Thermodynamics and kinetics hydrogen isotope effects of hydrogen/deuterium absorption in Pd-5wt.%Pt alloy

被引:4
作者
Liu, Ran [1 ]
Peng, Yating [1 ]
Rong, Wan [2 ]
Cao, Qigao [2 ]
机构
[1] North China Univ Technol, Coll Mech & Mat Engn, Beijing 100144, Peoples R China
[2] Northwest Inst Nonferrous Met Res, Xian 710016, Shaanxi, Peoples R China
关键词
Pd-Pt; Thermodynamic isotope effects; Kinetic isotope effects; p-c-T curve; Separation factor; GAS-CHROMATOGRAPHIC SEPARATION; DESORPTION; DEUTERIUM; HYSTERESIS; PERMEATION; SOLUBILITY; ADSORPTION; SIMULATION;
D O I
10.1016/j.ijhydene.2023.07.329
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Palladium-Platinum (Pd-Pt) alloys have excellent hydrogen isotope separation properties near room temperature compared to pure palladium (Pd), and are expected to be used as filling materials in thermal cyclic absorption (TCAP) columns. However, most studies on the thermodynamic and kinetic hydrogen isotope effects of hydrogen absorption/deuterium in Pd-Pt alloys have been conducted at temperatures of 273 K or above, with few studies involving the performance of TCAP in the cold-cycle operating temperature range (253 K-303 K). In this work, the performance of Pd-5wt.%Pt alloy for the absorption of hydrogen/deuterium at low temperatures (263 K-323 K) was investigated. The results show that the enthalpy and entropy of dissolution of hydrogen and deuterium in the a-phase of Pd-5wt.%Pt alloy are -11.77 kJ/mol (H), 104.00 J mol-1 K-1(H); -5.50 kJ/mol (D), 87.88 J mol-1 K-1 (D), respectively, which are lower than the enthalpy and entropy change values of pure Pd materials. The apparent reaction activation energies of protium and deuterium absorption are -4.14 kJ/mol (H2) and -11.87 kJ/mol (D2), respectively, which are lower than those of pure palladium. The excellent hydrogen isotope separation performance of Pd-Pt alloys may originate from the fast hydrogen absorption and discharge isotope kinetic performance. (c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:637 / 647
页数:11
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