Distribution of volatile organic compounds around a polluted river

The objectives of this study were to investigate the species and the concentration distribution of volatile organic compounds around a heavily polluted river. Air samples were collected seasonally at different locations near the polluted river. Samples were then analyzed by gas chromatography (electron capture detector for chlorinated organic compounds and flame ionization detector for ordinary hydrocarbons). The data was then analyzed by the statistical product and service solutions software. The results showed that total of 26 species of volatile organic compounds were identified. Each individual had its own concentration distribution pattern at different seasons and aliphatic volatile organic compounds displayed much higher concentrations than most benzenoic volatile organic compounds. In aliphatic volatile organic compounds, 1,2-dibromo-3-chloropropane, hexachlorobutadiene and 1,2-dibromoetane had much higher concentrations at the nearby environment of the river and they have been claimed to be carcinogenic to some experimental animals and possibly to human. Therefore, It is in doubt that for a long term, the volatile organic compounds evaporating out of the stream may threat the health of the residents living very close to the river. The concentrations of tetrachloroethene, 1,1,2,2-tetrachloroethane, hexachlorobutadiene, dibromoetane, dichlorobenzene and sec-butylbenzene appeared at the nearby environment of the river had significant correlations (P < 0.05) with those of each other or many other volatile organic compounds.     

Geochemistry of volatile organic compounds in seawater: Mesocosm experiments with 14C-model compounds

A series of ten radiotracer experiments were conducted in controlled experimental ecosystems (mesocosms) to investigate the behavior of volatile organic compounds (VOC) in seawater. Time-series measurements of the redistribution of ¹⁴C-activity within several major pools—dissolved, particulate, intermediate metabolite, and CO₂—in the ecosystem made possible an evaluation of the rates of processes—volatilization, biodegradation, Sorption and sedimentation—acting to remove VOC from seawater in summer. The behavior of the model ¹⁴C-VOC fell into three categories. Aromatic hydrocarbons (benzene, toluene, naphthalene) were subject to both volatilization and biodegradation, with mineralization dominating in summer. Chlorinated C₂-hydrocarbons (tetrachloroethylene) and chlorinated benzenes (chlorobenzene, 1,4-dichlorobenzene, and 1,2,4-trichlorobenzene) were affected only by volatilization and were relatively resistant to biodegradation. Of all the model VOC studied, only aliphatic hydrocarbons (decane and octadecane) were sorbed onto suspended paniculate matter; however, the primary route of loss from the water column appeared to be biodegradation rather than sedimentation. The mesocosm-derived removal rate constants were then applied to estimate summer VOC residence times in Narragansett Bay, Rhode Island of about 1 day for aromatic hydrocarbons, 1 week for the chlorinated VOC and about 1 day for aliphatic hydrocarbons. Residence times in winter might be on the order of 1 week for all VOC.     

水资源中氯代烃污染物的去除方法

随着工业化的发展。氯代有机溶剂使用越来越广泛。并且难于去除。在20世纪90年代初期，人们就已认识到用Fe^0恢复污染的地下水的潜力。国外正在研究帮使用扔几种还原挥发性氯代烃的还原反应介质，尤其要提高的是双金属反应系统，反应速度快，而且脱Cl中国难解产物少，目前国也只停留在实验室研究阶段，个别做了地上反应器的验证实验，它的脱Cl机理、介质钝化和完全脱Cl问题还有待于进一步研究。     

Modeling of packed absorption tower for volatile organic compounds emission control

Development of chemical industry and high vapor pressure of volatile organic compounds (VOCs) have been caused that these materials recently be considered as a source of air pollution. These are different methods for separation of VOC from air that absorption by suitable and selective solvent is an efficient method. In this research, mathematical modeling of a packed absorption tower for separation of VOCs from air has been presented. Then, acetone vapors separation in this tower and with Intalox saddle packing has been investigated. Concentration of acetone in inlet air stream was 1.5 mol % which has reduced to 150 ppm (0.015 mol %) in effluent air stream. The results show that the packed absorption tower with this type of packing can separate 99% of acetone vapors. Comparison of the results obtained by Intalox saddle packing with the results obtained by another type of packing (with trade mark of Kerapak patented by Sulzer Company) shows that the tower gives the same efficiency for acetone separation. Thus, the efficiency of absorption process, mainly, depends on solvent type, composition of VOC in feed air, desired composition of VOC in outlet air (or percentage of VOC separation) and pressure drop.     

某石油化工场地土层挥发性有机物的污染特征

在调查华北平原一个污染年限超过35年的石油化工场地时,采用便携式仪器土层测气方法,快速、准确地测定了场地内40多个钻孔不同深度土层中挥发性有机物(VOCs)的浓度。基于对场地地质水文地质条件的认识,以及通过对大量数据的分析对比和应用空间变异分析方法,得出了对场地土层介质中VOCs污染特征的如下认识:(1)土层VOCs浓度的垂向变化可概括为污染源淋滤型、包气带扩散污染型、地下水波动带污染型和混合污染型四种污染类型;(2)在包气带砂土层和粉土层中,VOCs的扩散规律可近似用指数模型描述;(3)包气带土层中VOCs优先积聚在渗透性强的砂性土层中,砂土层中VOCs浓度是粉土层中VOCs浓度的1.5～12倍,平均3.76倍;(4)土层VOCs浓度的水平变异性表现为包气带土层的变异性要比地下水波动带土层大,且水平变异性能在25m尺度内得到充分显示;而土层VOCs浓度的垂向变异性随地而异,变化复杂,很难用统一的一个量化尺度来表征。本文对这一典型污染场地的剖析,有助于从事污染场地调查人员认识我国华北平原石油化工类场地的污染特征,并为调查与治理类似污染场地提供技术依据。     

岩溶地区垃圾渗透液中36种挥发性有机物的测定

应用吹扫捕集-气相色谱-质谱法测定岩溶地区垃圾渗透液中36种挥发性有机物（VOCs）的含量。获取样品溶液5 mL于吹扫瓶中,利用TELEDYNE TEKMAR型吹扫捕集直接进样,经DB-VRX毛细管色谱柱分离、电子轰击电离（EI）全扫描检测,选择特征离子,再用外标法进行定量测定。结果表明:36种挥发性有机物的质量浓度在1～100 μg·L-1 范围内,与其峰面积呈线性关系,方法检出限在0.03～0.27 μg·L-1 之间,加标回收率在88%～110%之间,相对标准偏差（n=7）在2.32%～6.51%之间。      

Occurrence of selected volatile organic compounds in a bra cup manufacturing facility

This article presents a review of the types and levels of volatile organic compounds (VOC) detected in a bra cup manufacturing facility (considering the past 4 years) while conducting a human health risk assessment to selected VOCs. Most of the tested VOCs were undetected, except in the flocking section in 2014. However, from time to time dichloromethane and toluene were detected in the facility. Dichloromethane levels showed an increase with time in the laminating section (except during 2014) with drastically higher levels in 2015. SWIFT VS1 6016/5A (an adhesive) as per the material safety data sheet (MSDS) was the dichloromethane source. However, none of the MSDS revealed the occurrence of carcinogenic benzene (which was detected in 2014 in the flocking section) and 1,4-dichlorobenzene (which was detected in 2013 in the laminating and injection molding sections) and non-carcinogenic toluene indicating that MSDS do not accurately provide the identity of chemicals. Hazard Indices (HI) for non-carcinogenic VOCs and the total lifetime cancer risks (LCRs) and occupational exposure indices (E _i ) for carcinogenic VOCs varied during the different time periods. Toluene in many cases accounted for 100 % of the HI. LCRs and E _i of dichloromethane accounted for 100 % of the total LCR and total E _i , respectively (except in the flocking section in 2014). LCR and E _i of the individual VOCs (even the total LCR and E _i values) were simultaneously high whenever the levels of the individual VOCs had exceeded the regulatory limits posing a health risk. Some measures needed to prevent exposure to VOCs are discussed in this article.     

Modeling of air stripping from volatile organic compounds in biological treatment processes

The removal of volatile organic compounds from biological treatment processes occurs through several mechanisms. These include biodegradation, adsorption onto solids, and air stripping or volatilization to the atmosphere. Volatilization results in fugitive emissions to the atmosphere, which is largely uncontrolled. Recent regulations have called for increased evaluation and control of inadvertent volatile organic compounds emissions from treatment processes. The use oxygen as a parallel volatile compound is extremely useful for prediction of volatile organic compounds removal by air stripping. In this study, the simultaneous biodegradation and air stripping of volatile organic compounds, based on steady state mass balance are examined and a general approach to estimating the dominant removal mechanism is developed. A Monte Carlo simulation technique was used to estimate air stripping over a wide range of operating conditions. Several volatile organic compounds were selected for this study. The results showed the values drived from the model correspond with the experimental data for benzene, toluene, methylene chloride, trichloroethylene, and methyl isobutyl ketone.     

Detection of manure-derived organic compounds in rivers draining agricultural areas of intensive manure spreading

It is essential to have suitable tools able to trace the fate of manure organic matter in the environment to assess whether manure disposal on the soils of catchments could affect the organic quality of rivers. Sterol compounds – mainly expressed as C_29 + 28/C₂₇ and 5β/C₂₇ ratios – have been shown to be specific molecular tracers of pig, dairy and poultry manures in soils. The objective of this study was to measure C_29 + 28/C₂₇ and 5β/C₂₇ ratios in five Brittany rivers (Elorn, Yar, Léguer, Min Ran and Couesnon) draining agricultural catchments receiving massive annual inputs of pig, poultry and dairy manures and compare these ratios with ratios published for enriched soils and manure samples. The particulate organic fractions from the studied rivers yielded steroid signatures typical of animal manures. More specifically, a stanol compound diagnostic of pig slurry – the 5β-stanol known as coprostanol – was found to be very widespread, with particularly high concentrations in one of the rivers (Elorn). The C_29 + 28/C₂₇ and 5β/C₂₇ ratios of the particulate fractions of the rivers were compared with ratios measured directly in pig, dairy and poultry manure samples, as well as with the breeding activities on river catchments. These comparisons show that the steroid profiles of the five investigated rivers correlate closely with the types of manure (i.e. pig, poultry or dairy) spread on soils in their catchments. For instance, the C_29 + 28/C₂₇ and 5β/C₂₇ ratios in the Elorn river are similar to the values typical of pig slurry (e.g. 5β/C₂₇ > 4); compared with other catchments, the soils in this area receive by far the largest amount of pig slurry. By contrast, the Yar river drains a catchment receiving only poultry and dairy manures, and its soils exhibit C_29 + 28/C₂₇ and 5β/C₂₇ ratios similar to those of dairy and poultry manures (e.g. 5β/C₂₇ ∼ 1). Thus, this study indicates that the organic quality of rivers is modified in catchments where there is intense manure spreading on soils. It also provides evidence that rivers draining areas receiving different manure types may exhibit differences in the long-term evolution of their OM content. Indeed, two of the investigated river catchments receive dominantly dairy and poultry manure, and exhibit clear long-term upward trends in OM. On the other hand, one catchment receiving high proportions of pig slurry clearly shows a long-term downward trend in OM contents. A survey of the literature shows that the relative amount of OM and N received by soils in agricultural catchments could be the key parameter in determining the direction of the long-term OM trend of the river, rather than the absolute amount and/or type of manure that is applied to the soil. In any case, the present study suggests that sterol/stanol compounds may be of diagnostic value in determining whether a stream or a river is undergoing contamination by manure-derived organic matter.     

The influence of a heavily polluted urban river on the adjacent aquifer systems

 Ankara Creek is often subjected to overflowing of sewage caused by rainfall or direct discharge of raw sewage. Alluvial aquifers adjacent to Ankara Creek and its tributaries have considerable groundwater potential. The present status of groundwater quality is far from drinking water standards. Groundwater contamination in Ankara is suspected to be caused by Ankara Creek which is heavily polluted by raw sewage discharge, surface runoff and other common sources. In order to investigate the influence of heavily polluted Ankara Creek on the groundwater contamination in the adjacent alluvial aquifers, five sampling stations on Ankara Creek and 25 water wells were monitored during 1996. At five different sampling periods, water samples were collected from both surface water and groundwater. Chemical analyses of basic ions, pollution parameters and heavy metals in natural waters were carried out. The organic pollution prevails in Ankara Creek whereas total dissolved solids (TDS) and heavy metal concentrations are considerably low. Starting from the idea that Ankara Creek somewhat influences the groundwater quality and the contaminants in groundwater should attenuate with respect to distance, a series of water wells in a certain area, each having different distance from the creek, were examined using four pollution parameters. It is concluded that Ankara Creek barely influences the aquifer systems in connection. This is attributed to two reasons: rapid attenuation of contaminants due to dilution in groundwater and a blanket of very fine sized materials covering the bottom of Ankara Creek. Received: 28. April 1997 · Accepted: 23. February 1998     

Enhanced CE-QUAL-W2 model to predict the fate and transport of volatile organic compounds in water body: Gheshlagh reservoir as case study

Intentional and/or accidental volatile organic compound (VOC) spill into water bodies may lead to severe contamination and health problems in water infrastructures. The importance and widespread use of petroleum products and the threats posed by these products on surface water resources in Iran necessitates the access to numerical hydrodynamic and water quality simulation models with appropriate capabilities. Simulation the fate and transport of VOC in both flowing and standing water bodies is a fairly complex problem. In this research, CE-QUAL-W2 model is modified to simulate the fate and transport of VOC [i.e., Methyl tert-butyl ether (MTBE), benzene] in standing and flowing water bodies. The performance of the modified CE-QUAL-W2 model is evaluated in a MTBE pollution spill at Khalife-Tarkhan river along the headwaters of Gheshlagh reservoir, Kordestan, Iran. The results show the modified CE-QUAL-W2 model’s capability to depict the spatial and temporal variation of MTBE in comparison with recorded data from MTBE spill event of Gheshlagh reservoir. Based on the simulation results of modified CE-QUAL-W2 model, reservoir cleanup time in different meteorological and hydrological scenarios is evaluated. The results show Gheshlagh reservoir cleanup time reduced in scenarios that included air temperature reduction, wind speed increasing, and high inflow condition.     

Aromatic volatile organic compounds and their role in ground-level ozone formation in Russia

This paper reports proton mass spectrometry data on aromatic volatile organic compounds (VOCs) (benzene, toluene, phenol, styrene, xylene, and propylbenzene) obtained in different Russian regions along the Trans-Siberian Railway from Moscow to Vladivostok, based on expedition data retrieved using the TRO-ICA-12 mobile laboratory in the summer of 2008. The contribution of aromatic VOCs to ozone formation in the cities and regions along the measurement route has been estimated quantitatively. The greatest contribution of aromatic VOCs to ozone formation is characteristic of large cities along the Trans-Siberian Railway (up to 7.5 ppbv O₃) specified by the highest concentrations of aromatic VOCs (1–1.7 ppbv) and nitrogen oxides (>20 ppbv). The results obtained are indicative of a considerable contribution (30–50%) of anthropogenic emissions of VOCs to photochemical ozone generation in the large cities along the Trans-Siberian Railway in hot and dry weather against the background of a powerful natural factor such as isoprene emissions controlling the regional balance of ground-level ozone in warm seasons.

     

某石油化工污染场地地下水中挥发性有机物污染特征及成因分析

为了解典型污染场地浅层地下水微量有机污染特征,对西北某省会城市石油化工场地地下水中的挥发性有机污染物（VOCs）污染情况进行了调查。结果表明,污染场地地下水样品中挥发性有机污染物检出率为100%;检出率较高的是氯代烃和苯系物,检出率分别为60%和40%。超标组分为苯和1,2-二氯丙烷,苯超标率为30%,1,2-二氯丙烷超标率10%,苯最大检出浓度达1515μg/L。场地内的原油储存罐、污水隔油池的渗漏以及石油冶炼、机械加工过程工业废水不合理排放均为该场地地下水VOCs的重要来源;VOCs的理化性质以及污染场地地下水防污性能差是影响该场地地下水环境中VOCs归宿的主要因素。     

Volatile organic compounds in open ocean and coastal surface waters

Volatile organic compounds with volatilities ranging between those of n-hexane and n-pentadecane were identified in open ocean and coastal marine surface water samples taken in the north central part of the Gulf of Mexico. Approximately 40 organic compounds were found. The types and concentrations of the compounds found depended upon the extent of anthropogenic and terrestrial influences. Open ocean samples consisted mostly of aromatic hydrocarbons, whereas coastal samples included alkanes, cycloalkanes, cycloalkenes, aromatic hydrocarbons, aldehydes and chlorinated hydrocarbons. Unpolluted open ocean and coastal water samples had individual concentrations rarely exceeding 5 ng/kg; some aromatic hydrocarbons approached 15 ng/kg. n-Pentadecane dominated the hydrocarbons in these samples (50–100 ng/kg). The most polluted coastal water samples had individual volatile organic concentrations as great as 150 ng/kg with total concentrations approaching 1000 ng/kg. The terpene, limonene, was found extensively in the coastal samples (up to 40 ng/kg). Photooxidization of hydrocarbons in industrial/urban atmospheres was considered as a possible source of aldehydes present in coastal water. The dynamic headspace stripping/Tenax-GC adsorption method coupled with packed column gas chromatography, and gas chromatography-mass spectrometry were used for volatile organic analysis.     

Development of low-cost passive sampler from cow bone char for sampling of volatile organic compounds

A simple and low-cost passive sampler for collection of volatile organic compounds, specifically benzene, toluene, ethylbenzene and xylene (BTEX), from the ambient air has been developed by using cow bone char (CBC) as an adsorbent with desorption by solvent extraction prior to analysis by gas chromatography–mass spectrometry (GC–MS). The laboratory-made CBC was prepared by calcination process in a partially oxidative atmosphere. The developed passive sampler was tested for a suitable amount of CBC used, diffusion tube type and size, and sampling duration, in a closed chamber saturated with each of the BTEX vapors. With the optimum amount of 250 mg CBC packed in a glass bottle (82.6 mm height × 11.1 mm i.d.) and the exposure time of 168 h, detection limits (µg/m³) for BTEX determination using this developed sampler together with GC–MS were 0.28 (benzene), 0.79 (toluene), 0.58 (ethylbenzene), 0.28 (p-xylene) and 0.54 (o-xylene). The proposed method was applied to sampling BTEX from selected petrol stations, traffic congestion areas and a rural area in Chiang Mai Province, Thailand. The BTEX concentrations detected were well correlated with their sources as they were the highest at the petrol station sites, lower at the traffic congestion area sites and the lowest at the rural area site. The laboratory-made passive sampler containing CBC has thus opened up a possibility of having a simple and effective device for sampling of BTEX in the ambient air.     

岩溶区地表水体惰性有机碳研究

岩溶作用所产生的岩溶碳汇对全球碳循环有着重要的影响。岩溶水生生物通过CO₂富集机制（CCM）固定岩溶水中的HCO₃^-,将其转化为有机碳。惰性有机碳（RDOC）为水生生物和微生物不能利用和降解的溶解性有机碳。RDOC长时间滞留水体,形成稳定碳汇。多次培养实验发现可以用原位微生物法对岩溶区地表水中的RDOC进行检测。以桂林漓江为对象,研究由外源水补给并流经岩溶峰林平原区的岩溶地表水中的RDOC及其相关因子,结果显示：1）漓江水中Ca²⁺,HCO₃^-浓度从上游到下游逐渐升高,表明外源水进入岩溶区,发生了岩溶作用。漓江水的C/N为6.29~10.50,表明水中有机碳的来源为外源水和水生生物作用。受岩溶作用和水生生物光合作用双重影响,δ¹³C-DIC值从上游到下游逐渐偏正,水生生物优先利用无机碳中的¹²C使得δ¹³C-POC从上游到下游逐渐偏负。C/N与δ¹³C-DIC、δ¹³C-POC的变化以及相关性体现了岩溶地表水体中无机环境和有机环境相关联;2）岩溶区地表水中检测出RDOC且浓度远大于非岩溶区,RDOC浓度的时空变化与水生生物利用岩溶作用所产生的HCO₃^-有关。漓江地表水中DOC、BDOC、RDOC浓度与HCO₃^-浓度变化趋势一致,从上游到下游逐渐升高,下游L6（岩溶区）RDOC浓度为上游L1（非岩溶区）的3倍,在季节上表现出秋季>冬季>夏季>春季,RDOC的含量平均占水体中DOC含量的78%左右,体现了岩溶作用强度和水生生物活动对岩溶地表水中RDOC的影响;3）结合流量数据计算RDOC通量：桂林水文站RDOC的通量为0.75×10⁷ kg/a,阳朔水文站的RDOC通量为1.3×10⁷ kg/a,是桂林水文站断面的1.7倍。

     

潍河流域下游地表污水对地下水水质影响的状态分析

为了准确地建立莱洲湾南岸地区虞河段地表水与地下水污染质运移的数学模型,本文对研究区地下水及地表水污染特征及其污染现状进行了调查、分析,为地下水资源的合理利用开发提供了依据。     

Exploration for concealed orebodies by the analysis of volatile organic compounds contained in surface rocks: Trèves Zn-Pb deposit (Gard, France)

A previous study (Disnar et al., 1986a) indicated significant volatile hydrocarbon compounds (nC₁ to C₅) in mineralized carbonate rocks of the Trèves Pb-Zn deposit (Gard Dept., France) as well as an accumulation of methane, ethylene and ethane in the hanging wall of the deposit. The present study analyzed rock samples taken from outcrops vertically above and at a distance from the deposit and identified three anomalous zones indicating the presence of concealed mineralization. The first zone is due to methane (radius about 3 km), the second, to alkenes (about 2 km) and the third, to alkanes, higher homologues of methane (about 1 km). These anomalies are interpreted as resulting from migration of these compounds through the sedimentary cover from the deposit where they could have been generated during mineralizing events, or during subsequent diagenesis. Their specific signature with regard to that given by samples taken at a distance from the orebodies can be attributed to the hydrothermal and biological processes responsible for the deposition of the ore.     

Comparison of volatile organic compounds in stormwater and groundwater in Seoul metropolitan city,South Korea

Volatile organic compounds (VOCs) detected in stormwater were compared with VOCs present in emission sources, air, groundwater, and influent to sewage treatment plants in Seoul to understand their fate and transport in the urban hydrological system. Stormwater is a carrier of non-point source pollutants and contains VOCs from land surfaces and air. Samples of stormwater and influent to sewage treatment plants were collected and analyzed for 61 VOCs, while the VOCs in emission sources, air and groundwater were investigated through literature reviews for comparison. The results showed that the most frequently detected VOCs in stormwater were similar to those in air. However, the atmospheric concentrations of benzene, toluene, ethylbenzene, and xylenes (BTEX), and methyl tertiary-butyl ether (MTBE) were too low to explain their frequent detection and high concentrations in stormwater. As a result, land surfaces seem to be a primary source of these VOCs in stormwater. Comparison of the VOCs in stormwater and groundwater showed that toluene and MTBE were frequently detected in both media, but more often and at higher concentrations in stormwater. This finding indicates that stormwater recharge is a source of toluene and MTBE in groundwater. Regarding groundwater, land surfaces seem to be a primary source of toluene, while urban air is the primary source in the case of MTBE. Specifically, the MTBE values in air were sufficiently high to explain its levels in groundwater, which had continually increased and remained low afterward. Furthermore, the high ratios of TEX (toluene, ethylbenzene, and xylenes) to benzene and MTBE in stormwater indicated that TEX had additional sources other than vehicles, most likely hydrocarbon solvents. These solvents seem to be a primary source of TEX and other frequently detected VOCs in stormwater. However, trichloroethylene (TCE), tetrachloroethylene (PCE) and their dechlorination intermediates were far more frequently detected and at higher concentrations in groundwater than in stormwater. Additionally, their concentrations frequently exceeded the water-quality criteria. It seems that halogenated solvents had produced contamination plumes of these chlorinated VOCs in the Seoul aquifer. Based on VOCs detected in Seoul, stormwater was mixed with groundwater in combined sewers and flowed into sewage treatment plants. The results imply that organic solvents should be handled with extreme care to protect groundwater quality.     

Biofilms on the surface of gravels and aquatic plants in rivers and lakes with reusing reclaimed water

Reuse of reclaimed water for the eco-environmental water has become an effective measure to resolve the urban water crisis. However, it still contains large amounts of contaminants which may significantly affect the aquatic ecosystems. Biofilm attached on the surface of multiple matrixes in rivers and lakes is one of the indicators for describing the health of aquatic ecosystem. In this article, we chose eight rivers and lakes as the sampling locations, including three kinds of reclaimed water with different treatment processes and natural water. The morphology, structure and component characteristics of biofilms attached on the surface of aquatic plants and gravels in eight water bodies were evaluated. The results showed that the biofilm on the matrix surface were typical porous media with basic skeleton composed of inorganic particles, microorganisms and algae. The pores were filled with the viscous extracellular polymeric substances (EPS) secreted by microorganisms. The biofilms contained calcite, quartz, illite, alkali feldspar, dolomite, clinochlore, goethite and inorganic salt, and approximately 50 % of these compositions are calcite and quartz. The concentration of EPS was 20.78–500.44 μg/mL, and that of the gravel biofilms was less than that in aquatic plants by 18.1–75.3 %. In these three reclaimed waters, 4–7 kinds of PLFA (phospholipid fatty acid) were detected in aquatic plants biofilms, more than one or two kinds than in gravel biofilms. And the dominant PLFA were i15:0 and 18:0, the total contents of which were, respectively, 74.4, 62.9 and 85.9 % in the three kinds of reclaimed water. All biofilm samples contain major microorganisms such as Pseudomonas, Acinetobacter and Comamonas. This study is aimed to provide some support for assessing the health of river–lake ecosystem with biofilm indicator.