温州近海海域海水及滩涂沉积物中PFOS和PFOA污染特征分析

为了解温州近海海域全氟辛烷磺酸(PFOS)和全氟辛酸(PFOA)的污染状况和特征,采用固相萃取/高效液相串联质谱检测法分析了采自乐清湾、瓯江口、西湾、飞云江口及洞头半屏岛的近海海水和滩涂沉积物中PFOS和PFOA污染水平。结果显示,温州近海海水普遍存在PFOS和PFOA污染,其中,PFOS的浓度范围为<1.0～31.36 ng/L,中位浓度为2.29 ng/L;PFOA的浓度范围为<1.0～23.66 ng/L,中位浓度为5.29 ng/L。滩涂沉积物样品中PFOS和PFOA的浓度范围(干重)分别为(<1.0～11.91)×10-9(中位浓度为3.60×10-9)和(1.84～34.01)×10-9(中位浓度为6.83×10-9)。温州近海海水中PFOS和PFOA的污染水平明显高于香港沿岸、中国南海海水、韩国沿岸海水和近海珠江三角洲,与大连湾的海水相当,海岸滩涂沉积物中的PFOS和PFOA浓度远高于珠江和黄浦江沉积物中的浓度。     

基于事故统计分析的城市轨道交通运营安全和可靠性研究

本文通过对城市轨道交通运营事故的统计分析,研究了影响轨道交通运营安全和可靠性的主要因素,并构建了城市轨道交通运营安全保障体系,以为提高轨道交通运营安全和可靠性的研究提供依据。     

基于悬臂梁力学模型分析高边坡危岩体的稳定性——以四川省三清村高边坡W1危岩体为例

四川省苍溪县三清村高边坡的稳定性对当地居民的人身安全构成了威胁,需要对高边坡进行稳定性分析和评价。本文针对三清村高边坡自来水厂段W1危岩体,采用悬臂梁力学模型对其稳定性进行了定量计算及分析,结果表明:将计算所得的W1危岩体截面的最大剪切应力与截面允许的最大剪切应力进行对比,可以判断W1危岩体在自然条件下处于稳定状态,在暴雨和地震条件下处于不稳定状态,该结果与野外的宏观判断结论基本一致。     

北京市区春夏PM2.5和PM10浓度变化特征研究

通过对北京市2012年3月～6月PM2.5和PM10实时数据的整理和分析,结果表明,北京市区大气中细颗粒物PM2.5和可吸入颗粒物PM10浓度日变化趋势基本相同,PM2.5和PM10存在显著或极显著的正相关关系;3月～6月,PM2.5浓度随季节变化逐渐升高,PM10的浓度随季节变化先升高后减小;3月～6月PM2.5与PM10日平均浓度分别为62.77μg/m3和133.88μg/m3,分别为国家二级标准的83.69%和89.25%。     

兰州冬季城市烟雾层辐射效应的观测分析研究

冬季兰州城市上空形成浓厚的烟雾层。利用1990年11月兰州大学和离城市地面625m高南山顶的辐射和探空资料,分析和计算了烟雾层的辐射效应。兰州城市烟雾层具有浑浊度系数大波长指数小的特点。对到达地面的太阳辐射有很强的削弱。浑浊度系数最大时,烟雾层内的平均加热率为6.16℃/d,。大气层对各波段的消光强弱不同,对可见光削减最大。同时烟雾层使到达兰州地面的大气逆辐射比南山顶增加5.2％,总的入射辐射比南山顶小5.6％,地面辐射差额比南山顶小67.8％。烟雾层的存在增加了城市边界层的稳定性。     

柯树背岩体铀金成矿远景分析

本文在研究柯树背岩体矿物岩石学特征基础上 ,通过对该岩体的铀金成矿元素丰度、铀金矿化类型、铀金矿石物质成分及成矿阶段的划分、矿脉的铀金含量及其相关关系、围岩蚀变及原生晕特点、铀金矿化控制因素的详细研究 ,从岩体的放射性地质地球化学特点、岩体蚀变及剥蚀强度、岩石化学及稀土元素地球化学、矿脉向深部的变化趋势等几个方面分析了该岩体的铀金成矿远景及今后找矿工作的意见 ,指出该岩体西体南部断续出现的柯树背—隘高断裂上盘 1km范围与下寮—大坑里断裂夹持区为铀金成矿远景区。     

Size distributions of aerosol and water-soluble ions in Nanjing during a crop residual burning event

To investigate the impact on urban air pollution by crop residual burning outside Nanjing, aerosol concentration, pollution gas concentration, mass concentration, and water-soluble ion size distribution were observed during one event of November 4-9, 2010. Results show that the size distribution of aerosol concentration is bimodal on pollution days and normal days, with peak values at 60-70 and 200-300 nm, respectively. Aerosol concentration is 10⁴ cm^-3. nm^-1 on pollution days. The peak value of spectrum distribution of aerosol concentration on pollution days is 1.5-3.3 times higher than that on a normal day. Crop residual burning has a great impact on the concentration of fine particles. Diurnal variation of aerosol concentration is trimodal on pollution days and normal days, with peak values at 03:00, 09:00 and 19:00 local standard time. The first peak is impacted by meteorological elements, while the second and third peaks are due to human activities, such as rush hour traffic. Crop residual burning has the greatest impact on SO₂ concentration, followed by NO₂, O₃ is hardly affected. The impact of crop residual burning on fine particles (< 2.1 μm) is larger than on coarse particles (> 2.1 μm), thus ion concentration in fine particles is higher than that in coarse particles. Crop residual burning leads to similar increase in all ion components, thus it has a small impact on the water-soluble ions order. Crop residual burning has a strong impact on the size distribution of K⁺, Cl^-, Na⁺, and F^- and has a weak impact on the size distributions of NH₄⁺, Ca²⁺, NO₃^- and SO₄^2-.     

基于单颗粒质谱信息气溶胶分类方法的研究进展

气溶胶质谱仪在对气溶胶颗粒的监测过程中会产生大量单颗粒的化学成分和粒径信息,基于这些质谱数据能够推测颗粒的来源。而对气溶胶来源的分析,很大程度上是由颗粒的种类决定的,故对海量数据的分类就成为不可忽略的步骤。针对气溶胶质谱仪采集到的数据,概述了用于气溶胶分类的多种方法的理论核心、分类步骤及各自的优缺点等。据此可为今后气溶胶分类方法的研究提供建设性意见。     

聚合氯化铁-聚(环氧氯丙烷-二甲胺)复合絮凝剂在模拟水处理中的混凝特性研究

制备出一系列具有不同聚合氯化铁(PFC)的碱化度(B)、不同聚(环氧氯丙烷-二甲胺)[P(EPI-DMA)]质量分数[ω(E)]和黏度(η)的PFC-P(EPI-DMA)复合混凝剂,并将其用于模拟染料废水和模拟天然地表水的絮凝脱色处理,对比探讨了ω(E)、η和B对PFC-P(EPI-DMA)中铁的形态分布及其混凝效果的影响,以及混凝作用机制.结果表明,复合絮凝剂中铁的有效形态含量随ω(E)的增大而不断降低;η=850 mPa.s时,复合混凝剂中铁的有效形态含量最高;随B值的增大,Feb含量先增大后减少,而Fec含量逐渐增大.一定程度上使用预水解程度较低、有机成分黏度较大的PFC-P(EPI-DMA)有利于混凝效果的提高,复合混凝剂中有机成分质量分数对混凝效果的影响则与处理对象有关.在模拟水处理中,复合混凝剂依靠电性中和及架桥吸附能力发挥混凝特性.     

Homogeneous and heterogeneous reactions of anthracene with selected atmospheric oxidants

The reactions of gas-phase anthracene and suspended anthracene particles with O3 and O3-NO were conducted in a 200-L reaction chamber, respectively. The secondary organic aerosol (SOA) formations from gas-phase reactions of anthracene with O3 and O3-NO were observed. Meanwhile, the size distributions and mass concentrations of SOA were monitored with a scanning mobility particle sizer (SMPS) during the formation processes. The rapid exponential growths of SOA reveal that the atmospheric lifetimes of gas-phase anthracene towards O3 and O3-NO are less than 20.5 and 4.34 hr, respectively. The particulate oxidation products from homogeneous and heterogeneous reactions were analyzed with a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer (VUV-ATOFMS). Gas chromatograph/mass spectrometer (GC/MS) analyses of oxidation products of anthracene were carried out for assigning the time-of-flight (TOF) mass spectra of products from homogeneous and heterogeneous reactions. Anthrone, anthraquinone, 9,10- dihydroxyanthracene, and 1,9,10-trihydroxyanthracene were the ozonation products of anthracene, while anthrone, anthraquinone, 9-nitroanthracene, and 1,8-dihydroxyanthraquinone were the main products of anthracene with O3-NO.