On the applicability of the Redlich-Kister framework for viscosity estimation of molten halide salt mixtures

IF 4.1 2区 工程技术 Q2 ENGINEERING, CHEMICAL Chemical Engineering Science Pub Date : 2024-06-21 DOI:10.1016/j.ces.2024.120391
Anthony Birri, Nicholas Termini, N. Dianne Bull Ezell
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Abstract

For molten halide salt mixtures already being utilized or under consideration for carbon-free energy production systems, it is crucial that their viscosity is well understood so that system thermal hydraulics can be reliably assessed. Because of the difficulty in accurately measuring molten halide viscosity and the sheer size of the matrix of possible higher order salt mixtures that may be of interest to the energy industry, there are several gaps in the quantified understanding of molten halide viscosity across this matrix. As such, both first-principles and semi-empirical modeling techniques may be crucial for rapidly assessing this broad, complex compositional domain. Herein, the Redlich-Kister framework is applied to assess the feasibility of broadly interpolating and estimating the viscosity of several pseudobinary and pseudoternary molten halide salt systems that may be of key interest to the energy industry. The framework is based on the assumption that an ideal component and a nonideal component collectively describe the viscosity as a function of composition and temperature for a given molten halide system. Three different ideal models were considered for the ideal component, including Grunburg-Nissan, Katti-Chaudhri, and Gambill methods. Regarding the pseudobinary interpolations, the Redlich-Kister models with either the Grunburg-Nissan or Katti-Chaudhri models as the ideal component resulted in either highly (average error less than 5%) or reasonably (average error less than 15%) accurate interpolations of pseudobinary halide viscosity; BeF2- or UF4-bearing salts tended to result in reasonably accurate interpolations, whereas other pseudobinary mixtures tended to show high accuracy. Regarding the pseudoternary extrapolations, the Redlich-Kister framework shows reasonable success at estimating the extent to which a pseudoternary system may indicate deviations from ideal Grunburg-Nissan mixing, where discrepancies with comparative experimental data generally stay within 30%. The primary reasons identified for such discrepancies are (1) inaccuracy in the underlying experimental data, (2) different complexation behavior in the higher order systems compared to the pseudobinary subsystems, and (3) extrapolation into temperatures too far out of the domain, which is valid for the underlying experimental data feeding the Redlich-Kister model.

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论 Redlich-Kister 框架在熔融卤化盐混合物粘度估算中的适用性
对于已经使用或正在考虑用于无碳能源生产系统的熔融卤化盐混合物而言,充分了解其粘度至关重要,这样才能可靠地评估系统热水力学。由于难以精确测量熔融卤化物的粘度,以及能源行业可能感兴趣的高阶盐混合物矩阵的庞大规模,对整个矩阵中熔融卤化物粘度的量化理解存在若干空白。因此,第一原理和半经验建模技术对于快速评估这一广泛而复杂的成分领域至关重要。在本文中,Redlich-Kister 框架被用于评估广泛插值和估算几种假二元和假三元熔融卤化盐体系粘度的可行性,这些体系可能是能源行业的关键利益所在。该框架基于以下假设:对于给定的熔融卤化物体系,理想成分和非理想成分共同描述了粘度与成分和温度的函数关系。对于理想成分,考虑了三种不同的理想模型,包括 Grunburg-Nissan、Katti-Chaudhri 和 Gambill 方法。在假二元插值方面,以 Grunburg-Nissan 模型或 Katti-Chaudhri 模型作为理想成分的 Redlich-Kister 模型可得出高精度(平均误差小于 5%)或合理精度(平均误差小于 15%)的假二元卤化物粘度插值;含 BeF2- 或 UF4 的盐往往可得出合理精度的插值,而其他假二元混合物则往往显示出较高的精度。关于假ernary 推断,Redlich-Kister 框架在估计假ernary 系统可能偏离理想格伦堡-尼桑混合的程度方面取得了合理的成功,与比较实验数据的差异一般保持在 30% 以内。造成这种差异的主要原因是:(1) 基本实验数据不准确;(2) 与伪二元子系统相比,高阶系统的络合行为不同;(3) 外推温度超出领域太远,而这对于为 Redlich-Kister 模型提供支持的基本实验数据是有效的。
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来源期刊
Chemical Engineering Science
Chemical Engineering Science 工程技术-工程:化工
CiteScore
7.50
自引率
8.50%
发文量
1025
审稿时长
50 days
期刊介绍: Chemical engineering enables the transformation of natural resources and energy into useful products for society. It draws on and applies natural sciences, mathematics and economics, and has developed fundamental engineering science that underpins the discipline. Chemical Engineering Science (CES) has been publishing papers on the fundamentals of chemical engineering since 1951. CES is the platform where the most significant advances in the discipline have ever since been published. Chemical Engineering Science has accompanied and sustained chemical engineering through its development into the vibrant and broad scientific discipline it is today.
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