| Literature DB >> 30684761 |
Runlong Hao1, Xingzhou Mao2, Zheng Wang3, Yi Zhao4, Tianhao Wang2, Zhonghao Sun2, Bo Yuan2, Yankun Li2.
Abstract
The key step for nitric oxide (NO) removal using oxidation method is to efficiently oxidize NO. This study developed a novel advanced oxidation process (AOP) of ultraviolet light (UV) catalysis of chlorite (NaClO2) to oxidize NO. The production of nitric dioxide (NO2) and photo-production of chlorine dioxide (ClO2) were suppressed by adding ammonium hydroxide (NH4OH). The NO conversion efficiency was 98.1% using UV/NaClO2-NH4OH. Electron spin resonance (ESR) tests confirmed the roles of hydroxyl radical (HO) and oxychloride radical (ClO/Cl2O2) in the oxidation of NO. Kinetics analyses showed that NO flux was significantly enhanced by radical-induced (HO/ClO) oxidation of NO. In the presence of UV, the overall reaction rates (kov1*) were 3-8 times higher than those without UV. The Hatta number, namely the enhanced factor, was calculated in the range of 229-403 and 730-780 corresponding to without and with UV light, suggesting that NO oxidation belonged to fast and/or instantaneous reaction. Thus, the gas-film mass transfer resistance was the rate-determining step. N-containing product was determined as NH4+ and NO3- according to X-ray photoelectron spectroscopy (XPS).Entities:
Keywords: AOP method; Hydroxyl radical; Kinetics; NO removal; Oxychloride radical
Year: 2019 PMID: 30684761 DOI: 10.1016/j.jhazmat.2019.01.042
Source DB: PubMed Journal: J Hazard Mater ISSN: 0304-3894 Impact factor: 10.588