4.8 Article

Effects of Solution Chemistry on the Dechlorination of 1,2,3-Trichloropropane by Zero-Valent Zinc

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 45, Issue 9, Pages 4073-4079

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/es104081p

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Funding

  1. Strategic Environmental Research and Development Program (SERDP) [ER-1458]
  2. Navy Environmental Sustainability Development to Integration Program (NESDI) [N62583-09-C-0110]
  3. Department of Energy's Office of Biological and Environmental Research

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The reactivity of zerovalent zinc (ZVZ) toward 1,2,3-trichloropropane (TCP) was evaluated under a variety of solution conditions, including deionized water, groundwater, and artificial groundwater, over a pH range of about 6.5-12. In deionized water, first-order rate constants for TCP disappearance (kappa(obs)) exhibit abroad minimum between pH 8 and 10, with increasing kappa(obs) observed at lower and higher pH. The similarity between this trend and zinc oxide (ZnO) solubility behavior suggests pH related changes to the ZnO surface layer strongly influence ZVZ reactivity. Values of kappa(obs) measured in acidic groundwater are similar to those measured in DI water, whereas values measured in alkaline groundwater are much smaller (>1 order of magnitude at pH values >10). Characterization of the surfaces of ZVZ exposed to deionized water, acidic groundwater, and alkaline groundwater suggests that the rates obtained in alkaline groundwater are related to the presence of a morphologically distinct surface film that passivates the ZVZ surface. TCP degradation rates in artificial groundwater containing individual solutes present in groundwater suggest that silicate anions contribute to the formation of this passivating film.

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