An Analysis of Secondary Pollutants in Buenos Aires City

Air pollutant concentrations from a monitoring campaign in Buenos Aires City, Argentina, are used to investigate the relationships between ambient levels of ozone (O₃), nitric oxide (NO) and nitrogen dioxide (NO₂) as a function of NO _x (=NO + NO₂). This campaign undertaken by the electricity sector was aimed at elucidating the apportionment of thermal power plants to air quality deterioration. Concentrations of carbon monoxide (CO) and sulphur dioxide (SO₂) were also registered. Photo stationary state (PSS) of the NO, NO₂, O₃ and peroxy radicals species has been analysed. The ‘oxidant’ level concept has been introduced, OX (=O₃ + NO₂), which varies with the level of NO _x . It is shown that this level is made up of NO _x -independent and NO _x -dependent contributions. The former is a regional contribution that equates the background O₃ level, whereas the latter is a local contribution that correlates with the level of primary pollution. Furthermore, the anticorrelation between NO₂ and O₃ levels, which is a characteristic of the atmospheric photo stationary cycle has been verified.The analysis of the concentration of the primary pollutants CO and NO strongly suggests that the vehicle traffic is the principal source of them. Levels of continuous measurements of SO₂ for Buenos Aires City are reported in this work as a complement of previously published results.     

Spatial Characterization and Prioritization of Heavy Metal Contaminated Soil-Water Resources in Peri-Urban Areas of National Capital Territory (NCT), Delhi

Due to rapid industrialization and urbanization during last two decades, contamination of soils by heavy metals is on an increase globally. Lands under peri-urban agriculture are the worst affected. In NCT, Delhi about 14.4% of land area is chemically degraded. In order to take care of this problem, recently the Supreme Court of India ordered to shift various non-confirming (about 39,000 units) industries to regions outside NCT, Delhi. However in spite of this, there have been several reports and parliamentary debates on the phyto-toxicity and extensive accumulation of heavy metals in the region. Literature review revealed that the basis of these debates is a few studies on some point locations in/around Delhi. It was further observed that information on the distribution and extent of heavy metal pollution problem in the region was completely missing. The present study was thus basically aimed at assessing the spatial distribution/extent and type of heavy metal pollution in the study area, for enabling future designing of appropriate site-specific management measures by the decision makers.For this, detailed spatial information on bio-available heavy metal concentrations in the soils and surface/sub-surface waters of NCT (Delhi) was generated through actual soil/water surveys, standard laboratory methods and GIS techniques. The study showed that concentration of all micronutrients (viz. Zn: 0.05–0.18 ppm; Cu: in traces; Fe: 0–0.5 ppm; and Mn: 0–1.2 ppm) and most heavy metals (viz. Ni: 0–0.7 ppm; Pb: 0–0.15 ppm and Cd: in traces) in the surface/sub-surface irrigation waters were well within permissible limits. However Cr concentrations in irrigation waters of Alipur and Shahdara blocks were far above their maximum permissible limit of 1 ppm. It was further observed that Ni and Cr concentrations in the drinking waters of almost entire test area were far above maximum permissible levels of 0.02 and 0.01 ppm, respectively. Bio-available concentrations of several heavy metals (viz. Pb: 0.1–2 ppm; Cd: traces; Ni: 0.05–2 ppm and Cr: 0–0.4 ppm) in the study area soils were also observed to be well within the maximum permissible limits. However there were point Cu contaminations (5–10 ppm) in the sewage-sludge amended soils of vegetable growing areas near south Shahdara block. This was attributed to increased Cu availability due to oxidized acidic conditions generated by over-irrigation of agricultural lands. Available Mn concentrations in Kanjhawala, western Najafgarh and Alipur soils were also observed to be above maximum permissible limit of 10 ppm. This was observed to be mainly due to the geology (i.e. presence of Mn rich sedimentary rocks) and prevalence of reduced acidic conditions, due to paddy cultivation, in these areas. It was further observed that there is acute zinc (Zn) deficiency (< 0.6 ppm) in paddy growing soils of north Kanjhawala, Alipur and some parts of Najafgarh and Shahdara blocks due to extensive leaching of available Zn fractions to lower soil horizons. Similar available Zn deficiencies in high pH (8.5) soils of areas around Bamnoli village in E-Najafgarh block were also observed.     

Trace Metal Levels in Mussels (Mytilus Galloprovincialis L. 1758) from Turkish Aegean Sea Coast

Bio-monitoring of some heavy metal levels (Cd, Pb, Zn, Cu) in whole edible soft parts of Mytilus galloprovincialis (L. 1758) was conducted in Turkish Aegean Sea coast during the period of September 2002–August 2003 seasonally. Moreover, some physico-chemical environmental parameters, also have been analysed in the same region. The values of some physico-chemical environmental parameters in coastal waters of Turkish Aegean Sea were changed between; 9.0–27.0 ^∘C for temperature, 31.93–40.45 psu for salinity, 7.35–8.48 for pH and 4.05–9.50 mg/l for dissolved oxygen. The levels of trace elements in whole edible soft parts including interstitial fluids of Mediterranean mussels M. galloprovincialis (L. 1758), sampled from 6 different regions of Turkish Aegean Sea coast have ranged between; 0.04–0.52 μg Cd/g wet weight, 0.49–1.72 μg Pb/g w.w., 0.95–1.85 Cu/g w.w., 16.11–37.15 μg Zn/g w.w. The highest values for all trace metals (Cd, Pb, Zn, Cu) were measured in inner part of Izmir Bay (station 3) and lowest in Sigacik and Gulluk Bay (station 5, 6). Generally heavy metal levels are lower than the results in soft mussel tissues reported from Mediterranean regions.     

Characterization and Identification of the Sources of Chromium, Zinc, Lead, Cadmium, Nickel, Manganese and Iron in Pm10 Particulates at the Two Sites of Kolkata, India

Monitoring of ambient PM₁₀ (particulate matter which passes through a size selective impactor inlet with a 50% efficiency cut-off at 10 μm aerodynamic diameter) has been done at residential (Kasba) and industrial (Cossipore) sites of an urban region of Kolkata during November 2003 to November 2004. These sites were selected depending on the dominant anthropogenic activities. Metal constituents of atmospheric PM₁₀ deposited on glass fibre filter paper were estimated using Inductively Coupled Plasma Atomic Emission Spectrometer (ICP-AES). Chromium (Cr), zinc (Zn), lead (Pb), cadmium (Cd), nickel (Ni), manganese (Mn) and iron (Fe) are the seven toxic trace metals quantified from the measured PM₁₀ concentrations. The 24 h average concentrations of Cr, Zn, Pb, Cd, Ni, Mn and Fe from ninety PM₁₀ particulate samples of Kolkata were found to be 6.9, 506.1, 79.1, 3.3, 7.4, 2.4 and 103.6 ng/m³, respectively. The 24 h average PM₁₀ concentration exceeded national ambient air quality standard (NAAQS) as specified by central pollution control board, India at both residential (Kasba) and industrial (Cossipore) areas with mean concentration of 140.1 and 196.6 μg/m³, respectively. A simultaneous meteorology study was performed to assess the influence of air masses by wind speed, wind direction, rainfall, relative humidity and temperature. The measured toxic trace metals generally showed inverse relationship with wind speed, relative humidity and temperature. Factor analysis, a receptor modeling technique has been used for identification of the possible sources contributing to the PM₁₀. Varimax rotated factor analysis identified four possible sources of measured trace metals comprising solid waste dumping, vehicular traffic with the influence of road dust, road dust and soil dust at residential site (Kasba), while vehicular traffic with the influence of soil dust, road dust, galvanizing and electroplating industry, and tanning industry at industrial site (Cossipore).     

LB复合膜选择性检测水中痕量镉离子的方法研究

开发了一种利用LB复合膜选择性地检测水中痕量镉离子的技术方法,研究了最佳LB复合膜检测器的制作条件.用表面活性剂十二烷基-(2-噻唑偶氮)间苯二酚(DTAR)作显色剂,对乙烯基硬脂酸盐(PVS)、十八烷基异丁烯酸盐(PMOA)、乙烯基-N-氨基甲酸十八烷基酯(PVOC)和顺丁烯二酸酐-1-十八烯(PMO)4种聚合物进行了强度实验,得出稳定的检测器结构,即偶数层DTAR上附着单层PVOC的LB复合膜.经过灵敏度实验,制作出最佳LB复合膜检测器DTAR6-PVOC1,在pH为7.5,温度40℃且搅拌的反应条件下,该检测器可以在10 min之内检出10-7mol/L镉,并可目视定性及半定量检测出水中痕量镉离子.水中可能共存的离子中只有CU2+和Zn2+会干扰镉离子的检测,需要抑制.      

受污染原水中有机物去除中试集成系统的工艺对比研究

在中试集成系统水平上对比研究了常规工艺、预臭氧化工艺、粒状活性炭吸附工艺、臭氧-生物活性炭工艺对受污染源水中的有机物及消毒副产物前体的去除效果.结果表明,前2种工艺对有机物的去除效能大致在50%～60%,后2种则能达到75%～90%.与前2种相比,后2种为更有效地去除受污染原水中有机物的方法.建议采用Ⅱ类及更优水体为水源的水厂考虑使用常规处理或季节性水质变化时采用预氧化工艺;而对于那些以Ⅲ类或更差水体为主水源的水厂则应考虑增设GAC或BAC设备,以满足饮用水水质新标准要求.     

青藏铁路用空气弹簧橡胶胶料耐紫外线老化试验研究

我国正在建设的青藏铁路是世界上海拔最高、线路最长的高原铁路.其气候特点对橡胶制品提出了新的技术要求,为适应在该气候条件下的运用需要,进行了针对空气弹簧胶囊用橡胶的耐紫外线老化试验研究工作,试验表明随着紫外线老化时间的增加,其硬度和300%定伸强度均提高,但拉伸强度和扯断伸长率随着紫外线老化时间的增加而降低;通过与胶料的耐臭氧试验和大气老化试验比较,基本可以认为引起空气弹簧胶囊表面龟裂的主要原因是受力状况、臭氧和大气老化的作用,而紫外线对橡胶的表面龟裂影响作用不大,因此,为提高空气弹簧胶囊的耐老化性能,主要考虑降低橡胶的受力,提高耐臭氧和耐大气老化性能.     

多功能粉煤灰治理垃圾场渗滤液

以具絮凝、吸附、降解多功能粉煤灰污水处理材料,填充成絮凝沉降降解过滤箱,组合有鼓气、臭氧的连续式5级垃圾场渗滤液集成处理系统。垃圾渗滤液流量、鼓气量、臭氧量分别为40Lh、40L(m3·h)、15mgL的工艺条件下,渗滤液的悬浮物、色度、CODCr、BOD5、氨氮、硫化物等主要污染物指标分别降低93%、90%、96%、92%、86%和92%,达到垃圾场渗滤液二级控制标准。     

Ozone facilitated degradation of caffeine using Ce-TiO2 catalyst

The ozone initiated oxidation of 1,3,7-trimethylxanthine (caffeine), commonly found in wastewaters as model compound is reported using cerium (Ce)/titanium dioxide (TiO₂) as catalyst. The effect of pH and loading of ceria on titania were investigated. Effect of reaction conditions on degradation of caffeine based on their pseudo first-order rate constants were compared. The combination of catalyst Ce-TiO₂ and ozone aeration significantly enhanced the degradation of caffeine compared to uncatalysed ozonation. The oxidation of caffeine ensued via the free radical mechanism, through enhanced ozone decomposition into OH radicals. Ce/TiO₂(0.5?wt%) showed good activity in degradation of caffeine at pH 6, in both natural stream and river water samples showing about 60% total organic carbon removal in 2?h ozonation period. Using liquid chromatography-mass spectroscopy, degradation products were analysed. A reaction intermediate and one final product were positively identified. Nano-catalysts with different loadings of Ce on TiO₂ synthesized by sol-gel route were characterized by scanning electron microscope, transmission electron microscopy, BET and powder X-ray diffraction spectrum techniques. The results showed that the material retained a highly ordered mesoporous structure and possessed large surface area.     

衡阳市区和衡山背景站臭氧浓度变化规律的对比分析

选取衡阳市区和衡山背景站臭氧自动监测数据,分析两地的臭氧污染特征。对空气质量的优良率情况、臭氧作为首要污染物的变化情况、臭氧浓度的日变化特征、典型时段的浓度变化特征、臭氧浓度的月际变化特征和臭氧与PM_(2.5)的关联情况等进行了分析。结果表明,多云及阴雨天气时,衡阳市区的臭氧浓度日变化幅度大于衡山背景站。夏季,衡阳市区和衡山背景站的臭氧浓度的日变化特征规律差异较大,臭氧浓度分布比较分散,前者为典型的单峰形,后者则波动平缓。冬季,日变化幅度不大,但衡阳市区的臭氧浓度明显低于衡山背景站。衡山背景站和衡阳市区的臭氧基本同步变化,但日均值高于衡阳市区。