Disinfection By-product Formation Potential Research Articles

Release regularity and cleaning measures of magnetic anion exchange resin during application

Anion exchange resin is responsible for removing harmful anionic contaminants in drinking water treatment, but it may become a significant source of precursors for disinfection byproducts (DBPs) by shedding material during application without proper pretreatment. Batch contact experiments were performed to investigate the dissolution of magnetic anion exchange resins and their contribution to organics and DBPs. Dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) released from the resin were highly correlated with the dissolution conditions (contact time and pH), in which 0.7 mg/L DOC and 0.18 mg/L DON were distributed at exposure time of 2 h and pH 7. The formation potential of four DBPs in the shedding fraction was also revealed that trichloromethane (TCM), dichloroacetonitrile (DCAN), nitrosodimethylamine (NDMA), and dichloroacetamide (DCAcAm) concentrations could reach 21.4, 5.1, 12.1 μg/L, and 69.6 ng/L, respectively. Furthermore, the hydrophobic DOC that preferred to detach from the resin mainly originated from the residues of crosslinkers (divinylbenzene) and porogenic agents (straight-chain alkanes) detected by LC-OCD and GC-MS. Nevertheless, pre-cleaning inhibited the leaching of the resin, among which acid-base and ethanol treatments significantly lowered the concentration of leached organics, and formation potential of DBPs (TCM, DCAN, and DCAcAm) below 5 μg/L and NDMA dropped to 10 ng/L.

Characterization of DOM and disinfection by-products precursors in biological activated carbon filter backwash water from drinking water treatments

Abstract Biological activated carbon filter backwash water (BAC FBW) removes pollutants from BAC filters in drinking water treatment plants. Characterizing the dissolved organic matter (DOM) in BAC FBW is of great significance for the recycling and treatment of backwash water. DOM pollution was monitored over a year using three-dimensional excitation–emission matrix fluorescence spectra. The dissolved organic carbon (DOC) concentration and fluorescence results showed that the DOC concentration reached the lowest value of 1.95 mg/L in the summer. The relative abundances of fluorescence components had a direct relationship with temperature variations. The soluble microbial products were enhanced greatly during cold seasons, while fulvic-acid-like and humic-acid-like compounds remained constant. Disinfection by-products (DBPs) formation potential and cytotoxicity were evaluated. The total haloacetonitriles (HANs), trihalomethanes (THMs), halonitromethanes (HNMs), and haloacetaldehyde (HALs) formation potentials ranged from 35.5 to 47.3 μg/L, 95.1 to 126 μg/L, 4.95 to 8.06 μg/L, and 43.4 to 53.0 μg/L in BAC FBW, respectively. Among all DBPs included in the calculation, the order of contribution to cytotoxicity was HANs > HALs > THMs > HNMs, respectively. Especially, HANs were much higher than the other DBPs, which should be controlled to avoid the biological risk of effluent quality.

Identification of Toxicity Forcing Agents from Individual Aliphatic and Aromatic Disinfection Byproducts Formed in Drinking Water: Implications and Limitations.

Recently, a study found that aromatic DBP fractions dominate the overall toxicity of chlorinated drinking water. However, key toxicity drivers have not been reported via comprehensive evaluation based on the formation of aliphatic and aromatic DBPs in drinking water. In this study, the occurrence of 37 aliphatic and 19 aromatic DBPs in drinking samples with different water characteristics collected in a Chinese megacity was explored. According to the individual DBP concentrations and cytotoxicity potencies as well as the "TIC-Tox" method, haloacetonitriles and halonitrophenols were found to be the toxicity drivers among the measured aliphatic and aromatic DBPs, respectively. However, when aromatic and aliphatic DBPs are taken into consideration together, aliphatic DBPs were calculated to present higher toxicity contribution than aromatic DBPs, which is inconsistent with the previous study. TOX showed significant positive correlations with most aliphatic DBPs but no aromatic DBPs, and the overall toxicity of the water sample concentrates is significantly related to the total calculated cytotoxicity and aliphatic DBPs, suggesting that current selected aromatic DBPs are insufficient to represent the overall aromatic DBPs. UV254 and DOC rather than SUVA are better surrogates for predicting DBP formation potential for DOM with a lower humification degree as indicated by fluorescence results.

The estimation of DBPs formation potential depending on the molecular structure of natural organic matter

Objectives:Since natural organic matter(NOM) is generated from an ecosystem, it has various characteristics depending on its origin. Especially, aquatic NOM reduces an efficiency of water treatment system and forms disinfection-by-products(DBPs) as a precursor. In this study, DBP formation potential was estimated according to the molecular structure of NOMs resulted by pyrolysis-gas chromatography-mass spectrometer(py-GC-MS). Methods:Five NOM samples were characterized: Suwannee River NOM(SRNOM), Mississippi River NOM(MRNOM), Nakdong River NOM(NR), NOM in effluent of Jinhae wastewater treatment plant(WP), and NOM in a small stream(SG) in Changwon city. The various analytical instruments were used including TOC analyzer, UV spectrometer, fluorescence spectrometer, and size-exclusion chromatography. After freeze drying of NOMs, molecular structure of samples was identified by py-GC-MS. Results and Discussion:Molecular weights of SRNOM and MRNOM were similar each other (~1400Da). The others(NR,WP,SG) were larger than the SRNOM and MRNOM. Hydrophobicity of the samples followed the order: SRNOM≒MRNOM > NR > WP > SG. Py-GC-MS results showed that SRNOM and MRNOM contain high portion of humic components. Otherwise, NR, WP, SG have protein which is originated from microbials. The DBP formation potential of SRNOM and MRNOM were the highest.Conclusion:This research shows the different characteristics of NOMs originated from different source. The results confirmed that NOM contained high portion of humic components results in the formation of high concentration of DBPs.

Improvement of Fe(VI) oxidation by NaClO on degrading phenolic substances and reducing DBPs formation potential

Ferrate(VI) is a green oxidant and can effectively oxidize micropollutants. However, the instability of Fe(VI), i.e., self-decomposition, in the aqueous solution limited its application. Herein, it was found that the degradation of phenolic substances had been substantially improved through the combination of Fe(VI) with NaClO. At the condition of pH 8.0, 50 μM of Fe(VI) degraded 18.66 % of BPA (bisphenol A) at 0.5 min or 21.67 % of phenol at 2 min. By contrast, Fe(VI)/NaClO (50/10 μM) oxidized 38.21 % of BPA at 0.5 min or 38.08 % of phenol at 2 min with a synergistic effect. At the end of the reaction, the concentration of Fe(VI) in Fe(VI)/NaClO (50/10 μM) was 28.97 μM for BPA degradation, higher than the 25.62 μM of Fe(VI) group. By active species analysis, intermediate iron species [i.e., Fe(V) and Fe(IV)] played a vital role in the synergistic effect in Fe(VI)/NaClO system, which would react with the applied NaClO to regenerate Fe(VI). In natural water, the Fe(VI)/NaClO could also degrade phenolic substances of natural organic matter (NOM). Although the NaClO reagent was applied, disinfection by-products (DBPs) formation potential decreased by 22.75 % of the raw sample after Fe(VI)/NaClO treatment. Significantly, THMs, mainly caused by phenolic substances of NOM, even declined by 29.18 % of raw sample. Based on that, this study explored a novel ferrate(VI) oxidation system using the cheap NaClO reagent, which would present a new insight on ferrate(VI) application.

Improvements of ferrate(VI) pretreatment on membrane flux and membrane rejection using cheap NaClO reagent

Ferrate(VI) pretreatment can effectively alleviate membrane fouling during the ultrafiltration (UF) process, while instability and high expenditure limit its application. This study discovered that the cheap NaClO reagent would improve the performance of ferrate(VI) pretreatment, i.e., establishing Fe(VI)/NaClO (FC) process. 20 μM of Fe(VI) group can increase J/J0 from 0.323 to 0.391, while the optimization process of 20 μM Fe(VI)/4 μM NaClO [FC (5:1)] increased it to 0.491 at the end of cycle 1 filtration. Meanwhile, the reversible and irreversible membrane fouling resistance decreased by 50% and 56% in FC (5:1). This was attributed to the suppression of ferrate(VI) decomposing and in-situ formation of more dispersed ferric nanoparticles in FC process [730.33 nm in Fe(VI) and 606.80 nm in FC (5:1)] by applied NaClO. The rejection ratio of dissolved organic carbon (DOC) increased from 27.18% of Fe(VI) group to 40.34% of FC (5:1) due to the repulsive interaction amplification of acid-base (AB) interaction energy. That was derived from the hydrophilia promotion of the treated sample and the electrical property evolution of in-situ formed ferric nanoparticles by NaClO. It suggested that AB interaction energy, presenting repulsive interaction in membrane-foulants and foulants-foulants, was a major role in Fe(VI) group and FC process. There was no more side effect induced by FC pretreatment, which was confirmed by the result that FC caused no increase in the disinfection by-products (DBPs) formation potential. The present study provided insight into improving the effect of ferrate(VI) pretreatment without inducing side effect, and reduced the costs of ferrate(VI) pretreatment during the process of UF.

The change of amino acids samples under metalimnetic oxygen minimum condition: Characterization and mechanism

The metalimnetic oxygen minimum (MOM) is a common anaerobic phenomenon that occur between 5.00 and 40.00 m of reservoirs. Amino acids (AAs) are widely found in water, but their change in MOM remain unclear. In this study, four AAs with different side chain groups were selected to explore the change of their samples and related disinfection by-products formation potential (DBPFPs) under MOM condition. The results showed that the final degradation rate of dissolved organic carbon and dissolved organic nitrogen of four AAs samples were 11.71%−59.87% and 26.50%−100.00% under MOM condition. Aspartic acid samples were the easiest to be degraded, whereas glycine samples were the opposite. While the total fluorescence intensity increased by 6.30%−113.40% for the appearance of tryptophan-like substance. The total DBPFPs of glutamic acid, arginine and aspartic acid samples were finally decreased by 4.73%, 8.00% and 98.88% (glycine sample increased by 2.30 times). Compared with the surface condition, the degradation of AAs samples and the change of DBPFPs were significantly inhibited under MOM condition. In addition, the diversities of bacterial communities were significantly reduced under MOM condition, which was very unfavorable to the degradation of AAs samples, and in turn affected the control of DBPs and deteriorated the water quality.

Effect of Medium Pressure Ultraviolet/Chlorine Advanced Oxidation on the Production of Disinfection by-Products from Seven Model Benzene Precursors

UV/chlorine advanced oxidation process (AOP), as a potential alternative to UV/H2O2 in water treatment, may pose a potential risk of increased disinfection by-product (DBP) formation and is of great concern. In this paper, seven benzene derivatives, containing two chlorine-inert and five chlorine-active compounds, were selected as typical model DBP precursors, and the effects of medium pressure UV/chlorine (MPUV/chlorine) on their chlorine demand and DBP formation potential (DBPFP) were evaluated. The results showed that MPUV/chlorine could significantly increase the chlorine demand and DBPFP of the two inert precursors. For the four slow but active DBP precursors, MPUV/chlorine may accelerate their short-term DBP formation, whereas it showed an insignificant effect or even reduced their chlorine demand and DBPFP. For the only fast and active DBP precursor, MPUV/chlorine showed an insignificant effect on its short-term DBP formation or DBPFP. The overall effect of MPUV/chlorine was more significant at pH 6 than at pH 8. In the presence of Br−, MPUV/chlorine significantly increased the bromine substitution factors of THMs. In addition, linear fitting results indicated that the UV/chlorine-induced change in overall chlorine demand may be considered as a potential indicator for the prediction of DBPFP alteration.

Hydrochloric acid-modified algal biochar for the removal of Microcystis aeruginosa: Coagulation performance and mechanism

The unceasing algae blooms have led to the deterioration of water quality and ecological imbalance in the entire globe, it’s urgent to investigate its treatment and resource utilization technology. In this study, treated algae was prepared to produce the biochar and then it was utilized as a coagulant for the removal of Microcystis aeruginosa. To improve the pore structure of algae-derived biochar for improving the removal capacity of M. aeruginosa, hydrochloric acid (HCl) modification was applied and optimized by Box-Behnken model-based response surface methodology. After modification by HCl, the specific surface area, pore volume, and average pore diameter of modified algae-derived biochar (MAB) increased to 38.34 m2/g, 0.073 cm³ /g, and 7.42 nm, respectively. The removal efficiency of Microcystis aeruginosa (The initial cell density: 4 ×106 cells/mL) by the MAB reached 99.02%±0.18 under the optimum condition obtained with response surface experiment (dosage of 287.46 mg/L, pH of 8.2, stirring rate of 175 rpm, and stirring time of 6.4 min). At the same time, the removal efficiencies of Chl a, turbidity and total phosphorus of polluted waters reached more than 84%, 91% and 60%, respectively. The dissolved organic matters were removed synchronously, thereby reducing the disinfection by-products formation potential. Electrostatic adsorption has been determined as the predominant force during the coagulation process. In conclusion, the HCl has been proved to be an effective strategy to improve the pore structure and algal removal capacity of MAB, and the MAB could be applied as the suitable materials for the algal coagulation with the advantage of resource utilization.

NOM fractionation by HPSEC-DAD-OCD for predicting trihalomethane disinfection by-product formation potential in full-scale drinking water treatment plants

Chlorination is a common method for water disinfection; however, it leads to the formation of disinfection by-products (DBPs), which are undesirable toxic pollutants. To prevent their formation, it is crucial to understand the reactivity of natural organic matter (NOM), which is considered a dominant precursor of DBPs. We propose a novel size exclusion chromatography (SEC) approach to evaluate NOM reactivity and the formation potential of total trihalomethanes-formation potentials (tTHMs-FP) and four regulated species (i.e. CHCl3, CHBrCl2, CHBr2Cl, and CHBr3). This method combines enhanced SEC separation with two analytical columns working in tandem and quantification of apparent molecular weight (AMW) NOM fractions using C content (organic carbon detector, OCD), 254-nm spectroscopic (diode-array detector, DAD) measurements, and spectral slopes at low (S206–240) and high (S350–380) wavelengths. Links between THMs-FP and NOM fractions from high performance size exclusion chromatography HPSEC-DAD-OCD were investigated using statistical modelling with multiple linear regressions for samples taken alongside conventional full-scale as well as full- and pilot-scale electrodialysis reversal and bench-scale ion exchange resins. The proposed models revealed promising correlations between the AMW NOM fractions and the THMs-FP. Methodological changes increased fractionated signal correlations relative to bulk regressions, especially in the proposed HPSEC-DAD-OCD method. Furthermore, spectroscopic models based on fractionated signals are presented, providing a promising approach to predict THMs-FP simultaneously considering the effect of the dominant THMs precursors, NOM and Br−.

Beneficial role of pre- and post-ozonation in a low rate biofiltration-ultrafiltration process treating reclaimed water

Previous studies have shown that the combination of biological and ozone oxidation processes can achieve a greater performance in treating natural surface water than each process individually. In this work, we designed and tested an ozonation–gravity-driven up-flow slow rate (0.01 m/h) biofiltration–ozonation (O3–GUSB–O3) process for the pre-treatment of reclaimed water prior to ultrafiltration (UF), with the aim of producing high quality drinking water and a significantly reduced degree of UF fouling. Results showed that O3 coupled with GUSB can effectively remove aromatic compounds (∼ 84.8%), dissolved organic carbon (DOC, ∼ 83.4%), and biopolymers in surface water. In addition, post-ozonation greatly contributed to the reduction of the UF membrane fouling (∼ 6 times greater flux). With regard to the disinfection by-product formation potential (DBPFP) of the final treated water, both trihalomethane formation potential (THMFP) and haloacetic acid formation potential (HAAFP) were greatly reduced (86.4% and 84.8% for THMs and HAAs, respectively). The relationship between DBPFP and various spectral indexes revealed that aromatic compounds and amino acids were more likely to generate DBPs during the disinfection stage. Among these, humic substances were more likely to generate THMs, while low molecular weight carboxylate and carbonyl organic compounds were associated with the generation of HAAs. Moreover, the dosage of O3 during the post-ozonation stage was found to influence directly the generation of DBPs. Overall, this study has conducted a detailed evaluation of a novel multi-ozone biofilter UF process for treating surface water, and the results provide a valuable basis for subsequent studies at larger scale to demonstrate the potential of the treatment process for practical applications.

A new process to further remove dissolved organic matter and disinfection by-product formation potential during drinking water treatment.

Biological activated carbon (BAC) will produce soluble microbial products (SMPs), which affect effluent quality. To clarify the mechanism by which BAC affects effluent water quality, the processes of a drinking water plant in Jiangsu Province were investigated. It was found that during the O3-BAC process, although ozonation could remove dissolved organic matter (DOC) to a certain extent, the DOC increased from 4.44 to 4.47mg/L after BAC. Dissolved organic matter (DOM) in effluent from different processes was divided into five fractions based on hydrophilicity and hydrophobicity by resin fractionation. Through fluorescence excitation-emission matrix (EEM) spectroscopy combined with DOC analysis, it was found that SMPs are mainly included in transitional hydrophilic neutral (TPIN) fraction, which was the main cause of the DOC increase. Therefore, a new combined process was designed to remove TPIN effectively by coagulation after biological treatment, and found that coagulation had a good removal rate (13.2%) on TPIN. The trihalomethane formation potential (THMFP) of TPIN could be reduced effectively by 44.9% after coagulation. Compared with the old process, the new combined process had a higher removal rate (14.2-30.0%) of DOC, as well as a greater reduction of THMFP (29.0-78.6%) and haloacetic acid formation potential (HAAFP) (46.4-75.3%). This study aims to reveal the mechanism by which SMPs affect effluent water quality and exacerbate health risks, and to propose a solution to provide theoretical support for the design and optimization of drinking water treatment processes.

Change of algal organic matter under different dissolved oxygen and pressure conditions and its related disinfection by-products formation potential in metalimnetic oxygen minimum

Most of the reservoirs or lakes will form a metalimnetic oxygen minimum (MOM) with the characterization of a substantial fraction of dissolved oxygen (DO) depleted below the epilimnion. The effect of intracellular organic matter (IOM) of algal cells transformed under MOM conditions is completely different from that of the original IOM on water quality. In this study, the IOM changes of Microcystic aeruginosa under different MOM conditions and its related disinfection by-products formation potentials (DBPFPs) were investigated by changing the pressure and DO concentration of MOM. Total Fmax increased slightly and then decreased under different pressure conditions, finally decreasing by no more than 22.0%. Under aerobic condition, dissolved organic carbon (DOC) and total Fmax decreased significantly, and decreased by 60.4% and 38.8% within the first 2 days. The results of specific UV absorbance (SUVA) and UV250/UV365 indicated that aromatic compounds and average molecular weight of IOM were gradually increased under different MOM conditions. The total DBPFPs increased firstly and then decreased under different pressure conditions, and finally decreased by 26.2%-33.1%. The decrease of total DBPFPs was significantly higher under aerobic condition than that under anoxic condition, which finally decreased by 64.5%. Redundancy analysis showed that the fluorescence parameter (protein-like and humic-like fluorescence) could be expected as an index to predict the DBPFPs. Moreover, the results revealed that with the decrease of DO, the activity and diversity of natural microbial consortium decreased, which prevented the further degradation and utilization of organic matter by natural microbial consortium. Therefore, lower DO was a key player for the deterioration of water quality under MOM conditions.

Does Snowfall Introduce Disinfection By-product Precursors to Surface Water?

Snow with large specific surface area and strong adsorption capacity can effectively adsorb atmospheric pollutants, which could/might lead to the increase of disinfection by-product (DBP) precursors in surface water. In this study, the contents and characteristics of dissolved organic matter (DOM) in meltwater were investigated, and DBP formation and the DBP-associated cytotoxicity index during chlorination of meltwater was first explored. Overall, meltwater exhibited high nitrogen contents. Meltwater-derived DOM was mainly composed of organics with low molecular weights, low aromaticity, and high unsaturated degrees. DBP formation potentials and cytotoxicity indexes in chlorinated meltwater were positively correlated with air quality index and were significantly impacted by snowfall stages. The trihalomethane and haloacetic acid yields from meltwater were relatively low, while yields of highly cytotoxic DBPs, especially halonitromethanes (6.3-10.8 μg-HNMs/mg-DOC), were significantly higher than those of surface water (1.7 μg-HNMs/mg-DOC). Notably, unsaturated nonaromatic organic nitrates in meltwater were important precursors of halonitromethanes. The actual monitoring results showed that snowfall significant increased the haloacetaldehydes and nitrogenous DBP formation levels of surface water. Considering increased DBP formation and DBP-associated toxicity, it was demonstrated that DOM derived from snowfall in atmosphere-polluted areas could deteriorate surface water quality and pose potential risks to drinking water.

Fertilization regime shifts the molecular diversity and chlorine reactivity of soil dissolved organic matter from tropical croplands

Soil-derived dissolved organic matter (SDOM) is an important site-specific disinfection byproduct (DBP) precursor in watersheds. However, it remains unclear how fertilization regime shifts the molecular diversity and chlorine reactivity of SDOM in cropland-impacted watersheds. Here, we analyzed the spectroscopic and molecular-level characteristics of the SDOM from croplands that had different fertilization regimes (i.e., non-fertilization, chemical fertilization, straw return, and chemical fertilization plus straw return) for 5 years and evaluated the chlorine reactivity of the SDOM by determining the 24-h chlorine consumption and specific DBP formation potential (SDBP-FP). The SDOM level decreased by chemical fertilization and was not significantly altered by straw return alone or combined with chemical fertilizer. However, all fertilization regimes elevated the molecular diversity of SDOM by increasing the abundance of protein-, lignin-, and tannin-like compounds. The chlorine reactivity of SDOM was reduced by chemical fertilization, but was significantly increased by straw return. Typically, straw return increased the formation potential of specific trihalomethane and chloral hydrate by 339% and 56% via increasing the aromatics in SDOM, whereas chemical fertilization could effectively decrease about 231% of the increased specific trihalomethane formation potential caused by straw return. This study highlights that fertilization regime can significantly shape the molecular diversity and chlorine reactivity of the SDOM in croplands and that partially replacing chemical fertilizer with crop straw is an advantageous practice for reducing DBP risks in drinking water in cropland-impacted watersheds.

Effect of dissolved organic matter and its fractions on disinfection by-products formation upon karst surface water

In this study, disinfection by-products (DBP) formation from dissolved organic matter (DOM) and its fractions, including both hydrophilic and hydrophobic components, were investigated at a typical karst surface water. The subsequent DBP formation potential was evaluated by deducing chemical characteristics of DOM fractions and representative algal organic matter (Chlorella sp. AOM) under the influence of divalent ions (Ca2+ and Mg2+) via spectra analysis. Both terrigenous and autochthonous DOM performed as critical DBP precursors, and DBP formation patterns were tightly correlated to organic matter chemical variations. DBP formation was significantly higher in drought period compared to that in wet period (P < 0.05). Particularly, trichloromethane (TCM) and dichloroacetonitrile (DCAN) showed distinct formation patterns compared to the scenarios in non-karst water. For DOM fractions, hydrophobic components showed higher DBP formation compared to hydrophilic counterparts, hydrophilic neutral enriched more reactive organic nitrogen for N-DBPs production. It was preferable to enrich humic-like substances after Ca2+ and Mg2+complexation in Chlorella sp. AOM, TCM formation increased whereas DCAN production remained unchanged in the presence of divalent ions. This study innovatively provided a linkage between chemical characteristics of DOM and understanding of DBP formation in karst surface water.

Effects of biological activated carbon filter running time on disinfection by-product precursor removal.

Biological activated carbon (BAC) filtration is usually considered to be able to decrease formation potentials (FPs) of disinfection by-products (DBPs) in drinking water treatment plant (DWTP). However, BAC filters with long running time may release microbial metabolites to effluents and therefore increase FPs of nitrogenous DBPs with high toxicity. To verify this hypothesis, this study continuously tracked BAC filters in a DWTP for one year, and assessed effects of old (running time 8-9 years) and new (running time 0-13 months) BAC filters on FPs of 15 regulated and unregulated DBPs. Results revealed that dissolved organic carbon (DOC) removal was slightly higher in the new BAC than the old one. All fluorescent components of dissolved organic matter evidently declined after new BAC filtration, but fulvic acid-like and soluble microbial product-like substances increased after old BAC filtration, which could be caused by microbial leakage. Correspondingly, new BAC filter generally removed more DBP FPs than the old one. 46.5% HAA7 FPs from chlorination and 44.3% THM4 FPs from chloramination were removed by new BAC filter. However, some DBP FPs, especially HAN FPs, were poorly removed or even increased by the old BAC filter. Proteobacteria could be a main contributor for DBP precursor removal in BAC filters. Herminiimonas, most abundant genera in new BAC filter, may explain its better DOC and UV254 removal performance and lower DBP FPs, while Bradyrhizobium, most abundant genera in old BAC filter, might produce more extracellular polymeric substances and therefore increased N-DBP FPs in old BAC effluent. This study provided insight into variations of DBP FPs and microbial communities in the new and old BAC filters, and will be helpful for the optimization of DWTP design and operation for public health.

Insight into disinfection byproduct formation potential of aged biochar and its effects during chlorination.

Biochar can achieve multiple benefits including solid waste management, polluted water remediation, carbon sequestration, and emission reduction. However, various environmental factors (such as temperature variations and dry-wet alternation) and microbial activity may lead to the fragmentation, dissolution, and oxidation of biochar. These accelerate the dissolution of biochar-derived dissolved organic matter (DOM) and then influence disinfection byproducts formation potential (DBPFP) throughout the water treatment process. In this paper, biochars from six biomass feedstocks with five aging processes were prepared, and the DBPFP of biochar and its derived DOM were first studied systematically. Different aging processes might increase the DBPFP of biochar by increasing DOM content and changing the fraction distribution of DOM derived from biochar. Especially, the DBPFP of biochar increased apparently with the chemical aging process. Coexisting with the environmental concentration of humic acid, even aged biochar showed the potential to reduce DBPFP and integrated toxic risk value of the mixed system. In this study, the DBPFP of biochar-derived DOM during the disinfection process is confirmed, and the results can give information to the selection of biomass feedstocks of biochar and its service life in the water treatment process.

Low-energy high-rate flotation technology for reduction of organic matter and disinfection by-products formation potential: A pilot-scale study.

Despite operating complexity and high energy costs associated with its operation and maintenance, dissolved air flotation (DAF) is widely used in drinking water treatment processes. Recently, the focus has shifted to designing and developing DAF with high surface loading rates. This research compares the performance of pilot-scale high-rate DAF and low-energy high-rate flash-pressurized flotation (FPF) based on the removal behavior of natural organic matter, different molecular weight size fractions, and the formation potential of disinfection by-products. For a surface-loading rate of 30m/h, the residual dissolved organic matter (DOC) concentrations in treated samples from high-rate DAF and FPF were 1.35±0.02 (30.25±0.15% removal) mg/L and 1.37±0.03 (29.12±1.72% removal) mg/L, respectively. In contrast, the removal of high-molecular-weight fractions, i.e., biopolymers and humic substances, showed similar removal performance for both treatment processes but not for building blocks. The removal rates were 27.10% and 6.64% for high-rate DAF and FPF, respectively. The formation potential of trihalomethanes/DOC for high-rate DAF with reaction times of 1, 3, 6, and 9 days 14.12±0.18, 17.84±0.22, 23.04±0.29, and 29.73±0.37μg/mg C, respectively, and 16.83±0.34, 22.69±0.46, 27.08±0.55, and 28.54±0.58 for high-rate FPF. In the case of haloacetonitriles/dissolved organic nitrogen-humic substances and chloral hydrate/DOC, there were no significant differences. Thus, low-energy high-rate FPF with a reduction of energy of 55% provides an alternative to high-rate DAF.

Characteristics of dissolved organic matter in two alternative water sources: A comparative study between reclaimed water and stormwater

Reclaimed water and stormwater are two important alternative water sources to mitigate water resource shortage. They can be reused by discharging into drinking water sources. Due to different sources, characteristics of dissolved organic matter (DOM, a precursor of disinfection by-products, DBPs) present in reclaimed water and stormwater would be different. This study selected reclaimed water to compare with stormwater (including both stormwater runoff and rainwater) by investigating their DOM characteristics, including concentrations, aromaticity, molecular weight, hydrophobicity/hydrophilicity, composition and DBPs formation potential. The results showed that reclaimed water had higher dissolved organic carbon (DOC) concentrations (6.02–10.8 mg/L) than stormwater (3.62–5.48 mg/L) while SUVA254 values of stormwater runoff (1.92–2.53 L/(mg-C·m)) were higher than reclaimed water (1.11–1.24 L/(mg-C·m)). Additionally, reclaimed water is more hydrophobic while stormwater runoff and rainwater are more hydrophilic. Although all water types included the highest fraction of DOM with molecular weight <1 kDa (43.0 %–77.5 %), reclaimed water primarily contained soluble microbial products (SMPs)-like and humic acid-like substances while stormwater runoff primarily contained humic acid-like DOM. In terms of DBPs, reclaimed water showed relatively higher formation potential than stormwater runoff while rainwater had the lowest DBPs formation potential. These results can contribute to effective water resource management. Particularly, when reclaimed water or/and stormwater are discharged into drinking water sources, these outcomes can help on efficient drinking water treatment.