Characterisation of metal organic frameworks for adsorption cooling

被引:126
作者
Rezk, Ahmed [1 ]
Al-Dadah, Raya [1 ]
Mahmoud, Saad [1 ]
Elsayed, Ahmed [1 ]
机构
[1] Univ Birmingham, Dept Mech Engn, Birmingham B15 2TT, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
Adsorption cooling; Metal organic frameworks; Silica gel RD-2060/water; HKUST-1; MIL-100; ACTIVATED CARBON-FIBER; WATER-ADSORPTION; SILICA-GEL; REFRIGERATION CYCLE; WASTE HEAT; EQUILIBRIUM; PERFORMANCE; KINETICS; CHILLER; CHLORIDE;
D O I
10.1016/j.ijheatmasstransfer.2012.07.068
中图分类号
O414.1 [热力学];
学科分类号
摘要
Silica gel/water adsorption cooling systems suffer from size, performance and cost limitations. Therefore. there is a need for new adsorbent materials that outperform silica gel. Metal organic frameworks (MOFs) are new micro-porous materials that have extraordinary porosity and uniform structure. Due to the lack of published data that characterise MOF/water adsorption, this paper experimentally investigates the adsorption characteristics of HKUST-1 (Cu-BTC (copper benzene-1,3,5-tricarboxylate), C18H6Cu3O12) and MIL-100 (Fe-BTC (Iron 1,3,5-benzenetricarboxylate), C9H3FeO6) MOFs compared to silica gel RD-2060. The adsorption characteristics of Silica gel RD-2060, HKUST-1 and MIL-100 were determined using an advanced gravimetric dynamic vapour sorption analyser (DVS). Results showed that HKUST-1 performed better than silica gel RD-2060 with an increase of water uptake of 93.2%, which could lead to a considerable increase in refrigerant flow rate, cooling capacity and/or reducing the size of the adsorption system. However, MIL-100 MOF showed reduced water uptake comparable to silica gel RD-2060 for water chilling applications with evaporation at 5 degrees C. These results highlight the potential of using MOF materials to improve the efficiency of water adsorption cooling systems. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7366 / 7374
页数:9
相关论文
共 41 条
[41]   Adsorption Equilibrium of Water on Silica Gel [J].
Xia, Zai Z. ;
Chen, Chuan J. ;
Kiplagat, Jeremiah K. ;
Wang, Ru Z. ;
Hu, Jin Q. .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2008, 53 (10) :2462-2465