AERMOD模型在土壤环境影响预测中的应用

目的分析以大气沉降为主的土壤影响预测及评价。方法采用AERMOD模型进行有机废气干沉降量、湿沉降量、总沉降量的计算。结果该区域内甲苯干沉降量占总沉降量比在97%～99%之间,湿沉降对总沉降量的贡献值很小,甲苯在该区域干沉降过程沉降速度范围为0.0003～0.0033 m/s,平均沉降速度为0.0016 m/s。结论以甲苯为代表的有机废气大气沉降计算主要以干沉降为主,干沉降速度具有明显的日变化特征,一般在中午前后出现最大值,大气沉降对周围土壤环境影响较小。     

烟气干法脱硫技术

SO2是我国煤烟型大气污染的主要污染物之一，SO2对人体、植物、大气环境等都会产生很大危害；烟气脱硫技术是控制SO2污染最行之有效的途径，通过介绍高能电子活化氧化法等几种烟气干法脱硫技术的原理、工艺特点和应用现状，给出烟气干法脱硫技术在我国的发展趋势。     

元江干热河谷环境变迁与适应对策研究

元江是我国著名的干热区，当前的独特生态环境是由自然环境变化和人类活动作用共同影响而形成的。经过区域发展的纵向分析比较，不同时期的环境变化与适应对策都具有特异性，正确的社会行为适应、生产与技术适应是区域特色产业建设和可持续发展的重要保障。     

珠江三角洲表层土壤中的多环芳烃

多环芳烃是一类主要由人类活动排放的有毒有机污染化合物,对人和生物体具有致癌、致畸和致突变效应,是评价土壤生态污染的重要内容之一。文章利用螺旋钻采样、索氏抽提、硅胶氧化铝净化和GC-MS分析,研究了珠江三角洲不同功能区(城市点、郊区点、乡村点)的76个表层土壤样品(耕作土、非耕作土)中多环芳烃(PAHs)的含量、分布特征及其影响因素。结果表明,16种优控PAHs的总质量分数范围为31.5~791.6ng·g-1(平均279.1ng·g-1,以干质量计),以萘(44.4%)、菲(13.7%)、荧蒽(8.4%)、芘(4.9%)、■(6.6%)等化合物为主。与国内外其它地区的城市相比较,珠江三角洲地区土壤PAHs的污染程度较低,在组成上也表现出亚热带地区独特的中、低环化合物为主的特征。受人类经济活动的影响,地处珠江三角洲中部的经济工业中心地带,土壤中PAHs含量相对较高。珠三角表层土壤PAHs含量和组成分布主要受大气沉降控制,而与土壤有机碳、pH的相关性较小。高温潮湿的亚热带季风气候是影响珠三角土壤PAHs的降解和迁移的重要环境因素。     

Efficacy of a Biomonitoring (Moss Bag) Technique for Determining Element Deposition Trends on a Mid-Range (375 Km) Scale

National networks detect multi-state trends in element deposition using direct measurement methods. Biomonitoring techniques have been used to examine deposition in local areas and around point sources. We sought to determine the efficacy of a moss bag technique to detect element deposition trends on a mid-range (state) scale, and to compare these results with those of the National Acid Deposition Program/National Trends Network (NADP/NTN, 1999). We sampled heavy metals, sulfur, and nitrogen deposition (21 elements) using mesh bags containing Sphagnum russowii at nine sites, over a 375 km transect crossing southern Wisconsin (upper Midwest, USA). We found statistically significant trends of decreasing deposition in a northwesterly direction for 13 elements: Al, B, Ca, Cd, Co, Cu, Cr, Fe, Mg, Mn, Ni, S, and Zn. Six of these have moderate to large changes in concentration (14–37%). The trends for Ca, Mg, and S are consistent with regional deposition patterns in 1998 isopleth maps from the NADP/NTN (1999) which are derived from a sampling array far less dense than the transect sites. This national network indicates that Ca and Mg increase to the southeast, beyond Wisconsin borders. The fact that the present study demonstrates strong correlations between both of these elements (Ca and Mg) and Al, B, Cr, Cu, Fe, Mn, Ni, and Zn (mean r for all correlations = 0.75, p < 0.02) implies that these correlated elements also increase to the southeast in neighboring states.     

Losses of nitrogen and phosphorus from agricultural and forest areas in Finland during the 1980s and 1990s

The temporal changes and spatial variability of phosphorus andnitrogen losses and concentrations in Finland during the period1981–1997 were studied in 15 small agricultural and forestedcatchments. In addition, four coastal river basins with highagricultural land use located in southern Finland were includedin the study in order to assess the representativeness ofagricultural loss estimates from small agricultural catchments.The mean annual loss specific for agricultural land was estimatedto be on average 110 kg km^-2 a^-1 for total phosphorusand 1500 kg km^-2 a^-1 for total nitrogen. The resultsfrom small agricultural catchments were in agreement with thecorresponding loss estimates from rivers, with an average of137 kg km^-2 a^-1 for total phosphorus and 1800 kg km^-2a^-1 for total nitrogen. The results from the studiedagricultural catchments and rivers during the period 1981–1997suggest that weather-driven fluctuation in discharge was usuallythe main reason for changes in nutrient losses, and little or noimpact of changes in agricultural production or managementpractises can be observed. In forested areas the total phosphorusloss (average 9 kg km^-2 a^-1) and total nitrogen loss(average 250 kg km^-2 a^-1) were lower than inagricultural areas. In forested catchments the impact of forestryoperations, such as clear-cutting and fertilization, and theimpact of atmospheric nitrogen deposition can be seen in changesin nutrient losses.     

Transport,deposition and biodegradation of particle bound polycyclic aromatic hydrocarbons in a tidal basin of an industrial watershed

Polycylic aromatic hydrocarbons (PAHs) are commoncontaminants in industrial watersheds. Their origin,transport and fate are important to scientists,environmental managers and citizens. The Philadelphia NavalReserve Basin (RB) is a small semi-enclosed embayment nearthe confluence of the Schuylkill and Delaware Rivers inPennsylvania (USA). We conducted a study at this site todetermine the tidal flux of particles and particle-boundcontaminants associated with the RB. Particle traps wereplaced at the mouth and inside the RB and in the Schuylkilland Delaware Rivers. There was net particle deposition intothe RB, which was determined for three seasons. Spring andfall depositions were highest (1740 and 1230 kg ofparticles, respectively) while winter deposition wasinsignificant. PAH concentrations on settling particlesindicated a net deposition of 12.7 g PAH in fall and 2.1 gPAH in spring over one tidal cycle. There was nosignificant PAH deposition in the winter. Biodegradationrates, calculated from ¹⁴C-labeled PAH substratemineralization, could attenuate only about 0.25% of the PAHdeposited during a tidal cycle in fall. However, in thespring, biodegradation could be responsible for degrading50% of the settling PAHs. The RB appears to be a sink forPAHs in this watershed.     

干湿交替对自然沟渠沉积物反硝化速率的影响

以川中丘陵区自然沟渠沉积物为研究对象,设置低强度、中强度、高强度的干湿交替频率和长期淹水对照处理,运用室内原状土柱-乙炔抑制培养法和实时荧光定量PCR技术,研究了干湿交替对自然沟渠沉积物反硝化速率及相关功能基因的影响.结果表明：在试验模拟过程中,干湿交替显著降低了沉积物中NH₄⁺-N和DOC含量,沉积物中NO₃^--N含量则表现为先增加后减少的趋势.沉积物反硝化速率均值表现为中强度（266.42 μg·m^-2·h^-1） > 高强度（199.10 μg·m^-2·h^-1） > 低强度（152.93 μg·m^-2·h^-1） > 长期淹水（9.57 μg·m^-2·h^-1）.干湿交替增加了反硝化功能基因的拷贝数（p<0.05）,nosZ基因拷贝数在实验前后无显著差异;低强度和中强度处理的nirK基因拷贝数在实验前后差异显著,中强度处理的nirS基因拷贝数在实验前后差异显著.Pearson相关分析结果表明,沉积物的反硝化速率与NO₃^--N含量、ORP和nirK基因拷贝数呈显著正相关（p<0.05）.干湿交替可能主要通过改变沉积物的NO₃^--N含量、ORP和nirK基因拷贝数影响沉积物反硝化速率.     

敦煌地区干热与干冷环境特征研究

目的 建立大气环境干热、干冷环境特征的表征方法,以便定量表征大气环境干热、干冷的严酷性,为高分子材料及产品在该地区的老化试验与评估提供参考。方法 设置温度-相对湿度组合为临界值,统计给定时期内温度高于临界温度、相对湿度低于临界相对湿度的时间为干热时间,统计给定时间内温度低于临界温度、相对湿度低于临界相对湿度的时间为干冷时间,并以干热时间、干冷时间占给定时期总时间的百分比来表征干热、干冷环境特征,研究临界条件、数据间隔时间对干热、干冷特征的影响。结果 以25 ℃RH40%、5 ℃ RH40%为临界条件分别统计干热时间和干冷时间的月、年百分比,可表征大气环境的干热、干冷特征。敦煌6、7月份为干热严酷月,月干热时间百分比超过40%,1、2月份为干冷严酷月,月干冷时间百分比可超过70%。结论 临界温度、临界相对湿度、统计年份、数据间隔时间等对统计结果有较大的影响。     

Efficiency characterization of fire extinguishing compound superfine powder containing Mg(OH)2

To improve the fire extinguishing efficiency of existing dry powders, a new type of superfine dry powder was prepared using magnesium hydroxide as an additive. In our study, a thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were used to analyze the thermal decomposition of the synthesized powders. The temperature of thermal decomposition, weight loss, and other thermodynamic parameters of the fire extinguishing powders were analyzed to explain the performance advantages of the compound superfine powder. Through a small-scale fire experiment, the physical parameters of the extinguishing process—such as extinguish time, powder dosage, smoke concentration, and minimum extinguishing concentration—were quantified for the suppression of a diesel fire using the different powders; these parameters were used to evaluate the fire extinguishing capacity and toxic gas suppression ability of the powders. TGA demonstrated that the compound superfine powder decomposed more quickly and its thermal decomposition process was much shorter than those of the other powders. The DSC data indicated that the compound superfine powder could decrease the characteristic temperature at each stage and thus the powder absorbed the flame's heat more quickly and suppressed flame propagation. The fire extinguishing test demonstrated that the consumption of the three types of fire extinguishing powder decreased with an increase in the driving pressure, and the order of powder dosage was as follows: commercial dry powder > superfine powder > compound superfine powder. Similarly, the order of minimum extinguishing concentration was as follows: commercial dry powder > superfine powder > compound superfine powder. Furthermore, the compound superfine powder exhibited a greater capacity for controlling toxic and harmful gas emissions.