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In the light of the instability of trihalomethanes (THMs) in water, a fast and high accuracy method based on headspace gas chromatography-isotope dilution mass spectrometry (HS-GC-IDMS) technique was developed. The optimised method was validated using fortified water samples. Recoveries between 96.1% and 108.8% with an intermediate precision between 3.9% and 5.7% were achieved. The method was applied in the value assignment of THMs in water in an accuracy-based proficiency testing (PT) programme organised by the Health Sciences Authority (HSA) Singapore. The assigned values obtained for chloroform, bromodichloromethane, dibromochloromethane and bromoform were 73.6 ± 9.3 µg/L, 49.1 ± 5.2 µg/L, 47.7 ± 4.4 µg/L and 70.8 ± 6.8 µg/L, respectively. The PT programme was especially valuable and uncommon as it allowed local water testing laboratories to have access to traceable reference values for the benchmarking of their technical competencies. The procedure undertaken by the Laboratory to prepare a batch of PT sample comprising the unstable analytes, conduct homogeneity and stability testing, as well as value assignment, are presented. The between-samples relative standard deviations (RSDs) obtained in a feasibility batch of THMs concentrate in methanol were improved by four to six times compared to those from the first feasibility batch of THMs in water. Based on z-scores, evaluated using the assigned reference value determined by HS-GC-IDMS, 85% of the participating laboratories in the PT programme achieved satisfactory results. The provision of metrological assigned values heightened the testing laboratories' awareness on the importance of accuracy-based PT programmes for evaluation of true method biases, which is particularly valuable for analytes with regulated limits. [ABSTRACT FROM AUTHOR]

There is a rising concern about the safety risk that trihalomethanes (THMs) in drinking water pose. In this work, to adsorb THMs such as chloroform (TCM), dibromochloromethane (DBCM), bromodichloromethane (BDCM), and bromoform (TBM), we coated chitosan (CS) on coconut shell activated carbon (CAC). The adsorbents were characterized using BET, XRD, FTIR, and SEM techniques. The impact of various variables was examined, including contact time, quantity of adsorbent, initial pH, and initial THM concentrations. Under the same conditions, TCM was adsorbed most efficiently, followed by BDCM, DBCM, and TBM. When the pH was between 4 and 8, the adsorption of THMs onto the coconut shell activated carbon supported chitosan (CS/CAC) varied relatively little; however, when the pH increased above 8, the adsorption of THMs decreased. For THMs, CS/CAC adsorption was a chemical reaction and monolayer adsorption that fit better with the pseudo-second-order kinetic model and the Langmuir isotherm model. According to the thermodynamic study, THMs were adsorbed endothermically and spontaneously on CS/CAC. For column experiments, the adsorption of THMs was influenced by bed height and flow rate. After up to four cycles of adsorption and desorption, it was found that the adsorbent was reusable. The maximum adsorption capacities for Langmuir were 187.27, 114.29, 93.28, and 89.61 µg/g for TCM, BDCM, DBCM, and TBM, respectively. CS/CAC has a high adsorption capacity, especially for TCM, which is responsible for a major portion of THMs in drinking water. This indicates that CS/CAC has a lot of potential uses when it comes to removing THMs from water. [ABSTRACT FROM AUTHOR]

Trihalomethanes, the main drinking water disinfection byproducts, may be carcinogenic and are regulated to amaximum total trihalomethanes (TTHM) of 80 µg/l in the US. We aimed to determine whether total and individual trihalomethanes in drinking water across the US are associated with higher cancer mortality in 6,260 adult participants to the National Health and Nutrition Examination Surveys from 1999 to 2008 followed for mortality until 2019 (median: 14.4 years). At baseline, the geometric mean (standard error) of TTHM in drinking water was 9.61 (0.85) µg/l. During follow-up, 873 deaths occurred, including 207 from cancer. In Cox proportional hazards regression adjusted for relevant covariates, drinking water TTHM (HR: 1.45, 95% CI: 1.16–1.82), chloroform (HR: 1.35, 95% CI: 1.12–1.64), and bromodichloromethane (HR: 1.30, 95% CI: 1.05–1.59) were associated with 30% to 45% higher cancer mortality. Therefore, drinking water trihalomethanes, especially chloroform and bromodichloromethane maybe risk factors for cancer mortality. [ABSTRACT FROM AUTHOR]

The adsorption of trihalomethanes (THMs) from drinking water was investigated in the current study through comparison studies of kaolinite and ZnO@kaolinite nanocomposites. The clay structural network’s successful immobilization on the zincite hexagonal structure of ZnO nanoparticles’ lattice layers was verified by the SEM/EDX analysis. Under the optimum conditions, the maximum removal of THMs was achieved by kaolinite and ZnO@kaolinite nanocomposites after 60 min. The adsorption performance of the ZnO@kaolinite nanocomposites was greater than that of kaolinite because the former had a larger surface area than the latter. The Freundlich isotherm model best matched the adsorption experimental data, which also reveals the existence of multilayer adsorption on a diverse surface with the greatest correlation (R² ¼ 0.956 and 0.954, respectively) for both nanoadsorbents using the pseudo-first-order (PFO), pseudo-second-order (PSO), mixed 1, 2-order (MFSO), and intraparticle diffusion (IPD) models. The mechanism by which THMs in drinking water adsorb onto nanoadsorbents was examined. This revealed that both intraparticle and film diffusion were involved in the adsorption process. Kaolinite and ZnO@kaolinite nanocomposites can be used in water treatment to remove THMs due to their great recyclable and reusable properties, even after six cycles. [ABSTRACT FROM AUTHOR]

Background: Previous studies have demonstrated that there is a correlation between trihalomethanes and disease progression, such as allergic diseases. As we know, only few studies focused on the relationship between trihalomethanes and metabolic diseases, such as diabetes mellitus. Objective: The aim of this study was to further explore the associations between blood trihalomethane concentrations and diabetes mellitus in older adults in the US. Methods: Data were collected from the National Health and Nutrition Examination Study (NHANES) database in the survey cycle during 2013 to 2018, including 2,511 older adults in the US whose blood trihalomethane concentrations were measured, involving chloroform (TCM) and brominated trihalomethanes (Br-THMs). Br-THMs include bromodichloromethane (BDCM), dibromochloromethane (DBCM), and bromoform (TBM). Meanwhile, the concentration of total trihalomethanes (TTHMs) was also measured later. A multivariate logistic regression and restricted cubic spline were used to examine the relationship between blood THMs and diabetes mellitus. Meanwhile, we performed a subgroup analysis, which aims to explore the stability of this relationship in different subgroups. In order to further consider the impact of various disinfection by-products on diabetes, we also used weighted quantile sum (WQS). To explore the correlation in trihalomethanes, we plot a correlation heatmap. Results: Adjusting for potential confounders, we found that there was a significant negative association between chloroform and diabetes mellitus [Model 1 (adjusted for covariates including age, sex, and race, OR = 0.71; 95% CI: 0.50-1.02; p = 0.068; p for trend = 0.094); Model 2 (adjusted for all covariates, OR = 0.68; 95% CI: 0.48-0.96; p = 0.029; p for trend = 0.061)]. In the bromodichloromethane, we reached a conclusion that is similar to TCM [Model 1 (adjusted for covariates including age, sex, and race, OR = 0.54; 95% CI: 0.35-0.82; p = 0.005; p for trend = 0.002); Model 2 (adjusted for all covariates, OR = 0.54; 95% CI: 0.35-0.82; p = 0.003; p for trend = 0.002)]. Meanwhile, the restricted cubic spline curve also further confirms this result (p overall = 0.0027; p overall< 0.001). Based on the analysis in the subgroups, we found that the value p for interaction in the majority of subgroups is higher than 0.1. Trihalomethanes and diabetes were inversely associated, and in the WQS, chloroform and bromodichloromethane were found to be the major contributors to this relationship. In the correlation analysis, we found that most trihalomethanes have a weak correlation, except for TBM and TCM with a strong correlation. Conclusion: Our results in this study showed that blood chloroform, bromodichloromethane concentrations, and diabetes mellitus in older adults in the US are negatively correlated, suggesting that chloroform and bromodichloromethane can be protective factors for diabetes. [ABSTRACT FROM AUTHOR]

The presence of nonylphenol (NP) in bromide-containing water contributed to the formation of regulated disinfection by-products (DBPs): trihalomethanes-4 (THM4) and haloacetic acids-5 (HAA5). This study investigates the effects of ozonation pH on the degradation of NP, DBP formation, and DBP-estimated cytotoxicity. The ozonation pH was varied to 5, 7, and 9 to determine the effect of acidic, neutral, and alkaline conditions. The increase of ozonation initial pH improved the NP degradation. Ozonation of all initial pH conditions could decrease TCM, BDCM, and BDCM formation but increase the TBM formation at alkaline conditions. The formation of mono-HAA5 on the other hand, increased at all ozonation initial pH. Ozonation at acidic and neutral initial conditions can reduce the estimated cytotoxicity of the total formation of THM4 and HAA5 by 74.34 % and 93.31 %, respectively. In contrast, DBP's estimated cytotoxicity was raised by 33.72 % upon ozonation at an initial pH of alkaline. According to the study's findings, lowering the cytotoxicity of DBPs in acidic or alkaline environments can be achieved without changing the ozonation's pH. Based on these findings, pH changes are not required to reduce DBP during ozonation of NP-bromide-containing water. Future research on the impact of natural organic matter is recommended to investigate ozonation's capacity to reduce DBP production during ozonation of NP-containing natural water.

We characterized concentrations of trihalomethanes (THMs), a measure of disinfection byproducts (DBPs), in tap water samples collected from households with utility-supplied water in two rural counties in Appalachian Virginia, and assessed associations with pH, free chlorine, and metal ions which can impact THM formation. Free chlorine concentrations in all samples (n = 27 homes) complied with EPA drinking water guidelines, though 7% (n = 2) of first draw samples and 11% (n = 3) of 5-min flushed-tap water samples exceeded the US Safe Drinking Water Act (SDWA) maximum contaminant level (MCL) for THM (80 ppb). Regression analyses showed that free chlorine and pH were positively associated with the formation of THM levels above SDWA MCLs (OR = 1.04, p = 0.97 and OR = 1.74, p = 0.79, respectively), while temperature was negatively associated (OR = 0.78, p = 0.38). Of the eight utilities serving study households, samples from water served by three different utilities exceeded the EPA MCL for THM. Overall, these findings do not indicate substantial exposures to DBPs for rural households with utility-supplied water in this region of southwest Virginia. However, given the observed variability in THM concentrations between and across utilities, and established adverse health impacts associated with chronic and acute DBP exposure, more research on DBPs in rural Central Appalachia is warranted. HIGHLIGHTS 11% (n = 3) of tap water samples exceeded the EPA MCL threshold for THMs (>80 ppb).; Mean free chlorine residual in tap water samples was ≥0.2 ppm, aligning with regulatory guidance.; More research is warranted to characterize rural exposures and assess potential drivers of DBP formation in small rural systems.;

BackgroundThe Qingcaosha Reservoir is facing issues of algal blooms and eutrophication, and the resulting increase in the level of chlorination disinfection by-products in the water has been a major concern. ObjectiveTo evaluate the impact of "Algae Monitoring and Control Program in Qingcaosha Reservoir" (hereinafter referred to as the program) on the control of trihalomethanes (THMs) in conventional finished water. MethodsFrom 2011 to 2019, water samples were collected from the Lujiazui Water Plant once per season, one sample each time, and the concentrations of four THMs (trichloromethane, dichlorobromomethane, monochlorodibromomethane, and tribromomethane) were measured in the samples. Using 2014 when the program was implemented as a cut-off point, the entire study period was divided into two phases: pre-implementation (2011–2013) and post-implementation(2014–2019). Segmented linear regression with interrupted time series analysis was applied to assess the concentrations and trends of THMs in the finished water before and after the program launch. ResultsThe concentration of total THMs in finished water increased by 1.561 µg·L−1 (P=0.010) for each season of time extension before launching the program. The change in the concentration of total THMs in finished water was not statistically significant after the program launch, but the THMs concentration showed a decreasing trend as the slope was −0.626 (P=0.001). From 2017 until the end of 2019, the average concentration of THMs in finished water of Lujiazui Water Plant dropped to 10 μg·L−1 or less.ConclusionsThe algae and eutrophication control measures in Qingcaosha Reservoir have achieved good results, controlling THMs in finished water at a low level, and the trend of THMs has changed from a yearly increase pattern before the program to a yearly decrease pattern after the program.

The performance capability of granular activated carbon (GAC) adsorption in terms of disinfection by-product (DBPs) removal was investigated with synthetic water containing 1) trihalomethanes (THMs), 2) haloacetronitriles (HANs), and 3) Mix-THMs & HANs. The initial 20 min of adsorption resulted in the maximum adsorption rate, with the total THMs, total HANs, and total Mix–THMs & HANs being 4.972, 2.071, and 6.460 µg/gGAC-min, respectively. GAC dosage affects the adsorption selectivity of THMs and HANs. Under a low GAC dosage, the selectivity of GAC adsorbs more bromo-THMs than chloro-THMs. The adsorption selectivity of THMs on GAC following bromoform > dibromochloromethane > bromodichloromethane > chloroform was investigated. As the GAC concentration increased, the selectivity of THM adsorption by GAC became comparable. Chloro-HAN, in contrast to THMs, has a higher adsorption selectivity than bromo-HAN. Trichloroacetonitrile was removed by GAC more rapidly than the other HAN species when the GAC dose was increased. The toxin of bromoform was primarily eliminated through GAC adsorption, caused by a greater removal rate than that of the other THMs. As an implemented measure, GAC is introduced to reduce THMs and HANs and the toxic contents associated with THMs and HANs. [ABSTRACT FROM AUTHOR]

We characterized concentrations of trihalomethanes (THMs), a measure of disinfection byproducts (DBPs), in tap water samples collected from households with utility-supplied water in two rural counties in Appalachian Virginia, and assessed associations with pH, free chlorine, and metal ions which can impact THM formation. Free chlorine concentrations in all samples (n = 27 homes) complied with EPA drinking water guidelines, though 7% (n = 2) of first draw samples and 11% (n = 3) of 5-min flushed-tap water samples exceeded the US Safe Drinking Water Act (SDWA) maximum contaminant level (MCL) for THM (80 ppb). Regression analyses showed that free chlorine and pH were positively associated with the formation of THM levels above SDWA MCLs (OR = 1.04, p = 0.97 and OR = 1.74, p = 0.79, respectively), while temperature was negatively associated (OR = 0.78, p = 0.38). Of the eight utilities serving study households, samples from water served by three different utilities exceeded the EPA MCL for THM. Overall, these findings do not indicate substantial exposures to DBPs for rural households with utility- supplied water in this region of southwest Virginia. However, given the observed variability in THM concentrations between and across utilities, and established adverse health impacts associated with chronic and acute DBP exposure, more research on DBPs in rural Central Appalachia is warranted. [ABSTRACT FROM AUTHOR]

There are no studies investigating the association of chlorinated drinking water with the risk of cardiovascular diseases (CVDs) among young and middle-aged adults. This study was aimed to assess the associations between trihalomethanes (THMs) in drinking water and the risk of CVDs in in the target group in Petropavlovsk, Kazakhstan. 448 dwellers of Petropavlovsk were asked about their demographic, socioeconomic, lifestyle, behavioural characteristics, and drinking water preferences. THMs exposure was assessed to each participant based on their residence address. We used multivariable logistic regression analysis to assess the risk of CVDs in young and middle-aged adults. The results showed that the risk of hypertension in the adjusted logistic regression model was increased by 68% and a 2.7-fold in the second and third THM tertiles, respectively. Participants in the second and third THM exposure tertiles had a 2.3-fold and a 4.8-fold increase in the risk of arrhythmia. [ABSTRACT FROM AUTHOR]

Background: Associations between maternal periconceptional exposure to disinfection by‐products (DBPs) in drinking water and neural tube defects (NTDs) in offspring are inconclusive, limited in part by exposure misclassification. Methods: Maternal interview reports of drinking water sources and consumption from the National Birth Defects Prevention Study were linked with DBP concentrations in public water system monitoring data for case children with an NTD and control children delivered during 2000–2005. DBPs analyzed were total trihalomethanes, the five most common haloacetic acids combined, and individual species. Associations were estimated for all NTDs combined and selected subtypes (spina bifida, anencephaly) with maternal periconceptional exposure to DBPs in public water systems and with average daily periconceptional ingestion of DBPs accounting for individual‐level consumption and filtration information. Mixed effects logistic regression models with maternal race/ethnicity and educational attainment at delivery as fixed effects and study site as a random intercept were applied. Results: Overall, 111 case and 649 control children were eligible for analyses. Adjusted odds ratios for maternal exposure to DBPs in public water systems ranged from 0.8–1.5 for all NTDs combined, 0.6–2.0 for spina bifida, and 0.7–1.9 for anencephaly; respective ranges for average daily maternal ingestion of DBPs were 0.7–1.1, 0.5–1.5, and 0.6–1.8. Several positive estimates (≥1.2) were observed, but all confidence intervals included the null. Conclusions: Using community‐ and individual‐level data from a large, US, population‐based, case–control study, we observed statistically nonsignificant associations between maternal periconceptional exposure to total and individual DBP species in drinking water and NTDs and subtypes. [ABSTRACT FROM AUTHOR]

The interaction-based hazard index (HIINT), a mixtures approach to characterizing toxicologic interactions, is demonstrated and evaluated by statistically analyzing data on four regulated trihalomethanes (THMs). These THMs were the subject of a multipurpose toxicology study specifically designed to evaluate the HIINT formula. This HIINT evaluation uses single, binary and quaternary mixture THM data. While this research is considered preliminary, the results provide insights on the application of HIINT when toxicology mixture data are available and on improvements to the method. The results for relative liver weight show the HIINT was generally not conservative but did adjust the additive hazard index (HI) in the correct direction, predicting greater than dose-additivity, as seen in the mixture data. For the liver serum enzyme endpoint alanine aminotransferase, the results were mixed, with some indices giving an estimated effective dose lower than the observed mixture effective dose and others higher; in general, the HIINT adjusted the HI in the correct direction, predicting less than dose-additivity. In addition, a methodological improvement was made in the calculation of maximum interaction magnitude. Suggested refinements to the HIINT included mixture-specific replacements for default parameter values and approaches for supplementing the usual qualitative discussions of uncertainty with numerical descriptions. [ABSTRACT FROM AUTHOR]

In this study, proportional response addition (Prop-RA), a model for predicting response from chemical mixture exposure, is demonstrated and evaluated by statistically analyzing data on all possible binary combinations of the four regulated trihalomethanes (THMs). These THMs were the subject of a multipurpose toxicology study specifically designed to evaluate Prop-RA. The experimental design used a set of doses common to all components and mixtures, providing hepatotoxicity data on the four single THMs and the binary combinations. In Prop-RA, the contribution of each component to mixture toxicity is proportional to its fraction in the mixture based on its response at the total mixture dose. The primary analysis consisted of 160 evaluations. Statistically significant departures from the Prop-RA prediction were found for seven evaluations, with three predications that were greater than and four that were less than the predicted response; interaction magnitudes (n-fold difference in response vs. prediction) ranged from 1.3 to 1.4 for the former and 2.6 to 3.8 for the latter. These predictions support the idea that Prop-RA works best with chemicals where the effective dose ranges overlap. Prop-RA does not assume the similarity of toxic action or independence, but it can be applied to a mixture of components that affect the same organ/system, with perhaps unknown toxic modes of action. [ABSTRACT FROM AUTHOR]

Various factors influence the formation of disinfection by-products (DBPs) in drinking water. Therefore, it is crucial to study the formation of DBPs and identify the associated influencing agents in water distribution networks (WDNs) to effectively prevent and control the health risks posed by DBPs. This research aimed to examine THM concentrations in the WDNs of Maragheh, Iran, focusing on seasonal variations. It also compared THM levels between new and old WDNs and assessed the health risks associated with exposure to THMs through various exposure routes. The mean concentrations of Chloroform, BDCM, DBCM, and Bromoform were 44.28 ± 18.25, 12.66 ± 5.19, 3.16 ± 0.89, and 0.302 ± 0.89 μg/L, respectively. Therefore, Chloroform was the predominant compound among the THM species, accounting for over 72 % of the total THMs (TTHMs). The average TTHMs concentration in summer (69.89 μg/L) was significantly higher than in winter (50.97 μg/L) (p

Trihalomethanes (THMs) are one of the main disinfection by-products generated in drinking water (DW). To control health risks caused by THMs several countries have established a maximum content of these chemicals in DW. THMs can be removed by granular activated carbon (GAC) and their adsorption processes have been studied by different authors. However, there are few studies on their desorption from GAC and no data are available on their desorption at a full scale. This paper summarises the results obtained in the monitoring of the adsorption and desorption processes of THMs at a full-scale DW plant considering different types and stages of GACs, as well as several types of influent waters. This research was carried out during 3 years in a full-scale advanced DW plant (6.25 m3·h−1) that can use four different pre-oxidants. An increase on THMs concentration in the outlet of the AC filters due to desorption processes were checked, although the obtained doses were always far below the established European limit (100 μg/L). HIGHLIGHTS Data on the real performance of activated carbon filters in a drinking water treatment plant under different conditions were provided.; Performance of different activated carbons and different ages of these carbons were compared.; Adsorption varies with the characteristics of water inlet, pretreatment applied and GAC type.; Desorption capacity depends on the type and previous usage of the GAC.; Desorption process was verified, for two different types of carbons, when the pre-oxidant was changed, and ozone was used instead of chlorine.;

This groundbreaking research delves into the intricate molecular interactions between MXene and trihalomethanes (THs) through a comprehensive theoretical study employing density-functional theory (DFT). Trihalomethanes are common carcinogenic chlorination byproducts found in water sanitation systems. This study focuses on a pristine MXene [Mn+1·Xn] monolayer and its various terminal [Tx] functional groups [Mn+1·XnTx], strategically placed on the surface for enhanced performance. Our investigation involves a detailed analysis of the adsorption energies of THs on different MXene types, with the MXene-Cl layer emerging as the most compatible variant. This specific MXene-Cl layer exhibits remarkable properties, including a total dipole moment (TDM) of 12.443 Debye and a bandgap of 0.570 eV, achieved through meticulous geometry optimization and computational techniques. Notably, THs such as trichloromethane (CHCl3), bromide-chloromethane (CHBrCl2), and dibromochloromethane (CHBr2Cl) demonstrate the highest TDM values, indicating substantial changes in electronic and optical parameters, with TDM values of 16.363, 15.998, and 16.017 Debye, respectively. These findings highlight the potential of the MXene-Cl layer as an effective adsorbent and detector for CHF3, CHClF2, CHCl3, CHBrCl2, and CHBr2Cl. Additionally, we observe a proportional increase in the TDM and bandgap energy, indicative of conductivity, for various termination atom combinations, such as Mxene-O-OH, Mxene-O-F, Mxene-O-Cl, Mxene-OH-F, Mxene-F-Cl, and Mxene-OH-Cl, with bandgap energies measured at 0.734, 0.940, 1.120, 0.835, and 0.927 eV, respectively. Utilizing DFT, we elucidate the adsorption energies of THs on different MXene surfaces. Our results conclusively demonstrate the significant influence of the termination atom nature and quantity on MXene's primitive TDM value. This research contributes to our understanding of MXene–THs interactions, offering promising avenues for the development of efficient adsorbents and detectors for THs. Ultimately, these advancements hold the potential to revolutionize water sanitation practices and enhance environmental safety. [ABSTRACT FROM AUTHOR]

The reactions between natural organic matter, anthropogenic contaminants, ions, and disinfectants lead to the formation of disinfection by-products (DBPs) such as trihalomethanes (THMs) in drinking water. The formation of THMs is strongly related to the chlorination of water. The study's central objective was to compare the concentration of THMs in twenty developed and developing countries and their disinfection techniques. The THM concentration in 11 developed and 9 developing countries ranged from 0.5 µg/L (Germany) to 215 µg/L (Russia) and 3 µg/L (China) to 439.2 µg/L (Bangladesh), respectively. The developed country has partially succeeded in reducing THM concentration in drinking water, whereas significant steps are needed in developing countries to reduce the existing high THM concentration. The concentration of THMs in water varies among these countries because of the different water sources, water quality, environmental conditions, and efficiency of water treatment technologies. A meaningful relationship has been observed between the properties of water and the THM formation. The use of chemical disinfectants will result in new forms of DBPs that are undesirable due to their carcinogenic and mutagenic effects on human health. The DBP guidelines by various national and international agencies have helped to control and manage the THM concentration in drinking water. However, these regulatory standards are not continuously monitored. Therefore, the formation of these compounds should be prevented either by removing THMs forming precursors or by using an integrated approach for controlling THM formation by implementing advanced water treatment technology. Extensive research is desirable in domains like THM minimization strategies which are easy to deploy, scalable, and cost-effective. [ABSTRACT FROM AUTHOR]

Disinfection is an important step in water treatment, but unpredictable compounds are produced as disinfection by-products (DBPs). DBPs are harmful products to human health so their formation must be prevented during treatment, especially for drinking water treatment. An organic compound such as natural organic matter (NOM) is the main precursor of DBPs due to its presence in river water. The Water Treatment Plant (WTP) in Indonesia, mostly uses river water as raw water. Analysis of the organic matter is very important as this research aims to determine the ability of the WTP units to reduce precursors and the formation of DBPs. The sample was filtered by a 0.45µm microfilter. The presence of NOM was evaluated by the dissolved organic carbon (DOC) parameters, ultraviolet at 254 nm absorbance (UV254), and specific UV absorbance (SUVA). Then measure the Trihalomethanes (THMs) as DBPs after the disinfection. The results of analysis from five WTPs, the DOC concentration is between 3.30-8.20 mg/L; UV254 is 0.70-0.10 cm-1; SUVA is 0.90-3.13 L/mg.m. The ability of conventional WTP units such as coagulation-sedimentation-filtration in removing DOC is around 7%-42%; UV254 is 17%-35%; SUVA is 6%-69%. For the THMs, the concentration after the disinfection is 4.50-127 µg/L. It can be concluded that conventional WTP units are not effective in reducing NOM and the potential of DBPs formation is still high. [ABSTRACT FROM AUTHOR]

Abstract This work presents a collaboration between the so-called Gasset Service Association (responsible for providing drinking water to 100,000 inhabitants from a surface water reservoir) and researchers from the University of Castilla-La Mancha (Spain). The main aim of this work was providing a comprehensive characterization of the formation and removal of disinfection by-products in a real drinking water treatment plant (DWTP) and water distribution network. According to the results obtained, it can be stated that bromate is formed on the pre-oxidation stage and it is not eliminated throughout the DWTP; meanwhile, total organic carbon is partially removed on the clarification process. Moreover, it demonstrates the key role of the residence time and the type of water storage throughout the distribution network (either in pipes or in tanks) due to the combined effect of, at least, four overlapped mechanisms: THMs chemical generation, air stripping, hydrolysis and biological removal. This comprehensive view of the drinking water production and distribution network represents an excellent framework for allowing the improvement in the drinking water quality for a very common water production case study: a medium-size city fed by a surface water source.

Disinfection by-products (DBPs), including trihalomethanes (THMs) and haloacetic acids (HAAs), have attracted attention due to their carcinogenic properties, leading to varying conclusions. This meta-analysis aimed to evaluate the dose-response relationship and the dose-dependent effect of DBPs on cancer risk. We performed a selective search in PubMed, Web of Science, and Embase databases for articles published up to September 15th, 2023. Our meta-analysis eventually included 25 articles, encompassing 8 cohort studies with 6038,525 participants and 10,668 cases, and 17 case-control studies with 10,847 cases and 20,702 controls. We observed a positive correlation between increased cancer risk and higher concentrations of total trihalomethanes (TTHM) in water, longer exposure durations, and higher cumulative TTHM intake. These associations showed a linear trend, with relative risks (RRs) and 95 % confidence intervals (CIs) being 1.02 (1.01–1.03), 1.04 (1.02–1.06), and 1.02 (1.00–1.03), respectively. Gender-specific analyses revealed slightly U-shaped relationships in both males and females, with males exhibiting higher risks. The threshold dose for TTHM in relation to cancer risk was determined to be 55 µg/L for females and 40 µg/L for males. A linear association was also identified between bladder cancer risk and TTHM exposure, with an RR and 95 % CI of 1.08 (1.05–1.11). Positive linear associations were observed between cancer risk and exposure to chloroform, bromodichloromethane (BDCM), and HAA5, with RRs and 95 % CIs of 1.02 (1.01–1.03), 1.33 (1.18–1.50), and 1.07 (1.03–1.12), respectively. Positive dose-dependent effects were noted for brominated THMs above 35 µg/L and chloroform above 75 µg/L. While heterogeneity was observed in the studies for quantitative synthesis, no publication bias was detected. Exposure to TTHM, chloroform, BDCM, or HAA5 may contribute to carcinogenesis, and the risk of cancer appears to be dose-dependent on DBP exposure levels. A cumulative effect is suggested by the positive correlation between TTHM exposure and cancer risk. Bladder cancer and endocrine-related cancers show dose-dependent and positive associations with TTHM exposure. Males may be more susceptible to TTHM compared to females.

This article, published in 1980, explores the connection between algae and the formation of trihalomethanes (THMs) in water supplies. The study conducted in northern Virginia found that THM concentrations varied seasonally and correlated with chlorophyll-a concentrations in the reservoir. Laboratory experiments confirmed that algal biomass and algal extracellular products can act as precursors for THMs. The article emphasizes the importance of understanding the role of algae in water quality and suggests that further research is needed to fully comprehend the relationship between algae and THMs. [Extracted from the article]

Swimming pools are popular entertainment and sport areas that people often use. For this reason, it is crucial to determine the physicochemical properties and Trihalomethanes (THMs) concentrations of swimming pools and the effect of THMs on swimmer health. This study focuses on the physicochemical parameters and THM concentrations of six swimming pools in Eskisehir and the impacts of THMs on human health. Within the study context, physicochemical parameters were examined and swimming pool water standards of various countries and organizations were evaluated. The alkalinity, pH, temperature, hardness, and free chlorine values of the swimming pools were determined to compare with the current standards. Concentrations of chloroform (TCM), bromodichloromethane (BDCM), and dibromochloromethane (DBCM) were also determined in the collected samples. Concentrations were found to be in the range of 11.6-100.1 mg/l for BDCM, 151.5-366.4 mg/l for TCM, ND6.95 mg/l for DBCM, and 172.1-380.7 mg/l for TTHM. From the results, it was determined that TTHM concentrations were above the limit values defined by WHO, while chloroform (except P1 and P5 pools), BDCM (except P3 pool), and DBCM concentrations were significantly below the limit values. TTHMs and chloroform concentrations were high in tap water using sodium hypochlorite as a disinfectant. BDCM and DBCM concentrations were high in pools where groundwater was used. Health risks of THMs in pools through ingestion and dermal absorption were also estimated for both women and men. In the interpretation of the result, it was also found that high concentrations of TTHMs increased the risk, and women’s ingestion-based risk values are slightly higher than men’s ingestion-based risk values. Fingerprints of THM formation in pool water are precursor parameters and it is of great importance to constantly control and take precautions. It has been observed that the use of groundwater as a water source and NaCl as a disinfectant significantly reduces THM formation in swimming pools. However, in order to reduce the BDCM and DBCM concentrations in the use of groundwater, it is recommended to measure the precursor bromide and establish the relevant limit values. The use of hypochlorite disinfectants in pools where tap water is used as a water source increases THM formation. For this reason, it is necessary to determine the amount of organic carbon as a precursor for pools using tap water as a water source and add it to the limit values. In addition, the use of calcium hypochlorite disinfectant instead of sodium hypochlorite reduces THM formation. [ABSTRACT FROM AUTHOR]

Chlorination is one of the most important methods used in water disinfection. Chlorine reacts with natural organic substances in water and causes the formation of disinfection byproducts that might cause health problems. The predominant by-product of chlorination is trihalomethanes. Humic substances, which make up the majority of natural organic substances, are the primary precursors of trihalomethanes. In this study, the effect of different doses of chlorine on the formation of chloroform, bromodichloromethane, dibromochloromethane and bromoform in the presence of natural organic matter and bromide in drinking water was evaluated. Artificial raw water samples prepared with the addition of 2, 3 and 5 mg/L humic acid representing natural organic matter were subjected to chlorination at doses of 1, 2 and 3 mg/L and analysed on the 0th, 3rd and 7th day. The only trihalomethane formed was chloroform with a concentration of 20.52-131.13 µg/L. Increased humic acid and chlorine levels resulted in increased chloroform content. Free chlorine in the water caused chloroform formation to continue even on the 7th day. Accordingly, the amount of chloroform formed increased with the contact time. While the chlorine dose was constant, increased humic acid resulted in decreased free chlorine. To evaluate the effect of bromide on trihalomethane formation, 200 µg/L bromide was added to 2 mg/L humic acid containing water, and 1 mg/L and 2 mg/L chlorination was applied. At the end of the chlorination process in bromide-free waters, only 23.46-41.90 µg/L of chloroform was formed. In the presence of bromide, chloroform, bromodichloromethane, dibromochloromethane and bromoform were formed and the total trihalomethane level increased to 50.03-85.59 µg/L. While the ratio of brominated trihalomethane increased, the amount of chlorinated species decreased. [ABSTRACT FROM AUTHOR]

Contamination of ground and surface water resources with Nitrate (NO3 ), Fluoride (F), Trihalomethanes (THMs), radon, and heavy metals is the most important global concern due to its possible health risks to people. This study reviews the drinking water contaminants and their health outcomes examined in Iran. A review search was conducted using Scopus, Web of Knowledge, PubMed, and Embase databases for associated released articles from 2014 to 2023, resulting in 86 articles relevant to the objective of this study. According to the results of this review, different emerging contaminants were found in potable water, including THMs, NO3, F, radon and heavy elements (i.e., As, Pb, Ni, Cd, Zn, Cu, and Cr). Health outcomes of exposure to radon, F, NO3, THMs, and heavy metals in potable water have been expressed in various epidemiological research studies. More than 65% of the studies reported hazard index (HI) or hazard quotient (HQ) of heavy elements to be greater than one in potable water in Iran for infants, children, teenagers, and adults. Children and infants are at higher health risk than adults in these areas. The level of Arsenic, Cadmium, Lead, Nickel, Zinc, and Chromium, in 26, 26, 17.39, 13.04, 8.69, and 4.3% of the papers was more than the allowable limits, respectively. Various groups of emerging pollutants have been found in potable water in Iran, while epidemiological research studies on their health outcomes are still insufficient. [ABSTRACT FROM AUTHOR]

BackgroundThe concentrations of disinfection by-products (DBPs) are varied by different water sources, disinfectants, or treatment processes in Wuxi, and the associated health risks are also different. ObjectiveTo understand the levels of trihalomethanes (THMs) and haloacetamides (HAcAms) in drinking water in Wuxi, and their variations by water sources, seasons, disinfectants or treatment processes, aiming to provide technical support for ensuring the safety of drinking water. MethodsIn dry period (December 2019) and wet period (July 2020), the finished water and tap water (from the beginning, middle, and end of the drinking water distribution network) from 12 centralized water treatment plants in Wuxi were collected to detect the concentrations of THMs and HAcAms in water samples. A purge and trap-gas chromatography-mass spectrometry method was applied to detect trichloromethane (TCM), bromodichloromethane (BDCM), dibromochloromethane (DBCM), and tribromomethane (TBM), and a solid-phase extraction-gas chromatography-mass spectrometry method to detect dichloroacetamide (DCAcAm), trichloroacetamide (TCAcAm), bromochloroacetamide (BCAcAm), dibromoacetamide (DBAcAm), bromodichloroacetamide (BDCAcAm), dibromochloroacetamide (DBCAcAm), and tribromoacetamide (TBAcAm). Analyses and comparisons were made on the concentrations of THMs and HAcAms in drinking water by water sources (the Yangtze River/the Taihu Lake/reservoir), wet/dry seasons, disinfection methods (liquid chlorine/sodium hypochlorite), and treatment processes (conventional treatment/conventional+advanced treatment). ResultsA total of 96 drinking water samples were collected in Wuxi. THMs were positive in all the water samples (100%), with concentration ranging from 1.027 to 40.225 μg·L−1 and the M (P25, P75) concentration being 24.782 (17.784, 30.932) μg·L−1. None of the 4 THMs exceeded the standard limit of the Standards for drinking water quality (GB 5749-2022 ), and the order of the 4 THMs concentrations from high to low was TCM > BDCM > DBCM > TBM. Five of the 7 HAcAms were detected, the total concentration ranged from 0.137 to 3.288 μg·L−1, and the M (P25, P75) was 0.808 (0.482, 1.704) μg·L−1. The DCAcAm concentration was the highest (2.448 μg·L−1), followed by BCAcAm, while TCAcAm and DBCAcAm were not detected. The M (P25, P75) of the total concentration of THMs in the drinking water from the Taihu Lake was 33.353 (26.649, 36.217) μg·L−1, that of the Yangtze River was 27.448 (24.312, 31.393) μg·L−1, and both were higher than the level of the reservoir [16.359 (2.305, 21.553) μg·L−1] (P0.05). The M (P25, P75) concentrations of THMs and HAcAms in drinking water after advanced treatment process involving ozone, activated carbon, and membrane were 20.565 (3.316, 27.185) μg·L−1 and 0.623 (0.452, 1.286) μg·L−1 respectively, and were lower than the corresponding values after conventional treatment process, 28.740 (23.431, 35.085) μg·L−1 and 0.934 (0.490, 2.116) μg·L−1 respectively (P＜0.05). ConclusionThe concentrations of THMs and HAcAms in drinking water in Wuxi are generally at a low level. The levels of controlled THMs meet the requirements of national standards, and the levels of uncontrolled HAcAms as new DBPs are up to μg·L−1. The concentrations of the two kinds of DBPs in drinking water vary by water sources. The concentrations of THMs and HAcAms produced by the advanced treatment process are lower than that by the conventional treatment process.

BackgroundNon-melanoma skin cancer (NMSC) is a prevalent skin malignancy. It has been indicated in many studies that trihalomethanes (THMs) exposure has a strong association with tumors but has not been associated with NMSC. Our investigation aims to explore the association between THMs exposure and NMSC.MethodsCross-sectional data from the 2011 to 2020 National Health and Nutrition Examination Survey (NHANES) was collected. Poisson regression and subgroup analyses were performed to evaluate the association between individual THMs components and NMSC. Fitted smoothing curves and generalized additive models were also used.ResultsThis study involved 5,715 individuals, 98 (1.7%) of whom self-reported NMSC. After adjusting for covariates, Poisson regression showed that higher blood TBM levels were associated with an increased likelihood of NMSC (OR = 1.03; 95% CI: 1.01–1.05, p = 0.002). However, the correlation between the blood levels of TCM, DBCM, and BDCM and the likelihood of NMSC was not statistically significant (all p > 0.05). Subgroup analysis and interaction tests showed no significant differences between blood TBM concentration and the likelihood of NMSC, indicating that age, gender, and race were significantly independent of this positive association (all p < 0.05).ConclusionsOur results implied that among adults older than 65 years old in the U.S., elevated blood TBM concentrations were positively associated with NMSC. More prospective investigations are required to validate this relationship with the early prevention of NMSC.

Disinfection by-products (DBPs) are formed in the water in swimming pools due to reactions between disinfectants (chlorine, bromine, ozone) and the organic matter introduced by bathers and supply water. High concentrations of DBPs are also reported in the air of indoor swimming pools. Based on a robust multisampling program, the levels and variations of DBPs in the air (trichloramine [TCAM] and trihalomethanes [THMs]) and water (THM) were assessed, as well as their precursors (total organic carbon, water temperature, pH, free, and total chlorine) and proxies (CO2 and relative humidity) in four indoor chlorinated swimming pools. High-frequency sampling was conducted during one high-attendance day for each pool. This study focused on parameters that are easy to measure in order to develop models for predicting levels of THMs and TCAM in the air. The results showed that the number of bathers had an important impact on the levels of THMs and TCAM, with a two-to-three-fold increase in air chloroform (up to 110 μg/m3) and a two-to-four-fold increase in TCAM (up to 0.52 mg/m3) shortly after pools opened. The results of this study for the first time showed that CO2 and relative humidity can serve as proxies for monitoring variations in airborne THMs and TCAM. Our results highlight the good predictive capacity of the developed models and their potential for use in day-to-day monitoring. This could help optimize and control DBPs formation in the air of indoor swimming pools and reduce contaminant exposure for both pool employees and users. [ABSTRACT FROM AUTHOR]

This work presents a collaboration between the so-called Gasset Service Association (responsible for providing drinking water to 100,000 inhabitants from a surface water reservoir) and researchers from the University of Castilla-La Mancha (Spain). The main aim of this work was providing a comprehensive characterization of the formation and removal of disinfection by-products in a real drinking water treatment plant (DWTP) and water distribution network. According to the results obtained, it can be stated that bromate is formed on the pre-oxidation stage and it is not eliminated throughout the DWTP; meanwhile, total organic carbon is partially removed on the clarification process. Moreover, it demonstrates the key role of the residence time and the type of water storage throughout the distribution network (either in pipes or in tanks) due to the combined effect of, at least, four overlapped mechanisms: THMs chemical generation, air stripping, hydrolysis and biological removal. This comprehensive view of the drinking water production and distribution network represents an excellent framework for allowing the improvement in the drinking water quality for a very common water production case study: a medium-size city fed by a surface water source. [ABSTRACT FROM AUTHOR]

Introduction Disinfection by-products are produced in water disinfected with chlorine-based products. One such group is trihalomethanes, and chloroform is the most abundant trihalomethane in swimming pool areas. Chloroform can be absorbed by inhalation, ingestion, and dermal absorption, and is classified as possibly carcinogenic. Aim To investigate if chloroform concentrations in air and water affect the chloroform concentration in urine samples of exposed swimming pool workers. Methods Workers from 5 adventure indoor swimming pools carried personal chloroform air samplers and provided up to 4 urine samples during one workday. Chloroform concentrations were analyzed with a linear mixed model analysis to investigate a possible correlation between air and urine concentrations. Results The geometric mean chloroform concentration was 11 μg/m3 in air and 0.009 µg/g creatinine in urine among individuals with ≤2 h at work, 0.023 µg/g creatinine among those with >2–5 working hours, and 0.026 µg/g creatinine in the group with >5–10 working hours. A risk of higher levels of chloroform in urine was associated with longer hours at work (≤2 h versus >5–10 h, odds ratio [OR] 2.04, 95% confidence interval [CI] 1.25–3.34), personal chloroform concentrations in air (≤17.00 µg/m3 versus >28.00 µg/m3, OR 9.23, 95% CI 3.68–23.13) and working at least half the working day near the swimming pools (OR 3.16, 95% CI 1.33–7.55). Executing work tasks in the swimming pool water was not associated with higher chloroform concentrations in urine compared to only working on land (OR 0.82, 95% CI 0.27–2.45). Conclusion There is an accumulation of chloroform concentrations in urine during a workday and a correlation between personal air and urine concentrations of chloroform among workers in Swedish indoor swimming pools. [ABSTRACT FROM AUTHOR]

Eutrophication in water reservoirs releases algal organic matter (AOM), which is an important precursor of disinfection by-products (DBPs) formed during water treatment. Chlorella sorokiniana is a microalgae which flourishes under conditions of high light intensity and temperature, thus its prevalence in algal blooms is expected to increase with climate change. However, Chlorella sorokiniana AOM has not been previously investigated as a DBP precursor. In this context, this study evaluated the effect of AOM concentration, humic acid (HA), and pH on DBP formation from chlor(am)ination of AOM Chlorella sorokiniana. DBP yields determined by linear regression for trichloromethane (TCM) and chloral hydrate (CH) were 57.9 and 46.0 µg·mg DOC−1 in chlorination, while the TCM, CH, dichloroacetonitrile (DCAN), 1,1,1-trichloropropanone (1,1,1-TCP), and chloropicrin (CPN) concentrations were 33.6, 29.8, 16.7, 2.1, and 1.2 µg·mg DOC−1 in chloramination. Chloramination reduced the formation of TCM and CH but increased CPN, DCAN, and 1,1,1-TCP yields. AOM Chlorella sorokiniana showed a higher DBP formation than 9 of 11 algae species previously investigated in the literature. At basic pH, the concentration of TCM increased while the concentration of other DBP classes decreased. Bromide was effectively incorporated into the AOM structure and high values of bromine incorporation factor were found for THM (1.81–1.89) and HAN (1.32) at 1.5 mg Br·L−1. Empirical models predicted successfully the formation of THM and HAN (R2 > 0.86). The bromide concentration had more impact in the model on the DBP formation than AOM and HA. These results provide the first insights into the DBP formation from AOM chlor(am)ination of Chlorella sorokiniana. [ABSTRACT FROM AUTHOR]

The goal of this study is to reveal the time dynamics of studies systematically and comprehensively on drinking water treatment and disinfection, as well as the situation in the literature, by using the bibliometric analysis method to examine scientific publications in the field of "Disinfection By-Products" between 2001 and 2022. The data gathered from the investigated articles is shown using the visual mapping approach. In this regard, the research provides for an evaluation of the disinfection by-products literature. The study's database contained 115 scientific papers retrieved from Web of Science. Istanbul Technical University is the most productive university with 23 published articles on Disinfection By-products, followed by Suleyman Demirel University with 18 published articles. Trihalomethanes, haloacetic acids are the most studied types of carbonaceous disinfection by-products in published articles, and N-nitrosodimethylamine is one of the most widely published nitrogenous disinfection by-products. The precursors of disinfection by-products or the removal of disinfection by-products are the two main focuses of the purpose of all studies. Coagulation, advanced oxidation processes and membrane processes constitute the methods used in the control of disinfection by-products. Brominated, and nitrogenous DBPs have attracted much attention due to their high toxicity. Future studies on disinfection by-products should focus on water quality standards, precursor controls, toxicity, and health effects. The necessity of bibliometric analysis of disinfection by-products is a necessity to fill the existing knowledge gaps in global and regional studies. [ABSTRACT FROM AUTHOR]

We investigated the effects of two California wildfires (Rocky and Wragg Fires, 2015) compared to an unburned reference watershed on water quality, dissolved organic matter (DOM), and precursors of disinfection by-products (DBPs) for two years' post-fire. The two burned watersheds both experienced wildfires but differed in the proportion of burned watershed areas. Burned watersheds showed rapid water quality degradation from elevated levels of turbidity, color, and suspended solids, with greater degradation in the more extensively burned watershed. During the first year's initial flushes, concentrations of dissolved organic carbon (DOC), dissolved organic nitrogen (DON), ammonium (NH4+/NH3), and specific ultraviolet absorbance (SUVA254) were significantly higher (67 ± 40%, 418 ± 125%, 192 ± 120%, and 31 ± 17%, respectively) in the more extensively burned watershed compared to the reference watershed. These elevated values gradually declined and finally returned to levels like the reference watershed in the second year. Nitrate concentrations were near detection limits (0.01 mg-N/L) in the first year but showed a large increase in fire-impacted streams during the second rainy season, possibly due to delayed nitrification. Changes in DOM composition, especially during the initial storm events, indicated that fires can attenuate humic-like and soluble microbial by-product-like (SMP) DOM while increasing the proportion of fulvic-like, tryptophan-like, and tyrosine-like compounds. Elevated bromide (Br-) concentrations (up to 8.7 μM]) caused a shift in speciation of trihalomethanes (THMs) and haloacetic acids (HAAs) to brominated species for extended periods (up to 2 years). Wildfire also resulted in elevated concentrations of N-nitrosodimethylamine (NDMA) precursors. Such changes in THM, HAA, and NDMA precursors following wildfires pose a potential treatability challenge for drinking water treatment, but the effects are relatively short-term (≤1 year).

Background & aim: The presence of natural organic substances (NOM) in aqueous solutions due to the creation of disinfection by-products (DBP) including trihalomethanes (THMs) and haloacetic acids (HAAs), as a result of the chlorination of aqueous solutions in the conventional purification process and according to Potential health risks for public health have attracted a lot of attention. Therefore, the aim of the present study was to determine and investigate the performance of combined Fenton-ultrasonic processes in removing the precursors of trihalomethanes from aqueous environments using zero iron. Methods: In the present experimental study conducted in 2021, the effect of independent variables included: the initial concentration of the pollutant, the reaction time, the concentration of the catalyst used, the amount of hydrogen peroxide used and the pH in the specified range to remove the precursors of trihalomethanes from water environments using zero iron with the surface-response method based on composite design. Central (CCD) was evaluated. Experiments were designed using Design expert software and CCD-RSM method. The graphs and figures required to determine the kinetics of the reactions were drawn using Excel software and the statistical parameters were analyzed to determine the optimal conditions of the process using analysis of variance, regression and Fisher tests. Results: The results indicated that by keeping the humic acid concentration at 64.75 mg/liter and the catalyst concentration at 106.76 mg/liter and the constant pH=4.39, the highest humic acid removal efficiency occurs when It happens that the hydrogen peroxide and the reaction time are at their maximum level of 35 mmol and 88.75 minutes, respectively, and in this condition, the removal rate has increased from 80% to 92%, and also with the increase in the amount of the catalyst, the reaction efficiency increases. find According to the reactions related to the Fenton process, the presence of iron causes an increase in hydroxyl radicals, this can be one of the reasons for increasing the removal efficiency. Conclusion: In the mentioned Ultrasonic-Fenton process under laboratory conditions, iron ion as a catalyst reacted with an oxidant such as hydrogen peroxide in an acidic environment and produces hydroxyl radicals. The efficiency of this method was influenced by various factors such as pH, concentration of iron and hydrogen peroxide, initial concentration of the pollutant and reaction time.

Absorbance differential spectra could be utilized to identify dissolved organic matter (DOM) characteristics such as the disinfection by products (DBPs) formation. This research purposed to establish the relationship between absorbance differential spectra and trihalomethanes-4 (THM4) formation potential, as well as the estimated cytotoxicity of tropical peat water DOM percentage. The ion exchange resin was used to separate the DOM components from peat water. In addition, the UV–Vis spectrum was examined between 200 and 700 nm. The hydrophobic-acid (HPOA) fraction contains the highest concentration of dissolved organic carbon (DOC), THM4 production potential, and calculated cytotoxicity. On the other hand, the hydrophilic-neutral (HPIN) fraction has the lowest potential THM4 production. The UV–Vis absorbance spectra of all DOM fractions showed a comparable peak at 277 nm. The differential spectra of 277 nm (ΔA277) indicated a significant association with DOC concentration (99.6 %), trichloromethane (TCM) creation (86.6 %), total-THM4 (TTHM4) (81.3 %) formation, THM4 estimated cytotoxicity (89.7 %), and a moderate correlation with bromodichloromethane (BDCM) formation (55.6 %). Meanwhile, ΔA277 had a poor correlation with brominated THM4 formation potential (chlorodibromomethane (CDBM): 2.59, tribromomethane (TBM): 2.78 %). The absorbance differential spectra might be employed as a surrogate measure for the peat water DOM fraction and its precursor properties to form THM4 during the chlorination process, as well as its estimated cytotoxicity.

Background: Trihalomethanes (THMs), a class of DBPs (disinfection byproducts) that includes chloroform, bromodichloromethane (BDCM), chlorodibromomethane (CDBM), and bromoform. To the best of authors’ knowledge, no study has addressed the relationship between the concentration of THMs and lifetime cancer risks (LCR) in drinking water supply system in Addis Ababa, Ethiopia. Therefore, this study aimed to determine the lifetime cancer risks of exposure to THMs in Addis Ababa, Ethiopia. Method: A total of 120 duplicate water samples were collected from 21 sampling points in Addis Ababa, Ethiopia. The THMs were separated by a DB-5 capillary column and detected by an electron capture detector (ECD). Cancer and non-cancer risk assessments were performed. Results: The average total THMs (TTHMs)concentration in Addis Ababa, Ethiopia, was 76.3 μg/L. Chloroform was the most dominant THM species identified. The total cancer risk for males was higher than that for females. The average LCR for TTHMs via ingestion in drinking water in this study was unacceptably high risk93.4×10−2. An average LCR through dermal routes was also of unacceptably high risk4.3×10−2. The LCR by chloroform contributes the highest (72%) of the total risk, followed by BDCM (14%), DBCM (10%) and bromoform (4%). Conclusions: The cancer risk of drinking water due to THMs in Addis Ababa was higher than the level recommended by the USEPA. The total LCR from the targeted THMs was higher via the three exposure routes. Males were at higher THM cancer risk than females. The hazard index (HI) indicated that the dermal route caused higher HI values than the ingestion route. It is essential to apply alternatives to chlorine, i.e., chlorine dioxide (ClO2), ozone and ultraviolet radiation, in Addis Ababa, Ethiopia. The monitoring and regulation of the THMs is required on a regular basis to analyse the trends and guide the water treatment and distribution system. Availability of data and materials: The datasets generated for this analysis are available from the corresponding author upon reasonable request.