Calibration and field performance of membrane-enclosed sorptive coating for integrative passive sampling of persistent organic pollutants in water

Membrane-enclosed sorptive coating (MESCO) is a miniaturised monitoring device that enables integrative passive sampling of persistent, hydrophobic organic pollutants in water. The system combines the passive sampling with solventless preconcentration of organic pollutants from water and subsequent desorption of analytes on-line into a chromatographic system. Exchange kinetics of chemicals between water and MESCO was studied at different flow rates of water, in order to characterize the effect of variable environmental conditions on the sampler performance, and to identify a method for in situ correction of the laboratory-derived calibration data. It was found that the desorption of chemicals from MESCO into water is isotropic to the absorption of the analytes onto the sampler under the same exposure conditions. This allows for the in situ calibration of the uptake of pollutants using elimination kinetics of performance reference compounds and more accurate estimates of target analyte concentrations. A field study was conducted to test the sampler performance alongside spot sampling. A good agreement of contaminant patterns and water concentrations was obtained by the two sampling techniques.     

Calibration of the Chemcatcher passive sampler for the monitoring of priority organic pollutants in water

An integrative passive sampler consisting of a C18 Empore disk receiving phase saturated with n-octanol and fitted with low-density polyethylene diffusion membrane was calibrated for the measurement of time-weighted average concentrations of hydrophobic micropollutants, including polyaromatic hydrocarbons and organochlorine pesticides, in water. The effect of temperature and water turbulence on kinetic and thermodynamic parameters characterising the exchange of analytes between the sampler and water was studied in a flow-through system under controlled conditions. It was found that the absorption of test analytes from water to the sampler is related to their desorption to water. This allows for the in situ calibration of the uptake of pollutants using offload kinetics of performance reference compounds. The sampling kinetics are dependent on temperature, and for most of the tested analytes also on the flow velocity. Sampler-water partition coefficients did not significantly change with temperature.     

Partitioning of selected environmental pollutants into organic matter as determined by solid-phase microextraction

Partitioning/sorption of selected environmental pollutants (PCBs, organochlorine insecticides, triazine and amide herbicides) into dissolved humic acids (HA), soil and mineral substances was evaluated by measuring their free concentrations by solid-phase microextraction (SPME). Compounds were chosen to cover a wide range of logK(ow) (2.2-7.6). Two different types of partitioning behaviour for dissolved HA were observed. Compounds with logK(ow)>5 partitioned almost instantly into HA fraction and the remaining free fraction remained rather constant. LogK(HA) and logK(DOC) were calculated and found to be similar for commercial HA, HA standard and isolated HA. The behaviour of these compounds in soil suspension was similar, but strong sorption on CaCO3 and Florisil was also noticed. For compounds with logK(ow)<5, we have not noticed significant changes in free concentrations in HA solutions over time. In soil suspension, however, some sorption/partitioning was observed over time for some compounds, but it was matching the sorption on CaCO3 and Florisil.     

声光催化降解水中有机污染物

声光催化是水处理降解有机污染物的一种新技术。在分析中 ,探讨了该技术降解有机污染物的机理 ,以及国内外研究现状 ,包括降解效果和主要的影响因素     

Ranking potential impacts of priority and emerging pollutants in urban wastewater through life cycle impact assessment

Life cycle impact assessment (LCIA), a feature of the Life cycle assessment (LCA) methodology, is used in this work outside the LCA framework, as a means to quantify the potential environmental impacts on ecotoxicity and human toxicity of wastewater containing priority and emerging pollutants. In order to do this, so-called characterisation factors are obtained for 98 frequently detected pollutants, using two characterisation models, EDIP97 and USES-LCA. The applicability of this methodology is shown in a case study in which wastewater influent and effluent samples from a Spanish wastewater treatment plant located in the Mediterranean coast were analysed. Characterisation factors were applied to the average concentration of each pollutant, obtaining impact scores for different scenarios: discharging wastewater to aquatic recipient, and using it for crop irrigation. The results show that treated wastewater involves a substantially lower environmental impact when compared to the influent, and pharmaceuticals and personal care products (PPCPs) are very important contributors to toxicity in this wastewater. Ciprofloxacin, fluoxetine, and nicotine constitute the main PPCPs of concern in this case study, while 2,3,7,8-TCDD, Nickel, and hexachlorobenzene are the priority pollutants with highest contribution. Nevertheless, it must be stressed that the new characterisation factors are based on very limited data, especially with regard to toxicology, and therefore they must be seen as a first screening to be improved in the future when more and higher quality data is available.     

水中有机污染物电化学清除的研究进展

介绍利用直接电解发、间接电解和电化学吸附等方法去除水中有机污染物的研究现状,并指出今后的工作方面。     

电化学催化降解水中有机污染物的研究进展

电化学法催化降解废水中的有机污染物已引起广泛兴趣。在电极的作用下 ,电化学反应和化学催化作用结合 ,可导致有机分子的电催化降解。选用合适的电极材料可以加速电化学反应速率 ,有助于有机物的电化学转化。本文讨论了提高电催化降解速率的方法 ,指出了在该领域的研究中存在的问题和发展方向     

Analysis of marine sediment, water and biota for selected organic pollutants

The concentrations of various organic pollutants (benzo(a)pyrene (BaP), hexachlorobenzene (HCB) and pentachlorophenol (PCP)) were determined in samples of water, sediment and biota (flounder, killifish, shrimp, crabs and squid) from San Luis Pass, Texas. Sediment was also analyzed for polychlorinated biphenyls (PCBs), phthalic acid esters (PAEs) and various pesticides. Only PCP was detectable in water. In sediment, the relative concentrations were PAEs > BaP > (PCBs HCB) > PCP. In biota, BaP was not detectable in any animal; HCB was highest in crabs and PCP was highest in all others (flounder, killifish, shrimp and squid). The relative concentrations of HCB and PCP were different in the different organisms. The differences between the relative concentrations in the biota and in sediment are discussed. The results of this study are compared to values measured at other sites. This study is part of a larger effort to identify and quantitate pollutants in various Texas estuaries and to serve as a basis for monitoring marine pollution.     

2种再生水深度处理工艺对有毒有机污染物去除效果的评价研究

采用固相萃取(SPE)技术和气相色谱/质谱联用(GC/MS)的方法对2个再生水厂的进水和不同深度处理工艺出水中的有毒有机污染物进行了定性和定量分析,讨论了这2种不同再生水深度处理工艺对有毒有机污染物的去除效果.结果表明,厌氧/缺氧/好氧(A2/O)+连续微滤技术(CMF)+加氯消毒处理工艺和水解酸化+膜生物反应器(MB...     

Matrix effect on the performance of headspace solid phase microextraction method for the analysis of target volatile organic compounds (VOCs) in environmental samples

Solid phase microextraction (SPME) is a fast, cheap and solvent free methodology widely used for environmental analysis. A SPME methodology has been optimized for the analysis of VOCs in a range of matrices covering different soils of varying textures, organic matrices from manures and composts from different origins, and biochars. The performance of the technique was compared for the different matrices spiked with a multicomponent VOC mixture, selected to cover different VOC groups of environmental relevance (ketone, terpene, alcohol, aliphatic hydrocarbons and alkylbenzenes). VOC recovery was dependent on the nature itself of the VOC and the matrix characteristics. The SPME analysis of non-polar compounds, such as alkylbenzenes, terpenes and aliphatic hydrocarbons, was markedly affected by the type of matrix as a consequence of the competition for the adsorption sites in the SPME fiber. These non-polar compounds were strongly retained in the biochar surfaces limiting the use of SPME for this type of matrices. However, this adsorption capacity was not evident when biochar had undergone a weathering/aging process through composting. Polar compounds (alcohol and ketone) showed a similar behavior in all matrices, as a consequence of the hydrophilic characteristics, affected by water content in the matrix. SPME showed a good performance for soils and organic matrices especially for non-polar compounds, achieving a limit of detection (LD) and limit of quantification (LQ) of 0.02 and 0.03 ng g⁻¹ for non-polar compounds and poor extraction for more hydrophilic and polar compounds (LD and LQ higher 310 and 490 ng g⁻¹). The characteristics of the matrix, especially pH and organic matter, had a marked impact on SPME, due to the competition of the analytes for active sites in the fiber, but VOC biodegradation should not be discarded in matrices with active microbial biomass.     

自然水体中主要有毒有机物的研究进展

介绍了主要有毒有机物多环芳烃(PAHs)、多氯联苯(PCBs)、有机氯农药(OCPs)在环境中的危害及其来源,着重评述了近年来中国自然水体中和沉积物中该类污染物的研究进展,指出新的检测技术的开发、有毒有机物的生殖毒性和生态环境风险影响方法学的研究及污染区域污染控制、消减及修复是今后该领域的工作重点.     

Behavior of selected priority organic pollutants in horizontal subsurface flow constructed wetlands: a preliminary screening

A discrete injection experiment was carried out in a constructed wetland to evaluate the behavior of selected priority pollutants. A horizontal subsurface flow pilot plant located in the NE of Spain was selected for this study. A total of eight European Priority Pollutants listed in the Water Framework Directive were considered, including a commonly used herbicide (mecoprop). The pollutants encompassed a variety of chemical classes and physicochemical properties. They included organochlorine, organophosphorus, phenols, chloroacetanilides, triazine, phenoxycarboxylic acid and phenylurea pesticides. A time series of composite effluent samples and discrete gravel bed samples from the wetland were analyzed. Response curves for all the pollutants injected from effluent concentrations were obtained and compared with the tracer (clofibric acid). On the basis of an analysis of the samples taken 21 days after the injection, priority pollutants were classified into four groups according to their removal efficiency. These groups were (i) the highly efficiently removed (>90%), namely lindane, pentachlorophenol, endosulfan and pentachlorobenzene; (ii) the efficiently removed (80-90%), namely alachlor and chlorpyriphos; (iii) poorly removed (20%), namely mecoprop and simazine; and (iv) recalcitrant to elimination, namely clofibric acid and diuron. Taking into account the poor accumulation of the injected contaminants in the gravel bed (0-20%), biodegradation and plant uptake are postulated as the most likely elimination pathways for the pollutants.     

Semiconductor-mediated photocatalysed degradation of two selected priority organic pollutants,benzidine and 1,2-diphenylhydrazine,in aqueous suspension

The photocatalysed degradation of two selected priority organic pollutants, namely benzidine (1) and 1,2-diphenylhydrazine (DPH, 2) has been investigated in aqueous suspensions of titanium dioxide (TiO2) under a variety of conditions employing a pH-stat technique. The degradation was studied by monitoring the change in substrate concentration of the model compound employing HPLC analysis and the decrease in total organic carbon content, respectively, as a function of irradiation time. The degradation kinetics were studied under different conditions such as reaction pH, substrate and photocatalyst concentration, type of TiO2 photocatalyst and the presence of alternative additives such as H2O2, KBrO3 and (NH4)2S2O8 besides molecular oxygen. The degradation rates and the photonic efficiencies were found to be strongly influenced by the above parameters. Toxicity tests for the irradiated samples of benzidine measuring the luminescence of bacteria Vibrio fischeri after 30 min of incubation were also performed. 4-amino-biphenyl (7) and hydroquinone (13) were identified as intermediate products by GC/MS technique and probable pathways for the formation of the products are proposed.     

Assessment of persistent organic pollutants in sediments from Lower Mekong River Basin

Organochlorine compounds (OCs) in sediments collected from various locations in Lower Mekong River Basin (MRB) in Laos and Thailand were examined to elucidate their occurrence, distribution and potential ecological risk. Concentration of PCBs and DDTs were higher than other OCs, ranging from 0.18 to 310 μg kg⁻¹ dry wt. and from 0.027 to 52 μg kg⁻¹ dry wt., respectively, whereas CHLs, HCHs and HCB were 1-3 orders of magnitude lower. Geographical distribution indicates that levels of PCBs, DDTs and CHLs in the Vientiane canal were significantly higher than those in mainstream of Mekong River, Phong River and its surrounding areas, indicating significant sources of these compounds in urbanized areas. Comparison with other parts of MRB indicates that PCBs were higher in Laos, whereas DDTs were more prevalent in Mekong Delta, indicating location specific contaminations of these compounds in MRB. The ratios of DDTs composition indicate possible difference in the historical input of DDT among locations in and around Mekong River. Hazard assessment of PCBs and DDTs indicate possible toxic potential particularly in areas close to point sources such as intensive human activities and agricultural areas which highlight the need for further study.     

混凝技术去除水中新兴污染物的研究进展

常规水处理工艺通常不能完全将水中新兴污染物(ECs)去除,残留的污染物仍然具有相当大的环境风险,如何有效地去除水中痕量新兴污染物是一个亟待解决的难题。本文概述了新兴污染物的来源、种类和危害,并分析了混凝工艺去除新兴污染物的可行性,重点介绍了新兴污染物性质、混凝剂种类和投加量、pH和水中溶解性物质对混凝效果的影响机制,并介绍了混凝与氧化、膜过滤及吸附等工艺的组合集成技术。在此基础上,对未来混凝技术去除新兴污染物的研究方向和发展趋势进行了展望。     

Estimation of octanol/water partition coefficients for organic pollutants using reverse-phase HPLC

Octanol/water partition coefficients (K_ow's) of organic solutes are estimated with reasonable accuracy (standard deviation ± 0.25 log K_ow units) by elution from a C-18 column with 75:25 (v/v) MeOH-H₂O, based on results with 37 test compounds. Changes in solute activity coefficients from water to 75% MeOH account for the slope of the log K_ow-log k' plot, where k' is the HPLC capacity factor. The method is used to estimate K_ow's for 25 additional organic compounds, and some disparities between the results and those calculated using group additivity-constitutive factors are noted.     

A biomimetic absorbent for removal of trace level persistent organic pollutants from water

A novel biomimetic absorbent containing the lipid triolein was developed for removing persistent organic pollutants (POPs) from water. The structural characteristics of the absorbent were obtained by SEM and a photoluminescence method. Under optimum preparation conditions, triolein was perfectly embedded in the cellulose acetate (CA) spheres, the absorbent was stable and no triolein leaked into the water. Dieldrin, endrin, aldrin and heptachlor epoxide were effectively removed by the CA--triolein absorbent in laboratory batch experiments. This suggests that CA-triolein absorbent may serve as a good absorbent for those selected POPs. Triolein in the absorbent significantly increased the absorption capacity, and lower residual concentrations of POPs were achieved when compared to the use of cellulose acetate absorbent. The absorption rate for lipophilic pollutants was very fast and exhibited some relationship with the octanol--water partition coefficient of the analyte. The absorption mechanism is discussed in detail.