4.5 Article

Effects of residual disinfectants on the redox speciation of lead(ii)/(iv) minerals in drinking water distribution systems

Journal

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ew00706d

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Funding

  1. U.S. National Science Foundation CAREER Program [CBET- 1653931]
  2. University of California Multicampus Research Programs and Initiatives award [MRP-17-455083]
  3. Department of Education GAANN Fellowship [P200A180038]
  4. National Institute of Health [T32 ES018827]

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This study investigated the reaction kinetics of lead(ii) minerals oxidation by free chlorine and free bromine in drinking water distribution systems. The results showed that the oxidation by bromine was orders of magnitude faster than chlorine. The addition of phosphate significantly inhibited lead(ii) mineral oxidation by chlorine, but had only modest effects in the presence of bromide.
This study investigated the reaction kinetics on the oxidative transformation of lead(ii) minerals by free chlorine (HOCl) and free bromine (HOBr) in drinking water distribution systems. According to chemical equilibrium predictions, lead(ii) carbonate minerals, cerussite PbCO3(s) and hydrocerussite Pb-3(CO3)(2)(OH)(2(s)), and lead(ii) phosphate mineral, chloropyromorphite Pb-5(PO4)(3)Cl-(s) are formed in drinking water distribution systems in the absence and presence of phosphate, respectively. X-ray absorption near edge spectroscopy (XANES) data showed that at pH 7 and a 10 mM alkalinity, the majority of cerussite and hydrocerussite was oxidized to lead(iv) mineral PbO2(s) within 120 minutes of reaction with chlorine (3 : 1 Cl-2 : Pb(ii) molar ratio). In contrast, very little oxidation of chloropyromorphite occurred. Under similar conditions, oxidation of lead(ii) carbonate and phosphate minerals by HOBr exhibited a reaction kinetics that was orders of magnitude faster than by HOCl. Their end oxidation products were identified as mainly plattnerite beta-PbO2(s) and trace amounts of scrutinyite alpha-PbO2(s) based on X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS) spectroscopic analysis. A kinetic model was established based on the solid-phase experimental data. The model predicted that in real drinking water distribution systems, it takes 0.6-1.2 years to completely oxidize Pb(ii) minerals in the surface layer of corrosion scales to PbO2(s) by HOCl without phosphate, but only 0.1-0.2 years in the presence of bromide (Br-) due the catalytic effects of HOBr generation. The model also predicts that the addition of phosphate will significantly inhibit Pb(ii) mineral oxidation by HOCl, but only be modestly effective in the presence of Br-. This study provides insightful understanding on the effect of residual disinfectant on the oxidation of lead corrosion scales and strategies to prevent lead release from drinking water distribution systems.

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