HPLC法测定饲料中维生素A、维生素D 3 和维生素E

建立了以w(C2H5OH)=95 %乙醇直接提取,高效液相色谱仪在波长280 nm和254 nm处连续测定饲料中维生素A、维生素D3和维生素E的方法.色谱柱为大连依利特Hypersil ODS C18(25 cm×4.6 mm×5 μm),流动相为甲醇-水,流速为1.2 mL/min.维生素A、维生素D3、维生素E的质量浓度分别在1.0 mg/L～20.0 mg/L、0.5 mg/L～15.0 mg/L 、2.5 mg/L～50.0 mg/L范围内与峰面积呈良好的线性关系,检测限分别为0.3×10-6 μg、0.04×10-6 μg、5.0×10-6 μg,相对标准偏差分别为1.6 %、2.7 %、2.4 %,平均回收率分别为99 %、102 %、98 %.     

DOAS大气环境质量监测系统与传统点式采样监测法可比性研究

系统比较了DOAS大气监测系统与传统点式采样设备在测定环境空气中二氧化硫的性能。     

Application of CFD Methods for Modelling in Air Pollution Problems: Possibilities and Gaps

Different urban air pollution problems deal with complex structure of air flows and turbulence. For such problems the Computer Fluid Dynamics (CFD) methods become widely used. However, this approach despite a number of advantages has some problems. Experience of use of CFD tools for development of models and suggestions of their applications for a local scale air pollution over a complex terrain and stable stratification are discussed in this paper, including: Topography and complex geometry: choose of the co-ordinate system and computer grid; Turbulence closure for air pollution modelling: modified k- model for stable stratified ABL; Boundary conditions for vertical profiles of velocity for stable-stratified atmosphere; Effects of the radiation and thermal budget of inclined surfaces to dispersion of pollutants; Artificial sources of air dynamics and circulation.Some examples of CFD applications for air pollution modelling for a flat terrain, mountainous area, mining open cast and indoor ventilation are discussed. Modified k- model for stably-stratified ABL is suggested. Due to the isotropic character of the k- model a combination of it in vertical with the sub-grid turbulence closure in horizontal can be more suitable for ABL. An effective scheme of boundary conditions for velocity profiles, based on the developed similarity theory for stable-stratified ABL, is suggested. Alongside with the common studies of atmospheric dispersion, the CFD methods have also demonstrated a good potential for studying anthropogenic and artificial-ventilation sources of air dynamic and circulation in local-scale processes of air pollution.     

Effect of temperature on single and competitive adsorptions of Cu(II) and Zn(II) onto natural clays

This study conducted a combined adsorption-sequential extractionanalysis (CASA), by which five phases (i.e., exchangeable, carbonate, Mn-Oxide, organic, and Fe-Oxide phases) of adsorbed heavy metals were analyzed, to investigate temperature effects on single and competitive adsorptions of Zn(II) and Cu(II) ontonatural clays. In the case of single adsorption of Zn, the exchangeable phase adsorption decreased from 65 to 40%, but thecarbonate phase adsorption increased from 30 to 40%, with an increase in temperature from 15 to 55 °C. However, in itscompetitive adsorption with Cu, Zn was mostly present in the exchangeable phase (over 90%), and with an increase in temperature, the exchangeable phase adsorption decreased only 10%. In the case of Cu, over 50% among the total amount of adsorption was present in the carbonate phase in both cases ofsingle and competitive adsorptions. The carbonate phaseadsorption of Cu increased from 56 to 61% and from 60 to 66% in single and competitive adsorptions, respectively, with atemperature increase. These results show that in the case of Zn,the major mechanism of retention in natural clay soils might beexchangeable phase adsorption, especially in the case of competitive adsorption with Cu. However, in the case of Cu, the major mechanism might be carbonate phase adsorption, which is known to be a more immobile phase than exchangeable phase adsorption. It seems that the adsorption of Zn and Cu onto natural clays is an endothermic reaction, which represents thatthe adsorption equilibrium constants and capacities increase with a temperature increase, with the exception of exchangeablephase adsorption.     

Geostatistical Uncertainty Modelling for the Environmental Hazard Assessment During Single Erosive Rainstorm Events

This paper presents an environmental hazard assessment to account the impacts of single rainstorm variability on river-torrential landscape identified as potentially vulnerable mainly to erosional soil degradation processes. An algorithm for the characterisation of this impact, called Erosive Hazard Index (EHI), is developed with a less expensive methodology. In EHI modelling, we assume that the river-torrential system has adapted to the natural hydrological regime, and a sudden fluctuation in this regime, especially those exceeding thresholds for an acceptable range of flexibility, may have disastrous consequences for the mountain environment. The hazard analysis links key rainstorm energy variables expressed as a single-storm erosion index (EI_sto), with impact thresholds identified using an intensity pattern model. Afterwards, the conditional probabilities of exceeding these thresholds are spatially assessed using non-parametric geostatistical techinques, known as indicator kriging. The approach was applied to a test site in river-torrential landscape of the Southern Italy (Benevento province) for 13 November 1997 rainstorm event.     

环境监测实验室信息管理系统建设——以上海市环境监测中心为例

简述了实验室信息管理系统(LIMS)的概念和建设LIMS的现实意义,着重介绍了上海市环境监测中心实施LIMS的过程和体会,分析了环境监测实验室在LIMS选型和实施过程中需要注意的问题及LIMS对现行工作的影响,并对需进一步完善的功能提出了建议.     

液相色谱法测定环境空气中酞酸酯类

制作了半挥发性有机物中流量采样装置,使用超细玻璃纤维滤膜采样,反相液相色谱法测定环境空气中酞酸酯类,并对样品净化方式、目标化合物在气相和颗粒物上的分布规律及采样器的捕集效率进行了试验.方法在0.50 mg/L～50.0 mg/L之间线性关系良好,当浓缩体积为1.0 mL、采样体积为144 m3时,目标化合物的检出限为0.4×10-3 μg/m3～6.0×10-3 μg/m3;当采样体积为6 m3时,检出限为0.008 μg/m3～0.145 μg/m3.     

灰色系统模型在总悬浮物预测中的应用

以１９８６－１９９４年东北某城市总悬浮物统计资料为依据，应用灰色系统理论ＧＭ（１，１）模型对总量浮物数值进行预测分析。     

超声波萃取-高效液相色谱法测定总悬浮颗粒物中的多环芳烃

研究了一种用中流量采样器采样,超声波萃取,硅镁型吸附剂柱层析预分离.高效液谱测定总悬浮颗粒物的实验方法,在16分内可分高萘、蒽、芘、苯并(a)芘、苯并(ghi)苝等15种多环芳烃.已在大气环境的实际监测中得到应用.     

我国内陆流域各类水体中天然放射性核素浓度

1985年～1989年由新疆、甘肃、青海、西藏、内蒙古、陕西、宁夏等省、自治区环境监测站(研究所)对内陆流域各类水体中U、Th、~(226)Ra、~(40)K浓度进行调查,由调查的29条内陆河、23个湖泊、15座水库、55处井泉和34个自来水的统计结果表明,流域内各水体中U和~(40)K浓度的平均值与同期调查的黄河水系同类水体的浓度相近,明显高于长江水系,与全国同类水体相比亦属偏高。Th和~(226)Ra的平均浓度与全国同类水体的浓度相近,甘、新内陆区浓度较低。调查发现,一些咸水湖、井水和自来水中U、~(226)Ra,或~(40)K浓度异常偏高。