4.7 Article

Insights into the corrosion of sulfidated microscale zero valent iron in the presence of benzoic acid: Inhibited oxidation capacity and promoted zinc immobilization

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2022.108950

关键词

Sulfidation; Microscale zero valent iron; Oxygen activation; Iron dissolution; Adsorption capacity

资金

  1. Scientific Research Fund of Zhejiang Provincial Education Department [Y202248895]
  2. China Postdoctoral Science Foundation Project [2022M712819]
  3. Key R&D Program of Zhejiang Province [2019C03G2051340]
  4. National Natural Science Foundation of China [41877357, 42077290]

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This study investigated the oxidation and adsorption capacity of zero valent iron (ZVI) and the effects of sulfidation on these processes. The results showed that sulfidation reduced the oxidation capacity of ZVI, while sulfidated ZVI exhibited enhanced heavy metal immobilization. This is valuable for assessing the oxidation capacity of sulfidated ZVI and heavy metal immobilization in wastewater treatment.
Under oxic environment, the corrosion of zero valent iron (ZVI) connects with its oxidation and adsorption capacity, but little is known about the effects of sulfidation on those processes of ZVI. To assess the oxidant production from ball-milling unsulfidated and sulfidated microscale ZVI (mZVI(bm) and S-mZVI(bm)), the transformation of benzoic acid (BA) to p-hydroxybenzoic acid (p-HBA) was used as the oxidation probe reaction. During the oxidation reaction, the concentration of p-HBA in S-mZVI(bm)/O-2 systems rapidly reached equilibrium (< 12 mu M) within 40 min regardless of sulfur loading content, whereas it could gradually reach 26 mu M in mZVIbm/O-2 system within 240 min despite the slower generation of p-HBA at initial stage. Combining with the characteristic analysis, the lower oxidation capacity of S-mZVI(bm)/O-2 system might be ascribed to the enhanced Fe(II) dissolution that caused a larger solution pH rise along with the loss of Fe(0) and FeSx sites and the formation of lepidocrocite, which was not beneficial for oxygen activation. Under the identical conditions such as material dosage and co-existing anions, the oxidation capacity of mZVI(bm)/O-2 system also exceeded S-mZVI(bm)/O-2 system. In addition, the comparative experiment of Zn2+ immobilization by S-mZVI(bm) and S-mZVI(bm) with or without BA was investigated. mZVI(bm) showed insignificant Zn2+ immobilization, whereas BA could enhance Zn2+ immobilization by S-mZVIbm due to the enhanced corrosion that could provide more adsorption sites. Overall, this work is valuable for assessing the oxidation capacity of S-mZVI(bm)/O-2 system and BA effect on heavy metal immobilization of S-mZVI in wastewater treatment.

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