Geochemical evidence of pollutants from coalfired generating stations in late Pleistocene palaeosols in the Dalijia Shan,northwestern China

Surface palaeosols in two tills and a diamicton from an area in northwestern China were analysed for geochemical pollutants. Elevated levels of Br, As and Sb indicate that pollution from coal-burning and/or coal-fired electricity generating stations is delivered by aeolian transport into palaeosols dating from the last glaciation. Because the climate in the field area is sub-humid (precipitation <760 mm) the relative movement of soluble elements in palaeosols dating from early and late stades of the last glaciation is not expected to be high. The glacial and aeolian parent materials of the palaeosols indicate differences that are probably related to their source areas and to the incorporation of geochemical pollutants.     

分子连接性指数对部分有机污染物溶解度及疏水参数的预测

以化学键为基础定义了键连接性指数和分子键连接性指数，分子键连接性指数与卤代烷、环烷烃、烷基苯和含氧原子醇、酮、醚及卤代苯等有机污染物的溶解度和辛醇／水分配系数都具有良好的线性关系，使用该模型对化合物的溶解度及疏水参数的估算结果接近实验值，能很好地反映有机化合物的结构特性，可应用于不饱和碳氢体系和各类杂原子体系，且具有良好的预测能力。     

Monitoring of waste deposit derived groundwater contamination with organic tracers

Specific anthropogenic substances derived from seepage and leakage water from a waste deposit landfill were analysed in groundwater and drainage effluents using gas chromatography-mass spectrometry (GC/MS). Here, we demonstrate the application of an organic marker approach to study lateral and vertical distribution of contamination as well as the long-term emission behaviour. Source-specific and environmentally-stable pesticides, plasticisers and pharmaceuticals, such as N,N-diethyl toluamide, N-butyl benzene sulfonamide, clofibric acid, mecoprop and bisphenol A, were quantitatively analysed. A distinct lateral expansion was detected. Although temporal variations were high, no significant trend was observed.     

一种用于空气压缩机的空气消声过滤器

介绍了组合式空气消声过滤器的用途、结构、工作原理和使用效果,它是空气压缩机前级的专用理想设备,推广使用后可获得良好的综合效益。     

煤烟型复合污染物相互作用与转移过程及其特点

粉尘,ＳＯ２,ＮＯｘ等的煤烟型复合污染是我国尤其是南方我的主要类型。本文根据实验观测,详细分析了主要污染物间的相互作用过程及其复污染物从产生,转移至植物界面的运动过程及其特点。     

沙尘天气对环境空气中PM_(10)影响分析

利用2002年沈阳市沙尘天气时的环境监测资料和气象资料进行分析得出浮尘天气时环境空气中PM10浓度最大,空气污染最严重,空气中的尘主要来源于我国西北沙漠地区;沙尘暴出现频率低,持续时间短,但强度大,空气中PM10主要来源科尔沁沙漠、省内荒漠地带及本市地表沙尘;扬沙天气污染相对较轻,空气的PM10以本地地表尘为主。     

Progress in developing an ANN model for air pollution index forecast

An air pollution index (API) reporting system is introduced to selected cities of China for public communication on air quality data. Shanghai is the first city in China providing daily average API reports and forecasts. This paper describes the development of an artificial neural network (ANN) model for the API forecasting in Shanghai. It is a multiple layer perceptron (MLP) network, with meteorological forecasting data as the main input, to output the next day average API values. However, the initial version of the MLP model did not work well. To improve the model, a series of tests were conducted with respect to the training method and structure optimization. Based on the test results, the training algorithm was modified and a new model was built. The new model is now being used in Shanghai for API forecasting. Its performance is shown reasonably well in comparison with observation. The application of the old model was only weakly correlated with observation. In 1-year application, the correlation coefficients were 0.2314, 0.1022 and 0.1710 for TSP, SO₂ and NO_x, respectively. But for the new model, for over 8 months application, the correlation coefficients are raised to 0.6056, 0.6993 and 0.6300 for PM₁₀, SO₂, and NO₂. Further, the new algorithm does not rely on manpower intervention so that it is now being applied in several other Chinese cities with quite different meteorological conditions. The structure of the model and the application results are presented in this paper and also the problems to be further studied.     

生物接触氧化结合气浮法处理卷烟综合废水

某卷烟厂采用生物接触氧化结合气浮法处理卷烟综合废水,经过3年的运行实践表明,工艺运行稳定可靠,在进水COD为300～1 500 mg/L、SS为100～600 mg/L、BOD5为100～900 mg/L、NH3-N为10～20 mg/L、水温为20～30 ℃时,出水COD《70 mg/L、BOD5《20 mg/L、SS《30 mg/L、NH3-N《3 mg/L,完全实现达标排放.     

Ozone pollution and ozone biomonitoring in European cities. Part I: Ozone concentrations and cumulative exposure indices at urban and suburban sites

In the frame of a European research project on air quality in urban agglomerations, data on ozone concentrations from 23 automated urban and suburban monitoring stations in 11 cities from seven countries were analysed and evaluated. Daily and summer mean and maximum concentrations were computed based on hourly mean values, and cumulative ozone exposure indices (Accumulated exposure Over a Threshold of 40 ppb (AOT40), AOT20) were calculated. The diurnal profiles showed a characteristic pattern in most city centres, with minimum values in the early morning hours, a strong rise during the morning, peak concentrations in the afternoon, and a decline during the night. The widest amplitudes between minimum and maximum values were found in central and southern European cities such as Düsseldorf, Verona, Klagenfurt, Lyon or Barcelona. In the northern European cities of Edinburgh and Copenhagen, by contrast, maximum values were lower and diurnal variation was much smaller. Based on ozone concentrations as well as on cumulative exposure indices, a clear north–south gradient in ozone pollution, with increasing levels from northern and northwestern sites to central and southern European sites, was observed. Only the Spanish cities did not fit this pattern; there, ozone levels were again lower than in central European cities, probably due to the direct influence of strong car traffic emissions. In general, ozone concentrations and cumulative exposure were significantly higher at suburban sites than at urban and traffic-exposed sites. When applying the newly established European Union (EU) Directive on ozone pollution in ambient air, it was demonstrated that the target value for the protection of human health was regularly surpassed at urban as well as suburban sites, particularly in cities in Austria, France, northern Italy and southern Germany. European target values and long-term objectives for the protection of vegetation expressed as AOT40 were also exceeded at many monitoring sites.     

Isotopic modelling of the significance of bacterial sulphate reduction for phenol attenuation in a contaminated aquifer

A Triassic sandstone aquifer polluted with a mixture of phenolic hydrocarbons has been investigated by means of high-resolution groundwater sampling. Samples taken at depth intervals of 1 m have revealed the presence of a diving pollutant plume with a sharply defined upper margin. Concentrations of pollutant phenols exceed 4 g/l in the plume core, rendering it sterile but towards the diluted upper margin evidence for bacterial sulphate reduction (BSR) has been obtained. Groundwaters have been analysed for both delta34S-SO4 and delta18O-SO4. Two reservoirs have been identified with distinct sulphate oxygen isotope ratios. Groundwater sulphate (delta18O-SO4 = 3-5/1000) outside the plume shows a simple linear mixing trend with an isotopically uniform pollutant sulphate reservoir (delta18O-SO4 = 10-12/1000) across the plume margin. The sulphur isotope ratios do not always obey a simple mixing relation, however, at one multilevel borehole, enrichment in 34SO4 at the plume margin is inversely correlated with sulphate concentration. This and the presence of 34S-depleted dissolved sulphide indicate that enrichment in 34SO4 is the result of bacterial sulphate reduction. Delta34S analysis of trace hydrogen sulphide within the plume yielded an isotope enrichment factor (epsilon) of -9.4/1000 for present-day bacterial sulphate reduction. This value agrees with a long-term estimate (-9.9/1000) obtained from a Rayleigh model of the sulphate reduction process. The model was also used to obtain an estimate of the pre-reduction sulphate concentration profile with depth. The difference between this and the present-day profiles then gave a mass balance for sulphate consumption. The organic carbon mineralisation that would account for this sulphate loss is shown to represent only 0.1/1000 of the phenol concentration in this region of the plume. Hence, the contribution of bacterial sulphate reduction to biodegradation has thus far been small. The highest total phenolic concentration (TPC) at which there is sulphur isotope evidence of bacterial sulphate reduction is 2000 mg/l. We suggest that above this concentration, the bactericidal properties of phenol render sulphate-reducing bacteria inactive. Dissolved sulphate trapped in the concentrated plume core will only be utilised by sulphate reducers when toxic phenols in the plume are diluted by dispersion during migration.