用于CSP应用的商用三元熔盐在不同气氛下的降解

F. Pérez, M. Miguel, M. I. Lasanta, V. Encinas-Sánchez, G. García-Martin, Rubén De Arriba
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引用次数: 1

摘要

本研究旨在研究一种称为Hitec的三元熔盐混合物与氮气和空气环境接触时的降解和物理化学性质的变化。通过化学分析NO3-和NO2-阴离子,DSC测定混合物的熔点和冰点来确定盐的降解。为此,在500°C下进行了1000小时的等温试验。直到2000年,对大气中盐的演化进行了更深入的研究。结果表明,在N2气氛下运行时,所研究的混合物性能保持不变。由于亚硝酸盐转化为硝酸盐,使用大气空气导致熔点和冰点逐渐增加。在试验初期可以观察到降解的效果,试验2000 h后,系统尚未达到稳定状态,降解过程仍在继续。本研究旨在研究一种称为Hitec的三元熔盐混合物与氮气和空气环境接触时的降解和物理化学性质的变化。通过化学分析NO3-和NO2-阴离子,DSC测定混合物的熔点和冰点来确定盐的降解。为此,在500°C下进行了1000小时的等温试验。直到2000年,对大气中盐的演化进行了更深入的研究。结果表明,在N2气氛下运行时,所研究的混合物性能保持不变。由于亚硝酸盐转化为硝酸盐,使用大气空气导致熔点和冰点逐渐增加。在试验初期可以观察到降解的效果,试验2000 h后,系统尚未达到稳定状态,降解过程仍在继续。
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Degradation of a commercial ternary molten salt under various atmospheres for CSP applications
This research aims to study the degradation and the changes in physicochemical properties of a ternary molten salt mixture, commercially known as Hitec, in contact with a nitrogen and an air atmosphere. The degradation of the salt was determined by chemical analysis of the NO3- and NO2- anions and DSC determination of the melting and freezing point of the mixture. To this end, isothermal tests at 500 °C were performed for 1000 h. A deeper study of the evolution of the salt under air atmosphere was carried out until 2000 h. It was found that the mixture properties studied remain invariable when it was operated under N2 atmosphere. The use of atmospheric air resulted in a progressive increase in melting and freezing points due to the nitrite transformation to nitrate. The effect of the degradation could be observed in the early hours of the test and after 2000 h of test, the system had not reached and steady state and the degradation progress was still ongoing.This research aims to study the degradation and the changes in physicochemical properties of a ternary molten salt mixture, commercially known as Hitec, in contact with a nitrogen and an air atmosphere. The degradation of the salt was determined by chemical analysis of the NO3- and NO2- anions and DSC determination of the melting and freezing point of the mixture. To this end, isothermal tests at 500 °C were performed for 1000 h. A deeper study of the evolution of the salt under air atmosphere was carried out until 2000 h. It was found that the mixture properties studied remain invariable when it was operated under N2 atmosphere. The use of atmospheric air resulted in a progressive increase in melting and freezing points due to the nitrite transformation to nitrate. The effect of the degradation could be observed in the early hours of the test and after 2000 h of test, the system had not reached and steady state and the degradation progress was still ongoing.
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