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Characteristics of zero-valent iron surface oxide films under the catalytic interface reactions by assisting ligands in nitrate-contaminated groundwater.

作者信息

Zhang Wen, Qi Liang, Li Ling, Guo Chengchen, Xiao Liwen

机构信息

Zhejiang University of Water Resources and Electric Power, No. 508, 2nd Street, Qiantang District, Hangzhou 310018, Zhejiang Province, China.

School of Engineering, Westlake University, Hangzhou 310024, China.

出版信息

J Hazard Mater. 2024 Jul 5;472:134433. doi: 10.1016/j.jhazmat.2024.134433. Epub 2024 Apr 29.

DOI:10.1016/j.jhazmat.2024.134433
PMID:38718503
Abstract

The surface passivation layer coating on zero-valent iron (ZVI) particles impedes the electron transfer from ZVI to nitrate. To enhance the efficiency of nitrate reduction by Fe(0), we tested the chemical process and the thickness of the iron oxide film on the surface of Fe(0) particles, utilizing Fe in aqueous solution and wheat straw as ligands. A novel principal surface catalyzing reaction was formulated as follows: [Formula: see text] . When Fe concentration increased from 0 - 200 mg·L, the NO removal rate increased from 6.95% to 82.6% respectively during 12 h and it was 48%, 72%, 79% and 94% respectively in Fe/WS ratio of 0, 0.25, 0.5 and 1 system. Uniform surface iron oxide films formed around the Fe(0) particles within 12 h after the adding Fe or wheat straw to the Fe(0) system. The composition and thickness of these films were dependent on the quantity of added materials. X-ray diffraction (XRD) analysis revealed that surface oxide iron mainly consisted of Fe or Fe oxides, with FeO being predominant. The X-ray photoelectron spectroscopy (XPS) etching indicated that the addition of Fe(0)/straw at mass ratios of 1 or system with 20 mg·L Fe resulted in the thinnest surface iron oxide layer. The study demonstrated that reducing the oxide layer's thickness was achieved through partial catalysis and enhanced complexation capacity. This reduction was facilitated by the introduction of Fe or wheat straw into the Fe(0) system, potentially improving proton dissociation and promoting the ligand-assisted dissolution of Fe oxides.

摘要

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