High Bromide Concentrations Research Articles

Formation and health risk assessment of trihalomethanes in coastal wells impacted by seawater intrusion

The formation of trihalomethanes (THMs) in coastal wells impacted by seawater intrusion (SWI) is relatively understudied. Coastal wells, unlike typical groundwater sources, frequently exhibit elevated levels of chloride and bromide ions, potentially influencing the formation and speciation of THMs. The current study investigated the THM formation in coastal well water from a location affected by SWI. Samples were chlorinated with 2.5 mg L−1 and 5 mg L−1 chlorine doses to replicate field conditions. The THM concentration in the samples exceeded the maximum permissible limit for drinking water. The well with the highest chloride-to-bromide (Cl/Br) ratio (Cl/Br = 645) exhibited the highest total THM concentration (503.2 μg L−1). Samples with high bromide concentration had more brominated THMs over the 5-day reaction period. The bromine substitution factors for wells after 24 h with a chlorine dose of 2.5 mg L−1 were 1.89, 2.21, and 2.78, corresponding to bromide concentrations of 0.098, 0.109, and 1.275 mM, respectively. The average cancer risk associated with the well water was estimated to be 20.9 × 10−06 through dermal contact and 6.84 × 10−04 through inhalation. The study area had an estimated average cancer risk of 705 cases per million population. The study area's common diseases and cancer incidence data for the past four decades indicated a decreasing trend for waterborne diseases and a steep increase in cancers. While several factors may contribute to increasing cancer cases, our study highlights chlorinated coastal well water as an additional potential cancer risk agent.

Pourbaix diagrams for iron-chromium alloys in lithium bromide absorption machines

The influence of lithium bromide concentration on the Pourbaix diagrams for iron-chromium alloys is evaluated in this work, which allows for predicting the corrosion to stainless steels exposed to the aggressive operating conditions of lithium bromide absorption machines (concentrations ranging from: 400–992 g/L). The novelty of this work is found in the development of Pourbaix diagrams for the Fe-Cr-Br–-H2O quaternary system in aqueous solutions with a high concentration of lithium bromide, a topic which has not yet been studied. Results show that the corrosion region at acid pH corresponding to the aqueous species FeBr2(aq), FeBr3(aq), Cr+2, CrOH+2, Cr+3 or CrBr+2 shifts to higher pHs with increasing lithium bromide concentration, which decreases the immunity region of iron and chromium and decreases the passivation region of the solid species FeCr2O4, Fe2O3 and Cr2O3.

Revision of the genus Robbea (Stilbonematinae: Desmodoridae), worldwide abundant marine nematodes with chromophoric Fe–Br inclusions and the description of a new stilbonematine genus

Abstract Nematodes are one of the most widespread and abundant animal taxa across aquatic and terrestrial environments. In marine shallow-water, porous sediments, members of the subfamily Stilbonematinae may be found in high numbers. Stilbonematinae are characterized by their coat of symbiotic bacteria, which give the nematodes a white appearance, while the nematodes themselves are usually colourless. We identified several species of the genus Robbea (Desmodoridae: Stilbonematinae) in which live specimens had a conspicuous dark purple coloration of the glandular sense organs (GSOs), highly specialized epidermal glands that are prominent in the Stilbonematinae. The dark inclusions in the GSOs of Robbea contained high concentrations of iron and bromide, regardless of their habitat. Morphological and phylogenetic analyses show that the genus Robbea is paraphyletic and we define the new genus Cyathorobbea gen. nov. for species with sucker-shaped post-pharyngeal supplements in males. Furthermore, we describe five new Robbea species from around the world. Some Robbea species are morphologically very similar and required the use of principal component analysis of morphometric data to untangle the diversity in this taxon. Our work emphasizes the value of live animal observations that enable the identification of important characters and highlights the overlooked diversity within the Stilbonematinae.

Unexpected trends for the formation of chlorate and bromate during the photolysis of chlorine in bromide-containing water

Solar photolysis of free chlorine (solar/chlorine) in bromide-containing water occurs under various scenarios, such as chlorinated reservoirs and outdoor swimming pools, and the formation of chlorate and bromate is an important issue in the system. We reported unexpected trends for the formation of chlorate and bromate in the solar/chlorine system. Excess chlorine inhibited the formation of bromate, i.e., increasing chlorine dosages from 50 to 100 μM reduced the bromate yield from 6.4 to 1.2 μM in solar/chlorine at 50 μM bromide and pH 7. The yield of bromate in solar/chlorine at 100 μM chlorine and 50 μM bromide in 240 min was 18.8% of that at 50 μM bromine only. The underlying mechanism was that HOCl can react with bromite (BrO2−) to form HOClOBrO−, whose multi-step transformation finally formed chlorate as the major product and bromate as the minor product. This reaction overwhelmed the oxidation of bromite to form bromate by reactive species, such as •OH, BrO• and ozone. On the other hand, the presence of bromide greatly enhanced the formation of chlorate. Increasing bromide concentrations from 0 to 50 μM enhanced the chlorate yields from 2.2 to 7.0 μM at 100 μM chlorine. The absorbance of bromine was higher than that of chlorine, thus the photolysis of bromine formed higher levels of bromite at higher bromide concentrations. Then, bromite rapidly reacted with HOCl to form HOClOBrO− and it further transformed to chlorate. Additionally, 1 mg L−1 NOM had a negligible effect on bromate yields in solar/chlorine at 50 μM bromide, 100 μM chlorine and pH 7. This study demonstrated a new pathway of chlorate and bromate formation in the solar/chlorine system with bromide.

Evaluation and strategy for improving the quality of desalinated water.

Seawater desalination is practiced in many coastal countries, which is accepted as clean water by the general populations. The untreated seawater reported high concentrations of bromide (50,000 - 80,000µg/L) and iodide (21 - 60µg/L) ions, which are reduced to non-detectable levels during thermal desalination while the concentrations of bromide and iodide ions were reduced to 250-600µg/L and < 4-16µg/L, respectively during reverse osmosis processes. During the treatment and/or disinfection, many brominated and iodinated disinfection byproducts (Br-DBPs and I-DBPs) are formed in desalinated water, some of which are genotoxic and cytotoxic to the mammalian cells and possible/probable human carcinogens. In this paper, DBPs' formation in desalinated and blended water from source to tap, toxicity to the mammalian cells, their risks to humans and the strategies to control DBPs were investigated. The lifetime excess cancer risks from groundwater, and desalinated and blended water sourced DBPs were 4.15 × 10-6 (4.72 × 10-7 - 1.30 × 10-5), 1.75 × 10-5 (2.58 × 10-6 - 5.25 × 10-5) and 2.59 × 10-5 (4.02 × 10-6 - 8.35 × 10-5) respectively, indicating higher risks from desalinated and blended water (2.56 and 4.51 times respectively) than groundwater systems. Few emerging DBPs in desalinated/blended water showed higher cyto- and genotoxicity in the mammalian cells. The findings were compared with safe drinking water standards and strategies to produce cleaner desalinated water were demonstrated.

Kinetic and mechanistic study of the effect of Cu(II) on monochloramine stability in bromide-containing waters

Naturally occurring bromide can reduce the stability of monochloramine (NH2Cl) by forming brominated halamines, the most abundant being bromochloramine (NHBrCl). Cu(II) is found in drinking water distribution systems from copper pipes leaching or added as a biocide. This study showed that Cu(II) can catalyse the decay of NHBrCl (proved by Membrane Introduction Mass Spectrometry) during the chloramination process. 11 % of the total oxidant (chloramines, bromamines and NHBrCl) was consumed during chloramination in bromide-containing waters at pH 6.5 after 6 h, while the presence of Cu(II) remarkably accelerated the total oxidant decay with 65 % consumption. Higher bromide concentrations and lower pH led to an increasing total oxidant decomposition. This was primarily ascribed to the higher formation of NHBrCl and its further catalytic degradation from Cu(II) under these conditions. The nitrogen by-products in the presence of bromide and Cu(II) were identified. Nitrogen gas and ammonia were shown to be the main degradation products and a mechanism involving NHBrCl decomposition is proposed. It was also verified that Cu(II) enhanced the disinfectant decay in the absence/presence of bromide when natural organic matter was present. These findings can provide useful information to water utilities to better manage and maintain the stability of disinfectant residual allowing safe distribution of drinking water over a wide geographical area.

Operational stability, low light performance, and long-lived transients in mixed-halide perovskite solar cells with a monolayer-based hole extraction layer

Due to their tunable bandgap and low manufacturing cost, metal halide perovskite solar cells are attractive for ambient/indoor light-harvesting applications. In this work, we evaluate p-i-n perovskite solar cells fabricated with MeO-2PACz, a molecular monolayer hole extraction layer, as potential candidates for ambient light-harvesting applications. Two triple-cation mixed halide lead perovskite absorbers are compared, one with high bromide content (Br/I ratio 1:2, bandgap 1.72 eV, 16.1% power conversion efficiency) and one with low bromide content (Br/I ratio 1:11, bandgap 1.57 eV, 19.1% power conversion efficiency). Both materials demonstrated good stability while operating under simulated sunlight at the maximum power point for 100 h, a cumulative light dose comparable to over two years of ambient use. After 100 h operation, however, the measured device efficiency fell temporarily due to a transient loss of output current before returning to the nominal level after a long recovery period in the dark. These transient losses were more apparent in the wide bandgap device under strong light and were likely caused by light-induced halide segregation. After recovery, both devices retained good performance under a wide range of light intensities. Under a simulated ambient light source (835 lx white LED), the power conversion efficiency of the wide bandgap device reached 30.4%.

Non targeted screening of nitrogen containing disinfection by-products in formation potential tests of river water and subsequent monitoring in tap water samples.

The generation of disinfection by-products during water chlorination is a major concern in water treatment, given the potential health risks that these substances may pose. In particular, nitrogen-containing DBPs are believed to have greater toxicological significance than carbon-based DBPs. Hence, high performance liquid chromatography coupled to high-resolution mass spectrometry (HPLC-HRMS) in positive mode was employed to identify new non-volatile nitrogen containing disinfection by-products (DBPs) and to assess their presence in potable water. Nine water samples were taken in the Llobregat river, in the context of a water reuse trial, near the catchment of a drinking water treatment plant (DWTP) in 2019. River samples were disinfected with chlorine under controlled formation potential tests conditions and analysed with a non-target approach. The peak lists of raw and chlorinated samples were compared exhaustively, resulting in an extensive list of 495 DBPs that include bromine and/or chlorine atoms. 172 of these species were found frequently, in three or more chlorinated samples. The empirical formulae of these DBPs were unambiguously annotated on the basis of accurate m/z measurements, isotopic patterns and common heuristic rules. Most of the annotated species (310) contained bromide, which is consistent with the relatively high bromide content of the Llobregat basin (>0.3mg/l). Drinking water samples were taken at the outlet of the DWTP during the same sampling period. According to their analysis, a large portion of the DBPs detected after the formation potential tests do not reach real-life drinking water, which suggests that the treatment train successfully removes a significant fraction of DBP precursors. However, 131 DBPs could still be detected in the final product water. A larger sampling was carried in the Barcelona water distribution network, during six consecutive weeks, and it revealed the presence of 78 halogenated DBPs in end-consumer water, most of which were nitrogen-containing. MS/MS fragmentation and retention times were employed to tentatively suggest molecular structure for these recalcitrant DBPs.

Occurrence of brominated disinfection by-products in thermal spas

Thermal spas are gaining more and more popularity among the population because they are used for recreational purposes. Disinfecting these baths without losing the health benefits poses a challenge for swimming pool operators. Previous studies have mainly focused on regulated chlorinated DBPs in freshwater pools with no bromide or seawater pools with very high bromide content. Thermal water pools have a low bromide content and in combination with chlorine can lead to chlorinated, brominated and mixed halogenated DBP species. The occurrence of brominated and mixed halogenated DBPs in these types of pools is largely unexplored, with very few or limited studies published on regulated DBPs and even fewer on emerging DBP classes. In the field of swimming pool water disinfection, apart from extensive studies in the field of drinking water disinfection, only a few studies are known in which >39 halogenated and 16 non-halogenated disinfection by-products, including regulated trihalomethanes (THM) and haloacetic acids (HAA), were investigated in swimming pool water. Calculated bromine incorporation factor (BIF) demonstrated that even small amounts of bromide in swimming pool water can lead to a large shift in DBP species towards brominated and mixed halogenated DBPs. Dihaloacetonitriles (DHANs) accounted for >50% of the calculated cytotoxicity and genotoxicity on average. Comparison of the target analysis with the TOX showed that a major part of the measured TOX (69% on average) could be explained by the regulated classes THMs, HAAs, and the unregulated class of HANs. This study aims to help operators of swimming pools with bromide-containing water to gain a better understanding of DBP formation in future monitoring and to fill the knowledge gap that has existed so far on the occurrence of DBPs in thermal water pools.

Bromide occurrence in Croatian groundwater and application of literature models for bromate formation

Bromide in water can form undesirable by-products such as bromate when treated by ozonation during drinking water production. The maximum contaminant level (MCL) for bromate is 10µg/L in most countries because it is suspected of being carcinogenic. In this paper, the geographical distribution of bromide concentration in Croatian groundwater is presented covering the Pannonian basin and the Dinarides (Adriatic Sea). Groundwater in Croatian wellfields predominantly has a bromide content of less than 50µg/L and thus belongs to the group with low potential for bromate formation. Waters with higher bromide concentrations were found mainly in the coastal regions of Croatia, probably due to seawater intrusion. In addition, bromide concentration showed a positive correlation of 0.6 with conductivity, chloride, and sodium. In addition, the potential of 123 groundwaters analyzed in this study to form bromate when treated with ozone was evaluated using models available in the literature. Analysis of water from Croatian wellfields indicated that the potential for bromate formation above the MCL during ozonation was relatively low. The models used from the literature predicted quite different values of bromate concentration when applied to the same water, with some values exceeding those theoretically possible. Selected models may be useful as a general warning of possible bromate formation.

Tough, Anti-Swelling Supramolecular Hydrogels Mediated by Surfactant-Polymer Interactions for Underwater Sensors.

It is a great challenge for traditional hydrogel-based sensors to be effective underwater due to unsatisfactory water resistance and insufficient wet adhesion. Herein, a tough supramolecular hydrogel aiming at underwater sensing is prepared by the modification of hydrophilic poly(acrylic acid) (PAA) with a small amount of hydrophobic lauryl methacrylate (LMA) in the presence of high concentrations of the cationic surfactant cetyltrimethylammonium bromide (CTAB). Owing to the synergistic effects of the electrostatic interactions and hydrophobic associations of CTAB with the P(AA-co-LMA) copolymer, the hydrogel with a water content of approximately 58.5 wt % demonstrates outstanding anti-swelling feature, superior tensile strength (≈1.6 MPa), large stretchability (>900%), rapid room-temperature self-recovery (≈3 min at 100% strain), and robust wet adhesion to diverse substrates. Moreover, the strain sensor based on the hydrogel displays keen sensitivity in a sensing range of 0-900% (gauge factor is 0.42, 3.44, 5.44, and 7.39 in the strain range of 0-100, 100-300, 300-500, and 500-900%, respectively) and pronounced stability both in air and underwater. Additionally, the hydrogel can be easily recycled by dissolving in anhydrous ethanol. This work provides a facile strategy to fabricate eco-friendly, tough supramolecular hydrogels for underwater sensing.

Microbial bromate reduction following ozonation of bromide-rich wastewater in coastal areas

Ozonation of wastewater can reduce the release of organic micropollutants, but may result in the formation of undesirable by-products, such as bromate from bromide. Bromide is one of the most abundant ions in seawater, the primary precursor of bromate during ozonation, and the end product in microbial bromate reduction. Investigations were carried out to compare the concentration of bromide in wastewater in coastal and non-coastal catchment areas, to monitor bromate formation during ozonation, and to assess the potential for subsequent bromate reduction with denitrifying carriers. Higher bromide concentrations were systematically observed in wastewater from coastal catchment areas (0.2–2 mg Br−/L) than in wastewater from non-coastal areas (0.06–0.2 mg Br−/L), resulting in elevated formation of bromate during ozonation. Subsequent investigations of bromate reduction in contact with denitrifying carriers from two full-scale moving bed biofilm reactors (MBBRs) showed that 80 % of the bromate formed during ozonation could be reduced to bromide in 60 min with first-order rate constants of 0.3–0.8 L/(gbiomass·h). Flow-through experiments with denitrifying carriers also showed that combined reduction of bromate and nitrate could be achieved below a concentration of 2 mg NOx−-N/L. These findings indicate that bromide-rich wastewater is more likely to be of concern when using ozonation in coastal than in non-coastal areas, and that bromate and nitrate reduction can be combined in a single biofilm reactor.

Intraarticularly injectable silk hydrogel microspheres with enhanced mechanical and structural stability to attenuate osteoarthritis

A silk fibroin (silk) hydrogel was prepared by using diglycidyl ether (BDDE), a chemical crosslinker commonly used to generate Food and Drug Administration (FDA)-approved hyaluronic acid (HA) medical products. The silk/BDDE hydrogels exhibited high elasticity (compressive modulus of 166 ± 15.0 kPa), anti-fatigue properties, and stable structure and mechanical strength in aqueous solution. Chemical crosslinking was conducted in a high concentration (9.3 M) of lithium bromide (LiBr) solution, a salt that is commonly used to dissolve degummed silk fibers during silk solubilization. The unfolded and extended structure of silk molecules with these reaction conditions, as well as the unique ionic environment provided by LiBr facilitated a high degree of crosslinking in the hydrogel. Similar hydrogels were not obtained when the silk was dissolved in other silk fiber-dissolving reagents (e.g., Ajisawa's, formic acid (FA)/LiBr, FA/CaCl2 solutions), likely because partially folded silk structures and the ionic conditions with these reagents were less favorable for the crosslinking reaction. Based on these findings, silk/BDDE hydrogel spheres were prepared using an oil/water (o/w) emulsification method and biocompatibility and biodegradation were evaluated in vivo, along with other silk gel control systems (e.g., enzyme-catalyzed di-tyrosine and pulverized silk/BDDE gel particles with irregular shapes). Histological and immunohistochemical analyses demonstrated that the silk/BDDE hydrogel spheres were biocompatible and served as a bio-lubricant to treat osteoarthritis (OA). The intra-articular injection of the gel spheres reduced pain as measured with OA rats, reduced cartilage damage and resisted the digestive environment in the articular cavity for extended time frames (>4 weeks), suggesting utility for pain relief and sustained drug release for future OA treatments.

Photothermal Conversion Profiling of Large-Scaled Synthesized Gold Nanorods Using Binary Surfactant with Hydroquinone as a Reducing Agent.

Photothermal application of gold nanorods (AuNRs) is widely increasing because of their good photothermal conversion efficiency (PCE) due to local surface plasmon resonance. However, the high concentration of hexadecyltrimethylammonium bromide used in the synthesis is a concern. Moreover, the mild and commonly used reducing agent-ascorbic acid does not reduce the Au(I) to A(0) entirely, resulting in a low yield of gold nanorods. Herein we report for the first time the PCE of large-scaled synthesized AuNRs using the binary surfactant seed-mediated method with hydroquinone (HQ) as the reducing agent. The temporal evolution of the optical properties and morphology was investigated by varying the Ag concentration, HQ concentration, HCl volumes, and seed solution volume. The results showed that the seed volume, HQ concentration, and HCl volume played a significant role in forming mini-AuNRs absorbing in the 800 nm region with a shape yield of 87.7%. The as-synthesized AuNRs were successfully up-scaled to a larger volume based on the optimum synthetic conditions followed by photothermal profiling. The photothermal profiling analysis showed a temperature increase of more than 54.2 °C at 2.55 W cm−2 at a low optical density (OD) of 0.160 after 630 s irradiation, with a PCE of approximately 21%, presenting it as an ideal photothermal agent.

Multivariate experimental design provides insights for the optimisation of rechloramination conditions and water age to control disinfectant decay and disinfection by-product formation in treated drinking water

The stability of drinking water disinfectant residuals is known to be influenced by multiple variables. To evaluate the effects of various influencing variables on disinfectant stability, a multivariate analysis of chloramine decay and associated disinfection by-products (DBPs) formation was investigated in a series of bench-scale experiments. Of nine water quality variables previously identified, monochloramine dose, pH, and bromide concentration were selected as key water quality variables based on previous investigations and modelling. Co-effects of these key variables on monochloramine decay and formation of 33 halogenated and nitrogen-containing DBPs were investigated using response surface experimental design.Rechloramination conditions, including monochloramine dose, pH and bromide concentration, were optimised via a 3-factorial multivariate analysis of monochloramine stability in post-treatment drinking water. Effects of influencing variables on disinfectant decay and DBP formation were assessed and graphically presented as response surfaces with minimal experiments using Doehlert matrix experimental design compared to other multivariate experimental designs. Concentrations of trihalomethanes (THMs), haloacetic acids (HAAs), and N-nitrosamines were found to increase with water age, whereas opposite phenomenon was observed in the net production of haloacetonitriles (HANs). Increasing pH was found to stabilise monochloramine but it could cause DBP speciation to shift. Furthermore, increasing bromide concentration elevated Br-DBP formation. In bromide-containing water, pH = 7.8–8.0 should be considered as higher pH increases Br-THMs formations and lower pH increases formations of Br-HAAs and Br-HANs. However, water age or pH has insignificant impacts on DBP formation after significant monochloramine decay or at low initial monochloramine dose.These findings indicate that effective combined control measures to maintain monochloramine stability should include the application of high monochloramine dose (>1.5 mg-Cl2.L−1) under conditions of moderate to high pH (pH = 7.8–8.0) and minimal bromide concentration. This study provides relevant insights to water utilities aiming to design effective disinfectant residual management strategies for controlling monochloramine decay and DBP formation.

Geo-Temporal Signatures of Physicochemical and Heavy Metals Pollution in Groundwater of Khulais Region—Makkah Province, Saudi Arabia

Seawater has intruded into many of Saudi Arabia’s Red Sea coastal aquifers, with varying degrees of extension depending on location, hydrogeology, and population density. This study aimed to evaluate and comprehend the processes that influence the hydrogeochemical characteristics of the coastal aquifer in Saudi Arabia’s Khulais region. Groundwater samples were taken from nineteen locations during the winter and summer of 2021, and data from major ions and trace elements were examined and interpreted using ArcGIS software. The total dissolved solids (TDS) concentrations ranged between 480 and 15,236 mg/L and 887–18,620 mg/L in winter and summer, respectively. Groundwater TDS concentration was observed to be influenced by groundwater flow, lithogenic, anthropogenic, and seawater intrusion in this study (2021) when compared to 2016. The concentration of nitrate (NO3−) and strontium (Sr) in most samples exceeds the drinking guidelines. The occurrence of high concentrations of bromide (Br), Fluoride (F), Iron (Fe) (winter and summer) and Aluminum (Al), Boron (B), Chromium (Cr), Nickel (Ni), lead (Pb), cadmium (Cd), cobalt (Co), copper (Cu) and manganese (Mn) (winter) was also exhibited and observed up to more than drinking and irrigation limits. The central part of the study area was affected by seawater intrusion. The hydraulic conductivity of the topsoil was measured, and it ranged from 0.24 to 29.3 m/day. Based on electrical conductivity (EC) and sodium absorption ratio, most aquifer samples were unsuitable for irrigation (SAR).

Influence of Various Concentrations of Cetyltrimethylammonium Bromide on the Properties of Nickel Oxide Nanoparticles for Supercapacitor Application

In this paper, the impact of the crystallite sizes of nickel oxide nanoparticles (NiO NPs) on their efficiency for electrochemical capacitors (EC) has been investigated. NiO NPs were prepared without and with low and high concentrations (0.02[Formula: see text]M and 0.1[Formula: see text]M) of cetyltrimethylammonium bromide (CTAB) using the hydrothermal process that represent NiO, NiO-1, NiO-2, respectively. The crystallite size of NiO, NiO-1, NiO-2 NPs was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) analysis. The thermogravimetry/differential thermal analysis (TG/DTA) was used to investigate the thermal observation of as-prepared precursor to transform as NiO NPs. HRTEM revealed spherical seed-like morphologies, which consist of aggregated NiO-1 NPs with an average particle size of 9[Formula: see text]nm. The NiO-1 shows the large specific capacitance value of 168[Formula: see text]Fg[Formula: see text] at a current density of 0.5[Formula: see text]Ag[Formula: see text] compared with other NiO and NiO-2 NPs. The study suggests that the low concentration of surfactant CTAB of NiO NPs plays an important role in supercapacitor applications because of the smaller crystallite sizes of the materials as well as a large number of active sites for faradic reaction.

Pool water disinfection by ozone-bromine treatment: Assessing the disinfectant efficacy and the occurrence and in vitro toxicity of brominated disinfection by-products

Pool water is continuously circulated and reused after an extensive treatment including disinfection by chlorination, ozonation or UV treatment. In Germany, these methods are regulated by DIN standard 19643. Recently, the DIN standard has been extended by a new disinfection method using hypobromous acid as disinfectant formed by introducing ozone into water with naturally or artificially high bromide content during water treatment.In this study, we tested the disinfection efficacy of the ozone-bromine treatment in comparison to hypochlorous acid in a flow-through test rig using the bacterial indicator strains Escherichia coli, Enterococcus faecium, Pseudomonas aeruginosa, and Staphylococcus aureus and the viral indicators phage MS2 and phage PRD1. Furthermore, the formation of disinfection by-products and their potential toxic effects were investigated in eight pool water samples using different disinfection methods including the ozone-bromine treatment. Our results show that the efficacy of hypobromous acid, depending on its concentration and the tested organism, is comparable to that of hypochlorous acid. Hypobromous acid was effective against five of six tested indicator organisms. However, using Pseudomonas aeruginosa and drinking water as test water, both tested disinfectants (0.6 mg L−1 as Cl2 hypobromous acid as well as 0.3 mg L−1 as Cl2 hypochlorous acid) did not achieve a reduction of four log10 levels within 30 s, as required by DIN 19643.The formation of brominated disinfection by-products depends primarily on the bromide concentration of the filling water, with the treatment method having a smaller effect. The eight pool water samples did not show critical values in vitro for acute cytotoxicity or genotoxicity in the applied assays. In real pool water samples, the acute toxicological potential was not higher than for conventional disinfection methods. However, for a final assessment of toxicity, all single substance toxicities of known DBPs present in pool water treated by the ozone-bromine treatment have to be analyzed additionally.

Electrode for selective bromide removal in membrane capacitive deionisation

Due to the shortage of freshwater around the world, seawater is becoming an important water source. However, seawater contains a high concentration of bromide that can form harmful disinfection by-products during water disinfection. Therefore, the current seawater reverse osmosis (SWRO) has to adopt two-pass reverse osmosis (RO) configuration for effective bromide removal, increasing the overall desalination cost. In this study, a bromide selective composite electrode was developed for membrane capacitive deionisation (MCDI). The composite electrode was developed by coating a mixture of bromide selective resin and anion exchange polymer on the surface of the commercial activated carbon electrode, and its performance was compared to that of conventional carbon electrode. The results demonstrated that the composite electrode has ten times better bromide selectivity than the conventional carbon electrode. The study shows the potential application of MCDI for the selective removal of target ions from water sources and the potential for resource recovery through basic modification of commercial electrode.

Formation and control of C- and N-DBPs during disinfection of filter backwash and sedimentation sludge water in drinking water treatment

Drinking water treatment plants (DWTPs) produce filter backwash water (FBW) and sedimentation sludge water (SSW) that may be partially recycled to the head of DWTPs. The impacts of key disinfection conditions, water quality parameters (e.g., disinfection times, disinfectant types and doses, and pH values), and bromide concentration on controlling the formation of trihalomethanes (THMs), haloacetic acids (HAAs), haloacetonitriles (HANs), and haloacetamides (HAMs) during disinfection of FBW and SSW were investigated. Concentrations of most disinfection byproducts (DBPs) and associated calculated toxicity increased with extended chlorination for both FBW and SSW. During chlorination of both FBW and SSW, elevated chlorine doses significantly increased THM yields per unit dissolved organic carbon (DOC), but decreased HAN and HAM yields, with minimum effect on HAA yields. Chloramine disinfection effectively inhibited C-DBP formation but promoted N-DBPs yields, which increased with chloramine dose. Calculated toxicities after chloramination increased with chloramine dose, which was opposite to the trend found after free chlorine addition. An examination of pH effects demonstrated that C-DBPs were more readily generated at alkaline pH (pH=8), while acidic conditions (pH=6) favored N-DBP formation. Total DBP concentrations increased at higher pH levels, but calculated DBP toxicity deceased due to lower HAN and HAM concentrations. Addition of bromide markedly increased bromo-THM and bromo-HAN formation, which are more cytotoxic than chlorinated analogues, but had little impact on the formation of HAAs and HAMs. Bromide incorporation factors (BIFs) for THMs and HANs from both water samples all significantly increased as bromide concentrations increased. Overall, high bromide concentrations increased the calculated toxicity values in FBW and SSW after chlorination. Therefore, while currently challenging, technologies capable of removing bromide should be explored as part of a strategy towards controlling cumulative toxicity burden (i.e., hazard) while simultaneously lowering individual DBP concentrations (i.e., exposure) to manage DBP risks in drinking water.