区域空气质量模拟中查表法的应用研究

在自行开发完善的区域空气质量模式系统RegSRRMS中应用查表法,模拟中国典型城市群对流层大气主要污染物的浓度变化,评估该方法在大气复合污染事件预测和控制中的有效性.首先,利用具有国际先进水平的空气质量模式WRF-CHEM中的化学模块建立了包含完善气相化学、气溶胶过程的箱模式WRFBOX.其次,利用WRFBOX进行化学反应敏感性分析,基于影响污染物的重要因子分别建立了臭氧(O3)及其前体物、无机盐气溶胶和二次有机气溶胶(SOA)查算表数据库,并检验其有效性.最后,将此查算表数据库引入RegSRRMS,建立简化的查表算法.利用直接耦合机制法和查表法对2000年3月珠三角地区污染个例中主要大气污染物浓度进行模拟.通过比较2种方法的模拟结果,显示查表法计算效率提高了57%,能够反映大气光化学反应的非线性特征、气溶胶及其前体物的平衡关系,具有高分辨率、高时效性,能够方便快捷地给出源和受体之间的响应关系,结果可靠.在区域空气质量模式中应用查表法有利于大气污染事件的快速预测以及大气污染控制的快速决策.     

春季黄渤海大气气溶胶的离子特征与来源分析

于2010年春季在黄海、渤海海域采集大气气溶胶总悬浮颗粒物（TSP）样品,并运用离子色谱法对其中主要的水溶性阴离子（Cl-、NO3-、SO24-、CH3SO3-（MSA））和阳离子（Na＋、K＋、NH4＋、Mg2＋、Ca2＋）浓度进行了测定.分析结果显示,黄海、渤海气溶胶样品中主要水溶性离子总浓度分别为10.2～47....     

粗粒子气溶胶远距离输送造成华南严重空气污染的分析

2009年4月末,发生了一次罕见的粗粒子气溶胶远距离输送造成华南地区出现严重的空气污染事件,其特征主要是气溶胶质量浓度超标,而能见度没有明显恶化,对这次空气污染事件进行分析的结果表明.在过程中,粗细粒子质量比(PM2.5/PM10)有明显的3次下降,最低达到0.3,即PM2.5仅占PM10的30%,这与珠江三角洲地区通常以细粒子为主的污染特征有很大不同,反映了外来粗粒子的侵入特征.长江流域浮尘天气的沙尘粒子变性后,长距离输送污染物叠加本地污染物,造成这次严重空气污染事件.     

青岛大气气溶胶中氨基化合物的分布特征

氨基化合物是大气气溶胶和雨水中常被检出的一类有机氮化合物,由于其可作为生物生长直接的氮源,因此可能对海洋生态系统产生直接作用.利用2008年1～12月在青岛采集的66个总悬浮颗粒物样品,采用邻苯二甲醛/N-乙酰-L-半胱氨酸柱前衍生高效液相色谱法,分析了其中溶解态(DAC)和颗粒态氨基化合物(PAC)的浓度.气溶胶中DAC浓度为2.4～40.9nmol·m-3,在春季最高,夏季次之,秋季、冬季最低.PAC浓度为0.7～76.1nmol·m-3,呈现春季冬季秋季夏季的变化趋势.不同季节氨基化合物的组成不同.依据气团的后向轨迹,气溶胶样品可分为受北方陆源、南方陆源和海洋源影响,DAC和PAC在受南方陆源影响的气溶胶中浓度最高,北方陆源次之,海洋源气溶胶中最低.不同来源的气溶胶中氨基化合物的组成不同,蛋白质类氨基化合物对总氨基化合物的贡献在海洋源气溶胶中最高,在南方源气溶胶中最低.     

Effect of platinum on the photocatalytic degradation of chlorinated organic compound

TiO2 nanoparticles, doped with di erent Pt contents, were prepared by a modified photodeposition method using Degussa P-25 TiO2, H2PtCl6 6H2O and methanol as the solvents. The physicochemical properties of Pt/TiO2 were investigated by the nitrogen adsorption and desorption isotherm measurement technique, X-ray di raction analysis and photoluminescence spectra, respectively. Reaction rates from photocatalytic removal of dichloromethane over Degussa P-25 TiO2 and Pt/TiO2 were evaluated. The average diameter and BET surface area of the TiO2 catalyst particles were 300 nm and 50 m2/g, respectively. The degradation e ciency was 99.0%, 82.7%, 55.2%, and 57.9% with TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. And the degradation e ciency was 99.3%, 79.7%, 76.5%, and 73.4% with a 0.005 wt.% Pt/TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. In addition, we found that the photoluminescence emission peak intensities decreased with increases in the doping amount of Pt, which indicates that the irradiative recombination was weakened. Furthermore, the results showed that the UV/0.005 wt.% Pt/TiO2 process was capable of e ciently decomposing gaseous DCM in air.     

物理界两大实验室宣称 或已瞥见“上帝粒子”

7月28日,物理界的两大圣殿级实验室——欧洲核子物理研究中心（CERN）和美国费米实验室（Fermilab）,先后宣称或已“瞥见”了希格斯玻色子的蛛丝马迹,即是说著名的“上帝粒子”有可能已现身世间。不过,由于数据尚未足够也未经严格验证,两实验室都不敢言之凿凿。     

亚微米气溶胶高效过滤装置的设计

针对亚微米气溶胶颗粒进入大气中危害环境及人类的健康的问题,设计了一种移动式亚微米气溶胶高效过滤装置,采用最易穿透粒径法(MPPS)测试了装置的过滤效率,结果表明:该装置具有较高的过滤效率,在0.1~0.25μm粒径范围内,装置的过滤效率在99.999%以上,该设备可用于亚微米气溶胶颗粒的过滤净化。     

Catalytic bubble-free hydrogenation reduction of azo dye by porous membranes loaded with palladium nanoparticles

Catalytic bubble-free hydrogenation reduction of azo dye by porous membranes loaded with palladium （Pd） nanoparticles was studied for the first time. The effects of Pd loading, dye concentration and reuse repetitions of membranes were investigated. In reduction, the dye concentration decreased whereas the pH rose gradually. An optimal Pd loading was found. The catalytic membranes were able to be reused more than 3 times.     

Reduction and characterization of bioaerosols in a wastewater treatment station via ventilation

Bioaerosols from wastewater treatment processes are a significant subgroup of atmospheric aerosols. In the present study,airborne microorganisms generated from a wastewater treatment station(WWTS) that uses an oxidation ditch process were diminished by ventilation.Conventional sampling and detection methods combined with cloning/sequencing techniques were applied to determine the groups,concentrations,size distributions,and species diversity of airborne microorganisms before and after ventilation. There were 3021 ± 537 CFU/m3 of airborne bacteria and 926 ± 132 CFU/m3 of airborne fungi present in the WWTS bioaerosol.Results showed that the ventilation reduced airborne microorganisms significantly compared to the air in the WWTS. Over 60% of airborne bacteria and airborne fungi could be reduced after4 hr of air exchange. The highest removal(92.1% for airborne bacteria and 89.1% for fungi) was achieved for 0.65–1.1 μm sized particles. The bioaerosol particles over 4.7 μm were also reduced effectively. Large particles tended to be lost by gravitational settling and small particles were generally carried away,which led to the relatively easy reduction of bioaerosol particles0.65–1.1 μm and over 4.7 μm in size. An obvious variation occurred in the structure of the bacterial communities when ventilation was applied to control the airborne microorganisms in enclosed spaces.     

Compositions and sources of organic acids in fine particles (PM2.5) over the Pearl River Delta region, south China

Organic acids as important constituents of organic aerosols not only influence the aerosols' hygroscopic property, but also enhance the formation of new particles and secondary organic aerosols. This study reported organic acids including C14–C32fatty acids, C4–C9dicarboxylic acids and aromatic acids in PM2.5collected during winter 2009 at six typical urban, suburban and rural sites in the Pearl River Delta region. Averaged concentrations of C14–C32fatty acids, aromatic acids and C4– C9 dicarboxylic acids were 157, 72.5 and 50.7 ng/m3, respectively. They totally accounted for 1.7% of measured organic carbon. C20–C32fatty acids mainly deriving from higher plant wax showed the highest concentration at the upwind rural site with more vegetation around, while C14–C18fatty acids were more abundant at urban and suburban sites, and dicarboxylic acids and aromatic acids except 1,4-phthalic acid peaked at the downwind rural site. Succinic and azelaic acid were the most abundant among C4–C9dicarboxylic acids, and 1,2-phthalic and 1,4-phthalic acid were dominant aromatic acids. Dicarboxylic acids and aromatic acids exhibited significant mutual correlations except for 1,4-phthalic acid, which was probably primarily emitted from combustion of solid wastes containing polyethylene terephthalate plastics. Spatial patterns and correlations with typical source tracers suggested that C14–C32fatty acids were mainly primary while dicarboxylic and aromatic acids were largely secondary. Principal component analysis resolved six sources including biomass burning, natural higher plant wax, two mixed anthropogenic and two secondary sources; further multiple linear regression revealed their contributions to individual organic acids. It turned out that more than 70% of C14–C18fatty acids were attributed to anthropogenic sources, about 50%–85% of the C20–C32fatty acids were attributed to natural sources, 80%–95% of dicarboxylic acids and 1,2-phthalic acid were secondary in contrast with that 81% of 1,4-phthalic acid was primary.