基于DOC+CDPF后处理技术的公交车实际道路颗粒物排放特性

利用车载排放测试系统,对柴油公交车安装氧化催化转化器(DOC)+催化型颗粒捕集器(CDPF)前后的实际道路工况颗粒物排放特性进行了研究。安装DOC+CDPF前后,稳态工况下,颗粒物数量排放(PN)、质量排放(PM)分别在车速为25,30 km/h降幅最大;瞬态工况下,随着加速度的增加,PN、PM排放率降幅逐渐增大;颗粒粒径分布规律不同,安装前呈单峰或双峰分布,而安装后呈三峰分布,粒径124.1 nm左右降幅最大。     

DOC/CCRT老化对柴油公交车气态物排放特性的影响

基于重型底盘测功机,研究新鲜及老化氧化型催化器(DOC)、氧化型催化器耦合催化型颗粒捕集器(DOC+CDPF,CCRT)对在用国Ⅲ柴油公交车进行中国典型城市公交车循环CCBC时一氧化碳(CO)、总碳氢化合物(THC)、一氧化氮(NO)、二氧化氮(NO_2)和氮氧化物(NO_x)、二氧化碳(CO_2)等气态物排放特性的影响.结果表明:采用新鲜及老化DOC/CCRT,均可以降低CO、THC、NO排放,增加NO_2排放,NO_x及CO_2排放基本不变;在怠速、加速、减速及匀速这4种工况下,新鲜DOC比老化DOC对CO、THC氧化效率好,新鲜CCRT比老化CCRT对THC氧化效率好,但老化CCRT对CO氧化效率更好,新鲜DOC/CCRT比老化DOC/CCRT对NO减少幅度高,对NO_2增加幅度高,但对NO_x排放总量基本无影响.     

DOC+CDPF对生物柴油公交车排放特性的影响

采用便携式排放测试系统PEMS,研究某加装催化型连续再生颗粒捕集器(DOC+CDPF)的柴油公交车长期燃用生物柴油混合燃料B5时,整车常规气态物和颗粒物排放性能随行驶里程的变化规律.结果表明:随行驶里程的增加,一氧化碳(CO),总碳氢化合物(THC),颗粒物质量(PM)减排率均呈先增后减的趋势,THC减排率在行驶里程达到2.5×104km之前呈上升趋势,之后呈降低趋势,至8×104km时THC减排率较DOC+CDPF初装时减少41.05%,CO和PM减排率在行驶里程到达3.5×104km之前均呈上升趋势,之后呈降低趋势,至8×104km时CO和PM减排率较DOC+CDPF初装时分别减少20.24%和11.74%;氮氧化物(NOx)和颗粒物数量(PN)减排率整体上均呈降低趋势,在行驶里程8×104km处,NOx和PN减排率较DOC+CDPF初装时分别降低33.83%和10.35%.B5生物柴油公交车在行驶里程到达8×104km左右时,污染物的减排率明显降低,需对DOC+CDPF后处理装置进行保养,以延长其工作寿命.     

不同后处理装置对柴油车排放特性的影响——基于行驶里程的后处理装置对柴油公交车气态物排放特性的影响

三辆柴油公交车分别安装柴油机氧化催化器（DOC）,催化型颗粒捕集器（CDPF）与DOC+CDPF三种后处理装置,采用便携式排放测试系统PEMS进行测试,研究整车THC,CO与NO_x等气态物排放性能随行驶里程的变化规律.研究结果表明：对于加装了DOC的公交车,行驶里程达到8万km时DOC性能劣化,应进行保养,此前CO,THC与NO_x的平均转化效率分别为78%,43%和27%;CDPF有效工作时间短,需要定期进行高温保养,周期应为1万km左右,加装CDPF的公交车CO,THC与NO_x平均转化效率分别为74%,16%与15%;DOC+CDPF在行驶里程达12万km时才出现性能劣化现象,此前加装该后处理装置后的公交车CO,THC与NO_x平均转化效率分别为87%,76%与21%.DOC+CDPF的连续再生效果可有效延长后处理装置的工作寿命.     

DOC+CDPF对重型柴油车排放特性的影响

基于重型转毂试验平台对比研究国Ⅲ重型柴油车加装催化型连续再生颗粒捕集器(DOC+CDPF)前后的气态物及颗粒物排放性能,结果表明从市区循环、公路循环到高速循环,原车的CO、THC、CO_2及颗粒质量(PM)排放因子依次减小,NO_x及颗粒数量(PN)排放因子依次增大,颗粒数量浓度随粒径呈双峰分布并且以聚集态颗粒排放为主;加装DOC+CDPF后,各污染物排放因子均有所下降,且下降趋势从市区循环、公路循环到高速循环依次增大,从整个C-WTVC循环来看,CO排放因子下降70.36%,THC排放因子下降72.73%,CO_2排放因子下降17.00%,NO_x排放因子下降7.76%,PM、PN排放因子分别下降93.77%和98.91%,颗粒数量浓度随粒径仍呈双峰分布,但排放以核模态颗粒为主,并且聚集态峰值对应粒径减小.     

DOC+CDPF对生物柴油燃烧颗粒排放特性的影响

以一台满足国五排放法规的车用柴油机为样机,研究加装氧化催化转化器DOC与催化型颗粒捕集器CDPF(DOC+CDPF后处理装置)前后,柴油机燃用B20燃料(燃料含20%体积掺混比的生物柴油)的颗粒排放特性.结果表明,在未加装该后处理装置时,该机排气颗粒数量浓度的粒径分布呈双峰形态,B20燃料的排气颗粒数量浓度的峰值粒径在10nm和50nm附近,纯柴油的排气颗粒数量浓度的峰值粒径在50nm和200nm附近.在颗粒粒径小于120nm的区域,该机燃用B20燃料的排气颗粒数量浓度大于纯柴油.加装该后处理装置后,该机排气颗粒数量浓度的粒径分布呈多峰形态,峰值粒径在10nm、20nm和60nm附近.加装DOC+CDPF后,不论是柴油还是B20燃料,与原机相比,柴油机排气颗粒总数量下降明显,其中60~200nm粒径范围的颗粒数量浓度降幅更为显著.在相同工况下,DOC+CDPF对柴油机燃用B20燃料的颗粒总数量净化效率高于纯柴油.     

基于DOC+CDPF+SCR技术的国Ⅴ排放重型柴油机气态物排放特性研究

基于DOC+CDPF+SCR后处理技术,在国V排放重型柴油机平台上研究了后处理装置三个测点:本机后、DOC+CDPF后以及SCR后的NOx、THC、CO、SO2、CO2以及醛类等气态物排放特性。研究结果表明:DOC+CDPF+SCR联合工作能够有效降低柴油机的NOx、THC、CO及SO2的排放,转化率分别达到91.8%、96.9%、99.9%和90.5%。SCR对柴油机排放中的NOx和SO2净化起主导作用,DOC+CDPF对THC和CO净化起主导作用。SCR对发动机背压的影响以及尿素的分解引起柴油机的CO2和醛类排放上升分别为3.1%和22.8%。     

DMDF电控单体泵柴油机结合简单后处理装置实现国Ⅴ排放的研究

在一台原机为满足国Ⅲ排放法规的增压中冷电控单体泵四缸发动机上采用柴油/甲醇双燃料(DMDF)燃烧方式,结合废气再循环(EGR)技术及不同后处理装置进行台架试验.结果表明:加装DMDF系统并经过精细标定,在不添加任何后处理器的情况下,仅结合EGR,氮氧化物(NO_x)和颗粒物(PM)的排放即可满足国V规定法规,但总碳氢化合物(THC)和一氧化碳(CO)排放高于法规限值;增加采用氧化催化转化器(DOC)或DOC+颗粒氧化催化转化器(POC)简单的后处理装置可以使电控单体泵DMDF发动机排放全面满足国V排放标准要求.其中,仅采用DOC的方式,THC和CO十三点加权比排放与后处理之前相比的降幅可分别达98.0%和99.8%,且分别仅为国V限值的35.2%和2.4%,采用DOC+POC的方式,HC和CO十三点比排放较原机的降幅分别达99.2%和99.9%,且分别仅为国V限值的13.5%和1.2%.     

DOC+CDPF对国III重型柴油货车实际道路排放的影响

利用便携式车载排放测试系统（PEMS）对2辆加装氧化催化转化器（DOC）和催化型柴油颗粒捕集器（CDPF）与否的国III重型柴油货车进行实际道路排放测试.结果表明,2辆改造重型柴油车的CO、THC、固态颗粒物粒数（SPN）和黑碳（BC）实际道路排放因子分别为（1.31±0.37）g/（kW×h）、（0.20±0.03） g/（kW×h）、（7.13×10¹⁰±5.27×10¹⁰）个/（kW×h）和（0.69±0.06）mg/（kW×h）,相对于原始排放（拆除DOC+CDPF）分别降低52.48%、55.69%、99.91%和99.22%.从低速、中速到高速,CO和THC减排比例呈现上升趋势,然而运行工况对SPN和BC减排比例则无显著影响.加装DOC+CDPF会导致NO₂在NO_x中的占比升高,且从低速、中速到高速涨幅依次增大,但对NO_x无明显减排效益,其排放因子为9.53~9.83g/（kW×h）,远高于实验室排放限值.     

不同后处理器对DMCC发动机PM排放的影响

在一台整车排放达到国Ⅲ标准的YC4D140电控单体泵增压中冷柴油机上加装甲醇喷射系统,改成柴油甲醇组合燃烧(DMCC)发动机.使用AVL 415S烟度计和DMS 500快速颗粒物光谱仪研究不同后处理器对DMCC发动机颗粒物(PM)排放的影响.试验结果表明,各工况下单独CDPF、DOC+CDPF基本可以消除发动机产生的干炭烟.DOC+CDPF后处理方式与单独CDPF相比,颗粒物捕集效率明显提高,且前者对颗粒物中核态部分的捕集效果更加突出.甲醇掺烧后,炭烟和颗粒物几何平均直径降低.经CDPF和DOC+CDPF处理,415S烟度计测得的炭烟进一步降低;DMS颗粒物光谱仪显示的颗粒物粒径,因其中核态部分大部被氧化捕集而仅余较大几何平均直径的部分.小负荷时经CDPF和DOC+CDPF处理,颗粒物的几何平均直径会增大,大负荷时则相反.各工况下相比于CDPF,DOC+CDPF对核态颗粒物捕集更有效.     

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.     

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.     

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.     

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.     

Effects of two sludge application on fractionation and phytotoxicity of zinc and copper in the soil

The potential harm of heavy metals is a primary concern in application of sludge to the agricultural land. A pot experiment was conducted to evaluate the effect of two sludges on fractionation of Zn and Cu in soil and their phytotoxicity to pakchoi. The loamy soil was mixed with 0%, 20%, 40%, 60% and 80% (by weight) of digested sewage sludge (SS) and composted sludge (SC). The additions of both sludges caused a significant raise in all fractions, resulting in that exchangeable (EXCH) and organic bound (OM) became predominance of Zn and organic bound Cu occupied the largest portion. There was more available amount of Zn and Cu in SS treatments than SC treatments. During the pot experiment, the concentration of Zn in EXCH, carbonate (CAR) and OM and Cu in EXCH and OM fractions decreased in all treatments, so their bioavailability reduced. Germination rate and plant biomass decreased when the addition rate was high and the best yield appeared in 20% mixtures at the harvest of pakchoi. The two sludges increased tissue contents of Zn and Cu especially in the SS treatments. Zn in pakchoi was not only in relationship to ΔEXCH and ΔCAR forms but also in ΔOM forms in the sludge-soil mixtures. Tissue content of Cu in pakchoi grown on SC-soils could not be predicted by ΔEXCH. These correlation rates between Zn and Cu accumulation in pakchoi and variation of different fractions increased with time, which might indicate that sludges represented stronger impacts on the plant in long-term land application.     

Intraspecific differences in effects of co-contamination of cadmium and

A hydroponic experiment was carried out to study intraspecific differences in the effects of different concentrations of cadmium (Cd)(0-10 mg/L) and arsenate (As(V)) (0-8 mg/L) on the growth parameters and accumulation of Cd and As in six wheat varieties Jing-9428, Duokang-1, Jingdong-11, Jing-411, Jingdong-8 and Zhongmai-8. The endpoints of wheat seedlings, including seed germination,biomass, root length and shoot height, decreased with increasing the Cd and As concentrations. Significant differences in seed germination, biomass, root length, shoot height and the accumulation of Cd and As were observed between the treatments and among the varieties (p ＜ 0.05). The lethal dosage 50% were about 20, 80, 60, 60, 80 and 20 mg As/L for Jing-9428, Duokang-1, Jingdong-11,Jing-411, Jingdong-8 and Zhongmai-8, respectively, and the corresponding values for Cd were about 30, 80, 20, 40, 60 and 10 mg Cd/L, respectively. Among the six varieties, Duokang-1 was found to be the most resistant to Cd and As toxicity, and Zhongmai-8 was the most sensitive to Cd and As co-contamination. The resistance of the six varieties was found dependant on the seedling uptake of Cd and As. Duokang-1 was the most suitable for cultivation in Cd and As co-contaminated soils.     

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

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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.     

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.