Influence of Cycle Temperatures on the Thermochemical Heat Storage Densities in the Systems Water/Microporous and Water/Mesoporous Adsorbents |
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Authors: | H. Stach J. Mugele J. Jänchen E. Weiler |
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Affiliation: | (1) ZeoSys GmbH, Volmerstr. 13, 12489, Berlin;(2) TU-Berlin, Institut für Haustechnik, Berlin;(3) ZeoSys GmbH, Volmerstr. 13, 12489, Berlin |
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Abstract: | The adsorption equilibrium of water on microporous adsorbents (zeolites of NaA-, NaY- and NaX-type as well as their ion exchanged forms) and on mesoporous adsorbents (different silica gels and composite material i.e. silica gel + salt hydrate) has been studied experimentally and theoretically. Using the Dubinin theory of pore filling the characteristic curves of the adsorption systems and other relevant dependences such as isotherms, isobars, isosteres and the curve of the differential heat of adsorption were calculated. For all systems investigated the adsorption were calculated. Aads and the desorption potential Ades of the closed heat storage system were estimated. These values define the working range of the adsorption/desorption cycle and allow to calculate the specific heat storage density Δ hsp. On the basis of Δ hsp the different adsorbents were compared in order to select the optimal porous storage material for a given application. The presented experimental and theoretical investigations show that the adsorption systems water-zeolite and water-composites are promising working pairs for thermochemical heat storage processes for hot tap water supply and space heating of single family dwellings. The advantage of the water-composite system is the low desorption temperature (solar energy) the main shortcoming the low temperature lift. The advantage of the water zeolite system is the high temperature lift, the shortcoming are the relative high desorption temperatures. |
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Keywords: | thermochemical heat storage water adsorption equilibrium thermo-dynamical data heat storage density zeolites composite adsorbents |
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