我国固定源大气颗粒物监测技术的现状与改进建议

针对国内固定源大气颗粒物监测技术的现状及不足,通过对资料总结发现国内固定源排放颗粒物的监测技术现状中存在国标精度要求较低和技术细节不足等问题,并重点从分级采样和大气低浓度颗粒物检测方面深入剖析相关技术的不足与需求,并结合国内外的经验,从国标的修订与补充、分级采样技术体系的建立和低浓度大气颗粒物采样方法的改进等3个方面提出技术与设备方面的改进建议。     

国内外烟气流速测量标准比较分析

比较了国内外燃煤电厂烟气流速测量技术及相关标准,分析了测量仪器、矩形烟道采样位置及采样点位置和数目等方面的异同,结合我国电厂现场烟气流速测量的实际情况,提出了修改《固定污染源排气中颗粒物测定与气态污染物采样方法》相关内容的建议。     

固定污染源排放可凝结颗粒物采样方法综述

综述了国内外固定污染源可凝结颗粒物(CPM)冲击冷凝法和稀释冷凝法2种采样方法,指出CPM是固定污染源排放颗粒物的重要组成部分,国内对于固定污染源CPM排放的监测和研究尚处于起步阶段,缺乏必要的CPM采样标准方法。通过分析2种采样方法的优缺点,提出冲击冷凝采样法需进一步降低SO_2等水溶性气体的影响,提高气相CPM冷凝效果及超细颗粒态CPM的捕集效率;稀释冷凝法需提高采样装置的便携性实现可过滤颗粒物(FPM)和CPM的分离采样,提高采样管路壁面颗粒物回收率。同时,针对我国固定污染源如燃煤电厂大量使用湿法脱硫设备的情况,CPM采样方法需提高对低温高湿且夹带液滴烟气采样的适用性。     

固定源排气中可凝结颗粒物排放与测试探讨

阐述了可凝结颗粒物的定义及国内外颗粒物的测定方法,并就可凝结颗粒物的量级及危害进行了初步讨论,提出可凝结颗粒物应为被忽略的固定源颗粒状污染物,揭示出我国现存颗粒物采样方法存在的问题,并对此问题进行探讨,指出下一步工作的方向。     

发展我国大气颗粒物标准样品的国际经验和建议

介绍了国内外大气颗粒物标准样品体系构成及制备技术,分析了我国大气颗粒物标准样品存在的种类和目标组分单一、研制技术薄弱等问题。在借鉴国外发展经验和考虑我国需求和研究能力的基础上,提出了拓宽大气颗粒物标准样品基质和污染物种类、完善标准样品体系、加强合作与科研投入、逐步攻克研制技术难点等对策和建议。     

环境空气颗粒物来源解析受体采样频率优选方法初探

环境空气颗粒物来源解析受体样品化学组成的时空差异,除受采样点位分布制约外,主要还受采样时间的制约。如何选取时间段及采样周期显得尤为重要。通过青岛市空气自动监测系统近几年获取的颗粒物连续时均值数据,采用统计优化组合选择法,筛选出日均值、年均值的最佳采样时段,可供类似研究参考。     

固定源低浓度颗粒物监测技术现状与思考

简述了固定源颗粒物监测技术的国内外现状,建议从规范现有方法和研发新方法入手,对低浓度颗粒物监测方法加以研究和改进。     

大气连续采样的质量保证工作——兼论《大气环境质量考核实施细则》执行中的有关问题(二)

本文简要分析颗粒物及空气湿度对大气24小时连续采样的影响。重点阐明在我国东南部地区的湿热季节大气采样时,应在《大气环境质量考核实施细则》规定的采样仪器基础上,增加过滤除湿单元以提高大气待测成分的吸入效率。     

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。     

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.     

Assessment of elemental concentrations in the urban air (case study: Tehran city)

Tehran is one of the megacities of the world with a population of over eight million. Its air is highly polluted mainly due to the suspended particulate matters, which encompasses a wide spectrum of chemical elements. These elements based on their type, size, and impact on the life cycle have various environmental and heath risks. In this research, the neutron activation method is used to determine the concentration levels of Al, Ba, Fe, Mg, and V in the urban air. Thus, two districts of Tehran with different characteristics are selected. District 21 includes much of the industries located in Tehran metropolitan and is considered as an industrial area. In contrast, district 22 lacks any significant industrial activity. It is a newly established and expanding district adjacent to district 21 with a great deal of constructional activities. For the measurement of the suspended particulate matters in the air, the various sections of the aforesaid districts with industrial, residential, heavily congested traffic, residential/commercial, residential/heavily congested traffic, and residential/industrial classifications were identified. Subsequently, 24 sampling stations were selected. The sampling of the suspended particulate matters was conducted with the aid of a high volume pump containing 125 mm cellulose filters in two different time intervals. After completion of the sampling process, the samples were prepared and sent to the research reactor of the Iran Nuclear Energy Organization for Neutron Activation. During the next steps, the radiations emitted from the samples were registered, the radiation curves were plotted, and the amounts of the trace elements were determined. As a result, the average concentration levels of Al, Ba, Fe, Mg, and V were identified to be 3.301140, 2.273658 × 10, 4.0681696 × 10^???1, 3.5525475 × 10^???1, and 3.04075 × 10^???2 μg/m³, respectively. Moreover, the emission sources of the aforesaid elements into the air were identified. The concentration levels of these elements in the industrial and heavily congested traffic sections were higher. Finally, it was concluded that the statistical analysis of these elements presents a meaningful correlation among them.     

各国环境空气质量评价中污染物浓度表示方法比较

对不同国家在环境空气质量评价中主要污染物浓度表示方法进行了比较和分析,发现各国对于气态污染物浓度的表示方法主要有体积比浓度和质量浓度2种方法,对于颗粒物浓度的表示方法则普遍采用了质量浓度;颗粒物的质量浓度有标况浓度和实况浓度2种表示方法,在中国标况浓度和实况浓度的数值存在较大差异,在不同地区和不同季节此差异大小亦不同,一般情况下,实况浓度低于其标况浓度,且实况浓度能够更加客观反映颗粒物污染状况;建议修订中国环境空气质量标准中颗粒物浓度的表示方法,使用实际状况下的质量浓度来表示空气中颗粒物的浓度,以保证中国与其他国家之间监测数据的可比性。     

灰霾期间气溶胶的污染特征

从颗粒物的时空分布和浓度水平方面综述了灰霾期间气溶胶的污染特征,介绍了灰霾期间气溶胶中金属元素、水溶性离子、有机碳和元素碳的浓度特征,以及颗粒物与能见度的相关性研究进展。指出:灰霾天气多发生在冬季,且气溶胶中PM2.5占的比重大;气溶胶污染与地理环境、气候条件、经济发展水平等有密切关系;水溶性离子多集中在PM2.5中;能见度的下降与气溶胶特别是细颗粒物有很大关系。提出目前灰霾研究中主要存在3大问题:一是对灰霾期间气溶胶中含有的有机物类别及其对不同季节发生灰霾的贡献率仍需进一步研究;二是灰霾期间气溶胶中有机物的形成机理尚不明确;三是不同源排放的气溶胶对灰霾形成的贡献率有待探讨。建议系统地开展大气细颗粒物有害成分的鉴定、源排放颗粒物的物理化学特性、扩散过程中各种物质间的反应和转化等方面的研究,为大气污染防治法规的制定提供依据。     

全流稀释风道机动车排放颗粒物采集系统的集成及其流量控制和调节

以机动车排放颗粒物采集和分析为主要目的,开发了全流稀释风道机动车排放颗粒物采集系统.文章阐述了全流稀释风道的系统集成以及流量控制系统的设计和调节,其中包括设计应用范围、主要技术参数、系统检定等.流量控制系统采用的关键技术,即文丘里管组合装配方式具有控制流量范围广、变更灵活的特点,可以适应小到摩托车,大到重型柴油车等不同类型车辆检测的需要.     

天津市颗粒物中元素化学特征及来源

2006年的8月—12月采集天津市PM2.5和PM10样品,分析了Na、Al等17种元素质量浓度及月变化特征,PM2.5中元素平均质量浓度为17.2μg/m3,占PM2.5的10.3%。微量元素Zn、Pb在PM10和PM2.5中含量较高,Cr、V、Ni、As等则在细粒子中有明显分布。用富集因子法分析发现,PM2.5中元素富集程度高于PM10。地壳元素除Ca外,均无明显富集,微量元素则呈现不同程度的富集,以Cd富集最为明显。颗粒物分析表明,土壤尘、燃煤、机动车尾气及化工行业是PM2.5中无机元素的主要来源。     

采样罐和气袋保存116种挥发性有机物效果研究

为了提高挥发性有机物(VOCs)分析的准确性,笔者考察了3种采样罐和2种气袋对116种VOCs的保存效果。结果表明:VOCs在不同种类采样罐和气袋中的保存情况有一定差异,整体上Silonite采样罐的保存效果相对更稳定,罐内水分含量会对部分VOCs的保存效果造成影响(特别是对含氧有机物);保存实际样品时,能保证VOCs分析准确性的时间为12 d。     

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.     

核算间接冷却水污染当量数的研讨

针对间接冷却水的特点和核算其污染当量数过程中存在的问题，阐述了间接冷却水的界定，水源水的采样监测技术，本底值的扣除以及超标排放的判别等环节的技术要求和注意事项，并就与之密切相关的几个问题进行了讨论，为核算间接冷却水的污染当量提供了一定的参考依据，并建议增加水温排放指标，以切实控制间接冷却水造成的主要污染－热污染。     

广州市空气可吸入性颗粒物的污染水平

报告了中美合作“广州市大气污染对儿童肺功能影响研究”课题可吸入性颗粒物的两年监测结果。用安德森双道采样器、Ｔｅｆｌｏｎ膜采集细颗粒物（＜２５μｍ,ＰＭ２５）和粗颗粒物（２５≤＜１０μｍ,ＰＭ２５１０）,两者之和为ＰＭ１０,每季度采１５天,每天采一个２４小时样品。结果表明,广州市城区大气可吸入性颗粒物的污染相当严重,尤其是细颗粒物（ＰＭ２５）的污染,应引起公众和政府有关部门的重视。     

Seasonal variation, risk assessment and source estimation of PM 10 and PM10-bound PAHs in the ambient air of Chiang Mai and Lamphun, Thailand

Daily PM10 concentrations were measured at four sampling stations located in Chiang Mai and Lamphun provinces, Thailand. The sampling scheme was conducted during June 2005 to June 2006; every 3 days for 24 h in each sampling period. The result revealed that all stations shared the same pattern, in which the PM10 (particulate matters with diameter of less than 10 microm) concentration increased at the beginning of dry season (December) and reached its peak in March before decreasing by the end of April. The maximum PM10 concentration for each sampling station was in the range of 140-182 microg/m(3) which was 1.1-1.5 times higher than the Thai ambient air quality standard of 120 microg/m(3). This distinctly high concentration of PM10 in the dry season (Dec. 05-Mar. 06) was recognized as a unique seasonal pattern for the northern part of Thailand. PM10 concentration had a medium level of negative correlation (r = -0.696 to -0.635) with the visibility data. Comparing the maximum PM10 concentration detected at each sampling station to the permitted PM10 level of the national air quality standard, the warning visibility values for the PM10 pollution-watch system were determined as 10 km for Chiang Mai Province and 5 km for Lamphun Province. From the analysis of PM10 constituents, no component exceeded the national air quality standard. The total concentrations of PM10-bond polycyclic aromatic hydrocarbons (PAHs) are calculated in terms of total toxicity equivalent concentrations (TTECs) using the toxicity equivalent factors (TEFs) method. TTECs in Chiang Mai and Lamphun ambient air was found at a level comparable to those observed in Nagasaki, Bangkok and Rome and at a lower level than those reported at Copenhagen. The annual number of lung cancer cases for Chiang Mai and Lamphun Provinces was estimated at two cases/year which was lower than the number of cases in Bangkok (27 cases/year). The principal component analysis/absolute principal component scores (PCA/APCS) model and multiple regression analysis were applied to the PM10 and its constituents data. The results pointed to the vegetative burning as the largest PM10 contributor in Chiang Mai and Lamphun ambient air. Vegetative burning, natural gas burning & coke ovens, and secondary particle accounted for 46-82%, 12-49%, and 3-19% of the PM10 concentrations, respectively. However, natural gas burning & coke ovens as well as vehicle exhaust also deserved careful attention due to their large contributions to PAHs concentration. In the wet season and transition periods, 42-60% of the total PAHs concentrations originated from vehicle exhaust while 16-37% and 14-38% of them were apportioned to natural gas burning & coke ovens and vegetative burning, respectively. In the dry period, natural gas burning & coke ovens, vehicle exhaust, and vegetative burning accounted for 47-59%, 20-25%, and 19-28% of total PAHs concentrations. The close agreement between the measured and predicted concentrations data (R(2) > 0.8) assured enough capability of PCA/APCS receptor model to be used for the PM10 and PAHs source apportionment.