Efficient Atrazine Degradation through ZnFe2O4-Catalyzed Peroxymonosulphate Activation

Author:

Gao Junyi1,zhao xuying2,Li Caibin1,Luo Zhenbao1,long Zhang1,Xiao Zhipeng3,Mu Tingting3,Liu Furong2,Gao Ruikang2,Zhang Jiguang2,Sun Xiwen1

Affiliation:

1. Bijie Tobacco Branch Company of Guizhou Province

2. Chinese Academy of Agricultural Sciences

3. Hengyang Tobacco Company of Hunan Province

Abstract

Abstract

Atrazine (ATZ) is widely used as an herbicide in agricultural production. However, its extensive application results in contaminated residues that can adversely affect ecosystems because rainwater washes them into and contaminates water bodies. Therefore, there is a pressing need to remove ATZ from the aquatic environment. Using transition metals as catalysts for the persulfate degradation of organic pollutants has received much attention because of their strong ability to oxidize pollutants, including ATZs, and their selectivity for these pollutants. A novel technique for ATZ removal using a catalyst (ZnFe2O4) to activate peroxymonosulfate (PMS) was developed in this study . The ZnFe2O4 catalyst was prepared through co-precipitation, which involves the doping of zinc in iron-based materials. And this process accelerated the redox cycle, which energized the PMS and promoted the generation of free radicals. Electron paramagnetic resonance analysis revealed that ZnFe2O4 activates PMS and generates SO4-, HO•, O2-, and 1O2 to eliminate ATZ. In this study, a new approach is proposed for the development of efficient heterogeneous catalysts capable of activating PMS and eliminating the ATZ. Moreover, The ATZ degradation pathway was proposed based on the products identified by UPLC-MS. The results highlighted the efficiency of the as-prepared ZnFe2O4 catalyst in ATZ removal and its excellent performance. Given its environmentally friendly and efficient performance, The ZnFe2O4 catalyst has significant potential implications for agricultural environmental remediation.

Publisher

Research Square Platform LLC

Reference33 articles.

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