南京北郊冬夏季大气PM2.5中水溶性有机碳的研究

为研究南京北郊大气PM_(2.5)中水溶性有机碳(WSOC)的浓度及来源特点,在冬、夏季分别采集PM_(2.5)样品,还同步收集臭氧(O_3)浓度与相对湿度(RH)数据,分析了PM_(2.5)、有机碳(OC)、水溶性有机碳(WSOC)浓度特征,并对WSOC冬、夏季来源及其二次来源差异进行了探讨.结果显示,南京北郊冬季大气污染水平明显高于夏季且来源更复杂,与冬季静稳的天气条件及化石燃料和生物质燃烧排放较严重有关.冬季PM_(2.5)平均值为(136.7±42.4)μg·m~(-3),OC、WSOC浓度分别为(13.4±4.4)、(8.5±3.1)μg·m~(-3);夏季PM_(2.5)、OC、WSOC平均浓度分别为(61.5±14.6)、(6.7±2.1)、(4.6±1.7)μg·m~(-3).冬、夏季WSOC/OC值分别为67%±20%、69%±13%,且二次有机碳(SOC)与WSOC显著正相关,说明二次来源对WSOC有显著影响.冬季WSOC与O_3的负相关性不显著,与RH显著正相关;而夏季WSOC与O_3、RH的相关性正好与冬季相反,说明冬、夏季二次WSOC形成途径存在差异.冬季二次WSOC可能主要来自液相氧化,夏季可能主要来自光化学氧化.通过主成分因子分析法进一步确定南京北郊冬、夏季WSOC分别主要来源于二次来源和生物质燃烧、汽车尾气和扬尘.     

利用轨迹模式模拟近地层臭氧日变化

提出在多条轨迹上应用轨迹模式，以实现对固 区臭氧浓度日变化的模拟，应用该方法对北京燕山石化炼油厂地区的Ｏ３浓度日变化进行了模拟，结果表明模拟值和实测值十分吻和。进一步模拟了当地的臭氧生物特征，并讨论了当地的气象条件和源排放对Ｏ３生成浓度的影响。结果说明削减ＮＯｘ的排放量是控制该地区光化学烟雾形成的关键，而降低燃烃和芳香烃在排放物中所占的比例也是控制该地区光学烟雾的重要手段。     

The spatial and temporal distribution of total ozone over China

In this paper the grid data of total ozone mapping spectrograph (TOMS) installed on Nimbus-7 satellite (1978 to 1994) was used and the spatial and temporal distribution of total ozone over China was analyzed. The research indicates that the Qinghai-Tibet Plateau destroyed the latitudinal distribution of total ozone of China and the low value closed center emerged over Qinghai-Tibet Plateau. Long time change trends of seasonal total ozone of Qinghai-Tibet plateau are provided. It shows that the most obvious decrease of total ozone occurs in winter (Jan.), then in summer (Jul.), the relevant slow change occurs in autumn (Oct.) and spring (Apr.).     

兰州西固工业区夏季光化学烟雾污染的气象条件

通过对兰州西固工业区光化学烟雾污染规律与气象条件的关系的研究表明,在高空槽后的低空弱高压控制下,西固区出现高的臭氧浓度值,此时大气层结稳定,风很小,天气晴朗,但中午有浓重烟雾,臭氧浓度峰值在中午出现。该区盆地内形成的光化学烟雾烟团水平面积达几十公里,臭氧浓度的日变化取决于太阳总辐射和大气边界层的日变化。     

国际环境保护公约中技术转让障碍问题的探讨

随着世界各国对全球资源与环境问题认识的逐步提高 ,发展中国家必将签署越来越多的国际环境公约 ,参与到国际环境保护合作中。尽管许多国际环境公约都明确规定了发达国家在资金和技术上支持发展中国家保护环境履行国际公约的义务 ,但是实际履约过程中技术转让的问题并未得到良好的解决。论文将讨论国际环境公约履约中的技术转让障碍问题 ,并以中国履行《关于消耗臭氧层物质的蒙特利尔议定书》 ,实施臭氧层保护行动过程中所存在的实际问题为例 ,对国际环境公约履行中技术转让障碍的原因及其后果进行分析 ,最后对发展中国家所应采取的立场和对策提出建议。     

Degradation of nitrobenzene in aqueous solution by ozone-ceramic honeycomb

IntroductionAs a promising advanced oxidation technology for watertreatment ,catalytic ozonation has received great attentionforthe efficient degradation of organic compoundsinrecent years(Legube , 1999) . Some studies showed that homogeneousand heterogen…     

Spatial and temporal distribution of total ozone over China

In this paper the grid data of total ozone mapping spectrograph (TOMS) installed on Nimbus 7 satellite (1978 to 1994) was used and the spatial and temporal distribution of total ozone over China was analyzed. The research indicates that the Qinghai Tibet Plateau destroyed the latitudinal distribution of total ozone of China and the low value closed center emerged over Qinghai Tibet Plateau. Long time change trends of seasonal total ozone of Qinghai Tibet Plateau are provided. It shows that the most obvious decrease of total ozone occurs in winter (Jan.), then in summer (Jul.), the relevant slow change occurs in autumn (Oct.) and spring (Apr.).     

臭氧和模拟酸雨对冬小麦气体交换、生长和产量的复合影响

为探明酸雨和臭氧(O3)对作物是否存在复合影响,运用田间原位开顶气室研究了pH4.0模拟酸雨(SAR)和O3对冬小麦气体交换、生长和产量的影响.该实验包括3种处理:CF处理采用经活性炭过滤后的空气,作为对照;CF100处理采用经活性炭过滤后的空气加人恒定浓度为100 nL·L-1的O3;CF100 SAR处理为在CF100的基础上对冬小麦喷施pH 4.0模拟酸雨,喷施量为150 mL·m-2,每10d一次.结果表明:①CF100和CF100 SAR组冬小麦叶片细胞膜系统受到破坏,光合色素含量和气体交换参数降低,抑制了作物生长,导致生物量和产量下降.与CF相比,CF100和CF100 SAR处理下冬小麦产量分别降低了68.2%和63.6%;②与CF100组相比,CF100 SAR组对冬小麦细胞膜系统和叶绿素a含量产生显著的复合影响(p＜0.05),而对叶绿素b和类胡萝卜素含量、气体交换、小麦生长、生物量和产量的复合影响不显著.     

芳香化合物的光催化-臭氧联用降解研究

研究了几种芳香化合物的光催化 臭氧联用降解。探讨了光催化 臭氧联用技术降解有机物作用机理,分析了芳香化合物结构与反应活性的关系。实验结果表明,光催化 臭氧联用对芳香化合物的降解都存在一定的协同效应,而且符合表观准一级反应动力学规律;203#膜光催化臭氧的作用机理是催化臭氧产生了更多的高活性氧化剂,芳香化合物结构对其光催化 臭氧联用降解活性有很大影响。     

Catalysts for decomposing ozone tail gas

The preparation of immobilizing-catalysts for decomposing ozone by using dipping method was studied. XRD, XPS and TEM were used to characterize the catalysts. The three kinds of catalysts were selected preferentially, and their catalytic activities were investigated. The results showed that the catalyst with activated carbon dipping acetate( active components are Mn:Cu = 3:2, active component proportion in catalyst is 15%, calcination temperature is 200℃ ) has the best catalytic activity for ozone decomposing. One gram of catalyst can decompose 17.6g ozone at initial ozone concentration of 2.5g/m^3 and the residence time in reactor of 0.1s. The experimental results also indicated that humidity of reaction system had negative effect on catalytic activity.