Could Sulfidation Enhance the Long-Term Performance of Nano-Zero Valent Iron in the Peroxymonosulfate Activation to Degrade Pcb1?

硫化 零价铁 纳米- 期限(时间) 零(语言学) 降级(电信) 化学 化学工程 材料科学 冶金 复合材料 工程类 有机化学 硫黄 物理 吸附 电信 语言学 哲学 量子力学
作者
Weijian Xu,Jin Zhang,Tao Xu,Xinyi Hu,Chaofeng Shen,Liping Lou
出处
期刊:Social Science Research Network [Social Science Electronic Publishing]
标识
DOI:10.2139/ssrn.4183197
摘要

Sulfidation can enhance the hydrophobicity of nano-zero valent iron (nZVI) and improve its long-term degradation performance in reduction technology. However, whether sulfidation can enhance its long-term performance in sulfate radical-based advanced oxidation processes hasn’t been systematically studied. Herein sulfide-modified nZVI (S-nZVI) was prepared by different sulfidation methods and S/Fe ratios. The behavior of S-nZVI on the peroxymonosulfatec (PMS) activation to degrade PCB1 for continuous 5 rounds was investigated. The results showed that sulfidation couldn’t always promote the long-term degradation performance. S-nZVI prepared by one-step sulfidation method with high S/Fe ratio (7%, 14%) exhibited inferior degradation performance than unmodified nZVI (52.2%). This was because that the electron donor Fe0 was consumed rapidly and the iron oxides accumulated on the surface, thus inhibited PMS activation. In contrast, S-nZVI prepared by post-sulfidation method (S-nZVIpost) with high S/Fe ratio exhibited more Fe0 residual, less iron oxides accumulation, and more catalytic Fe2+ regeneration. Consequently, S-nZVIpost exhibited superior degradation capacity (69.3%). Moreover, the radical quenching experiments revealed that the primary free radicals involved in the degradation were transformed from SO4•- to •OH with prolongation of the degradation. Additionally, Fe (IV) contributed to the degradation through non-radical mechanism, especially in the S-nZVIpost-7%/PMS system.
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