The removal of nitrobenzene in the zerovalent iron-persulfate (ZVI-PS) system was investigated in this study. During the process of nitrobenzene reduction by pristine ZVI
fast adsorption of nitrobenzene was observed at pHini 3.0 and the removal rate was accelerated with the decrease of initial pH values. The increase of ZVI dosage enhanced the removal effectively and PS added to the system significantly promoted the removal rate of nitrobenzene. The cost of PS added was far less than the increase of counterpart of ZVI dosage to achieve the same removal effect. By XRD characterization of the precipitates after reaction
PS was supposed to enhance nitrobenzene removal by promoting ZVI corrosion and transformation of ZVI corrosion products. By FTIR characterization
it was determined that PS accelerated the nitrobenzene reduction process only
but did not change its reduction pathway. GC-MS results verified that the main product of nitrobenzene reduction by ZVI/ZVI-PS was aniline.
Hydrogenation of nitrobenzene to aniline on amorphous Ni-Mo-P catalysts and mechanism of catalyst deactivation
Research progress on persulfate-based advanced oxidation technology regulated by chelating agents
Research on application of alloy catalysts in electrochemical ammonia synthesis
Boosting persulfate activation via carbon dots-mediated Cu²⁺/Cu⁺ redox cycling under visible light for efficient tetracycline removal
Optimized preparation of carbon black/PTFE composite-modified graphite felt cathode and the mechanism on high-efficiency electrochemical production of H2O2
Related Author
LIU Zili1
2
QIN Zuzeng2
ZHANG Jianjie1
XIE Songru
CHEN Haoyun
YUAN Xingzhong
JIANG Longbo
Related Institution
1School of Chemistry and Chemical Engineering,Guangzhou University
School of Chemistry and Chemical Engineering, Guangxi University
School of Resource and Environment, Hunan University of Technology and Business
Xiang Jiang Laboratory
College of Environmental Science and Engineering, Hunan University