Publications by authors named "Daniel E Giammar"

Lead(IV) oxide (PbO) is an important component of the scale in many lead pipes used for water supply. Promoting conditions that maintain its stability could be an effective method for limiting lead release. In this study, we applied a method that combined electrochemical and free chlorine conditioning to form PbO scales on coupons.

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Anthropogenic and biogenic ligands may mobilize uranium (U) from tetravalent U (U(IV)) phases in the subsurface, especially from labile noncrystalline U(IV). The rate and extent of U(IV) mobilization are affected by geochemical processes. Competing metals and humic substances may play a decisive role in U mobilization by anthropogenic and biogenic ligands.

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The dynamics of Pb(II) at mineral surfaces affect its mobility in the environment. Pb(II) forms inner- and outer-sphere complexes on mineral surfaces, and this adsorbed pool often represents a large portion of the bioaccessible Pb in contaminated soils. To assess the lability of this potentially reactive adsorbed Pb(II) pool at metal oxide surfaces, we performed Pb(II) isotope exchange measurements between dissolved Pb(II) enriched in Pb and natural isotopic abundance Pb(II) adsorbed to rutile at pH 5, 6, and 7.

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Lead(IV) oxide (PbO) is one of the lead corrosion products that forms on the inner surface of lead pipes used for drinking water supply. It can maintain low dissolved Pb(II) concentrations when free chlorine is present. When free chlorine is depleted, PbO and soluble Pb(II) will co-occur in these systems.

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Microbial reduction of soluble hexavalent uranium (U(VI)) to sparingly soluble tetravalent uranium (U(IV)) has been explored as an strategy to immobilize U. Organic ligands might pose a potential hindrance to the success of such remediation efforts. In the current study, a set of structurally diverse organic ligands were shown to enhance the dissolution of crystalline uraninite (UO) for a wide range of ligand concentrations under anoxic conditions at pH 7.

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Adsorption and subsequent reduction of U(VI) on Fe(II)-bearing clay minerals can control the mobility of uranium in subsurface environments. Clays such as montmorillonite provide substantial amounts of the reactive surface area in many subsurface environments, and montmorillonite-containing materials are used in the storage of spent nuclear fuel. We investigated the extent of reduction of U(VI) by Fe(II)-bearing montmorillonite at different pH values and sodium concentrations using X-ray absorption spectroscopy and chemical extractions.

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Phosphate addition is commonly applied as an effective method to remediate lead contaminated sites via formation of low solubility lead phosphate solids. However, subsequent transport of the lead phosphate particles may impact the effectiveness of this remediation strategy. Hence, this study investigates the mechanisms involved in the aggregation of lead phosphate particles and their deposition in sand columns as a function of typical water chemistry parameters.

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The stability of RNA in aqueous systems is critical for multiple environmental applications including evaluating the environmental fate of RNA interference pesticides and interpreting viral genetic marker abundance for wastewater-based epidemiology. In addition to biological processes, abiotic reactions may also contribute to RNA loss. In particular, some metals are known to dramatically accelerate rates of RNA hydrolysis under certain conditions (i.

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Removing dissolved selenium (i.e., selenate and selenite) from wastewater is a challenging issue for a range of industries.

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A local preschool installed NSF/ANSI 42 and 53 certified point-of-use (POU) filters in its classroom sinks and drinking fountains to protect children from the possibility of elevated lead (Pb) levels in drinking water. We examined the effects of these filters during flowing water and immediately following stagnation periods on Pb, chlorine, and bacterial concentrations in the field and the laboratory. Before and after typical school stagnation periods, we collected samples from filtered classroom sinks, a filtered drinking fountain and nearby unfiltered sinks for a year.

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Lead oxide (PbO) has the lowest solubility with free chlorine among Pb corrosion products, but depletion of free chlorine or a switch from free chlorine to monochloramine can cause its reductive dissolution. We previously reported that Cu(II) and Zn(II) inhibited PbO reductive dissolution within 12 h. Here, we expanded on this work by performing longer duration experiments and further exploring the underlying mechanisms.

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Adsorption of uranium onto goethite is an important partitioning process that controls uranium mobility in subsurface environments, for which many different surface complexation models (SCMs) have been developed. While individual models can fit the data for which they are parameterized, many perform poorly when compared with experimental data covering a broader range of conditions. There is an imperative need to quantitatively evaluate the variations in the models and to develop a more robust model that can be used with more confidence across the wide range of conditions.

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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.

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The effect of sodium silicate addition on lead release from lead service lines (LSLs) was investigated using laboratory-based pipe loop experiments with LSLs harvested from a water utility that has one of the Great Lakes as its source water. The LSLs were first conditioned with a synthetic water similar to that of Buffalo Water that matched the major water chemistry that the pipes had experienced in the field; the one exception was the absence of dissolved organic carbon in the synthetic water. After conditioning, the LSLs were used in tests with the same synthetic water and with sodium silicate added to the water for half of the LSLs.

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The occurrence of aluminum in scales on lead pipes is common. This study aimed to identify factors that influence Al accumulation on oxidized lead surfaces and to determine whether the presence of Al impacts Pb release from corrosion products to water. Al accumulation and Pb release were monitored both with and without the addition of phosphate as a corrosion inhibitor.

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This study explored the ability of orthophosphate addition to limit lead release from lead service lines delivering high pH, low alkalinity water. We built pipe loop reactors with lead pipes harvested from Providence, RI, and we operated them with high pH and low alkalinity water of a composition similar to that in Providence. Orthophosphate addition decreased the release of both dissolved and particulate lead to the water.

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Natural organic matter-iron (NOM-Fe) colloids are ubiquitous at anoxic-oxic interfaces of subsurface environments. Fe(II) or NOM can chemically reduce Cr(VI) to Cr(III), and the formation of Cr(III)-NOM-Fe colloids can control the fate and transport of Cr. We explored the formation and transport of Cr(III)-humic acid (HA)-Fe colloids upon reaction of Cr(VI) with HA-Fe(II) colloids over a range of environmentally relevant conditions.

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The chemical oxidation of dissolved Mn(II) to Mn(III/IV) oxides (MnO) can lead to the accumulation of Mn deposits in drinking water distribution systems. However, Mn(II) oxidation by free chlorine is quite slow under mild conditions (e.g.

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For lead pipes that contain PbO as a major component of their scales, a change in the residual disinfectant from free chlorine to monochloramine can destabilize the PbO and result in dramatic increases in aqueous lead concentrations. Such a scenario occurred in Washington, D.C.

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Surface-functionalized magnetic nanoparticles are promising adsorbents due to their large surface areas and ease of separation after contaminant removal. In this work, the affinity of Cr(VI) adsorption to 8 nm surface-functionalized superparamagnetic magnetite nanoparticles was determined for surface coatings with amine (trimethyloctadecylammonium bromide, CTAB) and carboxyl (stearic acid, SA) functional groups. Cr(VI) adsorbed more strongly to the CTAB-coated nanoparticles than to the SA-coated materials due to electrostatic interactions between positively charged CTAB and anionic Cr(VI) species.

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Dissolved Mn(III) species have recently been recognized as a significant form of Mn in redox transition zones, but their speciation, stability, and reactivity are poorly understood. Besides acting as the intermediate for Mn redox chemistry, Mn(III) can undergo disproportionation producing insoluble Mn oxides and aqueous Mn(II). Using pyrophosphate(PP) as a model ligand, we evaluated the thermodynamic and kinetic stability of Mn(III) complexes.

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