全二维气相色谱/飞行时间质谱联用监测环境空气中VOCs

采用全采样系统-全二维气相色谱/飞行时间质谱联用技术监测环境空气中的VOCs,优化了调制周期、升温程序、进样体积等分析条件.39种目标化合物在0 μg/m3～10.0 μg/m3范围内线性良好,检出限范围为0.03 μg/m3～0.09 μg/m3,标准气体平行测定的RSD为1.1％ ～5.3％.应用于化工园区环境空气样品测定,与热脱附-气相色谱/质谱法相比,目标物的分离效果更佳.     

全国环境空气质量数值预报预警系统建立探析

随着雾霾天气的大范围、长时间发生,全国环境空气质量预报预警系统的建立迫在眉睫。集合数值预报模式成为当今预报预警模式发展的主流。介绍了现代化的环境空气质量预报预警系统框架,该系统包括4个子系统,并覆盖城市-区域-背景地区,预报项目要尽量完善。同时应注意预报产品的开发和健康指导信息的发布。     

The influence of the North-Föhn on tracer organic compounds in ambient air PM10 at a pre-alpine site in Northern Italy

The ambient air in Northern Italy is characterised by relatively high PAH and PM₁₀ concentrations in relation to calm wind and intensive temperature inversions, especially during cold periods. These stagnant conditions are occasionally interrupted by North-Föhn events, which cause a drop in relative humidity and an increase in O₃ levels, indicating the mixing of local and free troposphere air flows. In this study the influence of the North-Föhn on concentrations of tracer organic compounds, including polycyclic aromatic hydrocarbons (PAHs), PM₁₀, O₃ and black carbon (BC) was studied during a North-Föhn event in November 2007. Large fluctuations in the concentration of these compounds, as well as changes in PM₁₀ composition due to daytime and night-time variations of local source emissions were observed. Although these events occur at low frequencies (6-10%) they can for short periods, strongly affect the regional air quality by quickly decreasing the concentrations of these tracer organic compounds.     

PCDDs/PCDFs in ambient air (<1 fg m(-3)) - the CTDEP long term sampling (30 d) method

The Connecticut Department of Environmental Protection (CTDEP) commenced monitoring for PCDDs/PCDFs (polychlorinated dibenzodioxins and polychlorinated dibenzofurans) in ambient air in 1987 and adopted the long term (30 d) sampling approach in 1993. The CTDEP method represents the first use of isotopically labeled PCDDs/PCDFs as field surrogates to monitor the behavior of native PCDDs/PCDFs present in actual ambient air samples. This feature first introduced in 1987 was later adopted by US EPA in revisions to sampling methods for PCDDs/PCDFs in ambient air (EPA Method TO9A) as well as development of EPA Reference Method 23 for measurement of PCDDs/PCFDs in stationary source emissions. Results are provided here for a total of twenty-three (23) samples (reported as pairs) representing twelve (12) 30 d sampling events conducted at a site located in metropolitan Hartford CT. Samples were collected in winter months during calendar years 2002-2008. PCDDs/PCDFs concentration data (pg m⁻³) are reported as both congener sums (Cl₄-Cl₈) and 2378-substitued congeners. Total PCDDs/PCDFs concentrations for these twelve (12) sampling events ranged from 0.68 pg m⁻³ (2003) to 4.18 pg m⁻³ (2004) with a mean concentration of 2.04 pg m⁻³.Method performance was monitored through use of collocated samples, in field isotopically labeled compounds, isotopically labeled laboratory applied internal standards and field blank samples. Method performance consistently exceeded goals established in USEPA Method TO9A for these same parameters. Average recoveries of in field labeled PCDDs/PCDFs ranged from 97.5% to 104.2%. Average (mean) recoveries for each of the ten (10) isotopically labeled internal standards ranged from 77.0% (¹³C-OCDF) to 95.5% (¹³C-2,3,7,8-TCDF). Method precision defined as % RPD data for collocated sampler pairs ranged from 8% to 14% for PCDDs and from 5% to 12% for PCDFs. The mean RPD for all PCDDs/PCDFs combined is 9.6%. Field monitoring results demonstrate method sensitivity for all PCDDs/PCDFs congeners and 2378-substituted congeners to be well below concentrations typically found for these compounds in ambient air (all reported data represent measured concentrations). Quantities (pg) found in field blanks represent the major determinant to achieving further enhancements in method sensitivity for selected congeners (OCDD < 42 fg m⁻³; 1,2,3,4,6,7,8-HpCDD < 5.7 fg m⁻³; and 1,2,3,4,6,7,8-HpCDF < 2.1 fg m⁻³). The CTDEP method represents a highly sensitive and reliable technique for monitoring of PCDDs/PCDFs congeners and other persistent organic pollutants (POPs) at ultra trace levels in ambient air (fg m⁻³).     

丹东市环境空气SO_2总量控制初探

采用GB13201-91中的大气污染物总量控制方法总量计算公式,计算丹东市建成区环境空气SO2总量及污染状况。结果表明,整个采暖季全市SO2总量不需要削减,但低架源排放污染物较多,应进行削减。     

Performance of a combined anaerobic reactor for municipal wastewater treatment at ambient temperature

A bench-scale experimental study was carried out to investigate the overall performance of a combined anaerobic reactor for treating pre-settled municipal wastewater at ambient temperature (18–28°C) in terms of substrate removal efficiencies, biogas, methane production, volatile fatty acid (VFA) profiles and effluent suspended solids (SS) concentration, etc. The tested reactor was a modified anaerobic baffled reactor (ABR). The second and third compartments were partly packed with supporting media. The experimental results were similar to, or compared favourably with, other anaerobic reactor systems for municipal wastewater treatment at ambient temperature and proved the technical feasibility of this compartmentalised reactor. Considering its simple structure and operation, it could be considered a potential reactor system for treating municipal and domestic wastewaters in tropical and sub-tropical areas of developing countries.     

围压作用下自振空化射流脉动特性实验研究

就围压下自振空化射流动压力特性进行了实验研究,其实验结果表明：在围压作用下,自振空化射流脉动幅度存在最优喷距,并且最优喷距随围压的增大而增大;在压降一定情况下,脉动幅度随围压的增加而减小;在围压和压降一定时,自振空化射流的最大冲击压力明显高于普通连续射流;自振空化射流的脉动频率,基本不随围压、压降和喷距的变化而变化,在本实验条件下,基本保持在１．３８ＫＨｚ 左右     

DASIBI 1000系列环境空气自动监测系统常见故障分析及系统改进建议

目前,环境空气自动监测已成为我国城市环境空气监测的主要技术手段,我国已有百余个城市拥有这类监测系统。针对美国DASIBI 1000系列环境空气自动监测系统日常运行中的一些常见故障进行分析,并提出解决方法和改进建议,以期与同类机型性能进行可比性分析和探讨。     

β射线衰减法与微量振荡天平法测定PM 10的比较

对现场监测环境空气中PM10 的两种测定方法—β射线衰减法和微量振荡天平法的测量作了对比实验。实验表明 ,两种测定方法的结果具有一致性、相关性和可比性 ,能用回归直线方程来描述两者之间的关系。β射线衰减法的测定结果平均高于微量振荡天平法 15 8% ,它们之间平均偏差为 7 5 %。微量振荡天平法在现场测定中受干扰物和不确定因素的影响较少 ,其测量准确性优于 β射线衰减法。两种监测仪的运行费用大致相同 ,维护量和故障率均 较低     

气相色谱法测定环境空气和废气中乙酸

以蒸馏水吸收环境空气或工业废气中的乙酸,用5%PEG20M+0 5%H3PO4ChromosorbHP80目～100目、2m×2mm玻璃填充柱分离,氢火焰离子化检测器检测,样品直接进气相色谱仪测定。方法最低检出质量浓度为0 16mg/m3,相对标准差为2%～5%,加标回收率在85%～106%之间。方法操作简便、快速。