长江河口表层沉积物中PAHs的生态风险评价

2005年11月26—29日对长江河口部分表层沉积物中多环芳烃类化合物(PAHs)的污染现状进行了调查和研究,分析了其中16种PAHs单体含量. 结果表明,长江河口表层沉积物中属于美国优先控制的16种PAHs共检出15种,仅萘未被检出,w(PAHs)为355.72～2 480.85 ng/g,平均值为1 040.29 ng/g. 表层沉积物中以4环和5～6环PAHs为主,二者之和占w(PAHs)的80%以上. 长江河口表层沉积物中PAHs污染主要来源于矿物燃料的高温燃烧,但部分区域也不排除石油源输入的可能性. 与沉积物风险评估值相比,严重的生态风险在长江河口表层沉积物中不存在,然而排污口附近沉积物存在一定的生态风险.      

商业空间的照明设计构思

主要讨论基于商业空间的特殊性,利用合理的照明设计来改善环境质量,从而达到强化商业空间和商品特性的目的,有效的引导和提高消费者的购买欲望,并产生兴趣和信赖．图1,表1,参2．     

广州市室内尘土中多溴联苯醚的分布特点及来源

随机采集了广州市46个家庭和12个办公室内尘土样品,同时采集了17个室外尘土样品、2个电视机和2个电脑尘土样品并分析了室内尘土中多溴联苯醚(PBDEs)的含量、单体分布及来源.结果表明,家庭尘土中∑10PBDEs(BDE28,47,66,85,99,100,153,154,183,209之和)的含量为 564.3~9654ng/g,中值和均值分别为 2686,3407ng/g;办公室尘土中∑10PBDEs 的含量为 1737~4408ng/g,中值和均值分别为3133,3179ng/g.室内尘土中PBDEs的最主要单体为BDE209,分别占家庭尘土和办公室尘土∑10PBDEs的97.4%和99.0%.BDE47、99和183在室内尘土中含量也较高.大多数室内尘土中∑10PBDEs的含量高于室外,说明室内可能有重要的PBDEs释放源.室内尘土中PBDEs的主要工业品来源为十溴联苯醚,五溴联苯醚次之,八溴联苯醚较少.     

大气颗粒物“二重源解析”技术的误差分析

"二重源解析"模型计算结果的误差是采样误差、样品处理误差、化学组分分析误差、数据处理误差以及数学模型误差等所有误差的积累。提出了"二重源解析"解析结果的相对误差和标准偏差表达式,并用之计算了某市利用"二重源解析"模型计算的源贡献值的相对误差和标准偏差,还针对从源排放出来的初始态颗粒物在传输过程中发生的扬尘态变化提出了扬尘转化率的概念和计算方法。     

生物预处理微污染水

金坛市主要水源钱资荡水 ,劣于二级饮用水水源水质 ,系微污染水源。常规水处理工艺已很难满足饮用水水质要求 ,拟采用生物预处理。比较了两种生物预处理池对藻类、氨氮、亚硝酸盐氮、色度、浊度等指标的去除效果 ,提出了生物预处理适宜的运行工况参数 ,为工程设计提供依据。     

NEAR‐STREAM LANDUSE EFFECTS ON STREAMWATER NUTRIENT DISTRIBUTION IN AN URBANIZING WATERSHED1

ABSTRACT: We investigated spatial and temporal relationships among surface and subsurface watershed attributes and stream nutrient concentrations in urbanizing Johnson Creek watershed in northern Oregon. We sampled stream water at eight urban and five nonurban locations from March 1998 through December 1999. We sampled eight wells distributed over the two primary aquifers in the watershed. Using a Geographic Information System (GIS), percentages of landuse attributes within a radius of 30, 91, and 152 m from each sample site were quantified. We analyzed relationships between (1) nutrient concentrations and percentage cover of different landuse attributes, and (2) nutrient concentrations and underlying hydrologic units. We did not find a significant relationship between ground water chemistry and stream water chemistry. We found elevated levels of phosphorus (P) concentrations correlated with urban landuse, while higher nitrogen (N) concentrations were correlated with nonurban (primarily agricultural) landuse. We concluded that elevated levels of N in nonurban areas of Johnson Creek watershed were associated with agricultural practices. We further concluded that urban development factors such as increases in storm drains, dry wells, and impermeable surfaces may be responsible for higher input of P to the stream in urbanizing areas of the Johnson Creek watershed.     

有机着色铝合金阳极氧化膜耐光性快速评价方法

为了建立一种快速评价有机染料着色的铝合金阳极氧化膜耐光性的方法,用于工厂生产工艺质量控制,对比研究了阳极氧化膜实验室光老化试验和户外暴露试验的颜色变化结果．建立了综合色差和试验时间的线性回归方程．并利用付利叶红外光谱仪证实氧化膜内有机染料在实验室光老化和户外暴露试验中的变化机理是一致的．该光老化试验方法能很好地模拟氧化膜在户外暴露的变色行为。     

Formation characteristics of polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans, and coplanar PCBs in fly ash from a gasification–melting process of municipal solid waste

PCDDs/DF and Co-PCB (dioxin) formations were studied with ash from a newly developed gasification and melting process for municipal solid waste. Ash samples were heated in a laboratory-scale fixed-bed reactor. Emphasis was placed on the effects of the type and composition of ash, temperatures, gas residence time, and gaseous organic precursors. Investigations using macroscopic and homologue distribution analyses led to the following conclusion. The ash from the gasification–melting process had the ability to generate dioxins in flue gas. A possible carbon source is unburned carbon in the ash samples, although this was very low (less than 0.01%). An experimental result that the level of dioxins generated from preheated fly ash obtained from a conventional incinerator was much lower than that from nonheated fly ash supported this conclusion. Dioxin concentrations obviously showed temperature dependence and peaked at 350°C. Dioxins formed in a gasification–melting process ash were readily desorbed from the surface, probably because of the low carbon content of the ash. There was no experimental evidence that gaseous organic precursors fed to the reactor generated dioxins. Therefore, an organic precursor was not essential for the formation of dioxins. A good linear relationship obtained between PCDDs/DFs and gas residence time also supported the assumption. Received: February 14, 2000 / Accepted: June 30, 2000     

注水残渣固化修路技术研究

针对注水残渣含碱量大,盐、油及其它杂质含量高,处理困难等特点,研究出注水残渣固化修路工艺技术。注水残渣固化后,既消除了污染源,保护了周围环境的土壤及地下水资源,又减少了土地占用面积,从而取得了显著的经济效益。     

ENHANCEMENTS OF NONPOINT SOURCE MONITORING OF VOLATILE ORGANIC COMPOUNDS IN GROUND WATER1

ABSTRACT: The U.S. Geological Survey (USGS) has compiled a national retrospective data set of analyses of volatile organic compounds (VOCs) in ground water of the United States. The data are from Federal, State, and local nonpoint‐source monitoring programs, collected between 1985–95. This data set is being used to augment data collected by the USGS National Water‐Quality Assessment (NAWQA) Program to ascertain the occurrence of VOCs in ground water nationwide. Eleven attributes of the retrospective data set were evaluated to determine the suitability of the data to augment NAWQA data in answering occurrence questions of varying complexity. These 11 attributes are the VOC analyte list and the associated reporting levels for each VOC, well type, well‐casing material, type of openings in the interval (screened interval or open hole), well depth, depth to the top and bottom of the open interval(s), depth to water level in the well, aquifer type (confined or unconfined), and aquifer lithology. VOCs frequently analyzed included solvents, industrial reagents, and refrigerants, but other VOCs of current interest were not frequently analyzed. About 70 percent of the sampled wells have the type of well documented in the data set, and about 74 percent have well depth documented. However, the data set generally lacks documentation of other characteristics, such as well‐casing material, information about the screened or open interval(s), depth to water level in the well, and aquifer type and lithology. For example, only about 20 percent of the wells include information on depth to water level in the well and only about 14 percent of the wells include information about aquifer type. The three most important enhancements to VOC data collected in nonpoint‐source monitoring programs for use in a national assessment of VOC occurrence in ground water would be an expanded VOC analyte list, recording the reporting level for each analyte for every analysis, and recording key ancillary information about each well. These enhancements would greatly increase the usefulness of VOC data in addressing complex occurrence questions, such as those that seek to explain the reasons for VOC occurrence and nonoccurrence in ground water of the United States.