Speciation of organotins in polyvinyl chloride pipe via X-ray absorption spectroscopy and in leachates using GC-PFPD after derivatisation

Three different polyvinyl chloride (PVC) pipe types were subjected to de-ionized water exposures over the course of at least 180 days. Water exposed to the pipe was analyzed for organotin speciation and concentration. Organotin concentrations were the highest during the first 1-5 days. The species and concentrations of organotins leached varied by pipe type. Data were normalized by surface area in order to compare laboratory results with results from a residential pipe system. For one pipe type, the lowest non-zero concentrations from the laboratory tests overestimated organotin concentrations in solution when compared with water samples from the same pipe type in a residence. For organotin exposure estimates, a range of 0.1 ng m(-2) to 10 ng m(-2) could be used for mature pipes (e.g. in use for 1 year). These estimates should be refined with more field study, however, due to the high variation in organotin species and concentrations leached as a function of pipe type, accuracy within an order of magnitude may be optimal as, in many instances, the type of pipe installed or buried may be unknown. X-ray absorption spectroscopy (XAS) was used to identify organic and inorganic tin species in reference materials and the PVC samples. Monobutyl tin was identified as the primary organotin species in the pipes. Results from the XAS analyses also indicate that the technique shows promise for distinguishing between inorganic tin and organotins. Furthermore, organotins may be distinguished between mono-, di-, and tri-ligand species using XAS.     

The distribution, solid-phase speciation, and desorption/dissolution of As in waste iron-based drinking water treatment residuals

Arsenic concentrations and solid-phase speciation were assessed as a function of depth through Fe-media beds for two commercially available products (Granular Ferric Hydroxide-GFH and Bayoxide E33-E33) from pilot-scale water treatment field tests. These results were compared with data from solution (de-ionized water-DI-H2O) concentrations of As equilibrated with Fe-media in an anoxic environment at 4 degrees C. The materials had a high capacity for As (GFH media 9620 mg kg(-1) As, E33 Media 5246 mg kg(-1)). Arsenic concentrations decreased with bed depth. For E33, X-ray absorption near-edge spectroscopy results showed that As(V) was the dominant solid-phase species. For GFH, As(III) was detected and the proportion (relative to As(V)) of As(III) increased with bed depth. Arsenic concentrations in DI-H2O equilibrated with the media were low (35 microg l(-1)) over a period of 50 d. Arsenic concentrations in the equilibrated solutions also decreased with depth. Results from tests on soluble As speciation show that As in solution is in the form of As(V). Kinetic desorption experiments carried out at different pH values (3, 5, 7, 8, and 9) show that the media exhibit some acid/base neutralization capacity and tend to bind As sufficiently. Concentrations of As in the pH desorption experiments were in the same order of magnitude as the toxicity characteristic leaching procedure extractions (tens of microgl(-1)) except at low pH values. For the GFH media tested at a pH of three, As increases in solution and is mainly associated with colloidal (operationally defined as between 0.1 and 1.0 microm) iron.     

建立我国生态环境标准体系的初步构想

我国的生态环境标准极其薄弱，建立生态环境标准体系是我国生态环境保护的迫切需要。借鉴我国目前针对污染防治的环境标准体系，提出了我国生态环境标准体系的基本框架，以及生态环境标准制订的原则和重点。     

A survey on the temporal and spatial distribution of perchlorate in the Potomac River

Samples of river water and treated drinking water were obtained from eight sites along the Potomac River between western Maryland and Washington DC. Samples were collected each month from October 2007 to September 2008 and analyzed for perchlorate by ion chromatography/mass spectrometry. Data on anions were also collected for seven of the twelve months. Data were analyzed to identify spatial and temporal patterns for the occurrence of perchlorate in the Potomac. Over the year of sampling, the largest monthly increase occurred from June to July, with levels then decreasing from July to September. Samples from the period between December and May had lower perchlorate concentrations, relative to the remainder of the study year. Spatially, higher levels of perchlorate were found at sites located in west-central Maryland, the eastern panhandle of West Virginia, and central northern Virginia, with levels decreasing slightly as the Potomac approaches Washington DC. Within the sampling boundaries, river (untreated) water perchlorate concentrations ranged from 0.03 μg L(-1) to 7.63 μg L(-1), averaged 0.67 ± 0.97 μg L(-1) over the year-long period and had a median value of 0.37 μg L(-1). There was no evidence that any of the existing drinking water treatment technologies at the sampling sites were effective in removing perchlorate. There were no correlations found between the presence of perchlorate and any of the anions or water quality parameters examined in the source water with the exception of a weak positive correlation with water temperature. Results from the summer (June-August) and fall (September-November) months sampled in this study were generally higher than from the winter and spring months (December-May). All but one of the locations had annual average perchlorate levels below 1 μg L(-1); however, 7 of the 8 sites sampled had river water perchlorate detections over 1 μg L(-1) and 5 of the 8 sites had treated water detections over this level.     

生态气象监测评估业务平台的设计与应用

  针对目前生态气象监测轨道业务的特点,结合工作的实际需要,运用C和C++语言建立了生态气象监测评估业务平台。在程序设计中,采用了生成中间交换文件的结构组织,能够对各模块的输出结果进行详尽直观的分析,并提供了等值线色斑图与区域填充等多种图形绘制方式。该系统可处理AVHRR和EOS/MODIS卫星遥感资料,对气象观测报文进行解译、数据分类管理和质量控制,统计计算水体密度指数、湿润指数、植被覆盖指数、土地退化指数、灾害指数和生态质量综合评价指标,以图形、图像的形式输出生态气象监测评估产品,实现了卫星遥感与生态气象地面监测数据的有效组织和智能化管理。将系统应用于湖南省生态质量气象评价,业务化运行的结果表明,该系统具有较好的业务实用性。〖HJ1〗〖HJ〗
〖HT5”H〗     

江西武夷成矿带铜多金属矿产资源远景评价与展望

华南武夷山地区处于扬子、华夏两大构造单元交接叠加地段,构造变形复杂,中生代岩浆活动强烈,具有十分优越的成矿条件,矿产资源潜力巨大.本文以正在武夷山成矿带开展的矿产远景调查工作和资源评价工作所取得的阶段性成果为基础,分析了武夷山成矿带的成矿地质背景、主要矿床类型及近几年的找矿勘查成果,并对武夷成矿带江西省境内铜多金属矿产资源潜力进行了初步评价,划分了十七个找矿远景区.     

基于层次分析法的城市河流生态修复评估

城市的发展改变了许多河流的自然水文环境,并导致河流生态系统中水质、物理生境和生物完整性下降。评估受损河流水体修复的效果,需要结合物理、化学的参数,以及对生物结构、多样性和过程的影响。构建了包含河流水力、水质、水生生物、河岸带及物理结构5个方面15个指标的城市河流生态修复评估指标体系,运用群组决策的层次分析法(AHP),确定了各指标的权重,重要性排序前5位依次为：水质污染指数、鱼类IBI、水源补给量、藻类多样性、透明度。并以我国南方城市岐江河整治修复状况为例进行综合评价,结果表明,河流生态系统修复评估结果为可以接受,体现了河流整治工程使河流水质、生态的状况有所改善,但河流生态系统恢复需要较长的周期,修复初期生态系统仍处于受损状态。〖     

Correlation of the partitioning of dissolved organic matter fractions with the desorption of Cd,Cu, Ni,Pb and Zn from 18 Dutch soils

Eighteen Dutch soils were extracted in aqueous solutions at varying pH. Extracts were analyzed for Cd, Cu, Ni, Pb and Zn by ICP-AES. Extract dissolved organic carbon (DOC) was also concentrated onto a macroreticular resin and fractionation into three operationally defined fractions: hydrophilic acids (Hyd), humic acids (HA) and fulvic acids (FA). In this manner, change in absolute solution concentration and relative percentage for each fraction could be calculated as a function of extraction equilibrium pH. The soils were also analyzed for solid phase total organic carbon and total recoverable metals (EPA Method 3051). Partitioning coefficients were calculated for the metals and organic carbon (OC) based on solid phase concentrations (less the metal or OC removed by the extraction) divided by solution concentrations. Cu and Pb concentrations in solution as a function of extract equilibrium pH are greatest at low and high pH resulting in parabolic desorption/dissolution curves. While processes such as proton competition and proton promoted dissolution can account for high solution metal concentrations at low pH, these processes cannot account for higher Cu and Pb concentrations at high pH. DOC increases with increasing pH, concurrently with the increase in Cu and Pb solution concentrations. While the absolute concentrations of FA and HA generally increase with increasing pH, the relative proportional increase is greatest for HA . Variation in HA concentrations spans three orders of magnitude while FA concentrations vary an order of magnitude over the pH range examined. Correlation analysis strongly suggests that HA plays a major role in increasing the concentration of solution Cu and Pb with increasing pH in the 18 soils studied. The percentage of the OC that was due to FA was nearly constant over a wide pH range although the FA concentration increased with increasing pH and its concentration was greater than that of the HA fraction at lower pH values (pH = 3-5). Thus, in more acidic environments, FA may play a larger role than HA in governing organo-metallic interactions. For Cd, Ni, and Zn, the desorption/dissolution pattern shows high metal solution concentrations at low pH with slight increases in solution concentrations at extremely high pH values (pH>10). The results presented here suggest that the effects of dissolved organic carbon on the mobilization of Cd, Ni, and Zn may only occur in systems governed by very high pH. At high pH, it is difficult to distinguish in this study whether the slightly increased solution-phase concentrations of these cations is due to DOC or hydrolysis reactions. These high pH environments would rarely occur in natural settings.     

接种不同普通活性污泥培养厌氧氨氧化污泥的研究

采用厌氧氨氧化反应器（ASBR）,分别以普通厌氧活性污泥、混合污泥、好氧活性污泥为种泥,通过对氨氮,NO2^--N等指标监测、分析及污泥颜色的观察,研究采用不同普通活性污泥为种泥启动ASBR的可行性及差异。结果表明．ASBR反应器A和B成功启动,C因反应器故障．启动失败。采用厌氧活性污泥为接种污泥（反应器A）,当进水N的容积负荷为kg／（m^3·d）时,氨氮平均去除率为14.4％。P（NO2^--N）：p（NH4^＋-N）变化量为1．24。采用混合污泥为接种污泥（反应器B）．N的容积负荷于前者相同时,氨氮去除率平均29．7％,p（NO2^--N）：p（NH4^＋-N）变化量为1．27。采用混合普通活性污泥作为种泥培养厌氧氨氧化污泥优于单一厌氧普通活性污泥。