Selective reduction of nitrite to nitrogen gas by CO2 anion radical from the activation of oxalate

Nitrite (NO2-) reduction by carbon dioxide anion radical (CO2 center dot-) from the activation of small molecule carboxylic acid was investigated to selectively reduce nitrite to nitrogen gas (N-2). However, the CO2 center dot- generation efficiency from the activation of small molecule carboxylic acid needs to be enhanced to increase the NO2- reduction efficiency. In this study, a novel and promising process for selective NO2- reduction was proposed based on activation of oxalic acid (OA) by UV radiation coupled with Fe3+. In Fe(III)/OA/UV system, the activation of OA by photo-induced electron transfer process of Fe(III)-oxalate complex and by center dot OH radical from the photolysis of Fe3+ or NO2- could promote the generation of CO2 center dot- radical, which enhanced the NO2- reduction. The 100% removal efficiency of NO2-, 94.72% of total nitrogen (TN) and 94.72% of selectivity for N-2 were achieved in Fe(III)/OA/UV/NO2- system, at the Fe3+ dosage of 8 mmol/L, initial pH of 1.70, OA dosage of 16 mmol/L, initial NO2- concentration of 30 mg N/L, and reaction time of 180 min. CO2 center dot- radical played a significant role in the reduction of NO2- by Fe(III)/OA/UV system based on the inhibition experiments in which methyl violet was used as a quenching agent of CO2 center dot- radical. Based on the results from batch experiments and FTIR analysis, the activation mechanism of OA and selective reduction mechanism of NO2- in Fe(III)/OA/UV system was proposed. (C) 2021 Elsevier Ltd. All rights reserved.

Automated summary

A novel process for selective NO2- reduction was proposed based on the activation of oxalic acid by UV radiation coupled with Fe3+, promoting the generation of CO2 center dot- radical to enhance the reduction efficiency. The Fe(III)/OA/UV/NO2- system achieved 100% removal of NO2-, 94.72% of total nitrogen (TN), and 94.72% selectivity for N-2.