通州市大气质量监测点数的设置

用比对方式分析拟设监测点和已设监测点的大气中SO2，NOx和TSP，得出拟设监测点和已设监测点的年日均值的相对偏差小于15％，并用F检验法和t检验法对已设监测点5年的大气监测结果进行方差和显著性差异检验，结果表明通州市环境监测站提出的拟在监测站设置1个空气自动监测点取代原有的两个监测点的想法是可行的。     

有机溶剂浸取石油污染土壤中的多环芳烃

采用索氏提取法和气相色谱分析了某炼油厂周边土壤中的多环芳烃的种类及含量,考察了6种有机溶剂对土壤中多环芳烃的浸取效果,探讨了溶剂与溶质溶解度参数差异对浸取效果的影响。结果表明：土壤试样中含有蒽、荧蒽、芘、 、苯并[a]蒽、苯并[b]荧蒽、苯并[k]荧蒽和苯并[a]芘8种多环芳烃,其含量分别为4.20,22.05,10.62,4.26,5.54,0.80,0.94,4.18 mg/kg;筛选出二氯甲烷作为土壤中多环芳烃的浸取溶剂;最佳浸取条件为浸取时间10 min、浸取温度30 ℃、溶剂与土壤的液固比5:1（mL/g）、土壤含水量8%,在此条件下,总多环芳烃浸出率为83.0%,各种多环芳烃的浸出率分别为蒽97.8%、荧蒽78.2%、芘99.9%、 98.5%、苯并[a]蒽81.1%、苯并[b]荧蒽47.6%、苯并[k]荧蒽14.8%、苯并[a]芘58.7%。     

用活性白土为吸附剂处理含铬电镀废水的初步实验

论述了用活性白土为吸附剂,处理含铬电镀废水的最佳吸附条件：吸附剂的用量、吸附时间以及试液pH值对铬去除率的影响。做出了吸附等温线,并且对其吸附机理作了初步的探讨。另外指出了需进一步研究的问题。     

Aerobic dechlorination of cis- and trans-dichloroethenes by some indigenous bacteria isolated from contaminated sites in Africa

IntroductionChlorinatedethenesareamongthemostcommoncontaminantsobservedingroundwatersystems (Bouwer,1994;McCarty,1994) .Thesecompoundsvaryinnumberofchlorinesubstituents,fromthemostchlorinated,terachloroethene (PCE ) ,tothemonochlorinatedvinylchloride (VC …     

Solubility and Potential Mobility of Heavy Metals in Two Contaminated Urban Soils from Stockholm,Sweden

The solubility and potential mobility of heavy metals (Cd, Cu,Hg, Pb and Zn) in two urban soils were studied by sequential andleaching extractions (rainwater). Compared to rural (arable) soils on similar parent material, the urban soils were highlycontaminated with Hg and Pb and to a lesser extent also with Cd,Cu and Zn. Metal concentrations in rainwater leachates were related to sequential extractions and metal levels reported fromStockholm groundwater. Cadmium and Zn in the soils were mainly recovered in easily extractable fractions, whereas Cu and Pb were complex bound. Concentrations of Pb in the residual fractionwere between two- and eightfold those in arable soils, indicatingthat the sequential extraction scheme did not reflect the solidphases affected by anthropogenic inputs. Cadmium and Zn conc. inthe rainwater leachates were within the range detected in Stockholm groundwater, while Cu and Pb conc. were higher, whichsuggests that Cu and Pb released from the surface soil were immobilised in deeper soil layers. In a soil highly contaminatedwith Hg, the Hg conc. in the leachate was above the median concentration, but still 50 times lower than the max concentration found in groundwater, indicating the possibilityof other sources. In conclusion, it proved difficult to quantitatively predict the mobility of metals in soils by sequential extractions.     

Stabilization effects of surplus soft clay with cement and GBF slag

Utilization of industrial waste and surplus construction soft clay as construction material was recommended, and many attempts at geotechnical waste utilization were undertaken. This study aimed at the application of cement and a kind of industrial wastes, i.e. granulated blast furnace slag, on stabilization of surplus soft clay. The results showed that the cement and slag can successfully stabilize Ariake clays even though this high organic clay fails to be stabilized by lime and cement. Addition of slag in cement for stabilization induces higher strength than cement alone for longer curing time. The application of the cement with slag is more suitable than cement alone for stabilization because of economical consideration.     

基于最优尺度地理探测的长三角有机污染物时空分布驱动因素分析

场地污染对人体健康和生态环境造成了严重危害,理解其时空分布规律是污染评估和场地修复的基础.为此基于场地采样数据,利用最优尺度地理探测器分析长三角地区有机污染物时空分布规律及其驱动因素.结果表明:①长三角场地有机污染物空间分布存在显著的尺度效应,其最佳地理探测尺度格网为8000 m;②长三角污染物空间分布的主控因子最主要来源于生物场,其次来源于化学场;③在土壤0~20 cm深度,蔗糖酶含量、脲酶含量、微生物量氮、全氮含量和离子交换量等对有机污染物空间分布的解释力较大.在土壤20~40 cm深度,对有机污染物空间分布解释力较强的因子是土壤湿度、人口和全氮含量等.随着土壤深度的加深,水动力场的因子解释力增强.④春季里人口、全氮含量和多酚氧化酶含量等对有机污染物空间分布解释力较强.秋季里有机污染物的空间分布更复杂,因子之间表现出更强烈的非线性增强现象和双因子增强现象.     

腐殖酸对生物炭去除水中Cr(Ⅵ)的影响机制研究

以污泥生物炭作吸附剂处理水中Cr(Ⅵ),研究了共存腐殖酸对生物炭吸附性能影响.结果表明,腐殖酸能显著促进生物炭对Cr(Ⅵ)的吸附,大幅提高吸附量以及缩短吸附平衡时间,生物炭吸附过程符合准二级动力学模型.在溶液初始pH4.0,生物炭浓度20 g·L-1,Cr(Ⅵ)初始浓度在50～800 mg·L-1范围下,Langmuir模型比Freundlich模型更好地描述等温吸附行为.加入腐殖酸(20 mg·L-1)后拟合得到的理论饱和吸附量达10.10 mg·g-1,较未加入腐殖酸的吸附量5.56 mg·g-1提高近1倍.在pH 2.0～8.0范围内,吸附量随溶液初始pH值升高而减小.腐殖酸浓度上升,生物炭吸附能力进一步提高.红外光谱显示,生物炭表面的羟基、羧基、酯基、芳香环上C—H和环状结构上的CC等化学活性官能团与Cr(Ⅵ)的吸附有关.结合XPS分析结果,推断腐殖酸共存促进生物炭吸附的机制是:腐殖酸提高了Cr(Ⅵ)在生物炭表面聚集浓度,有利于生物炭对Cr(Ⅵ)的直接吸附和还原,而腐殖酸本身具有的吸附能力增加了对溶液中Cr(Ⅵ)和Cr(Ⅲ)的去除.     

石油污染土壤生物修复的中试系统构建与运行效果

构建了石油污染土壤生物修复中试系统,考察了中试规模下石油烃生物降解效率、矿化过程在生物降解中的作用.揭示生物修复过程中的系统微生物特性及其降解活性的关系,为现场污染土层生物修复工程评价和关键技术参数选择提供技术依据.结果表明,经过93d的运行,石油烃去除率达25.8%,其中典型轻质组分烷烃生物降解率最高,可达43.12%.中试系统运行稳定后,与现场调研的土壤微生物相比,其数量提高了1个数量级,活性提高了1.5倍.     

炼钢精炼渣气固碳酸化反应吸附CO2

采用炼钢精炼渣,通过气固碳酸化反应吸附CO₂,考察了不同吸附温度下精炼渣对纯CO₂和模拟高炉煤气中CO₂的吸附能力。实验结果表明：吸附温度对精炼渣吸附CO₂反应有显著的影响,升高温度可以提高精炼渣对CO₂的吸附能力;在400 ℃时,精炼渣吸附纯CO₂和模拟高炉煤气中CO₂的量分别为4.7 mg/g和9.8 mg/g;吸附温度升高到500 ℃和550 ℃时,精炼渣对纯CO₂的吸附能力强于高炉煤气中CO₂;在550 ℃时,精炼渣吸附纯CO₂和模拟高炉煤气中CO₂的量达到最高,分别为14.7 mg/g和12.9 mg/g。