Drinking Water Samples Research Articles

Assessment of Water Quality and its Risk to Human Health Posed by Drinking Water from Open Sources in Jammu and Kashmir

Globally, the quality of the water has been connected to health outcomes. This study assessed the community practices surrounding water collection and storage, the physicochemical and bacteriological quality of drinking water supplied by the public health division from the point of use to the source in Anatnag, and the risks to human health associated with water consumption. A water quality assessment was performed on one hundred samples. To find out how the community moves water from its source to its point of use and stores it, questionnaires were employed. The majority of the homes (73%) do not purify their water before consumption, and many of them reported frequent interruptions in the water supply. Although total coliform and E. coli were not found in the water samples taken at the reservoir's source, It was discovered that there was significant E. Col and total coliform contamination in the samples taken from the street taps and the domestic storage containers at the point of use. During the rainy season, higher levels of E. Coli and total coliform were found than during the dry season. The amounts of trace metals in the drinking water samples fell below the World Health Organization's and Indian Standards' acceptable limit. Drinking water through ingestion and cutaneous channels has noncarcinogenic effects that are assessed using hazard quotient toxicity potential and cumulative hazard index. These effects are less than unity, which suggests that there may not be a major non-carcinogenic health risk associated with water intake. sporadic disruptions to the water supply as well as specific methods of water storage and transit by residents of the community raise the possibility of contaminated water. We suggest that the province of Kashmir receive a more steady supply of treated water and that its citizens be instructed in hygienic methods for carrying and storing drinking water from the point of origin to the place of use

Characterization of Nanoparticles in Drinking Water Using Field-Flow Fractionation Coupled with Multi-Angle Light Scattering and Inductively Coupled Plasma Mass Spectrometry

The current absence of well-established and standardized methods for characterizing submicrometer- and nano-sized particles in water samples presents a significant analytical challenge. With the increasing utilization of nanomaterials, the potential for unintended exposure escalates. The widespread and persistent pollution of water by micro- and nanoplastics globally is a concern that demands attention, not only to reduce pollution but also to develop methods for analyzing these pollutants. Additionally, the analysis of naturally occurring nano entities such as bubbles and colloidal matter poses challenges due to the lack of systematic and consistent methodologies. This study presents Asymmetric Flow Field-Flow Fractionation (AF4) separation coupled with a UV-VIS spectrometer followed by Multi-Angle Light Scattering (MALS) for detection and size characterization of nanometric entities. It is coupled with an Inductively Coupled Plasma Mass Spectrometer (ICP-MS) for elemental analysis. Water samples from different sources, such as untreated mountain spring water, groundwater, and bottled drinking water, were analyzed. The system was calibrated using pure particle standards of different metallic compositions. Our study demonstrates the capability of AF4-UV-MALS-ICP-MS to detect metals such as Al, Ba, Cu, and Zn in particles of around 200 nm diameter and Mg associated with very small particles between 1.5 and 10 nm in different drinking water samples.

Drinking Water and Biofilm as Sources of Antimicrobial Resistance in Free-Range Organic Broiler Farms.

Drinking water distribution systems (DWDSs) represent an ideal environment for biofilm formation, which can harbor pathogenic and antimicrobial-resistant bacteria. This study aimed to assess longitudinally the microbial community composition and antimicrobial resistance (AMR), as determined by 16S rRNA NGS and qPCR, respectively, in drinking water (DW) and biofilm from DWDSs, as well as faeces, of free-range organic broiler farms. The role of DWDSs in AMR gene (ARG) dissemination within the farm environment and transmission to animals, was also assessed. DW and biofilm microbial communities differed from those of faecal samples. Moreover, potentially pathogenic and opportunistic bacteria (e.g., Staphylococcaceae) were identified in water and biofilms. High prevalence and abundance of ARGs conferring resistance to carbapenems (i.e., blaNDM), 3rd and 4th generation cephalosporins (i.e., blaCMY-2), (fluoro)quinolones (i.e., qnrS), and polymyxins (i.e., mcr-3 and mcr-5) were detected in DW, biofilm, and faecal samples, which is of concern for both animal and human health. Although other factors (e.g., feed, pests, and wildlife) may contribute to the dissemination of AMR in free-range organic poultry farms, this study indicates that DWDSs can also play a role.

Low-Volume Electrochemical Sensor Platform for Direct Detection of Paraquat in Drinking Water

Direct testing of pesticide contaminants in drinking water is a challenge. Portable and sensitive sensor platforms are desirable to test water contaminants directly at farm and consumer levels. In this study, we have demonstrated the feasibility of an electrochemical sensor for the direct detection of paraquat (PQ) in drinking water samples. An immunoassay-based sensing platform was fabricated using PQ-specific antibody immobilized on the surface of the electrochemically reduced graphene oxide (rGO) modified screen-printed carbon electrode (rGO-SPCE). Using non-faradaic electrochemical impedance spectroscopy (EIS) as a detection tool, the sensor platform demonstrated a dynamic response for PQ concentration in drinking water ranging from 0.05 ng/mL to 72.9 ng/mL (0.19 to 243.8 nM), with a coefficient of determination (r2) of 0.997 and a limit of detection of 0.05 ng/mL (0.19 nM). Percentage recovery within ±20% error was obtained, and the sensor cross-reactivity test showed a selective response against glyphosate antigen. With the flexibility to use single-frequency EIS and low sample volume, the developed sensor demonstrated testing in water samples directly without any sample pre-processing. This low-volume electroanalytical sensor platforms can be translated into portable testing tools for the detection of various water contaminants.

Pathways of exposure to Vibrio Cholerae in an urban informal settlement in Nairobi, Kenya.

Cholera is a diarrhoeal disease caused by Vibrio cholerae (V. cholerae) bacterium, with strains belonging to serogroups 01 and 0139 causing a huge proportion of the disease. V. cholerae can contaminate drinking water sources and food through poor sanitation and hygiene. This study aimed to identify environmental routes of exposure to V. cholerae within Mukuru informal settlement in Nairobi. We collected nine types of environmental samples (drinking water, flood water, open drains, surface water, shaved ice, raw produce, street food, soil, and public latrine swabs) over 12 months. All samples were analysed for V. cholerae by culture and qPCR, then qPCR-positive samples were quantified using a V. cholerae DNA standard. Data about the frequency of contact with the environment was collected using behavioural surveys. Of the 803 samples collected, 28.5% were positive for V. cholerae by qPCR. However, none were positive for V. cholerae by culture. V. cholerae genes were detected in majority of the environmental water samples (79.3%), including open drains, flood water, and surface water, but were only detected in small proportions of other sample types. Vibrio-positive environmental water samples had higher mean V. cholerae concentrations [2490-3469 genome copies (gc) per millilitre (mL)] compared to drinking water samples (25.6 gc/mL). Combined with the behavioural data, exposure assessment showed that contact with surface water had the highest contribution to the total V. cholerae exposure among children while ingestion of municipal drinking water and street food and contact with surface water made substantial contributions to the total V. cholerae exposure for adults. Detection of V. cholerae in street food and drinking water indicates possible risk of exposure to toxigenic V. cholerae in this community. Exposure to V. cholerae through multiple pathways highlights the need to improve water and sanitation infrastructure, strengthen food hygiene practices, and roll out cholera vaccination.

Overview of the pesticide contamination provided by the last Brazilian water quality surveillance information system for human consumption (SISÁGUA 2022) report

The Water Quality Surveillance Information System for Human Consumption (SISÁGUA) is designed to manage the risks of water contamination for human consumption. This short communication focuses on data from the 2022 Report regarding pesticide analysis. The data centers on 27 active pesticide ingredients found in drinking water samples exceeding the maximum residual limits (MRLs) established by Brazilian legislation. Results indicate that 1609 municipalities (60 %) found at least one pesticide in their water. Two hundred ten municipalities detected all 27 pesticides tested, with 11 of these pesticides reported to have some carcinogenic potential. Nearly one and a half million people were exposed to levels above the Brazilian MRL, with the sum of maximum detected residues exceeding 80,000 ppb. Additionally, the report highlights that 53 % of Brazilian municipalities did not submit water monitoring data for human consumption. Thus, improving and expanding the scope of water analysis within the SISÁGUA framework is essential.

Exploring the potential of machine learning to understand the occurrence and health risks of haloacetic acids in a drinking water distribution system

Determining the occurrence of disinfection byproducts (DBPs) in drinking water distribution system (DWDS) remains challenging. Predicting DBPs using readily available water quality parameters can help to understand DBPs associated risks and capture the complex interrelationships between water quality and DBP occurrence. In this study, we collected drinking water samples from a distribution network throughout a year and measured the related water quality parameters (WQPs) and haloacetic acids (HAAs). 12 machine learning (ML) algorithms were evaluated. Random Forest (RF) achieved the best performance (i.e., R2 of 0.78 and RMSE of 7.74) for predicting HAAs concentration. Instead of using cytotoxicity or genotoxicity separately as the surrogate for evaluating toxicity associated with HAAs, we created a health risk index (HRI) that was calculated as the sum of cytotoxicity and genotoxicity of HAAs following the widely used Tic-Tox approach. Similarly, ML models were developed to predict the HRI, and RF model was found to perform the best, obtaining R2 of 0.69 and RMSE of 0.38. To further explore advanced ML approaches, we developed 3 models using uncertainty-based active learning. Our findings revealed that Categorical Boosting Regression (CAT) model developed through active learning substantially outperformed other models, achieving R2 of 0.87 and 0.82 for predicting concentration and the HRI, respectively. Feature importance analysis with the CAT model revealed that temperature, ions (e.g., chloride and nitrate), and DOC concentration in the distribution network had a significant impact on the occurrence of HAAs. Meanwhile, chloride ion, pH, ORP, and free chlorine were found as the most important features for HRI prediction. This study demonstrates that ML has the potential in the prediction of HAA occurrence and toxicity. By identifying key WQPs impacting HAA occurrence and toxicity, this research offers valuable insights for targeted DBP mitigation strategies.

Far-UVC 222 nm Treatment: Effects of Nitrate/Nitrite on Disinfection Byproduct Formation Potential.

Irradiation at far ultraviolet C (far-UVC) 222 nm by krypton chloride (KrCl*) excilamps can enhance microbial disinfection and micropollutant photolysis/oxidation. However, nitrate/nitrite, which absorbs strongly at 222 nm, may affect the formation of disinfection byproducts (DBPs). Herein, we evaluated model organic matter and real water samples and observed a substantial increase in the formation potential for trichloronitromethane (chloropicrin) (TCNM-FP), a nitrogenous DBP, by nitrate or nitrite after irradiation at 222 nm. At a disinfection dose of 100 mJ·cm-2, TCNM-FP of humic acids and fulvic acids increased from ∼0.4 to 25 and 43 μg·L-1, respectively, by the presence of 10 mg-N·L-1 nitrate. For the effect of nitrate concentration, the TCNM-FP peak was observed at 5-10 mg-N·L-1. Stronger fluence caused a greater increase of TCNM-FP. Similarly, the increase of TCNM-FP was also observed for wastewater and drinking water samples containing nitrate. Pretreatment using ozonation and coagulation, flocculation, and filtration or the addition of H2O2 can effectively control TCNM-FP. The formation potential of other DBPs was minorly affected by irradiation at 222 nm regardless of whether nitrate/nitrite was present. Overall, far-UVC 222 nm treatment poses the risk of increasing TCNM-FP of waters containing nitrate or nitrite at environmentally relevant concentrations and the mitigation strategies merit further research.

Identification of Key Toxic Substances Considering Metabolic Activation: A Combination of Transcriptome and Nontarget Analysis.

There have been numerous studies using effect-directed analysis (EDA) to identify key toxic substances present in source and drinking water, but none of these studies have considered the effects of metabolic activation. This study developed a comprehensive method including a pretreatment process based on an in vitro metabolic activation system, a comprehensive biological effect evaluation based on concentration-dependent transcriptome (CDT), and a chemical feature identification based on nontarget chemical analysis (NTA), to evaluate the changes in the toxic effects and differences in the chemical composition after metabolism. Models for matching metabolites and precursors as well as data-driven identification methods were further constructed to identify toxic metabolites and key toxic precursor substances in drinking water samples from the Yangtze River. After metabolism, the metabolic samples showed a general trend of reduced toxicity in terms of overall biological potency (mean: 3.2-fold). However, metabolic activation led to an increase in some types of toxic effects, including pathways such as excision repair, mismatch repair, protein processing in endoplasmic reticulum, nucleotide excision repair, and DNA replication. Meanwhile, metabolic samples showed a decrease (17.8%) in the number of peaks and average peak area after metabolism, while overall polarity, hydrophilicity, and average molecular weight increased slightly (10.3%). Based on the models for matching of metabolites and precursors and the data-driven identification methods, 32 chemicals were efficiently identified as key toxic substances as main contributors to explain the different transcriptome biological effects such as cellular component, development, and DNA damage related, including 15 industrial compounds, 7 PPCPs, 6 pesticides, and 4 natural products. This study avoids the process of structure elucidation of toxic metabolites and can trace them directly to the precursors based on MS spectra, providing a new idea for the identification of key toxic pollutants of metabolites.

Assessment of Radon Concentration and Health Hazards in Natural Spring Water of a Sub-Himalayan District

The objective of this study was to evaluate the extent of radon contamination in twenty-six drinking water samples from natural springs were collected from Dhirkot Azad Kashmir, along with four bottled mineral water samples. Radon gas escapes from the earth’s crust due to uranium ores and diffuses into the atmosphere. This study assessed the levels of radon concentration, the yearly effective radiation dose, and carcinogenic risk from radon exposure in drinking water samples. The radon concentration varied from 0.28 to 30.25 Bq/L. The mean radon concentration of all samples was found to be 7.86 ± 2.3 Bq/L. The radon concentrations in bottled drinking water were found to be lower than those in natural springs. The statistical and GIS analyses included the use of interpolation and Pearson’s correlation matrix. Seven samples had radon concentration that surpassed the standard limit established by the US-EPA, which is 11 Bq/L. The average annual effective dose from inhalation and ingestion was found to be lower than the value (0.1 mSv/y) provided by the WHO, but for some natural spring water samples, it exceeded the risk limit. The cancer risk revealed that 40% of the samples had an elevated lifetime cancer risk from radon exposure. Overall, the majority of the results obtained aligned with the worldwide guidelines established by the US-EPA. However, there were a few instances where the limits were exceeded, and constant monitoring is recommended. This study establishes a baseline for radon concentration in the area and provides a basis for future studies.

Occurrence of pharmaceutical residues in drinking water: a systematic review.

The aim of the present paper was to give a complete picture on the drinking water contamination by pharmaceutical residues all over the world. For this purpose, a systematic review was carried out for identifying all available research reporting original data resulting by sampling campaign and analysis of "real" drinking water samples to detect pharmaceutical residues. The investigated databases were PubMed, Scopus, and Web of Science. A total of 124 studies were included; among these, 33 did not find target analytes (all below the limit of detection), while the remaining 91 studies reported the presence for one or more compounds, in concentrations ranging from a few units to a few tens of nanograms. The majority of the studies were performed in Europe and the most represented categories were nonsteroidal anti-inflammatory drugs and analgesics. The most common analytical approach used is the preparation and analysis of the samples by solid-phase extraction and chromatography coupled to mass spectrometry. The main implications resulting from our review are the need for (a) further studies aimed to allow more accurate environmental, wildlife, and human health risk assessments and (b) developing integrated policies promoting less environmentally persistent drugs, the reduction of pharmaceuticals in livestock breeding, and the update of wastewater and drinking water treatment plants for a better removal of drugs and their metabolites.

Uranium in Drinking Water and Bladder Cancer: A Case-Control Study in Michigan.

Uranium is naturally occurring in groundwater used for drinking; however, health risks from naturally occurring concentrations are uncertain. Uranium can cause both radiological and chemical toxicity following ingestion. Bladder and kidneys receive a dose when uranium is excreted into the urine. Investigate the association between uranium in drinking water and bladder cancer risk in a case-control study. A population-based bladder cancer case-control study was conducted in 11 counties of southeastern Michigan. A total of 411 cases and 566 controls provided drinking water and toenail samples and answered questions about lifestyle and residential history. Uranium was measured in drinking water and toenails, and its association with bladder cancer was assessed via unconditional logistic regression models. Median uranium concentration in water was 0.12 μg L-1, with a maximum of 4.99 μg L-1, and median uranium concentration in toenails was 0.0031 μg g-1. In adjusted regression models, there was a suggestion of a protective effect among those exposed to the upper quartile of uranium in drinking water (HR = 0.64, 95% CI: 0.43, 0.96) and toenails (HR 0.66; 95% CI 0.45, 0.96) compared to those in the lowest quartile. Our objective is to investigate additional adjustment of drinking water source at home residence at time of recruitment to address potential selection bias and confounding attenuated results toward the null for drinking water uranium (HR = 0.68, 95% CI: 0.44, 1.05) and toenail uranium (HR = 0.80, 95% CI: 0.53, 1.20). This case-control study showed no increased risk of bladder cancer associated with uranium found in drinking water or toenails.

Unveiling the potential of Fe2O3/TiO2 system to produce clean water: An effective and low‒cost approach for arsenic removal from ground water

The aim of this project is to estimate and eliminate arsenic by using cost‒effective approach. For the purpose, anatase TiO2 has been synthesized and sensitized with Fe2O3 using hydrothermal approach. As‒synthesized adsorbents namely Fe2O3/TiO2 were employed to remove the arsenic (III and V) contents in the form of arsenomolybdate complex (AMC). The structural morphologies and optical characteristics have been examined and assessed by various advance approaches like XRD, FTIR, Raman, SEM and AFM techniques. The BET, EDX and XPS techniques have confirmed the porosity, phase purity and chemical compositions. The stability of adsorbents was evaluated using thermo–gravimetric analysis. To extend the utility of adsorbents for successful implementation, various ground drinking water samples have been collected from Tehsil Jahania‒PK. For the quick removal and spectroscopic quantifications, arsenic contents were first converted to the arsenomolybdate complex (AMC) and then extracted via adsorption. Langmuir and Freundlich isotherm models were employed to evaluate and confirm the adsorption efficiencies, whereas Temkin model was employed to assure the electrostatic attraction between Fe2O3/TiO2 and AMC. Results indicate that the maximum adsorption capacity of Fe2O3/TiO2 is 130.1 mg/g. On the basis of survey reports and results, it has been concluded that this approach hold potential to replace the traditional adsorbents used for arsenic removal technologies.

A Mixed Methods Approach to Understanding the Public Health Impact of a School-Based Citizen Science Program to Reduce Arsenic in Private Well Water.

Exposure to arsenic (As) in well water is a well-documented public health issue for Maine and New Hampshire, as well as for other states in the United States and abroad. Arsenic contamination of well water in these locations is primarily attributed to metasedimentary bedrock that leaches As into groundwater. However, As can also enter groundwater reserves from soils contaminated by the historical use of arsenical pesticides. Approximately half of the households in Maine and New Hampshire rely on private wells, many of which have elevated As. Arsenic exposure has been associated with an increased risk of cancer, cardiovascular disease, reduced infection resistance, and lower intelligence quotient in children. Despite these known health impacts, well water testing and treatment are not universal. We have approached the problem of low well water testing rates in Maine and New Hampshire communities by developing the All About Arsenic (AAA) project, which engages secondary school teachers and students as citizen scientists in collecting well water samples for analysis of As and other toxic metals and supports their outreach efforts to their communities. We assessed this project's public health impact by analyzing student data relative to existing well water quality datasets in both states. In addition, we surveyed private well owners who contributed well water samples to the project to determine the actions taken to mitigate As in well water. Students collected 3,070 drinking water samples for metals testing, and 752 exceeded New Hampshire's As standard of . The AAA data has more than doubled the amount of information available to public health agencies about well water quality in multiple municipalities across both states. Students also collected information about well types and treatment systems. Their data reveal that some homeowners did not know what type of wells they had or whether they had filtration systems. Those with filtration systems were often unaware of the type of system, what the system was filtering for, or whether the system was designed to remove As. Through interviews with pilot survey participants, we learned that some had begun mitigating their exposure to As and other toxic metals in response to test results from the AAA project. A school-based approach to collecting and analyzing private well water samples can successfully reach communities with low testing rates for toxic elements, such as As and other metals. Importantly, information generated through the program can impact household decision-making, and students can influence local and state policymaking by sharing information in their communities. https://doi.org/10.1289/EHP13421.

The impact of stagnation on the microbial quality of constructed water systems after COVID-19 shutdowns.

In response to COVID-19 pandemic, governments all over the world limited the movement of people and mandated temporary closure of different institutions. While, these measures helped to reduce the spread of COVID-19, stagnant water can cause water quality deterioration. Stagnation is considered in context with the proliferation of pathogenic and facultatively pathogenic bacteria which pose potential health risks to humans. The objective of this study was to document the hygienic microbiological status of different water systems after the first shutdowns (between 18th March 2020 and 18th May 2020) in Hungary in comparison with a reference period (between 3rd January 2020 to 17th March). During the reference period drinking waters were compliant > 95% of total samples to the parametric values. After the short period shutdowns, the ratio of tnon-compliant drinking water samples was 6.6%: mainly Pseudomonas aeruginosa (7%) and coliform bacteria (5%) resulted poor water quality. The microscopic analysis of drinking waters showed that after low water demand the values of non-compliant samples also increased due to the proliferation of Amoebozoa and other Protozoa species. The compliant pool waters' ratio was also high in the reference period (97-99%), while after the shutdowns more samples were positive in both pool operation type (fill-and-drain pools and pools with recirculation) due to the proliferation of P. aeruginosa (14%) and micrococci (12%). Legionella non-compliant samples in hot tap water did not show significant difference during both studied periods (15%) although after stagnation the Legionella CFU (colony forming unit) values of the samples increased markedly.

Enhanced detection of 4-nitrophenol in drinking water: ECL sensor utilizing velvet-like graphitic carbon nitride and molecular imprinting

In this work, a molecularly imprinted electrochemiluminescence (ECL) sensor was developed for selective detection of 4-nitrophenol (4-NP) in drinking water for the first time. By synthesizing velvet-like graphitic carbon nitride (V-g-C3N4) via one-step thermal polycondensation and integrating it with a molecularly imprinted polymer (MIP), the ECL sensor was fabricated. The MIP-modified V-g-C3N4 composites (MIP/V-g-C3N4) were synthesized using a sol-gel method with 4-NP as the template molecule. Under optimal conditions, the ECL sensor exhibited a wide detection range (5 × 10−10-1 × 10−5 mol/L) and a low detection limit (1.8 × 10−10 mol/L). In testing with actual drinking water samples, it displayed high accuracy (recoveries for intraday and inter-day: 93.50–106.2% and 97.00–107.3%, separately) and precision (RSDs for intraday and inter-day: 1.54–4.59% and 1.53–4.28%, respectively). The developed MIP-based ECL sensor demonstrated excellent selectivity, stability, and reproducibility, offering a promising and reliable approach for highly sensitive and selective determination of 4-NP in drinking water.

Label-free multi-line immunochromatographic sensor based on TCBPE for broad-spectrum detection Salmonella in food

BackgroundSalmonella, a foodborne pathogen poses significant threats to food safety and human health. Immunochromatographic (ICTS) sensors have gained popularity in the field of food safety due to their convenience, speed, and cost-effectiveness. However, most existing ICTS sensors rely on antibody sandwich structures which are limited by their dependence on high-quality paired antibodies and restricted sensitivity. For the first time, we combined multi-line ICTS strips with fluorescent bacterial probes to develop a label-free multi-line immunochromatographic sensor capable of detecting broad-spectrum Salmonella. Salmonella was labeled with the aggregation-induced luminescence material TCBPE, resulting in its transformation into a green fluorescent probe. ResultsUsing this sensor, we successfully detected Salmonella typhimurium within the concentration range of 104–108 CFU/mL with a visual detection limit of 6.0 × 104 CFU/mL. Compared to single-line sensors, our multi-line sensor exhibited significantly improved fluorescence intensity resulting in enhanced detection sensitivity by 50 %. Furthermore, our developed multi-line ICTS sensor demonstrated successful detection of 18 different strains of Salmonella without any cross-reaction observed with 5 common foodborne pathogens tested. The applicability and reliability were validated using milk samples, cabbage juice samples as well and drinking water samples suggesting its potential for rapid and accurate detection of Salmonella in real-world scenarios across both the food industry and clinical settings. SignificanceIn this experiment, we developed a TCBPE-based multiline immunochromatographic sensor. Specifically, Salmonella was labeled with the aggregation-induced luminescence material TCBPE, resulting in its transformation into a green fluorescent probe. Through the multi-line analysis system, the detection sensitivity and accuracy of the sensor are improved. In brief, the sensor does not require complex antibody labeling and paired antibodies, and only one antibody is needed to complete the detection process.

Analysis of Drinking Water Quality among Employees of Sulianti Saroso Infectious Disease Hospital

Drinking water is water through or without processing that meets health requirements and can be drunk directly. The aim of the study is to check the quality of drinking water for employees of Sulianti Saroso Infectious Disease Hospital (SSIDH) so that it is suitable or not for consumption in accordance with established quality standards. Drinking water sampling is carried out twice a year with a sampling point of 8 (eight) samples at every 6 (six) months. Based on the results of physical tests, namely smell, turbidity, taste, temperature, total dissolved solids, and color, it shows that the employee's drinking water has met the quality standards according to applicable regulations. Chemical drinking water quality requirements show pH concentrations ranging from 7.22 – 8 and other parameters including organic substances have met the quality standard requirements. Biological test results show the bacteriological quality of drinking water Total Coliform and Escherichia Coli is 0 according the required quality standard of 0 per 100 ml. The quality of drinking water for employees of RSPI Prof. Dr. Sulianti Saroso based on the results of laboratory examinations shows 100% of samples meet the requirements in accordance with the drinking water quality standard.

Low levels of per- and polyfluoroalkyl substances (PFAS) detected in drinking water in Norway, but elevated concentrations found near known sources

Per- and polyfluoroalkyl substances (PFAS) are ubiquitous contaminants which are also found in drinking water. Concentration levels in drinking water vary widely and range from a very low contribution to total daily exposure for humans to being the major source of uptake of PFAS. PFAS concentrations in Norwegian drinking water has been rarely reported. We investigated concentrations of 31 PFAS in 164 water samples, representing both source water (i.e., before drinking water treatment) and finished drinking water. Samples were taken from 18 different water bodies across Norway. The 17 waterworks involved supply drinking water to 41 % of the Norwegian population. Only four of the waterworks utilised treatment involving activated carbon which was able to significantly reduce PFAS from the source water. Samples of source water from waterworks not employing activated carbon in treatment were therefore considered to represent drinking water with regards to PFAS (142 samples). All samples from one of the water bodies exceeded the environmental quality standard (EQS) for perfluorooctane sulfonic acid (PFOS) according to the water framework directive (0.65 ng/L). No concentrations exceeded the sum of (20) PFAS (100 ng/L) specified in the EU directive 2020/2184 for drinking water. Several EU countries have issued lower guidelines for the sum of the four PFAS that the European Food Safety Authority (EFSA) has established as the tolerable weekly intake (TWI) for PFOS, perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), and perfluorohexane sulfonic acid (PFHxS). Denmark and Sweden have guidelines specifying 2 and 4 ng/L for the sum of these PFAS. Only one of the 142 drinking water samples exceeded the Danish TWI and contained a sum of 6.6 ng/L PFAS. A population exposure model, for individuals drinking water from the investigated sources, showed that only 0.5 % of the population was receiving PFAS concentrations above the Danish limit of 2 ng/L.

Sensitive Determination of Alkali Metals by Liquid Anode Glow Discharge-Atomic Emission Spectrometry (LAGD-AES)

Liquid anode glow discharge-atomic emission spectrometry (LAGD-AES) was employed for the determination of alkali metals in brine and bottled drinking water samples. The results demonstrated that the optimum operating conditions are a discharge voltage of 630 V, a flow rate of 2.0 mL min−1, a supporting electrolyte solution of pH 1.7 HNO3, and a discharge gap of 0.5 mm. Alkaline-earth ions (e.g., Ca2+, Mg2+, and Sr2+) and Cr3+ interfere with the determination of alkali metals. The limits of detection (LODs) for the alkali metals, namely cesium (Cs), potassium (K), lithium (Li), sodium (Na), and rubidium (Rb) are 135, 6.21, 3.15, 7.57, and 31.1 µg L−1, respectively. The relative standard deviations are less than 5%, and the power consumption is approximately 13 W. The obtained results are in good agreement with the certified standard value for Li in the certified reference material and are consistent with the values obtained by ICP-OES and reference standards for K and Na in real samples. The concentrations of the Cs and Rb are considerably below the LAGD-AES detection limit. Consequently, they can be considered negligible. The results of the spiked water analysis are broadly consistent with the spiked values, with recoveries from 82% to 112%. LAGD-AES is an excellent technique for the sensitive determination of alkali metals due to its compact design, no requirement for inert gas, and low energy consumption.