Fluorescence characteristics of natural organic matter in water under sequential exposure to UV irradiation/chlor(am)ination

2013 ◽  
Vol 14 (1) ◽  
pp. 22-30 ◽  
Author(s):  
Qianjun Guo ◽  
Zaili Zhang ◽  
Zhengbo Ma ◽  
Yongmei Liang ◽  
Wei Liu
Keyword(s):  
Organic Matter ◽  
Natural Organic Matter ◽  
Uv Irradiation ◽  
Fluorescence Intensity ◽  
Fluorescence Spectra ◽  
Low Molecular Weight ◽  
Subsequent Reaction ◽  
Fluorescence Characteristics ◽  
Major Reaction ◽  
Molecular Weight Fractions

The organic matter in International Humic Substances Society Natural Organic Matter (IHSS NOM) water exposed to ultraviolet (UV) irradiation and chlor(am)ine sequentially under practically relevant conditions was characterized based on fluorescence spectra. IHSS NOM water exposed to UV irradiation or chlor(am)ine alone was also evaluated. Both chlor(am)ine alone and UV/chlor(am)ine exposure showed similar chlor(am)ine demand and fluorescence spectra. UV irradiation and UV/chlorine exposure diminished the fluorescence intensity of IHSS NOM water, while UV/chloramine exposure resulted in increased fluorescence intensity. When compared with the results obtained following chlor(am)ination alone, IHSS NOM water showed decreased chlorine decay and increased chloramine decay after UV irradiation/chlor(am)ination. Additionally, IHSS NOM water exposed to UV/chloramine and chloramine showed less disinfection by-product (DBP) formation than water subjected to UV/chlorine and chlorine. Overall, these findings indicate that UV irradiation degrades NOM molecules to low-molecular-weight fractions, facilitating the subsequent reaction with chlor-(am)ine. However, chlorine and chloramine play different roles in the reaction. Chlorine degradation and substitution dominates the process of UV/chlorine exposure, while chloramine substitution is the major reaction during UV/chloramine exposure.

Influence of UV irradiation and UV/hydrogen peroxide oxidation process on natural organic matter fluorescence characteristics

2004 ◽  
Vol 4 (4) ◽  
pp. 41-46
Author(s):  
D.E.W. Hofbauer ◽  
S.A. Andrews
Keyword(s):  
Hydrogen Peroxide ◽  
Organic Matter ◽  
Natural Organic Matter ◽  
Uv Irradiation ◽  
Distribution Systems ◽  
Molecular Size ◽  
Peroxide Oxidation ◽  
Fluorescence Characteristics ◽  
Molecular Size Distribution ◽  
Uv Lamps

Natural organic matter is ubiquitous in aquatic systems, and has long been associated with disinfection by-product (DBP) formation during chlorination in water treatment plants and distribution systems. In this study modelled water was irradiated with either ultraviolet (UV) lamps or with UV combined with the addition of hydrogen peroxide (H2O2). The changes in the fluorescence intensity between the pretreated and post-treated samples were measured to determine the changes in the molecular size distribution of this reactive fraction of NOM. It was determined that the UV/H2O2 process reduces the concentration of these potential DBP precursors more effectively than UV irradiation alone.

Natural organic matter from catchment to drinking water: a case study of Pori waterworks, Finland

2008 ◽  
Vol 8 (6) ◽  
pp. 681-690 ◽  
Author(s):  
H. M. Szabo ◽  
I. Lindfors ◽  
T. Tuhkanen
Keyword(s):  
Drinking Water ◽  
Organic Matter ◽  
Natural Organic Matter ◽  
Dissolved Organic Nitrogen ◽  
Organic Nitrogen ◽  
Raw Water ◽  
Lake Waters ◽  
Molecular Weight Fractions ◽  
Uv And Fluorescence Detection

In this study Natural organic matter (NOM) characteristics and variations of catchment samples (brooks and collector lakes) from Western Finland, and drinking water produced from the same catchment were examined. Seasonal and spatial NOM variations were followed by means of DOC and HPLC-SEC with UV and fluorescence detection. NOM decreased from drains to lakes by 35 to 75% and from drains to drinking water by 73 to 94%. Drains had a higher NOM content in summer and a lower NOM content in winter and spring. Lakes showed inverse patterns and had a higher NOM content in winter and spring and a lower NOM content in summer. HPLC-SEC separated 8 molecular weight fractions. In drains the HMW fractions represented up to 80% of the NOM, in lake waters HMW fractions accounted for 50 to 70% of the NOM. In drinking water IMW fractions dominated. Increased NOM in raw water during winter was associated with increased IMW fractions and the appearance of HMW fractions in drinking water, DOC increasing from 1.4 mg C/L in summer to 5.8 mg C/L in winter. SPH-Tryptophan correlated with the dissolved organic nitrogen and DOC of the samples. The drain affected by agriculture generally presented higher SPH-Tryptophan values than the unaffected drain.

Comparison of disinfection byproduct (DBP) formation from different UV technologies at bench scale

2002 ◽  
Vol 2 (5-6) ◽  
pp. 515-521 ◽  
Author(s):  
W. Liu ◽  
S.A. Andrews ◽  
J.R. Bolton ◽  
K.G. Linden ◽  
C. Sharpless ◽  
...  
Keyword(s):  
Organic Matter ◽  
Carboxylic Acids ◽  
Natural Organic Matter ◽  
Uv Irradiation ◽  
Direct Action ◽  
Disinfection Byproduct ◽  
Pressure Medium ◽  
The Impact ◽  
As Effects

The impact of UV irradiation on disinfection byproduct (DBP) formation was investigated for low pressure, medium pressure and pulsed UV technologies using a broad range of UV doses. Four classes of DBPs (THMs, HAAs, aldehydes and carboxylic acids) were examined. This enabled the determination of effects resulting from the direct action of UV irradiation on natural organic matter (aldehydes, carboxylic acids) as well as effects on the ultimate formation of chlorinated DBPs (THMs and HAAs) from secondary chlorination. For doses of less than 1,000 mJ/cm2, UV irradiation did not affect THM and HAA formation in subsequent chlorination processes, however higher UV doses resulted in lower ultimate concentrations of THMs and HAAs. UV irradiation also resulted in the formation of aldehydes and carboxylic acids at UV doses above 500 mJ/cm2, compounds that are known to adversely effect drinking water biostability.

scholarly journals Removal of Trihalomethane Precursors by Nanofiltration in Low-SUVA Drinking Water

Water ◽  
2018 ◽  
Vol 10 (10) ◽  
pp. 1370 ◽  
Author(s):  
Yael Dubowski ◽  
Roni Greenberg-Eitan ◽  
Menachem Rebhun
Keyword(s):  
Molecular Weight ◽  
Organic Matter ◽  
Natural Organic Matter ◽  
Low Molecular Weight ◽  
Water Recovery ◽  
Formation Potential ◽  
Pressure Water ◽  
Membrane Type ◽  
Hydrophilic Organic Matter ◽  
By Products

Trihalomethanes (THMs) are prevalent disinfection by-products. High THM formation is usually associated with natural organic matter with high molecular weight and aromatic characteristics, which is efficiently removed by nanofiltration (NF). In the Sea of Galilee and the Israeli National Water Carrier (NWC), water shows high THM formation potential, although it mainly contains low molecular weight and hydrophilic organic matter with low aromaticity. In the present study, NF removal abilities were tested on treated NWC water using three different spiral wound membranes (NF90, NF270, and DL). Rejections and fluxes were tested as a function of pressure, water recovery, and membrane type. Feed and permeate dissolved organic carbon (DOC), UVA254, total THM formation (THMF), and total THM formation potential (THMFP), as well as alkalinity, conductivity, hardness, Ca2+, Mg2+, and Cl− were measured to evaluate rejection and THM formation reduction. The results demonstrated that NF can efficiently remove natural organic matter (NOM) and reduce THM formation, even in this challenging type of water. At low water recovery, membranes showed average rejection of about 70–85% for THMFP and THM. Upon elevating recovery, average THM and THMFP rejection decreased to 55–70%, with THM content still well below regulation limits. Of the membranes tested, the higher permeability of NF270 appears to make it economically favorable for the applications tested in this work.

Effects of dissolved organic matter on sorption of benzotriazole to soil

2020 ◽  
Author(s):  
Lin Wu ◽  
Jin’e Dai ◽  
Erping Bi
Keyword(s):  
Molecular Weight ◽  
Organic Matter ◽  
Dissolved Organic Matter ◽  
Organic Contaminants ◽  
Low Molecular Weight ◽  
Sorption Equilibrium ◽  
Solution Ph ◽  
Environmental Behaviors ◽  
Unsaturated Zones ◽  
Molecular Weight Fractions

<p>Dissolved organic matter (DOM) plays an important role in affecting the environmental behaviors of organic contaminants. Effects of two representative DOMs (dissolved humic acid (HA) and tannic acid (TA)) on sorption of benzotriazole (BTA) to a reference soil were investigated by batch experiments. The results indicated that TA had stronger sorption to soil than HA (initial solution pH=6.0±0.1). This is because that TA contains more carboxylic and phenolic groups than those of HA. In the solution with DOM, the enhanced sorption of BTA was caused by cumulative sorption resulting from sorbed DOM. Hydrogen bonding was proposed as the main binding mechanism between BTA and the sorbed DOM. When the solution pH at sorption equilibrium increased from 6.5 to 10.5, the electrostatic repulsion inhibited the sorption of BTA in solution with/without HA. In addition, less hydrogren bonds made the effect of HA in promoting BTA sorption decrease when solution pH changed from 6.5 to 10.5. Higher molecular weight fractions of HA could be preferentially sorbed by the soil, its enhancement on BTA sorption was more obvious than that of the low molecular weight fractions. These findings are conducive to a better understanding of environmental behaviors of BTA as well as other organic compounds with similar structure in the unsaturated zones.</p>

scholarly journals Effect of Changes in Physical Properties of Granular Activated Carbon (GAC) on the Adsorption of Natural Organic Matter (NOM) with Increasing the Number of Thermal Regeneration: Pore Size and NOM Molecular Weight

2021 ◽  
Vol 43 (7) ◽  
pp. 537-546
Author(s):  
Heejong Son ◽  
Sangki Choi ◽  
Byungryul An ◽  
Hyejin Lee ◽  
Hoon-Sik Yoom
Keyword(s):  
Molecular Weight ◽  
Organic Matter ◽  
Activated Carbon ◽  
Pore Structure ◽  
Adsorption Capacity ◽  
Natural Organic Matter ◽  
Volume Ratio ◽  
The Other ◽  
Low Molecular Weight ◽  
Thermal Regeneration

Objectives : The purpose of this study was to evaluate the effect of increasing the number of regeneration of granular activated carbon (GAC) on the adsorption capacity of natural organic matter (NOM), and to suggest the technical process options associated the limit number of regeneration and the efficient use of regenerated GAC.Methods : The physicochemical properties of virgin and thermally regenerated GAC were analyzed. To evaluate the NOM adsorption capacity of virgin- and regenerated-GAC, five laboratory-scale columns packed with virgin- and regenerated-GAC were used for treating effluent from pilot-scale drinking water treatment facility. The NOM concentration in the influent and the effluent treated by each column was analyzed by LC-OCD (liquid chromatography-organic carbon detector) to evaluate the adsorption capacity of each NOM fractions (humic substances (HS), building blocks (BB), low molecular weight organics (LMWs)).Results and Discussion : Due to the change in the pore structure of GAC by thermal regeneration, the volume of micropores (< 2 nm) decreased, while the volume of mesopores (> 2 nm) increased. The volume ratio of micropore in virgin-GAC was about 60%, but it gradually decreased as the number of regenerations increased, resulting that the volume ratio of micropore in the 5th-regenerated (5th-Re) GAC decreased to 23%. On the other hand, the volume ratio of mesopore increased in proportion to the number of regenerations from 40% of the virgin GAC to 77% of the 5th-Re-GAC. The DOC adsorption capacities of the regenerated GACs were higher than that of virgin GAC, and the DOC adsorption capacity increased as the number of regenerations increased. As a result of comparing the adsorption capacity of virgin- and regenerated-GAC by NOM fractions, the adsorption capacity of high molecular weight NOM, such as HS, increased by 1.5 to 1.7 times as the number of regenerations increased. In contrast, the adsorption capacity of low molecular weight NOM, such as BB and LMWs, decreased by 78% and 48% as the number of regeneration increased. The limit number of regeneration was evaluated based on that the adsorption capacity (qe) of each NOM fractions keep over than 70% relative to its virgin GAC. As a result, the adsorption capacity for low molecular weight NOM was greatly reduced in GAC regenerated over than 3rd time, so that the 2nd-Re-GAC was valid to keep 70% removal of whole NOM fractions. Low adsorption of low molecular weight NOM (BB and LMWs) by 3rd-Re-GAC could be complemented by using together with virgin-GAC, and low adsorption of high molecular NOMs (HS) could be compensated as well.Conclusions : Due to the change in the pore structure of GAC by thermal regeneration, the DOC adsorption capacity was higher in regenerated GAC than its virgin-GAC, and the adsorption capacity of DOC and high molecular weight NOM (HS) was enhanced as the number of regenerations increased. On the other hand, the pore volume of micropore was reduced by regenerations, and in more than 3rd times regenerations, the adsorption capacity of low molecular weight NOMs (BB and LMWs) was reduced by less than 70% compared to its virgin GAC, so that 2nd-Re-GAC was suggested for suitable GAC. When using a mixture of virgin- and 3rd-Re-GAC, low adsorption of low molecular weight NOM (BB and LMWs) by 3rd-Re-GAC could be complemented by using together with virgin-GAC, and low adsorption of high molecular NOMs (HS) could be compensated as well.

Removal of Natural Organic Matter (NOM) from Drinking Water Supplies by Ozone-Biofiltration

1999 ◽  
Vol 40 (9) ◽  
pp. 157-163 ◽  
Author(s):  
Raymond M. Hozalski ◽  
Edward J. Bouwer ◽  
Sudha Goel
Keyword(s):  
Molecular Weight ◽  
Organic Matter ◽  
Organic Carbon ◽  
Natural Organic Matter ◽  
Laboratory Experiments ◽  
Low Molecular Weight ◽  
Batch Experiments ◽  
Toc Removal ◽  
High Molecular Weight Material ◽  
Effects Of Temperature

Removal of natural organic matter (NOM) in biofilters can be affected by many factors including NOM characteristics, use of pre-ozonation, water temperature, and biofilter backwashing. Laboratory experiments were performed and a biofilter simulation model was developed for the purpose of evaluating the effects of each of these factors on NOM removal in biofilters. Four sources of NOM were used in this study to represent a broad spectrum of NOM types that may be encountered in water treatment. In batch experiments with raw NOM, the removal of organic carbon by biodegradation was inversely proportional to the UV absorbance (254 nm)-to-TOC ratio and directly proportional to the percentage of low molecular weight material (as determined by ultrafiltration). The extent and rate of total organic carbon (TOC) removal typically increased as ozone dose increased, but the effects were highly dependent on NOM characteristics. NOM with a higher percentage of high molecular weight material experienced the greatest enhancement in biodegradability by ozonation. The performance of laboratory-scale continuous-flow biofilters was not significantly affected by periodic backwashing, because backwashing was unable to remove large amounts of biomass from the filter media. Model simulations confirmed our experimental results and the model was used to further evaluate the effects of temperature and backwashing on biofilter performance.

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