGFE), a nonlinear nonadditive increase or decrease from a linear ideal mixing behavior, in ternary glass systems, where the two glass forming species are varied, whereas the glass modifier content remains constant across the system. In the next of our continuing studies of the MGFE in ternary glasses, the T and molar volumes of two ternary glass forming series, 0.5NaS + 0.5[ xSiS + (1 - x)PS], the 0.50 NSP series, and 0.67NaS + 0.33[ xSiS + (1 - x)PS], the 0.67 NSP series, have been determined across the full glass forming range in both series, 0 ≤ x ≤ 1. The 0.50 NSP glasses were found to have a strongly negative MGFE in the T and a weaker MGFE in the molar volume. The 0.67 NSP series of glasses exhibited weak negative and strong positive MGFEs in the T and molar volumes, respectively. Using the short-range order (SRO) structure model for each glass series that was previously developed, the number of bridging sulfurs (BS) and nonbridging sulfurs (NBS) was determined and analyzed for each of these two series of glasses. A clear linear correlation was observed between the T and both the fraction of BSs, BS/(BS + NBS), and the number of BS per glass former, BS/GF in both series. The molar volumes of both series of glasses were analyzed using both ideal and real solution models of mixing. The molar volumes of the glasses were best fit to the molar volumes of all of the individual molar volumes of the various SRO units. In the ideal solution model, the molar volumes of the SRO units were only fit to molar volumes of the end member glasses, x = 0 and 1. In the real solution model, the molar volumes were best fit to the full composition dependence of the molar volume of all of the glasses. In both cases, the same molar volumes for the SRO units were used to fit both sets of molar volumes of both glass series. It was found that the best-fit molar volumes of both the P and Si SRO units were essentially the same at the same number of NBS/GF. In this study, therefore, it was observed that the MGFE in the T of the glass was linearly correlated with the number of BS per glass former, BS/GF, whereas the MGFE in the molar volumes of the glasses was correlated with the number of NBS per glass former, NBS/GF.
玻璃化转变温度(T)和摩尔体积(\overline{V})是已知在三元玻璃体系中呈现混合玻璃形成剂效应(MGFE)的两种物理性质,即与线性理想混合行为相比呈现非线性非加和性的增加或减少,在该三元玻璃体系中,两种玻璃形成物种发生变化,而玻璃改性剂含量在整个体系中保持恒定。在我们对三元玻璃中MGFE的持续研究中,已经确定了两个三元玻璃形成系列的(T)和摩尔体积,即(0.5NaS + 0.5[xSiS + (1 - x)PS])(0.50 NSP系列)和(0.67NaS + 0.33[xSiS + (1 - x)PS])(0.67 NSP系列),涵盖了两个系列中整个玻璃形成范围,(0\leq x\leq1)。发现0.50 NSP玻璃在(T)方面具有强烈的负MGFE,在摩尔体积方面具有较弱的MGFE。0.67 NSP系列玻璃在(T)和摩尔体积方面分别呈现出弱负和强正的MGFE。使用先前开发的每个玻璃系列的短程有序(SRO)结构模型,确定并分析了这两个系列玻璃中桥连硫(BS)和非桥连硫(NBS)的数量。在两个系列中,均观察到(T)与BS的分数(BS/(BS + NBS))以及每个玻璃形成剂的BS数量(BS/GF)之间存在明显的线性相关性。使用理想和实际混合溶液模型对两个系列玻璃的摩尔体积进行了分析。玻璃的摩尔体积与各种SRO单元的所有单个摩尔体积的总和最匹配。在理想溶液模型中,SRO单元的摩尔体积仅与端元玻璃((x = 0)和(1))的摩尔体积匹配。在实际溶液模型中,摩尔体积与所有玻璃摩尔体积的完整组成依赖性最匹配。在两种情况下,均使用相同的SRO单元摩尔体积来拟合两个玻璃系列的两组摩尔体积。发现在相同数量的NBS/GF下,P和Si SRO单元的最佳拟合摩尔体积基本相同。因此,在本研究中观察到,玻璃(T)中的MGFE与每个玻璃形成剂中的BS数量(BS/GF)呈线性相关,而玻璃摩尔体积中的MGFE与每个玻璃形成剂中的NBS数量(NBS/GF)相关。