Doré E, Deshommes E, Laroche L, Nour S, Prévost M. Lead and copper release from full and partially replaced harvested lead service lines: Impact of stagnation time prior to sampling and water quality. Water Research 2018 Dec 3;150:380-391. doi: 10.1016/j.watres.2018.11.076.
Partial lead service line replacement (PLSLR) results in the addition of a new galvanic connection and can increase lead concentrations at the tap. Focus has been given to minimizing lead release after PLSLR, but little information is available on the impact of lead remedial actions on copper concentrations, especially before passivation occurs. The impact of water quality (decreased chloride-to-sulfate mass ratio from 0.9 to 0.3; addition of orthoP; pH increase to 8.3) on lead and copper concentrations was investigated after stagnation (30 min-336 h) in a pipe rig comparing full lead service line (LSL), and two configurations of partial LSLs (Cu-Pb and Pb-Cu). Results show different trends for lead and copper: maximum lead concentrations were reached in 16 h while copper concentrations continued to increase over 336 h. Lead release rates were also the highest in the first 16 h of stagnation and were strongly impacted by water quality and the configuration of PLSLR (Cu-Pb vs Pb-Cu). Increasing the sampling flow rate from 5 to 15 LPM drastically increased the particulate lead release (78-fold) in Pb-Cu configurations; this effect was however not observed in 100% Pb or Cu-Pb configurations. High velocity flushing prior to 16 h stagnation decreased total Pb release by a factor of 12-fold for Cu-Pb, 1.6-fold for Pb-Cu and 2.0-fold for 100% Pb. Results support the definition of sampling protocols targeted for the detection of lead and copper sources and the proscription of flushing prior to sampling.
Hu J, Dong H, Xu Q, Ling W, Qu J, Qiang Z. Impacts of water quality on the corrosion of cast iron pipes for water distribution and proposed source water switch strategy. Water research. 2017 Oct 31;129:428-435. doi: 10.1016/j.watres.2017.10.065.
Switch of source water may induce “red water” episodes. This study investigated the impacts of water quality on iron release, dissolved oxygen consumption (ΔDO), corrosion scale evolution and bacterial community succession in cast iron pipes used for drinking water distribution at pilot scale, and proposed a source water switch strategy accordingly. Three sets of old cast iron pipe section (named BP, SP and GP) were excavated on site and assembled in a test base, which had historically transported blended water, surface water and groundwater, respectively. Results indicate that an increasing Cl– or SO42- concentration accelerated iron release, but alkalinity and calcium hardness exhibited an opposite tendency. Disinfectant shift from free chlorine to monochloramine slightly inhibited iron release, while the impact of peroxymonosulfate depended on the source water historically transported in the test pipes. The ΔDO was highly consistent with iron release in all three pipe systems. The mass ratio of magnetite to goethite in the corrosion scales of SP was higher than those of BP and GP and kept almost unchanged over the whole operation period. Siderite and calcite formation confirmed that an increasing alkalinity and hardness inhibited iron release. Iron-reducing bacteria decreased in the BP but increased in the SP and GP; meanwhile, sulfur-oxidizing, sulfate-reducing and iron oxidizing bacteria increased in all three pipe systems. To avoid the occurrence of “red water”, a source water switch strategy was proposed based on the difference between local and foreign water qualities.
Jereb G, Poljšak B, Eržen I. Contribution of Drinking Water Softeners to Daily Phosphate Intake in Slovenia. International journal of environmental research and public health. 2017 Oct 6;14(10). pii: E1186. doi: 10.3390/ijerph14101186.
The cumulative phosphate intake in a typical daily diet is high and, according to several studies, already exceeds recommended values. The exposure of the general population to phosphorus via drinking water is generally not known. One of the hidden sources of phosphorus in a daily diet is sodium polyphosphate, commonly used as a drinking water softener. In Slovenia, softening of drinking water is carried out exclusively within the internal (household) drinking water supply systems to prevent the accumulation of limescale. The aim of the study was to determine the prevalence of sodium phosphates in the drinking water in Slovenia in different types of buildings, to determine residents’ awareness of the presence of chemical softeners in their drinking water, and to provide an exposure assessment on the phosphorus intake from drinking water. In the current study, the presence of phosphates in the samples of drinking water was determined using a spectrophotometric method with ammonium molybdate. In nearly half of the samples, the presence of phosphates as water softeners was confirmed. The measured concentrations varied substantially from 0.2 mg PO4/L to 24.6 mg PO4/L. Nearly 70% of the respondents were not familiar with the exact data on water softening in their buildings. It follows that concentrations of added phosphates should be controlled and the consumers should be informed of the added chemicals in their drinking water. The health risks of using sodium polyphosphate as a drinking water softener have not been sufficiently investigated and assessed. It is highly recommended that proper guidelines and regulations are developed and introduced to protect human health from adverse effects of chemicals in water intended for human consumption.
Vargas IT, Fischer DA, Alsina MA, Pavissich JP, Pastén PA, Pizarro GE.
Copper Corrosion and Biocorrosion Events in Premise Plumbing. Materials (Basel, Switzerland). 2017 Sep 5;10(9). pii: E1036. doi: 10.3390/ma10091036.
Corrosion of copper pipes may release high amounts of copper into the water, exceeding the maximum concentration of copper for drinking water standards. Typically, the events with the highest release of copper into drinking water are related to the presence of biofilms. This article reviews this phenomenon, focusing on copper ingestion and its health impacts, the physicochemical mechanisms and the microbial involvement on copper release, the techniques used to describe and understand this phenomenon, and the hydrodynamic effects. A conceptual model is proposed and the mathematical models are reviewed.
Stets EG, Lee CJ, Lytle DA, Schock MR. Increasing chloride in rivers of the conterminous U.S. and linkages to potential corrosivity and lead action level exceedances in drinking water. Sci Total Environ. 2017 Jul 25. pii: S0048-9697(17)31822-3. doi: 10.1016/j.scitotenv.2017.07.119.
Corrosion in water-distribution systems is a costly problem and controlling corrosion is a primary focus of efforts to reduce lead (Pb) and copper (Cu) in tap water. High chloride concentrations can increase the tendency of water to cause corrosion in distribution systems. The effects of chloride are also expressed in several indices commonly used to describe the potential corrosivity of water, the chloride-sulfate mass ratio (CSMR) and the Larson Ratio (LR). Elevated CSMR has been linked to the galvanic corrosion of Pb whereas LR is indicative of the corrosivity of water to iron and steel. Despite the known importance of chloride, CSMR, and LR to the potential corrosivity of water, monitoring of seasonal and interannual changes in these parameters is not common among water purveyors. We analyzed long-term trends (1992-2012) and the current status (2010-2015) of chloride, CSMR, and LR in order to investigate the short and long-term temporal variability in potential corrosivity of US streams and rivers. Among all sites in the trend analyses, chloride, CSMR, and LR increased slightly, with median changes of 0.9mgL-1, 0.05, and 0.01, respectively. However, urban-dominated sites had much larger increases, 46.9mgL-1, 2.50, and 0.53, respectively. Median CSMR and LR in urban streams (4.01 and 1.34, respectively) greatly exceeded thresholds found to cause corrosion in water distribution systems (0.5 and 0.3, respectively). Urbanization was strongly correlated with elevated chloride, CSMR, and LR, especially in the most snow-affected areas in the study, which are most likely to use road salt. The probability of Pb action-level exceedances (ALEs) in drinking water facilities increased along with raw surface water CSMR, indicating a statistical connection between surface water chemistry and corrosion in drinking water facilities. Optimal corrosion control will require monitoring of critical constituents reflecting the potential corrosivity in surface waters.
Trueman BF, Sweet GA, Harding MD, Estabrook H, Bishop DP, Gagnon GA. Galvanic Corrosion of Lead by Iron (Oxyhydr)oxides: Potential Impacts on Drinking Water Quality. Environmental science and technology. 2017 May 30. doi: 10.1021/acs.est.7b01671.
Lead exposure via drinking water remains a significant public health risk; this study explored the potential effects of upstream iron corrosion on lead mobility in water distribution systems. Specifically, galvanic corrosion of lead by iron (oxyhydr)oxides was investigated. Coupling an iron mineral cathode with metallic lead in a galvanic cell increased lead release by 531 µg L-1 on average-a nine-fold increase over uniform corrosion in the absence of iron. Cathodes were composed of spark plasma sintered Fe3O4 or α-Fe2O3 or field-extracted Fe3O4 and α-FeOOH. Orthophosphate immobilized oxidized lead as insoluble hydroxypyromorphite, while humic acid enhanced lead mobility. Addition of a humic isolate increased lead release due to uniform corrosion by 81 µg L-1 and-upon coupling lead to a mineral cathode-release due to galvanic corrosion by 990 µg L-1. Elevated lead in the presence of humic acid appeared to be driven by complexation, with 208Pb and UV254size-exclusion chromatograms exhibiting strong correlation under these conditions (R2average = 0.87). A significant iron corrosion effect was consistent with field data: lead levels after lead service line replacement were greater by factors of 2.3 – 4.7 at sites supplied by unlined cast iron distribution mains compared with the alternative, lined ductile iron.
Baig SA, Lou Z, Baig MA, Qasim M, Shams DF, Mahmood Q, Xu X. Assessment of tap water quality and corrosion scales from the selected distribution systems in northern Pakistan. Environ Monit Assess. 2017 Apr;189(4):194. doi: 10.1007/s10661-017-5907-5.
Corrosion deposits formed within drinking water distribution systems deteriorate drinking water quality and resultantly cause public health consequences. In the present study, an attempt was made to investigate the concurrent conditions of corrosion scales and the drinking water quality in selected water supply schemes (WSS) in districts Chitral, Peshawar, and Abbottabad, northern Pakistan. Characterization analyses of the corrosion by-products revealed the presence of α-FeOOH, γ-FeOOH, Fe3O4, and SiO2 as major constituents with different proportions. The constituents of all the representative XRD peaks of Peshawar WSS were found insignificant as compared to other WSS, and the reason could be the variation of source water quality. Well-crystallized particles in SEM images indicated the formation of dense oxide layer on corrosion by-products. A wider asymmetric vibration peak of SiO2 appeared only in Chitral and Abbottabad WSS, which demonstrated higher siltation in the water source. One-way ANOVA analysis showed significant variations in pH, turbidity, TDS, K, Mg, PO4, Cl, and SO4 values, which revealed that these parameters differently contributed to the source water quality. Findings from this study suggested the implementation of proper corrosion prevention measures and the establishment of international collaboration for best corrosion practices, expertise, and developing standards.