南宁市大气颗粒物TSP、PM10、PM2.5污染水平研究

2002年在南宁市的5个典型城市功能区内,共采集了125个大气样品(按季节分别采集),初步调查了大气中颗粒物TSP、PM10、PM2.5的污染状况。结果表明,南宁市TSP、PM10、PM2.5的污染很严重,超标率分别为67．5％、82．5％、92．5％,对人体健康危害更大的PM2．5占到了PM10的63．5％左右。重污染区PM2.5的浓度超过轻污染区近一倍。     

区域大气环境中PM2．5／PM10空间分布研究

提出了一种利用移动监测技术研究区域大气环境中PM2.5／PM10空间分布的方法，并在2004年12月进行了宁波市全市域PM2.5／PM10空间分布的研究。数据显示：相同路径所代表的地区PM2.5和PM10具有很好的相关性，多数路径上PM2.5与PM10数据的相关系数平方在0．95以上，而不同路径上PM2.5与PM10的比值不同。文中给出了宁波市PM2.5／PM10污染的空间分布图，直观地显示出PM2.5／PM10污染的空间分布情况，突出了污染的重点点位和地区。     

成都市降水对大气颗粒物湿清除作用的观测研究

为研究成都市降水对大气颗粒物(以下简称颗粒物)的湿清除作用,对2014—2016年成都市的颗粒物(PM_(2.5)、PM_(10))和气象观测数据进行分析。结果表明:月、季尺度下,降水对PM_(2.5)、PM_(10)均有削减作用。降水时段的PM_(2.5)、PM_(10)浓度较非降水时段分别降低17.1%和15.8%,且冬季降幅最为明显。考察472次降水过程对颗粒物的湿清除作用,发现单次降水过程后PM_(2.5)、PM_(10)浓度增长频次(243、234次)和削减频次(229、238次)接近,但颗粒物浓度总体呈削减趋势。对于单次降水过程,颗粒物的初始浓度与降水对颗粒物的湿清除作用关系密切,特别是降水持续时间超过8h后,颗粒物初始浓度越高,削减效果越好。     

杭州城市大气消光系数和能见度的影响因子研究

为了解杭州市能见度下降与大气污染之间的关系，在2001年5月至2002年5月对不同粒径的颗粒物（PM10、PM2.5）的质量浓度进行了观测，结合晴天天气条件下的大气能见度，推算污染物和水汽分子对大气的消光散射，发现细微颗粒物的散射消光特性对杭州市能见度下降起主要作用，并得到能见度与细微颗粒物浓度比值（PM2．5／PM10）的关系；分析了大气能见度和消光系数与PM2．5／PM10和相对湿度的相关系数。     

贵阳市冬季大气PM 2.5和PM 10浓度空间插值及分布研究

为了解贵阳市冬季大气污染现状,以贵阳市污染相对严重的白云区为研究对象,连续采集PM_(2.5)、PM_(10)浓度数据,利用普通克里金法进行空间插值获取PM_(2.5)、PM_(10)分布特征。通过留一法交叉验证,比较6种半变异函数模型(三角函数、高斯函数、球面函数、指数函数、J-Bessel函数和K-Bessel函数)的空间插值精度,选出最适的函数模型;采用分区统计和格网统计的方法,对不同土地利用类型、植被覆盖度下的PM_(2.5)、PM_(10)平均浓度进行比较分析。结果表明,三角函数是PM_(2.5)空间插值的最适模型,指数函数是PM_(10)空间插值的最适模型;贵阳市白云区冬季大气PM_(2.5)、PM_(10)浓度总体表现出城区浓度高,郊区浓度低的分布特征;土地利用类型和植被覆盖度对PM_(2.5)和PM_(10)浓度有着较强的影响。     

重庆市春季大气颗粒物浓度的对比监测分析

通过2012年春季在重庆大气超级站进行的PM10和PM2.5手工采样与自动仪器的对比监测,分析了自动监测与手工监测的一致性及造成偏差的原因,并对PM2.5与PM10浓度的比值关系进行了分析。结果表明:MP101M型颗粒物自动监测仪用于监测PM10时系统性误差偏高,仪器初始精密度存在负偏差;用于监测PM2.5时系统性误差在允许范围之内,仪器初始精密度存在较大负偏差;PM10和PM2.5的手工采样和自动仪器监测值之变化趋势具有非常高的一致性;PM2.5与PM10浓度比值范围在56.5%～90.4%,平均比值为(73.8±7.4)%。     

气象因素对大气污染物影响的季节差异分析及预测模型对比—— 以深圳为例

以深圳为例,通过收集其2014年9月至2017年8月的地面气象观测数据、大气污染物PM_(2.5)和PM_(10)浓度数据及空气质量指数(AQI),利用SPSS软件分别构建线性回归模型与非线性多层神经网络(MLP)模型,探讨了气象因素对PM_(10)、PM_(2.5)及AQI影响的季节性差异,并利用构建的两种模型对PM_(2.5)、PM_(10)和AQI进行预测和对比。结果表明,气温、湿度、风速及风向均对深圳PM_(2.5)、PM_(10)及AQI有较大影响,且影响因素存在季节差异性;两种模型中,MLP模型在对复杂多变的空气质量预测上更具优越性。研究结果可为深圳空气质量优化以及城市局部和整体规划提供科学依据,并为其他城市空气质量模拟分析提供参考。     

宁波市大气可吸入颗粒物PM1o和PM2.5的源解析研究

在宁波市布设4个代表性点位,于2010年春季、夏季和冬季进行大气PM10和PM2.s的采样,同时采集了多种颗粒物源样品,建立了PM10、PM2.5和源样品的化学成分谱.采用化学质量平衡模型(CMB)对宁波市PM10、PM2.5进行源解析.结果表明,城市扬尘、煤烟尘、机动车尾气尘是宁波市PM10、PM2.5的3大污染源,...     

Sources and fate of PCDD and PCDF

PCDD and PCDF were found in urban air particulates from St. Louis and Washington, D.C., and in sediments from the Great Lakes and Siskiwit Lake, Isle Royale. The similarity between the PCDD and PCDF found in air particulates and sediment samples and the presence of PCDD and PCDF in sediment from Siskiwit Lake (a location which can receive only atmospheric inputs) suggest that these compounds are emitted to the atmosphere from combustion sources. The historical input of PCDD and PCDF to dated sediment cores shows a strong increase since 1940, and this suggests that the incineration of chlorinated organic compounds is an important source of PCDD and PCDF to the environment.     

Meta-analysis of time-series studies of air pollution and mortality: effects of gases and particles and the influence of cause of death,age, and season

A comprehensive, systematic synthesis was conducted of daily time-series studies of air pollution and mortality from around the world. Estimates of effect sizes were extracted from 109 studies, from single- and multipollutant models, and by cause of death, age, and season. Random effects pooled estimates of excess all-cause mortality (single-pollutant models) associated with a change in pollutant concentration equal to the mean value among a representative group of cities were 2.0% (95% CI 1.5-2.4%) per 31.3 microg/m3 particulate matter (PM) of median diameter < or = 10 microm (PM10); 1.7% (1.2-2.2%) per 1.1 ppm CO; 2.8% (2.1-3.5%) per 24.0 ppb NO2; 1.6% (1.1-2.0%) per 31.2 ppb O3; and 0.9% (0.7-1.2%) per 9.4 ppb SO2 (daily maximum concentration for O3, daily average for others). Effect sizes were generally reduced in multipollutant models, but remained significantly different from zero for PM10 and SO2. Larger effect sizes were observed for respiratory mortality for all pollutants except O3. Heterogeneity among studies was partially accounted for by differences in variability of pollutant concentrations, and results were robust to alternative approaches to selecting estimates from the pool of available candidates. This synthesis leaves little doubt that acute air pollution exposure is a significant contributor to mortality.     

Field and laboratory studies of the fate and enantiomeric enrichment of venlafaxine and O-desmethylvenlafaxine under aerobic and anaerobic conditions

The stereoselectivity of R,S-venlafaxine and its metabolites R,S-O-desmethylvenlafaxine, N-desmethylvenlafaxine, O,N-didesmethylvenlafaxine, N,N-didesmethylvenlafaxine and tridesmethylvenlafaxine was studied in three processes: (i) anaerobic and aerobic laboratory scale tests; (ii) six wastewater treatment plants (WWTPs) operating under different conditions; and (iii) a variety of wastewater treatments including conventional activated sludge, natural attenuation along a receiving river stream and storage in operational and seasonal reservoirs. In the laboratory and field studies, the degradation of the venlafaxine yielded O-desmethylvenalfaxine as the dominant metabolite under aerobic and anaerobic conditions. Venlafaxine was almost exclusively converted to O-desmethylvenlafaxine under anaerobic conditions, but only a fraction of the drug was transformed to O-desmethylvenlafaxine under aerobic conditions. Degradation of venlafaxine involved only small stereoisomeric selectivity. In contrast, the degradation of O-desmethylvenlafaxine yielded remarkable S to R enrichment under aerobic conditions but none under anaerobic conditions. Determination of venlafaxine and its metabolites in the WWTPs agreed well with the stereoselectivity observed in the laboratory studies. Our results suggest that the levels of the drug and its metabolites and the stereoisomeric enrichment of the metabolite and its parent drug can be used for source tracking and for discrimination between domestic and nondomestic wastewater pollution. This was indeed demonstrated in the investigations carried out at the Jerusalem WWTP.     

Meta-Analysis of Time-Series Studies of Air Pollution and Mortality: Effects of Gases and Particles and the Influence of Cause of Death,Age, and Season

Abstract

A comprehensive, systematic synthesis was conducted of daily time-series studies of air pollution and mortality from around the world. Estimates of effect sizes were extracted from 109 studies, from single- and multipollutant models, and by cause of death, age, and season. Random effects pooled estimates of excess all-cause mortality (single-pollutant models) associated with a change in pollutant concentration equal to the mean value among a representative group of cities were 2.0% (95% CI 1.5-2.4%) per 31.3 μg/m³ particulate matter (PM) of median diameter <10 μm (PM₁₀); 1.7% (1.2-2.2%) per 1.1 ppm CO; 2.8% (2.1-3.5%) per 24.0 ppb NO₂; 1.6% (1.1-2.0%) per 31.2 ppb O₃; and 0.9% (0.7-1.2%) per 9.4 ppb SO₂ (daily maximum concentration for O₃, daily average for others). Effect sizes were generally reduced in multipollutant models, but remained significantly different from zero for PM₁₀ and SO₂. Larger effect sizes were observed for respiratory mortality for all pollutants except O₃. Heterogeneity among studies was partially accounted for by differences in variability of pollutant concentrations, and results were robust to alternative approaches to selecting estimates from the pool of available candidates. This synthesis leaves little doubt that acute air pollution exposure is a significant contributor to mortality.     

剩余污泥浓缩脱水投药量优化和模型建立

应用高分子阳离子絮凝剂（CPF-100）和聚丙烯酰胺（PAM）对污水厂剩余污泥进行浓缩脱水实验，研究表明：CPF-100的浓缩脱水效果优于PAM；当CPF-00投加量为1．16‰时，污泥沉降性能改善程度为37．51％；且在CPF-100投加量逐渐增大的初始阶段，污泥沉降性能改善程度随投加量的增加而增大，但CPF-100投加量也不宜过大，当CPF-100投加量超过1．16‰后，反而会使浓缩脱水效果变差。同时，建立了污泥沉降性能改善程度与絮凝剂CPF-100投加量、沉降时间之间的数学模型，其能较好地反映污水厂剩余污泥的浓缩脱水效果。     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

骆马湖富营养化和生态状况调查与评价

为了了解骆马湖水质状况，在2005年对骆马湖富营养化状态和生态特性进行了调查，并结合“十五”期间的监测资料进行了分析。2005年骆马湖水体中总氮和总磷的平均值超《地表水环境质量标准》（GB3838-2002）中Ⅲ类，超标情况分别为0．78倍和0．54倍，达到湖库特定项目Ⅳ类水标准，骆马湖处于轻度富营养化状态。对骆马湖生态特征分析表明，由于该湖泊的形态以及“藻型浊水状态”和“泥沙型浊水状态”交替出现，遏制了湖水从高营养盐含量向全面富营养化状态演变，保障了底栖动物的良好生长环境，从而形成了骆马湖独特的环境生态平衡。     

Experimental and statistical validation of SPME-GC-MS analysis of phenol and chlorophenols in raw and treated water

A procedure based on solid-phase microextraction (SPME) and gas chromatography coupled with mass spectrometry (GC-MS) was developed and validated in order to analyse 10 phenols in water samples. The optimised conditions were obtained using polyacrylate fibre (PA), 20ml of sample volume, 10% NaCl, pH 4.0 and direct extraction at 35 degrees C and 1000rpm, for 40min. The linear range and quantification limits for these compounds by SPME-GC-MS were defined. An evaluation of the main uncertainty sources of this method is included, which allows expanded uncertainties in the 9.4-35% range for the majority of the compounds. The main source of uncertainty is associated with matrix effects. The validated method is suitable for monitoring the production and distribution of potable water and was used, in field trials, for the analysis of samples from main intakes of water (surface or underground) and from water supply system of a large area (Lisbon and neighbour municipalities).     

Copper-catalyzed chlorination and condensation of acetylene and dichloroacetylene

The chlorination and condensation of acetylene at low temperatures is demonstrated using copper chlorides as chlorinated agents coated to model borosilicate surfaces. Experiments with and without both a chlorine source and borosilicate surfaces indicate the absence of gas-phase and gas-surface reactions. Chlorination and condensation occur only in the presence of the copper catalyst. C₂ through C₈ organic products were observed in the effluent; PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed that is consistent with the observed product distributions. Similar experiments with dichloroacetylene indicate greater reactivity in the absence of the copper catalyst. Reaction is observed in the gas-phase and in the presence of borosilicate surfaces at low temperatures. The formation of hexachlorobenzene is only observed in the presence of a copper catalyst. PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed for the formation of hexachlorobenzene from dichloroacetylene.