Investigation of optical properties and radiative transfer of sea water-based nanofluids for photocatalysis with different salt concentrations

被引:18
作者
Cheng Ziming [1 ]
Wang Fuqiang [1 ]
Xie Yinmo [1 ]
Ma Lanxin [1 ]
Xu Huijin [2 ]
Tan Jianyu [1 ]
Bai Fengwu [3 ]
机构
[1] Harbin Inst Technol Weihai, Sch Automobile Engn, 2 West Wenhua Rd,, Weihai 264209, Peoples R China
[2] China Univ Petr Huadong, Coll Pipeline & Civil Engn, 66 West Changjiang St, Qingdao 266580, Peoples R China
[3] Inst Elect Engn CAS, Key Lab Solar Thermal Energy & Photovolta Syst, 6 Beiertiao Rd, Beijing 100190, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Sea water; Complex refractive index; TiO2; nanofluids; Extinction coefficient; Transmittance; PARABOLIC TROUGH RECEIVER; HEAT-TRANSFER; SOLAR COLLECTOR; PERFORMANCE ANALYSIS; TIO2; PHOTOCATALYSIS; HYDROGEN-PRODUCTION; TEMPERATURE; ABSORPTION; MECHANISMS; GENERATION;
D O I
10.1016/j.ijhydene.2017.09.044
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalytic decomposition of sea water is an effective way to solve the future energy crisis. However, there is a great deal of controversy about seawater's effect on photo catalytic hydrogen production efficiency. In this paper, the catalyst particles are divided into large particles (x >1) and small particles (x < 1). The Mie theory combined with Monte Carlo method are used to analyze the influence of sea water on radiative transfer in the sea water-based nanofluids. The effects of the optical constants of the base fluid (fresh water and sea water) on the spectral extinction and spectral transmittance of the TiO2 nanofluids are calculated. Results indicate that, for sea water-based nanofluids with small particles (x < 1), the spectral extinction coefficient increases and spectral transmittance decreases with salt concentration increasing. For sea water-based nanofluids with large particles (x > 1), the spectral extinction coefficient and transmittance oscillate because of diffraction peaks. (c) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:26626 / 26638
页数:13
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