کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
764366 | 896981 | 2012 | 5 صفحه PDF | دانلود رایگان |
Silica gel and zeolite 13X were used as supports for the hygroscopic salts LiBr, MgCl2 and CaCl2. The silica- and zeolite-supported hygroscopic salts were characterized by N2 adsorption at −196 °C and X-ray diffraction. The silica support was mesoporous whereas the zeolite support was microporous. The dispersion of CaCl2 was much lower on the zeolite than on the silica support, and the microporosity of the zeolite was blocked by the salt. CaCl2 supported on silica was a superior water sorbent versus zeolite, and CaCl2 supported on zeolite was an inferior sorbent versus zeolite. Complete water desorption from silica-supported hygroscopic salts can be effectively reached at a relatively low temperature (100–110 °C), making them candidates for efficient cooling or air conditioning applications. The isosteric heat of water desorption was obtained from the isobars and was dependent on the amount of water adsorbed. Finally, the thermodynamic cooling cycle for the SCa33 (silica gel containing 33 wt.% CaCl2) – water vapour pair showed a coefficient of performance of 0.83.
► The silica- and zeolite-supported hygroscopic salts (SHS) were prepared.
► The water uptake was evaluated as function of the pore size and salt content.
► A novel method based on mass spectrometry (MS) was proposed and successfully used.
► The MS was applied to obtain the water sorption isobars on SHS.
► The thermodynamic cooling cycle for SHS–water pair showed a coefficient of performance of 0.83.
Journal: Energy Conversion and Management - Volume 53, Issue 1, January 2012, Pages 219–223