不同排放标准下大型柴油客车实测排放因子与MOBILE6预测值的对比分析

在利用先进的车载尾气检测技术（PEMS）收集了我国大型柴油客车尾气的实时排放数据的基础上,分析了不同排放标准下车辆（国Ⅰ、国Ⅱ、国Ⅲ）的CO、HC、NOx和PM排放因子与速度的关系;使用MOBILE6模型,经过模型参数校正,预测了相应车辆的排放因子,并与不同排放标准下的车辆排放实测值进行对比,从而验证了MOBILE6模型对我国大型柴油客车尾气排放预测的适用性。     

中巴车实测排放因子和MOBILE6预测值的对比分析

利用车载尾气检测(OEM)技术对在实际道路上行驶的中巴车辆进行测试，得到该车的实测排放因子；同时应用美国环保局(EPA)开发的MOBILE6模型，在对相关参数进行适当调整后计算相应的排放因子；对得到的排放因子进行比较和分析，并就MOBILE6模型在我国的适用性做出探讨。     

捷达车实测排放因子和MOBILE6预测值的对比分析

OEM是最新的基于车辆实际行驶路况的车载尾气检测系统，文中利用OEM在实际道路上对不同捷达车的实时尾气排放进行测量，得到10天测试车辆每秒的尾气排放数据，并利用数据库统计、排放数据匹配行驶周期等方法，计算出每天的平均尾气排放因子。同时使用了美国的MOBILE6软件，确定相对应的输入参数，得到相应排放因子。最终将两者进行比较分析，探讨MOBILE6在中国的适用性。     

MOBILE计算中国机动车CO排放因子时的计算年确定

在使用MOBILE计算机动车排放因子时,一个较为重要的计算参数——计算年,在美国是根据实际年份来确定的,但是由于我国机动车排放发展水平与美国的不同,其值的确定是比较困难的关键问题。文章利用我国的实测机动车排放因子数据,在同等条件下使用MOBILE计算排放因子,并与道路实测数据对比,得到不同测试年份对应的MOBILE计算年,从而回归出使用MOBILE计算机动车排放因子的计算年公式。在今后利用MOBILE计算机动车排放时,可以方便的使用公式得到对应的MOBILE计算年,从而提高计算的精确度。     

北京市机动车污染物排放特征

定量分析计算机动车污染物排放特征 ,对城市汽车污染控制决策具有重要意义 .在利用实测数据确定基本参数的基础上 ,用 MOBILE5模型计算了北京市机动车污染物排放因子 ,获得了城区和全市机动车污染物排放总量和排放分担率 ,并分析了不同车型车种在城市区域汽车污染中的贡献率 .结果表明 ,北京市城区 CO,HC和 NO_x 的排放总量中 ,汽车源排放分担率分别为 :78% ,83%和 46% .     

中国机动车排放模型的研究与展望

通过介绍美国环保局(USEPA)颁布的机动车源排放模型(MOBILE)的发展、分类及最新模型版本,提出了根据这一思路开发的中国机动车排放模型.重点介绍了机动车类型划分、基本排放因子测试及有关修正因子的确定等.      

机动车排放车载实验及模型模拟研究

研究机动车的排放特征及获得排放因子,是建立机动车排放清单和制定相应控制策略的基础,而路上的机动车排放车载测试被认为是实验室台架测试的一个重要补充.本研究利用AVL DiGas 4000 light五气分析仪,在澳门典型路段上对7辆汽油轿车样本开展了尾气排放车载实验.研究发现安装电喷加三元催化转化系统的车辆(以下称电喷车)在气态污染物排放上比旧的化油器车有显著降低,化油器车HC、CO和NO排放的体积浓度平均值分别为227×10^-6、1.57%和1477×10^-6,而电喷车则分别为33×10^-6、0.21%和131×10^-6,约是前者的1/11～1/7.但电喷车在冷启动阶段会出现高排放;对电喷车的CO和NO排放浓度做算术平均,其绝对值主要由出现频率少的高浓度值所贡献.研究进一步估算了汽油轿车的排放因子,同时利用MOBILE5模型计算了澳门2000年汽油轿车的平均排放因子,模型计算值和实验数据估算结果的比值在59%～139%之间,如果仅比较年平均排放因子,这个比值则在68%～132%之间.结果表明,车辆采用电喷加催化转化系统,对控制污染物排放的作用显著,但催化设备存在冷启动时起燃缓慢的问题;对电喷车的技术改进,减少其在行驶过程中出现高浓度的污染物排放,将能进一步大大降低平均排放水平;应用修正的MOBILE5模型计算澳门地区汽油轿车的排放因子,结果是比较可信的.     

应用COPERTⅢ模型计算中国机动车排放因子

介绍了计算机动车污染物排放因子的COPERTⅢ模型,并根据中国机动车实际构成、行驶工况和燃油特征确定了模型所需参数,然后应用该模型计算得到了2002年中国机动车排放CO、NO_x、NMVOC和PM的排放因子.通过比较COPERTⅢ模式、MOBILE模式和台架测试得到的中国机动车排放因子发现,应用COPERTⅢ模型计算获得的排放因子更接近中国机动车实际排放情况.     

基于PEMS技术的交叉口尾气排放特性分析

利用车载尾气检测设备(PEMS)OEM-2100收集了在交叉口和路段上的实时尾气排放数据,利用GIS和相应二次开发工具构造了排放数据的分析平台,提出了交叉口尾气排放的空间分析方法,并对所收集的数据进行了对比分析。在此基础上,得到了交叉口处车辆各转向下的不同排放物的排放特征,计算了交叉口各转向相对于路段的排放系数,并对PEMS技术交叉口尾气排放进行了探讨。     

机动车排放模型的研究进展

综述了美国机动车的排放模型，讨论了美国环保局(USEPA)颁布的机动车源排放模型(MOBILE)、加州空气资源局(CARB)认证的排放因子模型(EMFAC)以及由加州大学河边分校和密西根大学主持研究的综合模式排放模型(CMEM)的发展、分类及最新重点模型版本，提出了建立基于我国情况的排放因子模型组的思路。     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Degradation of metabolites accumulated of benzo[a]pyrene by coupling Penicillium Chrysogenum with KMnO4

Several main metabolites of benzo[a]pyrene （BaP） formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone （BP 1,6- quinone）, trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene （BP 7,8-diol）, 3-hydroxybenzo[a]pyrene （3-OHBP）, were identified by high-performance liquid chromatography （HPLC）. The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that （1） the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; （2） the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; （3） the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% （w/v）, concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.     

Impact of atrazine and nitrogen fertilizers on the sorption of chlorotoluron in soil and model sorbents

Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.