TiO2光催化降解微污染水中腐殖酸的研究

为探讨TiO2光催化法处理微污染水中腐殖酸的规律,利用悬浮状的TiO2颗粒在紫外光的照射下催化降解含有腐殖酸污染物的水样,设计正交试验研究pH值、TiO2的投加量、腐殖酸溶液初始浓度、曝气量和温度等对腐殖酸降解效果的影响及规律。结果表明:pH=3.5时,TiO2的投加量为1.0 g/L、曝气量为0.12 m3/h、温度为18℃时,最佳有机物降解效果为96.83%;TiO2光催化法对微污染水中的腐殖酸能够有效降解。     

南京四季大气粗细粒子中PAHs的污染特征及来源

研究了南京2009—2010年大气粗、细粒子中PAHs(多环芳烃,Polycyclic Aromatic Hydrocarbons)在四季不同的组成特征及来源。结果表明,南京细粒子中PAHs的浓度范围是19.11~131.31 ng/m~3,而粗粒子是17.77~134.85 ng/m~3。局地排放与区域传输的综合作用,使得南京不同采样点的PAHs浓度相关度较高,具有相同的污染源及污染过程。除了秋季PAHs主要分布于粗粒径段,南京大气中PAHs以细粒子为主。春、冬季分别受到了来自ENE-S和NNW-NE方向污染气团的远距离输送影响,夏季局地排放的污染物受到了西南清洁气团的稀释作用,秋季不同于其他季节,仅以局地贡献为主。源解析结果显示,不同季节PAHs来源存在差异,最主要的排放源是机动车源,其次是燃煤/焦化,秋季受较多的生物质燃烧贡献。秋季特殊的排放源贡献,以及局地贡献为主的污染形式,可能是其浓度分布不同于其他季节的根本原因。     

北京市部分地区土壤和植物中多环芳烃的分布

研究了北京市区东部、东南部和西南部不同功能区土壤和绿化植物中多环芳烃（PAHs）的分布特征，讨论了土壤和植物叶片中多环芳烃质量分数的相关性。结果表明：车流量较多的路边土壤PAHs质量分数很高，西城区北京杨叶片中PAHs质量分数较高；相同采样点的土壤与植物叶片中多环芳烃的质量分数相关显著。     

中国部分清洁地区大气中N2O的浓度

１９９３年４月—１９９５年８月对中国部分清洁地区大气的Ｎ２Ｏ浓度进行了现场观测，结果表明：农田（玉米田和麦田）大气的Ｎ２Ｏ平均浓度高达３２２．１－３４３．４ｐｐｂｖ，这是土壤排放Ｎ２Ｏ的结果；临安、龙风山和瓦里关山大气本底观测站（ＷＭＯ／ＧＡＷ）Ｎ２Ｏ的平均浓度分别为３１８．８±８．４ｐｐｂｖ，３１７．４±４．７ｐｐｂｖ和３１４．０±４．２ｐｐｂｖ。在此基础上，分析了大气Ｎ２Ｏ的分布及变化特征。另外，还对现场取样及Ｎ２Ｏ浓度测量技术作了初步分析和评价     

南京北郊气溶胶中多环芳烃的污染特征及来源解析

利用2010年8月采集的南京北郊气溶胶样品,使用GC-MS对美国环保总局推荐的16种优先控制的多环芳烃含量、分布特征进行了研究。在此基础上,用特征比值法、主因子分析法分析得到南京市北郊大气中PAHs的主要来源为车辆尾气、燃煤、天然气和草木秸秆燃烧,并应用绝对因子分析法进一步定量计算主要源对PAHs的浓度贡献率。结果表明:1)大气颗粒物中16种多环芳烃的平均总质量浓度为135.85 ng/m~3,多环芳烃以4环为主,在可吸入颗粒物中的浓度占总浓度的88.7%;2)PM10中多环芳烃呈双模态分布,在9~10μm的粗模态和0.65~1.10μm的积聚模态上各出现一个峰值;3)天然气等对PAHs的贡献率为5.7%~44.1%,燃煤源的贡献率为20.7%~57.8%,汽车尾气的贡献率为4.6%~46.7%,木材燃烧的贡献率为2.9%~38.1%。本地交通排放和燃料燃烧是南京北郊大气颗粒物中PAHs的主要来源,远距离输送也对南京北郊气溶胶中的PAHs有重要贡献。     

藏东南大气中多环芳烃的污染特征及来源分析

为探究青藏高原东南部大气中多环芳烃(Polycyclic Aromatic Hydrocarbons,简称PAHs)的污染、源及输送特征,利用鲁朗地区(29.77°N,94.73°E)总悬浮颗粒物(Total Suspended Particles,简称TSP)和大气中的14种PAHs含量,结合同期气象环境数据进行了综合分析。结果表明,该地区TSP中PAHs和气相的PAHs质量浓度变化范围分别为0.22～5.05 ng m^-3和0.83～63.75 ng m^-3,平均值分别为2.13 ng m^-3和11.33 ng m^-3。薪柴和柴油的燃烧是污染的主要方式,汽油燃烧等其他排放为次要方式。PAHs来自本地污染和远距离传输(Long Range Transmission,简称LRT)共同的影响。本地污染在四季各个源地均不相同。冬春季本地污染大,源在东南及正南方,夏秋季受本地和外来输送共同作用,本地源在东南方且占比小,LRT占比大。LRT受西北气流、西风气流和西南气流三支气流影响,污染严重时西南气流占主导...     

石家庄市采暖期与非采暖期PM2.5中多环芳烃的来源解析及健康风险评价

为研究石家庄市采暖期与非采暖期大气细颗粒物(PM_2.5)中多环芳烃(Polycyclic Aromatic Hydrocarbons,PAHs)的污染特征及其人群健康效应,采集了石家庄市2017年1月—2019年12月每月10—16日PM_2.5样品,使用气相色谱-质谱联用仪测定PM_2.5中优先控制的16种多环芳烃的浓度,分析采暖期与非采暖期PM_2.5中多环芳烃的污染水平及组成特征,利用特征比值法和主成分分析法对其来源进行定性判断,并采用健康风险评估模型以及预期寿命损失评估多环芳烃对人群的健康风险。结果表明：(1)PM_2.5及其中多环芳烃浓度平均水平在采暖期分别为106.00μg/m³、44.17 ng/m³,非采暖期分别为73.00μg/m³、40.17 ng/m³。16种多环芳烃中含量最高的是苯并[a]芘,其次为苯并[k]荧蒽、苯并[b]荧蒽、?。多环芳烃单体环数越高其致癌作用越强,不同环...     

IPCC AR4中海气耦合模式对中国东部夏季降水及PDO、NAO年代际变化的模拟能力分析

利用1880—1999年中国东部35站的观测降水资料、英国Hadley中心的海温和海平面气压资料以及IPCC第4次评估报告（AR4）中20世纪气候模拟试验（20C3M）的模式输出结果,对IPCCAR4中22个耦合模式所模拟的我国东部夏季降水的年代际变化情况以及太平洋年代际涛动（PDO）和北大西洋涛动（NAO）的年代际变化情况进行了分析。结果显示,这些模式对20世纪我国东部夏季降水年代际变化的模拟结果并不理想,但对降水在20世纪70年代中期前后的突变具有一定的模拟能力。其中IAP_FGOALSL_0_G可以大致模拟出20世纪70年代中期前后降水型的突变特征,而BCCR_BCM2_0和UKMO_HadGEM1则可以模拟出华北地区降水在20世纪70年代中期之后减少的现象。对于引起我国东部夏季降水年代际变化的重要因子PDO和NAO,模式对它们年代际变化的模拟效果略好于降水。多数模式都可以模拟出PDO和NAO的空间模态,其中CNRM_CM3和UKMO_HadGEM1对PDO年代际变化（8 a以上）的模拟与实际情况比较相似,并可以模拟出20世纪70年代中期之后PDO由负位相转变为正位相的情况,而模式UKMO_HadGEM1也对NAO的年代际变化以及1980年以来不断加强的趋势模拟较好。     

ＩＰＣＣＡＲ４中海气耦合模式对中国东部夏季降水及ＰＤＯ、ＮＡＯ年代际变化的模拟能力分析

利用１８８０—１９９９年中国东部３５站的观测降水资料、英国Ｈａｄｌｅｙ中心的海温和海平面气压资料以及ＩＰＣＣ第４次评估报告（ＡＲ４）中２０世纪气候模拟试验（２０Ｃ３Ｍ）的模式输出结果,对ＩＰＣＣＡＲ４中２２个耦合模式所模拟的我国东部夏季降水的年代际变化情况以及太平洋年代际涛动（ＰＤＯ）和北大西洋涛动（ＮＡＯ）的年代际变化情况进行了分析。结果显示,这些模式对２０世纪我国东部夏季降水年代际变化的模拟结果并不理想,但对降水在２０世纪７０年代中期前后的突变具有一定的模拟能力。其中ＩＡＰ＿ＦＧＯＡＬＳＬ＿０＿Ｇ可以大致模拟出２０世纪７０年代中期前后降水型的突变特征,而ＢＣＣＲ＿ＢＣＭ２＿０和ＵＫＭＯ＿ＨａｄＧＥＭ１则可以模拟出华北地区降水在２０世纪７０年代中期之后减少的现象。对于引起我国东部夏季降水年代际变化的重要因子ＰＤＯ和ＮＡＯ,模式对它们年代际变化的模拟效果略好于降水。多数模式都可以模拟出ＰＤＯ和ＮＡＯ的空间模态,其中ＣＮＲＭ＿ＣＭ３和ＵＫＭＯ＿ＨａｄＧＥＭ１对ＰＤＯ年代际变化（８ａ以上）的模拟与实际情况比较相似,并可以模拟出２０世纪７０年代中期之后ＰＤＯ由负位相转变为正位相的情况,而模式ＵＫＭＯ＿ＨａｄＧＥＭ１也对ＮＡＯ的年代际变化以及１９８０年以来不断加强的趋势模拟较好。     

季节内印度洋-西太平洋对流涛动对次季节-季节尺度大气可预报性的影响

利用非线性局部Lyapunov指数和条件非线性局部Lyapunov指数定量估计了季节内印度洋-西太平洋对流涛动（IPCO）和实时多变量Madden-Julian指数（RMM指数）可预报期限,量化了季节内IPCO对S2S尺度大气可预报性的贡献,深入研究了季节内IPCO演变下S2S尺度可预报期限空间分布的变化规律。结果表明：（1）与RMM指数相比,季节内IPCO指数可预报性更强,可预报期限达到31天左右,比RMM指数高出2周以上;（2）印度洋-西太平洋区域S2S尺度大气可预报性最强,可预报期限达到30天以上,其中季节内IPCO是该地区的主要可预报性来源之一,其贡献达到6天,占总可预报期限的25%以上;（3）随着季节内IPCO的演变,印度洋-西太平洋地区S2S尺度大气可预报性有空间结构变化,表现为可预报期限异常的传播和振荡。S2S尺度大气可预报期限正负异常沿季节内IPCO传播路径,一支以赤道中西印度洋为起点北传至印度半岛,一支向东传播,经过海洋性大陆到赤道西太平洋后向北传播,到达日本南部。同时,可预报性异常的传播在在东印度洋和西太平洋表现出反向变化的特征,形成东西两极振荡,当季节内IPCO向正位相发展时,东印度洋具有更强的可预报性,西太平洋具有更弱的可预报性,反之亦然。季节内IPCO的发展（衰退）可使东印度洋（西太平洋）S2S尺度大气可预报性更强,表明模式预报技巧对此具有更大的提升空间。     

Influence of UV-B Radiation and Temperature on Photodegradation of PAHs: Preliminary Results

The joint impact of UV-B radiation and temperature on photodegradation of polycyclic aromatic hydrocarbons (PAHs) sorbed to an organic solvent was assessed in this study. This approach was experimentally performed in a laboratory investigation by means of comparison of two different environments: Atlantic (Lancaster, UK) and Mediterranean (Tarragona, Catalonia, Spain) climatic conditions. The concentration of 10 PAHs contained in a tetradecane solution was compared under two different temperatures (10 and 20°C) and UV-B doses (6.5 and 22.5 kJ m⁻² day⁻¹). No photodegradation was observed for the heaviest hydrocarbons (benzo(a)anthracene, chrysene, benzo(a)pyrene, dibenzo(g,h,i)perylene and coronene). In general terms, the half-life of PAHs was highly dependent on their molecular weight. Significant faster photodegradation rates were detected specially for light PAHs. It indicates that a synergistic effect occurred when both temperature and UV-B dose increased. This synergism might have a great implication on the long-range transport of environmental organic pollutants taking into account that low-latitude areas are the hottest and most irradiated of the planet.     

Seasonal variation of PM10-bound PAHs in the atmosphere of Xiamen, China

PM₁₀ samples from a garden site (site A), an industrial-traffic intersection (site B), a residential site (site C) and an island site (site D) were collected at December 21–29, 2004; March 18–22, 2005; July 4–13, 2005 and October 24–28, 2005 in Xiamen. 15 priority PAHs compounds were analyzed by using a gas chromatograph/mass spectrometer (GC/MS). The abundance and origin of PAHs are discussed to reveal seasonal variations in Xiamen air quality. Average concentrations of Σ15PAHs were 17.5 ng/m³, 3.7 ng/m³, 32.6 ng/m³ and 10.5 ng/m³ from spring to winter with the highest value in autumn. The dominant PAHs components in every season were low and middle molecular weight PAHs including phenanthrene, pyrene, fluoranthene and chrysene. Diagnostic ratios and PCA analysis identified the main sources of particle bound PAHs: mainly from both gasoline and diesel vehicles exhaust, with some contribution from coal combustion, industry emission and cooking sources.     

Polycyclic aromatic hydrocarbons (PAHs) associated with atmospheric particles in Higashi Hiroshima, Japan: Influence of meteorological conditions and seasonal variations

This work studied the influence of meteorological conditions on particulate polycyclic aromatic hydrocarbons (PAHs) in the atmosphere of Higashi Hiroshima, Japan. The seasonal variation of particulate PAHs was also covered. It was found that ambient temperature, solar intensity and weekly rainfall had significant influence on the particulate PAH concentration based on correlation studies. Correlation of particulate PAHs with ambient temperature, solar intensity, weekly rainfall, wind speed and humidity was studied by using Pearson correlation analysis. Particulate PAHs had a strong negative correlation with ambient temperature and solar intensity. A moderate negative correlation with weekly rainfall was also observed. There was no significant correlation between particulate PAHs with wind speed as well as humidity. Besides, particulate PAHs were found to have significant positive correlation with sulfur dioxide and nitrogen dioxide while having a moderate negative correlation with ozone. The particulate PAHs in Higashi Hiroshima exerted distinct seasonal variation with a higher concentration in winter and lower concentration in summer. When compared among PAHs with different numbers of aromatic rings; 5-ring PAHs was found to exert the most distinct seasonal variation. The contribution of carcinogenic PAHs to total particulate PAH concentration was fairly constant at about 50% throughout the year.     

辽河水中PAHs的污染水平及源解析

在辽河的干支流选择12个例行监测断面,分别于2007年8月和11月采集水样,分析16种US EPA（美国环保署）优控多环芳烃（PAHs）的浓度变化。结果表明：辽河丰水期16种PAHs总量的浓度范围为216—848 ng/L,平均值为430 ng/L,枯水期16种PAHs总量的浓度范围为221—1360 ng/L,平均值为660 ng/L。特征指数表明,辽河水中PAHs主要来源于燃料的高温不完全燃烧,燃烧源为机动车、煤和生物质等。     

瓦里关及西宁PM_(10)和多环芳烃谱分布的观测研究

为了研究青海瓦里关和西宁PM10中多环芳烃污染特征及其来源,于2007年5月24日～6月1日在青藏高原东北部的瓦里关大气本底站和青海气象台进行了观测并各采集7组气溶胶样品,分析了PM10质量浓度、粒径分布和多环芳烃谱分布特征。结果表明,瓦里关PM10日均浓度为24.85μg.m-3,粒径分布呈三模态;西宁PM10日均浓度为65.25μg.m-3,呈明显双模态。瓦里关积聚态颗粒物质量百分比大于西宁观测点。瓦里关PM10中多环芳烃含量远低于同季节西宁地区,浓度值为8.38ng.m-3;高分子量的PAHs主要集中在细颗粒上,而粗颗粒上低分子量PAHs相对较多。两地区高分子量多环芳烃均为单峰分布。后向轨迹分析表明,瓦里关PM10中PAHs污染与西宁市以及黄河河谷工业带方向的输送密切相关。     

Distribution and source apportionment of Polycyclic aromatic hydrocarbons from atmospheric particulate matter PM<Subscript>2.5</Subscript> in Beijing

A total of 11 PM2.5 samples were collected from October 2003 to October 2004 at 8 sampling sites in Beijing city. The PM2.5 concentrations are all above the PM2.5 pollution standard （65 μg m^-3） established by Environmental Protection Agency, USA （USEPA） in 1997 except for the Ming Tombs site. PM2.5 concentrations in winter are much higher than in summer. The 16 Polycyclic aromatic hydrocarbons （PAHs） listed as priority pollutants by USEPA in PM2.5 were completely identified and quantified by high performance liquid chromatography （HPLC） with variable wavelength detector （VWD） and fluorescence detector （FLD） employed. The PM2.5 concentrations indicate that the pollution situation is still serious in Beijing. The sum of 16 PAHs concentrations ranged from 22.17 to 5366 ng m^-3. The concentrations of the heavier molecular weight PAHs have a different pollution trend from the lower PAHs. Seasonal variations were mainly attributed to the difference in coal combustion emission and meteorological conditions. The source apportionment analysis suggests that PAHs from PM2.5 in Beijing city mainly come from coal combustion and vehicle exhaust emission. New measures about restricting coal combustion and vehicle exhaust must be established as soon as possible to improve the air pollution situation in Beijing city.     

Particle Size Distribution and Gas-Particle Partition of Polycyclic Aromatic Hydrocarbons in Helsinki Urban Area

Ambient concentrations of polycyclic aromatic hydrocarbons (PAHs) were measured in Helsinki (Finland). Particle mass size distributions were obtained with a cascade impactor (12 stages) with glass fibre filters as substrates. Simultaneously with the impactor measurements, particulate and gaseous PAHs were collected on a quartz filter and XAD-2 adsorbent, respectively, for evaluation of gas-partition coefficients. Samples were analysed for PAHs by on-line coupled supercritical fluid extraction — liquid chromatography — gas chromatography — mass spectrometry. The impactor results showed that most of the PAHs in Helsinki urban area were concentrated in fine particles (<2.5 μm diameter) with unimode peak at about 1 μm. The results were comparable with the number distribution measured with a differential mobility particle sizer. Total amounts of PAHs (gas + particle) varied from 15 (acenaphthylene) to 1990 (fluorene) pg/m³. The PAHs lighter than 202 amu (pyrene and fluoranthene) were exclusively in gas phase, whereas those heavier than 202 amu were mostly associated with particles. A plot of the partition coefficients (logKp) versus the temperature dependent sub-cooled vapour pressures (logp _L ⁰ ) showed a gradient of −0.66, which deviated from equilibrium state (gradient = −1).     

锌锡复合掺杂纳米二氧化钛的光催化性能研究

采用溶胶—凝胶法制备了Zn2+、Sn4+复合掺杂的TiO2光催化剂,通过XRD、TEM、UV—Vis测试手段对样品进行分析,以对硝基苯酚为研究对象,对其进行光催化降解。结果表明:复合掺杂Zn2+、Sn4+提高了催化剂对波长在200—450 nm范围内的光的吸光度,发生"红移"。在氙灯激发下,其催化活性优于纯TiO2。