一种PM_(2.5)辅助监测系统的设计与实现

为解决目前国内外PM2.5监测仪器价格昂贵,运行成本高,单点负责区域大,监测点少的问题,提出以国家监测网络为基础,以低成本、高精度为特点的PM2.5辅助监测方法。系统采用DSM501A作为PM2.5浓度采集传感器,完成粒子数量浓度到质量浓度的转换,通过在一定区域内布置监测终端,并借助于GPRS网络和参数曲面构建方法,建立了一定区域内PM2.5质量浓度网络图,填补了国家监测点间的监测盲区,并利用高斯消元法建立了从历史数据到未来浓度的预测算法。实验结果表明:实测数据与国家监测点数据基本一致,具有广阔的应用前景。     

Probability distributions of arsenic in soil from brownfield sites in Beijing (China): statistical characterization of the background populations and implications for site assessment studies

A probabilistic analysis was performed on soil arsenic concentration data from 4 brownfield sites at Beijing (Chaoyang and Haidian Districts), involved in environmental assessment studies. The available data sets were processed to provide a statistical characterization of the background populations and differentiate “anomalous data” from the natural range of variation of arsenic concentrations in soil. The site-specific background distributions and the existing wide-scale background values defined for the Beijing area were compared, discussing related implications for the definition of metal contamination soil screening levels (SSLs) in site assessment studies. The statistical analysis of As data sets discriminated site-specific background populations, encompassing 88% to 94% of the sample data, from outliers values, associated with either subsoil natural enrichments or possible anthropogenic releases. Upper Baseline Concentration (UBC) limits (+ 2σ level), including most of the site-specific metal background variability, were derived based on the statistical characterization of the background populations. Sites in the Chaoyang South District area had UBC values in the range 10.4–12.6 mg·kg^-1. These ranges provide meaningful SSL values to be adopted for As in local site assessment studies. Using the wide-scale background value for the Beijing area would have erroneously classified most of the areas in the subject sites as potentially contaminated.     

蒸汽相变促进可溶PM2.5凝结增长的数值分析

为利用蒸汽相变原理促进氨法脱硫系统排放细颗粒物(PM2.5)的脱除,建立多分散颗粒的凝结增长动力学模型,利用数值模拟方法研究了可溶硫酸铵颗粒的凝结增长规律,并将典型粒径可溶与不可溶颗粒的凝结增长过程进行对比分析.结果表明:不同粒径硫酸铵颗粒的增长速率相近,等温系统的凝结增长效果优于绝热系统;对于同一初始粒径分布下的可溶和不可溶颗粒,微米尺度可溶颗粒的增长速率始终大于不可溶颗粒,亚微米尺度可溶颗粒的增长速率先大于而后小于不可溶颗粒,使得二者的增长曲线存在一个交叉点;蒸汽饱和度增大能显著促进硫酸铵颗粒的增长;等温系统中温度对硫酸铵颗粒的增长影响显著,绝热系统中温度的影响较弱.     

基于油耗调查的2010年天津市农业机械排放研究

通过问卷调查,采用基于燃油消耗量的方法估算出天津市2010年农业机械氮氧化物(NOx)和颗粒物(PM)的总排放量.2010年天津市农业机械总保有量为57.5万台,其中种植业机械最大约占52.5%;总动力为588万kW,运输机械占比最大为47.3%.估算出2010年天津市农业机械总油耗(主要为柴油)为6.7万t,其中运输机械耗油量为4.5万t.再根据燃油消耗量估算了天津2010年农业机械污染物排放量,NOx和PM年排放量分别为3470t和303t.     

PM10中重金属的提取方法及生物可利用性研究

分别运用模拟生物提取法与化学连续提取法对PM10标准参考样品城市源（NIST-1648A）和工业源（BCR-038）中6种重金属（Cd、Co、Cu、Mn、Ni、Pb）质量分数及赋存形态进行分析。其目标是验证2种提取大气固体颗粒物中重金属方法的有效性,并比较2种方法的优缺点,为将来提取PM10中重金属的方法选取提供依据。模拟生物提取法中,使用Gamble溶液模拟人体肺液对 PM10样品进行溶解,实验方法操作较为简单快捷;化学连续提取法中,不同溶解步骤则可确定重金属的不同赋存形态。在需要快速确定 PM10中某种重金属总量时,应优先使用模拟生物提取法。化学连续提取结果表明,城市源PM10中重金属赋存形态分布没有统一规律,工业源PM10中重金属多以残渣态存在。通过对2种来源的PM10样品中重金属生物可利用性分析,城市源的大气颗粒物对人体的毒性更大,其中标准参考样品城市源 PM10中生物可利用性较高的是重金属Cd（BIBio为61.65%±3.45%;BISE为69.02%±3.82%）和Cu,最低的是重金属Co和Pb;标准参考样品工业源PM10中重金属的生物可利用性最高的是Cd（BIBio为27.66%±1.52%;BISE为15.05%±2.13%）,而Ni、Co和Pb的生物可利用性较低。     

2004年春季北京一次沙尘暴的理化特性分析

2004-03-27～2004-03-29北京发生沙尘暴天气期间,监测了气溶胶TSP、PM10和PM2.5的浓度,利用撞击式采样器采集了8级膜样品,并用ICP-MS分析了气溶胶中元素的含量,同时监测了地面辐射和风速的变化.结果显示,此次沙尘暴导致TSP浓度比平时增加3～4倍,PM10浓度增加2～3倍,PM2.5浓度有所降低.研究还表明:地壳元素Na、Mg、Al、Mn和Fe主要分布在粗粒子上.而污染元素Zn、Pb主要分布在细粒子上,污染元素主要是本地源.沙尘暴对总辐射有明显的影响,导致地面总辐射衰减了37.8%.受大风影响粗粒子浓度增加显著,细粒子浓度明显减少.     

Screening for acute ocular toxicity of commercialized products of cartap,an insecticide,and correlation to blood concentrations in rabbits

Cartap is an insecticide known to produce contraction and damage to mouse and rabbit diaphragms, and plays a pivotal role in respiratory paralysis and mortality in rabbits. The aim of this study was conducted to screen for the toxic properties and blood concentrations of commercialized cartap products in New Zealand White (NZW) rabbits. Five granular formulations (GRs) with different concentrations (4, 6, 6.5, 6.66 or 10%) and seven water-soluble powders (SPs, 50%) of commercialized cartap products were chosen to study toxicity following ocular instillation. Furthermore, ocular instillation (5, 12.5, 25 or 50 mg kg^?1) and oral administration (25 mg kg^?1) of the technical material (TC) cartap was also performed to compare blood concentration changes in rabbits. There was no death or eye irritation with all GR products; however, soluble powder (SP) products produced severe toxicity and mortality in rabbits. The blood concentration of TC cartap in rabbits started to increase from 2 min and reached peak levels at 7–9 min after ocular instillation in a dose-related pattern. For comparison of the blood distribution of cartap via different administration routes, oral exposure exhibited a higher absorption of cartap than ocular instillation. It was suggested that the commercialized GR products of cartap were safe but 50% SP products were highly toxic to rabbits following ocular exposure. This study provides valuable data to screen for potential acute toxicity of cartap to farmers and animals in the field.     

Statistical interpolation model for the description of ground pollution due to the TCDD produced in the 1976 chemical accident at seveso in the heavily contaminated zone “A”;

The influence of NTA on chromium genetic activity was studied in the D7 strain of Saccharomyces cerevisiae. At low dose (subgenotoxic) of sodium chromate (CrVI) (5mM), NTA increased the point mutation while at higher dose (25 mM) of chromate in the presence of NTA a decrease of point reverse mutation was observed. Probably NTA affected either the uptake of Cr(VI) favouring the intracellular reduction to Cr(III), or the recombinational repair of DNA breaks induced by chromate oxiding activity.

An increase of point (reverse) mutation was obtained in the experiments with NTA and chromium chloride, suggesting the hypothesis that NTA might interact with Cr(III) forming NTA‐Cr(III) complexes able to permeate cellular membranes and bind to DNA. In addition NTA genetic inactivity was confirmed.     

广州市交通干线附近细颗粒污染特征

利用中山大学大气环境监测平台数据,对广州市交通干线附近的ρ(PM_2.5)和ρ(PM₁)进行了统计学分析,以研究交通干线附近细颗粒污染特征及变化规律. 结果表明:2008—2012年广州市PM_2.5超标严重,但ρ(PM_2.5)有所下降. 受季节性污染源及气象因素影响,广州市夏季ρ(PM_2.5)平均值为42μg/m3,明显低于春、秋、冬三季. ρ(PM_2.5)在工作日与周末差异明显,周末明显高于工作日,而ρ(PM₁)在工作日与周末差异不明显. ρ(PM_2.5)与ρ(PM₁)日变化趋势基本一致,整体上呈白天低、夜晚高,上午低、下午高的特征. ρ(PM_2.5)日变化呈单峰,19:00左右达到最大值(53μg/m3);而ρ(PM₁)呈双峰变化,在20:00左右达到高峰值(43μg/m3),上午09:00左右也有一小峰值(37μg/m3). ρ(PM_2.5)和ρ(PM₁)的相关性较好,R(相关系数)为0.94,PM₁是PM_2.5的主要构成颗粒,所占比重平均值为0.65. ρ(PM_2.5)和ρ(PM₁)均与交通流量存在相关性,在白天和夜晚变化趋势相一致,但交通流量白天与ρ(PM_2.5)更为密切,夜晚则与ρ(PM₁)更为密切.      

大气PM_（2.5）在线监测仪对SO_4~（2-）、NO_3~-和NH_4~＋的测定评价

通过两套大气细颗粒物（PM2.5）水溶性离子在线监测仪与蜂巢式固气分离器膜采样系统作对比,评估了在线监测仪器对主要水溶性组分SO24-、NO3-和NH4＋的测定结果.美国URG公司生产的在线连续监测分析系统（AIM URG-9000B）对NH4＋和NO3-的监测结果较好,但对SO24-的测定结果存在明显高估,其原因是AIM的平板溶蚀器系统无法完全去除大气中高浓度SO2,从而对SO24-的测定结果有干扰.为解决这一问题,进行了一系列实验,结果表明采用两个溶蚀器串联并用5 mmol.L-1H2O2＋5 mmol.L-1NaOH混合溶液作吸收液时,高浓度的SO2（甚至达到260μg.m-3）可以被完全吸收而对SO24-的测定结果不产生影响.由荷兰能源研究所（ECN）、Metrohm和Applikon共同研制的在线气体组分及气溶胶监测系统（MARGA,ADI2080）对NH4＋和SO24-的监测结果较好,可以满足实验要求;但NO3-的测定结果偏高,其准确性需作进一步评估.新型监测仪器在不同大气环境中投入使用前需进行对比测试,以确定其准确性和精确性.