春节期间烟花爆竹燃放对乌鲁木齐市区PM2.5及其组分影响分析

为了解春节期间烟花爆竹燃放对乌鲁木齐市区PM2.5及其组分的影响,利用超级站在线监测仪器(包括颗粒物分析仪、在线离子色谱、激光雷达和重金属分析仪)对环境空气中的PM2.5浓度、颗粒物水溶性离子和重金属浓度进行连续监测.结果表明,大量烟花爆竹的集中燃放造成了PM2.5短时严重污染,最高质量浓度达到了423μg/m3.烟花...     

春节烟花爆竹燃放期间苏州市区PM2.5中水溶性离子特征分析

使用在线离子色谱分析了苏州市区春节期间PM2.5中水溶性离子.结果表明：春节期间存在2个空气污染高峰时段（初一和初五）,其中初一凌晨PM2.5达到最高峰,小时质量浓度为571μg/m3;烟花爆竹集中燃放时段,PM2.5中K＋、Cl-、Mg2＋质量浓度明显上升,初-凌晨与腊月三十凌晨相比,K＋、Cl-、Mg2＋质量浓度分别增加了117倍、80.7倍、18.0倍;相关性分析表明,PM2.5中K＋、Mg2＋、Na＋、Ca2＋在烟花爆竹燃放时段可能具有相同的来源.     

烟花燃放对空气中PM2.5及水溶性离子的影响研究

于2013年2月9日—2月16日在南京城区连续观测PM10、PM2.5、PM1的质量浓度、能见度、PM2.5中水溶性离子浓度等参数,探讨了因春节期间烟花爆竹的燃放导致大气中颗粒物浓度出现短时峰值,同时能见度急剧降低,空气质量下降的原因。研究发现:因烟花爆竹的燃放,PM2.5局地短时间浓度可达863μg/m3,能见度仅为1.2km;PM2.5中Cl-、K+与SO2-4浓度短时间上升,这与烟花爆竹中氧化剂、还原剂等组分的燃烧释放有关。由春节期间观测结果统计发现,因烟花爆竹燃放对PM2.5中水溶性离子的贡献约占50%。     

一种评估烟花爆竹燃放对大气PM2.5影响的新方法

基于北京市空气质量自动监测系统2013年2月常规污染物监测数据,提出了定量估算烟花爆竹燃放对大气PM2.5影响的污染物相对比值(PM2.5/CO)法。利用该方法研究表明,2013年北京除夕烟花爆竹燃放使PM2.5单站1小时平均浓度最大增加709μg/m3(石景山古城监测点);全市24小时平均浓度增加88μg/m3,达到159μg/m3,空气质量由良好升级为重度污染。元宵节夜间烟花爆竹燃放使PM2.5单站1小时平均浓度最大增加469μg/m3(海淀万柳监测点),全市24小时平均浓度增加54μg/m3。除夕夜、元宵夜全市平均烟花爆竹PM2.5浓度超过75μg/m3的时间分别为5、7 h,达到峰值后半衰期分别为0.9、1.7 h。城区烟花爆竹PM2.5浓度高于郊区,并可导致下风向郊区的PM2.5浓度显著增加。除夕、元宵节北京市区烟花爆竹排放PM2.5总量分别约为1.91×105kg、1.17×105kg。     

杭州城区春节PM2.5中水溶性离子在线观测

利用大气细颗粒物水溶性组分在线连续监测分析系统(AIM-URG9000D),考察了杭州城区春节期间PM2.5中无机水溶性离子的浓度变化范围,探讨了这些离子的日变化特征和影响因素,同时分析了集中燃放烟花爆竹对水溶性离子浓度的影响。结果表明,SO2-4、NO-3、NH+4是PM2.5中水溶性离子的主要成分,分别占全部水溶性组分的33.3%、28.4%、19.4%;强致癌物质NO-2浓度为2.07μg/m3,远大于膜采样结果;NO-3与SO2-4的质量比为0.85,表明机动车尾气排放导致的大气污染正逐步加重;各水溶性离子有着各自不同的日变化规律。相关性分析表明,NH+4与NO-3、SO2-4的相关系数分别为0.92、0.81;K+、Cl-、Mg2+3者之间的相关系数均在0.9以上。烟花爆竹燃放期间,PM2.5浓度急剧上升,Cl-、SO2-4、K+、Mg2+浓度分别达到燃放前的18、6、53、76倍。     

烟花爆竹燃放对北京市空气质量的影响研究

结合常规污染物浓度和PM_(2.5)化学组分浓度,分析了2015年春节期间烟花爆竹燃放对北京市空气质量的影响。结果表明:烟花爆竹燃放会在短时间内造成严重的大气污染,其中对SO2、PM_(2.5)和PM10的影响最为显著。除夕夜间良乡、官园和怀柔3个监测站点的PM_(2.5)质量浓度峰值分别达730.5、343.4、762.2μg/m~3,为2月17—25日和3月4—8日(观测期间)平均值的5.2、3.1、7.1倍。烟花爆竹燃放对PM_(2.5)组分中的SO_4~(2-)、K+和Cl-的影响最为显著,除夕夜间监测中心点位的SO_4~(2-)、K~+和Cl~-质量浓度峰值分别达92.2、95.6、57.4μg/m~3,为观测期间平均值的4.5、10.5、6.8倍。烟花爆竹燃放产生的气态前体物和NO_3~-、SO_4~(2-)、NH+4、OC等PM_(2.5)二次化学组分在不利的气象条件下会发生化学反应和物理积累,造成PM_(2.5)浓度升高,产生持续性的大气污染。根据各污染物与NH+4的质量浓度比推算得出,除夕、"破五"和元宵节3个时段烟花爆竹燃放对K~+、Cl~-、SO_4~(2-)、SO_2和PM_(2.5)浓度的平均贡献率分别为78.4%、61.1%、37.4%、38.7%和30.1%。     

石家庄市春节期间大气颗粒物有机碳和元素碳的变化特征

为研究石家庄市大气颗粒物的污染特征及其来源,于2013年2月6—19日春节期间在石家庄市采集大气颗粒物TSP、PM10、PM2.5样品,对其有机碳、元素碳进行分析测定。结果表明,石家庄TSP、PM10、PM2.5日平均质量浓度分别为389、330、245μg/m3,颗粒物污染严重;碳组分在颗粒物中占有较大比重,且随着粒径的减少,碳组分比重逐渐增加;存在不严重的次生有机碳污染;OC与EC的相关系数较高,说明两者有较为相似的污染源,主要为燃煤、机动车排放源。各种气象条件对PM2.5、OC、EC浓度和OC/EC的变化都有不同程度的影响。     

合肥市春季大气PM10和PM2.5中碳组分的污染特征

2014年4月，应用热/光碳分析仪测定合肥市春季大气PM10和PM2.5中的有机碳（OC）、元素碳（EC）。结果显示，PM10、PM2.5的平均质量浓度分别为(124.0±34.3)μg/m3和(96.3±29.2) μg/m3,PM10中OC、EC的平均质量浓度分别为(15.1±5.5)μg/m3和(6.0±2.1) μg/m3，PM2.5中OC、EC的平均质量浓度分别为(12.1±3.5）μg/m3和(5.5±2.1) μg/m3。OC、EC在PM2.5中所占的比例均高于在PM10中的比例，说明合肥市春季PM2.5中碳的含量更高。通过分析8个碳组分及OC/EC比值，发现燃煤、机动车尾气和生物质燃烧是主要贡献源； OC易形成二次污染，EC排放以焦炭为主。     

安徽省春节期间烟花爆竹燃放对环境空气质量的影响研究

为研究烟花爆竹集中燃放对江淮地区环境空气质量的影响,基于近地面常规空气质量参数、颗粒物组分参数、激光雷达监测等数据资料,系统分析了2022年春节期间烟花爆竹燃放对安徽省主要城市和县域环境空气质量的影响。研究表明,2022年春节期间安徽省环境空气质量总体好于2019—2021年平均水平,但受局部烟花爆竹燃放和不利气象条件(低温、小风、高湿、静稳)的叠加影响,产生的环境效应(颗粒物浓度峰值较高、影响范围较广)依然较为严重。重点区域(合肥和淮北)大气颗粒物组分中硝酸根离子(NO^(-)_(3))、硫酸根离子(SO ^(2-)_(4))和铵根离子(NH_(4)^(+))等主要离子占比有所下降(降幅为3.4%~12.1%),烟花爆竹燃放示踪组分(钾离子、氯离子、金属元素等)均出现了明显的峰值过程,且金属元素浓度占比涨幅明显高于水溶性离子。烟花爆竹燃放对颗粒物的垂直分布和传输沉降过程产生显著影响,燃放排放主要以球形细颗粒物为主;不利气象条件下的本地烟花爆竹燃放叠加周边污染传输影响是造成主城区空气质量显著恶化的主要原因。基于ρ(PM_(2.5))/ρ(CO)的比值法估算,集中燃放时段,烟花爆竹燃放对城建区PM_(2.5)质量浓度的绝对贡献范围为4~701μg/m^(3),平均值达159μg/m^(3);烟花爆竹燃放对PM_(2.5)质量浓度的贡献量和贡献率呈现皖中>皖北>皖南的分布特征。主城区的禁燃措施对于春节期间空气质量的改善起到了关键作用,同时需要加强城市周边区域的烟花爆竹燃放管控措施。     

宁波市PM10、PM2.5中水溶性无机阴离子浓度水平及分布特征

研究了宁波市PM10、PM2.5中无机阴离子浓度水平及分布特征。结果表明,PM10中Cl-为1.00μg/m3,具有较明显的海洋特征,SO24-、NO3-离子浓度为9.90、3.70μg/m3;Cl-主要存在于粒径为2.5-10μm的颗粒物中,而NO3-、SO42-主要存在于PM2.5中,成为PM2.5的重要组成部分。PM10中水溶性无机阴离子季节变化明显,呈冬天高,夏天低的趋势。     

锅炉烟尘测试中锅炉负荷率的计算方法探讨

GB5468 -91规定 ,锅炉烟尘测试时 ,必须对锅炉的运行负荷进行测试 ,而实际监测过程中 ,许多锅炉房不具备测试的计量条件 ,为了解决这一问题 ,文章提出利用烟气量和空气过剩系数计算锅炉负荷率。在实际监测工作中 ,该方法方便、易于操作 ,所得结果和标准规定方法所得结果有很好的一致性     

城市空气质量周报效用分析

介绍了世界上一些发达国家的空气污染预报的做法和采取的措施,阐述了我国开展空气质量预报的方针和方法,指出了周报是预报的基础工作。叙述了我国空气质量周报的污染参数的选取、污染指数的分级及其浓度限值和污染指数计算及确定,分析并总结了开展城市空气质量周报所发挥的效用是提高公众的环保意识,加大了治理污染的力度,转变了环境监测的职能,促进了环境监测事业的发展     

水中总硬度测量不确定度的评定

采用EDTA滴定法测定水质总硬度的测量不确定度评定。充分考虑测量重复性、标准溶液的配制、滴定等过程对测量的影响,计算水中总硬度的测量相对合成标准不确定度为1·81×10-3。     

贵州黔东南州三板溪水库春季拟多甲藻水华特征

2011年3月13日对贵州省黔东南州三板溪水库进行春季浮游植物调查的结果表明,三板溪水库Ⅱ号采样点(下革东)发生以佩纳形拟多甲藻为优势种的拟多甲藻水华,细胞密度高达1.15×10⁷cell/L;板溪水库总氮的最低值为2.09 mg/L,总磷的最低值为0.95 mg/L,三板溪水库的总氮、总磷含量较丰富,不存在总氮或总磷是限制性因子;通过SPSS16.0统计软件分别进行Pearson 积距相关系数分析表明,氮磷比是三板溪水库发生拟多甲藻水华的主要影响原因。     

Environmental Assessment of the Impact of Ozone to the Neuston of the Sea-Surface Microlayer of the Gulf of Mexico

Substantial amounts of NOx (146 000 t/y) and total hydrocarbons (294 000 t/y) are released to the marine atmosphere by the large number of oil and gas operations over Federal waters of the Gulf of Mexico (GOM). Under appropriate meteorological conditions these emissions react to form ozone (0–54 g/m3 over-water) which can affect the marine environment. Using a dry deposition model, this work examines the amount of ozone derived from oil and gas offshore operations and deposited in the sea surface of the Gulf of Mexico, and assesses its impact on the neuston of the sea-surface microlayer. Surface integrated estimates of ozone deposited from oil and gas operations over the sea surface ranges from 400 kg to 1800 kg which results in sea surface concentrations of 15 g/m3. This estimate and the actual toxic ozone levels suggest no acute, toxic impacts to the neuston. However, indirect effects may occur through changes to the pelagic foodwebs and organic carbon pathways. Another potential pathway for ozone impacting the environment is through the production of bromate. Based on the concentrations and time scales (11–139 days) only sublethal effects appear to occur, but uncertainties associated with this assessment need to be further studied. From an ecological perspective, the environmental impacts and risks of NOx and VOC discharges from offshore platforms need to be assessed for neuston and other components of the marine ecosystem.     

Fractionation of heavy metals and assessment of contamination of the sediments of Lake Titicaca

Chemical weathering is one of the major geochemical processes that control the mobilization of heavy metals. The present study provides the first report on heavy metal fractionation in sediments (8–156 m) of Lake Titicaca (3,820 m a.s.l.), which is shared by the Republic of Peru and the Plurinational State of Bolivia. Both contents of total Cu, Fe, Ni, Co, Mn, Cd, Pb, and Zn and also the fractionation of these heavy metals associated with four different fractions have been determined following the BCR scheme. The principal component analysis suggests that Co, Ni, and Cd can be attributed to natural sources related to the mineralized geological formations. Moreover, the sources of Cu, Fe, and Mn are effluents and wastes generated from mining activities, while Pb and Zn also suggest that their common source is associated to mining activities. According to the Risk Assessment Code, there is a moderate to high risk related to Zn, Pb, Cd, Mn, Co, and Ni mobilization and/or remobilization from the bottom sediment to the water column. Furthermore, the Geoaccumulation Index and the Enrichment Factor reveal that Zn, Pb, and Cd are enriched in the sediments. The results suggest that the effluents from various traditional mining waste sites in both countries are the main source of heavy metal contamination in the sediments of Lake Titicaca.     

二乙氨基二硫代甲酸银试剂质量对测砷的影响

用简单合成了二乙氨基二硫代甲酸银试剂，并比较了自制和市售的二乙氨基二硫人 银对测砷的影响。结果表明，采用自制的二乙氨基二硫代甲酸银能大大降低试剂空白，提高方法的灵敏度和降低检出限，试剂质量明显优于市售产品。     

氨氮测量不确定度的评定

采用纳氏试剂光度法测定水质氨氮的测量不确定度评定,应该考虑工作曲线、测量重复性、标准溶液、仪器读数分辨率等对测量的影响.     

Evaluation of method of preparation of passive diffusion tubes for measurement of ambient nitrogen dioxide

This study was carried out in response to suggestions that the measurement of NO(2) by Palmes-type passive diffusion tubes (PDT) is affected by the method of preparation of the triethanolamine (TEA) absorbent coating on the grids. The following combinations of factors were investigated: TEA solvent (acetone or water), volume composition of TEA in solvent (50% or 20%), and grid coating method (dipping in solution prior to assembly or pipetting solution on after assembly). Duplicate PDTs prepared by each of the 8 methods were exposed in parallel, in urban air, for a total of 80 separate 1 week exposures. NO(2) concentrations derived from PDTs prepared by pipetting methods were significantly less precise than concentrations from dipping methods, with mean RSDs for duplicate measurements of 13.8% and 8.5%, respectively (n= 316 each category). Pipetting methods using solutions of 50% TEA composition were particularly imprecise (mean RSD 17.2%). Data from PDTs prepared by pipetting methods were systematically more poorly correlated with each other and with data from co-located chemiluminescence analysers, than corresponding data from PDTs prepared by dipping methods, indicating that more consistent accuracy was also obtained by the latter PDTs. The statistical evidence suggested that PDTs prepared by pipetting 50% TEA in water generally gave lower NO(2) concentrations. Although this is in agreement with a previous study, it is also possible that such an observation here may be a statistical artefact given the demonstrably poorer precision of this method. The general tendency of PDTs to show positive bias in NO(2) measurement in urban air in 1 week exposures was again evident in this study (mean biases at roadside and urban centre locations of +35% (n= 475) and +18% (n= 112), respectively) consistent with augmentation of within-tube NO(2) flux by chemical reaction between co-diffusing NO and O(3). Overall, it is recommended that the pipetting method of PDT grid preparation is avoided, or at least investigated further, because of the apparent degradation in precision and accuracy of NO(2) measurement. Potential reasons for the effect are discussed.     

污染物总量控制中载体水流量的测定

示踪剂法测定河水流量是较为准确的办法 ,利用河流动力模型计算出示踪剂投放点 ,利用示踪剂投放量与测定浓度之间的关系可方便地获得河水流量结果