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重新审视用于太阳能热化学储能的BaO₂/BaO氧化还原循环。

Revisiting the BaO2/BaO redox cycle for solar thermochemical energy storage.

作者信息

Carrillo A J, Sastre D, Serrano D P, Pizarro P, Coronado J M

机构信息

Thermochemical Processes Unit, IMDEA Energy Institute, Avenida Ramón de la Sagra, 3, Parque Tecnológico de Móstoles, 28935, Móstoles, Madrid, Spain.

出版信息

Phys Chem Chem Phys. 2016 Mar 21;18(11):8039-48. doi: 10.1039/c5cp07777j.

DOI:10.1039/c5cp07777j
PMID:26922970
Abstract

The barium peroxide-based redox cycle was proposed in the late 1970s as a thermochemical energy storage system. Since then, very little attention has been paid to such redox couples. In this paper, we have revisited the use of reduction-oxidation reactions of the BaO2/BaO system for thermochemical heat storage at high temperatures. Using thermogravimetric analysis, reduction and oxidation reactions were studied in order to find the main limitations associated with each process. Furthermore, the system was evaluated through several charge-discharge stages in order to analyse its possible degradation after repeated cycling. Through differential scanning calorimetry the heat stored and released were also determined. Oxidation reaction, which was found to be slower than reduction, was studied in more detail using isothermal tests. It was observed that the rate-controlling step of BaO oxidation follows zero-order kinetics, although at high temperatures a deviation from Arrhenius behaviour was observed probably due to hindrances to anionic oxygen diffusion caused by the formation of an external layer of BaO2. This redox couple was able to withstand several redox cycles without deactivation, showing reaction conversions close to 100% provided that impurities are previously eliminated through thermal pre-treatment, demonstrating the feasibility of this system for solar thermochemical heat storage.

摘要

基于过氧化钡的氧化还原循环在20世纪70年代末被提出作为一种热化学储能系统。从那时起,这种氧化还原对很少受到关注。在本文中,我们重新探讨了BaO₂/BaO体系的氧化还原反应在高温热化学蓄热中的应用。通过热重分析研究了还原和氧化反应,以找出与每个过程相关的主要限制因素。此外,通过几个充放电阶段对该系统进行了评估,以分析其在反复循环后可能的降解情况。通过差示扫描量热法还测定了储存和释放的热量。氧化反应被发现比还原反应慢,使用等温试验对其进行了更详细的研究。观察到BaO氧化的速率控制步骤遵循零级动力学,尽管在高温下观察到偏离阿累尼乌斯行为,这可能是由于形成了BaO₂外层导致阴离子氧扩散受阻。这种氧化还原对能够承受几个氧化还原循环而不失活,只要通过热预处理预先去除杂质,反应转化率就接近100%,这证明了该系统用于太阳能热化学蓄热的可行性。

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