Metal oxide composites and structures for ultra-high temperature solar thermochemical cycles

被引:217
作者
Miller, James E. [1 ]
Allendorf, Mark D. [2 ]
Diver, Richard B. [1 ]
Evans, Lindsey R. [1 ]
Siegel, Nathan P. [1 ]
Stuecker, John N.
机构
[1] Sandia Natl Labs, Albuquerque, NM 87185 USA
[2] Sandia Natl Labs, Livermore, CA 94551 USA
关键词
D O I
10.1007/s10853-007-2354-7
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Conceptually, thermochemical cycles are heat engines that drive endothermic chemical reactions, e.g., splitting water into hydrogen and oxygen. The two-step metal oxide cycles (typically ferrite-based) are particularly attractive since they are relatively simple, use non-corrosive materials, and involve gas-solid reactions requiring no difficult separations. Additionally, they are potentially the most efficient renewable-energy driven processes for hydrogen production. We are developing a novel concentrating solar power (CSP) driven metal-oxide-based heat engine, the CR5, at the heart of which are rings of a reactive solid that are thermally and chemically cycled to produce oxygen and hydrogen from water in separate and isolated steps. The monolithic ring structures must have high geometric surface area for gas-solid contact and for adsorption of incident solar radiation, and must maintain structural integrity and high reactivity after extensive thermal cycling to temperatures of at least 1,400 degrees C. We have demonstrated through laboratory and on-sun testing that cobalt ferrite/zirconia mixtures fabricated into monolithic structures suitable for the CR5 are mechanically robust and maintain productivity over tens of cycles. We have also demonstrated that carbon dioxide splitting (CDS) to carbon monoxide and oxygen is a thermodynamically favorable alternative to water splitting that can be conducted with both iron- and cerium-based materials.
引用
收藏
页码:4714 / 4728
页数:15
相关论文
共 30 条
[1]   Thermochemical hydrogen production from a two-step solar-driven water-splitting cycle based on cerium oxides [J].
Abanades, Stephane ;
Flamant, Gilles .
SOLAR ENERGY, 2006, 80 (12) :1611-1623
[2]  
Abanades S, 2006, ENERGY, V31, P2805, DOI 10.1016/j.energy.2005.11.002
[3]  
ALLENDORF MD, 2006, P 2006 INT SOL EN C
[4]  
ALLENDORF MD, ENERGY FUEL UNPUB
[5]  
AOKI H, 2004, P 2004 INT SOL EN C, P515
[6]   Effect of mild re-oxidation treatments with CO2 on the chemisorption capability of a Pt/CeO2 catalyst reduced at 500°C [J].
Bernal, S ;
Blanco, G ;
Gatica, JM ;
Larese, C ;
Vidal, H .
JOURNAL OF CATALYSIS, 2001, 200 (02) :411-415
[7]   The oxidizing role of CO2 at mild temperature on ceria-based catalysts [J].
Demoulin, O. ;
Navez, M. ;
Mugabo, J. -L. ;
Ruiz, P. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2007, 70 (1-4) :284-293
[8]  
DIVER RB, 2006, P 2006 INT SOL EN C
[9]  
DIVER RB, 2008, P 2008 14 BIENN CSP
[10]   Burning buried sunshine: Human consumption of ancient solar energy [J].
Dukes, JS .
CLIMATIC CHANGE, 2003, 61 (1-2) :31-44