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。     

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.).     

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.     

臭氧控制膜污染的研究进展

本文对臭氧在控制膜污染方面的研究现状进行了综述,重点放在臭氧用于膜冲洗和臭氧用于过滤液预处理这两个方面;指明了在一定的条件下,臭氧可以有效地减缓、降低膜污染;臭氧控制膜污染的作用主要通过臭氧降解造成膜污染的有机物质来实现.此外,还介绍了一些臭氧与膜联用的开发应用情况.     

碱性环境中臭氧破解污泥的效果研究

实验研究发现,在碱性环境中臭氧破解污泥的效果下降;将污泥pH调至11,24 h后,MLSS减少率=38.3%、MLVSS减少率=45.1%;通入臭氧18 min后,MLSS减少率=18.3%、MLVSS减少率=27.2%;污泥减量过程中pH呈下降趋势.     

臭氧-生物活性炭深度处理黄浦江水源水中试研究

以黄浦江水源水厂的滤后水为试验对象，进行饮用水O3-BAC深度处理工艺影响因素的中试研完。针对进水水质的试验结果表明，最优臭氧投加量为3mg／L左右，空床停留时间为15min左右。试验结果可为工程设计提供有益的参考。     

The GaNE programme in a global perspective

This paper provides the background to this special issue, outlining the extent to which the global atmospheric nitrogen cycle has been modified by human activity and outlining the range of effects. The global total emissions of reduced and oxidized nitrogen, amount to 124 Tg N, and exceed those from natural sources (34 Tg N) by almost a factor of four showing the extent to which anthropogenic activity has taken over the global N cycle. Of the 124 Tg N, 70 Tg N is emitted in the oxidized form, largely as NO and 70% of which results directly from anthropogenic activity. The remaining 54 Tg N is emitted as NH₃, (66% anthropogenic). The enhanced nitrogen emissions are associated with a range of local, regional and global issues including, acidification, eutrophication, climate change, human health and tropospheric O₃. The paper also places the Global Nitrogen Enrichment (GaNE) research programme in the UK in a wider perspective.     

低浓度臭氧在含钴盐硅胶上的吸附研究

常压下对含钴盐硅胶进行低浓度臭氧的吸附实验，吸附达到饱和后用氮气作为载气加热解吸。结果显示，含钴盐的硅胶对臭氧具有较强的吸附能力；臭氧解吸量随着解吸温度的上升而增加；吸附了臭氧的含钴硅胶粒子在常温(313．15K)下可在60min内不问断解吸出臭氧。     

北京市郊区夏季臭氧重污染特征及生成效率

为研究北京郊区夏季O₃(臭氧)重污染过程特征及O₃生成的光化学敏感性,基于2016年夏季在北京郊区开展的针对O₃及其相关污染物的强化观测试验(7月23日—8月31日,共计40 d),分析了观测期间O₃浓度[以φ(O₃)计]变化特征、O₃重污染过程主控因素与O₃敏感性化学特征.结果表明:观测期间φ(O₃)超标时有发生,最大小时φ(O₃)为151.1×10-9,其中有15 d的φ(O₃)最大8 h滑动平均值(O₃-max-8h)超过了GB 3095—2012《环境空气质量标准》二级标准限值,占观测天数的37.5%;不同O₃重污染过程成因有所不同,城市烟羽传输的污染物对郊区O₃重污染过程影响显著(观测期间臭氧重污染过程:过程1,7月27—29日;过程3,8月9—11日;过程4,8月16日;过程5,8月21—24日),区域光化学污染对郊区O₃重污染过程也有贡献(观测期间O₃重污染过程2:8月4—6日);结合后向气流轨迹进一步辅助说明了不同重污染过程中O₃的来源不同.研究还发现,观测区域存在反“周末效应”现象,说明观测区域周末受人为影响较为明显;基于观测数据计算的OPE(O₃生成效率)分析了O₃光化学敏感性表明,在有OPE值的22 d内NO_x控制区和VOCs控制区出现的概率(41%)相等,即观测区域O₃对NO_x和VOCs均敏感;此外还发现,在O₃重污染过程中光化学敏感性会随其反应进程发生改变,由NO_x控制区逐渐转变为VOCs控制区.      

重庆市夏秋季VOCs对臭氧和二次有机气溶胶生成潜势的估算

为估算重庆市夏秋季VOCs（挥发性有机物）对O₃和SOA（二次有机气溶胶）的生成潜势,利用在线GC-MS/FID在2015年8月22日-9月23日对重庆市区点和郊区点VOCs开展了为期一个月的实时观测,获得市区点和郊区点$ \varphi $（TVOCs）（总挥发性有机物）分别为41.35×10-9和22.72×10-9,其中市区点以烷烃（35.2%）和烯炔烃（25.2%）为主,郊区点以含氧挥发性有机物（oxygenated volatile organic compounds,OVOCs）（30.6%）和烷烃（26.0%）为主.结合最大增量反应活性量化市区点和郊区点VOCs的OFPs（臭氧生成潜势）分别为149.11×10-9和71.09×10-9,市区点OFPs最大的是乙烯、丙烯、甲苯、C8和C9的芳香烃等,郊区点OFPs最大的VOCs是丙烯醛、异戊二烯和甲基乙烯基酮.结合气溶胶生成系数量化郊区点和市区点VOCs对SOA的生成贡献分别为0.36和1.26 μg/m3,相比国内其余城市VOCs的SOAP（二次有机气溶胶生成潜势）较小,主要以甲基环己烷、正壬烷、正葵烷和十一烷等高碳烷烃,以及甲苯、苯、二甲苯和乙苯等芳香烃的SOAP为主.研究显示,控制烯炔烃和芳香烃的浓度有助于控制重庆市O₃的生成,控制高碳烷烃和芳香烃则有助于控制重庆市SOA的生成.