基于TEM-EDS对四川盆地大气单颗粒气溶胶的研究

为了解四川盆地大气中单颗粒气溶胶理化特征,分别在该区域典型城市（成都市）和背景地区（峨眉山）进行了大气单颗粒样品采集.基于带能谱的透射电子显微镜（TEM-EDS）对两地累计3923个单颗粒的化学组成、形貌特征及混合状态等进行了全面观测和分析,并对两地颗粒物差异性进行了对比分析.结果发现：两地气溶胶颗粒主要包括有机物、富硫、矿物、烟尘和飞灰/金属颗粒,除了以单独的外混形式存在外,大多数颗粒以两种及两种以上颗粒类型混合（即内混）形式存在.通过对成都市不同污染状况下单颗粒特征对比发现,"污染天"的内混颗粒占比高于"清洁天",分别为74.2%和68.6%;相比"清洁天","污染天"颗粒物粒径分布范围更广且峰值区间更大,表明污染过程中颗粒物的大气混合趋于更强.对比成都市与峨眉山分析结果得知,成都市以内混的有机物-硫颗粒为主导（占比为50.2%）,而峨眉山以外混的有机物颗粒为主导（占比为50.5%）;成都市含硫类颗粒物（如有机物-硫颗粒）贡献高于峨眉山,而峨眉山两种含碳类颗粒（如烟尘和有机物-烟尘颗粒）占比高于成都市;此外,成都市与峨眉山两地大气颗粒物粒径分布范围及峰值区间均存在一定差异,进一步体现了两地颗粒物来源和老化混合的差异.在峨眉山,与非降雨天相比,一些易溶于水的颗粒物（如含硫类颗粒）在降雨天占比明显降低,而源自当地燃烧过程、粒径较小且疏水性强的颗粒物（如烟尘和有机物-烟尘颗粒）占比相应升高.     

由贵金属取代的钙钛矿催化剂对碳烟的催化性能

用柠檬酸法制备了不同贵金属取代的钙钛矿LaCo0.96X0.04O3(X为Pt、Pd、Rh、Au、Ag)催化剂,用热重法测试了催化剂对碳烟的催化活性,采用程序升温还原法(H2-TPR)、X-射线衍射仪(XRD)、能量谱仪(EDS)和红外光谱(FTIR)对催化剂进行了测试.结果表明,催化剂LaCo0.96Ag0.04O3催化活性最高,起燃温度为449℃,远低于LaCoO3的504℃;各贵金属取代的钙钛矿LaCoO3的TPR还原峰变化各异;XRD特征峰的衍射角向高角度偏移,说明各贵金属进入了钙钛矿结构相;能谱图显示各贵金属进入钙钛矿相的量不同.     

柴油车排气微粒后处理器的研究

通过同种典型微粒过滤器的比选试验,表明高效袋式消烟器微粒捕集效率最高.其结构简单,成本低,耐热性好,因此具有很好的推广价值.如果应用在公路隧道中,能降低隧道内能见度的影响,具有较大的开发前景.      

Interfacial effects of suspended particles on biodegradation of N (2,4 dimethyl phenyl) N'' methylformamidine hydrochloride and dibutyl phthalate in waters

ＩｎｔｅｒｆａｃｉａｌｅｆｅｃｔｓｏｆｓｕｓｐｅｎｄｅｄｐａｒｔｉｃｌｅｓｏｎｂｉｏｄｅｇｒａｄａｔｉｏｎｏｆＮ（２，４ｄｉｍｅｔｈｙｌｐｈｅｎｙｌ）Ｎ’ｍｅｔｈｙｌｆｏｒｍａｍｉｄｉｎｅｈｙｄｒｏｃｈｌｏｒｉｄｅａｎｄｄｉｂｕｔｙｌｐｈｔｈ...     

北京市大气细粒子的来源分析

细粒子(空气动力学直径小于2.5μm的颗粒物)污染是许多城市重要的大气环境问题.从1999年至2000年对北京市细粒子展开了4次采样和化学分析,有效采样天数为40d.利用正定矩阵分解(PMF)方法对细粒子的来源进行了分析.化学成分包括EC(元素碳)、有机物、SO₄^2-、F^-、Cl^-、Fe、Ca、K、Mg、Al、Na、Zn、Mn、Ti、Pb、Ba和P等17种.发现主要来源有6类:地面扬尘、建筑源、生物质燃烧、二次源、机动车排放和燃煤.     

2000~2020年天津PM2.5质量浓度演变及驱动因子分析

基于中国大气成分实时追踪数据集、天津气象局和生态环境局长序列PM_2.5质量浓度和气象观测,结合MEIC排放清单和环境模式构建的细颗粒气象条件扩散指数,研究2000～2020年天津地区PM_2.5质量浓度演变规律及驱动因子,以期更科学地分析气象对大气环境影响,为“十四五”期间深度环境治理提供支撑.结果表明,2000～2020年天津PM_2.5质量浓度呈现3个阶段变化,第一阶段2000～2007年,呈现持续地上升,其变化速率为4.58μg·（m³·a）^-1,该阶段排放量的快速增加是主导因素,其作用是气象条件年际波动影响的4倍,排放量增加使得PM_2.5质量浓度增加45.3%;第二阶段为2007～2013年,该阶段PM_2.5质量浓度呈现波动变化,出现了两个浓度峰值年（2007年和2013年）,该阶段排放稳定,气象条件年际波动对PM_2.5质量浓度年际波动产生重要影响,两者相关系数0.81;第三阶段为2013～2020年,PM<...     

夏季持续高温天气对北京市大气细粒子(PM2.5)的影响

在1999-06-23北京市出现长达13d的持续高温期间对细粒子(PM_2.5)质量浓度进行了观测.数据表明,持续高温期间细粒子质量浓度比非高温期间要高出2～3倍.但是通过对持续高温期间的气象数据进行分析,发现还是很利于污染物扩散.进一步分析同步监测的O₃浓度、颗粒物中SO₄^2-的粒径范围及其含量等数据,发现夏季持续高温期间活跃的光化学反应应该是北京市细粒子的主要来源.     

Second organic aerosol formation from the ozonolysis of -pinene in the presence of dry submicron ammonium sulfate aerosol

An indoor chamber facility is described for investigation of atmospheric aerosol chemistry. Two sets of α-pinene ozonolysisexperiments were conducted in the presence of dry ammonium sulfate seed particle: ozone limited experiments and α-pinene limitedexperiments. The concentration of gas phase and particle phase species was monitored continuously by on-line instruments andrecorded automatically by data sampling system. The evolution of size distribution was measured by a scanning mobility particlesizer (SMPS), and α-pinene consumed was measured using GC-FID. Secondary organic aerosol (SOA) produced for seed-free systemis 100% organic in content, resulting from a sufficient supersaturation of low volatility organics to produce homogeneous nucleationfollowed by condensation to the aerosol. Secondary organic aerosol produced in seeded system is a mixture of organic and inorganicconstituents, initially forms via condensation onto the inorganic particles, and subsequent growth occurs via absorption into the organicsurface coating the inorganic core. Although the formation process and the size distribution for seed-free system and seeded system isdifferent, the ultimate mass of SOA formed is equal, and SOA yield for the two system located in the same regression line when usingone-product model, suggesting that the presence of dry ammonium sulfate seed has no measurable effect on the total aerosol yield, and the dry seed particle acts solely as a site upon which organic deposition occurs.     

工业燃煤链条炉细粒子排放特征研究

链条燃煤锅炉是当前我国工业锅炉的最主要应用炉型,其容量占到了工业锅炉总容量的85%,是重要的大气污染物排放源之一.本研究在3个地区选取了5种典型容量的链条炉,应用自行设计的二级稀释系统现场测试其细粒子（PM_2.5）和各种气态污染物的排放特征.结果表明,链条炉烟气中的PM_2.5质量粒径呈单峰或双峰分布,第1个峰值在0.14 μm处,第2个峰值在1 μm后;湿法除尘和旋风除尘对PM_1.0的细粒子仍具有有效的去除效率;在相同或相似除尘控制技术的条件下,PM_2.5的排放水平随锅炉容量的增大而减小.在PM_2.5中,SO^2-₄是最丰富的离子,质量分数在20%～54%范围内;C是最丰富的元素,质量分数在7.5%～31.8%之间,其次是S,质量分数为8.4%～18.7%.采用碳平衡法计算得出PM_2.5、NO_x和SO₂的排放因子分别为0.046～0.486 　g·kg^-1、 1.63～2.47　g·kg^-1、 1.35～9.95　g·kg^-1,这为建立我国的工业锅炉排放清单及大气污染来源分析提供了必要的基础数据.     

Dry deposition velocity of total suspended particles and meteorological influence in four locations in Guangzhou, China

Dry deposition velocity of total suspended particles (TSP) is an effective parameter that describes the speed of atmospheric particulate matter deposit to the natural surface. It is also an important indicator to the capacity of atmosphere self-depuration. However, the spatial and temporal variations in dry deposition velocity of TSP at different urban landscapes and the relationship between dry deposition velocity and the meteorological parameters are subject to large uncertainties. We concurrently investigated this relationship at four different landscapes of Guangzhou, from October to December of 2009. The result of the average dry deposition velocity is (1.49 ± 0.77), (1.44 ± 0.77), (1.13 ± 0.53) and (1.82 ± 0.82) cm/sec for urban commercial landscape, urban forest landscape, urban residential landscape and country landscape, respectively. This spatial variation can be explained by the difference of both particle size composition of TSP and meteorological parameters of sampling sites. Dry deposition velocity of TSP has a positive correlation with wind speed, and a negative correlation with temperature and relative humidity. Wind speed is the strongest factor that affects the magnitude of TSP dry deposition velocity, and the temperature is another considerable strong meteorological factor.We also find out that the relative humidity brings less impact, especially during the dry season. It is thus implied that the current global warming and urban heat island effect may lead to correlative changes in TSP dry deposition velocity, especially in the urban areas.