Likely near-term solar-thermal water splitting technologies

被引:210
作者
Perkins, C [1 ]
Weimer, AW [1 ]
机构
[1] Univ Colorado, Dept Chem & Biol Engn, Ctr Engn, Boulder, CO 80309 USA
基金
美国国家科学基金会;
关键词
thermochemical; water splitting; solar; thermal; hydrogen;
D O I
10.1016/j.ijhydene.2004.02.019
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
Thermodynamic and materials considerations were made for some two- and three-step thennochemical cycles to split water using solar-thermal processing. The direct thermolysis of water to produce H-2 using solar-thermal processing is unlikely in the near term due to ultra-high-temperature requirements exceeding 3000 K and the need to separate H-2 from O-2 at these temperatures. However, several lower temperature ( < 2500 K) thermochemical cycles including ZnO/Zn, Mn2O3/MnO, substituted iron oxide, and the sulfur-iodine route (S-I) provide an opportunity for high-temperature solar-thernial development. Although zirconia-based materials are well suited for metal oxide routes in terms of chemical compatibility at these temperatures, thermal shock issues are a major concern for solar-thermal applications. Hence, efforts need to be directed towards methods for designing reactors to eliminate thermal shock (ZrO2 based) or that use graphite (very compatible in terms of temperature and thermal shock) with designs that prevent contact of chemical species with graphite materials at high temperatures. Fluid-wall reactor configurations where inert gases provide a blanket to protect the graphite wall appear promising in this regard, but their use will impact process efficiency. For the case of S-I up to 1800 K, silicon carbide appears to be a suitable material for the high-temperature H2SO4 dissociation. There is a need for a significant amount of work to be done in the area of high-temperature solar-thermal reactor engineering to develop then-nochemical water splitting processes. (C) 2004 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1587 / 1599
页数:13
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