CO2埋地管道泄漏区土壤形貌及温度场研究

通过建立DN25规格的小尺度埋地管道试验装置,开展了气相和超临界相CO_2通过2 mm口径的埋地管道向上泄漏试验,通过改变管道埋地深度(0 mm、200 mm、400 mm),研究了气相和超临界相CO_2埋地管道发生泄漏时土壤表面和泄漏口区域的形貌,以及泄漏口附近管壁和土壤区温度的分布。结果表明:气相和超临界相CO_2埋地管道发生泄漏时,在不同相态和管道埋地深度下,土壤表面会呈现"土壤喷射"、"小孔射流"和"土壤隆起"3种不同形貌;当土壤表面不发生"土壤喷射"时,泄漏口附近会形成冻土球;管道埋地深度越大,管壁温降速率增大,管壁最低温度降低;土壤区温度与埋地管道距泄漏口的距离呈指数函数关系,且在泄漏口附近土壤区射流方向的温降最大,管道埋地深度增加使得泄漏口附近土壤区在射流背向的温降幅度明显增加。     

新型絮凝剂聚合氯化铝钙中铝形态表征及钙含量测定

以Al2O3和CaCO3为原料经高温焙烧酸溶制备工艺合成新型高效絮凝剂——聚合氯化铝钙。采用Al-Ferron逐时络和比色法研究产品中的铝形态;络合滴定法研究钙含量。结果表明:焙烧工艺对钙含量的影响较大,酸溶工艺对钙含量的影响较小。在最佳配比条件下,生成的Alb为最佳;焙烧温度提高Ala、Alc含量减小,Alb含量增大;增长酸溶反应时间Alb含量减少;增加酸用量,Ala、Alc含量减少,Alb含量增大。     

活性炭吸附苯过程数值计算

为了研究活性炭吸附挥发性有机物工艺过程参数,采用实验方法测得活性炭吸附苯的吸附量和吸附速率,然后在实验数据的基础之上建立了活性炭吸附苯过程的三维非稳态数学模型,并利用该数值模型研究了混合气体入口速度和入口苯浓度对吸附过程中U型管内的苯浓度、温度和压力分布的影响。结果表明:被吸附气体苯的入口浓度和混合气体入口速度增大时,多孔介质区及其周围区苯的摩尔分数和压力差均增大;与多孔介质区下游管段相比,上游的温度梯度更大,热阻更大;入口苯浓度越大,热量在多孔介质下游管段传递的距离更长。     

电子废物酸浴处置区附近农田土壤重金属污染特征

分析了我国南方某典型电子废物酸浴提取贵重金属场地周围农田土壤剖面pH,重金属含量以及重金属的形态分布特征.结果表明:酸浴提取贵重金属场地周围土壤酸化现象明显,随着距酸浴源距离的增大以及土层深度的增加,酸化程度均减弱;底层土壤酸污染范围较小,仅限于距离污染场地很近的范围内.调查区土壤Cu和Ni 2种重金属的污染较为严重,Cd和Pb污染相对较轻.与酸污染相似,土壤中Cu和Ni的污染随着距酸浴源距离的增大以及土层深度的增加而减弱,表层最高分别超过对照点6倍和4倍.酸浴污染土壤中重金属活性态比例普遍较高,活性态比例随距酸浴场地距离和土层深度的变化趋势与土壤酸污染相似.      

椭圆纤维过滤压降与惯性捕集效率数值分析

采用数值方法求解了描述椭圆截面纤维绕流特征的Navier-Stokes方程,并计算了椭圆纤维对粒子惯性捕集效率及纤维过滤压降.分析讨论了椭圆纤维迎风角度θ、长短轴比ε和填充率C等参数对惯性粒子过滤性能的影响.结果表明,在大迎风角度时,过滤压降随长短轴比增大而增大,而在小迎风角度下,过滤压降则随长短轴比增大而减小;在相同纤维长短轴比条件下,过滤压降均随迎风角增大而增加.粒子惯性捕集效率计算结果则表明,对于中高惯性粒子捕集,大迎风角度和高长短轴比的椭圆纤维的捕集效率高于圆截面纤维,而对弱惯性粒子,小迎风角度和高长短轴比的椭圆纤维则表现出较高的捕集效率.在椭圆纤维过滤压降和捕集效率计算基础上,采用纤维过滤质量因子（定义为捕集效率比过滤阻力）评价综合过滤性能.结果表明,对于中高惯性粒子过滤,扁长型椭圆纤维（即为高长短轴比ε）在迎风角约为θ=45°时质量因子总体较高,即具有较优的综合过滤性能;而对弱惯性粒子,则扁长型椭圆纤维长轴平行来流方向（θ=0°）时,总体过滤性能较优.     

活性焦表面化学性质对其脱硫性能的影响

在氧气及水蒸汽存在的情况下 ,烟道气中低浓度的SO2 被活性焦吸附并被催化氧化为硫酸 .考察了活性焦表面化学性质对其脱硫性能的影响 .结果表明 ,活性焦的微孔面积及表面碱性位含量是影响其脱硫能力的主要因素 .同时 ,由XPS数据可知 ,随着活性焦表面的氧含量的减少 ,离域π电子 (Cπ)趋于活跃 ,活性焦的碱性增加 ,证实了碳原子平面层上的离域π电子 (Cπ)是影响活性焦脱硫能力的主要因素 .     

烟道气生物脱硫厌氧段影响因素的研究

采用UASB对烟道气生物脱硫厌氧段中的主要影响因素如水力停留时间、进水浓度和温度进行实验研究。分别从亚硫酸根去除效果和硫化物生成情况两方面考查对反应器运行效果的影响。结果表明,水力停留时间为36h时,SRB对SO32-的还原效果良好;进水SO32-浓度范围在500～800mg/L时,SO32-还原率在88%左右;在实验考察的温度范围内,反应温度为33℃时SO32-还原速率和硫化物产生量最大。     

预混喷雾增效细颗粒去除的电除尘实验研究

为提高电场对细颗粒物的捕集效率,实现颗粒物超低排放要求,本试验采用喷雾与电场分区设计,搭建了预混喷雾湿式电除尘试验装置,以增强颗粒与液滴之间的凝聚作用,试验探究了电场电压、极板间距、电场风速、喷雾压力及入口浓度等参数对除尘效率的影响规律.结果表明;除尘效率随着电场电压增加,除尘效率提升,增幅先升高后降低,最后趋于平稳;减小极板间距或电场风速,能够提高除尘效率,但降低了处理风量;随着喷雾压力增大,除尘效率先增加后减小,当压力值为6MPa时,除尘效果最佳;粉尘入口浓度对除尘效率的影响程度较低,对于粒径小于2.5μm的颗粒物去除效率最高达98.5%.综上,预混喷雾湿式电除尘效果相比单一喷雾或静电除尘具有显著的增强,对于颗粒物超低排放装置的设计具有重要参考价值.     

接触式污泥干化过程中SO_2吸收率的动态变化

根据接触式污泥干化工艺的实际运行参数,通过模拟试验,研究了污泥在干化过程中对烟气中二氧化硫(SO2)吸收率的动态变化及其影响因素,并对导致吸收率变化的原因进行了理论分析.结果表明,污泥对SO2的吸收率随干化温度的升高和气体流速的增大而减小,含水率为55%和75%的污泥对SO2的吸收率分别从干化温度80℃的16.0%和25.0%降至干化温度160℃的6.0%和7.0%,这是因为干化温度升高和气体流速增大,促使污泥水分加速蒸发,从而影响SO2从气相通过气膜向气液界面传递和扩散的过程,最终导致污泥对SO2吸收率的下降;污泥对SO2的吸收率随SO2浓度的增加没有明显的变化;污泥吸收SO2后,pH值降低表明了污泥吸收SO2发生了酸碱中和反应,污泥红外光谱证明污泥对烟气中SO2的吸收是一个化学吸收过程.     

车用锂离子电池组冷却系统传热仿真分析

目的解决电动汽车锂离子电池组在高温下的安全性和热失控问题。方法建立锂离子电池组冷却系统的三维分析模型,应用计算流体动力学(Computational Fluid Dynamics,CFD)方法,结合热传导和热对流理论,对电池组进行仿真分析。结果锂离子电池组的温度场分布基本相同,呈现出中间低、两侧高的分布特点,且层次变化。冷却液温度越低,电池组最高温度也越低;增大冷却液入口流速,电池组内部最高温度略微降低;冷却板材料对电池组的冷却效果影响很小。采用铝合金冷却板,冷却液温度20℃,入口流速2 m/s时,电池组的冷却效果最好。结论对于本文所设计的冷却系统,冷却液入口流速和冷却板材料的变化对电池组散热效果的影响较小,冷却液入口温度的变化对电池组散热效果的影响较大。应当选择铝合金为冷却板材料,以及合理的冷却液入口温度和流速,以满足轻量化要求,防止电池组过度冷却,减小流道内的阻力损失,提高冷却系统的散热效率。     

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.     

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.     

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.     

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.     

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.     

Effects of chitosan on growth of an aquatic plant (Hydrilla verticillata) in polluted waters with different chemical oxygen demands

Effects of chitosan on a submersed plant, Hydrilla verticillata, were investigated. Results indicated that H. venicillata could prevent ultrastructure phytotoxicities and oxidativereaction from polluted water with high chemical oxygen demand (COD). Superoxide dismutase (SOD) activity and malondialdehyde (MDA) contents in H. verticillata treated with 0.1% chitosan in wastewater increased with high COD (980 mg/L) and decreased with low COD (63 mg/L), respectively. Ultrastructural analysis showed that the stroma and grana of chloroplast basically remained normal. However, plant cells from the control experiment (untreated with chitosan) were vacuolated and the cell interval increased. The relict of protoplast moved to the center, with cells tending to disjoint. Our findings indicate that wastewater with high COD concentration can cause a substantial damage to submersed plant, nevertheless, chitosan probably could alleviate the membrane lipid peroxidization and ultrastructure phytotoxicities, and protect plant cells from stress of high COD concentration polluted water.     

Removal of cadmium using MnO2 loaded D301 resin

MnO2 loaded weak basic anion exchange resin D301 （Anion exchange resin, macroreticular weak basic styrene） as adsorbent has been prepared and applied to the removal of cadmium. The adsorption characteristics have been investigated with respect to effect of pH, equilibrium isotherms, removal kinetic data, and interference of the coexisting ions. The results indicated that the Cd^2＋ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions. The saturate adsorption capacity of the Cd^2＋ was 77.88 mg/g. The adsorption process followed the pseudo first-order kinetics. The equilibrium data obtained in this study accorded excellently with the Langmuir adsorption isotherm.     

Effect of coagulation pretreatment on the fouling of ultrafiltration membrane

The purpose of this study is to understand the effect and mechanism of preventing membrane fouling, by coagulation pretreatment, in terms of fractional component and molecular weight of natural organic matter （NOM）. A relatively higher molecular weight （MW） of hydrophobic compounds was responsible for a rapid decline in the ultrafiltration flux. Coagulation could effectively remove the hydrophobic organics, resulting in the increase of flux. It was found that a lower MW of neutral hydrophilic compounds, which could remove inadequately by coagulation, was responsible for the slow declining flux. The fluxes in the filtration of coagulated water and supernatant water were compared and the results showed that a lower MW of neutral hydrophilic compounds remained in the supernatant water after coagulation could be rejected by a membrane, resulting in fouling. It was also found that the coagulated flocs could absorb neutral hydrophilic compounds effectively. Therefore, with the coagulated flocs formed on the membrane surface, the flux decline could be improved.     

Penetration analysis of elements and bioleaching treatment of spent refractory for recycling

Acidithiobacillus ferrooxidans ATCC23270 and Acidithiobacillus thiooxidans TM-32 were used for bioleaching of spent refractories of aluminium and copper melting furnaces for their recycling.Firstly,penetration of elements into aluminium melting furnace refractory was investigated and it was found that up to 7 cm from surface was contaminated.Comparison on leaching efficiency by the strains ATCC23270 and TM-32 found that the strain ATCC23270 could treat larger amount of the refractories than the strain TM-32 could do.In the experiment of bioleaching of spent refractory aluminium melting furnace by the strain ATCC23270,high leaching efficiency were obtained on Al,Si,and Ca,and extremely low leaching performance was,however,shown on the rest of elements i.e.,Na,Mn,and Zn.Under the strain TM-32 use,relatively high leaching performance was recognized on Al,Si,Ca,Na,Mn,and Zn.In the experiment of bioleaching for spent refractory copper melting furnace,almost the same leaching trends were shown on Cu,Zn,Al,and Si under the strains ACTT23270 and TM-32 uses.     

Simultaneous removal of ammonium and phosphate by zeolite synthesized from coal fly ash as influenced by acid treatment

Zeolite synthesized from fly ash （ZFA） without modification is not efficient for the purification of NH4＋ and phosphate at low concentrations that occur in real effluents, despite the high potential removal capacity. To develop an effective technique to enhance the removal efficiency of ammonium and phosphate at low concentrations, ZFA was modified with acid treatment and the simultaneous removal of ammonium and phosphate in a wide range of concentration was investigated. It was seen that when compared with untreated ZFA, only the treatment by 0.01 mol/L of H2SO4 significantly improved the removal efficiency of ammonium at low initial concentrations. The behavior was well explained by the pH effect. Treatment by more concentrated H2SO4 led to the deterioration of the ZFA structure and a decrease in the cation exchange capacity. Treatment by 0.01 mol/L H2SO4 improved the removal efficiency of phosphate by ZFA at all initial P concentrations, while the treatment by concentrated H2SO4 （≥0.9 mol/L） resulted in a limited maximum phosphate immobilization capacity （PIC）. It was concluded that through a previous mild acid treatment （e.g. 0.01 mol/L of H2SO4）, ZFA can be used in the simultaneous removal of NH4＋ and P at low concentrations simulating real effluent.