TSP-PM10-PM2.5-2型中流量大气颗粒物采集系统的开发和应用

自行开发并研制了TSP-PM10-PM2.5-2型中流量TSP、PM10、PM2.5大气颗粒物采集系统,是目前中国唯一可以采集TSP、PM10、PM2.5样品并提供足够的样品量进行大气颗粒物化学成分分析的中流量大气颗粒物采集器.该系统精心设计和加工的限流孔可以保持完全固定的流量,保证切割粒径的稳定,减小采样的误差并方便操作.该系统已经成功地应用于20多个城市和地区大气颗粒物的监测和研究中,为研究大气颗粒物的污染状况和来源提供了有效的技术手段和支持.     

多通道PM_(2.5)采样器的设计及与进口采样器比对测试

设计了多通道大气颗粒物采样器,可同时采集4个通道的PM_(2.5)样品,灵活配置采样通道的开启,每个通道单独设置质量流量计,采用闭环反馈技术,通过比例阀、流量传感器及流量控制板共同控制和校正采样流量,保证通道流量的稳定性。与单通道采样器(BGI PQ 200)进行了为期30 d的比对测试,结果表明,多通道采样器斜率、截距和相关系数均符合《环境空气颗粒物(PM10和PM_(2.5))采样器技术要求及检测方法》(HJ 93—2013)的要求,可满足实际应用需求。     

用于挥发性颗粒物连续测量的冲击式采样器设计

为了实现滤膜式PM2.5测量仪中挥发性颗粒物的连续补偿测量,根据挥发性颗粒物加热挥发、冷却凝结的物理特性,利用冷凝装置和串级冲击采样器原理,设计了双通道的挥发性颗粒物连续采样测量装置。按照采样粒径为10、5、2.5μm的颗粒物设计了3级冲击采样器,通过理论计算得到了采样器的孔径、孔数等相关参数;对采样器中采集的样品使用石英晶体微天平(QCM)直接测量,并采用加热清洗的方式结合双通道的设计实现挥发性颗粒物的连续采样测量。该装置不但可以应用于目前滤膜式颗粒物监测仪中的挥发性颗粒物补偿测量,使测量结果更加准确可靠;也可直接应用于挥发性颗粒物的测量分析。     

矩形喷嘴PM2.5惯性冲击采样器的研制

惯性冲击器是最重要的颗粒物采样器之一,被广泛用于大气颗粒物的分级采样。设计了一种中流量的矩形喷嘴PM2.5惯性冲击采样器。根据Marple准则设计了冲击器的结构参数,用CFX软件进行了惯性冲击器内部气固两相流场的CFD模拟,得出了惯性冲击器的最优结构参数。根据得出的最优设计参数,进行了PM2.5惯性冲击器样机的结构设计,并在实验室用APS气溶胶空气动力学粒度仪进行了标定。实验标定和CFD数值模拟的结果基本吻合,当采样流量为100L/min,冲击器的切割粒径dp50=2.55μm,切割锐度σg=1.4,满足设计要求。     

大气颗粒物粒度分布规律的研究

我们从一九八七年秋开始到一九八八年夏,对沈阳市区内四种功能区和对照区,按四季进行了大气颗粒物粒度分布的测定和其规律的研究.1.实验颗粒物的粒度分布对于大气环境多用质量表示,即大气颗粒物某个粒径区间的质量占质量的百分数.测定粒度分布有多种方法.但目前质量分布普遍应用的是大流量多段冲击采样器,大流     

自动(仪器法)和手工(化学法)监测二氧化硫的相关性及两种方法对比试验的探讨

(一)实验仪器:自动仪器采用美国TE公司的43型二氧化硫分析仪、化学法采样器,因当时尚无专用采样器,采用真空泵作动力、限流孔控制流量,用大口冷藏瓶盛水维持采样吸收液(TCM)8—12℃的温度.样品分析用721型分光光度计、盐酸副玫瑰苯胺法.(二)对比试验方法:采用两种监测方法各用两套仪器平行对比的方法.对比前先校正仪器.自动仪器校零校标.然后两套仪器平行测定空气中二氧化硫,使平行日平均浓度连续3天,每天相差不大于15%.化学法采样装置首先选择合乎要求的采样管,在装     

澳门地区PM_(10)粒度分布的分形特征研究

采集澳门地区不同区域大气PM10样品,根据单颗粒图像分析方法分析了PM10的粒径分布,计算了各采样点PM10粒度分布的分形维数,分析讨论了PM10粒度分布分形维数的变化与粒度分布的关系,分析了粒度分布分形维数表征的澳门大气PM10不同采样点、不同季节的粒度整体分布及其影响因素之间的关系。结果表明,澳门地区PM10粒度分布的分形维数在2.05~3.95之间,夏季PM10的粒度分布分形维数(2.88)大于冬季(2.63),表明夏季PM10的粒度普遍较冬季的细。同一季节不同区域大气PM10的粒度也有较大变化,夏季时,澳门岛的总体颗粒物、矿物颗粒和烟尘颗粒物的分形维数较氹仔岛的偏大,即澳门岛的颗粒物比氹仔岛偏细,而冬季则相反,冬季时,澳门岛的总体颗粒物、矿物颗粒和烟尘颗粒物的分形维数较氹仔岛的偏小。     

一次连续在线观测分析天津市细颗粒物污染特征

根据2005年的5月17日—5月23日GR IMM(1.109#)谱分析仪在线观测结果考察天津市细颗粒物浓度和质量浓度特征。观测期间,天津市颗粒物数浓度平均值为1 124 cm-3,粒径分布为0.25μm~0.60μm,98.5%粒子的粒径0.65μm。同期PM10日均质量浓度值为204μg/m3,ρ(PM2.5)为104μg/m3,ρ(PM1.0)为82.9μg/m3。ρ(PM1.0)/ρ(PM2.5)超过80%,粒径1μm超细颗粒物为天津城市大气颗粒物的主要成分。     

主动采样技术在中国大气POPs监测中的应用

为了履行斯德哥尔摩公约,查明持久性有机污染物(POPs)在中国大气环境介质的存在水平,该研究首次采用主动采样技术,在中国境内大尺度范围内进行了环境大气中POPs的监测工作.利用主动采样技术,可以在短时间内采集数百立方米的大气样品.分别利用玻璃纤维滤膜采集大气颗粒物(固相)中的POPs,同时使用聚氨酯泡沫(PUF)吸附气态的POPs.该采样技术还便于样品的运输和保存.研究表明,大气主动采样技术可以很好地运用于区域大气POPs的监测工作并填补了我国在POPs履约监测中专用仪器设备的空白.     

β射线吸收法双通道PM_(2.5)/PM_(10)监测装置性能探究

根据中国环境保护产品认证标准(CCEP)的技术规范,结合美国环境保护署(EPA)关于环境空气监测参考指标和等效检测方法,对赛默飞世尔最新开发的双通道颗粒物自动监测装置的主要性能指标进行分析表征。用3台待测双通道5028i型和2台参照单通道5014i型颗粒物自动监测装置连续2个月自动监测大气颗粒物PM2.5和PM10,考察双通道颗粒物自动监测装置关于仪器精度、仪器准确度、流量稳定性和准确性等方面的性能。     

灰霾污染和清洁过程中污染物垂直结构特征

针对无锡地区2013年11月6—13日经历的灰霾污染和清洁过程,采用地基遥感激光雷达对空气中的气溶胶颗粒物垂直分布进行垂直探测,发现污染时段气溶胶颗粒物主要积聚在1.8 km以下,消光系数的日均值统计表明,从近地面至高空1.5 km,颗粒物产生的峰值消光系数稳定在0.2 km~(-1);而清洁时段,由于垂直扩散条件改善,颗粒物随高度增加明显减少,1.5 km处的消光系数不足0.05 km~(-1)。同时发现污染时段中,近地面PM_(10)、PM_(2.5)、碳黑(BC)的平均浓度分别是清洁时段的2.48、2.76、3.66倍;大气氧化剂(O3和NO_x的总和)平均值水平是清洁时段的1.73倍。气象条件分析发现,锋面的移动使大气水平、垂直对流运动加剧,污染物得以迅速扩散,空气质量转好,这也是此次污染清除的主要原因。     

相似案例比对法在空气质量精细化预报中的应用

2018年首届中国国际进口博览会期间,为开展精细化的空气质量保障预报,以2015年11月13-16日为相似案例,与2018年11月8-11日上海地区的天气要素和PM2.5浓度变化进行相似性分析。结果显示,2个案例中地表压强、地表温度、相对湿度、混合层高度和风向5项主要天气要素的相关系数为0. 66~0. 93,相似离度为0. 09~0. 26,PM2.5浓度的相关系数达0. 8左右,相似离度为0. 2。针对2015年案例的污染过程分析,不仅为2018年案例中的污染时段预报提供了参考,也为空气质量保障工作的管控决策提供了支持。     

从大运会期间浓度变化来分析污染物削减措施效果

运用深圳以及周边城市的环境空气污染物浓度资料,分析了NO2、PM10、PM2.5的分布特征,重点讨论了大运会期间NO2、PM10和PM2.5浓度的变化规律,应用相似气象条件的概念,采取多种空间、时间对比分析的方法,排除客观因素,分析了大运会期间人为减排的具体效果,结果表明:大运会期间控制措施效果显著,PM10削减比例更大,也即大运会期间关停了一些高污染排放企业对污染浓度的影响更明显。大运会期间控制措施对各污染浓度的下降起一定作用,作用在白天时段更明显,且对PM2.5的控制效果更显著。大运会期间南山区管控效果最明显,中心福田区PM2.5控制最好。大运会期间的区域联合控制成效显著。大运会后期控制措施的解除,致使污染物浓度快速上升到较高水平,且工业布局密集的区域及机动车流量最大的区域上升幅度相应较大。     

Atmospheric aerosols at a regional background Himalayan site—Mukteshwar, India

Continuous aerosol measurements were made at a regional background station (Mukteshwar) located in a rural Himalayan mountain terrain from December 2005 to December 2008 for a period of 3 years. The average concentrations of particulate matter less than or equal to 10 μm (PM₁₀), particulate matter less than or equal to 2.5 μm (PM_2.5) and black carbon (BC) are 46.0, 26.6 and 0.85 μg/m³ during the study period. Majority of the PM₁₀ values lie below 100 μg/m³ while majority of the PM_2.5 values lie below 30 μg/m³. It is further seen that during the monsoon months, especially July and August, the average values are comparatively low. It is also noted that the PM_2.5/PM₁₀ ratios between 0.50 and 0.75 have the maximum frequency distribution in the data set. Furthermore, the monthly mean ratio of BC to PM_2.5 mass lies between 3.0 and 7.5 % during the study period. Though the average PM₁₀ and PM_2.5 concentrations during the study period are less than the respective Indian ambient air quality standards, however, they are still above the WHO guidelines and would have adverse health impacts. This shows that even in rural/background regions that are far away from major pollution sources or urban areas, the aerosol concentrations are significant and require long-term monitoring, source quantification and aerosol model simulations.     

广州市春季一次沙尘天气过程综合观测

2017年4月21—23日广州市经历了一次远距离传输的沙尘天气过程,为了解沙尘过程对广州市空气质量的影响,基于广州市大气超级站,利用单颗粒气溶胶质谱(SPAMS)、气溶胶激光雷达观测数据并结合HYSPLIT后向轨迹模型分析了沙尘过程细颗粒物组分及污染来源贡献变化和沙尘气溶胶的来源及路径。结果表明:受沙尘过境影响,PM_(10)浓度大幅升高,PM_(2.5)/PM_(10)最小值仅为12.1%;沙尘过境期间影响近地面颗粒物的沙尘高度主要分布在1 km以下区域,近地面颗粒物消光系数均值为100.11 Mm~(-1),探测到最大退偏振比为0.28。SPAMS研究发现沙尘过境期间含硅酸盐颗粒物(SI)的细颗粒物数浓度比例达25.9%,是沙尘过境前的1.4倍;PM_(2.5)中扬尘贡献率明显增大,达到了17.3%,是沙尘过境前的1.9倍。后向轨迹模型HYSPLIT显示此次沙尘为典型的北方沙尘传输,沙尘源自中国西北地区,传输方向为自西北输送至华东地区后,转为东南方向影响广州市。     

Aerosol characteristics of different types of episode

Daily and hourly average data from nine air-quality monitoring stations distributed across central Taiwan, which include ten items (i.e., PM₁₀, PM_2.5, wind direction, wind speed, temperature, relative humidity, SO₂, NO₂, NO, and CO), were collected from 2005 to 2009. Four episode types: long-range transport with dust storms (DS), long-range transport with frontal pollution (FP), river dust (RD), and stagnant weather (SW), and one mixed type of episode were identified. Of these four episode types, the SW was the dominant type, averaging about 70 %. The mean ratio of PM_2.5/PM₁₀ was the lowest during the RD episodes (0.42), while the mean ratio of PM_2.5/PM₁₀ was the highest during the SW episodes (0.64). Fine aerosol (PM_2.5) and coarse aerosol (PM_10–2.5) samples were collected by high-volume samplers for chemical composition analysis, from only three stations (Douliou, Lunbei, and Siansi) during the days of SW, RD, DS, and FP. The concentrations of PM_2.5 and three ionic species (NH₄ ⁺, NO₃ ^?, and SO₄ ^2?) all showed significant differences among the four episode types. The highest levels of NO₃ ^? (12.1 μg/m³) and SO₄ ^2? (20.5 μg/m³) were found during the SW and FP episodes, respectively. A comparison on the spatial similarity of aerosol compositions among the episodes and/or non-episodes (control) was characterized by the coefficient of divergence (CD). The results showed higher CD values in PM_10–2.5 than in PM_2.5, and the CD values between RD episodes and the other three episodes were higher than those between two types of episode for the other three episodes. The ratios of SOR (sulfur oxidation ratio), SO₄ ^2?/EC (elemental carbon), NOR (nitrogen oxidation ratio), and NO₃ ^?/EC showed that sulfate formation was most rapid during the FP, while nitrate formation was most rapid during the SW.     

Concentrations of PM2.5-associated OC, EC, and PCDD/Fs measured during the 2003 wildfire season in Missoula, Montana

Throughout August and September, 2003, wildfires burned in close proximity to Missoula, Montana, with smoke emanating from the fires impacting the valley for much of the summer. This presented the perfect opportunity to measure the levels of polychlorinated dibenzodioxins and dibenzofurans (PCDD/F) comprising ambient forest fire smoke particles impacting the Missoula Valley. An air sampler at the Montana Department of Environmental Quality's (DEQ) compliance site in Missoula measured hourly averages of PM₁₀ throughout the fire season. Three collocated PM_2.5 cyclones collected 24-h smoke samples using quartz filters and Polyurethane Foam (PUF) sorbent cartridges. From the quartz filters, concentrations of Organic and Elemental Carbon (OC/EC) were measured, while PCDD/F were measured from one set of a filter (particle phase) and PUF (vapor phase) aggregate of samples in an attempt to also investigate the different phases of PCDD/F in forest fire smoke impaired communities.Hourly PM₁₀ concentrations peaked at 302.9 μg m⁻³ on August 15. The highest OC concentration (115.6 μg m⁻³) was measured between August 21–22, and the highest EC concentration of 10.5 μg m⁻³ was measured August 20–21. Measurable concentrations of PM_2.5 associated PCDD/Fs were not detected from a representative aggregate sample, with the exception of small amounts of 1,2,3,4,6,7,8-heptachlorodibenzodioxin and octachlorodibenzodioxin. PM_2.5 samples collected during the smoke events were composed of approximately 65% OC. However, the OC fraction of the particles collected in the smoke impaired Missoula valley was not composed of significant amounts of PCDD/F.     

Influence of Meteorological Parameters on Particulates and Atmospheric Pollutants at Taichung Harbor Sampling Site

Atmospheric aerosol particles and metallic concentrations, ionic species were monitored at the Experimental harbor of Taichung sampling site in this study. This work attempted to characterize metallic elements and ionic species associated with meteorological conditions variation on atmospheric particulate matter in TSP, PM_2.5, PM_2.5–10. The concentration distribution trend between TSP, PM_2.5, PM_2.5–10 particle concentration at the TH (Taichung harbor) sampling site were also displayed in this study. Besides, the meteorological conditions variation of metallic elements (Fe, Mg, Cr, Cu, Zn, Mn and Pb) and ions species (Cl⁻, NO₃ ⁻, SO₄ ²⁻, NH₄ ⁺, Mg²⁺, Ca²⁺ and Na⁺) concentrations attached with those particulate were also analyzed in this study. On non-parametric (Spearman) correlation analysis, the results indicated that the meteorological conditions have high correlation at largest particulate concentrations for TSP at TH sampling site in this study. In addition, the temperature and relative humidity of meteorological conditions that played a key role to affect particulate matter (PM) and have higher correlations then other meteorological conditions such as wind speed and atmospheric pressure. The parameter temperature and relative humidity also have high correlations with atmospheric pollutants compared with those of the other meteorological variables (wind speed, atmospheric pressure and prevalent wind direction). In addition, relative statistical equations between pollutants and meteorological variables were also characterized in this study.     

杭州秋冬季PM2.5污染特征分析

为研究杭州PM_2.5污染来源特征,利用2013—2019年杭州市PM_2.5监测数据和气象观测数据,分析了杭州市2013—2019年PM_2.5浓度变化,选取本地积累型和输入型2种PM_2.5污染过程,结合单颗粒气溶胶飞行时间质谱仪（SPAMS）和在线离子色谱数据,探讨杭州市PM_2.5化学组分和污染来源。结果表明：每年秋冬季（11月至次年3月）杭州以东北风、西北风及偏南风为主,风速低于4 m/s时,大气扩散条件差,受本地污染物积累影响,PM_2.5浓度容易出现超标;风速较大且为东北风和西北风时,受上游污染输入影响,易出现PM_2.5重度污染。本地积累型和输入型案例中,PM_2.5化学组分中占比最大的为NO₃^-、SO₄^2-和NH₄⁺;PM_2.5浓度上升过程中,二次NO₃^-和SO₄^2-转换率明显上升,其中NO₃^-上升更为显著,二次气溶胶污染严重。2次案例中,PM_2.5来源贡献占比前3位均为机动车尾气源、燃煤源和工业工艺源,其中本地积累型PM_2.5浓度上升阶段,机动车尾气源占比会明显上升;输入型案例中,输入阶段机动车尾气源占比显著上升,燃煤源贡献也小幅上升。     

APEC期间京津冀及周边地区PM2.5中碳组分变化特征及来源

在APEC会议期间和会期之后,分别采集北京、天津、石家庄、保定、济南5个采样点的PM2.5样品,通过分析碳组分的变化特征,研究京津冀地区污染物减排的影响以及减排后各指标的变化特征,分析大气颗粒物中碳气溶胶的可能来源。采用重量法测定组分中PM2.5的含量,利用热/光碳分析仪测定组分中OC、EC的含量,结果表明,由于采取了污染源减排措施,会议期间PM2.5、OC、EC的质量浓度均低于会期之后;会议期间和会期之后OC与EC均表现出了较好的相关性,r2为0.789~0.983,说明OC与EC的排放源基本相同;会议期间OC/EC为3.11~3.62,表明含碳气溶胶的来源主要是机动车排放,同时也存在一定的燃煤排放,会期之后为3.08~6.10,表明燃煤的排放在碳气溶胶中的比重明显增加,另外OC/EC也表明APEC会议期间和会期之后二次有机碳在各采样点均普遍存在。