Characterization Of Natural Organic Matter Research Articles

Characterization of natural organic matter in Wyoming-type bentonites irradiated at varied moisture levels

Wyoming-type bentonite clay (MX-80; Wyoming, USA) will be used in a deep geological repository (DGR) for the long-term storage of used nuclear fuel in Canada. The natural organic matter (NOM) found in bentonite may serve as a microbial nutrient source and potentially compromise the performance of the used fuel containers. Previous investigations indicate that NOM is present in low concentrations in MX-80 and has undergone extensive diagenetic alteration, though limited knowledge is available regarding NOM chemistry under simulated DGR conditions. Of particular concern is the possibility for gamma-radiation to alter NOM dissolution and reactivity due to the presence of reactive species generated by water radiolysis in Wyoming-type bentonites. In this study, NOM chemistry was investigated using complementary molecular-level techniques following exposure to a total gamma-radiation dose of 100 kGy (1.08 kGy/h for 93 h) at varied moisture levels (20%, 40%, 60% and 80%) and room temperature. Treated samples exhibited relatively low total organic carbon concentrations (0.074–0.232%), with no evidence of any major changes in total, organic, and inorganic carbon concentrations. Solid-state 13C NMR spectroscopy detected no changes in solid-phase NOM chemistry after irradiation. Solubilization of NOM increased significantly with radiation exposure at 80% moisture, suggesting higher levels of water saturation may enhance dissolved organic matter (DOM) production. Solution-state 1H nuclear magnetic resonance (NMR), and UV–Vis analyses did not identify any significant differences in DOM composition. More sensitive, targeted compound analysis revealed significant decreases in total n-alkanol concentration at lower moisture content levels (20% and 40%). Several individual compound concentrations also differed significantly at the nanogram-level, including n-octacosanol and several n-alkanoic acids at elevated moisture levels (60% and 80%). These findings suggest the majority of NOM in MX-80 remains chemically stable under the anticipated initial conditions of the proposed DGR.

Electro-sorption and -desorption characteristics of electrically conductive polyacrylonitrile membranes to remove aqueous natural organic matter in dead-end ultrafiltration system

Electrically conductive (EC) membranes have emerged as an innovative approach in removing natural organic matter (NOM) by electro-sorption (e-sorption) when external anodic potential (AP) is applied. In this study, the EC membranes were established by a forming a porous nanolayer of Pt nanoparticles via magnetron sputtering on both sides of virgin and chemically modified PAN ultrafiltration (UF) membranes. The modified PAN membranes were functionalized with ethylenediamine (PAN-EDA) and sodium hydroxide (PAN-NaOH). The virgin PAN membrane material contains nitrile group and demonstrated a negative zeta potential in the analyzed pH range. The PAN-EDA membrane owned amidine and amine groups, whereas PAN-NaOH membrane possessed carboxyl and amide groups in the membrane matrix. The PAN-NaOH and PAN-EDA membranes exhibited isoelectric points at 3.7 and 7.8, respectively. Electrical field-assisted UF experiments were conducted with Suwannee River NOM in dead-end mode and NOM removal was monitored using different methods of NOM characterization (e.g., SEC, DOC and UV254 absorbance). The results revealed that the non-electrically conductive (NEC) and EC virgin PAN membranes exhibited almost no intrinsic adsorption (at 0 V external potential) and e-sorption of NOM at 2.5 V AP respectively. However, NEC PAN-NaOH and PAN-EDA membranes showed DOC intrinsic sorption loadings of 17 mg·m−2 and 258 mg·m−2 at permeate flux 100 L·m−2·h−1 and pH 7 respectively. In comparison, the DOC e-sorption loadings of the EC PAN-NaOH and EC PAN-EDA membranes at 2.5 V AP were 197 mg·m−2 and 525 mg·m−2 under same test conditions respectively. The NOM e-desorption characteristics of the EC modified PAN membranes were also investigated to regenerate membranes for a sustainable filtration process. The results indicated that the EC PAN-NaOH and PAN-EDA membranes can be regenerated by reversing the electrical polarity almost completely. In conclusions, the outcomes of this work confirm that the presence of the derivatives of amines (e.g., amines, amidine and amide groups) and carboxyl group are necessary in the membrane matrix to induce e-sorption and -desorption characteristics.

Pilot-scale study on the performance of high-rate DAF based on removal of organic precursors and formation characteristics of disinfection by-products

In recent years, there has been an increased focus on the design and development of dissolved air flotation (DAF) with a high surface loading rate (SLR), but little research has been conducted using advanced natural organic matter characterization techniques. This research thus investigates the performance of pilot-scale DAF (10–30 m h–1) and compares them with those for a full-scale coagulation–flocculation–sedimentation (CFS) system based on the reduction of organic precursors, different molecular weight (MW) fractions characterized by liquid chromatography with organic carbon detection, and disinfection by-products. The removal of dissolved organic carbon (DOC) decreased with increasing SLR, ranging from 29 % to 38 %. This may be because of the short flocculation retention time for high SLR. Thus, achieving a similar removal of DOC by high SLR required higher coagulant doses. Furthermore, the organic precursors were measured lower in the high-rate DAF effluent than the CFS, maybe because of the high coagulation pH of the CFS effluent (7.5–8). Similarly, the concentration of different MW fractions, especially biopolymers and building blocks, was lower in the high-rate DAF effluent than in the CFS. The removal of biopolymers was 74.64 % and 87.20 % for the CFS and high-rate DAF, respectively. Likewise, 2.78 % and 27.09 % for the CFS and high-rate DAF, respectively, for building blocks. The normalized trihalomethanes/DOC and chloralhydrate/DOC were higher for the CFS than the high-rate DAF. Coagulation chemistry (pH, coagulant doses, and retention time) strongly influences the DAF and CFS unit performance and should not be neglected.

Seasonal variations of natural organic matter (NOM) in surface water supplied to two coal-fired power stations.

Global issues such as pollution and global warming have resulted in changes in water characteristics over the past 20years. Natural organic matter (NOM) which is a major component in water systems has shown an increase globally. This increase in NOM concentration has negatively affected both water treatment processes and drinking water quality. It is subsequently critical to understand the seasonal variations and composition of NOM to be able to address issues related to NOM. In this study, techniques such as ultraviolet-visible spectroscopy, total organic carbon and liquid chromatography-organic carbon detection (LC-OCD) were used for characterisation and quantification of NOM. Two coal-fired power stations were selected for this study with each power station receiving water from a different source, i.e. power station A receives water from the Vaal River and power station B from the Nkomati River. Results from this study demonstrated that composition and concentration of NOM from these two water sources varied seasonally. Characterisation of NOM using the LC-OCD indicated that the different fractions of NOM, i.e. low molecular weight neutrals, low molecular weight acids, building blocks, humic substances and biopolymers, varied seasonally. The dissolved organic carbon concentration and specific ultraviolet absorbance values of the raw water at both power stations showed an increment amid the wet seasons and a decrease amid the dry seasons.

Molecular-level characterization of natural organic matter in the reactive electrochemical ceramic membrane system for drinking water treatment using FT-ICR MS

Applications of electrochemical advanced oxidation processes are rising in drinking water treatment for effective mitigation of refractory organic compounds. This study explored the fate of natural organic matter (NOM) (lake water and standard NOM (SRNOM solution)) at molecular-level in the reactive electrochemical membrane (REM) system utilizing Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). Fluorescence spectroscopy showed above 90 % removal of the humic-like component in both lake water and SRNOM solution in 10 min of REM operation compared to 70–80 % removal of the fulvic-like component after 30 min. REM-based treatment effectively eliminated (>70 %) the disinfection byproduct precursors. The lake water, sharing ~70 % of similar compounds with SRNOM, displayed a different propensity toward electrochemical oxidation, and its finished water was characterized with relatively lower double-bond equivalent (DBE), nominal oxidation state of carbon (NOSC), and aromaticity compared to that of SRNOM. The chloride ions in the water matrix of lake water impacted the electrochemical oxidation and generated significantly different transformation products than SRNOM solution. The heteroatoms (N and S) containing compounds (CHON and CHOS) were preferentially degraded in lake water; however, CHOS compounds were removed fewer in SRNOM. The electrosorption and electrochemical oxidation on the REM surface were the significant contributors for NOM removal. The newly formed compounds were mostly retained on the REM surface and fewer were released in finished water. This study is believed to help understand the fate of NOM in real source drinking water during electrochemical treatment.

Characterization of natural organic matter in South African drinking water treatment plants: Towards integrating ceramic membrane filtration.

This work presents the first comprehensive investigation of natural organic matter (NOM) fraction removal using ceramic membranes in South Africa. The rate of removal of bulk NOM (measured as UV254 and DOC % removal), the biodegradable dissolved organic carbon (BDOC) fraction, polarity-based fractions, and fluorescent dissolved organic carbon (FDOM) fractions was investigated from water abstracted from drinking water treatment plants (WTPs) in South Africa. Further, mechanisms of ceramic membrane fouling by waters of South Africa were studied. Ceramic membranes removed more than 80% DOC from samples from coastal WTPs, whereas for inland plants, the removal was between 60% and 75% of DOC. FDOM was removed to at least 80% regardless of the site of the plant. The BDOC removal by the ceramic membranes was above 85%. The hydrophobic fraction was the most amenable to removal by ceramic membranes regardless of the site of sample abstraction (above 60% for all sites). The freshness index (β:α) correlated strongly to UV254 removal (R2 = 0.96), thus UV254 removal can serve as a proxy for the susceptibility to removal of such class of NOM by ceramic membranes. This investigation demonstrated that ceramic membranes could be a valuable technology if integrated into the existing WTPs. PRACTITIONER POINTS: The removal of bulk parameters by ceramic membrane was greater than unit conventional processes used in all the sampled water treatment plants. The hydrophobic polarity-based fraction of NOM was the most amenable to removal by ceramic membranes regardless of the site of the WTP. Polarity-based fractions, aromaticity, and initial DOC had a combined influence on the removal of organic matter by ceramic membranes as explained by principal component three.

Data-Based Chemical Class Regions for Van Krevelen Diagrams.

Ultrahigh resolution mass spectrometry (UHR-MS) is commonly used to characterize natural organic matter (NOM). The complexity of both NOM and the data set produced make data visualization challenging. Van Krevelen diagrams─plots of component hydrogen/carbon (H/C) against oxygen/carbon (O/C) elemental ratios─have become a popular way to visualize the chemical formulas identified by UHR-MS. Different regions on the van Krevelen diagram have been attributed to different chemical classes; however, the classifications vary between studies and the regions lack standard definitions. Here, chemical formulas were obtained from public databases to create H/C and O/C ranges for amino sugar, carbohydrate, lignin, lipid, peptide, and tannin chemical classes on van Krevelen diagrams. The recommended H/C and O/C ranges are presented in a table and can be adapted to any data analysis software programs. The regions recommended here agreed reasonably well with previous literature for amino sugar, carbohydrate, lignin, lipid, and peptide regions. However, the recommended tannin region appears at lower H/C ratio values and with a wider range of O/C ratio values compared to previous studies. The regions presented herein are strongly recommended for use as consistent reference points in future NOM characterization studies to aid in the discussion of data and to readily compare studies.

Tracking Br-DBPs and bromine substitution factors by two-stage differential characterization of water matrix and NOM during chlorination

Tracking disinfection byproducts (DBPs) upon chlorination becomes challenging whenever bromides occur because they alter DBP formation from chlorinated to brominated DBPs (Br-DBPs). Although epidemiological studies have emphasized the need to control Br-DBPs because of their notable carcinogen effects, work on Br-DBP monitoring is timely, since limited attention has to date been paid to this. This study proposes a two-stage differential characterization approach to a water matrix and natural organic matter (NOM) surrogates as a more robust way to trace Br-DBP precursors and bromine substitution factors (BSF). This two-stage approach monitors the differential variations (Δ) of both inorganic and organic precursors, e.g., dissolved organic carbon (DOC), bromide levels, Cl2 content, specific ultraviolet absorbance (SUVA), fluorescent spectra, before and after chlorination. To mimic practical conditions, chlorination experiments were conducted with two principle NOMs, including Suwannee River fulvic (SW) and M. aeruginosa organic matter (MA), with Br− levels from 0 to 2000 μg/L and chlorination times from 15 min-24 h. When Br− levels increased, all Br-DBP yields and BSF values correspondingly magnified, accounted for 70–90% of the total DBP yields from chlorinated SW or MA water. At each Br− level, prolonging chlorination time also increased the overall Br-DBPs and varied BSF values, but these differences were of no significance (p > 0.05). Correlation tests highlighted the significant insufficiency of the conventionally-used DBP surrogates (initial DOC, Cl2 dose, and SUVA) for Br-DBPs and BSF monitoring. By contrast, our two-stage characterization parameters are superior, with correlation coefficients ρ > 0.8 (p < 0.01), especially for those parameters including ΔBr as a numerator. Accordingly, regression models of Br-DBPs and BSFs built by our two-stage tertiary parameters exhibited high adjusted R2 values mostly >0.7 and >0.8 (n = 60), indicating a promising application for effective Br-DBPs and BSF monitoring.

Characterization of Natural Organic Matter in Spring Water

Interest in aspects of industrialization relating to human health has increased. Accordingly, the use of labels such as ‘natural foods’ and ‘organic ingredients’ has become more widespread, and greater emphasis is being placed on improving quality of life. Water is an essential element for human life, and water quality has a significant impact on human health. However, technology that can precisely determine the substances present in water is still lacking. This study was conducted to establish a complete mass spectrometry process, from pretreatment to analysis, to measure and characterize natural organic matter (NOM) in Korean spring water samples. Salts and other matrices were removed from the samples using solid-phase extraction (SPE) with two different columns (PPL and C18). After establishing an accurate analysis method, the experimental results were evaluated based on Van Krevelen diagrams and analysis of molar O/C and H/C ratios. The method for characterizing NOM introduced herein should facilitate evaluation of water quality.

Assessment of the molecular-level compositional heterogeneity of natural organic matter in bentonites intended for long-term used nuclear fuel storage

Bentonite-rich clays have been chosen as the sealing material in the engineered barrier system of the deep geological repository (DGR) for the long-term storage of used nuclear fuels. Natural organic matter (NOM) found in these bentonites can serve as a source of nutrients for microbial growth. Although high density bentonite does not support microbial activity within its matrix, it is possible that microbial growth will occur at interface of the DGR rock wall and the bentonite; the availability of nutrients is therefore a design consideration. Furthermore, it is unclear if NOM is similar in composition within bentonite samples collected from different locations from the same naturally-occurring clay deposit, or whether NOM chemistry will vary within different batches.Here, we report the detailed geochemical characterisation of different nutrients and NOM in five different MX-80 bentonites from the same location, but collected in different lots. Our results show that total carbon comprises <1% and that organic carbon constitutes less than one-fifth of this total carbon content. Statistical analyses revealed no significant differences in the NOM composition, or the other geochemical characteristics, of these samples. Targeted organic compound analyses indicated a predominance of long-chain homologues in the aliphatic lipids of the bentonites, suggesting that NOM in MX-80 bentonites is primarily terrestrially-derived. We detected nanogram-level variabilities in the concentrations of selected compounds between samples, but these variabilities were not statistically significant. Analysis by solid-state 13C nuclear magnetic resonance (NMR) spectroscopy also showed consistency between the NOM of the different MX-80 samples and a predominance of aliphatic, as well as aromatic compounds, which suggests that the NOM has undergone extensive diagenesis.Overall, all analyses consistently indicated that the NOM composition exhibits low heterogeneity between the different bentonites mined from the same source. These results provide confidence in the potential use of MX-80 as a buffer material for widespread use in DGRs and they build upon past research on the NOM composition of bentonite clays.

Disinfection by-products in Croatian drinking water supplies with special emphasis on the water supply network in the city of Zagreb

The occurrence of disinfection by-products (DBPs) was investigated in 48 drinking water systems across Croatia. Eleven DBPs were studied: chlorite (ClO2−), chlorate (ClO3−), four trihalomethanes (THMs), and five haloacetic acids (HAAs). Furthermore, an intensive sampling program was conducted in the distribution system in the city of Zagreb where, aside from DBP analyses, natural organic matter (NOM) was characterized using fluorescence spectroscopy. In the drinking waters examined across Croatia, DBP values were found in the range from 0.7 μg/L to 32.8 μg/L for THMs, below LOQ to 17.2 μg/L for HAAs (primarily di- and trichloroacetic acids), below LOQ to 720 μg/L for ClO2− and below LOQ to 431 μg/L for ClO3−. The results obtained showed higher chlorite concentrations in the systems treated with hypochlorite compared to systems treated with chlorine dioxide. DBPs in the Zagreb distribution network were generally low (the average values were below 6 μg/L and 2 μg/L for total THM and total HAA respectively). In contrast to our observations throughout Croatia, dibromoacetic acid (DBAA) was found to be the predominant HAA within Zagreb, most likely due to the degradation of chlorinated carboxylates (di-/tri-chloroacetic) in the network. Characterization of NOM by Parallel Factor Analysis (PARAFAC) fluorescence spectroscopy across the Zagreb network showed distinct temporal variations arising from groundwater inputs, as evident from variable humic-, tyrosine-, and tryptophan-like peaks. Statistical correlations between fluorescence data and DBPs highlight its potential for monitoring the presence of DBPs in distribution networks.

Molecular Tagging for the Molecular Characterization of Natural Organic Matter.

Natural organic matter (NOM) is the product of microbial and abiotic decay of plant and animal remains in terrestrial and aquatic ecosystems. On a molecular level, NOM is a complex mixture of organic molecules, of which the vast majority of structures are unknown. By identifying these molecules, our understanding of the many functions of NOM could be greatly enhanced. However, given that they are chromatographically inseparable and number in the thousands, traditional analytical techniques have proven unable to achieve this goal. A promising approach to enumerate functional groups and elucidate molecular structures within NOM is based on a combination of molecular tagging and high resolution spectroscopic techniques, such as nuclear magnetic resonance spectroscopy and mass spectrometry. Molecular tagging involves the selective modification of particular functional groups, inserting nuclei to act as reporters on their surrounding chemical environment. This allows examination of only the tagged molecules within NOM, thereby reducing the complexity of the mixture. In this review, the effectiveness of molecular tagging methods incorporating carbon, silicon, nitrogen, phosphorus, and deuterium into NOM are discussed. Some potential tagging methods which have not yet been applied to NOM are also presented.

Characterization of natural organic matter and assimilable organic carbon from an advanced full-scale drinking water treatment plant to tap

Characterization of natural organic matter and assimilable organic carbon from an advanced full-scale drinking water treatment plant to tap

Fractionation and molecular characterization of natural organic matter (NOM) by solid-phase extraction followed by FT-ICR MS and ion mobility MS

Electrospray ionization (ESI) coupled with Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) has been widely used for the characterization of dissolved organic matter (DOM) extracted by solid-phase extraction (SPE) from various environmental waters. It is known that common SPE generally has a relatively low recovery and the non-polar and weakly polar components are less likely to be ionized due to ionization discrimination. However, the molecular selectivity during SPE is not clear so far. In this study, the Suwannee River natural organic matter (SRNOM) was fractionated by multi-step SPE with different solvents and the fractions were characterized by negative ESI FT-ICR MS and trapped ion mobility spectrometry-mass spectrometry (IMS-MS). The sequential solvent elution increased the extraction recovery of DOM in water by SPE and enabled the characterization of a weakly polar component, which cannot be detected in common SPE separation. The weakly polar component accounts for 5.7% in TOC for the SRNOM, which has complex but different molecular composition with methanol- and/or water-eluted fractions. Lipid-like compounds were enriched in this fraction. Compared with the polar molecules directly eluted by one-step SPE from the SRNOM, the weakly polar fractions exhibit larger molecular size. The results are helpful for understanding of the molecular composition of SRNOM, as well as other environmental waters. In addition, the study demonstrates that the combination of FT-ICR MS and IMS-MS has potential to characterize the chemical composition of a complex mixture, like DOM, to a new depth. Graphical abstract.

Multi-spectral characterization of natural organic matter (NOM) from Manitoba surface waters using high performance size exclusion chromatography (HPSEC)

The main objective of this research was to develop an algorithm that would be able to relate ultraviolet absorbing moieties in potable water to trihalomethanes (THMs) and other water quality parameters. The characterization was carried out using high performance size exclusion chromatography (HPSEC) to separate water samples based on apparent molecule weight (AMW); while the developed algorithm utilized multi-spectral information extracted from 7 Manitoba source waters, and from samples treated with strong base ion-exchange (IX). AMW components between 2.2-4 k Da were strongly associated with the formation of THMs, and more strongly with chlorinated byproducts, determined using Spearman and Pearson coefficients. associations were not improved upon removal of the raw samples from the dataset, indicating that the applied methodology is not specific to IX treatment. Strong associations were also found between initial wavelengths of 226–239 nm and final wavelengths of 257–273 nm, which suggests that absorbing moieties in these ranges are prime precursors in the reaction mechanism to form THMs. A closer look noted that chlorinated THMs were more strongly associated than THMs in general; with brominated byproducts following closely to profiles of UV254 - indicating these parameters are closely related.

Molecular weight-dependent adsorption fractionation of natural organic matter on ferrihydrite colloids in aquatic environment

Natural organic matter (NOM), a heterogeneous mixture with various organic components and continuous molecular weight (MW) distribution, is omnipresent in natural waters. To date, understanding of the MW-dependent adsorption fractionation of NOM samples on colloids is limited due to the lack of NOM fractionation and characterization methods. In this study, the ultrafiltration technique was applied to fractionate the bulk NOM samples into low MW (LMW-, <1 kDa) and high MW (HMW-, 1 kDa–0.45 μm) fractions, whose adsorption behaviors on ferrihydrite colloids were comparatively examined via using total organic carbon, chromophoric, fluorescent emission-excitation matrix-parallel factor (EEM–PARAFAC), and two dimension FTIR correlation spectroscopy (2D–FITR–COS). The adsorption behaviors of all samples can be reasonably explained by Langmuir and Frendlich isotherm models, and the HMW-NOM exhibited higher adsorption capacities and affinities (4.71 mg-C/g) than the bulk (3.88 mg-C/g) and LMW- (2.44 mg-C/g) counterparts. Irrespective of MWs, the non-aromatic moieties were preferentially adsorbed by ferrihydrites, causing an enhanced aromaticity for the residual solutions. Two humic-like and one protein-like component were identified by EEM–PARAFAC, and a increase and decrease trend of Ka (adsorption affinity) were observed for humic- and protein-like components, respectively, in the order of LMW-, bulk, and HMW-NOM, showing obvious MW- and component-dependent adsorption fractionation of NOM on ferrihydrite colloids. 2D–FTIR–COS provided further information that, with increasing site limitation, the C–O in carbohydrate was adsorbed prior to the amide I in proteins, which testified the MW-dependent adsorption fractionation of NOM samples and accounted for the enhanced aromaticity in the residual solutions. This study highlighted the importance of MWs in NOM adsorption, which can enhance our understanding of the biogeochemical cycles of colloids and contaminants in aquatic environments.

Electrochemical characterization of natural organic matter by direct voltammetry in an aprotic solvent.

The complex and indeterminant composition of NOM makes characterization of its redox properties challenging. Approaches that have been taken to address this challenge include chemical probe reactions, potentiometric titrations, chronocoulometry, and voltammetry. In this study, we revisit the use of direct voltammetric methods in aprotic solvents by applying an expanded and refined suite of methods to a large set of NOM samples and model compounds (54 NOM samples from 10 different sources, 7 NOM model compounds, and 2 fresh extracts of plant materials that are high in redox-active quinonoid model compounds dissolved in DMSO). Refinements in the methods of fitting the data obtained by staircase cyclic voltammetry (SCV) provided improved definition of peaks, and square wave voltammetry (SWV), performed under the same conditions as SCV, provided even more reliable identification and quantitation of peaks. Further evidence is provided that DMSO improves the electrode response by unfolding some of the tertiary structure of NOM polymers, thereby allowing greater contact between redox active functional groups and the electrode surface. We averaged experimental peak potentials for all NOM compounds and calculated potentials in water. Average values for Epa1, Epc1, and Ep1 in DMSO were -0.866 ± 0.069, -1.35 ± 0.071, and -0.831 ± 0.051 V vs. Ag/Ag+, and -0.128, -0.613, and -0.0930 V vs. SHE in water. In addition to peak potentials, the breadth of SCV peaks was quantified as a way to characterize the degree to which the redox activity of NOM is due to a continuum of contributing functional groups. The average breadth values were 1.63 ± 0.24, 1.28 ± 0.34, and 0.648 ± 0.15 V for Epa1, Epc1, and Ep1 respectively. Comparative analysis of the overall dataset-from SCV and SWV on all NOMs and model compounds-revealed that NOM redox properties vary over a narrower range than expected based on model compound properties. This lack of diversity in redox properties of NOM is similar to conclusions from other recent work on the molecular structure of NOM, all of which could be the result of selectivity in the common extraction methods used to obtain the materials.

Assessment of trihalomethane (THM) precursors using specific ultraviolet absorbance (SUVA) and molecular size distribution (MSD)

It is well known that natural organic matter (NOM) is the major precursor of disinfection by-products (DBPs) when inadequately removed NOM reacts with the disinfectant during chlorination and chloramination. Special interest in the DBP precursors is justified as it is essential to understand the reactivity and character of the precursors responsible for the formation of DBPs. This is vital in order to develop processes that will enhance precursor removal during drinking water treatment. The aim of this study was to investigate the impact of the characteristics of NOM within an oligotrophic water source on the formation of trihalomethanes (THMs) during drinking water treatment at Rand Water. Specific ultraviolet absorbance (SUVA) and molecular size distribution (MSD) were the main NOM characterisation techniques utilised during this study. The MSD was investigated by making use of high-performance size-exclusion chromatography (HPSEC). The MSD results showed a significant correlation between the high-molecular-weight (HMW) fraction of NOM and TTHM formation, specifically during the summer months. The positive correlation existing between SUVA and full scale NOM removal indicates that SUVA can be used to indicate NOM treatability during water treatment. A link between chloroform formation and the HMW fraction of NOM was also observed; however, the formation of bromodichloromethane (BDCM) was not due to the HWM fraction, as indicated by a weak regression coefficient. The results displayed are an indication that the aromatic fraction of NOM was the main precursor to TTHM formation, more prominently during summer.

Characterization of Natural Organic Matter by FeCl3 Coagulation

Natural organic matter (NOM) is heterogenous mixture of organic compounds that enter the water from various decomposition and metabolic reactions, including animal, plant, domestic and industrial wastes. NOM refers to group of carbon-based compounds that are found in surface water and ground water. The aim of the study is to assess organic matter characteristics in Jagir River as drinking water source and to characterize the organic components that could be removed during coagulation. Coagulation is the common water treatment process can be used to remove NOM with FeCl3 coagulant in various dosage. NOM surrogates, including total organic carbon (TOC), ultraviolet absorbance at 254 nm (UV254) and specific UV absorbance (SUVA) were chosen to assess the organic removal. Results of jar test experiments showed that NOM can be removed about 40% of NOM surrogates with 200 mg/L FeCl3. About 60% removal of total organic fraction, which is mainly humic substances, as detected by size exclusion chromatography (SEC).

Testing the Underlying Chemical Principles of the Biotic Ligand Model (BLM) to Marine Copper Systems: Measuring Copper Speciation Using Fluorescence Quenching.

Speciation of copper in marine systems strongly influences the ability of copper to cause toxicity. Natural organic matter (NOM) contains many binding sites which provides a protective effect on copper toxicity. The purpose of this study was to characterize copper binding with NOM using fluorescence quenching techniques. Fluorescence quenching of NOM with copper was performed on nine sea water samples. The resulting stability constants and binding capacities were consistent with literature values of marine NOM, showing strong binding with [Formula: see text] values from 7.64 to 10.2 and binding capacities ranging from 15 to 3110nmolmg[Formula: see text] Free copper concentrations estimated at total dissolved copper concentrations corresponding to previously published rotifer effect concentrations, in the same nine samples, were statistically the same as the range of free copper calculated for the effect concentration in NOM-free artificial seawater. These data confirms the applicability of fluorescence spectroscopy techniques for NOM and copper speciation characterization in sea water and demonstrates that such measured speciation is consistent with the chemical principles underlying the biotic ligand model approach for bioavailability-based metals risk assessment.