串联氧化塘中氮、磷去除的容积分配效应的研究

在人工模拟条件下,串联厌氧 好氧塘在总容积相同,不同的容积分配的情况下,污水中的氮、磷去除效率不同,存在最佳容积分配比：V_厌/V_总约为0.27。在最佳容积分配比处,COD、氮、磷的去除率可分别提高11.4％、26.0％、51.6％。随着负荷、污水C/N比、温度、光照时间等因素的变化,氮磷去除呈一定的变化规律。说明了串联厌氧 好氧塘氮、磷去除的容积分配效应是客观存在的,合理的容积分配对氮、磷去除尤其重要     

Comparison of constant volume balloons, model trajectories and tracer transport during ETEX

In the field phases of the European Tracer EXperiment (ETEX), an inert tracer was released for 12 h into the atmosphere and samples taken at several locations downwind. During the same time, several Constant Volume Balloons (CVB) (10 and 6 for ETEX first and second release, respectively) were launched into different altitudes and followed as far as 21–188 km, to indicate the initial dispersion directions of the tracer puff. A model simulating the CVB behaviour in hydrostatic meso-scale model forecasts is applied to ETEX data to demonstrate its capability to predict the tracer puff mean axis over long distances (−2000 km). CVB model results are first compared to air parcels trajectories and 2D (i.e. isentropic, isobaric and isodensity) trajectories. Then they are compared to the measured CVB trajectories and finally to the tracer puff trajectories. As expected, the CVB model and isodensity model trajectories are found to be identical. The 16 CVBs calculated trajectories nearly overlap the real ones over 21–188 km with mean absolute horizontal transport deviations less than 20 km (average value of 8.2 km). The corresponding relative transport deviations are less than 45% with an average value of 20.6%. Better predictions are obtained for the ETEX second release. During the 60 h following ETEX’s first release start, the simulated CVBs are mainly found in the area of the maximum surface concentrations of the released tracer, up to 2000 km. Up to 36 h after ETEX second tracer release start, the simulated CVB trajectories predict well the mean axis of the tracer puff, but failed later.     

取样量与烘干时间对总悬浮物测定结果的影响

就取样量和烘干时间两个因素的变化对总悬浮物测定结果的影响程度进行了探讨。结果表明 ,取样量是造成悬浮物测定结果准确与否的主要因素 ,而不同的烘干时间对测定结果的精密度不会造成明显的影响。随着取样量的逐步减少 (从 2 0 0 0 ml减至 50 ml) ,平行样的相对偏差则从 2 7%上升到 4 5 5%。为了使相对偏差≤ 1 5% ,取水量必须满足其中的总不可滤残渣达到 6 2 mg以上。     

液液小体积萃取气相色谱法测定水中丙烯酰胺

文章建立了溴化衍生-液液小体积萃取-气相色谱法-电子捕获检测器(GC-ECD)测定水中丙烯酰胺的方法。优化了前处理步骤,缩短了样品的处理时间,减少了试剂和样品的使用量。取20 mL水样,分别加入H2SO4、KBrO3、KBr,4℃下反应至少30 min,丙烯酰胺与新生溴反应生成2,3-二溴丙酰胺。加入Na2S2O3去除多余的溴,加无水硫酸钠于室温下溶解盐析,用2.0 mL乙酸乙酯萃取,取上层萃取液GC-ECD分析。用衍生物2,3-二溴丙酰胺的响应峰面积对水中丙烯酰胺的质量浓度绘制工作曲线,相关系数达到0.999 47。方法适用于饮用水、地表水中丙烯酰胺的测定,检出限可达到0.026μg/L,相对标准偏差RSD为2.70%,加标回收率为80.67%¹00.43%。     

活性炭吸附有机蒸气性能的研究

吸附法在油气回收技术中运用很广泛.吸附剂的选择对吸附分离效果起到了决定性作用.选用3种商用活性炭,以正己烷和正庚烷为吸附质,在温度为293.15 K下进行了静态和动态吸附实验,并研究了活性炭孔结构对其吸附性能和吸附能的影响,同时利用Logistic模型的回归公式对活性炭的吸附穿透曲线进行拟合.结果表明,活性炭的比表面积和孔容是其吸附性能主要影响因素;正己烷和正庚烷的吸附行均符合Langmuir吸附等温模型;3种活性炭对正己烷和正庚烷的吸附能都随其比表面积变大而变大;Logistic模型拟合曲线与实验结果具有高度相似性,可用于活性炭吸附穿透曲线的预测.     

2015年南京市城区挥发性有机物组成特征及大气反应活性

采用GC-FID自动在线监测系统对南京市2015年环境大气中56种VOCs开展了为期1a的连续观测.结果表明,南京市城区大气VOCs小时平均体积分数为（17.49±11.35）×10^-9,其中4月最高（22.21×10^-9）,7月最低（12.39×10^-9）,日均体积分数变化特征不明显.烷烃、烯烃、芳香烃和乙炔占比分别为56.51%、11.06%、24.62%和7.81%,丙烷（15.26%）、乙烷（14.14%）、乙炔（7.81%）、甲苯（6.97%）、正丁烷（6.23%）、乙烯（5.23%）、异丁烷（4.34%）、丙烯（4.13%）、异戊烷（4.12%）和间/对-二甲苯（4.06%）是含量最丰富的VOCs物种.T/B（甲苯/苯）均值为2.02,表明南京市城区大气VOCs主要受机动车尤其是汽油车排放的影响.E/E（乙烷/乙炔）均值为2.24,表明观测站点区域大气老化程度较严重.利用·OH消耗速率（L^·OH）和臭氧生成潜势（OFP）评估了大气VOCs的反应活性.南京市城区大气VOCs冬春季大气反应活性较夏秋季强.芳香烃和烯烃的活性最高,对L^·OH和OFP的贡献依次为46.96%和41.58%、33.73%和39.86%,丙烯、乙烯和二甲苯等苯系物是活性最高的VOCs物种.     

围湖垦殖对湖泊调蓄功能的累加效应分析

计算了长湖、洪湖在围垦前后湖泊容量在水位变化时的容量增长率和四个涝灾年份降雨条件下汛期湖泊水位逐日增加值，对四湖流域尚存的18个湖泊的围垦强度与容量损失情况进行了分析。结果发现，围垦后的长湖容量平均增长率、相对增长率、最大增长率分别从1.8436、0.1834、2.4979(10^8m^3/m）减少到了1.4321,0.1802,1.7569(10^8m^3/m0，洪湖容量平均增长率、相对增长率、最大增长率分别从5.8506、0.3000、6.5095(10^8m^3/m）减少到了3.3970、0.2900、3.4440(10^8m^3/m），围垦导致的湖泊容量损失随着水位上升呈加速增加趋势，随着围垦强度的增加呈加速增加趋势，围垦后这两个湖泊在同样降雨条件下的水位逐日增加值都有不同程度的增加且这种增加值随着雨量和围垦强度的增加而增加。18个湖泊容量变化率随着围垦强度的增加而增加且在围垦强度为40％左右时表现出门槛效应。表明围湖垦残对湖泊调蓄功能的影响具有明显的累加效应。从累加效应的角度对四湖流域围湖垦残的合理性和退田还湖问题进行了讨论。     

A CFD based explosion risk analysis methodology using time varying release rates in dispersion simulations

A full probabilistic Explosion Risk Analysis (ERA) is commonly used to establish overpressure exceedance curves for offshore facilities. This involves modelling a large number of gas dispersion and explosion scenarios. Capturing the time dependant build up and decay of a flammable gas cloud size along with its shape and location are important parameters that can govern the results of an ERA. Dispersion simulations using Computational Fluid Dynamics (CFD) are generally carried out in detailed ERA studies to obtain these pieces of information. However, these dispersion simulations are typically modelled with constant release rates leading to steady state results. The basic assumption used here is that the flammable gas cloud build up rate from these constant release rate dispersion simulations would mimic the actual transient cloud build up rate from a time varying release rate. This assumption does not correctly capture the physical phenomena of transient gas releases and their subsequent dispersion and may lead to very conservative results. This in turn results in potential over design of facilities with implications on time, materials and cost of a project.In the current work, an ERA methodology is proposed that uses time varying release rates as an input in the CFD dispersion simulations to obtain the fully transient flammable gas cloud build-up and decay, while ensuring the total time required to perform the ERA study is also reduced. It was found that the proposed ERA methodology leads to improved accuracy in dispersion results, steeper overpressure exceedance curves and a significant reduction in the Design Accidental Load (DAL) values whilst still maintaining some conservatism and also reducing the total time required to perform an ERA study.     

用小波方法识别并提取通河体应变震前异常

基于小波变换理论可以识别、清除数字化资料干扰。本文利用小波方法对通河体应变2006年以来资料进行分析,并结合黑龙江及邻区4.0级以上地震震例资料探讨该方法对于提取体应变数据的震前异常信息的有效性,结果表明在一些地震前2～5个月,体应变都接收到了周期10～30天左右的异常信号,该方法能有效地提取震前异常。     

Validation and application of an analytical method for determining pesticides in the gas phase of ambient air

A method for determining atmospheric concentrations of eight pesticides applied to corn and soybean crops in Mato Grosso state, Brazil is presented. The method involved a XAD-2 resin cartridge coupled to a low volume air pump at 2 L min^?1 over 8 hours. Pesticides were recovered from the resin using sonication with n-hexane:ethyl acetate and determined by GC-MS. Good accuracy (76–128%) and precision (CV < 20%) were obtained for atrazine, chlorpyrifos, alpha- and beta-endosulfan, endosulfan sulfate, flutriafol, malathion, metolachlor and permethrin. Method detection ranged from 9.0 to 17.9 ng m^?3. This method was applied to 61 gas phase samples collected between December 2008 and June 2009. Atrazine and endosulfan were detected both in urban and rural areas indicating the importance of atmospheric dispersion of pesticides in tropical areas. The simple and efficient extraction method and sampling system employed was considered suitable for identifying pesticides in areas of intense agricultural production.