鼎湖山臭氧、氮氧化物和太阳可见光辐射相互关系的研究

给出了１９９６年了在广东肇庆鼎湖山自然保护区对太阳可见光 段辐射，地面臭氧、ＮＯ、ＮＯ２浓度的观测结果，对影响地面臭氧、ＮＯ、ＮＯ２的主要因子进行了分析，并得到了较好的结果，晴天条件下，地面臭氧浓度、ＮＯ、ＮＯ２浓度有明显的日变化；阴天条件下，地面臭氧浓度、ＮＯ、ＮＯ２浓度的日变化要复杂一些。     

臭氧污泥减量过程中混合液各参数的变化

实验用污泥的初始浓度(MLSS)分别限定为4g/L、7g/L和11g/L,用以探讨不同浓度下臭氧氧化过程中COD、N和P浓度的变化。结果表明:臭氧氧化过程中,MLSS和MLVSS基本呈线性下降;臭氧对污泥细胞的溶解可以引起混合液中COD、N和P浓度的升高,升高速率受污泥浓度和臭氧浓度影响较大;TKN和硝态氮是N的主要存在形式,TKN和TN随时间均呈先增加后趋缓的变化规律;臭氧对氨氮和亚硝酸盐氮有较强的氧化能力,二者浓度均呈先增大后减小的规律;而硝酸盐氮呈一直增加趋势;臭氧对COD的氧化也很明显,表现为COD的增加速率随氧化时间的增加而不断降低;总磷的浓度基本呈线性增加,单位质量污泥的总磷释放量差异不大;臭氧对MLSS的彻底减量会引起臭氧溶胞利用率的降低,因此应该合理控制臭氧化反应的时间。     

氟氯碳化合物的分解及对其损耗O3和臭氧消耗潜势的影响

采用计数物种法模拟氟氯碳化合物在大气中的分解行为，研究结果表明，ＨＣＦＣ－２２及ＣＦＣ－１１在在气中分解总量的２．７７％６和９８．２３％是在２０ｋｍ以上区域分解，正是这一部分的分解产物向平流层引入了Ｃｌ原子、破坏了Ｏ３，对其臭氧消耗潜势（ＯＤＰ）有着主要的贡献；研究结果还表明，ＨＣＦＣ－２２与ＣＦＣ－１１在平流层破坏Ｏ３的效率有极大的差别，在本计算的条件下，平流层上部单个Ｃｌ原子破坏Ｏ３的相差近６     

Air pollution effects on hospital admissions: a statistical analysis of parallel time series

A statistical model for longitudinal count data is used to examine the potential adverse health effects of ambient air pollution. Daily respiratory admissions to 164 acute care hospitals in Ontario are obtained for the period 1983 to 1988. Estimates of ozone levels in the vicinity of each hospital are determined from air pollution monitoring stations maintained by the Ontario Ministry of the Environment. Generalized estimating equation methods are used to make inferences about the regression and overdispersion parameters. The admission data display little evidence of serial correlation and extra Poisson variation. However, admission rates vary considerably among hospitals. This latter source of variation needs to be taken into account in examining the effects of air pollution on respiratory health status.     

炼油厂含油冷却水处理回用技术研究

开展了O3 氧化和强碱性阴离子交换组合工艺用于炼油厂含油冷却水回用处理的实验研究。结果表明 ,O3 氧化过程中的最佳pH值约为 10 .5 ,O3 氧化的除油效率为 86 .7% (紫外法测定 ) ,去除 1mg石油类约需消耗 5 .7mgO3 ,O3 氧化后产物以乙酸和丙酸等挥发性脂肪酸为主。离子交换处理后油的含量达到未检出的水平。研究结果表明 ,O3 氧化和离子交换组合处理技术能使炼油厂含油冷却水达到回用水水质标准。     

采用塔式反应器处理地面水中亚硝酸盐的研究

考察了塔式反应器中臭氧对地面水中亚硝酸盐氧化的工艺条件 ,得到了将亚硝酸盐氮含量为 0 .2 1mg/L的地面水处理到符合“地面水环境质量标准”Ⅰ、Ⅱ、Ⅲ类水的最佳工艺条件。研究表明 ,该工艺不受水温影响 ,有较好稳定性 ,且设备简单、处理费用低     

Study on the formation and transport of ozone in relation to the air quality management and vegetation protection in Tenerife (Canary Islands)

An experimental study on the formation and transport of ozone in ambient air was performed in Tenerife (Canary Islands) in order to investigate the processes affecting ozone levels and air quality. The special features of Tenerife (prevalence of the trade wind pattern (NE), orography and the specific location of the local ozone sources) permit to quantify the role of the ‘long-range transport from northern latitudes' versus the ‘formation and transport of ozone downwind of the main urban areas' of Tenerife. Levels of O₃, NO₂ and O_X were monitored in different types of environments to achieve this purpose. The results showed that: (1) upwind of the urban areas ozone is mainly transported from the ocean by trade winds, (2) local ozone titration (by NO) and ozone replenishment from the ocean are the main causes of ozone variations in urban and suburban areas, and (3) photochemical ozone production occurs downwind of the urban areas. Photochemical production causes daylight O₃ and O_X levels downwind of urban areas to be frequently (60% and 35% days/year, respectively) higher than upwind of the urban sites (O₃ and O_X excess frequently in the range 5–20 ppbv). Due to the above processes, different daily ozone cycles occur in short distances (<30 km), with maximum O₃ levels during daylight or night depending on the site. Ozone phytotoxicity was assessed by calculating the AOT40 index upwind and downwind of the main urban areas. The critical value for the 5-day-AOT40 index was simultaneously exceeded at the two sites (few times/year) during long-range transport events. During the additional exceedances of the critical value downwind of the urban area, relatively high 5-day-AOT40 values were recorded upwind of the urban site. Thus, long-range transport from northern latitudes may produce relatively high 5-days-AOT40 levels in the oceanic boundary layer. These results are important for the protection of the large number of endemic plants in the Canaries. The conceptual model discussed in this study may be qualitatively applied to other islands which possess features similar to those of Tenerife.     

多相催化-臭氧氧化法处理模拟有机磷农药废水

实验通过臭氧氧化法来降解模拟废水中的有机磷农药，将其转化为无害物质，并试验研究了在废水中加入2种自制的催化剂对降解结果的影响。采用气相色谱法测定水中有机磷农药的量。结果表明，只用臭氧处理的情况下1周后有机磷的去除率为78．03％；在催化剂A存在下，去除率可达93．85％；在催化剂B存在下，去除率可达为88．35％。结果表明，臭氧氧化法对此类污水：具有较好的降解作用，尤其在有催化剂存在的情况下处理效果更好，在室温和中性介质中均属于一级反应。     

臭氧-曝气生物滤池处理酸性玫瑰红染料废水

在实验室配制含酸性玫瑰红染料的印染废水,采用臭氧氧化-曝气生物滤池工艺开展处理试验.试验运行结果表明,臭氧氧化处理能提高模拟废水的可生化性,BOD/COD值由原水的0.18上升到0.36.经组合工艺处理后出水COD＜40 mg/L,色度40倍以下,SS约50 mg/L,处理效果良好.     

Halogenated compounds and climate change: future emission levels and reduction costs

OBJECTIVES: This work assesses the contribution to climate change resulting from emissions of the group of halogenated greenhouse gases. METHODS: A bottom-up emission model covering 22 technological sectors in four major regions is described. Emission estimates for 1996 and projection for 2010 and 2020 are presented. The costs for deep cuts into projected emission levels are calculated. RESULTS: The substances covered by this study have contributed emissions of 1100 +/- 800 MT CO2 equivalents per year in 1996. In terms of their relative contribution to emissions of CO2 equivalents, this corresponds to 3 +/- 2% of global emissions of all anthropogenic greenhouse gases. The wide range of uncertainty is due to the poorly quantified net global warming potential of the ozone depleting substances, which have an indirect cooling effect on climate through the destruction of stratospheric ozone. For annual emissions of HFCs, PFCs and SF6 (which are regulated under the Kyoto Protocol and for which global warming potentials are well defined), the relative contribution is projected to increase to 2% (600 MT CO2 eq.) of global greenhouse gas emissions by 2010. This trend is expected to continue, emissions are projected to grow to a contribution of roughly 3% (870 MT CO2 eq.) in 2020 compared to 0.9% (300 MT CO2 eq.) in 1996. For HFCs, PFCs and SF6, this study identifies global emission reduction potentials of 260 MT CO2 eq. per year in 2010 and 640 MT CO2 eq. per year in 2020 at below US$ 50 per ton. These values correspond to roughly 40% and 75% of projected emissions in 2010 and 2020, respectively.