TY - JOUR
T1 - Tuning mZVI surface species through synergistic Sulfur-Graphite incorporation via Mechanochemistry technique for High-Efficiency TCE Dechloridation and electron utilization
AU - Jiang, Wenqiang
AU - Dong, Dianxiao
AU - Zhang, Ling
AU - Zhang, Xiutian
AU - Li, Xingyi
AU - Gu, Yawei
AU - Zhang, Honglei
AU - Liu, Xiaoying
AU - Xiao, Yunyi
AU - Bi, Runze
AU - Hao, Jun
AU - Wu, Haili
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/12/5
Y1 - 2025/12/5
N2 - Zero-valent iron (ZVI) technology has gained significant attention for the in situ dechlorination of trichloroethylene (TCE), a typical organic pollutant commonly found in soils and groundwater. However, ZVI technology faces several critical challenges, such as insufficient reactivity, easy passivation, limited selectivity, and unclear mechanisms. In this study, a ball-milled S&C-mZVIbm material was synthesized by co-incorporation strategy and demonstrated a significant improvement in the degradation efficiency of ZVI. This enhancement occurs alongside a reduction in the hydrogen evolution reaction (HER), thereby increasing the electron selectivity during TCE dechlorination. Through comprehensive characterization techniques, we have shown that the co-incorporation of carbon and sulfur into mZVI results in improved affinity for TCE, accelerated electron transfer, and reduced charge-transfer resistances. The S&C-mZVIbm also exhibited excellent long-term stability, with degradation efficiency higher than 90% even after 12 repeated cycles. The pathway for TCE dichlorination can be precisely adjusted by the S addition, i.e., the addition of S simultaneously promoted the acetylene production by β-elimination and DCEs production by hydrogenolysis, while suppressed the acetylene transformation to other hydrocarbon products. These findings not only advance the development of ZVI-based materials but also broaden their applicability in the remediation of groundwater contaminated with chlorinated hydrocarbons.
AB - Zero-valent iron (ZVI) technology has gained significant attention for the in situ dechlorination of trichloroethylene (TCE), a typical organic pollutant commonly found in soils and groundwater. However, ZVI technology faces several critical challenges, such as insufficient reactivity, easy passivation, limited selectivity, and unclear mechanisms. In this study, a ball-milled S&C-mZVIbm material was synthesized by co-incorporation strategy and demonstrated a significant improvement in the degradation efficiency of ZVI. This enhancement occurs alongside a reduction in the hydrogen evolution reaction (HER), thereby increasing the electron selectivity during TCE dechlorination. Through comprehensive characterization techniques, we have shown that the co-incorporation of carbon and sulfur into mZVI results in improved affinity for TCE, accelerated electron transfer, and reduced charge-transfer resistances. The S&C-mZVIbm also exhibited excellent long-term stability, with degradation efficiency higher than 90% even after 12 repeated cycles. The pathway for TCE dichlorination can be precisely adjusted by the S addition, i.e., the addition of S simultaneously promoted the acetylene production by β-elimination and DCEs production by hydrogenolysis, while suppressed the acetylene transformation to other hydrocarbon products. These findings not only advance the development of ZVI-based materials but also broaden their applicability in the remediation of groundwater contaminated with chlorinated hydrocarbons.
KW - Dechlorination
KW - Electron efficiency
KW - Groundwater
KW - Synergistic effect
KW - Trichloroethylene
KW - Zero-valent iron
UR - http://www.scopus.com/inward/record.url?scp=105006874383&partnerID=8YFLogxK
U2 - 10.1016/j.seppur.2025.133814
DO - 10.1016/j.seppur.2025.133814
M3 - Article
AN - SCOPUS:105006874383
SN - 1383-5866
VL - 375
JO - Separation and Purification Technology
JF - Separation and Purification Technology
M1 - 133814
ER -