Impacts of orthophosphate-polyphosphate blends on the dissolution and transformation of lead (II) carbonate.

Orthophosphate-polyphosphate blends are commonly used to control lead release into drinking water, but little is known about how they interact with lead corrosion scale. Conventional corrosion control practice assumes that orthophosphate controls lead release by forming insoluble Pb-phosphate minerals, but this does not always occur, and under certain conditions, phosphate blends may increase lead release. Here, we used continuously-stirred tank reactors to compare orthophosphate-polyphosphate blends with orthophosphate on the basis of lead (II) carbonate dissolution and transformation at environmentally relevant phosphate concentrations.

Early phase effects of silicate and orthophosphate on lead (Pb) corrosion scale development and Pb release.

Orthophosphate is widely used to control lead (Pb) release in drinking water distribution systems, but phosphorus addition is not sustainable. Alternative corrosion control treatments are needed, and sodium silicate is one possibility. Here, pre-corroded Pb coupons-with and without free chlorine-were used to examine early-phase corrosion scale development after silicate addition, with orthophosphate as a reference corrosion inhibitor.

Pilot-scale comparison of sodium silicates, orthophosphate and pH adjustment to reduce lead release from lead service lines.

Sodium silicate is thought to mitigate lead release via two mechanisms: by increasing pH and by forming a protective silica film. A pilot-scale study using an excavated lead service line (LSL) fed with water from a Great Lakes source was undertaken to: (1) clearly distinguish the pH effect and the silica effect; (2) compare sodium silicate to orthophosphate and pH adjustment; (3) determine the nature of silica accumulation in the pipe scale. The LSL was cut into segments and acclimated with water at pH 7.

Controlling lead release due to uniform and galvanic corrosion - An evaluation of silicate-based inhibitors.

Silicates have been added to drinking water for decades, both to sequester iron/manganese and as a corrosion control treatment for lead. But the mechanisms by which they might act to limit lead release are not well understood. We evaluated the effects of two silicate formulations on lead release due to uniform and galvanic corrosion over a wide range of pH and dissolved inorganic carbon concentrations.

Impact of sodium silicate on lead release and colloid size distributions in drinking water.

Sodium silicates have been used in drinking water treatment for decades as sequestrants and corrosion inhibitors. For the latter purpose they are poorly understood, which presents a potential public health risk. We investigated a common sodium silicate formulation as a treatment for lead release and compared it to orthophosphate, a well-established lead corrosion control treatment.

Inorganic contaminants in Canadian First Nation community water systems.

While previous Canadian studies have examined microbiological water quality in First Nations, there is little published information on inorganic contaminants. In Atlantic Canada, the lead, manganese, and arsenic content of First Nations' drinking water has been measured for more than a decade, but the data have not been analyzed comprehensively. These contaminants are linked with health problems, and high levels in drinking water are a cause for concern.

Source Water Characteristics and Building-specific Factors Influence Corrosion and Point of Use Water Quality in a Decentralized Arctic Drinking Water System.

Access to clean and safe drinking water is a perpetual concern in Arctic communities because of challenging climatic conditions, limited options for the transportation of equipment and process chemicals, and the ongoing effects of colonialism. Water samples were gathered from multiple locations in a decentralized trucked drinking water system in Nunavut, Canada, over the course of one year. The results indicate that point of use drinking water quality was impacted by conditions in the source water and in individual buildings and strongly suggest that lead and copper measured at the tap were related to corrosion of onsite premise plumbing components.

Manganese Increases Lead Release to Drinking Water.

Lead and manganese are regulated in drinking water due to their neurotoxicity. These elements have been reported to co-occur in drinking water systems, in accordance with the metal-scavenging properties of MnO. To the extent that manganese is a driver of lead release, controlling it during water treatment may reduce lead levels.

Fluorescence Spectra Predict Microcystin-LR and Disinfection Byproduct Formation Potential in Lake Water.

Disinfection byproducts (DBPs) and algal toxins can be expensive to monitor and represent significant potential risks to human health. DBPs, including haloacetic acids and trihalomethanes, are possible or probable human carcinogens. Microcystin-LR-produced by cyanobacteria-is linked with various adverse health effects.

Understanding the Impact of Extracellular Polymeric Substances on Lead Release in Drinking Water Systems.

Lead release in a lead (Pb, anode)-iron oxide (α-FeO, cathode) galvanic system was studied under the influence of synthetic extracellular polymeric substances (sEPS). Sodium alginate, bovine serum albumin (BSA), and cytochrome c represented extracellular polysaccharides, proteins, and electrochemically active components, respectively. Microbiologically influenced corrosion was investigated using sEPS and pelleted and resuspended cells.

Galvanic Corrosion of Lead by Iron (Oxyhydr)Oxides: Potential Impacts on Drinking Water Quality.

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 on average-a 9-fold increase over uniform corrosion in the absence of iron.

Lake Recovery Through Reduced Sulfate Deposition: A New Paradigm for Drinking Water Treatment.

This study examined sulfate deposition in Nova Scotia from 1999 to 2015, and its association with increased pH and organic matter in two protected surface water supplies (Pockwock Lake and Lake Major) located in Halifax, Nova Scotia. The study also examined the effect of lake water chemistry on drinking water treatment processes. Sulfate deposition in the region decreased by 68%, whereas pH increased by 0.

Understanding the Role of Particulate Iron in Lead Release to Drinking Water.

Lead service lines (LSLs) are a major source of drinking water lead, and high iron levels are frequently observed along with elevated lead release. A model distribution system, dosed with orthophosphate, was used to evaluate the effect of corroded iron distribution mains on lead release from recovered LSLs. Lead release was higher by 96 μg L(-1), on average, from LSLs supplied by corroded iron compared to the inert reference material (PVC).

Evaluating the Effects of Full and Partial Lead Service Line Replacement on Lead Levels in Drinking Water.

Lead service line replacement (LSLR) is an important strategy for reducing lead exposure via drinking water, but jurisdictional issues can sometimes interfere with full replacement of the lead line. The effects of full and partial LSLR on lead levels were assessed using 5 × 1-L sample profiles collected at more than 100 single-unit residences. Profiles comprised four sequential standing samples (L1-L4) and a free-flowing sample (L5) drawn after a 5 min flush of the outlet.

A new analytical approach to understanding nanoscale lead-iron interactions in drinking water distribution systems.

High levels of iron in distributed drinking water often accompany elevated lead release from lead service lines and other plumbing. Lead-iron interactions in drinking water distribution systems are hypothesized to be the result of adsorption and transport of lead by iron oxide particles. This mechanism was explored using point-of-use drinking water samples characterized by size exclusion chromatography with UV and multi-element (ICP-MS) detection.