城市污水处理过程中溶解性有机物及荧光物质的变化规律

以锦州市W污水处理厂为研究对象,利用三维荧光光谱分析技术和荧光区域积分(FRI)方法考察了城市污水处理过程中溶解性有机物及荧光物质的去除状况.利用XAD树脂将DOM分为5个部分:疏水性有机酸(HPO-A)、疏水性中性有机物(HPO-N)、过渡亲水性有机酸(TPIA)、过渡亲水性中性有机物(TPI-N)和亲水性有机物(HPI).结果表明,HPO-A和HPI是该污水处理厂进水中的主要DOM组分,并且DOM中的荧光物质主要为类芳香族蛋白质荧光物质和类富里酸荧光物质.在该污水处理厂内,生物降解作用是TPI-A和HPI的主要去除机制,HPO-N和TPI-N主要是由深度处理工艺(絮凝-沉淀-过滤)去除的,生物处理工艺和深度处理工艺对HPO-A的去除能力接近,而生物处理工艺和深度处理工艺对TPI-N的去除效果均较差.生物处理工艺对HPO-A、TPI-A和HPI中的荧光物质有较强的去除能力,而对HPO-N和TPI-N中荧光物质的去除效果较差.深度处理工艺能够有效去除HPO-A和HPO-N中的荧光物质,而对TPI-A、TPI-N和HPI中的荧光物质无明显去除作用.     

USE OF X-RAY FLUORESCENCE TO DETERMINE TRACE METALS IN WATER RESOURCES1

ABSTRACT. The X-ray fluorescence method was used to analyze trace metals collected in particulate form on filter papers and from the ionic state by ion exchange filter papers. The samples were prepared by allowing water to pass through these filter papers. The procedures necessary for using the X-ray fluorescence method are described. A number of samples were taken from the Great Miami River in Dayton, Ohio over one year showing the presence of the following metals, Ca, Ti, Cr, Fe, Cu, Zn, Sr, and Cd. Elements in the periodic table between Ti and Cs were detectable to a sensitivity limit of the order of 30 ppb for metals in the particulate form and 0.4 ppm for metals in the ionic form.     

Dynamics of Bacterial Abundance,Biomass, Activity,and Community Composition in the Oligotrophic Traunsee and the Traun River (Austria)

The holomictic Traunsee is the deepest and second largest lakein Austria. The special characteristic of this ecosystem isthe fact that local salt and soda industries presumably alterthe lake by the discharge of waste materials. Since thebeginning of the 20th century salt and soda works areannually releasing up to 50,000 tons of solid wastes and up to150,000 tons of chloride into Traunsee. To assess potentialeffects of these anthropogenic impacts on the bacterioplanktonthree sampling sites, influenced as well as not influenced bythe industrial discharge, were chosen for comparison andsampled monthly from November 1997 to October 1998. Bacterialabundance ranged between 0.4 to 3.0 × 10⁶ cells ml^-1 with decreasing numbers along the depth profile. Theproportion of actively respiring bacteria, i.e. INT [2-(4-iodophenyl)-3-(4-nitrophenyl)-5-phenyltetrazolium chloride]reducing cells, never exceeded 10% of DAPI (4',6'-diamidino-2-phenylindole) stained cells. Fluorescence in situ hybridization (FISH) was used to examine the seasonal and spatial distribution of dominant phylogenetic groups of thebacterioplankton. Up to 84% of bacteria detected with DAPIcould be detected via FISH applying the universal bacterialprobe EUB338. Percentages of alpha- and beta-Proteobacteriaand members of the Cytophaga-Flavobacterium cluster did notexceed 60% of DAPI-stained cells.Beta-Proteobacteriaappeared to be the most abundant group, not only in Traunsee butalso in two reference lakes, Attersee and Hallstättersee. No significant differences in any of the bacterial parameters couldbe detected between the three sampling sites and all measurementswere found in the range reported for oligotrophic lakes. The highdischarge of the Traun River, resulting in a lake water renewaltime of only one year, may diminish possible effects of industrial waste discharge in the pelagic zone.     

提高环境水中纳克级超痕量汞测定灵敏度的研究

对ｎｇ／Ｌ级超痕量汞测定中的消解、测定各步骤对灵敏度的影响进行了研究。得出结论：采用高纯氩气作载、屏气，选择高负压值和高扩展倍率能明显提高灵敏度；选择合适的消解时间和缩短测定时间能使灵敏度略有提高；试剂和玻璃器皿所带给空白的痕量汞对提高灵敏度不利，应作除汞处理。     

流动注射-氢化物发生-原子荧光光谱法测定土壤中铅

采用流动注射-氢化物发生-原子荧光光谱法测定土壤中的铅,工作曲线线性关系良好,检出限为0.25 mg/kg,相对标准偏差＜3.5%,加标回收率为93.0%～105%.该方法简便快速,测定结果准确可靠.     

氢化物发生原子荧光法测定饮用水中的微量硒

氢化物发生原子荧光法测定饮用水中的微量硒时。仪器条件和试剂的浓度选择很重要。本文对条件的最佳化进行了实验。并对方法的精密度、准确度和检出限进行了讨论。     

高灵敏XRF测定废水中痕量砷

本文提出了在硫酸介质中，以锌粒还原产生氢化物，溴化铜溶液吸收，微孔滤膜过滤制成薄样，Ｘ射线荧光测定水中痕量砷的分析方法。     

龙岩市区大气颗粒物中多环芳烃的种类和时空分布特征及来源

采用恒能量同步荧光法检测了龙岩市大气颗粒物样品中的多环芳烃(PAHs),比较了龙岩市区大气颗粒物中多环芳烃含量的差异以及不同季节对多环芳烃含量的影响,讨论了其分布规律及污染源。     

AFS-830型双道原子荧光光度计同时测定饮用水中砷、汞

主要探讨应用AFS-830型双道原子荧光光度计，在饮用水监测中同时测定水中砷、汞的方法和技术。此法是在硝酸介质，以硼氢化钠作还原剂，进行原子化，被测元素原子激发出荧光强度值在一定范围内与被测元素的浓度成正比。砷与汞的检出限分别为0．0618和0．0158ug／L。     

Determination of arsenic in grain and soil by hydride nondispersive atomic fluorescence method

Quantity of trace arsenic in grain and soil was determined by hydride nondispersive atomic fluorescence method.Optimum conditions of measurement were selected in the experiment including the pH of the medium, reductive agent, the concentration and flowing velocity of KBH4, rate of carrier gas and atomized temperature. The reference sample of rice C was determined and the linear relationship of the calibration curve was plotted, indicating that the method was highly precise. In the experiment of recovery rate, the method was quite satisfactory.Based on the determination of hundreds of samples, it is proved that atomic fluorescence method is rapid, sensitive and low in interference. It is very efficient on determination of trace arsenic in soils and grains, especially in grains.