太湖某湖区高锰酸盐指数变化趋势的平滑处理

应用数理统计检验，移动平均法和指数平滑法，对太湖的某湖区九年的高锰酸盐指数平均值的数据进行了处理，发现统计检验在０．０５置信水平上无意义。移动平均法虽然有数学上的统计意义，但与实际变化趋势差距很大。而指数平滑法，所得的处理数据，其预测的趋势与实测的比较符合。     

房地产用地土壤污染环境风险评价——以江苏某搬迁企业原址用地为例

许多房地产项目都是在工业企业原址上进行开发建设,可能存在不同程度的土壤污染。土壤污染的评估和修复方案已成为房地产开发项目环评的重点,文中采用单因子指数法、内梅罗指数法和土壤背景值对照法对江苏某房地产用地土壤进行了环境风险评价,结果表明该地块不需要进行土壤修复和处置。     

提升“小康社会”环境质量综合指数的对策措施

环境质量综合指数是南京市建设“小康社会”的难点、核心指标,通过分析环境质量状况和环境保护工作的现状,提出了创建期间有关环保工作的机制、管理的重点和工程措施等对策与措施.     

Seres2000型高锰酸盐指数仪器监测数据质量分析

水质自动站测定的高锰酸盐指数（CODMn）数据与实验室标准方法测定结果常常产生较大的偏差。作者旨在通过自动仪器与实验室标准方法的比对测试，查找自动监测结果的偏差原因，同时分析和探讨如何保障仪器的正常运行，保持自动仪器监测的数据质量，达到与实验室标准监测结果的统一。     

滇池入湖河流“十一五”综合整治效果分析

滇池是中国“三河三湖”治理的重点湖泊之一,是中国著名的高原淡水湖泊.“十一五”期间,昆明市政府加大对滇池入湖河流的综合整治力度.纳入水质监测的29条主要入湖河流中,通过分析综合污染指数和有机污染指数,评价“十一五”期间的入湖河流水污染综合整治效果.结果表明,经过大力整治,滇池大部分主要入湖河流的水质改善明显,综合污染指数和有机污染指数均大幅下降,河流污染整治效果显著;但部分河流的综合污染指数和有机污染指数仍明显升高,河流水质有进一步恶化趋势,入湖河流综合整治工作仍任重而道远.     

内梅罗污染指数在运河水质评价中的应用

应用内梅罗污染指数公式,计算了１９９４－１９９８年运河（杭州段）各监测点位的污染指数,用较直观的数据来评价运河（杭州段）的污染状况。     

测定高锰酸盐指数考核样品时的计算方法修正

针对测定高锰酸盐指数考核样品时的结果偏高现象，经过查找，其原因是由于按公式计算没有考虑稀释用纯水的空白值响应。经修正公式后计算，其考核样品的结果则均为正确。     

不同加热法对地表水中高锰酸盐指数测定影响的探讨

对高锰酸盐指数标准测定法进行探讨。以直火加热回流反应代替水溶锅加热反应，快速测定地表水中的高锰酸盐指数。与标准法比较，加热煮沸时间由３０ｍｉｎ缩短至１０ｍｉｎ，耗电费用降低４８％；避免了室内环境的污染。     

琼脂碳源生物反硝化去除水源水中硝酸盐

针对受硝酸盐污染的水源水,以琼脂为反硝化细菌的碳源和微生物载体,通过生物反硝化作用脱除水源水中的硝酸盐,并利用曝气生物滤池(BAF)去除琼脂反应器出水中残留的少量CODMn和NO2--N等污染物。实验结果表明,水源水自然接种的条件下,可以顺利启动琼脂反应器;在温度为25℃左右,琼脂反应器在进水NO3--N约25 mg/L、水力停留时间1.5 h时,能获得70%的硝酸盐氮去除率;曝气生物滤池在水力停留时间0.5 h、气水比2.8时,可控制最终出水的CODMn和NO2--N分别在5.0 mg/L和0.10 mg/L以下;琼脂反应器的脱氮效果与温度、进水NO3--N浓度及水力停留时间等有关。研究指出,琼脂反应器与曝气生物滤池构成的组合系统能较好地脱除水源水中的硝酸盐并且能控制最终出水水质,不会导致二次污染,从而获得合格的饮用水源水。     

“控源-截污-资源化”模式处理面源污染

针对农村面源污染的时空范围广,不确定性大,成分、过程复杂,难以控制的特点,同时考虑废物资源化的问题,提出了"控污-截污-资源化(再利用)"CIR模式,包括三方面:通过改变不良用水习惯及耕作方式等从源头上控制污染排放;利用植物缓冲带、自然塘、沟渠湿地和表面流湿地等达到截污的目的;将畜禽养殖废水及生活黑水集中处理,产生沼气,变废为宝,于湿地内种植经济类水生植物,兼性塘内水产养殖,最终实现废物资源化(再利用)。经过将近一年半的运行测试,测试结果表明,整个模式不仅除污效率高,而且可产生良好的经济效益。     

Cooperative identification for critical periods and critical source areas of nonpoint source pollution in a typical watershed in China

Environmental Science and Pollution Research - Critical periods (CPs) and critical source areas (CSAs) refer to the high-risk periods and areas of nonpoint source (NPS) pollution in a watershed,...     

Nonpoint source pollution of urban stormwater runoff: a methodology for source analysis

The characterization and control of runoff pollution from nonpoint sources in urban areas are a major issue for the protection of aquatic environments. We propose a methodology to quantify the sources of pollutants in an urban catchment and to analyze the associated uncertainties. After describing the methodology, we illustrate it through an application to the sources of Cu, Pb, Zn, and polycyclic aromatic hydrocarbons (PAH) from a residential catchment (228 ha) in the Paris region. In this application, we suggest several procedures that can be applied for the analysis of other pollutants in different catchments, including an estimation of the total extent of roof accessories (gutters and downspouts, watertight joints and valleys) in a catchment. These accessories result as the major source of Pb and as an important source of Zn in the example catchment, while activity-related sources (traffic, heating) are dominant for Cu (brake pad wear) and PAH (tire wear, atmospheric deposition).     

Revealing source signatures in ambient BTEX concentrations

Management of ambient concentrations of Volatile Organic Compounds (VOCs) is essential for maintaining low ozone levels in urban areas where its formation is under a VOC-limited regime. The significant decrease in traffic-induced VOC emissions in many developed countries resulted in relatively comparable shares of traffic and non-traffic VOC emissions in urban airsheds. A key step for urban air quality management is allocating ambient VOC concentrations to their pertinent sources. This study presents an approach that can aid in identifying sources that contribute to observed BTEX concentrations in areas characterized by low BTEX concentrations, where traditional source apportionment techniques are not useful. Analysis of seasonal and diurnal variations of ambient BTEX concentrations from two monitoring stations located in distinct areas reveal the possibility to identify source categories. Specifically, the varying oxidation rates of airborne BTEX compounds are used to allocate contributions of traffic emissions and evaporative sources to observed BTEX concentrations.     

Temporal evolution of DNAPL source and contaminant flux distribution: impacts of source mass depletion

We investigated, using model simulations, the changes occurring in the distribution of dense non-aqueous phase liquid (DNAPL) mass (Sn) within the source zone during depletion through dissolution, and the resulting changes in the contaminant flux distribution (J) at the source control plane (CP). Two numerical codes (ISCO3D and T2VOC) were used to simulate selected scenarios of DNAPL dissolution and transport in three-dimensional, heterogeneous, spatially correlated, random permeability fields with emplaced sources. Data from the model simulations were interpreted based on population statistics (mean, standard deviation, coefficient of variation) and spatial statistics (centroid, second moments, variograms). The mean and standard deviation of the Sn and J distributions decreased with source mass depletion by dissolution. The decrease in mean and standard deviation was proportional for the J distribution resulting in a constant coefficient of variation (CV), while for the Sn distribution, the mean decreased faster than the standard deviation. The spatial distributions exhibited similar behavior as the population distribution, i.e., the CP flux distribution was more stable (defined by temporally constant second moments and range of variograms) than the Sn distribution. These observations appeared to be independent of the heterogeneity of the permeability (k) field (variance of the log permeability field=1 and 2.45), correlation structure (positive vs. negative correlation between the k and Sn domains) and the DNAPL dissolution model (equilibrium vs. rate-limited), for the cases studied. Analysis of data from a flux monitoring field study (Hill Air Force Base, Utah) at a DNAPL source CP before and after source remediation also revealed temporal invariance of the contaminant flux distribution. These modeling and field observations suggest that the temporal evolution of the contaminant flux distribution can be estimated if the initial distribution is known. However, the findings are preliminary and broader implications to sampling strategies for remediation performance assessment need to be evaluated in additional modeling and experimental studies.     

Line source emission modelling

Line source emission modelling is an important tool in control and management of vehicular exhaust emissions (VEEs) in urban environment. The US Environmental Protection Agency and many other research institutes have developed a number of line source models (LSMs) to describe temporal and spatial distribution of VEEs on roadways. Most of these models are either deterministic and/or statistical in nature.This paper presents a review of LSMs used in carrying out dispersion studies of VEEs, based on deterministic, numerical, statistical and artificial neural network techniques. The limitations associated with deterministic and statistical approach are also discussed.     

微污染水源水中消毒副产物前体物的去除

采用生物接触氧化法对北京某水库的微污染水源水中消毒副产物前体物的去除进行了研究。结果表明,水源水和生物接触氧化柱(简称生化柱)出水中的消毒副产物前体物氯化后形成的消毒副产物三卤甲烷(THMs)以CHCl3,CHCl2Br和CHBr2Cl为主,其中CHCl3含量最高,约占THMs的70％。水温对THMs前体物的去除有很大的影响,水温15．8℃时,生化柱对THMs前体物的去除率为65．2％;当水温由15．8℃降至12．8℃时,THMs前体物的去除率由65．2％降至18．8％。2002年11月至2003年1月间,生化柱UV254吸收值的平均去除率为11％。     

Concentrations of mobile source air pollutants in urban microenvironments

Human exposures to criteria and hazardous air pollutants (HAPs) in urban areas vary greatly due to temporal-spatial variations in emissions, changing meteorology, varying proximity to sources, as well as due to building, vehicle, and other environmental characteristics that influence the amounts of ambient pollutants that penetrate or infiltrate into these microenvironments. Consequently, the exposure estimates derived from central-site ambient measurements are uncertain and tend to underestimate actual exposures. The Exposure Classification Project (ECP) was conducted to measure pollutant concentrations for common urban microenvironments (MEs) for use in evaluating the results of regulatory human exposure models. Nearly 500 sets of measurements were made in three Los Angeles County communities during fall 2008, winter 2009, and summer 2009. MEs included in-vehicle, near-road, outdoor, and indoor locations accessible to the general public. Contemporaneous 1- to 15-min average personal breathing zone concentrations of carbon monoxide (CO), carbon dioxide (CO₂), volatile organic compounds (VOCs), nitric oxide (NO), nitrogen oxides (NO_x), particulate matter (<2.5 μm diameter; PM_2.5) mass, ultrafine particle (UFP; <100 nm diameter) number, black carbon (BC), speciated HAPs (e.g., benzene, toluene, ethylbenzene, xylenes [BTEX], 1,3-butadiene), and ozone (O₃) were measured continuously. In-vehicle and inside/outside measurements were made in various passenger vehicle types and in public buildings to estimate penetration or infiltration factors. A large fraction of the observed pollutant concentrations for on-road MEs, especially near diesel trucks, was unrelated to ambient measurements at nearby monitors. Comparisons of ME concentrations estimated using the median ME/ambient ratio versus regression slopes and intercepts indicate that the regression approach may be more accurate for on-road MEs. Ranges in the ME/ambient ratios among ME categories were generally greater than differences among the three communities for the same ME category, suggesting that the ME proximity factors may be more broadly applicable to urban MEs.

Implications:Estimates of population exposure to air pollutants extrapolated from ambient measurements at ambient fixed site monitors or exposure surrogates are prone to uncertainty. This study measured concentrations of mobile source air toxics (MSAT) and related criteria pollutants within in-vehicle, outdoor near-road, and indoor urban MEs to provide multipollutant ME measurements that can be used to calibrate regulatory exposure models.     

水环境多环芳烃源解析研究进展

城市化和工业化给环境带来的潜在危害引起人们对环境质量的重视.污染物来源解析研究的成果为环境管理提供了有效的工具.在查阋大量文献的基础上,综述了应用于水环境尤其是沉积物中多环芳烃源解析的主要理论方法和应用模型,并初步提出了沉积物中多环芳烃源解析方法.