大气污染物排放总量控制管理机制的探讨

阐述实施大气污染物总量控制的特点及作用，分析研究现行的总量控制管理模式，进行总量控制监控机制设计，提出总量控制政策体系的改进建议。     

喹啉的微波辅助光催化氧化降解研究

对微波辅助紫外光催化(MV/UV/P25)处理喹啉模拟废水的工艺条件进行了实验研究,并比较了MW、UV、UV/曝气、MW/UV/曝气、MW/UV/P25等五种体系下喹啉的降解,结果表明,微波辐射与紫外光催化(MV/UV/P25)在喹啉的降解过程中具有很好的协同作用,在反应进行到lh时,喹啉的去除率达到了64.9%。实验还对MW/UV/P25体系中喹啉降解的影响因素进行了研究。     

建设项目审批数据管理系统的设计与实现

本系统根据葫芦岛市环境保护的需要,整合各种环境保护建设项目审批数据,建立Oracle数据仓库,利用PowerBuilder技术完成对环境保护建设项目数据的管理、统计与发布。     

哈尔滨道路附近大气可吸入颗粒物浓度及其成份分析

采集了2005年8月具有代表性的道路附近空气中可吸入颗粒物(PM10),分析了PM10中的离子、重金属及碳成分含量。结果表明,哈尔滨市道路附近PM10离子组分中SO42-、NH4+、Ca2+浓度较高,其主要来源于交通尘污染;富集因子法表明元素Cr、Zn和Pb来源于人为污染;EC/TC大于0.36,主要来自于汽车尾气等一次污染源的排放。     

辽宁省辽河流域污染现状与对策

分析辽河流域地表水、地下水及水库水质现状,从保证生态需水、提高水体自净能力出发提出了适当减小开发利用率和合理安排工业布局等措施,并提出了污染物总量控制、加强工业点源与农业面源污染的综合治理,针对辽河流域地表水质已经严重污染的事实提出了实施水生态修复工程的建议。     

巢湖污染现状与水质恢复措施

巢湖是属于国家"三河三湖"重点水污染防治流域之一。近年来,湖体营养过程加剧,生态环境受到明显损害,制约了流域社会经济的可持续发展。巢湖湖区水中高锰酸钾、总氮、总磷含量分别为4.9、2.48、0.227mg/L,水质类别为劣ⅴ类(重度污染);表层沉积物中总氮、总磷含量平均值为1065、587 mg/kg。要实现流域水资源的可持续利用,必须加快水污染综合治理。文章分析了巢湖污染现状,结合实际情况提出了治理对策。     

SBR与SBBR法处理制药废水对比试验

制药废水属于高浓度含微生物难降解,对微生物有抑制作用的有机废水,水质水量波动大,本文对制药厂厌氧处理出水,分别采用SBR和SBBR法进行对比试验,研究其COD去除效果。当曝气量控制在0.02m3/h,沉淀时间在2h时,在2~10h反应时间段内,对比了SBR和SBBR法对CODCr的去除率。试验结果表明:总体上,SBBR法CODCr去除效果优于SBR,且更稳定,CODCr去除率能达到90%以上,而SBR在反应时间6h时达到CODCr最大去除率:82.03%后,出水中CODCr不降反升。     

Particle number size distribution and new particle formation: New characteristics during the special pollution control period in Beijing

New particle formation is a key process in shaping the size distribution of aerosols in the atmosphere.We present here the measurement results of number and size distribution of aerosol particles (10-1...     

Characteristics and recent trends of sulfur dioxide at urban, rural, and background sites in North China: Effectiveness of control measures

SO₂ measurements made in recent years at sites in Beijing and its surrounding areas are performed to study the variations and trends of surface SO₂ at different types of sites in Northern China. The overall average concentrations of SO₂ are (16.8 ± 13.1) ppb, (14.8 ± 9.4) ppb, and (7.5 ± 4.0) ppb at China Meteorological Administration (CMA, Beijing urban area), Gucheng (GCH, relatively polluted rural area, 110 km to the southwest of Beijing urban area), and Shangdianzi (SDZ, clean background area, 100 km to the northeast of Beijing urban area), respectively. The SO₂ levels in winter (heating season) are 4-6 folds higher than those in summer. There are highly significant correlations among the daily means of SO₂ at different sites, indicating regional characteristics of SO₂ pollution. Diurnal patterns of surface SO₂ at all sites have a common feature with a daytime peak, which is probably caused by the downward mixing and/or the advection transport of SO₂-richer air over the North China Plain. The concentrations of SO₂ at CMA and GCH show highly significant downward trends (-4.4 ppb/yr for CMA and -2.4 ppb/yr for GCH), while a less significant trend (-0.3 ppb/yr) is identified in the data from SDZ, reflecting the character of SDZ as a regional atmospheric background site in North China. The SO₂ concentrations of all three sites show a significant decrease from period before to after the control measures for the 2008 Olympic Games, suggesting that the SO₂ pollution control has long-term effectiveness and benefits. In the post-Olympics period, the mean concentrations of SO₂ at CMA, GCH, and SDZ are (14.3 ± 11.0) ppb, (12.1 ± 7.7) ppb, and (7.5 ± 4.0) ppb, respectively, with reductions of 26%, 36%, and 13%, respectively, compared to the levels before. Detailed analysis shows that the differences of temperature, relative humidity, wind speed, and wind direction were not the dominant factors for the significant differences of SO₂ between the pre-Olympics and post-Olympics periods. By extracting the data being more representative of local or regional characteristics, a reduction of up to 40% for SO₂ in polluted areas and a reduction of 20% for regional SO₂ are obtained for the effect of control measures implemented for the Olympic Games.     

Novel Co-Mg-Al-Ti-O catalyst derived from hydrotalcite-like compound for NO storage/decomposition

Catalysts of Co_1.5Mg_1.5/Al_0.9Ti_0.1O and Co_1.5Mg_1.5/AlO were successfully prepared by calcinations of corresponding hydrotalcite-like compounds at 800℃ for 4 hr. The derived oxides were of spinel phase and a small quantity of Ti substitution did not change the crystal purity. Their catalytic performance for the NO storage/decomposition was investigated. Ti incorporation enhanced the NO decomposition activity while has an opposite effect on the storage capacity of catalyst. In situ FT-IR spectra of the catalysts showed that the final adsorption species on the catalysts was coordinated nitrates/nitrites. In addition, NO storage/decomposition mechanism has been discussed on the basis of these observations.