长江中下游洪水灾害成因及洪水特征模拟分析

长江中下游地区洪水灾害的发生是自然地理条件及人类活动共同作用的结果。流域水系构造和地理特征决定了其洪水多发性,气候变化和土地利用/地表覆盖变化导致该地区水循环过程发生较大改变,而大量水库、堤防的建设以及城市化的发展使得洪水过程发生显著变化,因此在各种因素的综合作用下,长江中下游地区近年来洪水灾害频繁发生。综述了气候变化对长江中下游降水的影响,探讨了长江中下游水系特征与洪水灾害的关系,分析了人类活动对洪水灾害的影响规律,在此基础上,开展了气候和下垫面特征变化条件下的暴雨洪水模拟研究,以长江下游太湖东苕溪流域的南苕溪为研究区,进行了流域降雨径流过程的动态模拟验证和特征分析,并取得了较满意的成果,从而为长江中下游地区防洪减灾研究打下了基础。     

基于RS/GIS的四湖地区湖泊水域百年变迁研究

四湖地区是长江中游江汉平原的重要湖泊分布区,在历史时期湖泊分布广阔,是著名的云梦泽的主体。由于江湖关系演变和人类活动的影响,湖泊面积变化迅速,尤以20世纪为甚。在野外调查和历史文献分析的基础上,利用不同时期的水利图、地形图、遥感影像图作为基本信息源,在GIS技术支持下,提取湖泊面积信息,对四湖地区近百年湖泊水域变化进行了研究。结果显示,从20世纪20年代开始湖泊面积和个数呈先增加后减少的趋势,50年代处于鼎盛时期,50年代初期到70年代初期迅速减少,70年代至2000年减幅明显减缓。这种动态变化是自然因素和人类活动综合作用的结果,人类活动的作用更为突出。针对湖泊水域日益减少的现状,应加强对湖泊资源的保护力度,并在此基础上进行合理开发和利用。     

工业废水对洹河有机污染的调查与分析

采用适当的样品前处理技术,利用GC/MS对洹河水及焦化厂、染料厂废水进行有机污染物的分析,确定了工业废水对洹河造成有机污染的主要化合物,从而为企业污水的处理和洹河治理提供依据.     

典型流域土地利用/覆被变化及对水质的影响--以太湖上游浙江西苕溪流域为例

利用1985、1995和20D0年的TM数据及水质资料，运用GIS和水质指数法研究西苔溪流域的土地利用／覆被变化及其水环境效应。结果表明：流域内耕地不断减少，建设用地持续扩大，林地前期减少后期缓慢增加；林地和耕地是流域内的主要土地利用类型，二者面积之和占流域面积的比例在三个时段均在92％以上；空间集中性及斑块碎化是土地利用空间格局变化的主要表现，建设用地斑块数量增多且斑块面积明显增大，饼地面积减少但斑块数量增多。研究时段内流域水质在时间上呈逐步恶化趋势，在空间上则表现为自上游至下游逐渐下降，其中，1996-2000年，研究河段内水质指数下降幅度达30％左右；只治理点污染源仅使水质指数增加6．5％左右，表明影响水质的主要因素是土地利用变化导致的面源污染。     

UV/H2O2光化学氧化降解对氯苯酚废水的反应动力学

研究了UV/H₂O₂体系降解对氯苯酚废水的过程及动力学结果表明,反应降解速率与双氧水加入量、污染物初始浓度及载气种类有关.在双氧水理论投加量一半的情况下,通入氧气或空气,总酚的降解率可达到96%,COD_Cr去除率接近50%.反应体系加入载气,显著影响污染物的去除率.在本实验中,总酚降解为拟一级反应.     

位阻胺混合甘氨酸盐溶液吸收CO2的研究

在双搅拌反应釜中研究了位阻胺2-氨基-2-甲基-1-丙醇(AMP)与甘氨酸钠(SG)混合溶液吸收CO2的性能.实验温度293~313K,混合溶液的浓度为AMP(1.5kmol/m3)+SG (0.2,0.4,0.6,0.8kmol/m3),SG浓度每增加0.2kmol/m3,200min内的平均吸收速率分别提高11.47%,10.07%,9.18%和5.33%.与AMP单一溶液相比,混合溶液在200 min时的吸收容量增加了11.5%~41.1%.在293~313K,吸收速率随温度上升而提高.使用加热的方法进行再生实验,得到1.5 kmol/m3 AMP + 0.6 kmol/m3 SG混合液的最适再生温度为378K.AMP + SG混合溶液的再生效率高于单一SG溶液及AMP + MEA/DEA混合溶液.     

海藻酸钠/锆@钙水凝胶的制备及其对磷的吸附研究

利用简便的方法制备了一种新型的海藻酸钠/锆@钙(SA/Zr@Ca)水凝胶材料,采用SEM、XRD对该材料进行了表征,并通过拟合吸附等温模型及吸附动力学模型,结合XPS和Zeta电位分析,研究了该材料对磷酸盐吸附的性能和机理.结果表明,该材料为非晶态的无定型材料.在溶液初始pH为2～7时,SA/Zr@Ca对磷酸盐(以PO...     

Decolorization and degradation of acid dyes mediated by salt fractionated turnip ( Brassica rapa ) peroxidases

Peroxidases from turnip roots (524?U?g^?1 of vegetable) were highly effective in decolorizing acid dyes having wide spectrum chemical groups. Dye solutions, containing 40–170?mg?dye?L^?1, were treated by turnip peroxidases (TP) (specific activity of 122.0?U?mg^?1 proteins). These enzymes were able to decolorize most of the acid dyes in the presence of 2.0?mM 1-hydroxybenzotriazole (HOBT). Increasing concentration of enzyme and time in the absence of HOBT did not influence dye decolorization. The rate of decolorization was significantly enhanced when HOBT was added to the decolorizing solutions. The decolorization of all the used dyes was maximum at pH 5.0 and 40°C. Complex mixtures of dyes were significantly decolorized when treated with enzyme in the presence of HOBT (2.0?mM). Phytotoxicity test based on Allium cepa root growth inhibition has shown that majority of the TP-treated dye product were not more toxic than their parent dye. Kinetic parameters of the TP with various dyes showed that this enzyme has highest affinity for Acid Yellow 42. This study demonstrates that the peroxidase/mediator system was an effective biocatalyst for the treatment of industrial effluents from textile, dye manufacturing, dyeing and printing industries or complex mixtures of dyes.     

Toxicity of cadmium to the green alga Parachlorella kessleri: Producing Cd-loaded algae for feeding experiments

The effects of Cd at environmental concentrations (0–32 µg/L) on the green alga Parachlorella kessleri were investigated. At about 3 µg Cd/L, toxic effects of Cd are becoming evident, much lower than reported previously. At 8 µg/L and higher, pronounced adverse effects on growth, cell morphology, size, and physiological state are seen. Therefore, levels lower than 2 µg Cd/L should be employed to produce Cd-carrying algae for feeding experiments with organisms on the next trophic level, e.g. mussels, to avoid reduced food uptake. These findings also suggest that aquatic ecosystem conditions can be indirectly influenced via the impairment of the nutritional value of algae since they are the basic organisms of aquatic food chains.     

Standard purity and response factors of perfluorinated compounds

It has been reported that the relative response factors of isotopically labeled standards and unlabeled standards of the same perfluorinated compounds could be different. Individual (100 ng mL^?1) solutions of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) were analyzed using high-performance liquid chromatography tandem mass-spectrometry under negative-ion electrospray to detect any impurities present down to 0.5%–0.1% relative to the major component. Purity of the standards ranged from approximately 86% to ≥ 97%. Standard solutions of unlabeled and isotopically labeled materials were analyzed to compare the response factors of isotopically labeled analytes versus their nonlabeled counterparts in three different matrices at equivalent concentrations: organic solvent (methanol), serum extract, and water present individually and concurrently. Not all labeled analytes have the same response factor as their nonlabeled complement, and in at least one case the matrix in which the standard is present may cause significant suppression of response. Standard solutions of electrochemical fluorination produced PFOA and PFOS were quantified under multiple reaction monitoring mode, using calibration curves prepared from standards consisting primarily of linear standards only. The use of linear only standards may cause under-prediction of concentrations, and that the working range of these standards may be limited.