Determination of volatile organic compounds pollution sources in malaysian drinking water using multivariate analysis

A field investigation was conducted at all water treatment plants throughout 11 states and Federal Territory in Peninsular Malaysia. The sampling points in this study include treatment plant operation, service reservoir outlet and auxiliary outlet point at the water pipelines. Analysis was performed by solid phase micro-extraction technique with a 100 μm polydimethylsiloxane fibre using gas chromatography with mass spectrometry detection to analyse 54 volatile organic compounds (VOCs) of different chemical families in drinking water. The concentration of VOCs ranged from undetectable to 230.2 μg/l. Among all of the VOCs species, chloroform has the highest concentration and was detected in all drinking water samples. Average concentrations of total trihalomethanes (THMs) were almost similar among all states which were in the range of 28.4--33.0 μg/l. Apart from THMs, other abundant compounds detected were cis and trans-1,2-dichloroethylene, trichloroethylene, 1,2-dibromoethane, benzene, toluene, ethylbenzene, chlorobenzene, 1,4-dichlorobenzene and 1,2-dichloro - benzene. Principal component analysis (PCA) with the aid of varimax rotation, and parallel factor analysis (PARAFAC) method were used to statistically verify the correlation between VOCs and the source of pollution. The multivariate analysis pointed out that the maintenance of auxiliary pipelines in the distribution systems is vital as it can become significant point source pollution to Malaysian drinking water.     

Monitoring the Trihalomethanes Present in Water After Treatment with Chlorine Under Laboratory Condition

In this work assays involving chlorinated water samples, which were previous spiked with humic substances or algae blue green and following the production of the THMs for 30 days is described. To implement the assays, five portions of 1,000 ml of water were stored in glass bottles. The water samples were treated with solutions containing 2, 3, 4 and 5 mg l⁻¹ chlorine. The samples aliquots (60 ml) were transferred into the glass vials, 10 ml were removed to have a headspace and 100 μl of the 10 mg l⁻¹ pentafluortoluene bromide solution was added to each vial. The extraction step was performed by adding 10 g of Na₂SO₄ followed by 5 ml of n-pentane. The vials were stopped with a TFE-faced septum and sealed with aluminum caps. The generated THMs were determined by gas chromatography with electron capture detector using reference solutions with concentration ranging from 8 to 120 μg l⁻¹ THMs. Three assays were monitored during 30 days and chloroform was the predominant compound found in the water samples, while other species of THMs were not detected. The results showed that when the chlorine concentration was increased in water samples containing algae the concentration of THM varied randomly. Nevertheless, in water samples containing humic substances the increase of the THM concentration presented a relationship with the chlorine concentration. It was also observed that chloroform concentration increased with the elapsed time up to one and six days to water samples spiked with humic substances and algae blue green, respectively and decreased along 30 days. By other hand, assays performed using water samples containing decanted algae material showed that THM was not generated by the chlorine addition.     

N-nitrosodimethylamine and trihalomethane formation and minimisation in Southeast Queensland drinking water

This study assesses the prevalence of disinfection by-product (DBP) precursors in some Southeast Queensland drinking water sources by conducting formation potential experiments for the four regulated trihalomethanes (THMs), and the potent carcinogen, N-nitrosodimethylamine (NDMA). NDMA formation potentials were consistently low (<5-21 ng/L), and total THM (tTHM) formation potentials were consistently below the Australian Drinking Water Guideline (250 μg/L). NDMA concentration of finished drinking waters was also monitored and found to be <5 ng/L in all cases. The effect of coagulation and advanced oxidation on the formation of NDMA and THMs is also reported. UV/H(2)O(2) pre-treatment was effective in producing water with very low THMs concentrations, and UV irradiation was an effective method for NDMA degradation. H(2)O(2) was not required for the observed NDMA degradation to occur. Coagulation using alum, ferric chloride or poly(diallyldimethylammonium chloride) (polyDADMAC) was ineffective in removing DBPs precursors from the source water studied, irrespective of the low dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) attained. Rather, coagulation with polyDADMAC caused an increase in NDMA formation potential upon chloramination, and all coagulants led to an increased tTHM formation potential upon chlorination due to the high bromide concentration of the source water studied.     

Reduction of dissolved organic matter in terms of DOC, UV-254, SUVA and THMFP in industrial estate wastewater treated by stabilization ponds

The aim of this research was to monitor the influent and effluent water quality of the aeration, facultative and oxidation water treatment ponds of an industrial estate. This industrial estate, the largest in northern Thailand, has proposed to utilization of reclaimed treated wastewater in their raw water supply so as to cope with the yearly water shortage during the dry season. Water samples were collected four times from four sampling points and evaluated for their dissolved organic matter (DOM) content in terms of dissolved organic carbon (DOC), ultraviolet light absorbance at 254 nm (UV-254), specific ultraviolet absorption (SUVA), trihalomethane formation potential (THMFP) and trihalomethane (THM) species. Average values of DOC, UV-254, SUVA and THMFP in the influent wastewater of 12.9 mg L⁻¹, 0.165 cm⁻¹, 1.29 L mg⁻¹m⁻¹ and 1.24 mg L⁻¹, respectively, were observed. The aeration ponds produced the best results: a 54% reduction of DOC, a 33% reduction of UV-254, and a 57% reduction of THMFP. However, SUVA in the aeration pond effluent showed a moderate increase. The facultative ponds and oxidation ponds did not take part in the reduction of DOC, UV-254, SUVA and THMFP. Average DOC, UV-254, SUVA and THMFP value of the treated wastewater were 5.8 mg L⁻¹, 0.107 cm⁻¹, 1.85 L mg⁻¹m⁻¹ and 468 μg L⁻¹, respectively. Chloroform, at 72.6% of total THMFP, was found to be the predominant THM species.     

Size and resin fractionations of dissolved organic matter and trihalomethane precursors from four typical source waters in China

Dissolved organic matter (DOM) and its potential to form disinfection by-products (DBPs) during drinking water treatment raise challenges to water quality control. Understanding both chemical and physical characteristics of DOM in source waters is key to better water treatment. In this study, the DOM from four typical source waters in China was fractionated by XAD resin adsorption (RA) and ultrafiltration (UF) techniques. The trihalomethane formation potential (THMFP) of all fractions in the DOM were investigated to reveal the major THM precursors. The fraction distributions of DOM could be related to their geographical origins in a certain extent. The dominant chemical fraction as THM precursors in the DOM from south waters (East-Lake reservoir in Shenzhen and Peal rivers in Guangzhou) was hydrophobic acid (HoA). The size fraction with molecular weight (MW) <1 kDa in both south waters had the highest THMFP. The results of cluster analysis showed that the parameters of fractions including DOC percentage (DOC%), UV₂₅₄%, SUVA₂₅₄ (specific UV₂₅₄ absorbance) and THMFP were better for representing the differences of DOM from the studied waters than specific THMFP (STHMFP). The weak correlation between SUVA₂₅₄ and STHMFP for either size or XAD fractions suggests that whether SUVA₂₅₄ can be used as an indicator for the reactivity of THM formation is highly dependent on the nature of organic matter.     

Lead and cadmium concentrations in shorebirds from the Yeongjong Island, Korea

This study presents concentration levels of pollutants (lead, and cadmium) in tissues (livers, kidneys, muscles, and bones) of shorebirds (Kentish Plovers (n = 5), Mongolian Plovers (n = 2), Dunlins (n = 6), Great Knots (n = 10), Terek Sandpipers (n = 10)) from Yeongjong Island, Korea in the East Asian–Australian migration flyways during the autumn migration in 1994–1995. Lead concentrations in livers, in kidneys, in muscles, and in bones were significantly different among shorebird species. Lead concentrations in livers of Kentish Plovers (4.76 ± 2.72 μg/wet g), Mongolian Plovers (2.05 μg/wet g), Dunlins (3.77 ± 1.07 μg/wet g), and Great Knots (4.27 ± 3.19 μg/wet g) were less than the toxic level, and lead concentrations in livers of Terek Sandpipers (1.20 ± 0.94 μg/wet g) were at the background level. Cadmium concentrations in livers, in kidneys, in muscles, and in bones did not vary among shorebirds, and concentrations of cadmium in livers and in kidneys were at background level (respectively, approximate 1 μg/wet g, approximate 2.67 μg/wet g) in all shorebird species. We suggest that interspecific differences of lead and cadmium concentrations were attributed to differences in exposure time and differences of diet, microhabitats in wintering ground. In livers and kidney of shorebirds from Yeongjong Island, lead and cadmium concentrations were higher than other locations previously reported.     

Monitoring of Coliforms and chlorine residual in water distribution network of Rawalpindi, Pakistan

The present study was undertaken to examine the drinking water quality of Rawal Treatment Plant, Rawalpindi and its distribution network by collecting samples from eight different locations. The aim was to determine potential relationship between the presence of microorganisms and chlorine residual in the distribution network. Quantification of chlorine residual, turbidity, standard plate count (SPC), fecal and total coliforms by Most Probable Number (MPN) was performed. Three different forms of chlorine were measured at each sampling station such as free chlorine, residual chlorine, chloramines and total chlorine residual. A critical evaluation of data presented indicated that pH generally ranged from 7.02–7.30; turbidity varied from 0.34–2.79 NTU; conductivity fluctuated from 359–374 μS/cm; and TDS values were found to be ranging between 180–187 mg/l. Station # 7 was found to be most contaminated. The value of total chlorine was found to be 0.86 to1.7 mg/l at Station # 3 and 6, respectively. Highest standard plate count was 62 CFU/ml at Station # 7. Total coliforms were less than 1.1 MPN/100 ml at almost most of the stations except at Station # 3 where it was found to be greater than 23.0 MPN /100 ml. Overall aim of this study is to create awareness about contamination of drinking water in the water distribution networks and to make recommendations to provincial agencies such as EPA, CDA and WASA that regular monitoring should be carried out to ensure that the chlorine residual is available at consumer end.     

Effects of Cadmium (CdCl2) on development and hatching of eggs in European squid (Loligo vulgaris Lamarck, 1798) (Cephalopoda: Loliginidae)

This is the first study related to the effects of cadmium (Cd) on the development and hatching of eggs of Loligo vulgaris. The eggs were exposed to concentrations varying from 10 to 100,000 μg Cd/l for up to 1 month. During the study period natural sea water salinity (37 PSU), ambient temperature (ranging 16.5–21.5°C) and light conditions of 12-h light: 12-h dark for 744-h were used prior to the hatching. For 96-h, mortality rate of 100% of the eggs was found at cadmium concentration of 100,000 μg Cd/l, and the same mortality rate of the eggs were found at 1,000 and 10,000 μg Cd/l for 744-h and 696-h, respectively. Hatching took place between hours 456 and 576 in the control group and between hours 480 and 576 in 10 and 100 μg Cd/l groups. Total hatching rates were calculated to be 98.2 ± 1.6% for control group, 99.4 ± 0.6% for 10 μg Cd/l group and 98.6 ± 1.2% for 100 μg Cd/l group. Hatching successes were estimated as 69.5 ± 13.8% for control group, 84.5 ± 8.2% for 10 μg Cd/l group and 76.9 ± 5.9% for 100 μg Cd/l group. In the 100,000 μg Cd/l treatment, the egg degeneration began from animal pole of the eggs in 16 h, and 50% and 100% of them died in the initial stage at 72-h and 96-h, respectively. In the 10,000 μg Cd/l group, the eggs which reached at stage 19 (IX) were deformed and 50% and 100% of them died at 312-h and 696-h, respectively. In 1,000 μg Cd/l group, however, the eggs developed abnormally from stage 21 (X–XI) and reached at stage 29 (XIX), and 50% and 100% of them died in 624-h and in 744-h, respectively. There were significant differences in survival rates of the eggs among the concentrations (p < 0.05). The current study demonstrated that Cd adversely affects the development, survival and hatching of L. vulgaris eggs; however, no mortality was observed in 10 μg Cd/l and 100 μg Cd/l groups.     

Modeling the Formation of Chlorination By-Products During Enhanced Coagulation

Because of increasing need to balance health risks for pathogen control and disinfection by-products (DBP) formation in drinking water supplies, water utilities are forced to closely examine and optimize their disinfection practices. This research was designed to investigate the effects of independent variables of dissolved organic carbon (DOC), ferric chloride dosage, chlorine dose, and reaction time on trihalomethanes (THMs) formation in Terkos Lake Water (TLW) of Istanbul City. A statistically-based empirical model was developed for predicting THM formation during enhanced coagulation. The R ² and F value of model were 0.762 and 460, respectively. The model was found to be statistically significant for all four variables, and model predictions appear to be most accurate for this study. A multiple linear model exhibited the best fit of data. It was observed that THM formation depended primarily on DOC removal. Model calibration, testing and validation were accomplished by using independent data set.     

Application of a Larval Medaka Assay to Evaluate the Fish Safety Level in Sagami River, Japan

Physico-chemical characteristics of some river and hand-dug well waters used for drinking and domestic purposes in the oil rich Niger Delta area of Nigeria were assessed using standard methods. The concentrations of the parameters in the river water samples ranged in the following order: pH (5.6–6.9), temperature (26.90–28.60°C), turbidity (23–63 NTU), electrical conductivity (52–184 μs/cm), DO (5.4–7.2 mg/l), BOD (21–57 mg/l), TDS (6.0–217 mg/l), PO₄ ³⁻ (0.19–1.72 mg/l), SO₄ ²⁻ (25–36.8 mg/l), NO₃ ⁻ (20.3–28 mg/l), Fe (6.07–15.71 mg/l), Zn (0.04–0.24 mg/l), Pb (0.01–0.17 mg/l), Ni (0.01–0.13 mg/l), Vn (0.01–0.20 mg/l) and Hg (0.001–0.002 mg/l). The concentrations of these parameters in the hand-dug well water ranged in the following order: pH (5.7–6.8) temperature (26–30°C), turbidity (134–171 NTU), electrical conductivity (160–340 μs/cm), DO (5.4–6.4 mg/l), BOD (13–34 mg/l), TDS (110–190 mg/l), PO₄ ³⁻ (0.84–1.84 mg/l), SO₄ ²⁻ (10.6–28.1 mg/l), NO₃ ⁻ (11.3–23 mg/l), Fe (13.17–16.31 mg/l), Ni (0.01–0.02 mg/l), Vn (0.01–0.04 mg/l) and Hg (0.001–0.004 mg/l). The concentrations of BOD, turbidity, NO₃ ⁻ and Fe in the water samples were above WHO and FMENV permissible limits for safe drinking water. The results suggest that the use of such waters for drinking and domestic purposes pose a serious threat to the health of the users and calls for the intervention of government agencies.     

Evaluation of biological stability and corrosion potential in drinking water distribution systems: a case study

The appearance of assimilable organic carbon (AOC), microbial regrowth, disinfection by-products (DBPs), and pipe corrosion in drinking water distribution systems are among those major safe drinking water issues in many countries. The water distribution system of Cheng-Ching Lake Water Treatment Plant (CCLWTP) was selected in this study to evaluate the: (1) fate and transport of AOC, DBPs [e.g., trihalomethanes (THMs), haloacetic acids (HAAs)], and other organic carbon indicators in the selected distribution system, (2) correlations between AOC (or DBPs) and major water quality parameters [e.g. dissolved oxygen (DO), free residual chlorine, and bacteria, and (3) causes and significance of corrosion problems of the water pipes in this system. In this study, seasonal water samples were collected from 13 representative locations in the distribution system for analyses of AOC, DBPs, and other water quality indicators. Results indicate that residual free chlorine concentrations in the distribution system met the drinking water standards (0.2 to 1 mg l(-1)) established by Taiwan Environmental Protection Administration (TEPA). Results show that AOC measurements correlated positively with total organic carbon (TOC) and UV-254 (an organic indicator) values in this system. Moreover, AOC concentrations at some locations were higher than the 50 microg acetate-C l(-1) standard established by Taiwan Water Company. This indicates that the microbial regrowth might be a potential water quality problem in this system. Higher DO measurements (>5.7 mg l(-1)) might cause the aerobic biodegradation of THMs and HAAs in the system, and thus, low THMs (<0.035 mg l(-1)) and HAAs (<0.019 mg l(-1)) concentrations were observed at all sampling locations. Results from the observed negative Langelier Saturation Index (LSI) values, higher Ryznar Stability Index (RSI) values, and high Fe3+ concentrations at some pipe-end locations indicate that highly oxidative and corrosive conditions occurred. This reveals that pipe replacement should be considered at these locations. These findings would be helpful in managing the water distribution system for maintaining a safe drinking water quality.     

Iron content in groundwaters of Visakhapatnam environs, Andhra Pradesh, India

Trace elements are essential for human health. However, excess concentrations of these elements cause health disorders. A study has been carried out in Visakhapatnam environs, Andhra Pradesh, India to ascertain the causes for the origin and distribution of iron content in the groundwaters. Fifty groundwater samples are collected and analyzed for iron. The content of iron ranges from 400 to 780 μg/l. A comparison of groundwater data with rock and soil chemistry suggests that the concentration of iron (400–530 μg/l) in the groundwaters is derived from the rocks and soils due to geogenic processes. This concentration is taken as a natural occurrence of iron in the groundwaters of the study area for assessing the causes for its next higher content (>530 μg/l). Relatively higher concentration of iron (540–550 μg/l) is observed at some well waters, where the wells are located nearby municipal wastewaters, while the very high concentration of iron (610–780 μg/l) is observed in the industrially polluted groundwater zones, indicating the impact of anthropogenic activities on the groundwater system. These activities mask the concentration of iron caused by geogenic origin. Hence, both the geogenic and anthropogenic activities degrade the groundwater quality. Drinking water standards indicate that the iron content in all the groundwater samples exceeds the permissible limit (300 μg/l) recommended for drinking purpose, causing the health disorders. Necessity of close monitoring of groundwater quality for assessing the impact of geogenic and anthropogenic sources with reference to land use/land cover activities is emphasized in the present study area to protect the groundwater resources from the pollution.     

Water quality assessment: surface water sources used for drinking and irrigation in Zaria,Nigeria are a public health hazard

We assessed the quality and pollution status of source surface waters in Zaria, Nigeria by monitoring the nature, cause and extent of pollution in Samaru stream, Kubanni River and Kubanni dam over a period of 10 months, between March and December 2002. A total of 228 water samples was collected from 12 sites and analysed for a total of ten physicochemical and one bacteriological quality indicators, using standard methods. Aesthetic water quality impairment parameters were also observed. The mean values of most water quality parameters were significantly higher (P < 0.05) in both the stream and river than in the dam. There was no significant correlation between faecal coliform counts (FCC) and water temperature (in the range 15–33°C); pH (5.77–7.32); and turbidity (1.4–567 NTU). The high FCC ranged from 2.0 × 10¹ to 1.6 × 10⁶ MPN/100 ml and exceeded the WHO standards for drinking water and water used for fresh-produce irrigation, and correlated positively (P < 0.05) with conductivity (in the range 68–1,029 μS/cm); TDS (10.0–70.0 mg/l); TSS (10.0–70.0 mg/l); Cl (7.5–181 mg/l); PO₄⁻P (0.01–0.41 mg/l); NO₃⁻N (0.6–3.8 mg/l) and BOD₅ (0.1–14.9 mg/l). The main pollution sources were municipal wastewater, stormwater runoffs, the ABU sewage treatment plant, abattoir effluents and irrigation farms treated with chemical fertilisers. We conclude that these water bodies are potentially hazardous to public health and that proper sewage treatment and river quality monitoring are needed to warn against hazards to public health.     

Distribution of heavy metals in surface water of Ranipet industrial area in Tamil Nadu, India

Ranipet industrial area is about 120 km from Chennai on Chennai-Bangalore highway and is a chronic polluted area identified by Central Pollution Control Board of India. It is one of the biggest exporting centers of tanned leather in India. The total number of industries located in and around Ranipet town are 240 tanneries along with ceramic, refractory, boiler auxiliaries plant, and chromium chemicals. Studies were carried out to find out the contamination of surface water bodies due to industrial effluents. The results reveal that the surface water in the area is highly contaminated showing very high concentrations of some of the heavy/toxic metals like Cadmium ranging from 0.2 to 401.4 μg/l (average of 51.1 μg/l), Chromium 2.4–1,308.6 (average of 247.2 μg/l), Copper 2.1–535.5 μg/l (average of 95.5 μg/l), Nickel 1.6–147.0 μg/l (average of 36.7 μg/l), Lead 6.4–2,034.4 μg/l (average of 467.8 μg/l) and Zinc 20.8–12,718.0 μg/l (average of 3,760.4 μg/l). The concentration levels of these metals are much above the permissible limits in surface water and are health hazards especially for the people working in the tannery industries. It was observed that the people in the area are seriously affected and suffering from occupational diseases such as asthma, chromium ulcers and skin diseases. Distribution of metals, their contents at different locations, and their effects on human health are discussed in this paper.     

Trace Metal Levels in Mussels (Mytilus Galloprovincialis L. 1758) from Turkish Aegean Sea Coast

Bio-monitoring of some heavy metal levels (Cd, Pb, Zn, Cu) in whole edible soft parts of Mytilus galloprovincialis (L. 1758) was conducted in Turkish Aegean Sea coast during the period of September 2002–August 2003 seasonally. Moreover, some physico-chemical environmental parameters, also have been analysed in the same region. The values of some physico-chemical environmental parameters in coastal waters of Turkish Aegean Sea were changed between; 9.0–27.0 ^∘C for temperature, 31.93–40.45 psu for salinity, 7.35–8.48 for pH and 4.05–9.50 mg/l for dissolved oxygen. The levels of trace elements in whole edible soft parts including interstitial fluids of Mediterranean mussels M. galloprovincialis (L. 1758), sampled from 6 different regions of Turkish Aegean Sea coast have ranged between; 0.04–0.52 μg Cd/g wet weight, 0.49–1.72 μg Pb/g w.w., 0.95–1.85 Cu/g w.w., 16.11–37.15 μg Zn/g w.w. The highest values for all trace metals (Cd, Pb, Zn, Cu) were measured in inner part of Izmir Bay (station 3) and lowest in Sigacik and Gulluk Bay (station 5, 6). Generally heavy metal levels are lower than the results in soft mussel tissues reported from Mediterranean regions.     

Occurrence of haloacetic acids (HAAs) and trihalomethanes (THMs) in drinking water of Taiwan

In this study, water samples were collected from 86 water treatment plants for analysis of haloacetic acids (HAAs) and trihalomethanes (THMs) from February to March, 2007 and from July to August, 2007. Both seasonal and geographical variations of disinfection by-products (DBPs) in drinking water of Taiwan were presented. The results showed that the five HAA concentrations (HAA5) were 1.0–38.9 μg/L in the winter and 0.2–46.7 μg/L in the summer; and the total THMs were ND-99.4 μg/L in the winter and ND-133.2 μg/L in the summer. For samples taken from the main Taiwan island, dichloroacetic acid (29.4–31.7%) and trichloroacetic acid (25.3–27.6%) were the two major HAA species, and trichloromethane was the major THM species (49.9–62.2%) in finished water. For water treatment plants located on the offshore islands outside of Taiwan, high bromide concentration was found in raw water, and higher percentage of brominated THMs and HAAs were formed in the overall formation. A statistically significant (P?<?0.005) logarithmic linear regression model was found to be useful to describe the correlations between TTHM and HAA5 or nine HAAs (HAA5?=?1.219 ×TTHM ^0.754, R ²?=?0.658; HAA9?=?1.824 ×TTHM ^0.735, R ²?=?0.678). No apparent difference was observed for DBPs concentrations between finished water and distribution samples in this study.     

Arsenic and Other Metal Contamination of Groundwaters in the Industrial Area of Thessaloniki, Northern Greece

In groundwater, used for drinking water supply in the greater industrial area of Thessaloniki, in Northern Greece, concentrations of total arsenic exceeded the WHO provisional guideline value and the EU maximum contaminant level (MCL) of 10 μg/L. The concentration of total arsenic was in the range between 4–130 μg/L, whereas the median value was 36 μg/L and the average concentration 46 μg/L. Nine out of the eleven wells contained total arsenic at concentration higher than 10 μg/L and it should be stressed that 6 of them contain arsenic at concentrations between 10 (new MCL) and 50 μg/L (previous MCL). The examined groundwaters were found to contain elevated concentrations of manganese and phosphate. Arsenic had a positive correlation with the pH, indicating the possible effect of pH on arsenic mobilisation. These findings emerge the problem of contamination from arsenic, since, according to the EU directive 98/83, all drinking water sources within the European Union should have achieved compliance with the new limits by 12/2003, implying that the situation requires urgent remedial action.     

Comparative Metal Distribution in Hair of Pakistani and Libyan Population and Source Identification by Multivariate Analysis

Using nitric acid-perchloric acid wet digestion based FAAS method ten selected metals (Cd, Co, Cr, Fe, K, Mn, Na, Ni, Pb and Zn) were determined in the scalp hair of male Pakistani and Libyan donors (n = 62), between 3–54 years age and residing in typical urban areas. The study was taken up to identify sources of metal distribution in two diverse population segments exposed to different environments. Sodium emerged with the highest mean hair concentration of 511.0 μg/g and 496.9 μg/g for Libyan and Pakistani donors respectively, followed by K, at 266.2 μg/g and 242.4 μg/g for the two donor categories. Cadmium showed the lowest mean hair concentration for both Pakistani (0.380 μg/g) and Libyan (0.530 μg/g) donors. Levels of Na, K, Pb, Cr and Cd were higher in hair of Libyan donors compared with Pakistani counterparts which showed higher comparative levels of Zn, Fe, Co, Ni and Mn. Strong metal-to-metal correlations were found between Na–K (r = 0.638) and Cd–Co (r = 0.574) for Pakistani donors, while for Libyan donors, Na–K (r = 0.680) and Fe–Mn (r = 0.624) correlations emerged as strongly significant. Only K was found to have a strong positive correlation (r = 0.611) with age for Pakistani donors while this correlation was significantly negative (r = −0.500) for Libyan donors, probably arising from individual food habits. Other metals showed no viable relationship with age. Principal Component Analysis (PCA) and Cluster Analysis (CA) of the data evidenced food, industrial emissions and automobile emissions as possible sources of metal distribution. The results of the present study are compared with those reported for subjects from other regions of the world.     

Trihalomethane formation potential in treated water supplies in urban metro city

Trihalomethane (THM) formation potential (TFP) is very useful test to assess the level of the formation of trihalomethanes in worst case scenario. Organics in water have the potential to generate harmful disinfection by-products (DBPs) such as THMs, as a result of their reaction with disinfectant chlorine used in drinking water. DBPs are increasingly recognized as cancerous agents. TFP of postchlorinated treated water were investigated at six water treatment plants (WTPs) in Delhi City (India). The present paper presents the current trends of TFP so that prevention and control measures can be initiated by the regulating agencies responsible for drinking water supply. Liquid–liquid extraction method, followed by qualitative and quantitative estimation by gas chromatograph equipped with electron capture detector, had been used for the determination of THMs in water samples collected at the outlet just before supplying to the consumers during 2000–2007. The TFP values from 2004 onward of all WTPs did not exceed the WHO guideline value of ≤1.     

Hydrogen Peroxide and Ultraviolet Irradiations in Water Treatment

Trihalomethanes (THMs) the by-products of chlorination in water treatment are recognised as a threat to public health due to their carcinogenicity. The photodegradation of THMs using hydrogen peroxide has been found to give increased removal efficiency and the outcome of the study may find, its application in designing a unit process for water treatment. Batch experiments were carried out using UV lamp of 83 W and 40% w/w Hydrogen peroxide (H₂O₂) in test waters between 2.5–10 pH range of chloroform, bromodichloromethane, dibromochloromethane and bromoform at 50–200 μg L⁻¹ initial concentration. 92–100% removal of chloroform, bromodichloromethane, dibromochloromethane and bromoform were found with 0.1% of H₂O₂ and 90 min of UV exposure.