Characterization of Two-Step Tin-Based Redox System for Thermochemical Fuel Production from Solar-Driven CO2 and H2O Splitting Cycle

被引:27
作者
Leveque, Gael [1 ]
Abanades, Stephane [1 ]
Jumas, Jean-Claude [2 ]
Olivier-Fourcade, Josette [2 ]
机构
[1] PROMES CNRS UPR 8521, Proc Mat & Solar Energy Lab, F-66120 Font Romeu, France
[2] Univ Montpellier I, Inst Charles Gerhardt UMR 5253, F-34095 Montpellier 5, France
关键词
KINETIC-ANALYSIS; HYDROGEN-PRODUCTION; DISPROPORTIONATION; REDUCTION; ZNO;
D O I
10.1021/ie500206u
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The solar thermochemical dissociation of H2O and CO, for renewable fuel production from two-step SnO2/SnO cycle is considered. This cycle is based on the solar production of SnO phase in a first endothermic step that is subsequently used for splitting CO2 and H2O in a second exothermic step. The reactivity of tin-based species was studied in order to elucidate the phenomena occurring during its heating and subsequent reoxidation in a H2O or CO2 atmosphere to produce H-2 or CO. Two main types of reactant were considered for comparing their reactivity: SnO nanopowder obtained via solar sublimation and condensation of commercial SnO powder, and Sn/SnO2 nanopowder obtained via disproportionation of nanosized SnO. The reaction rate was quantified via thermogravimetry analysis and the reaction products were characterized using Mossbauer spectrometry and X-ray diffraction. The SnO and Sn/SnO2 nanopowders are more reactive with H2O than with CO2 in the range 550-650 degrees C. SnO is also more reactive with oxidants than Sn/SnO2. The disproportionation reaction starts significantly around 600 degrees C, giving rise to a particular Sn-II phase that reacts faster with the oxidants but is more prone to passivation. A kinetic study yields an activation energy of 101 +/- 10 kJ mol(-1) and 53 +/- 1 kJ mol(-1) for the Sn/SnO2 oxidation with CO2 and H2O, respectively.
引用
收藏
页码:5668 / 5677
页数:10
相关论文
共 23 条
[11]   Experimental study of SnO2/SnO/Sn thermochemical systems for solar production of hydrogen [J].
Charvin, Patrice ;
Abanades, Stephane ;
Lemont, Florent ;
Flamant, Gilles .
AICHE JOURNAL, 2008, 54 (10) :2759-2767
[12]  
D'Souza L, 2013, MATER RENEW SUSTAIN, V2, DOI 10.1007/s40243-013-0007-0
[13]   X-RAY-DIFFRACTION AND MOSSBAUER ANALYSES OF SNO DISPROPORTIONATION PRODUCTS [J].
GAUZZI, F ;
VERDINI, B ;
MADDALENA, A ;
PRINCIPI, G .
INORGANICA CHIMICA ACTA-ARTICLES AND LETTERS, 1985, 104 (01) :1-7
[14]   Kinetics of the disproportionation of SnO [J].
Giefers, H ;
Porsch, F ;
Wortmann, G .
SOLID STATE IONICS, 2005, 176 (1-2) :199-207
[15]   Kinetic analysis of solid-state reactions: The universality of master plots for analyzing isothermal and nonisothermal experiments [J].
Gotor, FJ ;
Criado, JM ;
Malek, J ;
Koga, N .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (46) :10777-10782
[16]   Recent advances in the photocatalytic conversion of carbon dioxide to fuels with water and/or hydrogen using solar energy and beyond [J].
Izumi, Yasuo .
COORDINATION CHEMISTRY REVIEWS, 2013, 257 (01) :171-186
[17]   TIN OXIDE-SN3O4 [J].
LAWSON, F .
NATURE, 1967, 215 (5104) :955-&
[18]   Kinetic analysis of high-temperature solid-gas reactions by an inverse method applied to ZnO and SnO2 solar thermal dissociation [J].
Leveque, Gael ;
Abanades, Stephane .
CHEMICAL ENGINEERING JOURNAL, 2013, 217 :139-149
[19]  
LUXMANN L, 1980, METALL BERLIN, V34, P821
[20]   Kinetic analysis of the dismutation of tin monoxide [J].
Machado-Bailly, C ;
Delalu, H ;
Létoffé, JM ;
Metz, R .
JOURNAL DE PHYSIQUE IV, 2004, 113 :135-138