The Formation of Filter-Removable Biodegradable Organic Matter During Ozonation

Biodegradable organic matter formed during the ozonation of natural waters was fractionated into rapidly and slowly degradable components based on measurements of biodegradable organic carbon (BDOC). The rapidly degradable fraction (BDOC_rapid) was defined using the specific BDOC reactor incubation time that resulted in biodegradation similar to that in a pilot scale biofilter. Ozone dose was found to increase the formation of BDOC_rapid up to a transferred dose of 1.0 to 1.5 mg O₃/mg DOC. This fraction was insensitive to DOC quantity or character. The formation of BDOC_slow was not sensitive to ozone dose but was sensitive to DOC quantity.     

Formation and Removal of Biodegradable Ozonation By-Products during Ozonation-Biofiltration Treatment: Pilot-Scale Evaluation

An ozonation-biological filtration pilot-scale study was performed to evaluate the formation and removal of biodegradable ozonation by-products. The formation of aldehydes and ketoacids was found to be proportional to the DOC concentration and ozone dosage, and a strong relationship between the formation of aldehydes, ketoacids, and biodegradable dissolved organic carbon (BDOC) was observed. Four types of granular activated carbon (GAC) and one nonadsorbing medium, biolite, were employed to evaluate the performance of biofiltration for removing ozonation by-products. It was observed that GAC filters developed biological activity sooner than the biolite filter. Once developed, biofilters, either GACs or biolite, were particularly effective in the removal of aldehydes, ketoacids and BDOC.     

Pilot study of the removal of THMs, HAAs and DOC from drinking water by GAC adsorption

The objective of this pilot study was to evaluate the performance of a GAC postfilter-adsorber for the removal from the drinking water of Athens, Greece, of the two main groups of chlorination by-products, trihalomethanes (THMs) and haloacetic acids (HAAs), as well as of dissolved organic carbon (DOC). The analyses performed during the whole operation period (638 days) showed that the GAC breakthrough capacity for DOC was much higher than the capacity for total HAAs, which was higher than that for total THMs. The removal of THMs and the most part of the removal of HAAs and DOC should be attributed to adsorption by GAC, while that of a smaller part of HAAs and DOC may be attributed to biodegradation in the adsorber bed, where dechlorination, caused catalytically by the carbon surface, favoured microbial growth. Additionally, the GAC postfilter-adsorber showed a much higher adsorption efficiency than a GAC filter-adsorber, due to the smaller size of the carbon and the lower hydraulic loading rate. Also, observed desorption incidents of THMs (mainly) and HAAs, especially during the postfilteradsorber operation, were favoured by the same factors. Formation of THMs within the GAC bed was also indicated by the mass balance of total THMs during the whole cycle.     

Application of hybrid photocatalysis systems coupled with flocculation and adsorption to biologically treated sewage effluent for organic removal

The application of a photocatalysis hybrid system coupled with flocculation and adsorption in treating biologically treated sewage effluent (BTSE) was investigated. The removal of organic matter was studied in terms of dissolved organic matter (DOC), removal of hydrophobic (HP), transphilic (TP) and hydrophilic (HL) fractions, and molecular weight (MW) distribution. The photooxidation removed the majority of MW (263, 580, 865, and 43109 daltons) within the first 30 minutes of operation. The removal of MW range of organic matter of 330 daltons was low. DOC removal of HP and TP was high (80%). DOC removal from HL fraction was, however, minimum. The photocatalytic system with simultaneous PAC adsorption and FeCl₃ flocculation removed the effluent organic matter (EfOM) up to 90%. Therefore, photocatalysis with the ferric chloride (FeCl₃) flocculation and PAC adsorption hybrid system can be a possible option in the removal of DOC from BTSE for water reuse.     

Effects of Ozonation on Natural Organic Matter Reactivity in Adsorption and Biodegradation Processes – A Case Study: The Úzquiza Reservoir Water

In this paper the influences of preozonation on the effectiveness of NOM adsorption and biodegradation processes are studied. Three different types of water have been used in this study: A natural water from the Úzquiza Reservoir (Burgos, Spain), synthetics waters prepared using natural humic substances (fulvic and humic acids extracted from the Úzquiza Reservoir) and a synthetic water prepared using a commercially supplied humic acid. The effect of preozonation on NOM adsorption by activated carbon is evaluated: adsorption of humic acids (hydrophobic, high molecular weight compounds) is improved following preozonation; however, for the fulvic acids (hydrophilic, low molecular weight compounds), no net appreciable effect of preozonation on adsorption was observed. Preozonation increases the biodegradability of NOM: biodegradable dissolved organic carbon (BDOC), which was determined using two different bioassays (Billen-Servais method and Joret-Lévi method), increases with increasing ozone dosage. A characterization of humic substances based on their adsorption and biodegradability properties is also reported, showing the effect of ozone.     

Effluent organic matter removal from reverse osmosis feed by granular activated carbon and purolite A502PS fluidized beds

Applying pre-treatments to remove dissolved organic matter from reverse osmosis (RO) feed can help to reduce organic fouling of the RO membrane. In this study the performance of granular activated carbon (GAC), a popular adsorbent, and purolite A502PS, an anion exchange resin, in removing effluent organic matter (EfOM) from RO feed collected from a water reclamation plant located at Sydney Olympic Park, Australia were evaluated and compared through adsorption equilibrium, kinetics and fluidized bed experiments. The maximum adsorption capacity (Q_max) of GAC calculated from the Langmuir model with RO feed was 13.4 mg/g GAC. The operational conditions of fluidized bed columns packed with GAC and purolite A502PS strongly affected the removal of EfOM. GAC fluidized bed with a bed height of 10 cm and fluidization velocity of 5.7 m/h removed more than 80% of dissolved organic carbon (DOC) during a 7 h experiment. The average DOC removal was 60% when the bed height was reduced to 7 cm. When comparing GAC with purolite A502PS, more of the later was required to remove the same amount of DOC. The poorer performance of purolite A502PS can be explained by the competition provided by other inorganic anions present in RO feed. A plug flow model can be used to predict the impact of the amount of adsorbent and of the flow rate on removal of organic matter from the fluidized bed column.     

Effects Of Ozone On Biodegradable Dissolved Organic Carbon And Heterotrophic Plate Counts In The Distribution System

The impacts of ozone dose in the formation of biodegradable dissolved organic carbon (BDOC) were studied at the North Bay Regional Water Treatment Plant (NBR). Increasing the ozone to total organic carbon ratio to 0.45 (mg/mg) resulted in the formation of BDOC. Sedimentation and filtration/adsorption were effective in removing BDOC to non-measurable levels prior to the water entering the distribution system. Data from an on-going distribution system monitoring program indicate no discernible adverse impacts on microbiological parameters from using ozone during water treatment. Heterotrophic plate count (HPC) levels were similar before and after the use of ozone. Maintaining chlorine residual levels above 0.3 mg/L appears to be important for controlling HPC levels.     

磁性离子交换树脂强化水源中有机物去除性能研究

在调查某水厂水源水质及传统工艺处理效能的基础上,对比探讨了粉末活性炭和磁性离子交换树脂分别以预吸附、预吸附-混凝、混凝沉淀-吸附等不同工艺对水源水中溶解性有机物的去除效能,确定了最佳工艺。该水源存在季节性有机物污染,亲水性有机质占比80%。水厂传统工艺对有机物的去除能力约20%~30%。与其他工艺相比,树脂预吸附-混凝对有机物的去除功效最好,DOC和UV254的去除率分别达到41.48%和80.0%,与单独强化混凝相比,该工艺可将DOC和UV254的去除效率分别提高17.7和35.49个百分点,且可减少86.67%的混凝剂投加量。Langmuir等温线模型和拟二级动力学方程可定量描述树脂吸附有机物平衡和动力学。磁性离子交换树脂预吸附可作为该水厂强化去除水源中溶解性有机物的可靠技术。     

Ozonation of C.I. Reactive Yellow 3 and Further Decrease in Dissolved Organic Carbon Concentration by Post-Biodegradation

Using C.I. Reactive Yellow 3 as the target compound, the effect of the combined use of ozonation and post-biodegradation on the decrease in dissolved organic carbon (DOC) concentration was investigated, and the synergistic effect (the difference in the amounts of DOC removed by the biological process between solutions with and without ozonation) was estimated. A decrease in DOC concentration was observed during ozonation and ΔO₃/ΔDOC was decreased from 16.0 to 5.2 with increasing ozonation time. Moreover, an enhancement of biodegradability was shown. A further decrease in DOC concentration was observed during the biodegradation after ozonation. The total amount of DOC removed by the combined method was increased from 73.6 mg at 30 min to 159.9 mg at 4 h. The synergistic effect was in the range of 22.7 to 39.2 mg. BOD₅ was a better indicator of the synergistic effect than BOD₅/DOC.     

常规处理与深度处理工艺对南京长江原水中有机物去除效能比较

以长江南京段原水为研究对象,通过常规处理及深度处理工艺(强化过滤工艺和生物活性炭工艺)对长江南京段水源水中有机物的去除效能进行对比研究。结果表明常规工艺对CODMn、UV254、DOC及BDOC的去除率分别为30%、41%、27%及25%。强化常规工艺和生物活性炭工艺各指标的去除率分别为34%和52%、48%和50%、37%和40%及74%和82%。强化过滤工艺及生物活性炭工艺对1,2,4-三氯苯的去除效果明显,能显著提高出水水质。常规工艺对MW大于5 kDa的有机物去除效果明显,强化过滤工艺对MW小于1 kDa的有机物去除率大于25%,生物活性炭工艺对各个分子量区间的去除效果都比较好,特别是对原水中占多数的MW小于1 kDa的有机物去除率大于30%。     

Ozonation of Dyestuffs and Intermediates and Further Decrease in Dissolved Organic Carbon by Post-Biodegradation

Four each of water-soluble dyestuffs, intermediates and reference compounds were examined to determine the effect of the combined use of ozonation and post-biodegradation on the decrease in the amount of dissolved organic carbon (DOC) and the synergistic effect induced by ozonation. The amount of DOC removed by ozonation was increased initially with increasing ozonation time, and showed a plateau thereafter. The amount of ozone required to remove 1 mg of DOC (ΔO₃/ΔDOC) ranged from 5.2 to 18.6 mgO₃/mgC for the dyestuffs and the intermediates. The DOC concentrations of all the ozonized solutions were decreased with incubation time. In the case of the dyestuffs and the intermediates, the total amounts of DOC removed were increased with increasing ozonation time and showed a plateau thereafter. The synergistic effect (the ozonation-induced increase in the amount of DOC removed by the biological process) was dependent on the initial biodegradability, and was observed in all the dyestuffs and the intermediates in the range of 0.2 to 42.7 mgDOC. On the other hand, no synergistic effect was observed in the reference compounds of high biodegradability.     

臭氧-活性炭组合工艺对污水处理厂二级出水中β-内酰胺类抗生素的去除

采用臭氧-活性炭组合工艺去除污水厂二级出水中的β-内酰胺类抗生素。试验选取6种常见β-内酰胺类抗生素作为目标抗生素,考察了臭氧投加量、反应时间、活性炭炭层高度以及空床停留时间(EBCT)对目标抗生素去除效果的影响。试验表明,在臭氧投加量为8 mg/L,臭氧与目标物质反应时间为20 min,活性炭炭层高度为750 mm,EBCT为10 min时,臭氧-活性炭组合工艺对目标抗生素的平均去除率为69.24%,对头孢他啶(CAZ)的去除率最高,为75.13%,头孢曲松(CRO)的去除率最低,为62.14%。     

生物活性炭工艺去除长江原水中有机成分的研究

以长江南京段原水为研究对象,以提高水处理出水水质和生物稳定性为目标,研究了生物活性炭工艺对有机物指标和氯苯类化合物的去除效果,并从有机物分子量的角度研究了生物活性炭工艺对有机物的去除机制。中试试验结果表明：生物活性炭工艺能有效地去除水中的有机物,对CODMn,UV254,溶解性有机碳（DOC）及可生物降解溶解性有机碳（BDOC）的去除率可分别达到52％,50％,40％和82％,对氯苯类化合物的去除效果也较为明显,去除率为40％左右。生物活性炭工艺对各个分子量区间的去除效果都比较好,对原水中占多数的小于1k的溶解性有机物（DOM）去除效果尤为显著。     

Operation of Fixed‐bed Bioreactor for Polluted Surface Water Treatment

Abstract

Dissolved organic matters and ammonia nitrogen are serious contaminants of surface water in Taiwan. These contaminants can interfere with the water treatment process and cause biological instability in the finished water. One solution is to employ a biological treatment stage prior to the conventional water treatment process. A continuous flow biological filter packed with reticulated PU foam was used to remove ammonia nitrogen and organic materials before the conventional water treatment practice. The effect of its operation mode, namely, empty bed contact time (EBCT) and backwash, on the removal efficiencies of ammonia and organic matter was examined. The results suggested that ammonia nitrogen and organic nitrogen can be effectively removed by controlling the operation mode of the biological fixed bed. Efficient ammonia nitrogen removal was achieved upon the combination of the backwash mode with short EBCT or extended EBCT without the backwash. Efficient organic nitrogen and DOC removals were observed at short EBCT without the backwash. This study provides insights into the function of biofiltration, which benefits the design of a fixed‐bed bioreactor for the treatment of polluted surface water.     

Effects Of Ozone On The Production Of Biodegradable Dissolved Organic Carbon (BDOC) During Water Treatment

This article deals with the oxidation effect of ozone on the increasing fraction of biodegradable organic matter with the “ozotest” method, a laboratory technique which simulates the effect of ozonation and allows a complete oxidation assessment. Ozone treatment was performed on river water samples and sand filter effluent samples. Ozone consumption, reduction of UV absorbance and BDOC formation were monitored with applied ozone doses from 0 to 10 mg/L and with contact times from 0 to 60 min. The BDOC formation was optimum at an applied ozone dose of 0.25-0.5 mg O₃ per mg DOC (contact time = 5 min) corresponding to apparition of traces of residual ozone and maximum UV reduction. Maximum ozone consumption, UV reduction and BDOC formation occurred simultaneously during the first two minutes of treatment. Concerning BDOC formation, applied ozone dose showed a greater effectiveness than contact time. For the same quantity of consumed ozone, a short contact time associated with a high ozone dose was preferable to a long contact time and a low ozone dose.     

Systematic Approach to Quantify Adsorption and Biodegradation Capacities on Biological Activated Carbon Following Ozonation

The goal of this research was to develop a systematic approach to quantify adsorption and biodegradation capacities on biological activated carbon (BAC). The role of absorption and biodegradation on BAC was studied using a continuous column. Several media, i.e., granular activated carbon (GAC), seeded glass bead and seeded GAC, and a target compound (p-hydroxybenzoic acid) were selected. Before breakthrough, the effluent of the GAC column contained a small amount of p-hydroxybenzoic acid that contributed the greatest amount of organic carbon to the effluent of the glass bead column, which suggests that adsorption should be the prevailing mechanism for removal the p-hydroxybenzoic acid, and biodegradation should be responsible for reducing the ozonation intermediates. Also, the bioactivity approach (biomass respiration potential, BRP) of BAC can not only reveal the importance of biodegradation mechanisms for the intermediates of ozonation, but also quantify the extent of the adsorption or biodegradation reaction occurring on BAC.     

Application of combined coagulation-ultrafiltration membrane process for water treatment

The objectives of this research are to identify the membrane fouling potential due to different fractions of NOM and correlate the physicochemical properties of NOM and membranes with the adsorption of humic substances on membrane and investigate the mechanism of coagulation affecting UF, and find the optimum conditions of the combined of coagulation with UF membrane filtration for NOM removal. For Nakdong river water, the humic acid fraction was the most reactive precursor fraction for the formation of the ratio of THMFP/DOC (STHMFP) and TOXFP/DOC (STOXFP). The result of adsorption kinetics tests showed that hydrophobic organics adsorbed much more quickly than hydrophilic organics on both membranes. Thus, hydrophobic compounds exhibited a preferential adsorption onto membrane. In case of the effect of membrane properties on the adsorption of organic fractions, the adsorption ratio (C₁/C_e) was greater for the hydrophobic membrane than for the hydrophilic membrane regardless of the kind of organic fractions. For combined coagulation with membrane process, flux reduction rate showed lower than the UF process alone. Also, the rate of flux decline for the hydrophobic membrane was considerably greater than for the hydrophilic membrane. Applying the coagulation process before membrane filtration showed not only reduced membrane fouling, but also improved removal of dissolved organic materials that might otherwise not be removed by the membrane. That is, during the mixing period, substantial changes in particle size distribution occurred under rapid and slow mixing conditions due to the simultaneous formation of microflocs and NOM precipitates. Therefore, combined pretreatment using coagulation (both rapid mixing and slow mixing) improved not only dissolved organic removal efficiency but also DBP (Disinfection By-Product) precursor's removal efficiency.     

臭氧氧化对可溶性有机物构成的研究

实验目的在于对溶解性有机物进行分类及考察，研究臭氧氧化影响四种溶解性有机物：1．可生物降解不可吸附；2．可生物降解可吸附；3．可吸附不可生物降解；4．不可吸附不可生物降解。（NA＆BDOC、B＆ADOC、NB＆ADOC、NRDOC）的因素及趋势。实验结果表明臭氧不能同时去除四种溶解性有机物。而是影响它们所占比例．使可生物降解性有机物增加，可吸附性有机物减少。根据实验结果可优选出后续生物活性炭净水效果的最佳的臭氧投加量和停留时间。实验结果可为工程设计提供有益的参考价值。     

Characterization procedure for adsorption of DOC (Dissolved Organic Carbon) from synthetic wastewater

A characterization method to evaluate the composition of background organic matters in terms of adsorbability was presented and applied to synthetic and domestic wastewater. The binomial distribution of DOC (Dissolved Organic Carbon) fraction in relation of a characterizing variable, the Freundlich coefficient, k, was proposed to describe the initial composition of wastewater by a finite number of pseudospecies. This method was tested for removal of DOC by using granular and powdered activated carbons. These experiments enable us to get information on the distribution function of species in the solution. From the results obtained in this work, kinetic experimental data were predicted on the assumption that the diffusion coefficients were unchanged during the experiments. It was confirmed to be effective in determining the initial composition and describing the equilibria of the DOC. From the experiments, it was found that this synthetic solution has a sigmoid type isotherm on activated carbons. This implies that there are two different adsorption regions in a system, favourable and unfavourable cases, depending on the solution concentration. This unfamiliar problem can be solved by using a characterization method based on IAST-Freundlich model.