Experimental determination of high energy density lithium nitrate hydrate eutectics

被引:3
作者
Ahmed, Sophia [1 ]
Hoe, Alison [1 ]
Alamo, Fabiola [1 ]
Turner, Nathan [1 ]
Shamberger, Patrick J. [1 ]
机构
[1] Texas A&M Univ, Dept Mat Sci & Engn, College Stn, TX 77843 USA
关键词
Phase change material; Salt hydrate; Eutectic; Thermophysical properties; PHASE-CHANGE MATERIALS; HEAT-TRANSFER; STORAGE; SALT; NUCLEATION; DIAGRAM; WATER; TETRAHYDRATE; ELECTROLYTE; ENTHALPIES;
D O I
10.1016/j.est.2022.104754
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Congruently melting salt hydrates absorb and release heat reversibly upon melting and solidification, and have among the highest energy density and thermal conductivity of low melting point (< 50 ?C) phase change ma-terials. However, very few salt hydrate systems have been identified that congruently melt near room temper-ature, which limits their utility in environmental control applications. Here we present thermochemical and thermophysical properties of three near-room temperature ternary eutectic salt hydrate systems based on lithium nitrate trihydrate with high specific energy densities: LiNO3.3(H2O)-LiNO3-MgNO3.6(H2O) (T-eu = 25.3 +/- 0.3 ?C; delta(Heu )= 249 +/- 9 J.g(-1)), LiNO3.3(H2O)-LiNO3-NaNO3 (T-eu = 25.8 +/- 0.5 ?C; delta H-eu = 285 +/- 15 J.g(-1)), and LiNO3.3 (H2O)-LiNO3-Zn (NO3)(2).6(H2O) (T-eu = 13.4 +/- 0.5 ?C; delta H-eu = 197 +/- 11 J.g(-1)). Thermal conductivity of the liquid LiNO3.3(H2O)-LiNO3-NaNO3 ternary eutectic is k/W.m(- 1).?C-( 1 )= 0.498 + 0.000523 x T/?C over the temperature range 25 to 65 ?C. Finally, we report undercooling in the presence of multiple nucleation agents in the LiNO3.3(H2O)-LiNO3-NaNO3 eutectic, and demonstrate the effectiveness of including multiple nucleation agents to nucleate the three phases, which solidify simultaneously in these ternary eutectics. Isothermal solid-ification data, as well as aging of salt hydrates together with nucleation agents for up to 100 days demonstrate that this is a robust and stable system.
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页数:10
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