scholarly journals Photocatalytic Oxidation of Natural Organic Matter in Water

Water ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 288
Author(s):  
Dan C. A. Gowland ◽  
Neil Robertson ◽  
Efthalia Chatzisymeon
Keyword(s):  
Drinking Water ◽  
Organic Matter ◽  
Water Treatment ◽  
Natural Organic Matter ◽  
Photocatalytic Oxidation ◽  
Municipal Wastewater ◽  
Complex Mixture ◽  
Chemical Properties ◽  
Water Supplies ◽  
Treatment Technologies

Increased concentrations of natural organic matter (NOM), a complex mixture of organic substances found in most surface waters, have recently emerged as a substantial environmental issue. NOM has a significant variety of molecular and chemical properties, which in combination with its varying concentrations both geographically and seasonally, introduce the opportunity for an array of interactions with the environment. Due to an observable increase in amounts of NOM in water treatment supply sources, an improved effort to remove naturally-occurring organics from drinking water supplies, as well as from municipal wastewater effluents, is required to continue the development of highly efficient and versatile water treatment technologies. Photocatalysis has received increasing interest from around the world, especially during the last decade, as several investigated processes have been regularly reported to be amongst the best performing water treatment technologies to remove NOM from drinking water supplies and mitigate the formation of disinfection by products. Consequently, this overview highlights recent research and developments on the application of photocatalysis to degrade NOM by means of TiO2-based heterogeneous and homogeneous photocatalysts. Analytical techniques to quantify NOM in water and hybrid photocatalytic processes are also reviewed and discussed.

scholarly journals Natural organic matter removal by ion exchange at different positions in the drinking water treatment lane

2013 ◽  
Vol 6 (1) ◽  
pp. 1-10 ◽  
Author(s):  
A. Grefte ◽  
M. Dignum ◽  
E. R. Cornelissen ◽  
L. C. Rietveld
Keyword(s):  
Water Quality ◽  
Drinking Water ◽  
Organic Matter ◽  
Water Treatment ◽  
Organic Carbon ◽  
Natural Organic Matter ◽  
Drinking Water Treatment ◽  
Biological Stability ◽  
Sand Filtration ◽  
Slow Sand Filtration

Abstract. To guarantee a good water quality at the customers tap, natural organic matter (NOM) should be (partly) removed during drinking water treatment. The objective of this research was to improve the biological stability of the produced water by incorporating anion exchange (IEX) for NOM removal. Different placement positions of IEX in the treatment lane (IEX positioned before coagulation, before ozonation or after slow sand filtration) and two IEX configurations (MIEX® and fluidized IEX (FIX)) were compared on water quality as well as costs. For this purpose the pre-treatment plant at Loenderveen and production plant Weesperkarspel of Waternet were used as a case study. Both, MIEX® and FIX were able to remove NOM (mainly the HS fraction) to a high extent. NOM removal can be done efficiently before ozonation and after slow sand filtration. The biological stability, in terms of assimilable organic carbon, biofilm formation rate and dissolved organic carbon, was improved by incorporating IEX for NOM removal. The operational costs were assumed to be directly dependent of the NOM removal rate and determined the difference between the IEX positions. The total costs for IEX for the three positions were approximately equal (0.0631 € m−3), however the savings on following treatment processes caused a cost reduction for the IEX positions before coagulation and before ozonation compared to IEX positioned after slow sand filtration. IEX positioned before ozonation was most cost effective and improved the biological stability of the treated water.

scholarly journals Biodegradation Behavior of Ozonated Natural Organic Matter in Sand Filters

2005 ◽  
Vol 9 (1) ◽  
pp. 3-16 ◽  
Author(s):  
J. Z. Wang ◽  
R. S. Summers
Keyword(s):  
Drinking Water ◽  
Organic Matter ◽  
Organic Carbon ◽  
Natural Organic Matter ◽  
Glyoxylic Acid ◽  
Complex Mixture ◽  
Drinking Water Treatment ◽  
Sand Filters ◽  
Substrate Removal ◽  
Exchange Resins

Natural organic matter (NOM) in drinking water is a complex mixture of organic compounds. Some of the compounds are not biodegradable, while others are quickly biodegradable and a third group is more resistant to biodegradation. To have a better understanding of the biofiltration process in drinking water treatment, it is important to identify the elements of the quickly and slowly biodegradable NOM and to characterize the biodegradation rate of each element. In this study, an ozonated NOM solution was used as the substrate. The NOM was isolated from a groundwater in Germany using ion-exchange resins. The ozone dose was 0.35 mg O3/mg DOC (dissolved organic carbon). Previously bioacclimated sand was used as filter media and biomass source and was homogeneously distributed in the filter prior to each run. The substrate removal was evaluated by DOC, biodegradable DOC (BDOC), assimilable organic carbon (AOC), aldehyde and ketoacid analyses. When expressed in terms of the empty bed contact time (EBCT), the results showed that filter velocity in the range of 1.5 to 15 m/hr had no impact on substrate removal. This implies that substrate utilization, not external mass transfer, is the rate limiting step for substrate removal in drinking water biofilters. In this study, compounds or NOM fractions are termed quickly biodegradable if they are removed in the first three minutes of EBCT. 15% of the DOC was removed by the biofilter within three minutes of EBCT and was termed the quickly biodegradable fraction. The BDOC fraction of the ozonated solution was determined to be 40 to 45% of the DOC. In terms of BDOC, about one third of the total BDOC was quickly biodegradable. The AOC results show that about 90% of the total AOC was utilized by Spirillum sp. NOX (AOC-NOX). Most of the AOC was quickly biodegradable and was removed within one minute of EBCT. For aldehydes, glyoxal and methyl glyoxal were removed to below the detection limit after two minutes of EBCT. However, only 60% of formaldehyde removal was achieved in the first two minutes of EBCT, and no additional removal was achieved with increasing EBCT. Additionally, no significant removal of acetaldehyde was observed. The results of ketoacids show that their utilization rates were very high. More than 90% of glyoxylic acid and pyruvic acid were removed within one minute of EBCT.

scholarly journals Fouling analysis of polysulfone ultrafiltration membranes used for drinking water treatment

2011 ◽  
Vol 11 (6) ◽  
pp. 668-674 ◽  
Author(s):  
B. Q. Zhao ◽  
C. P. Huang ◽  
S. Y. Chen ◽  
D. S. Wang ◽  
T. Li ◽  
...  
Keyword(s):  
Drinking Water ◽  
Organic Matter ◽  
Water Treatment ◽  
Fulvic Acid ◽  
Humic Substances ◽  
Natural Organic Matter ◽  
Drinking Water Treatment ◽  
Ultrafiltration Membranes ◽  
Fluorescence Excitation ◽  
Hydrophobic Fraction

Natural organic matter (NOM) plays a significant role in the fouling of ultrafiltration membranes in drinking water treatment processes. For a better understanding of the interaction between fractional components of NOM and polysulfone (PS) ultrafiltration membranes used for drinking water treatment, fouling and especially the physically irreversible fouling of natural organic matter were investigated. Resin fractionation, fluorescence excitation–emission matrix (EEM) spectroscopy, fourier transform infrared spectroscopy (FTIR), contact angle and a scanning electron microscope (SEM) were employed to identify the potential foulants. The results showed that humic acid and fulvic acid of small size were likely to permeate the membrane, while the hydrophobic fraction of humic and fulvic acid and aromatic proteins tended to be rejected and retained. Organic compounds such as proteins, humic substances, and polysaccharide-like materials, were all detected in the fouling layer. The physically irreversible fouling of the PS membrane seemed to be mainly attributed to the hydrophobic fraction of humic substances.

Evaluation of drinking water treatment processes focusing on natural organic matter removal and on disinfection by-product formation

2002 ◽  
Vol 2 (5-6) ◽  
pp. 459-464 ◽  
Author(s):  
S. Chae
Keyword(s):  
Drinking Water ◽  
Organic Matter ◽  
Water Treatment ◽  
Natural Organic Matter ◽  
High Performance ◽  
Drinking Water Treatment ◽  
Molecular Size ◽  
Product Formation ◽  
Size Exclusion ◽  
Activated Carbon Adsorption

The aim of this study was to characterize and compare natural organic matter (NOM) removal and disinfection by-product (DBP) formation in the drinking water treatment train that can give valuable information, while optimizing the treatment process. In this study, the determination of the hydrophobic (HPO), transphilic (THP) and hydrophilic (HPI) NOM distribution was used in parallel with more related drinking water parameters to compare the selected waters. High-performance size-exclusion chromatography (HPSEC) was applied to evaluate the relative changes of molecular size distribution of NOM in different treatment steps and source waters. This showed that the quantity, speciation and activated carbon adsorption of DBPs could vary not only by water quality, but also by the distribution and properties of the organic molecules that comprise NOM.

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