TY - JOUR
T1 - Novel photo-sulfite system
T2 - Toward simultaneous transformations of inorganic and organic pollutants
AU - Guo, Yaoguang
AU - Lou, Xiaoyi
AU - Fang, Changling
AU - Xiao, Dongxue
AU - Wang, Zhaohui
AU - Liu, Jianshe
PY - 2013/10/1
Y1 - 2013/10/1
N2 - An efficient and green advanced oxidation process (i.e., photo-sulfite reaction) for the simultaneous oxidation of sulfite and organic pollutants in water is reported. The photo-sulfite system (UV-Fe(III)-sulfite) is based on the Fe-catalyzed sulfite oxidation and photochemistry of Fe(III) species. SO 4•- and •OH radicals were identified in the photo-sulfite system with radical scavenging experiments using specific alcohols. This novel technology was consistently proven to be more favorable than the alternative Fe(III)-sulfite systems for the degradation of 2,4,6-trichlorophenol (2,4,6-TCP) and other organic pollutants at all conditions tested. The reactivity of photo-sulfite system was sustained due to the spontaneous switch of photoactive species from Fe(III)-sulfito to Fe(III)-hydroxo complexes with the depletion of sulfite and the decrease in pH. In contrast, in the absence of light the performance of the Fe(III)-sulfite system was greatly diminished after the consumption of sulfite. The formation of the Fe(III)-sulfito complex is a necessary step for initiating the photo-sulfite reaction. Inhibition of the oxidation of 2,4,6-TCP and methyl orange (MO) was observed in the presence of ligands that can stabilize one or more of the reactants: Fe(III), Fe(II), or sulfite. Our study provides a new facile route for the generation of SO4•- and simultaneous removal of organic and inorganic pollutants.
AB - An efficient and green advanced oxidation process (i.e., photo-sulfite reaction) for the simultaneous oxidation of sulfite and organic pollutants in water is reported. The photo-sulfite system (UV-Fe(III)-sulfite) is based on the Fe-catalyzed sulfite oxidation and photochemistry of Fe(III) species. SO 4•- and •OH radicals were identified in the photo-sulfite system with radical scavenging experiments using specific alcohols. This novel technology was consistently proven to be more favorable than the alternative Fe(III)-sulfite systems for the degradation of 2,4,6-trichlorophenol (2,4,6-TCP) and other organic pollutants at all conditions tested. The reactivity of photo-sulfite system was sustained due to the spontaneous switch of photoactive species from Fe(III)-sulfito to Fe(III)-hydroxo complexes with the depletion of sulfite and the decrease in pH. In contrast, in the absence of light the performance of the Fe(III)-sulfite system was greatly diminished after the consumption of sulfite. The formation of the Fe(III)-sulfito complex is a necessary step for initiating the photo-sulfite reaction. Inhibition of the oxidation of 2,4,6-TCP and methyl orange (MO) was observed in the presence of ligands that can stabilize one or more of the reactants: Fe(III), Fe(II), or sulfite. Our study provides a new facile route for the generation of SO4•- and simultaneous removal of organic and inorganic pollutants.
UR - https://www.scopus.com/pages/publications/84885100204
U2 - 10.1021/es403199p
DO - 10.1021/es403199p
M3 - 文章
C2 - 24015851
AN - SCOPUS:84885100204
SN - 0013-936X
VL - 47
SP - 11174
EP - 11181
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 19
ER -