4.7 Article

Sulfidation extent of nanoscale zerovalent iron controls selectivity and reactivity with mixed chlorinated hydrocarbons in natural groundwater

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 431, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2022.128534

Keywords

Corrosion; Metallic iron; Remediation; Iron sulfide; Chlorinated ethenes; ethanes and methanes

Funding

  1. Metal-Aid Innovative Training Network (ITN) - European Commission [675219]
  2. Helmholtz Recruiting Initiative [I-044-16-01]
  3. DOE Office of Science [DE-AC02-06CH11357]
  4. Marie Curie Actions (MSCA) [675219] Funding Source: Marie Curie Actions (MSCA)

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This study investigates the reactivity of sulfidated nanoscale zerovalent iron (S-nZVI) when exposed to complex mixtures of chlorinated hydrocarbons (CHCs). The results show that different S-nZVI materials exhibit varying trends in CHC removal, which are influenced by the thickness and crystallinity of the iron sulfide (mackinawite, FeSm) shell. These findings provide important insights for advancing S-nZVI synthesis strategies in specific CHC treatment scenarios.
Sulfidated nanoscale zerovalent iron (S-nZVI) exhibits low anoxic oxidation and high reactivity towards many chlorinated hydrocarbons (CHCs). However, nothing is known about S-nZVI reactivity once exposed to complex CHC mixtures, a common feature of CHC plumes in the environment. Here, three S-nZVI materials with varying iron sulfide (mackinawite, FeSm) shell thickness and crystallinity were exposed to groundwater containing a complex mixture of chlorinated ethenes, ethanes, and methanes. CHC removal trends yielded pseudo-first order rate constants (k(obs)) that decreased in the order: trichloroethene > trans-dicloroethene > 1,1-dichlorethene > trichloromethane > tetrachloroethene > cis-dichloroethene > 1,1,2-trichloroethane, for all S-nZVI materials. These k(obs & nbsp;)trends showed no correlation with CHC reduction potentials based on their lowest unoccupied molecular orbital energies (E-LUMO) but absolute values were affected by the FeSm shell thickness and crystallinity. In comparison, nZVI reacted with the same CHCs groundwater, yielded k(obs) that linearly correlated with CHC E-LUMO values (R-2 = 0.94) and that were lower than S-nZVI k(obs). The CHC selectivity induced by sulfidation treatment is explained by FeSm surface sites having specific binding affinities towards some CHCs, while others require access to the metallic iron core. These new insights help advance S-nZVI synthesis strategies to fit specific CHC treatment scenarios.

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