Assessing the removal potential of soil-aquifer treatment system (soil column) for endotoxin

Soil-aquifer treatment (SAT) of wastewater is an increasingly valued practice for replenishing aquifers due to ease of operation and low maintenance needs and therefore low cost. In this study, we investigated the fate of endotoxins through laboratory-scale SAT soil columns over a four month period. The effluent of rapid sand filtration was run through the columns under gravity flow conditions. Four SAT columns were packed with four different filter materials (fine sand, medium sand, coarse sand and very coarse sand). The effluent of rapid sand filtration (average dissolved organic carbon (DOC) = 4 mg l(-1) and average endotoxin concentration = 4 EU ml(-1)) was collected from a domestic wastewater treatment plant in Sapporo, Japan. DOC removal ranged from 12.5% to greater than 22.5% during the study, with DOC levels averaging 3.1 and 3.5 mg l(-1) for the SAT columns packed with different soils. Endotoxin transformation exhibited different profiles, depending on the time and soil type. Reduction in endotoxin concentration averaged 64.3% and was as high as 86.7% across the soil columns 1, 2, 3 and 4, respectively. While DOC removal was gradual, the reductions in endotoxin levels were rather rapid and most of the removal was achieved in the top layers. Soil with a larger grain size had lower efficiency in removing endotoxin. Tests were performed to evaluate the transformation of organic matter showing endotoxicity and to determine the mechanisms responsible for changes in the structural and size properties of dissolved organic matter (OM) during SAT. Dissolved OM was fractionated using Sep-Pack C18 Cartridges into hydrophobic and hydrophilic fractions. Dialysis tubes with different molecular weight cut-offs were used to perform size fractions of OM showing endotoxicity. Evaluation of the transformation of organic matter showing endotoxicity during SAT indicated that both hydrophobic and large molecules were reduced. Moreover, experimental findings showed that adsorption test data fit to the Freundlich isotherm and were affected by the particle grain size with higher adsorption capacity for fine and medium sand.     

Fluorescence spectroscopic characterization of dissolved organic matter fractions in soils in soil aquifer treatment

This work investigated the effect of soil aquifer treatment (SAT) operation on the fluorescence characteristics of dissolved organic matter (DOM) fractions in soils through laboratory-scale soil columns with a 2-year operation. The resin adsorption technique (with XAD-8 and XAD-4 resins) was employed to characterize the dissolved organic matter in soils into five fractions, i.e., hydrophobic acid (HPO-A), hydrophobic neutral (HPO-N), transphilic acid (TPI-A), transphilic neutral (TPI-N), and hydrophilic fraction (HPI). The synchronous fluorescence spectra revealed the presence of soluble microbial byproduct- and humic acid-like components and polycyclic aromatic compounds in DOM in soils, and SAT operation resulted in the enrichment of these fluorescent materials in all DOM fractions in the surface soil (0–12.5 cm). More importantly, the quantitative method of fluorescence regional integration was used in the analysis of excitation–emission matrix (EEM) spectra of DOM fractions in soils. The cumulative EEM volume (Φ _{T, n} ) results showed that SAT operation led to the enrichment of more fluorescent components in HPO-A and TPI-A, as well as the dominance of less fluorescent components in HPO-N, TPI-N, and HPI in the bottom soil (75–150 cm). Total Φ _{T, n} values, which were calculated as $ {\Phi_{{T,n}}} \times {\mathrm{DOC}} $ , suggested an accumulation of fluorescent organic matter in the upper 75 cm of soil as a consequence of SAT operation. The distribution of volumetric fluorescence among five regions (i.e., P _{i, n} ) results revealed that SAT caused the increased content of humic-like fluorophores as well as the decreased content of protein-like fluorophores in both HPO-A and TPI-A in soils.     

焦化废水生化处理过程中溶解性有机物及毒性变化规律

焦化废水中的溶解性有机物(DOM)作为废水污染物和毒性的主要来源受到广泛关注。厌氧-缺氧-好氧(A-A-O)生物法联合混凝沉淀工艺在焦化废水处理中被广泛应用。于2018年4,7和11月分别采集4座焦化废水处理厂废水,采用光谱学分析手段和水生生物急性毒性试验对A-A-O联合混凝沉淀处理过程中焦化废水的DOM和毒性变化进行分析。结果表明,焦化废水中含有大量不饱和芳香性物质,其中类色氨酸、络氨酸物质占主导,其次为类溶解性微生物代谢产物、类富里酸物质和类腐殖酸类物质;未经处理的焦化废水对藻类和大型溞的急性毒性等级为中毒至高毒。A-A-O联合混凝沉淀处理可去除90%以上的类色氨酸、络氨酸和类富里酸物质,但对类腐殖酸类物质去除率相对较低,仅为约80%,关键去除段为缺氧段和好氧段;该工艺对焦化废水急性毒性削减率为80.51%~94.30%,关键削减段为厌氧段。Pearson相关性分析结果显示,焦化废水溶解性总有机碳(TOC)、类腐殖酸类物质荧光组分C1和类富里酸类物质荧光组分C4与废水急性毒性存在显著正相关关系,可利用其作为水样急性毒性初筛的指示性指标。可为焦化废水生化处理的效能优化和废水毒性控制及安全评估提供科学支撑。     

Measurement of wastewater treatment efficiency by fluorescence and UV absorbance

The degree of chemical treatment in terms of removal of organic matter from different wastewaters has been investigated by employing potassium ferrate (K₂FeO₄) and ozone in various combinations. The study was performed in both the batch and the continuous flow systems. The treatment efficiency was determined through three different methods, i.e., chemical oxygen demand (COD), fluorescence and ultraviolet (UV) absorption. Fluorescence and UV absorption techniques were employed due to their specificity in measurement of humic substances, aromatic compounds and heterocyclic systems, whereas COD is a general parameter for the estimation of total organic matter. Fluorescence and UV absorbance values were correlated with respective COD values.Abdul Bari is with the Department of ChemistryShaukat Farooq is with the Department of Civil Engineering     

Changes in the sorption and rate of 17β-estradiol biodegradation by dissolved organic matter collected from different water sources

The potential biodegradation and subsequent transformation of 17β-estradiol (E2) to estrone (E1) were examined in the presence of various dissolved organic matter (DOM) isolated from effluent, river and lake waters. In addition, estrogenicity was estimated in association with the removal of E2 via its sorption onto DOM and biodegradation. The more biodegradable lake-derived DOM promoted more extensive transformation of E2 into E1 than the effluent organic matter through a biodegradation process. Overall, under all conditions, biodegradation dominated the removal of E2 in water. The increased dissolved organic carbon (DOC) concentrations in river and lake-derived DOM (e.g. 6.5 mg C L(-1)) reduced the removal of E2 by decreasing its biodegradation due to the moderate sorption of E2 onto DOM. The effluent organic matter showed greater removal of E2 via biodegradation, as well as significantly high sorption. This was associated with a large amount of hydrophobic fulvic acid (FA)- and humic acid (HA)-like organic components, as shown by the small increase in the specific UV absorbance at 254 nm (SUVA(254)). An increase in the DOC concentration reduced the removal of E2, resulting in high estrogenicity. The present study suggests that both organic composition and DOC concentration influenced the removal of E2 and, therefore, should be fully considered when assessing estrogenicity and its impacts on the aquatic environment.     

气相色谱-质谱法分析污水中溶解态有机物

采用0.45μm玻璃纤维滤膜将污水分离为悬浮态和溶解态有机物质,以二氯甲烷为萃取剂,采用液液萃取-气质联用法对污水中溶解态有机物进行测定,同时还对萃取条件(萃取次数,萃取时间,无机盐加入量)进行优化.结果表明:萃取回收率最高的是每个pH范围各萃取2次、静置5 min,氯化钠加入15g.该方法分析时间短,准确度好(样品平均加标回收率为91.1％ ～ 103％),精密度高(相对标准偏差小于5％),易于操作.     

BDE-47在土壤矿物质与有机质上的吸附解吸特征

以多溴联苯醚典型单体2,2′,4,4′?四溴联苯醚（BDE?47）为研究对象,阐明了其在土壤矿物质与有机质上的吸附解吸行为及特征。结果表明：土壤中无机矿物质对BDE?47的吸附贡献不大,而有机质是调控BDE?47在土壤中吸附行为的关键组分;有机质对BDE?47的吸附能力与其有机碳含量和物理化学特性相关;BDE?47在腐殖酸上的解吸存在显著的滞后现象。     

Investigation of 15-year-old municipal solid waste deposit profiles by means of FTIR spectroscopy and thermal analysis

Five profiles of a 15-year-old bank containing over three weeks composted municipal solid waste were characterized by means of different parameters habitually applied in waste management (loss on ignition, total organic carbon, total nitrogen, NH(4)-N, pH), and in addition by humic acid determination, FTIR spectroscopy and thermal analysis. Stabilization processes are revealed by humic acid contents. Over the 15 year period organic matter had developed in various ways. Highest humic acid contents were found at 0.5 m below the surface. Below 1.0-1.5 m anaerobic conditions dominated causing a strong decline of humic acid concentrations. Despite similar contents of organic matter at 0.5 m and at 3.0 m organic matter quality differed. These differences were verified by infrared spectroscopic investigations and thermal analyses (differential scanning calorimetry DSC). The spectral pattern of 15-year-old profile samples (municipal solid waste including the biogenic fraction) was compared to current municipal solid waste and abandoned landfill materials. Current municipal solid waste samples comprised different degradation stages from fresh materials to stabilized waste, suitable for landfilling according to Austrian standards. Municipal solid waste originating from abandoned landfills closed in the seventies represented stable material. Principal component analysis was performed to detect similarities and differences. It is evident that the profile samples constitute a particular group in between municipal solid waste and abandoned landfill material. Some differences can be attributed to the divergent composition of municipal solid waste in the eighties when the organic fraction was not separated. Otherwise, landfill materials from the seventies with the same composition regarding the organic fraction were deposited together with construction waste. Heat flow curves (DSC profiles) of municipal solid waste, representing different decomposition stages, illustrate the development of enthalpies and reveal the status of the profile samples. It is evident that mechanical-biological pretreatment leads to a faster stabilization of waste organic matter.     

Transport of Cryptosporidium parvum oocysts in sandy soil: impact of length scale

The objective of this study was to investigate the impact of length scale (travel distance) on the retention and transport of Cryptosporidium oocysts in a sandy soil. Long columns (1 and 2 meters) and an in situ lysimeter (4 m) were used to allow investigation of larger-scale transport under controlled conditions. Significant retention of oocysts was observed, with the magnitude of removal from solution ranging between 2 to 5 logs. While the removal was greater for longer travel distances (or residence times), the increase was not log-linear. This observation indicates that oocyst transport was not consistent with standard colloid filtration theory. The observed behavior is speculated to arise, at least in part, from intrapopulation variability in oocyst properties. The results of this study indicate that while Cryptosporidium oocysts may be expected to experience significant retention and removal during transport in sandy soil, the magnitude of retention may be less than that which would be predicted by applying standard colloid filtration theory to the results of typical short-column experiments. Thus, a fraction of the oocysts may be more mobile than anticipated and thereby pose a greater than expected risk to groundwater.     

石油化工废水中有机组分剖析

采用二氯甲烷液—液萃取预处理水样，气相色谱—质谱联用技术分析了炼油厂生化曝气池进、出水，腈纶厂干法纺丝废水及其经ＳＢＲ小试处理的出水中二氯甲烷可萃取的有机组分，并半定量地评估了生化处理对这些有机组分的去除效果。结果表明，炼油厂生化曝气池对酚类及芳烃类化合物的去除效果较好，而长链脂肪烃的去除率相对较低；腈纶干法纺丝工艺废水中可萃取的有机组分主要为Ｎ，Ｎ二甲基甲酰胺，其相对含量大于９５％（ｍ／ｍ），该废水经ＳＢＲ小试处理后，原水中各种可萃取的有机化合物均得到分解，结构发生了变化，但不能全部彻底地转化为ＣＯ２和水。     

The distribution of organic matter in songkhla lake basin (SLB)

The concentrations and the distribution of organic matter in SLB (e.g. the outer part of Thale Sap Songkhla area) were examined during the period of September 1988 to September 1989. Organic matter in water samples were analyzed by gravimetry. Total organic matter and dissolved organic matter concentrations ranged from 74 to 7908 mg/L and from 23 to 7813 mg/L, respectively. Except for a set of observations which showed low concentrations during the flood season in November 1988, organic matter was regularly distributed throughout SLB. Domestic effluent and aquaculture are hypothesized as major sources of organic matter contamination. The levels of organic matter concentrations in SLB are significantly higher than would be expected for an area considered to be uncontaminated. The data also indicated a linear relationship between concentrations of suspended organic matter and suspended solids. This may be due to the organic matter associated with suspended solids.     

Preferential adsorption of fluorescing fulvic and humic acid components on activated carbon using flow field-flow fractionation analysis

Activated carbon treatment of drinking water is used to remove natural organic matter (NOM) precursors that lead to the formation of disinfection byproducts. The innate hydrophobic nature and macromolecular size of NOM render it amenable to sorption by activated carbon. Batch equilibrium and minicolumn breakthrough adsorption studies were performed using granular activated carbon to treat NOM-contaminated water. Ultraviolet (UV) absorption spectroscopy and flow field-flow fractionation analysis using tandem diode-array and fluorescence detectors were used to monitor the activated carbon sorption of NOM. Using these techniques, it was possible to study activated carbon adsorption properties of UV absorbing, fluorescing and nonfluorescing, polyelectrolytic macromolecules fractionated from the total macromolecular and nonmacromolecular composition of NOM. Adsorption isotherms were constructed at pH 6 and pH 9. Data were described by the traditional and modified Freundlich models. Activated carbon capacity and adsorbability were compared among fractionated molecular subsets of fulvic and humic acids. Preferential adsorption (or adsorptive fractionation) of polyelectrolytic, fluorescing fulvic and humic macromolecules on activated carbon was observed. The significance of observing preferential adsorption on activated carbon of fluorescing macromolecular components relative to nonfluorescing components is that this phenomenon changes the composition of dissolved organic matter remaining in equilibrium in the aqueous phase relative to the composition that existed in the aqueous phase prior to adsorption. Likewise, it changes the composition of dissolved organic matter remaining in equilibrium in the aqueous phase relative to the adsorbed phase. This research increases our understanding of NOM interactions with activated carbon which may lead to improved methods of potable water production.     

Evaluating the Efficiency of Coagulation in the Removal of Dissolved Organic Carbon from Reservoir Water using Fluorescence and Ultraviolet Photometry

The present study used ultraviolet absorption (UVa) and the florescence intensity (FI) to evaluate the coagulation efficiency for removing dissolved organic carbon (DOC) in the raw water from Min-Ter, Li-Yu-Ten and Yun-Ho-Shen reservoirs in Taiwan. The results indicated that the ratio of DOC removal rate and FI removal rate was maintained at about 1 at various coagulant dosages. However, the ratio of DOC removal rate and UVa removal rate decreased as the coagulant dosage increased. In addition, after coagulation, the use of florescence intensity instead of total organic carbon (TOC) is better than UVa for measuring the DOC removal rate of the raw waters gathered in different months from the three reservoirs. Furthermore, a good linear relationship between florescence intensity and DOC removal rate was observed, and the DOC/FI ratio of raw water from each reservoir can be used to predict the DOC residual concentration after enhanced coagulation. This result shows that fluorescence analysis can be used for on-line and continuous monitoring the effectiveness of organic matter removal in water treatment.     

Chemical constraints on new man-made lakes

The formation of reservoirs often affects water quality strongly, with the changes in the physicochemical properties being ascribed to decomposition of remaining organic matter arising from leaching and (biological and chemical) breakdown processes. In this study, experiments under laboratory conditions were performed to show that the nature of the course particulate organic matter (CPOM; i.e., leaves, branches, barks, and litter) determines the decomposition kinetics in new reservoirs. Effects on the water quality can be of short-, mid-, and long-term duration for all types of CPOM, as indicated in the mathematical modeling of the decomposition kinetics. Leaves and litter displayed the shortest half-life times (51 and 40 days, respectively) and the highest potential of leaching/oxidation of labile compounds (19 and 21 %, respectively). On the other hand, decomposition of branches and barks generated the lowest oxygen consumption (74 and 44 mg oxygen/g dry mass (DM), respectively). During formation of the reservoir, the incorporation and decomposition of organic matter prevailed over material exportation. Therefore, in addition to a decrease in oxygen availability the concentration of biochemical oxygen demand (BOD) and nutrients increased. After the filling stage, there was significant loss of organic matter via oxidation, sedimentation, biological assimilation, and export, thus causing the BOD concentration and the fertility of the water to decrease.     

Pharmaceuticals and personal care products in effluent matrices: A survey of transformation and removal during wastewater treatment and implications for wastewater management

Pharmaceuticals and personal care products (PPCPs) represent pollutants of emerging concern, originating in surface and drinking waters largely from their persistence in wastewater effluent. Accordingly, a wealth of recent investigations has examined PPCP fate during wastewater treatment, focusing on their removal during conventional (e.g., activated sludge) and advanced (e.g., ozonation and membrane filtration) treatment processes. Here, we compile nearly 1500 data points from over 40 published sources pertaining to influent and effluent PPCP concentrations measured at pilot- and full-scale wastewater treatment facilities to identify the most effective series of technologies for minimizing effluent PPCP levels. Available data suggest that at best a 1-log(10) concentration unit (90%) of PPCP removal can be achieved at plants employing only primary and secondary treatment, a performance trend that is maintained over the range of reported PPCP influent concentrations (ca. 0.1-10(5) ng L(-1)). Relatively few compounds (15 of 140 PPCPs considered) are consistently removed beyond this threshold at facilities using solids removal and conventional activated sludge (CAS), and most PPCPs are removed to a far lesser extent. Further, increases in CAS hydraulic retention time or sludge retention time do not appreciably increase removal beyond this limit. In contrast, plants employing advanced treatment methodologies, particularly ozonation and/or membranes, remove the vast majority of PPCPs beyond 1-log(10) concentration unit and oftentimes to levels below analytical detection limits in effluent. Data also indicate that passive approaches for tertiary treatment (e.g., wetlands and lagoons) represent promising options for PPCP removal. We conclude by addressing future challenges and frontiers in wastewater management posed by PPCPs including analytical needs for their real-time measurement, energy demands associated with advanced treatment technologies, and byproducts arising from transformation of PPCPs during treatment.     

Environmental monitoring of offshore drilling for petroleum exploration (MAPEM Project): shallow waters

This paper deals with the characteristics and composition of municipal solid waste (MSW) generated in Sangamner city. The composition of solid waste was studied by segregating it into different component, i.e., kitchen waste, paper, earth and fine material, slaughter house waste, leaves, metals, etc. These components were categorised into organic waste and inorganic waste. It was observed that Sangamner city produces around 61% organic waste, and the rest is inorganic waste. The characteristics of organic solid waste, i.e., pH, electrical conductivity, moisture content, organic carbon, nitrogen, phosphorus and potassium were evaluated. The analysis of organic content of MSW indicates that it is good source of nutrients for the agriculture sector whereas inorganic material can be used for landfill.     

Monitoring dissolved organic carbon in surface and drinking waters

The presence of natural organic matter (NOM) strongly impacts drinking water treatment, water quality, and water behavior during distribution. Dissolved organic carbon (DOC) concentrations were determined daily over a 22 month period in river water before and after conventional drinking water treatment using an on-line total organic carbon (TOC) analyzer. Quantitative and qualitative variations in organic matter were related to precipitation and runoff, seasons and operating conditions. Following a rainfall event, DOC levels could increase by 3.5 fold over baseflow concentrations, while color, UV absorbance values and turbidity increased by a factor of 8, 12 and 300, respectively. Treated water DOC levels were closely related to the source water quality, with an average organic matter removal of 42% after treatment.     

七虎林河流域上游溶解性有机质光谱特性分析

七虎林河源头区地表腐殖质随着径流的冲刷进入水体,形成了天然有机质(NOM),其中,溶解性有机质(DOM)易对河流水质造成影响。为了研究七虎林河中DOM的时空分布特征及其对水质的影响,开展了6次采样,分析了水体及土壤吸收光谱和荧光光谱特征参数,利用平行因子(PARAFAC)算法解析了水体DOM的特性及来源。结果表明：七虎林河上游水体五日生化需氧量(BOD₅)、高锰酸盐指数(COD_Mn)、化学需氧量(COD)、可溶性有机碳(DOC)的浓度分别为1.4 mg/L±0.2 mg/L、6.1 mg/L±3.0 mg/L、21 mg/L±8 mg/L、7.0 mg/L±3.2 mg/L,BOD₅/COD平均值为0.08,说明流域内水体DOM的可生化性差,对水质影响较小。光谱特征参数紫外吸收系数(SUVA₂₅₄)、荧光指数(FI)、腐殖化指数(HIX)、生物源指数(BIX)分析结果表明,七虎林河上游云山水库库上林区河段DOM的物质组成与水库及库下河段差异显著。库上河段DOM的芳香碳含量更高、分子量更大、自生源组分...     

Adsorption of antimony(V) by floodplain soils, amorphous iron(III) hydroxide and humic acid

Antimony (Sb) emissions to the environment are increasing, and there is a dearth of knowledge regarding Sb fate and behaviour in natural systems. In particular, there is a lack of understanding of sorption of the oxidised Sb(V) species onto soils and soil phases. In this study sorption of Sb(V) by two organic rich soils with high levels of oxalate extractable Fe was examined over the pH range of 2.5-7. Furthermore, the sorption behaviour of Sb(V) was examined in two phases mimicking those dominant in the experimental soils, namely a solid humic acid and an amorphous Fe(OH)3, across the same pH range. Sorption of Sb by the soils and the humic acid fitted a Freundlich type isotherm, with the equation parameters reflecting changes in bonding affinity corresponding to pH changes. The soils sorbed >75% of the added Sb in all trials, and 80-100% at pH values less than approximately 6.5. The Fe(OH)3 retained >95% of the added Sb in all experiments. The humic acid sorbed up to 60% of the added Sb at acidic pH values, but sorption decreased to zero at higher pH values. Further adsorption studies are recommended, such as examining the effects of ion competition and changes in ionic strength.     

Aerosol chemical characteristics of an island site in the Bay of Bengal (Bhola-Bangladesh)

Aerosol constituents (elemental carbon, organic carbon, soluble ions including organic acids, and selected trace metals) were investigated from samples of a field campaign taking place at Bhola Island in the Bay of Bengal (Bangladesh). The campaign took place in the pre-monsoon season (May 2001) using low volume samplers. Carbonaceous material comprised the majority of the analysed components. The average concentrations of EC and OC were 2.8 and 4.6 microg m(-3), respectively. Oxalic acid was the most abundant dicarboxylic acid (average 268 ng m(-3)) followed by malonic and malic acid. The contribution of carboxylic acids-carbon to organic carbon was 2.0%. Average concentrations observed for sulfate and nitrate were 3.7 microg m(-3) and 1.5 microg m(-3). Two different types of aerosol were identified at the rural background site on Bhola Island during southerly synoptic flow by means of trajectory analysis: air masses were transported from the Bay of Bengal to the sampling site in all cases. However, during "Period 1" they experienced longer residence times over the Indian Ocean, while the "Period 2" trajectories came along the Indian coast or passed over the Indian continent. During Period 1 the concentration levels of soluble ions were a factor of 4-6 lower than during Period 2. The concentrations of EC, OC and K differed less than a factor of 1.5 between the two periods. The Period 1 aerosol showed similarities to the haze layers observed during winter-monsoon conditions south of India during the INDOEX experiment. Based on EC/TC and K/EC ratios we find that around 80% of the carbonaceous aerosol from Period 1 in Bhola is from fossil fuel and only around 50% from Period 2. Absolute concentrations of carbonaceous species, soluble ions and trace metals indicate that the background site on Bhola Island is affected by emissions from urbanized regions of Southeast Asia.