水环境中天然溶解有机质分子量的研究现状及意义

溶解有机质存在于所有的水环境中,它是组成不均匀、结构复杂和分子量分布很宽的有机化合物混合体。本文综述了测量溶解有机质分子量的主要方法,各种方法的原理和优缺点,其中详细介绍了高效体积排阻色谱法的原理,平均分子量和分散系数的计算,以及分子量的校正;同时介绍了可能影响分子量分布的主要地球化学因素,以及天然水中溶解有机质的分子量分布的特征。     

模糊物元法综合评价福州市大气环境质量

大气环境质量的综合评价是城市环境质量考核的重要内容,鉴于大气环境质量评价中客观存在的不确定性和模糊性,将熵值理论与模糊物元分析法相结合应用于大气环境质量综合评价中,可有效解决这种不确定性和模糊性。应用该模型对福州市的大气环境质量进行综合评价,将评价结果与属性识别理论模型的评价结果相比较,二者基本吻合,结果证明该方法可行。     

失效锂离子电池有机物真空脱除和浸出研究

文章采用真空蒸发热处理的方法脱除废弃失效的锂离子电池中的有机物,加热温度为220~500℃,真空炉内压力150Pa,恒温处理时间1h。除有机物被脱除外,当处理温度为280℃时形成了CoO和Li2CO3。温度升高至350℃时,主要的物相为LiCoO2、CoO、Co3O4和Co,以及少量Li2CO3。在超声场中将电极材料与铝、铜箔集流体分离,然后分别用含亚硫酸钠的硫酸溶液和氨性溶液处理电极材料。当用含亚硫酸钠的硫酸溶液浸出经280℃脱除有机物的电极材料时,钴元素基本被浸出。而用氨性溶液浸出经350℃脱除有机物的电极材料时,钴元素的浸出率很低。为了提高钴的浸出率,真空热处理的温度应介于280~350℃之间。     

活性污泥对有机污染物的吸附研究

通过中试试验,分析了活性污泥对污染物吸附的影响因素,并考察了活性污泥对城市污水中污染物的吸附效果.试验研究表明,污泥浓度(MLSS)、水力停留时间(HPT)和污泥龄(SRT)对活性污泥吸附污染物的效果有一定的影响,但污泥龄影响较小.在污泥质量浓度为3～5 g/L,HRT为36 min和SRT为2 d的运行参数下,活性污泥时COD,SS,TN和TP吸附效果分别为70.7%,87.7%,30.2%和72.2%.     

Interactive effect of dissolved organic matter and phenanthrene on soil enzymatic activities

The investigation of dissolved organic matter (DOM) on urease, catalase and polyphenol oxidase activity in a phenanthrene (Phe)-contaminated soil was conducted under laboratory incubation conditions. Values of soil enzymatic activity depended mainly on incubation time. In the initial 16 days, urease activity increased, and was followed by a decrease. In the initial 8 days, catalase activity decreased and then increased. Variation of polyphenol oxidase activity was just the reverse of catalase activity. After 30 days of incubation, no pronounced difference among treatments with Phe, Phe and DOM, and control were detected in urease, catalase and polyphenol oxidase activity. Phe might inhibit urease and catalase, and stimulate polyphenol oxidase. DOM could improve inhibition of Phe in soil urease and catalase activity during the initial period of applying DOM. Nevertheless, DOM had no significant effect on polyphenol oxidase activity in the Phe contaminated soil. There was a negative correlation between catalase and polyphenol oxidase (r = -0.761~(***)), and catalase and urease (r = -0.554~(**)). Additionally, a positive correlation between polyphenol oxidase and urease was also detected (r = 0.701~(***)). It is implied that the formed DOM after application of organic wastes into soils may counteract the inhibition of polycyclic aromatic hydrocarbons in soil enzyme activities.     

河口区有色溶解有机物(CDOM)三维荧光光谱的影响因素

结合在厦门湾九龙江口的现场调查与实验室分析,对目前河口区CDOM三维荧光光谱(excitation-emission matrix spectroscopy,EEMS)分析的一些影响因素(主要是离子强度、浓度效应、不同孔径滤膜过滤)进行了探讨.结果表明,CDOM的EEMS与样品中离子强度关系不大,说明在河口区河海水混合过程中,仅仅由于水体盐度的变化不会造成CDOM光学特征的明显变化.河端CDOM的荧光强度随物理稀释倍数的增大成相应比例的减小,稀释对EEMS的影响仅仅体现在荧光强度上,显示河口区的CDOM样品不存在荧光淬灭效应.九龙江口河流端样品中共含有类腐殖质(C、A)及类蛋白质(T1、T2)4种荧光团,随着混合样品中海水体积分数的增大,样品荧光强度逐渐降低,代表海洋来源的类腐殖质荧光峰M逐渐显露,T1峰逐渐高于A峰.这说明从河端至外海CDOM的组成结构发生了一系列的变化,来源上逐渐完成了以陆源为主到海源为主的转变;性质上逐渐完成了以类腐殖质荧光团为主到类蛋白质荧光团为主的转变.在中、高盐度区,0.2μm的Millipore聚碳酸酯滤膜可以很好地去除水体散射对EEMS的干扰,EEMS(0.2μm)比EEMS(0.7μm)更为规则,各峰的显示更加清晰.不同荧光基团的划分更加容易.无论高、中、低盐度站位,0.7μm滤膜过滤的样品,其CDOM荧光强度都要略高于0.2μm滤膜过滤的样品,2种不同孔径滤膜过滤对CDOM荧光测定带来的差异不可忽略.     

土壤重金属形态与溶解性有机物的环境行为

土壤中重金属的污染已成为日趋严重的环境问题,重金属在土壤中的富集过程和迁移转化规律与土壤中重金属赋存形态有着密切的联系。文章阐述了土壤中重金属的赋存形态及其影响因素,并介绍了溶解性有机物质(DOM)与土壤中重金属间的环境化学行为,为更加科学合理利用和修复受重金属污染土壤以及为土壤环境污染风险评估与预测提供准确、可靠的理论支持。     

水体有色溶解有机质的研究进展

有色溶解有机质（CDOM）是溶解有机质（DOM）的重要组成部分,它影响着碳的生物地球化学循环,为水生微生物提供重要的碳源和能源。文章介绍了国内外CDOM的研究进展和动态．主要包括CDOM的紫外吸收光谱研究,荧光光谱研究,并对CDOM中主要成分的荧光峰位置及峰值变化、来源进行论述．最后对CDOM的研究重点作了展望。     

聚硅酸硫酸铁强化混凝去除微污染水源水中天然有机污染物

应用强化混凝技术,降低原水中有机物含量,是控制消毒副产物生成的有效途径之一。通过混凝搅拌试验,评价了聚硅酸硫酸铁混凝剂对原水中有机污染物的去除效果,考察了混凝剂投加量、pH值等对去除效果的影响。结果表明：聚硅酸硫酸铁去除有机物和除浊能力明显优于硫酸铁、聚合硫酸铁,其适宜的投药量范围和pH值范围宽;聚硅酸硫酸铁在混凝过程中形成的矾花较大,沉降速度快,因而可缩短处理水在构筑物中的停留时间,提高系统的处理能力;此外,通过正交实验确定了聚硅酸硫酸铁混凝剂的最佳水力条件。     

Influence of atmospheric stability on the mass concentration and chemical composition of atmospheric particles: a case study in Rome, Italy

PM(10) concentration and chemical composition (ions and carbon compounds) at three sampling stations in Rome and in its surroundings was determined daily during a one-month field study, carried out during December 2003. PM concentration at the traffic station was considerably higher than at the urban background and semi-rural stations; elemental carbon was detected as one of the chemical components responsible for this increase. The difference in the concentration of sulphate and ammonium was negligible, as it was expected for secondary pollutants. A negative artefact in the determination of ammonium nitrate by means of heated automatic monitors was highlighted. The dilution properties of the lower atmosphere were traced by means of a natural radioactivity monitor. This parameter has been found to play an essential role in pollution buildup. A considerable increase in PM concentration was observed to coincide with periods of atmospheric stability. The main difference in PM composition between periods of high concentration and periods of "clean" air was found to be in the increase of ammonium nitrate concentration.