苯胺降解菌的分离和特性研究

从活性污泥中分离到一株细菌ＡＮ３，能以苯胺为唯一碳源、氮源和能源生长．经鉴定为食酸丛毛胞菌（Ｃｏｍａｍｏｎａｓａｃｉｄｏｖｏｒａｎｓ）．该菌株可以在高达５０００ｍｇ／Ｌ以上的苯胺中生长．当苯胺浓度为２０００ｍｇ／Ｌ左右时，经３天培养即可全部被降解．该菌株还可以利用乙酰苯胺，但不能利用其他取代类苯胺化合物．ＡＮ３菌的生长和降解苯胺的最适温度为３０℃和ｐＨ为７０．９种金属离子对该菌的生长和苯胺的降解均有不同程度抑制作用，尤以Ａｇ＋和Ｈｇ２＋为明显．该菌与苯胺降解代谢有关酶类的测定结果表明，该菌含有的邻苯二酚－２，３加双氧酶是诱导酶．     

西湖底泥不同供氧条件下有机质降解及CO2与CH4释放速率的模拟研究

采用密闭培养实验装置于室温（２５℃左右）及ｐＨ为７５条件下，对西湖底泥中有机质完全降解及转化为ＣＯ２和ＣＨ４的速率进行了模拟研究．结果表明，在西湖湖水现有供氧水平（５０—８６ｍｇ（Ｏ２）／Ｌ）条件下，底泥中有机质完全降解的速率最为缓慢，培养期间（４２天）平均只有０７２ｍｇ（Ｃ）／（ｋｇ·ｄ）．当湖水供氧水平进一步上升（８６→１２０→１６０ｍｇ（Ｏ２）／Ｌ），ＣＯ２释放速率增加，最大值可达到８７ｍｇ（Ｃ）／（ｋｇ·周）；当湖水供氧水平下降（８６→０ｍｇ（Ｏ２）／Ｌ），ＣＨ４释放速率加快，最大值可达到４６ｍｇ（Ｃ）／（ｋｇ·周）．     

染料脱色菌的筛选及固定化脱色试验

从印染厂污水中筛选到７株高效脱色菌,其中Ｐｓｅ４、Ｐｓｅ２９两菌在非固定化条件下,分别对１０ｍｇ／Ｌ阳离子桃红ＦＧ、活性艳红Ｋ－２ＢＰ溶液３在染料为唯一碳源、能源时、１２ｄ脱以８０％以上,这２菌都属于公章民菌属,将各菌等量混合进行脱色,没有协同作用,采用凹凸棒粘土颗粒或塑料环为载体固定化脱色菌,能大大缩短反应时间,提高脱色率,凹凸棒颗粒固定化柱在６ｈ即对６０ｍｇ／Ｌ混合染料脱色９１％,是一种具有较     

沼泽红假单胞菌对活性紫KBR脱色的研究

研究了驯化后的沼泽红假单胞菌(Rhodopseudomonaspalustris)N菌株的生长细胞在不同条件下对活性紫KBR的脱色效果.结果表明,该菌株生长细胞脱色的最佳条件为温度25～30℃,pH值为7,厌氧条件下的脱色率远远高于好氧条件下的脱色率.染料作为该菌株唯一的碳源和能源脱色时,脱色率与细胞浓度呈极显著相关,细菌脱色比活率保持在较恒定的水平.此外,生长细胞脱色过程中对菌体生长的测定表明,该菌株生长的指数期明显滞后于染料脱色的指数期.     

硝基苯降解菌生长特性及其降解活性

从一些下水道底泥中筛选分离、驯化得到２株厌氧降解硝基苯高效菌吉氏拟杆菌（Ｂａｃｔｅｒｏｉｄｅｓ ｄｉｓｔａｓｏｎｉｓ）和屎拟杆菌（Ｂａｃｔｅｒｏｉｄｅｓ ｍｅｒｄａｅ）,能与葡萄糖共代谢还原硝基苯。实验确定了吉氏拟杆菌和屎拟杆菌的最适生长条件为：温度２８～３５℃;ｐＨ６．５～７．２;ＮａＣｌ浓度为０．４％～０．５％。该菌最大降解硝基苯的速率为９５ｍｇ／（Ｌ·ｄ）,ｌｇ葡萄糖能共代谢还原２００ｍｇ～     

一株酸性大红3R脱色菌的分离、鉴定及其脱色性能研究

通过浓度梯度驯化,从厌氧污泥中分离到一株酸性大红3R脱色菌M3,根据其形态学特征及16S rRNA基因序列分析,鉴定该厌氧菌株为阴沟肠杆菌(Enterobacter cloacae).同时,研究了该菌株在厌氧静置条件下对酸性大红3R的最适脱色条件.结果表明,菌株脱色的最佳营养源为酵母粉,最适宜脱色条件为酵母粉浓度1％、pH =6.5、温度35 ℃、盐度小于4％,在此条件下,对浓度为100 mg·L-1酸性大红3R溶液厌氧静置培养72 h,脱色率达到98％以上.菌株耐盐性良好,在6％ ～8％的盐度下具有较好的脱色效果.分光光谱表明,菌株脱色机制主要为生物降解脱色.毒性试验表明,脱色后的酸性大红3R毒性明显降低.     

一株苯胺降解菌的研究

报道了从自然界分离的一株能以苯胺为唯一氮源和碳源，同时降解苯胺的细菌４＾＃。该菌鉴定为节杆菌４＾＃（Ａｒｔｈｒｏｂａｃｔｅｒ．４＾＃）。该菌降解苯胺的最高浓度为２０４４ｍｇ／Ｌ。４＾＃菌株降解苯胺的最适ｐＨ值和温度分别为７．０和３０℃，最适苯胺浓度为１０２２ｍｇ／Ｌ。在此条件下，４８ｈ苯胺的降解率可达９４．７％。试验结果表明，重金属离子对４＾＃菌株降解苯胺都有不同程度的抑制作用，以Ｈｇ＾２＋、Ａｇ     

杀灭菊酯的微生物降解及酶促降解

测定了降解菌ＹＦ１１及其胞内酶对杀灭菊酯的降解特性,在纯培养系统中,菌量为ＯＤ４１５ｎｍ０．２０时,ＹＦ１１对大于３０ｍｇ／Ｌ的杀灭菊酯的降解呈零级动力学特征,浓度为３０￣１００ｍｇ／Ｌ时,降解速率为１．８７６－２．１２４ｍｇ／（Ｌ·ｈ）;浓度大于２００ｍｇ／Ｌ的杀灭菊酯对降解菌ＹＦ１１的降解产生抑制作用,降解速率与菌量近似成正比关系,１０ｍｇ／Ｌ杀灭菊酯的降解曲线呈一级动力学特征。从ＹＦ１１提取     

水泥负载TiO2光催化降解染料水溶液的研究

研究了以ＴｉＯ２为催化剂，且将ＴｉＯ２涂布在模拟工业水处理浅池的水泥质池底表面，以直管高压汞灯为光源，对有机染料酸性玫瑰红Ｂ和晒化绿Ｂ进行光催化降解的可行性。结果表明，在实验条件下，本系统对以上染料有显著的光降解作用，浓度为２５ｍｇ／Ｌ的上述二种染料溶液，经３０ｍｉｎ光照，其降解率分别达８８．２％，此外，还探讨了染料浓度，染料体积、染料溶液ＰＨ值等因素对光降解的影响。     

氧化还原介体厌氧催化酸性红B生物脱色研究

研究了筛选出的四种结构相似的醌类氧化还原介体对酸性红B厌氧脱色的促进作用,并以催化效果最佳的蒽醌-2-磺酸钠为醌介体模型,探讨了醌介体催化酸性红B厌氧生物降解路径。在35℃中温厌氧条件下,采用间歇批量实验法,测定不同体系中醌介体催化酸性红B脱色效果。结果表明:①在酸性红B浓度为150mg·L-1,醌介体浓度为0.16mmol/L,反应时间为4h时,结构相似的四种醌介体均可促进酸性红B脱色,反应效率提高了1.6².4倍,其大小顺序为AQS>2,7-AQDS>AQDS>α-AQS;②AQS在催化酸性红B降解过程中与传统厌氧微生物降解路径保持一致。     

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.