Performance analysis of a thermochemical based heat storage as an addition to cogeneration systems

被引:47
|
作者
Lele, Armand Fopah [1 ,2 ]
Kuznik, Frederic [2 ,3 ]
Opel, Oliver [1 ]
Ruck, Wolfgang K. L. [1 ]
机构
[1] Leuphana Univ Luneburg, Fac Sustainabil Sci, Sustainable Energy Res & Environm Chem Inst, D-21335 Luneburg, Germany
[2] INSA Lyon, CETHIL, F-69621 Villeurbanne, France
[3] Univ Lyon, CNRS, UMR5008, F-69622 Villeurbanne, France
关键词
Heat storage; Thermochemical process; Reaction front model; 3D reactor model; Thermal performance; ENERGY-STORAGE; PHASE; MODEL; SALT;
D O I
10.1016/j.enconman.2015.10.068
中图分类号
O414.1 [热力学];
学科分类号
摘要
A closed thermochemical heat storage system based on pure salt hydrate, namely SrBr2 center dot 6H(2)O is developed and its performance, numerically investigated. This paper focuses on system development as an addition to existing micro-combined heat and power (cogeneration). The originality of this work lies in the fact that it models the coupled heat and mass transfer with chemical reaction on a 3D geometry to be closed to reality. Besides, a reaction front model is also developed, in order to determine optimal parameters (bed porosity, bed thickness kinetic behaviour) and thermal power, required for system efficiency. Then, sensitivity of permeability and thermal conductivity on the reaction efficiency is numerically demonstrated, leading to some recommendations for future prototype development. Results exhibit a theoretical reactor energy storage density of 115 kWh m(-3), storage capacity of 61 kWh, thermal efficiency of 78% (at 90% of reaction conversion) and COPth of 0.97, highlighting system performances. An average output temperature of 52 degrees C is numerically obtained. A comparison simulation-experiment is then performed and discussed, showing encouraging results, even if limited at lab-scale. Performances are quite similar, consolidating the idea that, waste heat from cogeneration can be re-used with 78% of efficiency. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1327 / 1344
页数:18
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