TY - JOUR
T1 - A green and robust solid catalyst facilitating the magnesium sulfite oxidation in the magnesia desulfurization process
AU - Wang, Lidong
AU - Qi, Tieyue
AU - Wu, Siyu
AU - Zhang, Shihan
AU - Qi, Dan
AU - Xiao, Huining
N1 - Publisher Copyright:
© 2017 The Royal Society of Chemistry.
PY - 2017
Y1 - 2017
N2 - Oxidation of magnesium sulfite is a crucial step in the wet magnesia desulfurization process. In this study, a green and robust solid catalyst, a SBA-15 (SBA, Santa Barbara Amorphous)-supported cobalt catalyst, was developed to promote the oxidation of sulfite. Both Co(iii) and Co(ii) served as the active sites for the oxidation of sulfite and were mainly located in the inner pore of the SBA-15. The lattice defects formed via the reduction of Co(iii) to Co(ii) and the dispersion of cobalt played an important role in the catalytic activity. Excess loadings of cobalt resulted in the blockage of the pore and hence decreased the catalytic activity of the catalyst. The catalytic mechanism of sulfite oxidation by this solid catalyst was also proposed. Sulfite was oxidized by the active site, such as Co(iii) and Co(ii), and the spent catalyst was in situ regenerated by oxygen. Therefore, the diffusion of oxygen into the pore is important to sustain the catalytic activity of the catalyst. Even after four cycles of catalyst reclamation, the catalytic activity was still comparable with that of the aqueous Co2+ counterpart, indicating that the catalyst is robust and efficient. In addition, no leakage of cobalt from the catalyst was detected, implying that it is a green catalyst without risks of secondary pollution. This study is expected to aid in the development of a green and robust catalyst for reclaiming the desulfurization byproduct and downsizing the absorber.
AB - Oxidation of magnesium sulfite is a crucial step in the wet magnesia desulfurization process. In this study, a green and robust solid catalyst, a SBA-15 (SBA, Santa Barbara Amorphous)-supported cobalt catalyst, was developed to promote the oxidation of sulfite. Both Co(iii) and Co(ii) served as the active sites for the oxidation of sulfite and were mainly located in the inner pore of the SBA-15. The lattice defects formed via the reduction of Co(iii) to Co(ii) and the dispersion of cobalt played an important role in the catalytic activity. Excess loadings of cobalt resulted in the blockage of the pore and hence decreased the catalytic activity of the catalyst. The catalytic mechanism of sulfite oxidation by this solid catalyst was also proposed. Sulfite was oxidized by the active site, such as Co(iii) and Co(ii), and the spent catalyst was in situ regenerated by oxygen. Therefore, the diffusion of oxygen into the pore is important to sustain the catalytic activity of the catalyst. Even after four cycles of catalyst reclamation, the catalytic activity was still comparable with that of the aqueous Co2+ counterpart, indicating that the catalyst is robust and efficient. In addition, no leakage of cobalt from the catalyst was detected, implying that it is a green catalyst without risks of secondary pollution. This study is expected to aid in the development of a green and robust catalyst for reclaiming the desulfurization byproduct and downsizing the absorber.
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U2 - 10.1039/c7ta01513e
DO - 10.1039/c7ta01513e
M3 - Article
AN - SCOPUS:85021958607
SN - 2050-7488
VL - 5
SP - 8018
EP - 8028
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 17
ER -