利用IVE模型建立成都市轻型汽油客车排放清单

城市机动车污染物排放清单的建立是控制机动车污染的关键.本研究以2012年为基准年,通过对成都市轻型汽油客车技术水平分布、活动水平和保有量等数据的调查,将IVE模型本地化,计算了成都市2012年轻型汽油客车VOCs、PM、NOx、CO的排放清单,并分析了清单的不确定性.结果表明:成都市2012年轻型汽油客车排放的VOCs、PM、NOx和CO分别为2.23×104t、1.6×102t、1.26×104t和2.03×105t;轻型汽油客车中黄标车VOCs、PM、NOx、CO的排放量分别占排放总量的27.5%、18.1%、37.2%和42.5%,表明黄标车是轻型汽油客车污染物排放的主要来源;排放清单的不确定性主要来自于排放因子,VOCs、PM、NOx和CO清单的不确定性分别为-31.67%~32.35%、-54.75%~55.09%、-6.56%~6.76%和-12.22%~12.51%.     

天津市机动车尾气排放因子研究

通过调查研究天津市机动车车型构成、保有量、车辆行驶状况、气象数据和油品等基础数据,利用COPERT IV模型计算了在国1、国2、国3、国4和国5排放标准下机动车尾气中CO、NO_x、VOC和PM_(2.5)的排放因子.应用车载测试系统在实际道路上对国4柴油货车的排放因子进行了测量,并将模型结果与实测结果进行了比较,研究表明,国4排放标准下,污染物排放实测数据普遍高于模型模拟数据.对于轻型载货柴油车而言,实际道路测量的CO、NO_x、VOC和PM_(2.5)的排放因子分别是模型模拟数据的2.5、4.3、1.9和1.2倍;对于中型载货柴油车而言,以上污染物的实测排放因子分别是模型的1.3、2.1、1.0和1.2倍;对于重型载货柴油车而言,以上污染物的实测排放因子分别是模型的1.7、1.9、1.1和1.2倍.     

丹东市机动车尾气污染现状与控制措施

调查和研究了9种车型：轿车、出租车、摩托车、中型客车、小型面包车、大公共汽车、轻型货车、中型货车、重型货车的汽油和柴油的NOx，CO、HC、SO2、PM10污染排放量及分别在主干线、次干线、支路、街巷路中每条路段不同时间车流量密度及利用排放因子，求出每条路段机动车污染物排放量。同时分别汇总主干线、次干线、支路、街巷路中9种车型车流量密度及污染物排放量，最后估算出污染物排放总量。     

红河州机动车污染物排放特征研究

基于《道路机动车大气污染物排放清单编制技术指南》建立了红河州2019年机动车排放清单。结果表明:2019年红河州CO、HC、NOx、PM2. 5、PM10和SO2排放总量分别为29494、11908、13259、273、301和138t/a。机动车污染物分担率差别显著,小型汽油载客车、轻型汽油载货车和摩托车是CO的主要排放来源,小型汽油载客车和摩托车对HC排放贡献最大,对NOx、PM2. 5和PM10贡献最大的是大型柴油载货车。汽油车是CO和HC机动车污染物排放的主要贡献源,其排放量分别占排放总量的82. 01%和96. 64%,柴油车是NOx、PM2. 5和PM10的主要贡献源。     

运用CMEM模型计算北京市机动车排放因子

采用由美国加州大学Riverside分校开发的综合模式排放模型(CMEM)分析和研究北京市机动车污染物的排放特征,以9辆代表北京市典型技术类型的轻型机动车为实验车辆,收集了运行CMEM模型所需要的数据和参数.通过CMEM模型Access 2.02版本计算,得到了在不同交通行驶状况下北京市4类典型轻型机动车的CO2,CO,HC,NOx单车排放因子及各车型综合排放因子.通过与同一车辆的在路实测排放因子比较发现,用CMEM模型计算的CO,HC和NOx与实测排放因子及排放特征有较好的一致性,因此适用于计算北京市机动车CO,HC和NOx排放因子.      

西安市机动车尾气排放特征分析

根据车辆类型及排放因子计算西安市机动车尾气污染物排放CO、碳氢化合物(HC)、氮氧化物(NOx)及颗粒物(PM)的特征。结果显示,机动车排放污染物中一氧化碳含量远大于其他三者。CO和HC主要来自客车,尤其是小型客车,而颗粒物主要由重型货车排放;超过80%的CO和HC来自汽油车,而超过90%的PM排放来自柴油车;国Ⅰ前汽车在西安市汽车保有量中仅占3.48%,而四种污染物排放量在的比例分别为33.55%、29.68%、11.92%和21.43%。为减少机动车尾气污染物的排放,建议淘汰国Ⅰ前车辆,对柴油车尾气加强处理。     

中国机动车污染物排放因子及其修正方法研究

中国机动车污染物排放已成为影响空气质量的重要源。机动车污染的研究中,排放因子的确定是关键。根据机动车使用状况,车用燃料硫含量和行驶状况,运用MOBILE6．2的方法和原理确定了中国各类型机动车HC、CO、NOx的综合排放因子。小型汽油客车国0阶段CO、HC、NOx的综合排放因子分别为34．29g／km、3．45g／km和0．856g／km;国Ⅰ阶段CO、HC、NOx的综合排放因子分别为2．80g／km、0．25g/km和0．40g／km;国Ⅱ阶段CO、HC、NOx的综合排放因子分别为1．39g／km、0．16g／km和0．09g／km。     

乌鲁木齐市区机动车污染物排放特征研究

选择乌鲁木齐市125条道路调研测试得来的数据分析了乌鲁木齐市在用机动车的行驶分布的规律、污染物的排放特点和机动车道路的行驶特点。然后使用COPERT本地化模型计算CO、NMVOC、NOx和PM的排放因子,并计算了2012年CO、NMVOC、NOx和PM的排放量。通过估算得到2012年乌鲁木齐市机动车CO、NMVOC、NOx和PM的排放量分别为94 087,17 886,25 079,1 489 t。柴油机动车对NOx、PM的排放分担比率较大,而柴油机动车的保有量的贡献比率偏低;柴油汽车的CO、NMVOC的保有量的贡献比率跟它的排放分担率相比,贡献率要大;占保有量22.3%的国Ⅰ、国Ⅰ前标准的机动车辆对机动车CO、NMVOC、NOx、PM的排放分担比率分别为50.5%、41.0%、51.5%和55.0%;占保有量64.3%的国Ⅲ、和国Ⅳ车辆对CO、NMVOC、NOx和PM的贡献率分别为35.2%、42.7%、35.6%和33.9%。     

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。     

杭州市机动车污染物排放清单的建立

基于调研的基础数据,运用修正后的IVE排放模型及GIS系统建立了杭州市2010年1km×1km的高时空分辨率的机动车排放清单.结果表明,2010年杭州市机动车污染物CO、HC、NOx、PM的年排放量分别为44.06,2.31,4.43,0.65万t,主要来自线源道路的排放.各车型污染物分担率各不相同,汽油乘用车和公交车排放CO和HC最大,柴油重型货车和公交车是NOx和PM排放的主要来源,两种燃油下的机动车排放差异十分明显.机动车污染排放与路网密集程度及道路长度密切相关,因此西湖区和江干区排放总量远远高出其他区域.机动车各污染物排放强度空间分布均呈现由城市中心向城市边缘的递减趋势,各污染物中心城区排放量占总排量的70%以上.机动车污染物排放日变化十分明显,与人群出行规律有极大的相关性.     

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.     

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.     

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.     

Removal of heavy metals from sewage sludge by low costing chemical method and recycling in agriculture

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Single and joint effects of pesticides and mercury on soil urease

The influence of two pesticides including chlorimuron-ethyl and furadan and mercury （Hg） on urease activity in 4 soils （meadow burozem and phaeozem） was investigated. The soils were exposed to various concentrations of the two pesticides and Hg individually and simultaneously. Results showed that there was a close relationship between urease activity and organic matter content in soil. Chlorimuron-ethyl and furadan could both activate urease in the 4 soils. The maximum increment of urease activity by chlorimuronethyl was up to 14%-18%. There was almost an equal increase （up to 13%-21%） in the urease activity by furadan. On the contrary, Hg markedly inhibited soil urease activity. A logarithmic equation was used to describe the relationship （P〈0.05） between the concentration of Hg and the activity of soil urease in the 4 tested soils. Semi-effect dose （ED50） values by the stress of Hg based on the inhibition of soil urease in the 4 soils were 88, 5.5, 24 and 20 mg/kg, respectively, according to the calculation of the corresponding equations. The interactive effect of chlorimuron-ethyl or furadan with metal Hg on soil urease was mainly synergic at the highest tested concentrations.     

Isolation and preliminary characterization of a 3-chlorobenzoate degrading bacteria

A study was conducted to compare the diversity of 2-, 3-, and 4-chlorobenzoate degraders in two pristine soils and one contaminated sewage sludge. These samples contained strikingly different populations of mono-chlorobenzoate degraders. Although fewer cultures were isolated in the uncontaminated soils than contaminated one, the ability of microbial populations to mineralize chlorobenzoate was widespread. The 3- and 4-chlorobenzoate degraders were more diverse than the 2-chlorobenzoate degraders. One of the strains isolated from the sewage sludge was obtained. Based on its phenotype, chemotaxonomic properties and 16S rRNA gene, the organism S-7 was classified as Rhodococcus erythropolis. The strain can grow at temperature from 4 to 37℃. It can utilize several （halo）aromatic compounds. Moreover, strain S-7 can grow and use 3-chlorobenzoate as sole carbon source in a temperatures range of 10-30℃ with stoichiometric release of chloride ions. The psychrotolerant ability was significant for bioremediation in low temperature regions. Catechol and chlorocatechol 1,2-dioxygenase activities were present in cell free extracts of the strain, but no （chloro）catechol 2,3- dioxygenase activities was detected. Spectral conversion assays with extracts from R. erythropolis S-7 showed accumulation of a compound with a similar UV spectrum as chloro-cis,cis-muconate from 3-chlorobenzoate. On the basis of these results, we proposed that S-7 degraded 3-chlorobenzoate through the modified ortho-cleave pathway.     

Organochlorine pesticides in soils under different land usage in the Taihu Lake region, China

A field study was conducted in the Taihu Lake region, China in 2004 to reveal the organochlorine pesticide concentrations in soils after the ban of these substances in the year 1983. Thirteen organochlorine pesticides (OCPs) were analyzed in soils from paddy field, tree land and fallow land. Total organochlorine pesticide residues were higher in agricultural soils than in uncultivated fallow land soils. Among all the pesticides, ΣDDX (DDD, DDE and DDT) had the highest concentration for all the soil samples, ranging from 3.10 ng/g to 166.55 ng/g with a mean value of 57.04 ng/g and followed by ΣHCH, ranging from 0.73 ng/g to 60.97 ng/g with a mean value of 24.06 ng/g. Dieldrin, endrin, HCB and α-endosulfan were also found in soils with less than 15 ng/g. Ratios of p,p'-(DDD DDE)/DDT in soils under three land usages were: paddy field ＞ tree land ＞ fallow land, indicating that land usage inlfuenced the degradation of DDT in soils. Ratios of p,p'-(DDD DDE)/DDT ＞1, showing aged residues of DDTs in soils of the Taihu Lake region. The results were discussed with data from a former study that showed very low actual concentrations of HCH and DDT in soils in the Taihu Lake region, but according to the chemical half-lives and their concentrations in soils in 1980s, the concentration of DDT in soils seemed to be underestimated. In any case our data show that the ban on the use of HCH and DDT resulted in a tremendous reduction of these pesticide residues in soils, but there are still high amounts of pesticide residues in soils, which need more remediation processes.     

Sorption of 1-naphthol by plant cuticular fractions

The contribution of aliphatic-rich plant biopolymer to sorption of hydrophobic organic compounds is significantly important because of their preservation and accumulation in the soil environment,but sorption mechanism is still not fully understood.In this study, sorption of 1-naphthol by plant cuticular fractions was examined to better understand the contributions of respective fraction.Toward this end,cuticular materials were isolated from the fruits of tomato by chemical method.The tomato cuticle sheet consisted of waxes (6.5 wt%),cuticular monomer (69.5 wt%),and polysaccharide (24.0 wt%).Isotherms of l-naphthol to the cuticular fractions were nonlinear (N value (0.82-0.90)) at the whole tested concentration ranges.The KodKow ratios for bulk cuticle (TC1),dewaxed cuticle (TC2),cutin (TC4),and desugared cuticle (TC5) were larger than unity,suggested that tomato bulk cuticle and cutin are much powerful solption medium.Sorption capability of cutin (TC4) was 2.4 times higher than the nonsaponifiable fraction (TC3).The 1-naphthol interactions with tomato cuticular materials were governed by both hydrophobic-type interactions and polar (H-bonding) interactions. Removal of the wax and polysaccharide materials from the bulk tomato cuticle caused a significant increase in the sorption ability of the cuticular material.There was a linear negative trend between K_(oc) values and the amount of polysaccharides or fraction's polarities ((N O)/C);while a linear positive relationship between K_(oc) values and the content of cutin monomer (linear R~2=0.993) was observed for present in the cuticular fractions.Predominant sorbent of the hydrophobic organic compounds (HOCs) in the plant cuticular fraction was the cutin monomer,contributing to 91.7% of the total sorption of tomato bulk cuticle.     

Alterations of organ histopathology and metallolhionein mRNA expression in silver barb, Puntius gonionotus during subchronic cadmium exposure

Common silver barb,Puntius gonionotus,exposed to the nominal concentration of 0.06 mg/L Cd for 60 d,were assessed for histopathological alterations(gills,liver and kidney),metal accumulation,and metallothionein(MT)mRNA expression.Fish exhibited pathological symptoms such as hypertrophy and hyperplasia of primary and secondary gill lamellae,vacuolization in hepatocytes,and prominent tubular and glomerular damage in the kidney.In addition,kidney accumulated the highest content of cadmium,more than gills and liver.Expression of MT mRNA was increased in both liver and kidney of treated fish.Hepatic MT levels remained high after fish were removed to Cd-free water.In contrast,MT expression in kidney was peaked after 28 d of treatment and drastically dropped when fish were removed to Cd-free water.The high concentrations of Cd in hepatic tissues indicated an accumulation site or permanent damage on this tissue.     

Seed selections for crystallization of calcium phosphate for phosphorus recovery

Seed induces and promotes the crystallization of calcium phosphate, and acts as carrier of the recovered phosphorus （P）. In order to select suitable seed for P recovery from wastewater, three seeds including Apatite （AP）, Juraperle （JP） and phosphate-modified Juraperle （M-JP） were tested and compared. Batch and fixed-bed column experiments of seeded crystallization of calcium phosphate were undertaken by using synthetic wastewater with 10 mg/L P phosphate. It shows that AP has bad enduring property in the crystallization process, while JP has better performance for multiple uses, and M-JP is a hopeful seed for P recovery by crystallization of calcium phosphate.