Human biomonitoring of trace metals from different altitudinal settings of Pakistan.

Human biomonitoring of toxic trace elements is of critical importance for public health protection. The current study aims to assess the levels of selected trace metals (Cd, Co, Cr, Cu, Mn, Ni, Pb, and Zn) into paired human nail and hair samples (n = 180 each) from different altitudinal setting along the Indus River, and which were measured by using inductively coupled plasma mass spectrometry (ICP-MS). The human samples (hair and nail) were collected from four different ecological zones of Pakistan which include frozen mountain zone (FMZ), wet mountain zone (WMZ), riverine delta zone (RDZ), and low-lying southern areas (LLZ). Our results showed the following occurrence trends into studied hair samples: higher values (ppm) of Zn (281), Co (0.136), and Mn (5.65) at FMZ; Cr (1.37), Mn (7.83), and Ni (1.22) at WMZ; Co (0.15), Mn (11.89), and Ni (0.99) at RDZ; and Mn (8.99) and Ni (0.90) at LLZ. While in the case of nails, the levels (ppm) of Mn (9.91) at FMZ and Mn (9.38, 24.1, and 12.5), Cr (1.84, 3.87, and 2.33), and Ni (10.69, 8.89, and 12.6) at WMZ, RDZ and LLZ, respectively, showed higher concentration. In general, among the studied trace elements, Mn and Ni in hair/nail samples were consistently higher and exceeded the WHO threshold/published reference values in most of the studied samples (> 50-60%) throughout the Indus basin. Similarly, hair/nail Pb values were also higher in few cases (2-10%) at all studied zones and exceeded the WHO threshold/published reference values. Our area-wise comparisons of studied metals exhibited altitudinal trends for Cd, Cr, Zn, and Mn (p < 0.05), and surprisingly, the values were increasing from south to north (at higher altitudes) and indicative of geogenic sources of the studied toxic elements, except Mn, which was higher at lower floodplain areas. Estimated daily intake (EDI) values showed that food and drinking water had the highest contribution towards Zn, Cu, Mn, and Ni and accumulation at all studied zones. Whereas, dust also acts as the main exposure route for Mn, Co, Cr, and Cd followed by the food, and water.

Sustainable use of low-cost adsorbents prepared from waste fruit peels for the removal of selected reactive and basic dyes found in wastewaters.

Agricultural wastes are potential sustainable adsorbents since they are available in large quantities, are low-cost, and may require little or no treatment, in some cases. In this study, several fruit peels, such as banana, orange, and pomegranate, were collected from local markets and prepared by a simple and eco-friendly method and used as natural adsorbents for the removal of both anionic (Reactive Red 120 (RR120), Reactive Black 5 (RB5), Remazol Brilliant Blue R (RBBR)) and cationic Methylene Blue (MB) dyes found in wastewaters. Many industries, such as leather and textiles, can release huge amounts of synthetic dyes into the wastewater during dyeing processes. These are one of the most important pollutants of water pollution as they cause enormous damage to the water body and also affect the health of organisms due to their toxicity and carcinogenicity. The search for a sustainable and at the same time efficient material for the removal of a wide variety of dyes is the innovation of this work. These peels were prepared by washing, drying, grinding, and finally sieving, under natural sustainable conditions. Porosometry (BET analysis), FTIR, SEM/EDS, and XRD techniques were used to characterize the fruit peels before and after the adsorption process. Factors affecting the adsorption of dyes (adsorbent dosage, pH solution, initial concentration of dyes, contact time, and temperature) were investigated. According to the results, in terms of the effectiveness of fruit peels as (natural) adsorbent materials, for anionic dyes, 5.0-6.0 g/L of banana or orange dry peels was sufficient to remove near or even more than 90% anionic dyes at pH 2.0, and 4.0 g/L was sufficient to remove 98% of cationic MB dye at pH 9.0. Similar amount of pomegranate peels had lower efficiency for anionic dyes (50-70%), while cationic MB was still efficiently removed (98%) at pH 9.0. Moreover, the adsorption process in all cases was found to better fit to pseudo-second-order model, in comparison to pseudo-first-order model. According to isotherms, Freundlich model fitted better in some cases to the equilibrium data, while the Langmuir model in others. Finally, this study demonstrates the viability of reusing the banana, orange, and pomegranate peel adsorbents for eight, four, and five cycles, showing a gradual reduction of around 50% of their effectiveness.

Effective Usage of Biochar and Microorganisms for the Removal of Heavy Metal Ions and Pesticides.

The bioremediation of heavy metal ions and pesticides is both cost-effective and environmentally friendly. Microbial remediation is considered superior to conventional abiotic remediation processes, due to its cost-effectiveness, decrement of biological and chemical sludge, selectivity toward specific metal ions, and high removal efficiency in dilute effluents. Immobilization technology using biochar as a carrier is one important approach for advancing microbial remediation. This article provides an overview of biochar-based materials, including their design and production strategies, physicochemical properties, and applications as adsorbents and support for microorganisms. Microorganisms that can cope with the various heavy metal ions and/or pesticides that enter the environment are also outlined in this review. Pesticide and heavy metal bioremediation can be influenced by microbial activity, pollutant bioavailability, and environmental factors, such as pH and temperature. Furthermore, by elucidating the interaction mechanisms, this paper summarizes the microbe-mediated remediation of heavy metals and pesticides. In this review, we also compile and discuss those works focusing on the study of various bioremediation strategies utilizing biochar and microorganisms and how the immobilized bacteria on biochar contribute to the improvement of bioremediation strategies. There is also a summary of the sources and harmful effects of pesticides and heavy metals. Finally, based on the research described above, this study outlines the future scope of this field.

Chromium(VI) Removal from Water by Lanthanum Hybrid Modified Activated Carbon Produced from Coconut Shells.

Cr(VI) is considered to be the most hazardous and toxic oxidation state of chromium and hence the development of effective removal technologies, able to provide water with Cr(VI) below the drinking water limits (US EPA 100 µg/L, European Commission 50 µg/L, which will be reduced to 25 by 2036) is a very important issue in water treatment. This study aimed at examining the performance of activated carbon produced from coconut shells, modified by lanthanum chloride, for Cr(VI) removal from waters. The structure of the formed material (COC-AC-La) was characterized by the application of BET, FTIR and SEM techniques. The effect of the adsorbent's dosage, pH value, contact time, initial Cr(VI) concentration and water matrix was examined with respect to Cr(VI) removal. The results indicated that the maximum Cr(VI) removal was observed at pH 5; 4 h contact time and 0.2 g/L of adsorbent's dosage was adequate to reduce Cr(VI) from 100 µg/L to below 25 µg/L. Freundlich isotherm and pseudo-second order kinetic models fitted the experimental data sufficiently. The maximum adsorption capacity achieved was 6.3 µg/g at pH 5. At this pH value, the removal percentage of Cr(VI) reached 95% for an initial Cr(VI) concertation of 30 µg/L. At pH 7 the corresponding efficiency was roughly 60%, resulting in residual Cr(VI) concentrations below the anticipated drinking water limit of 25 µg/L of total chromium, when the initial Cr(VI) concentration was 50 µg/L. Consecutive adsorption and regeneration studies were conducted using 0.01 M of NaOH as an eluent to evaluate the reusability of the adsorbents, Results showed 20% decrease of adsorption capacity after 5 regeneration cycles of operation.

Applications of Up-Flow Anaerobic Sludge Blanket (UASB) and Characteristics of Its Microbial Community: A Review of Bibliometric Trend and Recent Findings.

The interest in research on up-flow anaerobic sludge blanket (UASB) reactors is growing. The meta-analysis of bibliometric data highlighted the growing interest in four diverse topics: (i) energy recovery production; (ii) combination with other treatments; (iii) the study of processes for the removal of specific pollutants and, (iv) characterization of microbial community and granular sludge composition. In particular, the papers published in the first 6 months of 2021 on this process were selected and critically reviewed to highlight and discuss the results, the gaps in the literature and possible ideas for future research. Although the state of research on UASB is to be considered advanced, there are still several points that will be developed in future research such as the consolidation of the results obtained on a semi-industrial or real scale, the use of real matrices instead of synthetic ones and a more in-depth study of the effect of substances such as antibiotics on the microbiota and microbiome of UASB granular biomass. To date, few and conflicting data about the environmental footprint of UASB are available and therefore other studies on this topic are strongly suggested.

Enhanced uranium removal from acidic wastewater by phosphonate-functionalized ordered mesoporous silica: Surface chemistry matters the most.

The removal of uranium species from aqueous phases using non-hazardous chemicals is still an open challenge, and remediation by adsorption is a prosperous strategy. Among the most crucial concerns regarding the design of an efficient material as adsorbent are, except the cost and the green character, the feasibility to be stable and effective under acidic pH, and to selectively adsorb the desired metal ion (e.g. uranium). Herein, we present a phosphonate functionalized ordered mesoporous silica (OMS-P), prepared by a one-step co-condensation synthesis. The physicochemical features of the material were determined by HR-TEM, XPS, EDX, N2 sorption, and solid NMR, while the surface zeta potential was also measured. The removal efficiency was evaluated at two different temperatures (20 and 50 °C) in acidic environment to avoid interferences like solid phase formation or carbonate complexation and the adsorption isotherms, including data fitting with Langmuir and Freundlich models and thermodynamic parameters are presented and discussed. The high and homogeneous dispersion of the phosphonate groups within the entire silica's structure led to the greatest reported up-todays capacity (345 mg/g) at pH = 4, which was achieved in less than 10 min. Additionally, OMS-P showed that the co-presence of other polyvalent cation like Eu(III) did not affect the efficiency of adsorption, which occurs via inner-sphere complex formation. The comparison to the non-functionalized silica (OMS) revealed that the key feature towards an efficient, stable, and selective removal of the U(VI) species is the specific surface chemistry rather than the textural and structural features. Based on all the results and spectroscopic validations of surface adsorbed U(VI), the main interactions responsible for the elevated uranium removal were proposed.

Mathematical modeling of arsenic(V) adsorption onto iron oxyhydroxides in an adsorption-submerged membrane hybrid system.

The adsorption of arsenic (V), As(V), on two porous iron oxyhydroxide-based adsorbents, namely, micro-sized tetravalent manganese feroxyhyte (µTMF) and granular ferric hydroxide (µGFH), applied in a submerged microfiltration membrane hybrid system has been investigated and modeled. Batch adsorption tests were carried out to determine adsorption equilibrium and kinetics parameters of As(V) in a bench-scale slurry reactor setup. A mathematical model has been developed to describe the kinetic data as well as to predict the As(V) breakthrough curves in the hybrid system based on the homogeneous surface diffusion model (HSDM) and the corresponding solute mass balance equation. The kinetic parameters describing the mass transfer resistance due to intraparticle surface diffusion (Ds) involved in the HSDM was determined. The fitted Ds values for the smaller (1-63 µm) and larger (1-250 µm) diameter particles of µGFH and µTMF were estimated to be 1.09 × 10-18 m2/s and 1.53 × 10-16 m2/s, and 2.26 × 10-18 m2/s and 1.01 × 10-16 m2/s, respectively. The estimated values of mass transfer coefficient/ kinetic parameters are then applied in the developed model to predict the As(V) concentration profiles in the effluent of the hybrid membrane system. The predicted results were compared with experimental data for As(V) removal and showed an excellent agreement. After validation at varying adsorbent doses and membrane fluxes, the developed mathematical model was used to predict the influence of different operation conditions on As(V) effluent concentration profile. The model simulations also exhibit that the hybrid system benefits from increasing the amount of adsorbent initially dosed and from decreasing the membrane flux (increasing the contact time).

Fluoride removal from water by composite Al/Fe/Si/Mg pre-polymerized coagulants: Characterization and application.

Fluoride, an anionic pollutant, is possibly to be found in excessive concentrations especially in groundwaters and can show detrimental effects on human health, in concentrations higher than the commonly applied legislation limit of 1.5 mg/L The most commonly applied method for water de-fluoridation is performed by Al-based coagulants, which however presents some important limitations, such as the applied relatively high dosage, producing rather excessive amounts of chemical sludge. In this study, the use of novel pre-polymerized Al-based coagulants was examined, regarding their efficiency towards fluoride removal, as compared with the conventionally applied AlCl3. The novel coagulants were characterized by measuring the main physico-chemical properties, the aluminum species distribution, the zeta potential, the particles' size distribution and the produced flocs' sizes. The results showed that the Mg-containing coagulant (PSiFAC-Mg30-10-15) was the most efficient, when applied in pH values relevant to fluoride-containing groundwaters; it was also the only coagulant, which increases its efficiency at pH values > 7. The uptake capacity of coagulants, regarding fluoride, to reach the residual/equilibrium concentration limit of 1.5 mg F/L (Q1.5-value) at the pH value 7.0 ±â€¯0.1 were found 170, 134 and 94 mg F/g Al for the cases of PSiFAC-Mg30-10-15, AlCl3·6H2O and PSiFAC-Na1.5-10-15, respectively. Accordingly, at the pH value 7.8 ±â€¯0.2 the Q1.5-values were found 189, 118 and 41 mg F/g Al for the same coagulants; whereas considering the residual aluminum concentration this was ranged at 15 ±â€¯5, 25 ±â€¯5 and 30 ±â€¯5 µg Al/L, respectively. In addition, (beneficial) increase of residual magnesium concentration, when applying the coagulant PSiFAC-Mg30-10-15 was 15 ±â€¯5 mg/L.

Application of a ceramic membrane contacting process for ozone and peroxone treatment of micropollutant contaminated surface water.

This study investigates the performance of membrane-based ozonation and peroxone processes, regarding the transformation of carbamazepine (CBZ), benzotriazole (BZT), p-chlorobenzoic acid (pCBA) and atrazine (ATZ) in natural surface waters, as well as the formation of bromates. Ozonation, performed with the use of ceramic membrane contactor, was able to diminish CBZ concentration below 0.1 µM at 0.4 mg O3/mg DOC, i.e. presenting >90% removal rate, whereas the transformation of BZT, pCBA and ATZ was not exceeded 70%, 57% and 49%, respectively, under the same experimental conditions. The addition of H2O2 reduced the removal efficiency of CBZ, since up to -8% transformation values were observed at 0.1 mg O3/mg DOC. In contrast, the transformation of ozone-resistant compounds pCBA and ATZ was slightly improved by approximately 5-10%, at 0.8 mg O3/mg DOC. Membrane-based oxidative treatment of surface water resulted to high bromate concentrations (49 µg/L and 28 µg/L for ozone and peroxone process, respectively, at 0.8 mg O3/mg DOC). The results obtained by using the membrane contactor were also compared with the corresponding from conventional batch experiments. These results suggest that the implementation of membrane contactors with the highest possible inner surface per volume along with the use of low ozone gas concentration are required to improve the removal of micropollutants and diminish bromate formation.

Reductive precipitation and removal of Cr(VI) from groundwaters by pipe flocculation-microfiltration.

Chromium (Cr(VI)) is a very toxic and carcinogenic element, which is widely present in groundwaters, mainly due to geogenic conditions. The limit of Cr(VI) in drinking water is expected to be reduced to 10 µg/L in both the USA and the European Union. Recent literature findings indicated that the most efficient process in reducing Cr(VI) levels to below 10 µg/L proved to be Cr(VI) reduction by Fe(II), by applying a molar ratio Fe(II)/Cr(VI) of around 9. In the present work, we investigated the reduction of Cr(VI) by Fe(II) in pipe flocculation reactors followed by filtration of insoluble products by microfiltration. The proposed technology involves re-circulation of a part of the sludge in the pipe reactors, in order to improve kinetics and efficiency of the process. The obtained results showed that with a Fe(II) dose of around 1 mg/L, Cr(VI) was reduced to below 10 µg/L, by even an initial concentration as high as 300 µg/L of Cr(VI), corresponding to a molar ratio Fe(II)/Cr(VI) of around 3, thus reducing the overall quantity of reductive reagents and of the produced sludge. This ratio was also confirmed by the XPS analysis, which also showed that Cr(VI) was reduced to Cr(III) and then precipitated either as Cr(OH)3 or associated with the produced iron oxides.

Impact of O3 or O3/H2O2 treatment via a membrane contacting system on the composition and characteristics of the natural organic matter of surface waters.

The present study aims to evaluate changes in the structure-composition of natural organic matter (NOM) that occur after the application of bubbleless ozonation or peroxone treatment of surface waters. The oxidation experiments (using 0.5-2 mg O3/mg DOC, or 2:1 O3:H2O2 molar ratio) were performed in a continuous mode, using a tubular ceramic membrane contactor. Fluorescence spectroscopy (emission-excitation matrix) and liquid chromatography-organic carbon detection (LC-OCD) were mainly used for the detailed DOC characterization. In brief, the application of single ozonation resulted to high reduction of humic-like peak fluorescence intensities (50-85%) and also to the formation of two new peaks in the region of protein-like components. The co-addition of H2O2 did not present the anticipated increase in the reduction of fluorescence intensity; however, it resulted to the further oxidation of protein-like fluorophores. LC-OCD measurements confirmed the decrease of average molecular weight of NOM during ozone treatment, due to the gradual degradation of biopolymers (14-23%) and humic substances (11-17%) towards building blocks and low molecular weight (LMW) neutrals. Advanced oxidation process (AOP) treatment by the mixture O3/H2O2 resulted in the simultaneous decrease of building blocks and LMW neutral concentrations. Conventional batch ozonation and AOP experiments were conducted using ozone-saturated solutions to investigate the effect of different contacting patterns. The results revealed that the different reaction pathways followed during bubbleless and conventional batch experiments may also influence the formation of NOM oxidation intermediates.

Occurrence of selected elements (Ti, Sr, Ba, V, Ga, Sn, Tl, and Sb) in deposited dust and human hair samples: implications for human health in Pakistan.

The current study determined, for the first time, the levels of titanium (Ti), strontium (Sr), barium (Ba), vanadium (V), gallium (Ga), tin (Sn), thallium (Tl), and antinomy (Sb), in deposited dust, and human hair collected from general population of different geographical areas of Pakistan. All the samples were prepared by microwave digestion and measured by ICP-MS. The results showed that on deposited dust samples, the detected elements followed the descending trend as: Ti > Sr > Ba > V > Ga > Sn > Tl > Sb similar to the upper continental crust. The deposited dust samples from low elevation areas exhibited highest levels of all studied elements (except antimony which was higher in soil samples from mountainous areas), followed by rive plains, mountainous areas, and highland valleys. In contrast, on human hair samples, the elements followed the descending trend as: Sr > Ba > Ti > Ga > V > Sn > Sb > Tl respectively. Ba, Ga, and V concentrations were higher in soil samples from lower elevation Indus plain, and Sr, Tl, Sb, and Ti were higher in samples from mountainous areas. The bioaccumulation trend of all studied elements was in descending order as follows: Sb, Ga, Sn, Ba, Sr, Ti, V, Tl, respectively. Principal component analysis (PCA) and correlation matrix evidenced both geological influences and anthropogenic activities as potential sources of these studied elements. On the other hand, the risk estimation (HI > 1) concluded that population were at higher health risk (non-carcinogenic) for Ga and Ti. All other studied rare elements were within safe limit for humans from all zones.

Production of demineralized water for use in thermal power stations by advanced treatment of secondary wastewater effluent.

The operation and efficiency of a modern, high-tech industrial full-scale water treatment plant was investigated in the present study. The treated water was used for the supply of the boilers, producing steam to feed the steam turbine of the power station. The inlet water was the effluent of municipal wastewater treatment plant of the city of Bari (Italy). The treatment stages comprised (1) coagulation, using ferric chloride, (2) lime softening, (3) powdered activated carbon, all dosed in a sedimentation tank. The treated water was thereafter subjected to dual-media filtration, followed by ultra-filtration (UF). The outlet of UF was subsequently treated by reverse osmosis (RO) and finally by ion exchange (IX). The inlet water had total organic carbon (TOC) concentration 10-12 mg/L, turbidity 10-15 NTU and conductivity 3500-4500 µS/cm. The final demineralized water had TOC less than 0.2 mg/L, turbidity less than 0.1 NTU and conductivity 0.055-0.070 µS/cm. Organic matter fractionation showed that most of the final DOC concentration consisted of low molecular weight neutral compounds, while other compounds such as humic acids or building blocks were completely removed. It is notable that this plant was operating under "Zero Liquid Discharge" conditions, implementing treatment of any generated liquid waste.

Quality of tube well water intended for irrigation and human consumption with special emphasis on arsenic contamination at the area of Punjab, Pakistan.

In the present study, the tube well water quality and the associated health risks, emphasizing on arsenic contamination, were investigated in rural and urban samples from Tehsil Mailsi located in Punjab, Pakistan. Arsenic concentrations (µg/L) were ranged from 12 to 448.5 and which exceeded the WHO recommended limit (10 µg/L) in all cases. The calculated average daily dose (3.3 × 10-0.4 to 1.2 × 10-0.2 mg/kg day) and hazard quotient (1.1-40) reflected the potential health risk to local population due to tube well water consumption as drinking purpose. Sodium percent (Na%), sodium absorption ratio, residual sodium carbonate, Kelly's index and magnesium absorption ratio were also determined to assess the suitability of tube well water for irrigation purpose. The resulting piper plot revealed the Na-Ca-HCO3 type water chemistry of the area and generally alkaline environment. The spatial distribution of arsenic in the tube well waters pinpoints the significant contribution of anthropogenic activities to arsenic pollution. Nevertheless, different statistical tools, including principal component analysis, hierarchical cluster analysis and correlation matrices, revealed the contribution of both natural and anthropogenic activities and alkaline type of aquifers toward the high level of arsenic contamination.

Human exposure to trace metals and arsenic via consumption of fish from river Chenab, Pakistan and associated health risks.

This study provided the first hand data of trace elements into fish muscles (N = 65) collected from river Chenab in Pakistan during 2013, using inductively coupled plasma mass spectrometry (ICP-MS). We monitored the health risk associated with consumption of contaminated fish of river Chenab, by the local population. The mean concentrations (µg/g, wet weight), in descending order were: Zn (35.5-54.4), Cu (1.38-4.57), Mn (2.43-4.5), As (0.23-1.21), Cr (0.21-0.67), Ni (0.14-0.34), Pb (0.14-0.31), Co (0.09-0.12), Cd (0.07-0.12) with higher concentration to be observed in the herbivore fish species (i.e., Cirrhinus reba and Catla catla). The levels of trace elements in different fish species found in this study were compared with similar data worldwide, and with the international standards for consumption. The concentration (µg/g) of arsenic in many cases (>65%) exceeded the FAO/WHO expert committee on food additives permissible limits. From the human health point of view, this study highlights that the local inhabitants, (i.e., fisher folk communities and population frequently consuming fish at about 100 g/day) along the river Chenab are exposed chronically to arsenic pollution with carcinogenic (10-4 to 10-6) and non-carcinogenic (THQ>1) risks, especially from the intake of Cirrhinus reba.

Human lead (Pb) exposure via dust from different land use settings of Pakistan: A case study from two urban mountainous cities.

The current study aims to determine the dust-borne lead (Pb) levels into outdoor dust, which were collected from the areas nearby the cities/districts of Islamabad and Swat in Pakistan. In general dust samples from all land use settings (industrial, urban and rural) showed significantly higher (p<0.05) Pb-levels (median, ppm) from Islamabad (110, 52, 24) than those of Swat district (75, 37, 21), respectively. Index of Geo-accumulation (Igeo values) indicated that industrial and urban areas of both sites were highly polluted due to severe anthropogenic influence, whereas the rural areas were in most parts unpolluted and where moderately polluted, this was mainly due to geological factors and short and/or long distance atmospheric deposition from surrounding polluted areas. According to the calculated chemical daily intake (mg/kg-day) values, dust ingestion is one of the major routes of human exposure for lead. Hazard Index (HI) values, calculated for both adult and children populations, were above unity in industrial and urban areas, indicating serious health risks especially to the children populations.

Enhanced As(III) oxidation and removal by combined use of zero valent iron and hydrogen peroxide in aerated waters at neutral pH values.

The oxidation and removal of As(III) by commercially available micro-scale zero-valent iron (mZVI) was studied in aerated synthetic groundwater with initially 6.7 µM As(III) at neutral pH values. Batch experiments were performed to investigate the influence of ZVI and H2O2 concentrations on As(III) oxidation and removal. Oxidation and removal kinetics was significantly increased by increasing ZVI concentration or by adding H2O2 in micromolar concentrations slightly higher than that of initial As(III). Observed half-lifes for arsenic removal without added H2O2 were 81-17 min at ZVI concentrations of 0.15-2.5 g/L, respectively. X-ray absorption spectroscopy (XAS) confirmed that almost all As(III) was converted to As(V) after 2 h of reaction in the pH range 5-9. Addition of 9.6 µM H2O2 to 0.15 g/L ZVI suspensions diminished half-lifes for arsenic removal from 81 to 32 min and for As(III) oxidation from 77 to 8 min, i.e., by approximately a factor of 10. The increased rate of As(III) oxidation is attributable to enhanced formation of oxidants by the Fenton reaction with higher initial concentrations of H2O2. In practice, results of this study suggest that addition of small amounts (<1 mg/L) of H2O2 in various forms (e.g. stable and widely available Na-percarbonate) to water prior to treatment could significantly enhance As(III) oxidation and removal with ZVI.

Arsenic levels from different land-use settings in Pakistan: Bio-accumulation and estimation of potential human health risk via dust exposure.

The present study aims at assessing arsenic (As) levels in outdoor dust and human exposure risks at different land use setting (i.e., rural, industrial, urban) from Punjab, Pakistan. The results showed higher As concentrations (mg/kg) in all the sample types ( i.e., dust, hair and nail) collected from industrial sites (9.78, 2.36, 2.5) followed by urban (7.59, 0.38, 0.88) and rural sites (6.95, 0.52, 1.12), respectively. In the current study, we also carried out human risk assessment via contaminated dust exposure, which suggested that dust ingestion is the major route of As contamination for the associated population, followed by the inhalation and dermal contact, at all studied land use settings. Hazard Index (HI) calculated for non-carcinogenic health risks for adults showed higher values at industrial (0.65) and urban (0.53) sites, which reflected that dust exposure is the major contributing source of human arsenic burden and may pose several adverse health effects. Carcinogenic risk values showed that at industrial areas the risk of carcinogenesis to the associated population is mainly due to As contaminated dust exposure. Hair (60%) and nail samples (70%) collected from industrial land use were found above the WHO threshold limit of 1mg/kg, suggested high risks for human health in the studied area. The results of the present study would be useful for assessing the human health risks due to arsenic contamination via dust exposure in different parts of country.