Ce_(0.65-x)Co_xK_(0.15)Zr_(0.2)O_2催化碳烟燃烧活性研究

采用柠檬酸络合燃烧法制备了不同铈钴摩尔比的Ce_(0.65-x)Co_xK_(0.15)Zr_(0.2)O_2(x=0,0.15,0.23,0.30,0.38,0.45,0.65)催化剂,采用XRD、SEM、FT-IR与H_2-TPR等技术对催化剂进行表征,并通过程序升温氧化反应(TPO)考察了催化剂不同Ce/Co比对碳烟颗粒物催化燃烧活性的影响。研究结果表明:在松散接触条件下,该系列催化剂催化碳烟颗粒物燃烧活性较高,T_m均小于400℃,当x=0.23时活性最高,T_i与T_m分别为321℃与355℃,催化剂所表现出的高活性受益于样品表面具有大量高活性的细小Co_3O_4颗粒物。     

复合氧化物催化材料上碳颗粒物的催化燃烧

针对柴油车排放碳颗粒物的控制 ,研制可应用于柴油车排放碳颗粒物催化再生复合氧化物催化材料 .通过运用热分析仪 (TGA)和程序升温氧化反应装置 (TPO)对复合氧化物催化材料的活性进行评价 ,研究了催化材料的组成、原子配比、催化材料与碳颗粒物质量比、H₂O的加入、焙烧温度对催化活性的影响 .实验结果表明 :双组分金属氧化物催化剂中 ,Cu-Mo-O有较好的活性 ;多组分金属氧化物催化剂中 ,Cu-K-Mo-O在原子比Cu∶K∶Mo =1∶1∶2 ,催化剂与碳颗粒物质量比为 5∶1时活性最好 ,其碳颗粒物起燃温度为 32.7℃ ,同时H₂O和焙烧温度对该催化剂的影响较小 ,是能够应用于柴油车排放碳颗粒物控制催化再生的良好催化材料 .     

新型汽车尾气净化催化剂的研究

研究Ｌａ－Ｃｏ－Ｃｕ－Ｍｎ－Ｃｅ－Ｐｄ催化剂的活性和热稳定性,结果表明,该催化剂具有低温活性良好、活性高以及热稳定性好的性能特点,对ＣＯ、ＨＣ氧化的Ｔ５０％和Ｔ１００％分别约为１８２℃,２３８℃和２４０℃、２６５℃,催化剂表面组分发生强相互作用形成３种活性中心,是催化剂低的起燃温度,高活性的原因。催化剂高温处理后未发生烧结,活性未下降,热稳定性良好。     

钯、铜、锰、铈三效催化剂性能研究

应用脉冲－火焰反应装置、ＸＲＤ、ＴＰＲ和氢氧滴定技术来研究Ｐｄ－Ｃｕ－Ｍｎ－Ｃｅ－Ｏ三效催化剂的性能。实验结果表明，不同的制备Ｐｄ－Ｃｕ－Ｍｎ－Ｃｅ－Ｏ催化剂的方法，则催化活性各不相同。在分层制备的催化剂中，催化性能主要以外层组分性能为主；以混合浸渍法制备的样品中，ＣｕＭｎ＿２Ｏ＿４相消失，Ｃｕ－Ｍｎ－Ｃｅ－Ｏ表面氧环境发生变化；表面活性剂的添加改变了Ｐｄ的分布，使催化剂表面易于还原；这些改变均对催化剂的三效性能发生影响。催化剂表面的有效贮氧量与三效活性没有明显的关系。     

呼和浩特市大气气态和颗粒物上正构烷烃的研究

采用聚氨基甲酸乙酯和玻璃纤维滤膜采集样品并测定。大气中总正构烷烃的浓度分布、气／固分布比与季节变化、污染源有关。在呼市大气中总正构烷烃（Ｃ１５－Ｃ３３），夏季主要存在气态中（７８％），而冬季主要存在于颗粒物上（８３％）。内蒙古草原大气对照样品中，气态中总正构烷烃在冬夏两季所占百分比都约为５０％。市区冬季大气颗粒物上的总正构烷烃浓度比其它城市结果高出１－２个数量级。     

催化氧化CS2的催化剂及其性能研究

以ＣＳ２作为含硫废气的处理对象，研究了Ｐｔ－Ｍｏ负载，在改性天然丝光沸石上对ＣＳ２的催化氧化活性，以及添加Ｖ对催化剂活性的影响。研究表明，Ｐｔ－Ｍｏ－Ｖ和改性载体之间存在着共催化作用，在Ｐｔ－Ｍｏ－Ｈ＾＋Ｍ催化剂上由于Ｖ的添加，使催化剂处理ＣＳ２的浓度和ＳＤＹ值明显提高。在反应温度３１０℃，空速５００ｈｒ＾－１和ＣＳ２浓度为３７０ｍｇ／ｍ＾３转化率达到１００％，ＳＯｘ放出率接近９５％－１００％。     

地表水中总有机碳的测定

该文提出了燃烧氧化－非分光红外吸收法测定地表水中总有机碳含量。水样连同净化空气分别导入高温燃烧管和低温反应管内，样品中的总碳和无机碳氧化分解ＣＯ２。定量试样中的总碳和无机碳之差即为样品总有机碳。     

南宁市区交通环境空气颗粒物中碳组分的污染特征分析研究

含碳颗粒物是大气颗粒物的重要组成部分,对人体健康产生很大的威胁.分别于2012年夏季及2013年冬季在南宁市选取六条主要交通干道采集了PM10、PM2.5样品,分析测定了其中的碳组分.结果表明,碳组分浓度季节变化明显.碳组分在细颗粒物中占有比重比在可吸入颗粒物中大.存在二次有机碳污染.对8种碳组分丰度分析说明南宁市大气颗粒物中碳组分的主要来源是燃煤、机动车尾气及生物质样品燃烧.     

空气颗粒物中有机污染物粒分布规律的研究

采用色谱一质谱联用技术（ＧＣ－ＭＳ），系统分析了１０００多个不同粒径颗粒物样品的有机污染物，结果表明，环境空气颗粒物中有机污染物集中分布于细颗粒物上，几乎所有的多环芳煤（ＰＡＨ）和一半以上的苯芘（ａ）芘Ｂ（ａ）ｐ）吸附在粒径小于０．３８μｍ的极细尘中。     

氢氟烃HFC－134a的分解实验研究

该研究进行了氢氟烃ＨＦＣ－１３４ａ的催化分解和化学分解实验。实验结果表明无催化剂时ＨＦＣ－１３４ａ很稳定，即使升温至５００℃时也下会分解：在空气和水蒸汽存在下ＨＦＣ－１３４ａ催化分解成ＣＯ和ＣＯ＿２。ＣＦＣ－１２比ＨＦＣ－１３４ａ易分解，反应产物只有ＣＯ＿２。分解产物ＨＦ对催化剂有强烈的失活作用；超氧离子（Ｏ＿２￣－）对液相中的ＨＦＣ－１３４ａ具有很强的氧化分解能力。在常温下几乎可完全分解高浓度的ＨＦＣ－１３４ａ。     

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.