镍/铁二元金属对莠去津脱氯特性的影响

为了考察Ni/Fe二元金属对莠去津的催化还原特性,分别以Fe粉和Ni/Fe体系作为还原和催化剂,在酸性条件下对莠去津的脱氯特性进行比较,并讨论了pH值,Ni/Fe配比以及金属添加量等因素对莠去津脱氯效率的影响.结果表明:与Fe粉比较,Ni/Fe体系对莠去津具有很明显的催化脱氯特性.在pH=2时,1.22%(W/W)Ni/Fe体系30min对莠去津的脱氯效率大于90%,相同条件下用Fe粉还原时,90min脱氯效率仅为22.21%通过Fe粉和Ni/Fe表面形态的比较以及实验结果的分析,对Ni/Fe体系的催化还原脱氯机理进行了初步探讨.     

Transfer and transport of aluminum in filtration unit

Aluminum salt coagulants were used prevalently in various water works.In this article,the effects of filtration on residual aluminum concentration and species distribution were researched by determining the concentration of diiferent aluminum species before and after single layer filter,double layer filter,and membrane filtration units.In the research,size exclusion chromatography(SEC)was used to separate colloidal and soluble aluminum,ion exchange chromatography(IEC)was used to separate organic and inorganic aluminum, and inductivity coupled plasma-atomic emission spectrometry(ICP-AES)was used to determine the aluminum concentration.The results showed that the rapid filtration process had the ability of removing residual aluminum from coagulant effluent water,and that double layer filtration was more effective in residual aluminum removal than single layer filtration,while nano filtration was more effective than micro filtration.It was found that when the residual aluminum concentration was below 1mg/L in sediment effluent,the residual aluminum concentration in treated water was above 0.2 mg/L.The direct rapid filtration process mainly removed the suspended aluminum.The removal of soluble and colloidal aluminum was always less than 10% and the natural small particles that adsorbed the amount of soluble or small particles aluminum on their surface were difficult to be removed in this process.Micro filtration and nano filtration were good technologies for removing aluminum;the residual aluminum concentration in the effluent was less than 0.05 mg/L.     

Heterogeneous uptake of NO2 on soils under variable temperature and relative humidity conditions

Heterogeneous reactions of nitrogen dioxide (NO₂) on soils collected from Dalian (S1) and Changsha (S2) were investigated over the relative humidity (RH) range of 5%-80% and temperature range of 278-328 K using a horizontal coated-wall flow tube. The initial uptake coefficients of NO₂ on S2 exhibited a decreasing trend from (10 ± 1.3) × 10^-8 to (3.1 ± 0.5) × 10^-8 with the relative humidity increasing from 5% to 80%. In the temperature effect studies, the initial uptake coefficients of S1 and S2 decreased from (10 ± 1.2) × 10^-8 to (3.8 ± 0.5) × 10^-8 and from (16 ± 2.2) × 10^-8 to (3.8 ± 0.4) × 10^-8 when temperature increased from 278 to 288 K for S1 and from 278 to 308 K for S2, respectively. As the temperature continued to increase, the initial uptake coefficients of S1 and S2 returned to (7.9 ± 1.1) × 10^-8 and (20 ± 3.1) × 10^-8 at 313 and 328 K, respectively. This study shows that relative humidity could influence the uptake kinetics of NO₂ on soil and temperature would impact the heterogeneous chemistry of NO₂.     

1~3 nm颗粒物在粒径分布测量仪中的通过效率研究

基于二甘醇的扫描电迁移率粒径谱仪(DEG-SMPS)是常用的1～3 nm颗粒物粒径分布测量系统.目前对1～3 nm颗粒物在该系统中通过效率的量化不够准确,这给大气颗粒物粒径分布的测量带来了较大的不确定性.本文研究了1～3 nm颗粒物和离子在直管、弯管以及气溶胶中和器等系统组件中的通过效率,并使用等效管长法来量化颗粒物在这些组件单元中的通过效率.研究表明,1～3 nm颗粒物在直管内的通过效率不受颗粒物电性影响,且可以由Gormley-Kennedy (G-K)方程估算.当采样流量为2.5 L·min~(-1)时,DEG-SMPS系统中总等效管长约为433 cm,其中气溶胶中和器的等效管长为160 cm,弯头的等效管长为33 cm.     

Size, composition, and mixing state of individual aerosol particles in a South China coastal city

Aerosol samples were collected in summer in Macao,a coastal city of the Pearl River Delta Region in China.Morphology,size,elemental composition,and mixing state of individual aerosol particles were determined by scanning electron microscopy coupled energy dispersive X-ray(SEM/EDX) and transmission electron microscopy(TEM).Based on the morphologies of 5711 aerosol particles,they consist of soot(32%),mineral(17%),secondary(22%),and unknown fine particles(29%).The sizes of these particles were mostly distributed between 0.1 and 0.4 μm.Compositions of 202 mineral particles were obtained by SEM/EDX.Mineral particles were mainly classified into three types:Si-rich,Ca-rich,and Na-rich.The compositions of typical mineral particles can indicate their sources in sampling location.For example,mineral particles,collected along the main street,were associated with trace amounts of heavy metals,such as Zn,Ti,Mn,Ba,Pb,and As.TEM observations indicate that most Na-rich particles were aged sea salt particles(e.g.,Na2SO4 and NaNO3) which formed through heterogeneous chemical reactions between sea salt and acidic gases.Additionally,aging time of soot was short in Macao due to high humidity,high temperature,and high levels of sunlight in Macao.Most of soot and fine mineral dust particles were internally mixed with secondary particles.     

基于细微粒子污染的灰霾判定方法的研究

本文从细微粒子污染导致灰霾形成的角度出发,首先开展了灰霾监测实验,并对实验数据进行频数和描述性分析,研究了以PM10为主的细微粒子污染与灰霾的影响关系。确定了以PM10日平均浓度为灰霾目的判定依据,并根据中国大陆PM10污染指数的分级标准建立了灰霾等级指数,从而形成了一套根据PM10日平均浓度来确定不同等级的灰霾发生概率的方法,为灰霾预测及灰霾治理提供一定的理论依据。     

大气细粒子的快速捕集及化学成分在线分析方法研究

本文介绍了一种新型的大气细粒子快速捕集及其化学成分在线分析方法。该方法中大气细粒子与过饱和水蒸气绝热混和而增长成大粒子 ,并在气流的带动下惯性撞击到一垂直玻璃板上 ,一含有内标物的去离子水流自上而下将撞击到玻璃板上的粒子收集 ,收集液被直接输送到离子色谱、总有机碳分析仪 ,在线分析其中的化学成分。该方法每 12min可完成单个样品分析 ,每小时可连续采集分析 5个样品。离子色谱最低检测限约为 0 .0 5 μg/m3(NH+4 )到 0 .2 0 μg/m3(SO2 -4 ) ,不确定度约为 3 % ,TOC最低检测限为 5× 10 -5μg/m3,不确定度约为 3 %。真实的大气细粒子观测结果表明 ,该方法快速、简捷、灵敏度高 ,是实时监测大气中细粒子化学成分的有效工具     

柴油车尾气碳烟颗粒物催化燃烧催化剂的最新研究进展

柴油车尾气排放的碳烟颗粒已经引起了严重的环境污染问题,必须加以净化处理.柴油车碳烟颗粒的低温燃烧离不开高活性的催化剂.针对柴油车排放的碳烟颗粒物后处理方法中的催化氧化技术,总结了近年来几种主要类型的碳烟燃烧催化剂(贵金属催化剂、碱金属催化剂、单组分过渡金属氧化物催化剂、多组分混合氧化物催化剂和固定结构复合氧化物催化剂)的最新研究进展,并对该研究方向存在的主要问题和应用前景进行了探讨.     

大气PM2.5对巨噬细胞的毒性作用研究

以上海市工业区，交通区、郊区3个功能区的大气PM2.5粒子，对腹腔巨噬细胞进行染毒培养，台酚蓝染色测定细胞存活率，酵母菌吞噬实验测定其吞噬功能，流式细胞仪检测凋亡情况，结果显示，随大气PM2.5粒子浓度增加，巨噬细胞存活率和吞噬功能下降，巨噬细胞出现凋亡，其中交通区大气PM2.5染毒组的观察指标改变较明显，提示了大气PM2.5粒子对巨噬细胞具有细胞毒性，而交通区大气PM2.5粒子的毒性较大。     

复合氧化物催化材料上碳颗粒物的催化燃烧

针对柴油车排放碳颗粒物的控制 ,研制可应用于柴油车排放碳颗粒物催化再生复合氧化物催化材料 .通过运用热分析仪 (TGA)和程序升温氧化反应装置 (TPO)对复合氧化物催化材料的活性进行评价 ,研究了催化材料的组成、原子配比、催化材料与碳颗粒物质量比、H₂O的加入、焙烧温度对催化活性的影响 .实验结果表明 :双组分金属氧化物催化剂中 ,Cu-Mo-O有较好的活性 ;多组分金属氧化物催化剂中 ,Cu-K-Mo-O在原子比Cu∶K∶Mo =1∶1∶2 ,催化剂与碳颗粒物质量比为 5∶1时活性最好 ,其碳颗粒物起燃温度为 32.7℃ ,同时H₂O和焙烧温度对该催化剂的影响较小 ,是能够应用于柴油车排放碳颗粒物控制催化再生的良好催化材料 .