A survey of organic contaminants in household and bottled drinking waters in Kuwait

Chemical analysis of volatile organic compounds (VOCs) and semivolatiles (SVs), including pesticides, was performed on 623 and 568 samples, respectively, of household drinking water, as well as on 113 samples from 71 brands of bottled water available in Kuwaiti markets. The analysis was performed according to United States Environmental Protection Agency (US-EPA) Methods 524.2 and 525.2. Nine VOCs and eight SVs were found in household water. Furthermore, between one and seven of 12 VOCs were detected in 93% of the bottled water brands. All bottled waters were found to be completely free of SVs. Styrene was the main pollutant found in all brands packaged in polystyrene containers of sizes 200-mL and 250-mL, with levels generally higher than the WHO guideline value of 20 µg/L. The levels of styrene, toluene, ethyl benzene and xylenes were found to increase with storage time, which indicates that these VOCs were migrating from the container material. No effect was detected due to changes in the storage temperature. All detected VOCs and SVs in household and bottled waters, except styrene, were found at concentrations much lower than those established as safe by WHO guidelines and US-EPA maximum contaminant levels (MCLs), respectively.     

Total selenium concentration in tap and bottled drinking water and coastal waters of Greece

The total selenium concentration in various waters from all over Greece was determined fluorimetrically. The concentration in most of the drinking water, either from the tap or bottled, was within the range 100-200 ng l-1 and showed no great seasonal fluctuations. Most Greeks receive 0.2-0.4 micrograms selenium per day from drinking water. Coastal surface water contains 100-250 ng Se l-1, while higher concentrations are found at locations regarded as polluted.     

饮用水水质标准与水系传染病

介绍了世界卫生组织 ( WHO)、欧盟 ( EC)和美国环保局 ( USEPA)所制订的饮用水水质标准的特点 ,指出了我国饮用水水质标准与这三部标准的差距与不足 .着重对饮用水标准中微生物指标的确定进行了讨论 ,指出了病原微生物 (如沙门氏菌、霍乱弧菌、军团菌、脊髓灰质炎病毒、隐孢子虫及贾第虫等 )所引起的一些水系传染病 ,介绍了控制原生动物的几项有效措施 .     

Removal of antimony(V) and antimony(III) from drinking water by coagulation-flocculation-sedimentation (CFS)

Antimony occurs widely in the environment as a result of natural processes and human activity. Although antimony is similar to arsenic in chemical properties and toxicity, and a pollutant of priority interest to the USEPA and the EU, its environmental behaviors, control techniques, and even solution chemistry, are yet barely touched. In this study, antimony removal from drinking water with coagulation-flocculation-sedimentation (CFS) is comprehensively investigated with respect to the dependence of both Sb(III) and Sb(V) removal on the initial contaminant-loading level, coagulant type and dosage, pH and interfering ions. The optimum pH for Sb(V) removal with ferric chloride (FC) was observed at pH 4.5-5.5, and continuously reduced with further pH increase. Over a broad pH range from 4.0 to 10.0, effective Sb(III) removal with FC was obtained. Contrary to the effective Sb removal with FC, the degree of both Sb(III) and Sb(V) removal with aluminum sulfate (AS) was very low, indicating the impracticability of AS application for antimony removal. The presence of phosphate and humic acid (HA) markedly impeded Sb(V) removal, while exhibited insignificant effect on Sb(III) removal. The effects of coagulant type, Sb species and pH are more pronounced than the effects of coagulant dose and initial pollutant concentration. After preliminarily excluding the possibility of precipitation and the predominance of coprecipitation, the adsorption mechanism is used to rationalize and simulate Sb/FC coagulation with good result by incorporating diffuse-layer model (DLM).     

The quality of groundwater in Bahrain

The quality of groundwater and house tap water throughout the State of Bahrain has been investigated with respect to pH, salinity, conductivity, bicarbonate, chloride, sulfate, sodium, potassium, magnesium, calcium, nitrite, nitrate, ammonia and phosphate. Groundwater showed elevated levels for salinity, chloride, sulfate, sodium and magnesium, with ranges of 1.40-9.30 ppt, and 110-4407, 239-1385, 247-2165, and 36-313 mg l-1, respectively. These values increased from western Bahrain reaching maximum values along the southeastern coastal zone. Nitrate concentration ranged from 1.3 to 23.3 mg l-1 with an average value of 4.4 mg l-1. The results of the study indicate deterioration of groundwater in localized areas. In the case of tap water, the observed ranges for salinity, chloride and sodium were 0.7-1.5 ppt, and 280-750 and 140-400 mg l-1, respectively. The quality of tap water was assessed by comparing values with WHO guidelines.     

Nitrate intake from drinking water on Tenerife island (Spain)

Although meat and vegetable products contain higher concentrations of nitrate, drinking water is the fastest and most direct form of nitrate consumption by the population. It becomes contaminated with nitrates when sea water infiltrates fresh water aquifers and when rain and irrigation water wash through soils that have been excessively treated with nitrated fertilizers. Nitrates are of great toxicological interest as they are involved in the origin of nitrites and nitrosamines and the development of metahaemoglobinaemia in infants. The objective of this study was to determine the quantities of NO(3)(-) in the water supply of each of the Island's municipalities and in the leading brands of bottled waters consumed by the population of Tenerife. This parameter is necessary for the determination of Acceptable Daily Intake (A.D.I.) of nitrates from drinking water. With one unremarkable exception, the nitrate levels found in the water analyzed were optimum for human consumption and amply complied with current European Legislation.     

Electrochemical degradation of 1,2- dichloroethane (DCA) in a synthetic groundwater medium using stainless-steel electrodes

The electrochemical degradation of 1,2-dichloroethane (DCA) was examined in a synthetic groundwater medium. An undivided electrolytic reactor constructed with 304 L-type stainless-steel plate electrodes was employed in all experiments. The removal of total organic carbon (TOC) content during the electrolysis of DCA was experimentally examined. Stainless-steel plate electrodes were effective in degrading DCA under experimental conditions including varying initial concentrations, chloride concentrations, electrolyte conductivities and applied current densities. A half-life method demonstrated TOC removal followed zero-order kinetics under the experimental conditions examined. Chlorides concentration and applied current affected the TOC removal rates. An increase in current density increased the rate of TOC removal but caused a reduction in mineralization current efficiency. Increase in electrolyte conductivity had no effect on TOC removal rates but it decreased the energy consumption by reducing the cell voltage. Reaction temperature was shown to affect the TOC removal and was modeled by the Arrhenius equation.     

Trace and ultratrace metals in bottled waters: survey of sources worldwide and comparison with refillable metal bottles

Bottled waters from diverse natural and industrial sources are becoming increasingly popular worldwide. Several potentially harmful trace metals (Ag, Be, Li, Ge, Sb, Sc, Te, Th, U) are not monitored regularly in such waters. As a consequence, there is extremely limited data on the abundance and potential health impacts of many potentially toxic trace elements. Containers used for the storage of bottled waters might also increase trace metal levels above threshold limits established for human consumption by the EPA or WHO. Applying strict clean room techniques and sector field ICP-MS, 23 elements were determined in 132 brands of bottled water from 28 countries. In addition, leaching experiments with high purity water and various popular metal bottles investigated the release of trace metals from these containers. The threshold limits for elements such as Al, Be, Mn and U in drinking water were clearly exceeded in some waters. Several bottled waters had Li concentrations in the low mg/L range, a level which is comparable to blood plasma levels of patients treated against manic depression with Li-containing drugs. The rate of release of trace metals from metal bottles assessed after 13 days was generally low, with one exception: Substantial amounts of both Sb and Tl were released from a commercially available pewter pocket flask, exceeding international guidelines 5- and 11-fold, respectively. Trace metal levels of most bottled waters are below guideline levels currently considered harmful for human health. The few exceptions that exist, however, clearly reveal that health concerns are likely to manifest through prolonged use of such waters. The investigated coated aluminium and stainless steel bottles are harmless with respect to leaching of trace metals into drinking water. Pocket flasks, in turn, should be selected with great care to avoid contamination of beverages with harmful amounts of potentially toxic trace metals such as Sb and Tl.     

The influence of the abandoned Kalecik Hg mine on water and stream sediments (Karaburun,Izmir, Turkey)

This study covers the geochemical investigations on water and stream sediments to evaluate the influence from the abandoned Kalecik Hg mine. The groundwater samples (S5, S8, S9, WW10) are neutral, slightly alkaline waters which have pH values varying between 7.3 and 7.5. Electrical conductivity (EC) values of groundwaters for spring samples are low (250-300 microS/cm). However, groundwater obtained from a deep well has a higher EC value of 950 microS/cm. Hg concentrations of groundwater samples vary between 0.01 and 0.13 microg/l. Hg concentrations of other water samples taken from mining area from surface waters and adits are between 0.10 and 0.99 microg/l. Adit water (A4) collected at the mine has the highest Hg content of 0.99 microg/l and a pH of 4.4. Trace element concentrations of mine water samples show variable values. As is observed only in MW1 (310 microg/l). A4 was enriched in Cd, Co and Cr and exceed the Turkish drinking water standards (Türk Standartlari Enstitüsü, 1997). Cu concentrations vary between 6.0 and 150 microg/l and are below the Turkish water standards. Mn concentrations in mine waters are between 0.02 and 4.9 mg/l. Only for sample A4 Mn value (4.9 mg/l) exceeds the standard level. Ni was enriched for all of the mine water samples and exceeds the safe standard level (20 microg/l) for drinking water. Of the major ions SO(4) shows a notable increase in this group reaching 650 mg/l that exceeds the drinking water standards. Stream sediment samples have abnormally high values for especially Hg and As, Sb, Ni, Cr metals. With the exception of sample Ss6 of which Hg concentration is 92 mg/kg, all the other samples have Hg contents of higher than 100 mg/kg. Pollution index values are significantly high and vary between 69 and 82 for stream sediment samples.     

Microscale fluctuation assay coupled with Sep-PakR concentration as a rapid and sensitive method for screening mutagens in drinking water

A sensitive short-term mutagenicity test, the microscale fluctuation test has been coupled with a concentration method based on adsorption on Sep-Pak^R C₁₈ cartridges as a method for screening drinking water mutagens. Comparison with XAD-2 concentration method showed that Sep-Pak adsorbed 5 times higher quantity of organics but was slightly less efficient for adsorbing TOX.Microscale fluctuation test was found to be more sensitive than Ames test by testing known direct-acting mutagens and concentrates of drinking water. Samples derived from conventional treatment including chlorination from eight surface water supplies in Norway were concentrated at pH 2 by adsorption on the disposable columns. The adsorbates were tested at different doses by the microscale fluctuation assay. The mutagenic properties of drinking water samples were also related to total organic carbon (TOC), total organic halogen (TOX) and trihalomethanes (THM) concentrations. Dose-related mutagenic responses were found for all the samples with S. typhimurium TA 100 and TA98 strains without metabolic activation. Good relationship was found between mutagenicity data and TOX and THM results. The method showed to be simple, rapid and suitable for routine screening of mutagens in drinking water.     

Influence of hydronium,sulfate, chloride and other non-carbonate ions on hydrogen generation by anaerobic corrosion of granular cast iron

Permeable reactive barriers are successfully applied for the removal of various contaminants. The concomitant reduction of hydrogen ions and the subsequent formation of hydrogen gas by anaerobic corrosion lead to decreased pore volume filled with water and thus residence times, so called gas clogging. Long term column experiments were conducted to elucidate the impact of ubiquitous water constituents on the formation of hydrogen gas and potential passivation due to corrosion products. The collected gas volumes revealed a relation to the hydronium concentration (pH) but were only slightly increased in the presence of chloride and sulfate and not significantly influenced in the presence of phosphate, silicate, humic acid and ammonium compared to deionized water. Significant gas volumes within the reactive filling were verified by gravimetry. The presence of nitrate completely eliminated hydrogen formation by competition for electrons. Solid phase analyses revealed that neither chloride nor sulfate was incorporated in corrosion products in concentrations above 0.1 weight percent, and they did not alter the formation of mainly magnetite in comparison to deionized water.     

阴离子交换膜生物反应器反硝化性能的研究

考察了进水硝酸盐浓度对阴离子交换膜生物反应器反硝化性能的影响。试验结果表明,当进水NO3-为47.01～168.55mg/L时,流动池出水中的NO3-N浓度满足我国生活饮用水水质标准中小于10mg/L的要求(NO3-≤44.29mg/L)。厌氧生物反应器对硝酸盐具有较高的反硝化性能。流动池出水中的Cl-浓度随着进水NO3-浓度的增加而升高,但出水pH值稳定在6.8左右。出水总有机碳浓度与进水的保持一致,表明其未受到"二次污染"和"微生物污染"。     

Chemical water quality in Thailand and its impacts on the drinking water production in Thailand

In Thailand, surface water and groundwater are the main water sources for tap water and drinking water production. Thirty-six different samples from surface waters from Chao Praya and Mae Klong rivers, tap waters, bottled drinking waters, groundwaters and commercial ice cubes from around the Bangkok area were collected. Water samples were also taken from two waterworks in the Chonburi province. The extensive survey showed that, overall in all water samples investigated, there was only a minor pollution which could be traced back to the analyses performed including amongst others total organic carbon, inorganics and heavy metals, pesticides, organochlorine compounds, volatile organic compounds, surfactants, pharmaceuticals and disinfection by-products. However, whenever organic micropollutants could be detected in surface water, such as, e.g. the herbicide atrazine, they were also present in the tap water produced thereof proving that the present treatment steps are not sufficient for removal of such pollutants. The concentration of disinfection by-products was higher in tap water produced from Chao Praya river than from Mae Klong river. Disinfection by-products were also found in bottled drinking water. Commercial ice cubes contained anionic surfactants and their metabolites at elevated concentrations. The data of this study constitute the first set of homogenous data for the chemical water quality and also aid development of new water quality criteria in Thailand.     

Antimony leaching from polyethylene terephthalate (PET) plastic used for bottled drinking water

Antimony is a regulated contaminant that poses both acute and chronic health effects in drinking water. Previous reports suggest that polyethylene terephthalate (PET) plastics used for water bottles in Europe and Canada leach antimony, but no studies on bottled water in the United States have previously been conducted. Nine commercially available bottled waters in the southwestern US (Arizona) were purchased and tested for antimony concentrations as well as for potential antimony release by the plastics that compose the bottles. The southwestern US was chosen for the study because of its high consumption of bottled water and elevated temperatures, which could increase antimony leaching from PET plastics. Antimony concentrations in the bottled waters ranged from 0.095 to 0.521 ppb, well below the US Environmental Protection Agency (USEPA) maximum contaminant level (MCL) of 6 ppb. The average concentration was 0.195+/-0.116 ppb at the beginning of the study and 0.226+/-0.160 ppb 3 months later, with no statistical differences; samples were stored at 22 degrees C. However, storage at higher temperatures had a significant effect on the time-dependent release of antimony. The rate of antimony (Sb) release could be fit by a power function model (Sb(t)=Sb 0 x[Time, h]k; k=8.7 x 10(-6)x[Temperature ( degrees C)](2.55); Sb 0 is the initial antimony concentration). For exposure temperatures of 60, 65, 70, 75, 80, and 85 degrees C, the exposure durations necessary to exceed the 6 ppb MCL are 176, 38, 12, 4.7, 2.3, and 1.3 days, respectively. Summertime temperatures inside of cars, garages, and enclosed storage areas can exceed 65 degrees C in Arizona, and thus could promote antimony leaching from PET bottled waters. Microwave digestion revealed that the PET plastic used by one brand contained 213+/-35 mgSb/kg plastic; leaching of all the antimony from this plastic into 0.5L of water in a bottle could result in an antimony concentration of 376 ppb. Clearly, only a small fraction of the antimony in PET plastic bottles is released into the water. Still, the use of alternative types of plastics that do not leach antimony should be considered, especially for climates where exposure to extreme conditions can promote antimony release from PET plastics.     

Attenuation of total organic carbon and unregulated trace organic chemicals in U.S. riverbank filtration systems

There is increasing concern regarding the presence of unregulated trace organic chemicals in drinking water supplies that receive discharge from municipal wastewater treatment plants. In comparison to conventional and advanced drinking water treatment, riverbank filtration represents a low-cost and low-energy alternative that can attenuate total organic carbon (TOC) as well as trace organic chemicals (TOrC). This study examined the role of predominant redox conditions, retention time, biodegradable organic carbon, and temperature to achieve attenuation of TOC and TOrC through monitoring efforts at three full-scale RBF facilities in different geographic areas of the United States. The RBF systems investigated in this study were able to act as a reliable barrier for TOC, nitrogen, and certain TOrC. Temperature (seasonal) variation played an important role for the make-up of the river water quality and performance of the RBF systems. Temperatures of less than 10 °C did not affect TOC removal but resulted in diminished attenuation of nitrate and select TOrC.     

Occurrence, oral exposure and risk assessment of volatile organic compounds in drinking water for Izmir

Concentrations of volatile organic compounds (VOCs) were measured in the drinking water in Province of Izmir, Turkey, and associated health risks due to ingestion of these compounds were investigated using population weighted random samples. A total of 100 houses were visited in different districts of Izmir and drinking water samples were collected from consumers' drinking water source. Questionnaires were administered to one participant in each house to determine demographics and drinking water consumption rates. Oral exposure and risks were estimated for each participant and Izmir population by deterministic and probabilistic approaches, respectively. The four trihalomethane (THM) species (i.e., chloroform, bromodichloromethane, dibromochloromethane, and bromoform), benzene, toluene, p-xylene, and naphthalene were the most frequently detected VOCs with concentrations ranging from below detection limit to 35 microg/l. The risk estimates were found to be less than the values reported in the literature with few exceptions. Noncarcinogenic risks attributable to ingestion of VOCs for Izmir population were negligible, whereas the mean carcinogenic risk estimates for bromodichloromethane and dibromochloromethane were above the de minimis level of one in a million (10(-6)). For all VOCs, the concentrations measured in metropolitan area were greater than those in other districts. All THM species were detected in higher concentrations in tap water, whereas nontap water contained more benzene, toluene, p-xylene, and naphthalene. Therefore, the concentrations of the latter four compounds and associated risks increased with increasing income and education level since bottled water was used in larger proportions within these subgroups. The results of this study showed that oral exposure to drinking water contaminants and associated risks may be higher than the acceptable levels even if the concentrations fall below the standards.     

Low concentrations of selenium in stream food webs of eastern Canada

Herbivorous and predatory invertebrates and two species of fish (brook trout and blacknose dace) were collected from 49 streams in New Brunswick, Canada to determine whether concentrations of selenium (Se) in the biota were affected by a point source (a coal-fired power plant), and stream water chemistry (pH, sulphate, conductivity, and total organic carbon), and to determine the trophic transfer of Se through these food webs. Total Se concentrations in the biota were generally low (0.2 to 4.8 μg g^− 1 dry weight) across sites and there was no relationship between distance from the coal-fired power plant and Se concentrations in invertebrates or fishes. Water chemistry was an equally poor predictor of Se concentrations in invertebrates and fish. Trophic position (determined using δ¹⁵N) was a significant predictor of Se concentrations in only five of the stream food webs, and two of these had negative slopes, indicating little or no trophic magnification across most systems; many fishes had lower concentrations than their invertebrate prey and trophic transfer was higher at sites with low invertebrate Se concentrations. Variability in Se concentrations in fishes was explained more by site of capture than microhabitat use within the site (as measured with δ¹³C), suggesting among-site differences in geological sources of Se. Because concentrations were below known toxicity thresholds for fish and other consumers, these results suggest that Se is not an environmental issue in New Brunswick streams that do not receive direct inputs from mining activities.     

A chemical profile of recycled irrigation water in North-East Israel

The use of recycled water for irrigation purposes in agriculture is probably the most effective response to the scarcity of water resources in Israel.Base-line studies of the quality of recycled irrigation water in the Beith Alpha basin (more than 1.2 million cubic meters of recycled water) have been carried out recently.The pH, conductivity and the concentration of the ions K⁺, Na⁺, Mg²⁺, Ca²⁺, PO₄^3?, NO₃^? and Cl^? have been determined. Relationships have been established between the concentrations determined, the conductivity and the sodium adsorption ratio (S.A.R.), these being the well-established criteria for irrigation water quality.Both the chloride content and the conductivity have been demonstrated to be far above the permitted standards for irrigation water in agriculture. Similarly, the S.A.R. was found to be approaching the “red line”.Clearly, these findings reflect the man-made changes in the natural level and distribution of chemical elements in the environment studied.This study should be considered not only as an illustrative case study for the crucial importance of on-going control and assessment of man-made systems in relation to environmental consequences, but also as scientific evidence that the re-use of untreated recycled water for flood-irrigation has its long-term environmental “trade offs”.     

European case studies supporting the derivation of natural background levels and groundwater threshold values for the protection of dependent ecosystems and human health

The EU Water Framework and Groundwater directives stipulate that EU member states have to assess groundwater chemical status by the use of groundwater threshold values derived for the protection of dependent ecosystems and human health. This paper presents a synthesis of main results of 14 European case studies evaluating a methodology for derivation of natural background levels (NBLs) and groundwater threshold values (TVs) proposed by the EU research project "BRIDGE". The 14 investigated groundwater bodies were selected to represent as many aquifer types, climate settings and European ecoregions as possible within the project group that included partners from 17 EU countries. The selected case study sites include transboundary groundwater bodies, EU Pilot River Basins and other important groundwater systems. Some are known to interact with associated ecosystems, while others do not. The proposed method derives groundwater threshold values based on environmental objectives for dependent ecosystems or groundwater "itself" using relevant reference criteria such as natural background levels, environmental quality standards and drinking water standards. Derived groundwater threshold values for dissolved Cl and As applying drinking water standards as examples of reference values, are compared for all 14 case studies. Additionally, more detailed analyses are conducted for the Odense Pilot River Basin and the Vouga River Basin, where groundwater threshold values for N and P and Cl, As, Cd, Ni, Pb, and Zn, respectively, are derived based on environmental objectives and quality standards for groundwater dependent ecosystems. Results demonstrate that the proposed methodology is operational and may be used to protect human health and the environment. Further they show that groundwater threshold values derived from environmental objectives and environmental quality standards for dependent ecosystems in some cases may be significantly lower than drinking water standards, e.g. for nitrate.     

Effects of time and point-of-use devices on arsenic levels in Southeastern Michigan drinking water, USA

Health effects associated with chronic, low-level exposures to arsenic in drinking water (<100 microg/L) remain unclear, in part due to uncertainties in assessing exposure. Drinking water concentrations have been used to assess past exposure to arsenic in epidemiological studies, under the assumption that a single measurement can be used to estimate historical exposure. This study aims to better understand (1) temporal variability in arsenic concentrations in drinking water and (2) the impact of point-of-use (POU) treatment devices on arsenic exposure measurements, and on reliability of the exposure measurement for population-level studies. Multiple drinking water samples were collected at two points in time (an average of fourteen months apart) for 261 individuals enrolled in a case-control study of arsenic exposure and bladder cancer in Michigan. Sources of drinking water included private wells (n = 221), public water supplies (n = 33), and bottled water (n = 7); mean arsenic concentration was highest in private wells (7.28 microg/L) and lowest in bottled water samples (0.28 microg/L). Arsenic concentrations in primary drinking water samples were highly correlated (r = 0.88, p < 0.0001, n = 196), with 3% of the water sources exceeding the United States Environmental Protection Agency's Maximum Contaminant Level (MCL) in one sample but not in the other sample. Measurement reproducibility did not vary by type of POU device (e.g., softener, filter, reverse osmosis system). Arsenic concentrations did differ, however, between samples treated with POU devices and untreated samples taken on the same day. Substantial differences in arsenic concentrations were consistently observed for reverse osmosis systems; other POU devices had variable effects on arsenic concentrations. These results indicate that while a single residential arsenic measurement may be used to represent exposure in this region, researchers must obtain information on changes in water source and POU treatment devices to better characterize population exposures over time.