MgCl2-石墨反应性化合物的渗透率

K. Udell
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摘要

由于吸收基质的渗透性降低而引起的传质限制已被观察到降低了热化学储能系统的性能。本文研究了由氨化氯化镁盐和石墨组成的反应性配合物的渗透性。结果表明,化合物的渗透性取决于化合物的容重,以及氯化镁基体中nh3的吸收量。此外,将氯化镁(MgCl2)氨化反应化合物的渗透率与其他研究者报道的氯化锰(MnCl2)反应化合物的渗透率进行了比较。这两种盐与氨气反应相似,反应动力学相似。虽然活性化合物的石墨含量不同,但两种化合物的渗透率在同一个数量级内。然而,研究表明,在吸收氨后,氯化镁化合物的渗透率下降幅度大于氯化锰化合物的渗透率下降幅度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Permeability of MgCl2- Graphite Reactive Compound
Mass transfer limitations due to decreasing permeabilities of the absorbing matrix has been observed to decrease the performance of thermochemical energy storage systems. In this study, the permeability of a reactive complex consisting ammoniated magnesium chloride salt and graphite was measured. It was shown that the permeability of the compound depends on the bulk density of the compound, as well as the amount of NH3absorbed in the magnesium chloride matrix. Additionally, the permeability of magnesium chloride (MgCl2) ammoniate reactive compound is compared with the permeability of the manganese chloride (MnCl2) reactive compound reported by other researchers. The two salts have similar reactions with ammonia gas with similar reaction kinetics. Although the graphite contents of the reactive compounds were different, it is shown that the permeabilities of both compounds are within the same order of magnitude. However, it is shown that upon absorbing ammonia, the permeability decrease in magnesium chloride compound was larger than the decrease of permeability in the manganese chloride compound.
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