滤膜对环境空气中砷测定的影响及改进

依据《环境空气和废气 颗粒物中砷、硒、铋、锑的测定 原子荧光法》（HJ 1133—2020）的要求,对采集环境空气中砷的9种滤膜的本底值、回收率、检出限、精密度和准确度进行了实验对比。根据实验各项性能指标及成本考虑,建议选择尼龙、硝酸纤维或混合纤维3种国产有机滤膜,其购买方便、价格较低,方法检出限均为0.2 ng/m³,精密度和准确度均能满足环境空气中砷的测定要求。     

Polybrominated diphenyl ethers in various atmospheric environments of Taiwan: their levels, source identification and influence of combustion sources

In this study, ambient air samples from different atmospheric environments were examined for both PBDE and PCDD/F characteristics to verify that combustion is a significant PBDE emission source. The mean ± SD atmospheric PBDE concentrations were 165 ± 65.0 pg Nm⁻³ in the heavy steel complex area and 93.9 ± 24.5 pg Nm⁻³ in the metals complex areas, 4.7 and 2.7 times higher than that (35.3 ± 15.5 pg Nm⁻³) in the urban areas, respectively. The statistically high correlation (r = 0.871, p < 0.001) found between the atmospheric PBDE and PCDD/F concentrations reveals that the combustion sources are the most likely PBDE emission sources. Correspondence analysis shows the atmospheric PBDEs of the heavy steel and metals complex areas are associated with BDE-209, -203, -207, -208, indicative of combustion source contributions. Furthermore, the PBDEs in urban ambient air experience the influence of the evaporative releases of the commercial penta- and octa-BDE mixtures, as well as combustion source emissions. By comparing the PBDE homologues of indoor air, urban ambient air, and stack flue gases of combustion sources, we found that the lighter brominated PBDEs in urban ambient air were contributed by the indoor air, while their highly brominated ones were from the combustion sources, such as vehicles. The developed source identification measure can be used to clarify possible PBDE sources not only for Taiwanese atmosphere but also for other environmental media in other countries associated with various emission sources in the future.     

临安大气本底站酸雨污染变化特征与影响因素分析

利用临安大气本底站酸雨观测数据,研究临安大气本底站降水pH,酸雨发生频率的时间分布特征、变化趋势及其影响因素;借助后向轨迹分析法分析输送形势对临安大气本底站酸雨的影响。研究表明:最近6年间临安大气本底站降水pH各月均值均小于4.5,均达到强酸雨的程度;临安大气本底站的酸雨发生频率表现为夏季低、秋季高;1985—2009年临安大气本底站降水的年均pH全部达到酸雨程度。根据Daniel趋势检验,临安大气本底站年均降水pH总体上呈逐年下降的趋势。风速越小,酸雨出现频率就越高;降水pH受降水量的影响较大。临安大气本底站的酸雨与降水前的大气中SO2浓度存在负相关的关系。根据气团的来向与酸雨污染程度的关系分析,临安大气本底站的酸雨污染受到其北部地区和浙西地区的酸雨气体物输送的影响较大。临安大气本底站的酸雨污染特征已由原来的硫酸型转为硫酸型与硝酸型并重。     

兰州市大气降尘中正构烷烃的分布特征及源解析

采集了2005年春季兰州市不同功能区大气降尘样品,采用气相色谱/质谱法测定样品中的正构烷烃。结果表明,降尘中正构烷烃主要有2种类型,一种是后峰型,以C29为主峰碳,大于C25正构烷烃具有明显的奇偶优势,碳优势指数(CPI)为1.25~1.40;另一种是双峰型,分别以C29,C20,C19,C15为主峰碳,在C25或C27后有明显的奇碳数优势,CPI为1.26~2.35。研究区内不同区域降尘中正构烷烃分布有明显的变化,相对清洁区正构烷烃分布为后峰型,主要来源于燃煤、高等植物的不完全燃烧。工业区、商业区、商业居民混合区正构烷烃分布属于双峰型,既有高等植物蜡的输入,也有汽车尾气、石油化工的输入,且人为源的贡献较大。     

KB-6C大气采样器故障维修几例

介绍了几例ＫＢ６Ｃ大气采样器常见故障现象以及排除方法。     

我国SO2排放总量控制方法探索与初步评估

介绍了我国SO     

浅析居民区大气污染特征及防治对策

对居民区大气的主要污染物、烟尘、SO_2、TSP等分布情况进行了分析和预测。结果表明，随着城市建设的发展，能源消耗的增加，将使大气环境进一步恶化。只有以强化管理为手段，以规划目标为导向，着重以改善市区能源结构入手，是改变大气环境质量的根本措施。     

天然气利用与环境效益

天然气是一种清洁燃料。加快天然气的开发利用，对改善能源结构，保护生态环境，提高人民生活质量，具有十分重要的战略意义。分析了我国大气污染和大气污染解决的可能性，探讨了天然气所能带来的环境效益。     

An experimental set up of a PAH vapour generator and its use to test an annular denuder

The aim of this work is to develop and test a dynamic gas generator for semi-volatile organic compounds (SVOC). A single compound, naphthalene, is used as a surrogate PAH to test the system. The dynamic generation of PAH is based on the permeation technique [Analyst 106 (1981) 817; Am. Ind. Hyg. Assoc. J. 38 (1977) 712]. Monitoring the temperature and measuring the mass of PAH present in the permeation chamber every 48 h gives a direct measurement of the sublimation rate of the PAH. Knowing the flow rate, gives an accurate value of the concentration of PAH from the generator. It was found stable over a period of time under constant operating conditions. This concentration is diluted down to between 0.3 and 30 ppbv by a controlled flow of pure air. The diluting airflow is a mixture of dry and wet air, making it possible to control the relative humidity of the flow from the generator as well as its concentration in PAH. We used this generator to calibrate an annular denuder tube, based on the study by Gundel et al. [Atmos. Environ. 29 (1995) 1719]. Although this technique has been shown to be artefact-free for sampling gaseous PAH [Polycyclic Aromatic Compounds 9 (1996) 67; Atmos. Environ. 28 (1994) 3083], its trapping efficiency still depends on environmental parameters (temperature, relative humidity and sampling duration). Accordingly, we used our generator to calibrate a single annular denuder under controlled conditions (T degrees C, HR%, CPAH, sampling duration). The trapping efficiency of the denuder was calculated by two independent methods. Firstly, by comparing the amount trapped on a denuder with the measured mass sublimated in the generator. Secondly, by putting two denuders in series and comparing the mass collected on the first and the second tube. These two methods gave similar results, within the 10% relative uncertainties of both methods. The first results obtained show that, in environmental conditions, the efficiency ranges between 90 and 100%.     

Vertical distribution of polycyclic aromatic hydrocarbons in atmospheric boundary layer of Beijing in winter

Air samples were collected using active samplers at various heights of 8, 15, 32, 47, 65, 80, 102, 120, 140, 160, 180, 200, 240, 280 and 320 m on a meteorological tower in an urban area of Beijing in two campaigns in winter 2006. Altitudinal distributions of polycyclic aromatic hydrocarbons (PAHs) in atmospheric boundary layer of Beijing in winter season were investigated. Meteorological conditions during the studied period were characterized by online measurements of four meteorological parameters as well as trajectory calculation. The mean total concentrations of 15 PAHs except naphthalene of gaseous and particulate phase were 667±450 and 331±144 ng m⁻³ in January and 61±19 and 29±6 ng m⁻³ in March, respectively. Domestic coal combustion and vehicle emission were the dominant PAH sources in winter. Although the composition profiles derived from the two campaigns were similar, the concentrations were different by one order of magnitude. The higher concentrations in January were partly caused by higher emission due to colder weather than March. Moreover, weak wind, passing through the city center before the sampling site, picked up more contaminants on the way and provided unfavorable dispersion condition in January. For both campaigns, PAH concentrations decreased with heights because of ground-level emission and unfavorable dispersion conditions in winter. The concentration ratio of PAHs in gas versus solid phases was temperature dependent and negatively correlated to their octanol–air partition coefficients.