Performance and Stability of Metal (Co, Mn, Cu)-Promoted La2O2SO4 Oxygen Carrier for Chemical Looping Combustion of Methane

被引:14
作者
Cimino, Stefano [1 ]
Mancino, Gabriella [1 ]
Lisi, Luciana [1 ]
机构
[1] Ist Ric Combust CNR, I-80125 Naples, Italy
来源
CATALYSTS | 2019年 / 9卷 / 02期
关键词
oxygen storage capacity; thermal stability; cyclic operation; deactivation; oxysulfate; oxysulfide; LANTHANIDE OXYSULFATE/OXYSULFIDE; STORAGE; CAPACITY; DECOMPOSITION; NANOPARTICLES; TEMPERATURE; CATALYSTS; PROGRESS; H-2; CO;
D O I
10.3390/catal9020147
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
Oxygen carrier materials based on La2O2SO4 and promoted by small amounts (1% wt.) of transition metals, namely Co, Mn and Cu, have been synthesized and characterized by means of X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), Temperature-programmed reduction/oxidation (TPR/TPO) and thermogravimetry-mass-Fourier transform infrared spectrometry (TG-MS-FTIR) experiments under alternating feeds in order to investigate their potential use for the Chemical Looping Combustion process using either hydrogen or methane as the fuel. The chemical looping reactivity is based on the reversible redox cycle of sulfur from S6+ in La2O2SO4 to S2- in La2O2S and entails a large oxygen storage capacity, but it generally requires high temperatures to proceed, challenging material stability and durability. Herein we demonstrate a remarkable improvement of lattice oxygen availability and activity during the reduction step obtained by cost-effective metal doping in the order Co > Mn > Cu. Notably, the addition of Co or Mn has shown a significant beneficial effect to prevent the decomposition of the oxysulfate releasing SO2, which is identified as the main cause of progressive deactivation for the unpromoted La2O2SO4.
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页数:15
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