Speciation of trace inorganic contaminants in corrosion scales and deposits formed in drinking water distribution systems

Sequential extractions utilizing the modified Tessier scheme (Krishnamurti et al., 1995) and measurements of soluble and particulate metal released from suspended solids were used in this study to determine the speciation and mobility of inorganic contaminants (As, Cr, V, U, Cd, Ni, and Mn) found in corrosion scales and particles mobilized during hydraulic flushing events. Arsenic, chromium and vanadium are primarily associated with the mobilization-resistant fraction that is resistant to all eluents used in this study and also bound in highly stable crystalline iron oxides. Very low concentrations of these elements were released in resuspension experiments. X-ray absorbance measurements demonstrated that arsenic in the sample with the highest As concentration was dominated by As(V) bound by iron oxides. Significant fractions of uranium and cadmium were associated with carbonate solids. Nickel and manganese were determined to be more mobile and significantly associated with organic fractions. This may indicate that biofilms and natural organic matter in the drinking water distributions systems play an important role in the accumulation and release of these inorganic contaminants.     

Trace inorganics in rural potable water and their correlation to possible sources

Ninety-eight water samples, comprising about 10% of the total sources available to rural homes in Hampton County, South Carolina, were randomly selected and analyzed for inorganic constituents. Chemical contamination is widespread in this area and many people are using substandard quality water.A noticeable number of water samples showed unacceptable levels of arsenic, iron, manganese and mercury. Iron and collodial material were chiefly responsible for turbidity in 19% of the water sources. Acceptable levels of cadmium, chloride, copper, lead, nitrate, phosphate, sodium, total solids and zinc were detected in most of the samples.Statistical analysis indicated that leachings from septic tanks were at least partially responsible for the contamination of shallow water supply sources with nitrate, phosphate, chloride and arsenic. Iron, lead and manganese appear to have come from corrosion of antiquated plumbing in older homes.     

Distribution of 23 elements in the kidney,liver and lungs of workers from a smeltery and refinery in north Sweden exposed to a number of elements and of a control group

The levels of antimony, arsenic, cadmium, caesium, chromium, cobalt, copper, gold, iron, lanthanum, lead, manganese, mercury, molybdenum, phosphorus, rubidium, scandium, selenium, silver, tellurium, tin, tungsten and zinc in the kidney, liver and lungs of autopsy specimens from exposed workers in North Sweden, as well as from a control group, have been assayed quantitatively. The workers had been exposed to several elements and their compounds, e.g. lead, mercury, arsenic and cadmium, for long periods in arsenic, lead or selenium plants and in a lead or copper smelter.The chemical analysis was by neutron activation analysis and atomic absorption spectrophotometry.Median levels of antimony, arsenic, cadmium, chromium, cobalt, lanthanum, lead or selenium in kidney, liver or lungs in the exposed worker group were found to be about 2 to 16 times as great as the corresponding levels for the control group. Long biological half-life values were observed for these elements, especially in lung tissue.     

Effects of blending of desalinated water with treated surface drinking water on copper and lead release

This study examined effects of desalinated water on the corrosion of and metal release from copper and lead-containing materials. A jar test protocol was employed to examine metal release from copper and lead-tin coupons exposed to water chemistries with varying blending ratios of desalinated water, alkalinities, pHs and orthophosphate levels. Increasing fractions of desalinated water in the blends resulted in non-monotonic changes of copper and lead release, with generally lower metal concentrations in the presence of desalinated water, especially when its contribution increased from 80% to 100%. SEM examination showed that the increased fractions of desalinated water were associated with pronounced changes of the morphology of the corrosion scales, likely due to the influence of natural organic matter. This hypothesis was corroborated by the existence of correlations between changes of the ζ-potential of representative minerals (malachite and hydrocerussite) and metal release. For practical applications, maintaining pH at 7.8 and adding 1 mg/L orthophosphate as PO₄ were concluded to be adequate to decrease copper and lead release. Lower alkalinity of desalinated water was beneficial for blends containing 50% or more desalinated water.     

Effects of gamma-sterilization on DOC, uranium and arsenic remobilization from organic and microbial rich stream sediments

Organic-rich sediments are known to be effective accumulators for uranium and arsenic. Much is known about the capacity for metal or metalloid fixation by microbes and organic compounds as well as inorganic sediment particles. Experiments investigating the effect of microbes on the process of metal fixation in sediments require sterilized sediments as control treatment which is often realized by gamma-sterilization. Only few studies show that gamma-sterilization has an effect on the remobilization of metal and metalloids and on their physico-chemical properties. These studies deal with sediments with negligible organic content whereas almost nothing is known about organic-rich sediments including a probably high microbial activity. In view of this, we investigated the effect of gamma-sterilization of organic-rich sediments on uranium and arsenic fixation and release. After ten days within an exposure experiment we found a significant higher remobilization of uranium and arsenic in sterile compared to unsterile treatments. In line with these findings the content of dissolved organic carbon (DOC), manganese, and iron increased to even significantly higher concentration in the sterile compared to unsterile treatment. Gamma-sterilization seems to change the physico-chemical properties of organic-rich sediments. Microbial activity is effectively eliminated. From increased DOC concentrations in overlaying water it is concluded that microbes are eventually killed with leaching of cellular compounds in the overlaying water. This decreases the adsorption capacity of the sediment and leads to enhanced uranium and arsenic remobilization.     

An investigation of trace element losses during lyophilization of marine biological samples

Trace element losses during lyophilization of selected macroalgae and marine flesh tissues were investigated. No significant losses (p > 0.1) of arsenic, cadmium, copper, iron, mercury, manganese, nickel, lead, selenium, tin and zinc were found. Significant losses of chromium (3–15%) occurred from several specimens. An all-glass freeze drying apparatus is also illustrated.     

陶瓷地理标志产品微量元素迁移量检测研究

利用电感耦合等离子体质谱仪对20种陶瓷地理标志产品中的砷、镉、铬、镍、铅、锑、锌、铜、锰等9种微量元素迁移量情况进行检测。结果显示,镉、铬、锑在20种地理标志产品陶瓷中均未检出;铅、锌、铜、锰迁移量在有釉瓷（陶）器的多数种类中检出,其中锌迁移量突出;砷、镍迁移量在无釉陶器中检出。     

Displacement of five metals sorbed on kaolinite during treatment with modified Fenton's reagent

The displacement of sorbed metals during the treatment of soils and groundwater with modified Fenton's reagent was investigated using five common metal contaminants (cadmium, copper, lead, nickel, and zinc) and kaolinite as a model sorbent. Modified Fenton's conditions included three H(2)O(2) concentrations (0.9, 1.8, 2.7 M) and two catalysts: soluble iron (III) at pH 3 and iron (III)-NTA chelate at pH 6. Iron (III)-catalyzed Fenton's reactions released significant amounts of zinc, cadmium, and copper. Modified Fenton's reactions catalyzed by iron (III)-NTA released zinc, cadmium, copper, and lead, and resulted in greater amounts of metals release than the iron (III)-catalyzed reactions. Metals release may have been mediated by transient oxygen species, such as superoxide, generated by propagation reactions, which become dominant at the relatively high hydrogen peroxide concentrations used. Metals release from kaolinite was undetectable when sufficiently low hydrogen peroxide concentrations were maintained to minimize propagation reactions. These results indicate that using dilute concentrations of hydrogen peroxide for Fenton's ISCO may minimize potential metals mobility when treating contaminated soils and groundwater containing a mixture of organic and metal contaminants.     

Secondary effects of anion exchange on chloride, sulfate, and lead release: systems approach to corrosion control

Water treatment processes can cause secondary changes in water chemistry that alter finished water quality including chloride, sulfate, natural organic matter (NOM), and metal release. Hence, the goal of this research was to provide an improved understanding of the chloride-to-sulfate mass ratio (CSMR) with regards to chloride and sulfate variations at full-scale water treatment plants and corrosion potential under simulated premise plumbing conditions. Laboratory corrosion studies were conducted using Pb-Sn solder/Cu tubing galvanic cells exposed to model waters with low (approx. 5 mg/L Cl⁻ and 10 mg/L SO₄^2-) and high (approx. 50 mg/L Cl⁻ and 100 mg/L SO₄^2-) concentrations of chloride and sulfate at a constant CSMR of ∼0.5. The role of NOM during corrosion was also evaluated by changing the type of organic material. In addition, full-scale sampling was conducted to quantify the raw water variability of chloride, sulfate, and NOM concentrations and the changes to these parameters from magnetic ion exchange treatment. Test conditions with higher concentrations of chloride and sulfate released significantly more lead than the lower chloride and sulfate test waters. In addition, the source of NOM was a key factor in the amount of lead released with the model organic compounds yielding significantly less lead release than aquatic NOM.     

Heavy metal and arsenic content in seabirds affected by the Prestige oil spill on the Galician coast (NW Spain)

Seabirds are top consumers in marine foodchains which offer opportunities to detect and assess the toxicological effects of different inorganic elements on the marine ecosystem. In order to provide baseline data concerning trace element levels in seabird species from NW Spain, zinc, copper, arsenic, chromium, lead, cadmium and mercury concentrations were analyzed in liver of three different seabird species (common guillemot, Atlantic puffin and razorbill) affected by the Prestige oil spill in September 2002 on the Galician coast. In general, with the exception of mercury, levels of all the analyzed elements were similar or lower in comparison with those reported for the same species in other Atlantic areas, and did not exceed levels indicative of increased environmental exposure.     

Records and sources of metal pollutants in a dated Loch Lomond sediment core

Lead, zinc, copper, chromium, arsenic and cadmium were measured in a sediment core from southern Loch Lomond for which ²¹⁰Pb dating indicated a sedimentation rate of 22±2 mg/cm²/yr corresponding to a mean accumulation rate of 0.36 mm/yr.While copper and chromium were enriched to only a minor extent, the lead, zinc, arsenic and cadmium concentrations were markedly enhanced in upper sections. Increasing anthropogenic input associated with industrial activity centred on Glasgow seems responsible for the vertical distribution of lead, zinc and cadmium but a high 0–1 cm level of arsenic (474 μg/g), strongly correlated with enhanced iron content in the surface oxidising layer of sediment, appears attributable to post-depositional diagenetic mobilisation and upward migration in the reducing zone of the sediment column.Leaching, using CH₃CO₂H/NH₂OH·HCl, released over 90% and 80% of the common metal pollutants, lead and zinc, from surface sediment. Onset of an approximately tenfold increase in lead and zinc concentrations above “background” levels of 13±2 μg/g and 47±13 μg/g to upper section levels of 140–170 μg/g and 450–460 μg/g respectively was placed at late-18th century, in accord with the records of the commencement of significant industrial activity in the Glasgow area. Current anthropogenic fluxes (μg/cm² /yr) of lead (2.51±0.34) and zinc (8.84±1.20) to the sediment are in agreement with recent atmospheric deposition data for the adjoining Clyde Sea Area.The general concordance between anthropogenic metal fluxes to Loch Lomond sediment and atmospheric deposition fluxes endorses the potential usefulness of Loch Lomond sediment data to the resolution of pollution sources in the adjoining sea lochs and firth of the Clyde Sea Area, illustrated here through consideration of the comparative distribution of chromium in relation to its historical use.     

The fate and transport of mercury, methylmercury, and other trace metals in Chesapeake Bay tributaries

Six tributaries to the Chesapeake Bay were analyzed for suspended particulate matter, dissolved organic carbon, particulate organic carbon, mercury, methylmercury, lead, nickel, zinc, cadmium, chromium, and copper. This study examined the importance of flow regime, suspended particulate concentration, and watershed characteristics on the transport of mercury, methylmercury, and other trace metals. Total mercury concentrations were higher under high flow conditions which is consistent with the tendency of this metal to bind strongly to particulate matter. Methylmercury showed less flow rate dependence. Nickel, lead, and zinc concentrations responded strongly to flow rate on the Potomac River, while weaker correlations were found on the other rivers sampled. Cadmium, copper, and chromium concentrations were the least influenced by flow. Partition coefficients calculated in this study were similar to those of other estuaries and overall decreased in the order of Hg > Ni-MMHg > Cr-Pb-Zn > Cd > Cu. Watershed yield estimates and associated retention factors were calculated for the various rivers. These calculations showed that for most of the rivers, mercury was the most strongly retained within the watershed.     

Effect of domestic effluents on groundwater quality: A case study

In order to evaluate the effects of seeping septic effluents on the quality of groundwater in a watershed, a number of contaminants such as nitrate, phosphorus, chloride, lead, copper, iron, and manganese, were studied. To determine the extent of contamination, a network of observation wells was established in the drainage area of the septic systems. Groundwater samples from the observation wells were collected in the spring, summer and fall of 1981, 1982 and 1983. The samples were extracted for the determination of various contaminants by standard methods.The results indicated that nitrate, phosphorus, and chloride were coming from septic systems and were moving into groundwater. Nitrate and chloride levels were less than the maximum allowable limits in drinking water, whereas phosphorus was above the limits in 41% of the wells. According to the data obtained, the concentrations of iron and manganese were above the recommended levels in 27 and 50% of the wells, respectively. The concentrations of lead and copper were below the allowable maximum levels in drinking water. The results indicate contamination of groundwater in the study area with phosphorus, which could be attributed to domestic use of detergents, and iron and manganese, which could be attributed to corrosion of household pipes.     

Metal concentration in cocoa seeds shell ash,liquid effluent,soil sediments and associated plants in a cocoa processing industry in Nigeria

Levels of iron, zinc, manganese, copper, tin, aluminium, magnesium, sodium, potassium, lead, arsenic, chromium, cadmium, titanium and calcium were determined in cocoa seeds shell ash, liquid effluent, soil sediments and associated plants (kokoyam and cassava parts) using an atomic absorption spectrophotometer from a cocoa processing industry located at Akure along the Akure–Owo express road, Ondo State, Nigeria. The soil sediments metals were more highly concentrated than the corresponding values in the liquid effluent; both samples showed evidence of metal bioaccumulation. The toxic trace metals determined were mostly above the permissible safe levels. Plants should not be planted along the effluent channel to avoid plant bioaccumulation of toxic metals.     

Addressing corrosion control and valve tuberculation in a water distribution system supplied by a silica-laden groundwater

Metal corrosion and valve tuberculation within a water distribution system supplied by groundwater containing 52 mg/L silica were studied using a corrosion test rack installed within a residence to determine the effectiveness of phosphate-based (PB) and silica-based (SB) corrosion inhibitor (CI). Results indicated that internal corrosion control based on the use of phosphate-based or silica-based CIs did not significantly decrease iron, lead, or copper corrosion rates, and in one case, caused a negative impact on copper corrosion rate. Evaluations of metal coupons using scanning electron microscopy, electron dispersive X-ray analysis, and X-ray photoelectron spectrophotometry confirmed these findings. Since CI failed to reduce corrosion rates, valve tuberculation within the water system could not be controlled. Consequently, a valve replacement plan was developed in place of an internal corrosion control method using CIs. An opinion of probable replacement cost for 200 tuberculated valves approximated $3.3 million expended over 20 years.     

Trace element analysis of Cretan wines and wine products

The object of this research is to investigate the ways and the degree of contamination of Cretan grapes from the area of Chania and their alcoholic products, with the elements aluminium, arsenic, cadmium, copper, chromium, iron, lead, manganese, nickel and zinc. Fifteen samples of grapes were collected and used for the production of experimental wines from rinsed and unrinsed grapes. A microwave furnace was used for the digestion and dissolution of the experimental wines, the precipitates that originated in these wines, as well as the wines of the corresponding producers. The analyses of all mentioned samples as well as 34 local alcoholic distillates were performed using total reflection X-ray fluorescence and graphite furnace atomic absorption spectrometry. The concentrations for all the elements that were determined were almost in all cases, well below the maximum permissible levels by the Greek and the European Union legislation.     

Distribution and mobility of chromium, copper, and arsenic in soils collected near CCA-treated wood structures in Korea

Chromated copper arsenate (CCA) is currently the most commonly used wood preservative in Korea. Questions, however, have been raised regarding the potential environmental impacts of metal leaching from CCA-treated wood to soil. Although a number of researchers from other countries have reported that chromium, copper, and arsenic do leach from CCA-treated wood over time, to date few field studies have been performed on those metals in soils adjacent to CCA-treated wood structures in Korea. The present study was conducted to determine the lateral and vertical distributions and accumulation of chromium, copper, and arsenic in soils collected from CCA-treated wood structures. A total of fifty-five composite soil samples were collected from four CCA-treated wood structures of approximately one year in age. The samples were analyzed for physicochemical properties as well as for the total chromium, copper, and arsenic concentrations. The chromium, copper, and arsenic concentrations in soil samples adjacent to the structures were as high as 79.0, 98.9, and 128 mg/kg, respectively, compared to background soil samples (48.2, 26.9, and 6.27 mg/kg, respectively). Arsenic was more mobile in soil than chromium and copper. The concentration gradient of arsenic in soil was observed only to the depth of approximately 5 cm in one year of outdoor exposure, whereas chromium and copper apparently remained near the surface (approximately less than 1 cm) after their release. Future efforts should be made to observe seasonal impacts on the release of metals and incorporate metal speciation into determining more detailed mobility and distribution.     

Elemental composition at different points of the rainwater harvesting system

Entry of contaminants, such as metals and non-metals, into rainwater harvesting systems can occur directly from rainfall with contributions from collection surfaces, accumulated debris and leachate from storage systems, pipes and taps. Ten rainwater harvesting systems on the east coast of Australia were selected for sampling of roof runoff, storage systems and tap outlets to investigate the variations in rainwater composition as it moved throughout the system, and to identify potential points of contribution to elemental loads. A total of 26 elements were screened at each site. Iron was the only element which was present in significantly higher concentrations in roof runoff samples compared with tank tap samples (P < 0.05). At one case study site, results suggested that piping and tap material can contribute to contaminant loads of harvested rainwater. Increased loads of copper were observed in hot tap samples supplied by the rainwater harvesting system via copper piping and a storage hot water system (P < 0.05). Similarly, zinc, lead, arsenic, strontium and molybdenum were significantly elevated in samples collected from a polyvinyl chloride pipe sampling point that does not supply household uses, compared with corresponding roof runoff samples (P < 0.05). Elemental composition was also found to vary significantly between the tank tap and an internal cold tap at one of the sites investigated, with several elements fluctuating significantly between the two outlets of interest at this site, including potassium, zinc, manganese, barium, copper, vanadium, chromium and arsenic.These results highlighted the variability in the elemental composition of collected rainwater between different study sites and between different sampling points. Atmospheric deposition was not a major contributor to the rainwater contaminant load at the sites tested. Piping materials, however, were shown to contribute significantly to the total elemental load at some locations.     

Heavy metals in the lagos lagoon sediments

Concentrations of cadmium, cobalt, copper, chromium, iron, manganese, nickel, lead and zinc were determined in surface sediments of the Lagos Lagoon, Nigeria. The results revealed largely anthropogenic heavy metal enrichment and implicated urban and industrial wastes and runoff water transporting metals from land‐derived wastes, as the sources of the enrichment. Higher levels (F < 0.05) of cadmium, iron, manganese, nickel and zinc occurred in sediment samples collected near industrialized‐urban areas than in those from unindustrialized‐rural areas only in the wet season. While iron constituted about 1% of dry sediment by weight, the other metals were present in trace amounts.     

Comparison of coagulation performance and floc properties using a novel zirconium coagulant against traditional ferric and alum coagulants

Coagulation in drinking water treatment has relied upon iron (Fe) and aluminium (Al) salts throughout the last century to provide the bulk removal of contaminants from source waters containing natural organic matter (NOM). However, there is now a need for improved treatment of these waters as their quality deteriorates and water quality standards become more difficult to achieve. Alternative coagulant chemicals offer a simple and inexpensive way of doing this. In this work a novel zirconium (Zr) coagulant was compared against traditional Fe and Al coagulants. The Zr coagulant was able to provide between 46 and 150% lower dissolved organic carbon (DOC) residual in comparison to the best traditional coagulant (Fe). In addition floc properties were significantly improved with larger and stronger flocs forming when the Zr coagulant was used with the median floc sizes being 930 μm for Zr; 710 μm for Fe and 450 μm for Al. In pilot scale experiments, a similar improved NOM and particle removal was observed. The results show that when optimised for combined DOC removal and low residual turbidity, the Zr coagulant out-performed the other coagulants tested at both bench and pilot scale.