Formation of Nitrate and Sulfate in the Plume of Berlin (8 pp)

Background, Aims and Scope Secondary inorganic aerosol (SIA), i.e. particulate sulphate (S(VI)), ammonium and nitrate (N(V)) is formed from gaseous precursors i.e., sulfur dioxide (S(IV)), ammonia and nitrogen oxides, in polluted air on the time-scale of hours to days. Besides particulate ammonium and nitrate, the respective gaseous species ammonia and nitric acid can be formed, too. SIA contributes significantly to elevated levels of respirable particulate matter in urban areas and in strongly anthropogenically influenced air in general. Methods The near-ground aerosol chemical composition was studied at two stationary sites in the vicinity of Berlin during a field campaign in summer 1998. By means of analysis of the wind field, two episodes were identified which allow to study changes within individual air masses during transport i.e., a Lagrangian type of experiment, with one station being upwind and the other downwind of the city. By reference to a passive tracer (Na+) and estimates on dry depositional losses, the influences of dispersion and mixing on concentration changes can be eliminated from the data analysis. Results and Discussion Chemical changes in N(-III), N(V) and S(VI) species were observed. SIA i.e., N(V) and S(VI), was formed from emissions in the city within a few hours. The significance of emissions in the city was furthermore confirmed by missing SIA formation in the case of transport around the city. For the two episodes, SIA formation rates could be derived, albeit not more precise than by an order of magnitude. N(V) formation rates were between 1.4 and 20 and between 1.9 and 59 % h-1 on the two days, respectively, and S(VI) formation rates were > 17 and > 10 % h-1. The area south of the city was identified as a source of ammonia. Conclusion The probability of occurrence of situations during which the downwind site (50 km downwind of Berlin) would be hit by an urban plume is > 7.4%. Furthermore, for the general case of rural areas in Germany it is estimated that for more than half of these there is a significant probability to be hit by an urban plume (> 8%). The S(VI) formation rates are higher than explainable by homogeneous gas-phase chemistry and suggest the involvement of heterogeneous reactions of aerosol particles. Recommendation and Outlook The possible contribution of heterogeneous processes to S(VI) formation should be addressed in laboratory studies. Measurements at more than two sites could improve the potential of Lagrangian field experiments for the quantification of atmospheric chemical transformations, if a second downwind site is chosen in such a way that, at least under particular stability conditions, measurements there are representative for the source area.     

Shifted power-law relationship between NO2 concentration and the distance from a highway: A new dispersion model based on the wind profile model

In this paper, a shifted power-law model, based on the wind profile model, had been supposed to simulate concentration gradient of nitrogen dioxide (NO₂) with distance from a highway. Field experiments were performed for NO₂ gradients from a highway in Shanghai by using passive samplers. The shifted power-law model was fitted well with experimental results of field experiments both in this study and in the literature. The results not only verified the validity of shifted power-law relationship between NO₂ concentration and the distance from a highway, but also partially demonstrated that there were some significant similarities between wind profile and air pollutants concentration profile near highway. With known concentration of chosen reference point and appropriate value of the parameter k, the model could be practically applied for predicting the NO₂ distributions near a highway. The methods of determining the parameter k were also discussed for further detailed studies.     

二氧化氯销毁氰化物的应用研究

在弱碱性条件下，二氧化氯消毒剂将氰化物氧化成无毒的氰酸盐（OCN）、二氧化碳和氮气。研究了影响二氧化氯销毁氰化物的几种因素：pH在8—11的范围内，不影响二氧化氯对氰化物的销毁率；在所试验的反应温度（0-40℃）内，温度对反应速率表现出有限的影响；二氧化氯与氰离子的最佳质量比为2：1；当氰离子最高使用浓度小于0．5g／L时，废水中氰离子浓度达一级以上的排放标准。     

微波解吸柠檬酸盐溶液中SO2实验研究

结合微波具有的热效应、非热效应特性，利用经改装的微波反应装置，研究了微波场下柠檬酸浓度、微波作用时间、微波功率、SO2初始浓度和搅拌速率对解吸柠檬酸盐溶液中SO2的影响，得出了影响SO2解吸率的基本规律和最佳解吸条件，并进行了分析。     

Characteristics of MnO2 catalytic ozonation of sulfosalicylic acid and propionic acid in water

The characteristics of different types of MnO₂ catalytic ozonation of sulfosalicylic acid (SSal) and propionic acid (PPA) have been investigated in this paper. The experimental results show the dependence of catalytic activity of MnO₂ on organic compounds and the pH of solutions, but it is independent on the type of MnO₂. For example, three types of MnO₂ have not any catalytic activity when ozonation of PPA under the condition of this experiment. All MnO₂ catalytic ozonation of SSal at pH=1.0 have a greater total organic carbon removal than ozonation alone has, however, at pH=6.8 and 8.5, catalytic efficiency is not observed. Furthermore, the batch experimental results indicate that there are no direct relationship between the activity of metal oxide catalytic decomposition of ozone and that of its catalytic degradation of organic compounds.     

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.     

COS,CS2 and SO2 in aluminium smelter exhaust

Measurements of carbonyl sulfide (COS) and carbondisulfide (CS₂) were carried out on samples drawn from a smoke stack of an aluminium smelter. Volume mixing ratios of 6 ppm COS and 0.1 ppm CS₂ were measured for gases from the electrolysis unit that had previously passed an Al₂O₃ fluid bed reactor and electrostatic precipitators. Specific emissions of 1.6 kg COS and 0.03 kg CS₂ per ton of primary aluminium were found. Extrapolating from this particular smelter’s conditions to a world mix specific COS emissions of about 4 kg/t(Al) are calculated resulting in emissions of annually 0.08 Tg COS into the atmosphere due to electrolytic aluminium production in 1995. Besides the photochemical conversion of anthropogenic CS₂ aluminium production is established to be the second major industrial source of COS probably exceeding automotive tire wear’s and coal combustion’s contributions.     

Poland’s environment - past,present and future state of the environment in the vistula and odra river basins

In the middle of the last century in the case of many river basins, it became obvious that the targets of the Helsinki-Commission (HELCOM) concerning a 50% reduction of nitrogen and phosphorus inputs to the Baltic Sea had not been reached. Such conclusions could be derived from the observed loads. But the measurements regarding the analysis were not sufficient to determine what the reasons for this report were, what has to be done to fulfil this agreement and to evaluate the time at which the targets can be reached. This contribution presents the current state of Polish surface water quality as well as results of modelling nutrient and heavy metal emissions into the two biggest Polish river basins: Vistula and Odra, which both cover approximately 90% of Poland's territory.     

Integrating models to predict regional haze from wildland fire

Visibility impairment from regional haze is a significant problem throughout the continental United States. A substantial portion of regional haze is produced by smoke from prescribed and wildland fires. Here we describe the integration of four simulation models, an array of GIS raster layers, and a set of algorithms for fire-danger calculations into a modeling framework for simulating regional-scale smoke dispersion. We focus on a representative fire season (2003) in the northwestern USA, on a 12 km domain, and track the simulated dispersion and concentration of PM_2.5 over the course of the season. Simulated visibility reductions over national parks and wilderness areas are within the ranges of measured values at selected monitoring sites, although the magnitudes of peak events are underestimated because these include inputs other than fire. By linking the spatial and temporal patterns of haze-producing emissions to climatic variability, particularly synoptic weather patterns, and the stochastic nature of fire occurrence across the region, we can provide a robust method for estimating the quantity and distribution of fire-caused regional haze under climate-warming scenarios.     

交通污染区城市绿化植物硫含量分布

为探讨城市绿化植物对交通环境中SO2的响应，以远离城市道路的相对清洁区公园生长的植物为对照植物，采集了广东省被广泛栽种的18种园林绿化植物的不同方位的叶片和树皮样品，用硫酸钡比浊法测定了每种植物样品在交通污染区面向机动车行驶方向、面向人行道方向及相对清洁区的植物样品等不同方位的植物叶片和树皮硫含量，分析了绿化植物在同一株植物的不同生长部位和不同环境中硫含量的分布特征。结果表明，交通污染区所有样品的叶片硫和树皮硫含量均高于相对清洁区的样品。其中，远离工厂的交通污染区生长的同一株植物，离机动车道越近，硫含量越高；靠近工厂的交通污染区的同一植物，离工厂近的部位的植物树皮硫含量高于面向机动车道一侧的植物硫含量。