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.     

混凝-氧化法处理印染废水

采用混凝 氧化法对印染废水进行处理 ,得出最佳混凝条件及氧化条件。实验结果表明 ,该法可使印染废水的CODCr与色度去除率分别达到 90 .2 %和 99.1%。该方法具有去除率高、操作方便、设备简单、不产生二次污染等优点。     

SO2的气相光催化氧化及催化剂的失活和再生研究

在模拟大气环境中，紫外光照射以及纳米TiO2光催化剂的作用下，气相无机污染物SO2被完全氧化为SO2或H2SO4。本文提出了SO2的非均相光催化氧化机理，并得出光催化反应速率符合一级动力学过程；经过连续使用之后，TiO2的光催化活性降低，最后活性消失；经过水洗之后，失活的TiO2可以得到再生。失活的TiO2和新鲜的TiO2的IR和XPS光谱差异表明，失活的TiO2表面存在H2SO4，其被认为是使催化剂失活的成分。     

低浓度硫化氢废气的液相催化氧化法净化实验研究

针对H2S浓度为750~1500mg/m3的气体的液相催化氧化技术进行了动力学实验研究。配制了以铁基离子作为主催化剂的复合吸收净化溶液,同时加入稳定剂和表面活性剂提高催化剂在碱性吸收溶液的活性。分别考察了原料气中H2S、O2含量以及吸收液中催化剂离子浓度、温度等因素对吸收速率的影响;确定了较为理想的吸收操作条件并获得了较好的吸收净化效果;饱和吸收液易于再生,净化性能恢复良好,可重复使用。     

粉煤灰-H2O2催化氧化水中对氨基苯酚的试验研究

研究了利用电厂粉煤灰作为非均相催化剂,催化H2O2氧化对氨基苯酚(PAP),讨论了各种因素对PAP去除率的影响.结果表明,在30℃,pH=1.5,H2O2和PAP的起始浓度分别为0.50 mol/L和0.10 mol/L,反应时间为100min,粉煤灰用量为6.0%,搅拌速度为1000r/min的条件下,粉煤灰具有良好的催化活性,能有效地催化H2O2氧化PAP,PAP的去除率可达81%左右.该法可用于预处理含PAP的工业废水.     

药物合成废水处理工程

针对氯唑沙宗、枸橼酸莫沙必利化学原料药合成过程中产生的有机废水浓度高、成分复杂及处理难度大等特点（COD高达80 000 mg/L左右）,采用催化氧化-生物化学方法,试验研究了药物合成废水处理.试验结果表明,该技术对合成废水的COD去除率可达98%,SS去除率可达96%,色度降到50倍左右,其去除率约为98%.该系统运行费用为0.4～0.5元/m^3废水.经过3个月的工程运行,表明催化氧化-生物化学处理药物合成废水系统是一种高效率、低能耗、运行管理方便、经济可行的处理方法.处理类似制药废水这样的高浓度有机废液,上述废水处理工艺具有广阔的应用前景.     

掺杂负载型纳米TiO2降解橙黄G的光催化活性及其动力学研究

采用溶胶-凝胶法和浸渍-焙烧法制备了掺杂Sn(Ⅳ)的TiO2/AC光催化剂,以偶氮染料橙黄G为目标降解物,对光催化反应条件进行了优化.结果表明:利用Sn(Ⅳ)掺杂量为2.5 at.%的TiO2/AC光催化剂,在进水浓度50 mg/L,催化剂的用量12.5 g/L,pH值2.0,H2O21.5 mL/L,主波长为365 nm的300W高压汞灯光照条件下,反应60 min,橙黄G的光催化去除率可达99.1%.该反应符合Langmuir-Hinshelwood动力学方程,其速控步为吸附反应.共存阴离子SO42-和H2PO4-,对橙黄G的光催化降解反应均有一定的抑制作用.     

水解-酸化法在味精废水处理中的应用

结合江苏南通天字味精厂的工程实例,介绍了以水解-酸化法为主体的味精废水处理工艺的原理、特点和应用中注意的问题.该工艺运行结果表明:在治理味精废水方面具有较佳的耐冲击性能;出水稳定达标;操作运行管理方便;投资成本和运行费用均较低.从其优势看有良好的应用前景.     

几种新式太阳能光催化反应器的探讨

本文综述了几种新式的太阳能光催化反应器 ,对其结构和处理效果进行了比较 ,并对该法处理水的经济性进行简单的概述 ,指出光催化法是一种可以充分利用太阳能、具有很大发展潜力的水处理方法