Continuous solid-state phase transitions in energy storage materials with orientational disorder - Computational and experimental approach

被引:35
|
作者
Singh, Harpreet [1 ]
Talekar, Anjali [1 ]
Chien, Wen-Ming [1 ]
Shi, Renhai [1 ]
Chandra, Dhanesh [1 ]
Mishra, Amrita [2 ]
Tirumala, Muralidhar [3 ]
Nelson, Daryl J. [3 ]
机构
[1] Univ Nevada, Dept Chem & Mat Engn, Reno, NV 89557 USA
[2] Dept Mech Engn, University, MS 38677 USA
[3] Intel Corp, Intel Labs, Hillsboro, OR 97124 USA
关键词
Continuous phase transitions; Orientationally disordered crystals; Pentaerythritol; Pentaglycerine; Neopentylglycol; CALPHAD modeling; SYSTEM; PENTAERYTHRITOL; PENTAGLYCERIN;
D O I
10.1016/j.energy.2015.07.130
中图分类号
O414.1 [热力学];
学科分类号
摘要
We report on TES (thermal energy storage) in new CT (continuous phase transitions) in multicomponent tetrahederally configured (orientationally disordered) crystals of NPG-neopentylglycol-C5H12O2, PG-pentaglycerine-C5H2O3, and PE-pentaerythritol-C5H12O4. This discovery is applicable in thermal energy storage in many systems which do not require conventional isothermal first-order phase transition energy storage. The above compounds exhibit polymorphs of orientationally disordered phases in which O-H center dot center dot center dot O bond rotation around the C-C bond stores significant amount of energy; for example, in PE 41.26 kJ/mol are absorbed isothermally during solid-solid transitions. In this paper we show, anisothermal continuous phase transitions (CT), due to compositional changes with changes in temperature, associated with a measurable amount of energy, not reported earlier. The correlation of phase stability regions in pseudo-binaries, calculated from ternary NPG-PG-PE phase diagrams, is validated by experimental ternary DSC (differential scanning calorimetry) and in-situ x-ray diffraction data. We established equations for determining the CT in a temperature range, and their respective enthalpies of transitions for any composition of the ternaries. Thermodynamic calculations of the Gibbs energies of the solution phases are modeled as substitutional solid solutions, in which the excess Gibbs energies are expressed by the Redlich-Kister-Muggianu polynomial. There is excellent agreement between the experimental and CALPHAD calculated data. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:334 / 349
页数:16
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