Tap Water Concentrations Research Articles

The effect of water filter pitchers on the mineral concentration of tap water.

To investigate the effect of water filter pitchers on the concentration of different minerals in tap water. Nine water filter pitchers (A-I) were chosen based on consumer preferences and Amazon reviews. Each filter was tested for its ability to modify the concentrations of fluoride, calcium, magnesium, potassium, and sodium in tap water. Tap water samples were collected before and after filtration, at various intervals (1, 5, 10, 30, 50, 75, and 100 L) during filtration, and analyzed using an ion-specific electrode (fluoride) and atomic absorption spectrometry (other minerals). Statistical analyses were conducted to compare filtered and unfiltered water mineral concentrations. Water filter pitcher effect: Filters F (p < 0.001) and G (p = 0.030) decreased fluoride concentrations. All filters except I (p = 0.235) and H (p = 0.717) decreased calcium concentrations (p < 0.01). Filters E (p = 0.018), D (p = 0.014), and G (p = 0.010) decreased magnesium concentrations. Filters I (p = 0.028) and D (p = 0.009) increased potassium concentrations. Filter A (p = 0.002) increased sodium concentrations, while C (p = 0.034) decreased sodium concentrations. Effect of filter aging: All filters affected mineral concentrations over time but to varying extents. Filter G had the most pronounced effect on reducing mineral concentrations compared to all others. No filter was able to completely remove fluoride from tap water, contrary to the claims made by three manufacturers. The present study highlighted that water filter pitchers vary greatly in their ability to affect mineral concentrations in tap water during their use. Further research is needed to develop more effective water treatment solutions.

Synthetic Microplastics in UK tap and bottled water; Implications for human exposure

There is increasing concern for public health over inadvertent human exposure to MPs due to potential adverse health effects linked to MPs polymeric composition, toxic chemical additives, and/or harmful microorganisms adsorbing onto their surfaces. While numerous studies have reported MPs occurrence and risk in the freshwater aquatic environment and drinking water sources (e.g., rivers, lakes, and reservoirs), the current state-of-knowledge on MPs pollution in drinking water (i.e., tap water and bottled water) remains limited at a global level. This paper provides the first comprehensive study of the occurrence, concentrations, size distribution, shape, and polymer type of MPs in 177 tap water samples from 13 cities in the United Kingdom, as well as 85 samples of bottled water from 17 popular brands, with various packaging materials, on the UK market.MPs were detected in all tap water samples (range 6–100 MP/L) and bottled water samples (range 12–62 MP/L). Average MPs concentration in tap water (40 ± 16 MP/L) was statistically indistinguishable from that in bottled water (37 ± 11 MP/L). However, the average MPs particle size in tap water (32.4 μm) exceeded significantly (p < 0.05) that in bottled water (26.5 μm), indicating the various purification processes applied to bottled water may help remove larger MPs, but raises concern over the potential adverse health effects from exposure to smaller MPs. The most frequently detected polymer types were: polypropylene (PP), polyethylene (PE), and polyvinyl chloride (PVC) in tap water, and PE, PP and polyethylene terephthalate (PET) in bottled water. A strong correlation was observed (r = 0.68, P = 0.049) between the plastic cap material (PE) and the predominant polymer type in the bottled water. In terms of morphology, fragments and fibres were the most abundant MPs, together constituting 92 % and 96 % of MPs detected in tap and bottled water samples, respectively.Using EFSA (European Food Safety Authority) recommended daily water intakes, the corresponding exposures to MPs in different UK age groups were estimated. On a body weight (BW) basis, infants and toddlers were exposed (4 MP/kg BW/day) at a higher level than adults (1 MP/kg BW/day). This raises concern, given the former's incompletely developed immune/nervous systems rendering them at higher risk of adverse health effects from such exposure.

Development of a Rapid Fluorescence Probe for the Determination of Aqueous Hypochlorite

Chlorine interacts with aqueous environments, including the mucosa and alveolar fluid in the lungs, causing its the immediate transformation to hypochlorous acid (HClO) and hydrochloric acid (HCl) which induces cellular damage and may produce systemic toxicity. There are multiple techniques to monitor hypochlorite (HClO/ClO−) from various matrices, however, they each have significant disadvantages, including limited sensitivity, complexity, and slow response. In this study, we developed a water-soluble fluorescein-based probe, called fluorescein thioacid (FSH), for the rapid and sensitive detection of HClO/ClO− in aqueous solutions via oxidation of FSH to produce fluorescein. FSH was synthesized via a simple, one-step procedure and exhibited excellent selectivity for ClO−, maintaining 82% signal stability for 24 h. FSH performed well over a wide pH range (4–10; optimum pH of 4), produced a linear range from 1 to 100 µM, and had a detection limit of 100 nM. The probe was able to accurately quantify HClO/ClO− concentrations in tap water (13.8 μM) and swimming pool water (56.9 μM) samples. Overall, FSH is simple to synthesize, highly selective, highly sensitive, has excellent water solubility, and produces a fast response for monitoring of aqueous ClO− levels.

Mapping the Environmental Risk of Fluoride Exposure of Drinking Water in a Community of Zacatecas, Mexico

Fluoride (iF) is an inorganic element commonly present in groundwater in central Mexico and is considered a health risk when it exceeds the Mexican drinking water standard of 1.5 mg/L. Prolonged exposure to iF can cause various adverse health effects, such as dental fluorosis and neurological effects, particularly in children. A rapid and cost-effective strategy to identify possible areas where the resident population may be at risk of exposure to this contaminant is the health risk estimation methodology of the Pan American Health Organization (PAHO). The aim of this study was to estimate the environmental risk of iF exposure in residents of Jerez, Zacatecas, Mexico, and subsequently construct risk maps to identify areas of the city where there is a higher risk of exposure. Fifty-five tap water samples were collected from households to determine iF concentrations using the ion-selective electrode method. Based on these environmental values, the hazard quotient (HQ) was estimated following the health risk estimation methodology. Subsequently, risk maps were generated from these values to visualize the spatial distribution of high-risk areas within the city. The iF concentrations in tap water ranged from 1.3 to 7.3 mg/L (ppm), with only one sample below the standard of 1.5 mg/L. We estimated HQ values ranging from 0.63 to 3.73. Exposure to iF in tap water is a health problem that must be addressed, necessitating risk communication actions that enable the population to safeguard its health through simple measures, thereby avoiding future health costs.

Assessing radon hazard in drinking water: A comprehensive approach integrating deterministic and probabilistic methods with water consumption routines

The research aimed to determine the spatiotemporal distribution patterns of radon activity concentrations in tap water of Yerevan city and assess radon-associated hazards using both deterministic and probabilistic approaches. This was accomplished by integrating one-year monitoring data of radon in water with water consumption habits among adult population clusters, which were identified through food frequency questionnaire in Yerevan.The study findings indicated variations in radon activity levels across administrative districts. The highest average activity concentrations were detected in Davtashen (7.07 Bq/L), while the lowest average was observed in Kanaker-Zeytun (1.57 Bq/L). The overall pattern of spatiotemporal variation during monitoring period revealed higher prevalence of radon in water in the northern and western parts of the city compared to the east and south, indicating different sources of drinking water. The radon-associated hazard assessment from water, using a deterministic approach (e.g., inhalation, ingestion, radon dissolution in blood, total effective dose), revealed values below the individual dose criterion (IDC) of 0.1 mSv/y. Monte Carlo simulation revealed a probability of exceeding IDC in specific water consumption-based groups. Residents of Yerevan who drink more than 3 L water daily with the highest observed activity concentration of 11.4 Bq/L, have an 86.26 % chance of exceeding IDC. Residents consuming 2.1 L water daily have a 7.02 % chance of exceeding IDC.The study highlights the importance of applied principles and methodologies for radon monitoring, particularly considering actual water consumption data and different risk assessment approaches. Considering the worst-case scenario results, it is recommended to keep tap water consumption up to 3 L per day, keeping the tap open longer to reduce radon levels. It also emphasizes the need for continued monitoring, given the variations in radon activity. The study provides valuable insights into radon exposure assessment, mitigation, and action plans in terms of water safety and public health.

The effect of using jug-type water filters on selected metals concentration in tap water – a case study

ABSTRACT In this study, the effect of the filtration process on Na, K, Mg, Ca, Fe and Zn concentration in water, using filters from one of the leading European manufacturers, was investigated. The increase in Na (up to 300%) and K concentration (up to 320%) at the beginning of jug filter usage was reported. A decrease in Ca, Fe and Zn concentration was observed. Standard filters remove 80–90% of Mg from tap water at the beginning of the usage, while magnesium-enriching ones slightly increase its concentration – from around 8 to 12–25 mg/L. Significant changes in the filter's operating characteristics were also observed for other studied elements as they wore out. Using Mg-enriching filters can increase magnesium intake from 4–5 to 6–15% of the recommended daily dose from water consumption. The results were also discussed regarding the amounts of macroelements found in commercially available bottled water. The magnesium concentration in tap water after filtration through magnesium-enriching filters was lower compared to bottled mineral waters. The authors note a scope for the development of water filter production technology, in particular, the need to develop filters that more efficiently enrich water with magnesium and do not increase sodium concentration.

Impacts of COVID-19 and climate change on wastewater-derived substances in urban drinking water: Evidence from gadolinium-based contrast agents in tap water from Berlin, Germany

Anthropogenic gadolinium from MRI contrast agents has been detected in surface waters worldwide. It is released with the treated effluents of wastewater treatment plants, similar to other wastewater-derived substances (WWDS) such as pharmaceuticals and personal care products. We determined concentrations of the rare earth elements in tap water from Berlin, Germany, using an automated preconcentration procedure that is both time- and cost-efficient. Anthropogenic gadolinium concentrations in Berlin's tap water increased on average 30-fold between 2009 and 2021. However, the tap water composition responded quickly to the reduced number of MRI scans during the COVID-19 pandemic, and some districts show a decrease from 2016 to 2021. Since climate change causes groundwater levels to decline in many regions, this needs to be mitigated by artificial groundwater recharge with surface water. This will inevitably lead to an increase in WWDS in potable water, which can be cost-efficiently monitored using anthropogenic gadolinium as tracer.

Preparation of PEI/La2O3/Polypropylene fiber filter for household water purifiers and investigation of its phosphate reduction and bacterial control

It has been accepted that limiting phosphate is a prerequisite for bacterial inactivation in tap water. La2O3 nanoparticles were loaded onto polypropylene (PP) fibers through the method of melt spinning. Hydrophilic modification of the adsorbent surface was performed using polyethyleneimine (PEI) to prepare PEI/La2O3/PP. The results indicated that the optimal loading amount of La2O3 was 1 %, and the optimal concentration of PEI was 1 %. The successful loading of La2O3 resulted in a roughened fiber surface and increased fiber diameters. After PEI modification the water contact angle was reduced from 98° to 50°. The pHzpc of PEI/La2O3/PP was determined to be 8.3. The co-existing ions have little effect on phosphate adsorption. Phosphate adsorption can be well described by Redlich-Peterson model with a maximum KR-P of 3.98 × 10−5 L/mg. Adsorption kinetics fit well with the pseudo-second-order reaction equation. The activation energy (Ea) is determined to be 57.9 kJ/mol, providing the evidence of chemical nature of the reaction involving phosphate ions on the surface of PEI/La2O3/PP. The PEI/La2O3/PP adsorbent can reduce the phosphate concentration in tap water to below 0.01 mg/L, leading to a reduction in Escherichia coli concentration from approximately 10,000 CFU/mL to around 10 CFU/mL. The survival rates of Escherichia coli in a multi-nutrient environment are higher than in a single phosphate source environment. Our research provides a new feasible approach for ensuring microbial water quality safety in household water purifiers.

Triangle-Shaped Cerium Tungstate Nanoparticles Used to Modify Carbon Paste Electrode for Sensitive Hydroquinone Detection in Water Samples.

In this study, we propose an eco-friendly method for synthesizing cerium tungstate nanoparticles using hydrothermal techniques. We used scanning, transmission electron microscopy, and X-ray diffraction to analyze the morphology of the synthesized nanoparticles. The results showed that the synthesized nanoparticles were uniform and highly crystalline, with a particle size of about 50 nm. The electrocatalytic properties of the nanoparticles were then investigated using cyclic voltammetry and electrochemical impedance spectroscopy. We further used the synthesized nanoparticles to develop an electrochemical sensor based on a carbon paste electrode that can detect hydroquinone. By optimizing the differential pulse voltammetric method, a wide linearity range of 0.4 to 45 µM and a low detection limit of 0.06 µM were obtained. The developed sensor also expressed excellent repeatability (RSD up to 3.8%) and reproducibility (RSD below 5%). Interferences had an insignificant impact on the determination of analytes, making it possible to use this method for monitoring hydroquinone concentrations in tap water. This study introduces a new approach to the chemistry of materials and the environment and demonstrates that a careful selection of components can lead to new horizons in analytical chemistry.

Effect of Community Water Service on Lead in Drinking Water in an Environmental Justice Community.

Multiple recent studies have found elevated lead (Pb) concentrations in tap water in U.S. homes relying on unregulated private wells. The main Pb source is dissolution from household plumbing, fixtures, and well components. Here, we leverage a natural experiment and citizen science approach to evaluate how extending community water service to an environmental justice community relying on private wells affects Pb in household water. We analyzed Pb in 260 first-draw kitchen tap water samples collected by individual homeowners over a 5-month period in residences that did and did not connect to the community system. Before the community water system was extended, 25% of homes had Pb > 15 μg/L (the U.S. regulatory action level for community water systems) in first-draw water samples. Pb was significantly correlated with nickel (ρ = 0.61), zinc (ρ = 0.50), and copper (ρ = 0.40), suggesting that corrosion of brass fittings and fixtures is the main Pb source. Among homes that connected to the community system, Pb decreased rapidly and was sustained at levels well below 15 μg/L over the study period. Overall, connecting to the municipal water supply was associated with a 92.5% decrease in first-draw tap water Pb.

Fluorescence and colorimetric analysis of β-estradiol based on aptamer assembled spherical nucleic acids.

Detecting β-estradiol (E2) in environmental monitoring is a complex task due to its status as a significant environmental contaminant. The detection methods require precision, sensitivity, and the ability to be conducted on-site without expensive instrumentation. Herein, we developed a novel approach using E2 aptamer assembled spherical nucleic acids (SNAs), which combines the sensitivity of fluorescence and the simplicity of colorimetry. Initially, a fluorescein (FAM)-labeled DNA aptamer is attached to the surface of gold nanoparticles (AuNPs) through hybridization with thiol-labeled DNA, resulting in fluorescence quenching. However, when E2 is present, the aptamer specifically binds to it, displacing from the thiol-DNA and releasing from the AuNP's surface. This leads to the recovery of fluorescence, allowing for quantitative detection of E2 by measuring the increase in fluorescence signal. Additionally, E2 detection can also be achieved visually using ultraviolet light. For colorimetric analysis, we introduce another set of AuNPs modified with thiol-DNA complementary to the DNA remaining on the surface of the previous AuNPs. When E2 triggers the release of the aptamer, the DNA on both AuNPs hybridized to each other, causing the aggregation of AuNPs and resulting in a distinct color change from red to purple. The detection limits for fluorescence and colorimetric analyses are 1 nM and 5 nM, respectively. We successfully applied this biosensing strategy to determine E2 concentrations in tap water and serum samples. Furthermore, our assay exhibits high selectivity towards E2 over other estrogens. Overall, this innovative approach provides an effective and versatile method for convenient on-site monitoring of E2.

Synthesis and characterization silica-MB@GO-NH2 particle as fluorescence-based chlorine sensor

In this research, we developed a fluorescence-based sensor to determine the sodium hypochlorite concentration (NaOCl) in tap water and swimming pool water samples. The detection of NaOCl was conducted by measuring the luminescence response of analyte in the paper-based sensor modified Silica-MB@GO-NH2 material were synthesized using Hummer's and Stober's methods under UV Light irradiation. Additionally, the prepared material exposed a couple peak 2D and 2G at 2938 cm-1 and 3286 cm-1 with ID/IG ratio 0.98 using Raman characterization which appropriate with the presence of GO structure in the mixture. This result was validated by the appearance of several functional groups like Si-O-Si, NH, OH, and C-C at 1079, 1391, 1611, and 3457 cm-1, respectively. Moreover, the existence of Si-O-Si bond indicates that the silica-MB interaction was perfectly formed, which plays the main role to absorb ultraviolet light that is used as sensor probe. The morphology of particles depicted an aggregated formation of spherical structure with 288 nm particle size, indicating the existence of silica-coated methylene blue. In this work, the paper-based sensor modified Silica-MB@GO-NH2 can detect the NaOCl species with concentration range 10-150 µM (R2 = 0.9757), a detection limit at 2.60 µM and quantification limit at 7.88 µM. Furthermore, this developed sensor has stable measurement with recovery performance 3.65%-6.67% for tap water and 0.05%–0.14% for swimming pool water. This result indicates that the prepared sensor can be potentially applied to calculate the hypochlorite species in the aquatic environment.

Density and proximity of oil and gas wells and concentrations of trace elements in urine, hair, nails and tap water samples from pregnant individuals living in Northeastern British Columbia

BackgroundOil and gas exploitation can release several contaminants in the environment, including trace elements, with potentially deleterious effects on exposed pregnant individuals and their developing fetus. Currently, there is limited data on pregnant individuals’ exposure to contaminants associated with oil and gas activity. ObjectivesWe aimed to 1)measure concentrations of trace elements in biological and tap water samples collected from pregnant individuals participating in the EXPERIVA study; 2)compare with reference populations and health-based guidance values; 3)assess correlations across matrices; and 4)evaluate associations with the density/proximity of oil and gas wells. MethodsWe collected tap water, hair, nails, and repeated urine samples from 85pregnant individuals, and measured concentrations of 21trace elements. We calculated oil and gas well density/proximity (Inverse Distance Weighting [IDW]) for 4buffer sizes (2.5 km, 5 km, 10 km, no buffer). We performed Spearman’s rank correlation analyses to assess the correlations across elements and matrices. We used multiple linear regression models to evaluate the associations between IDWs and concentrations. ResultsSome study participants had urinary trace element concentrations exceeding the 95th percentile of reference values; 75% of participants for V, 29% for Co, 22% for Ba, and 20% for Mn. For a given trace element, correlation coefficients ranged from −0.23 to 0.65 across matrices; correlations with tap water concentrations were strongest for hair, followed by nails, and urine. Positive (e.g., Cu, Cr, Sr, U, Ga, Ba, Al, Cd) and negative (e.g., Fe) associations were observed between IDW metrics and the concentrations of certain trace elements in water, hair, and nails. SignificanceOur results suggest that pregnant individuals living in an area of oil and gas activity may be more exposed to certain trace elements (e.g., Mn, Sr, Co, Ba) than the general population. Association with density/proximity of wells remains unclear.

Separating Measurement Error and Signal in Environmental Data: Use of Replicates to Address Uncertainty.

Measurement uncertainty has long been a concern in the characterizing and interpreting environmental and toxicological measurements. We compared statistical analysis approaches when there are replicates: a Naı̈ve approach that omits replicates, a Hybrid approach that inappropriately treats replicates as independent samples, and a Measurement Error Model (MEM) approach in a random effects analysis of variance (ANOVA) model that appropriately incorporates replicates. A simulation study assessed the effects of sample size and levels of replication, signal variance, and measurement error on estimates from the three statistical approaches. MEM results were superior overall with confidence intervals for the observed mean narrower on average than those from the Naı̈ve approach, giving improved characterization. The MEM approach also featured an unparalleled advantage in estimating signal and measurement error variance separately, directly addressing measurement uncertainty. These MEM estimates were approximately unbiased on average with more replication and larger sample sizes. Case studies illustrated analyzing normally distributed arsenic and log-normally distributed chromium concentrations in tap water and calculating MEM confidence intervals for the true, latent signal mean and latent signal geometric mean (i.e., with measurement error removed). MEM estimates are valuable for study planning; we used simulation to compare various sample sizes and levels of replication.

Ionic liquid-modified multi-walled carbon nanotube paste electrode for cadmium and lead ion determinations

The detection of trace heavy metal ions is important in monitoring water quality, a vital freshwater source. This study presents the preparation of a multi-walled carbon nanotube (MWCNTs) paste electrode using a pasting mixture of 1-butyl-3-methylimidazolium hexafluorophosphate ionic liquid ([Bmim][PF6] IL) and paraffin oil for the determination of Cd2+ and Pb2+. Scanning electron microscopy, Fourier-transform infrared spectroscopy, and Raman spectroscopy were applied to characterize the paste composites. The electrochemical behavior of the fabricated electrodes was analyzed by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) techniques. The [Bmim][PF6]-MWCNTs electrode showed enhanced sensitivity for Cd2+ and Pb2+ detections over linear sweep anodic stripping voltammetry (LSASV) performances. Experimental results showed that the MWCNTs-IL-1 electrode using a pasting mixture of 10 μL of [Bmim][PF6] and 190 μL of paraffin oil was the most suitable for Cd2+ and Pb2+ determinations. The LSASV conditions for Cd2+ and Pb2+ analysis at the MWCNTs-IL-1 electrode were optimized, including the deposition potential, deposition time, and pH of the working solution. The stripping peak currents were linearly correlated with the concentration ranges of Cd2+ (1–35 μg/L) and Pb2+ (1–90 μg/L) for both individual and simultaneous determinations. The MWCNTs-IL-1 electrode exhibited high repeatability, reproducibility, and stability over a 30-day storage period. The real applicability of the MWCNTs-IL-1 electrode was demonstrated by successful determinations of Cd2+ and Pb2+ concentrations in tap water and surface water samples, which agreed with the results obtained by inductively coupled plasma mass spectrometry.

Human health risk assessment of Triclosan in water: spatial analysis of a drinking water system.

Triclosan (TCS) has been increased in the water during the COVID-19 pandemic because it cannot remove by conventional water treatment. In addition, it can accumulate in the human body over time through long-term exposure. Therefore, the occurrence of TCS in the water treatment plant (WTP) and tap water, and its human health risk assessment through tap water ingestion, dermal absorption, and inhalation routes in Isfahan, Iran, were investigated. Moreover, spatial regression methods were used for the prediction of water quality parameters, TCS concentration, and total hazard quotient (HQ). The average TCS concentration in the influent and effluent of WTP and tap water was 1.6, 1.4, and 0.4 μg/L, respectively. Conventional WTP has low efficiency in the removal of TCS (12.6%) from water. The average values of total HQ for males were 7.79×10-5, 4.97×10-4, and 4.97×10-5 and for females were 3.31×10-5, 2.11×10-4, and 2.11×10-5 based on RfDEPA, RfDMDH, and RfDRodricks, respectively that were in the low-risk levels (HQ<1). Furthermore, TCS concentration in tap water and the ingestion rate of drinking water had the highest effect on the risk of TCS exposure from tap water. The non-carcinogenic health risk of TCS in water was low. The results of this study may be useful for promoting WTP processes to remove emerging pollutants.

Examining the influence of desalinated water on iodine concentration in tap water in Israel

IntroductionIn Israel, desalinated water is a major source of drinking water. Previous studies have suggested that the levels of iodine in water provided by authorities may not accurately reflect the levels reaching end-users. Materials and MethodsWe analyzed 21 tap water samples collected from different localities across Israel, 13 post-treated desalinated water samples from three of the largest Israeli desalination plants, and several natural water samples. An improved method of ICP-MS developed in our laboratory was used to analyze the content of iodine and other macro-elements, and determination of iodine was performed in alkaline media. ResultsOur results showed that it is possible to distinguish between sample groups based on iodine concentration, water hardness, and Ca/Mg ratio. The median iodine concentrations for four groups of tap water samples ranged from 0.3 to 12.3 µg/L, which is lower than the concentrations previously reported by other researchers in Israel. Based on typical consumption, the water samples can provide no more than 3.39% of the recommended dietary allowance level for iodine. The analysis of post-treated desalinated water samples indicated that these waters comply with industrial specifications but contain only trace concentrations of iodine and much less magnesium than recommended by different public health authorities for public consumption of drinking water. ConclusionThe total iodine concentrations found were lower than several observations reported in previous years in the literature. There are currently no strict regulations regarding iodine and magnesium levels in drinking and/or softened (desalinated) water, but the intensive desalination plant application is already exhibiting a negative impact on public health. Further investigations are needed, but the present study provides useful insights for developing an effective policy to ensure adequate iodine supply for the population of Israel through drinking water.

Colorimetric Paper-Based Analytical Devices (PADs) Backed by Chemometrics for Pd(II) Detection.

This paper presents the development of cheap and selective Paper-based Analytical Devices (PADs) for selective Pd(II) determination from very acidic aqueous solutions. The PADs were obtained by impregnating two cm-side squares of filter paper with an azoic ligand, (2-(tetrazolylazo)-1,8 dihydroxy naphthalene-3,6,-disulphonic acid), termed TazoC. The so-obtained orange TazoC-PADs interact quickly with Pd(II) in aqueous solutions by forming a complex purple-blue-colored already at pH lower than 2. The dye complexes no other metal ions at such an acidic media, making TazoC-PADs highly selective to Pd(II) detection. Besides, at higher pH values, other cations, for example, Cu(II) and Ni(II), can interact with TazoC through the formation of stable and pink-magenta-colored complexes; however, it is possible to quantify Pd(II) in the presence of other cations using a multivariate approach. To this end, UV-vis spectra of the TazoC-PADs after equilibration with the metal ions solutions were registered in the 300-800 nm wavelength range. By applying Partial Least Square regression (PLS), the whole UV-vis spectra of the TazoC-PADs were related to the Pd(II) concentrations both when present alone in solution and also in the presence of Cu(II) and Ni(II). Tailored PLS models obtained with matrix-matched standard solutions correctly predicted Pd(II) concentrations in unknown samples and tap water spiked with the metal cation, making the method promising for quick and economical sensing of Pd(II).

Determination of the radiation dose from radon ingestion and inhalation in different types of drinking water samples collected from Bethlehem province –Palestine

The objective of this study is to investigate the levels of radon gas and increase public awareness of its hazards to health in Bethlehem governorate- Palestine. The concentrations of radon-222 and radium- 226 in 79 different types of water samples were measured. The average values of radon and radium concentrations in tap water, rainwater, groundwater, and mineral water samples were 0.93 Bq/ℓ and 45.5 Bq/kg, 1.01 Bq/ℓ and 49.3 Bq/kg, 1.21 Bq/ℓ and 59.3 Bq/kg, and 0.60 Bq/ℓ and 29.2 Bq/kg, respectively. All the measured radon concentrations in the collected samples were within the limit of 11 Bq/ℓ established by UNSCEAR in 1982. The annual effective doses for ingestion and inhalation due to radon in water were calculated for adults, children, and infants using parameters introduced by UNSCEAR in 2000. The results show that there is no significant risk to public health from radon inhalation or ingestion through drinking water in the study region.

Lithium concentration in tap water, bottled mineral water, and Danube River water in Hungary

Due to increased manufacture and recycling of lithium batteries across the world, we may anticipate a rise in lithium pollution in the aquatic environment and drinking water reservoirs. In order to investigate the current status regarding the lithium content in Hungarian tap waters, samples were collected from the public drinking water supply systems of 19 county seats in Hungary during seasonally selected times. Depending on the water sources, such as bank-filtrated river water, surface water from open reservoirs, and groundwater, the lithium concentrations varied between 0.90–4.23, 2.12–11.7 and 1.11–31.4 µg/L, respectively, while the median values were 3.52, 5.02 and 8.55 µg/L, respectively. The lithium concentration in the bottled Hungarian mineral waters was also determined since the daily intake of lithium can be influenced by the consumption of mineral waters. The concentrations ranged from 4.2 to 209 µg/L, while the median value was only 17.8 µg/L. Additionally, a correlation was only found between lithium and potassium concentrations. The lithium concentration was also assessed at ten sampling locations in the Hungarian segment of the Danube River since the Danube water is also a water source for additional drinking water utilities using bank filtration technology. The mean and median lithium concentrations were 2.78 and 2.64 µg/L, respectively.