Thermodynamics of Aqueous Lithium Nitrate Solutions at 298.15 to 398.15 K and 0.1 to 60 MPa

IF 1.3 4区 化学 Q4 CHEMISTRY, PHYSICAL Journal of Solution Chemistry Pub Date : 2024-10-27 DOI:10.1007/s10953-024-01421-4
Somnath Pramanik, Bidyut Debnath, Bijan Das
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Abstract

The activity and osmotic coefficients of electrolyte solutions are relatively scarce under super-ambient conditions. This study computes the activity and osmotic coefficients of aqueous lithium nitrate solutions to a molality of 7 mol·kg−1, within the pressure range 0.1 to 60 MPa, and temperature range 298.15 K to 398.15 K. In particular, the pressure dependences of the activity and osmotic coefficients have been estimated with the equations derived by Rogers and Pitzer (J Phys Chem Ref Data 11:15–81, 1982) on the basis of the Pitzer ion-interaction approach using the literature apparent molar volume data. These pressure effects in conjunction with the low-pressure activity and osmotic coefficient data on aqueous lithium nitrate solutions provide estimates of the values of these coefficients under high pressures. Effects of temperature, pressure, and molality on the activity and osmotic coefficients have been discussed.

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298.15 至 398.15 K 和 0.1 至 60 MPa 下硝酸锂水溶液的热力学
在超环境条件下,电解质溶液的活度和渗透系数相对较少。在0.1 ~ 60 MPa、298.15 ~ 398.15 K的温度范围内,计算了质量摩尔浓度为7 mol·kg−1的硝酸锂水溶液的活度和渗透系数。特别是,活度和渗透系数的压力依赖性已经用Rogers和Pitzer (J Phys Chem Ref Data 11:15-81, 1982)在Pitzer离子相互作用方法的基础上,利用文献中的表观摩尔体积数据推导出的方程来估计。这些压力效应与低压活度和渗透系数数据结合在一起,提供了高压下这些系数的估计值。讨论了温度、压力和摩尔浓度对活性和渗透系数的影响。
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来源期刊
Journal of Solution Chemistry
Journal of Solution Chemistry 化学-物理化学
CiteScore
2.30
自引率
0.00%
发文量
87
审稿时长
3-8 weeks
期刊介绍: Journal of Solution Chemistry offers a forum for research on the physical chemistry of liquid solutions in such fields as physical chemistry, chemical physics, molecular biology, statistical mechanics, biochemistry, and biophysics. The emphasis is on papers in which the solvent plays a dominant rather than incidental role. Featured topics include experimental investigations of the dielectric, spectroscopic, thermodynamic, transport, or relaxation properties of both electrolytes and nonelectrolytes in liquid solutions.
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