RESUMEN
Pipe scales in drinking water distribution systems (DWDS) potentially adsorb chromium (Cr). Meanwhile, the fate of Cr in pipe scales and water could be influenced by the disinfectants used in DWDS since they might influence the valence state of Cr. Therefore, the adsorption of Cr (Cr(VI) and Cr(III)) on pipe scales, the transformation between different valence states, and the effects of disinfectants present in DWDS are important research topics for improving tap water quality but have not yet been sufficiently investigated. This study investigated the properties of layered pipe scales and conducted adsorption kinetic experiments in single and binary Cr(VI) and Cr(III) systems, as well as experiments related to the oxidation and adsorption of Cr(III) under the influence of decaying disinfectants. According to the results, pipe scales exhibited distinct layered structures with varying mechanisms for the adsorption of Cr(VI) and Cr(III). Cr(VI) was adsorbed through surface complexation on the surface and porous core layers, while redox reactions predominantly occurred on the shell-like layer. Furthermore, Cr(III) was adsorbed via surface precipitation on the three-layer pipe scales. Importantly, disinfectants promoted the transformation of Cr(III) to the less readily released Cr(VI) in pipe scales, reducing the Cr exposure risk from the pipe scale phase. Pipe scales also decreased the Cr(VI) concentration in water (almost 0 mg/L), enhancing the safety of DWDS. This study provides theoretical guidance on the safe operation of DWDS.
RESUMEN
Metal contaminants in corrosion products of drinking water distribution systems (DWDS) can be released into potable water under specific conditions, thereby polluting drinking water and posing a health risk. Under stagnation conditions, the release characteristics, occurring forms, and environmental risks of ten metals were determined in loose and tubercle scale solids of an unlined cast iron pipe with a long service history, before and after immersion. Most Al, As, Cr, Fe, and V in corrosion scales existed in the residual fraction, with the released concentration and pollution risk being low. Since more than 59% of Ca in pipe scales existed in the exchangeable fraction, Ca release was high. Although the Pb and Cd content of corrosion solids was low, a high proportion of Pb and Cd was present in non-residual fractions with high mobility. Sudden severe Pb or Cd pollution events in DWDS could result in high pollution and environmental risk levels. The total content and released amount of Mn and Zn in corrosion scales were both high. Therefore, while special attention should be paid to Mn and Zn, Pb and Cd also present a high risk in pipe scales, despite their low concentrations. During stagnation immersion, metal release from powdered pipe scales occurred via the processes of mass release, re-adsorption into scales, and slow release until equilibrium was reached. The levels of metal re-adsorption into scales were much higher than the concentrations dissolved into bulk water. However, the amount of metal re-adsorption into tubercle scale blocks was less. Importantly, these findings highlight that during DWDS operation, the sudden release of metal pollutants caused by pipe scale breakage should be avoided.