臭氧/活性炭协同作用去除二级出水中DON

为探讨臭氧氧化和活性炭吸附对城市污水厂二级出水中溶解性有机氮(DON)的去除机制,首先测定二级出水DON、溶解性有机炭(DOC)、UV254、pH值等指标.接着通过臭氧氧化试验和活性炭吸附试验来考察二级出水中DON、DOC和UV254变化,以及DON分子量分布和DON亲疏水性变化,并应用三维荧光光谱对二级出水中DON变化进行表征.结果表明,当臭氧投加量为8mg/L,DON的去除率大约为33.9%,DOC和UV254去除率约21.2%、66.7%;当活性炭投加量为2.0g/L,DON、DOC和UV254的去除率大约为43.4%、27.6%、92.2%;臭氧氧化和活性炭吸附组合试验时,对DON的去除率大约为83.3%和81.5%;臭氧氧化提高小分子量( 20kDa)的DON所占比例;活性炭吸附降低小分子量( 20kDa)DON所占比例为;臭氧氧化和活性炭吸附都提高亲水性DON所占比例,而降低疏水性和过渡性DON所占比例;三维荧光光谱证实,二级出水中DON变化与3个主要峰有关,分别代表物质为色氨酸类蛋白质、芳香族类蛋白质和富里酸类物质.     

山西夏季气溶胶空间分布飞机观测研究

以搭载了多种气溶胶观测仪器的飞机为观测平台,在2013年夏季首次对山西中部地区霾日及晴空大气气溶胶空间分布特性进行了观测,得到气溶胶粒子数浓度和尺度的垂直分布廓线以及不同高度气溶胶粒子谱分布特征.研究发现,山西夏季非降水天气条件下气溶胶粒子以核模态和积聚模态的细粒子为主,粗粒子很少.霾日气溶胶数浓度是晴空的2~3倍,主要是核模态的小粒子;气溶胶粒子数浓度随着高度逐渐减小,低空存在气溶胶累积区,逆温层的存在是导致气溶胶累积区形成的主要原因;气溶胶粒子尺度随高度增加,大粒子主要分布在2500m以上的高空;不同高度上的气溶胶粒子谱均呈双峰或三峰分布,谱型基本一致,从近地面到5000m高空,气溶胶粒子谱随高度的增加略有展宽.观测区域气团后向轨迹模拟结果显示,4000m以上高空气溶胶粒子主要是从中国西北地区远距离输送而来,3000m以下气溶胶粒子则主要来源于近地面排放.     

沸石滤池深度处理石化废水二级出水研究

采用小试规模沸石滤池,深度处理石化废水二级出水,通过考察滤池对CODCrNH4^-N和挥发酚的去除情况,分析了沸石去除污染物的规律和机理。结果表明：沸石滤池对CODCr,NH4^＋-N和挥发酚的平均去除率分别达到27．32％、94．67％和34．47％。在滤池运行初期,离子交换起主要作用。随着反应器的运行,离子交换因沸石饱和而减弱,而生物氧化逐渐起作用。由于沸石资源丰富、价格低廉和性能优越,所以沸石滤池作为三级深度处理技术具有广阔应用前景。     

Single particle analysis of ambient aerosols in Shanghai during the World Exposition, 2010: two case studies

ATSI Model 3800 aerosol time-of-flight mass spectrometer (ATOFMS) was deployed for single-particle analysis in Shanghai during the World Exposition (EXPO), 2010. Measurements on two extreme cases: polluted day (1st May) and clean day (25th September) were compared to show how meteorological conditions affected the concentration and composition of ambient aerosols. Mass spectra of 90496 and 50407 particles were analyzed respectively during the two sampling periods. The ART-2a neural network algorithm was applied to sort the collected particles. Seven major classes of particles were obtained: dust, sea salt, industrial, biomass burning, organic carbon (OC), elementary carbon (EC), and NH₄-rich particles. Number concentration of ambient aerosols showed a strong anti-correlation with the boundary layer height variation. The external mixing states of aerosols were quite different during two sampling periods because of different air parcel trajectories. Number fraction of biomass burning particles (43.3%) during polluted episode was much higher than that (21.6%) of clean time. Air parcels from the East China Sea on clean day diluted local pollutant concentration and increased the portion of sea salt particle dramatically (13.3%). The large contribution of biomass burning particles in both cases might be an indication of a constant regional background of biomass burning emission. Mass spectrum analysis showed that chemical compositions and internal mixing states of almost all the particle types were more complicate during polluted episode compared with those observed in clean time. Strong nitrate signals in the mass spectra suggested that most of the particles collected on polluted day had gone through some aging processes before reaching the sampling site.     

Mutagenicity of diesel engine exhaust in the Ames / Salmonella assay using a direct exposure method

The aim of this study was to investigate the potential mutagenic activity of diesel engine exhaust in the Ames/Salmonella assay using a direct aerosol exposure system. So, TA 98 and TA 100 strains, with or without added S9 mix, were exposed to diesel emissions after varying degrees of filtration. Variants of these two strains, deficient in nitroreductase (TA 98NR and TA 100NR) or over-expressing O-Acetyl Transferase (YG 1024 and YG 1029), were also exposed to total (unfiltered) diesel exhaust to highlight the putative mutagenicity of any nitro-PAHs present in these emissions. Mutagenic activity of the diesel exhaust was demonstrated on Salmonella typhimurium, strains TA 100 and variants TA 100 NR and YG1029. The use of a particle filter did not modify the genotoxicity of the diesel emissions, indicating a major contribution of the gas phase to the mutagenicity of these diesel emissions. The prominent role of the particulate-associated nitro-polycyclic aromatic hydrocarbons (nitro-PAHs) claimed by some authors working on diesel exhaust organic extracts was not confirmed by our results with native diesel exhaust exposure. Our results show that the gas phase is potentially more mutagenic than the particles alone.     

全球沙尘气溶胶源汇分布及其变化特征的模拟分析

根据全球沙尘气溶胶气候模式GEM-AQ/EC模拟的1995~2004年的沙尘起沙量和干湿沉降量,分析了沙尘气溶胶源汇的全球时空变化特征.全球沙尘起沙量集中在各个主要沙漠地区,北非对全球沙尘气溶胶贡献最大为66.6%.沙尘气溶胶沉降的高值区分布在沙漠源区及其紧临的下风地区.最大净沙尘气溶胶接收主要分布在沙漠周围地区并形成净接收量大于10t/(km2×a)的位于0°N~60°N之间的北非、欧亚大陆、西太平洋、北印度洋、北美和大西洋的带状分布.在北非、阿拉伯半岛、中亚、东亚和澳大利亚5个主要沙漠地区中,起沙量和沉降量都存在明显的季节变化,除中亚其他4个区域干湿沉降量和起沙的季节变化基本一致;东亚地区沙尘气溶胶起沙量和总沉降量的季节变化最为明显,而北非沙漠起沙量和总沉降量的季节变化最小,其他3个区域的季节变化幅度基本相同.中亚起沙峰值和阿拉伯半岛起沙次峰值出现在夏季,其他区域的峰值均出现在春季.10年间全球陆地年平均起沙量为(1500±94)Mt,保持略微上升趋势.以北非沙漠起沙量年际变化率最低(6.3%), 而以东亚(28.3%)和澳大利亚(45.0%)起沙量年际变化最为明显;全球陆地的沙尘气溶胶沉降量以约9.9Mt/a的速率递减,全球海洋的沙尘气溶胶沉降递增.     

Measurement of watershed phosphorus: A review

Eutrophication control programs are based on phosphorus management which, in turn, requires a detailed quantification of the watershed phosphorus budget. This involves an assessment of non‐point sources of phosphorus, a key element of which is determining the fraction of soil‐P and sediment‐P available to support algal growth. This paper presents a review of the state‐of‐the‐art of estimating algal available‐P from non‐point sources, and an analysis of pertinent data. The need to employ multi‐interval algal bioassays in developing phosphorus management systems is stressed.     

杭州无车日大气细颗粒物化学组成形成机制及光学特性

在世界无车日期间对PM2.5化学组分、光学参数及气态污染物进行同步监测,评估机动车尾气排放对杭州市细颗粒物污染及能见度的影响.结果表明:管制期间NO2、NOx、CO和PM2.5浓度分别为45.0, 50.8, 1119, 85.8μg/m3,比平日分别下降了17.5%、23.3%、20.6%和32.6%.管制期间PM2.5中OC、EC和二次无机组分浓度为8.58, 4.29, 25.95μg/m3,比管制前下降了13.8%、12.6%和15.7%,管制后则达到20.24, 10.85, 27.39μg/m3,上升了136.0%、152.7%和5.5%.管制期间较高的NO3-/PM2.5和NOR(0.15)表明PM2.5的形成更多受二次无机转化影响,管制后PM2.5中上升的OC、EC比例和较低的NOR(0.07)则说明PM2.5主要来自机动车排放的碳质组分的贡献.硫酸盐、硝酸盐、有机气溶胶和EC是最主要的消光组分,共解释了总消光系数的74.0%~89.7%.管制后,机动车排放的有机物和EC消光比例达到26.6%和24.6%,大气消光系数则达到438.7Mm-1,比管制期间上升了60.5%,表明机动车污染排放已成为影响杭州大气细颗粒物污染和能见度下降的重要因素.     

Lead-210 and Beryllium-7 in the Aerosol Particles Around Taiwan Off-Shore Areas

Abstract

Distributions of ²¹⁰Pb and ⁷Be in the aerosol particles of different size fractions were measured around Taiwan offshore areas from October, 1994 to October, 1995. the size distribution and abundance of the aerosol particles showed both spatial and temporal variations. the particle concentrations off northwestern Taiwan were more than twice as those off northeastern Taiwan both in November and March, and the values were much higher in November than in March for both areas. the measured particle concentrations, except for one sample with an unusually high value, ranged from 10 to 83 μOgm ^?3 in the study areas. the ²¹⁰Pb concentrations in the aerosol particles filtered from the air mass varied between 20 × 10^?3 and 72 × 10^?3 dpm m^?3 (1dpm = 0.45 pCi). the ²¹⁰Pb concentrations in the area off southwestern Taiwan appeared somewhat higher than in other areas and were probably contributed by the land air from Taiwan which contains higher ²¹⁰Pb in winter. the ²¹⁰Pb concentrations off northern Taiwan were low in November when the aerosol concentrations were high, but they were high in March when the aerosol concentrations were low.

Based on the ⁷Be monitoring records of 20 years on the aerosol particles of the island by the Taiwan Radiation Monitoring Center, the mean settling rate averaged 0.91, 0.79 and 0.68 cm s^?1, respectively, in northern, central and southern Taiwan. with these values and the ²¹⁰Pb concentrations in the aerosols, the ²¹⁰Pb flux was determined to be between 0.58 and 2.30 dpm cm^?2y^?1, with an average of 1.19 dpm cm^?2y^?1. Excluding the highest value due to its extremely high ²¹⁰Pb and aerosol concentrations, the average is reduced to 1.05 dpm cm^?2y^?1. the activity median diameters (AMD) for ²¹⁰Pb in the study areas were between 0.69 and < 0.49 μM with a mean of 0.5 öm based on ²¹⁰Pb distributions in different particle size fractions. Thus, ²¹⁰Pb was preferentially adsorbed on to the submicron particles. ⁷Be in the study areas showed a good correlation with ²¹⁰Pb in total activity although the two nucides had different sources.     

PCDD/Fs emission, risk characterization, and reduction in China’s secondary copper production industry

Secondary copper production is one of the key polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) emission sources in China, but research and data on this issue are rare. In 2004, when the Stockholm Convention entered into force in China, PCDD/Fs emissions from secondary copper production contributed to 32.2% of the total release. In this paper, PCDD/Fs emission dynamics from secondary copper industry were discussed and cumulative risks were characterized. From 2004 to 2009, industrial policies played an indirect role in PCDD/Fs reduction, but its effects are still limited. The Yangtze River Delta, Pearl River Delta and central regions were among the top three of dioxin emissions from secondary copper production in China. Shanghai, Shandong, Zhejiang, and Jiangxi had comparatively higher accumulated risk and were recommended as the priority regions for promoting PCDD/Fs emission control in China. From 2009 to 2015, the PCDD/Fs emission dynamics in the secondary copper industry were presented through simulation. PCDD/Fs emission equations were established, resulting in the recommendation of control technology conversion rate at 30% for small scale smelters and 51%–57% for large and medium-sized enterprises in 2015. In conclusion, both indirect policy and direct control technology retrofitting should be integrated for more effective PCDD/Fs emission reduction in secondary copper industry.