烟尘监测时采样滤筒的质量控制

介绍了合格滤筒的筛选方法和采样滤筒在实验室分析中的质量控制,分析了影响滤筒称量恒重的原因,指出空气湿度、冷却时间和烘干时间对滤筒称量恒重都有影响.     

烟尘测试中滤筒称重问题

烟尘测试中滤筒称重问题张萍萍（福建龙岩地区环境监测站，龙岩３６４０００）①当滤筒放入天平称重时，滤筒湿度较天平内空气湿度小，产生吸湿现象，天平显示不稳。实验表明，最初称量的５个滤筒应放回干燥器内重新干燥、重新称量。②干燥时间的确定：实验表明，在内径为...     

影响滤筒分析质量的主要因素和改进方法

介绍了影响滤筒称量恒重的原因,指出空气湿度、冷却时间和烘干时间等对滤筒称量恒重都有影响。提出使用标准空白滤筒、在平衡室中冷却、称量滤筒、并采用专用滤筒盒和刚玉滤筒采样减小系统误差。     

烟尘滤筒称重方法的改进

针对在烟尘测试中滤筒的称重存在天平显示不稳、恒重难的现象进行了探讨。比较了2种称量方法，提出在平衡室中冷却、称量滤筒，并采用标准滤筒来减小由于称重条件不同而产生的系统误差。结果表明，改进方法具有称量稳定、易恒重、失重少的优势。     

氨法脱硫废气中烟尘测试方法的实验研究

利用重量法测试原理,将氨法脱硫外排废气中烟尘监测滤筒用二次水经过超声波洗涤后过滤,在烘箱内于105℃烘干2 h后称量恒重,除去滤简中的硫酸铵成分,从而准确获得烟尘的含量.     

影响滤简分析质量的主要因素和改进方法

介绍了影响滤简称量恒重的原因，指出空气湿度、冷却时间和烘干时间等对滤简称量恒重都有影响。提出使用标准空白滤筒、在平衡室中冷却、称量滤筒、并采用专用滤简盒和刚玉滤筒采样减小系统误差。     

生活垃圾焚烧炉烟尘、金属元素项目采样测试方法探讨

一直以来,生活垃圾焚烧炉烟尘项目监测和金属元素颗粒物项目监测,样品的采集都是分开进行的,而且样品分析时,各金属元素样品也是分别消解,这样操作不但花费时间长,而且还浪费滤筒、试剂等资源.     

大气颗粒物手工比对监测体系滤膜称量质控技术探讨

健全大气颗粒物手工比对监测体系是"十三五"环境空气自动监测质量管理的一项重点任务,其中颗粒物滤膜的称量直接影响手工监测数据质量。研究调研了国内各级环保部门所属环境监测机构颗粒物滤膜称量工作情况,结合国内外方法标准、技术规范等,重点探讨了称量实验室环境、称量设备、称量影响因素等滤膜称量质控要点,并针对环境管理与监测需求对大气颗粒物手工比对监测滤膜称量质控提出建议。     

环境样品采集中的方差分析

环境样品的分析一般包括从野外采集样品然后经过一定的预处理,再带回实验室进行称量、测试分析等手续,最后根据所得的数据对研究的“总体”进行评价。在上述过程中,由于研究对象的“不均性”往往带入的采样误差称量误差、分析测试误差以及随机误差、但哪一种误差因素是起着主要的作用呢?采用方差分析对几种误差进行研究。可以判明引起误差的主次因素。从而对那些造成主要误差因素的环节加以严格控制。这对环境监测工作的合理安排以及保证结果的准确性都起着重要的作用。     

我国烟尘浓度监测的分析误差

烟造气烟尘浓度的则定一直处于只知道测,不知道准确到什么程度的状态,这就影响了我国烟尘测试技术的发展和提高,同时也不能为污染治理和防护提供科学的数据.本文就可以依据专题试验结论来探讨国产预测流速法烟尘测定仪、静压平衡烟尘测定仪和动压平衡烟尘测定仪监测结果的分析误差,同时依据众多工程技术人员的实践经验来分析产生误差的原因,并提出可行的减小测定误差的部分措施,还提出了烟尘浓度测定仲裁方法的建议.     

连续流动注射间接测定空气中的五氧化二磷

建立连续流动注射间接测定空气中五氧化二磷的方法。空气中的五氧化二磷用过氯乙烯滤膜或滤筒采样,加入去离子水反应生成正磷酸,过滤、洗涤、定容后运用连续流动注射仪进行测定。优化了抗坏血酸浓度、硫酸浓度、钼酸盐浓度以及恒温室温度等影响显色的因素。最佳条件下,实际样品五氧化二磷加标回收率为96.0%~102%,相对标准偏差在4%以下;采样体积为300 L时,方法检出限为0.001 6 mg/m~3。t检验结果表明,所建方法与现行国标法的测定结果无显著性差异。方法分析速度快、重现性好、灵敏度高,适用于空气中五氧化二磷的测定。     

餐饮业油烟排放监测模拟工况研究

在现行《饮食业油烟排放标准(试行)》(GB18483—2001)的执行过程中,工况难以控制,影响监测结果的准确性。在对不同餐饮业的主要烹饪方式(炸、煎、煮、炒)餐饮油烟的初始排放浓度进行实测的基础上,模拟出和以上4种烹饪方式相匹配的工况,分析各种类型餐饮业不同工况下的油烟排放规律,建立了一组能够由监测人员主动控制的油烟监测模拟工况。     

硫酸雾测试方法若干问题思考

简述了我国硫酸雾测试方法的发展历史,分析和总结了《固定污染源废气硫酸雾的测定离子色谱法》(HJ 544—2016)存在的一些争议和问题,包括硫酸雾的定义、测试方法的干扰控制等。分析认为,相比《硫酸工业污染物排放标准》(GB 26132—2010),HJ 544—2016对硫酸雾的定义更加合理。实验结果表明:硫酸盐是测试方法条件下的目标物,滤筒可以显著地捕捉硫酸盐。9组样品滤筒中,被测目标物所占比例为7.9%~69.1%;滤筒和前吸收液中,被测目标物所占比例为93.7%~97.8%。HJ 544—2016新增加的两级串联碱液吸收瓶可以较完全地捕集穿透滤筒后的硫酸雾,同时也会捕集SO2。SO2会对硫酸雾测试产生正干扰,约42.9%的SO2在被吸收后转化为硫酸雾。     

Wetting and hydration of insoluble soot particles in the upper troposphere

Wettability and hydration are determined for aircraft combustor and laboratory-made soots which are used as surrogates for the insoluble part of aircraft-generated black carbon particles in the upper troposphere (UT). The measured water/ice contact angles on the soot surfaces are in the range 60-80 degrees. Factors influencing the soot wetting show a tremendous dependence on the surface chemical composition and microstructure. Wetting characteristics of soots are directly related to its hydrophilicity. The inverse Kelvin effect is considered as a mechanism of ice nucleation which is facilitated by the soot agglomerated structure with interparticle cavities in which condensation takes place on the insoluble surface with a high water contact angle. Estimations of the critical supersaturations needed for the ice condensation growth of particles are provided to determine which of the wetting characteristics are required for cirrus cloud formation in ice saturated regions of the UT.     

The Adsorption of Formaldehyde on Suspended Particles investigated on model systems

Our laboratory investigation aimed at assessing to what extent suspended particles could adsorb formaldehyde, allowing it, when inhaled, to penetrate deeper into the lung. We used two types of pure soot, N-220 and N-660 (the former being a highly active oil furnace soot with smaller particles and a larger surface area than the latter), because of their chemical inactivity and the adsorptive properties. The results obtained in experimental conditions showed that soot particles could bind 2.3 to 50.2% of formaldehyde, depending on the particle size, relative humidity, amount of particles and the duration of the contact. The recovery of formaldehyde from the particles was also tested. Further investigation is planned under realistic conditions.     

饮用水中苯基脲除草剂的分子印迹固相萃取方法研究

以N-（4-异丙基苯基）-N-亚丁基脲分子印迹聚合物为吸附剂，建立了饮用水中苯基脲除草剂的分子印迹固相萃取方法。上样后固相萃取柱依次用2．5mL0．1mol／L盐酸和2．5mL去离子水淋洗，然后氮气吹干，再用1mL含8％乙腈的甲苯溶液淋洗，最后用2mL甲醇洗脱。将建立的方法用于自来水中异丙隆、非草隆、甲氧隆、绿麦隆、枯莠隆、灭草隆、伏草隆、草不隆等8种苯脲类除草剂的测定，除伏草隆和草不隆的回收率较低外，其余6种除草剂的回收率均〉60％。     

Indoor air sampling of organophosphate triesters using solid phase extraction (SPE) adsorbents

In this paper we demonstrate the use of SPE cartridges for sampling of organophosphate triesters in indoor air by adsorptive enrichment. The method has been optimised for the sampling and analysis of organophosphate triesters using a 25 mg aminopropyl silica SPE cartridge. The same cartridge is used for the active air sampling as well as for the subsequent extraction and clean-up of the sample. This makes the method fast and eliminates some tedious and time-consuming manual sample handling steps. Sampling and extraction efficiency was high for the investigated organophosphates, and limit of detection was in the range 0.1-0.3 ng m(-3). The method was applied to measurements of organophosphate triesters in two lecture halls and an electronics dismantling facility, and was compared with results from common filter/adsorbent sampling at each site. Analysis was made by GC with selective detection by NPD set in phosphorus mode, and by GC-MS. Thirteen organophosphate triesters (not counting isomers) were detected in the electronic dismantling facility. Chlorinated organophosphate triesters were detected in all locations with concentrations over 1 microg m(-3) in the lecture halls. This kind of adsorptive enrichment using an SPE cartridge could be adjusted to other types of analytes as well.     

Validation of a passive atmospheric deposition sampler for polybrominated diphenyl ethers

An atmospheric deposition sampler was validated with respect to polybrominated diphenyl ethers (PBDEs), a compound group that is widely used as flame retardants in many types of consumer products. The deposition sampler consists of an adsorption cartridge that is connected to a glass funnel. Extraction tests with spiked cartridges using soxhlet extraction with acetone revealed recoveries of >80% for all of the investigated PBDEs. Once adsorbed, PBDEs are stable, as proven by extractions of spiked cartridges that were stored outdoors and collected after different periods of time, up to 84 days. High recoveries indicate that degradation of adsorbed PBDEs does not play a role under realistic field conditions. Bulk deposition rates of PBDEs were determined in a field test with 3 replicates, and a possible breakthrough of target compounds was assessed in the field using a second adsorption cartridge in series. No breakthrough of target compounds could be observed within a sampling period of 61 days, and a bulk deposition rate of approximately 1 ng m(-2) day(-1) for the sum of all analysed PBDEs was measured. The highest deposition rates were measured for octa-brominated congeners, followed by BDEs 99, 183, 153, and 47. Overall, the sampler was successfully validated regarding the atmospheric deposition of PBDEs.     

微波消解石墨炉原子吸收法测定工业废气中铍及其化合物

采用玻璃纤维滤筒采集工业废气中铍及其化合物，硝酸-氢氟酸混酸体系微波消解滤筒、硝酸镁一硝酸混合液作为基体改进剂，石墨炉原子吸收法测定铍。本方法前处理操作过程简单、省时、酸用量少、环境污染小，方法的灵敏度和准确度都有很大的提高。当采样体积为30L，工业废气中铍的最低检出质量浓度为1×10μmg／m^3。     

Study of Trace Elements and Soot in Aerosols from a Coal-Fired Power Plant in Northern Vietnam

Two measurement campaigns were conducted in two sampling sites, An Thinh and Duy Minh, in northern Vietnam during the months of November–December 2000 and November 2001–February 2002 in order to investigate the extend of the particulate air pollution from the Pha Lai coal fired power plant. Fine particle samples were analyzed by Energy Dispersive X-Ray Fluorescence spectrometry and soot samples were analyzed by reflectometer. The result showed that high concentration of soot and elements mostly coincided with the air masses originating from the power plant. Sea spray aerosol was found to be the major source of chlorine at both sites. Ratios of specific elements and principal component analysis (PCA) revealed that coal combustion was the main contributor to the air pollution at both sites. PCA also indicated that there were other sources responsible for the elements emission, probably the influence of long distance transport and Asian Brown Cloud.