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1.
原子吸收光光度法测定矿石中铁   总被引:4,自引:1,他引:3  
运用石墨炉电热蒸发进行分子光谱研究,文献已有报道[1~3],但用原子吸收光度计代替紫外-可见分光光度计进行溶液分子光谱分析报道较少[4,5]。本文以原子吸收分光光度计代替紫外-可见分光光度计用原子吸收光光度法研究了测定铁的条件并实测了铜矿中铁含量。实...  相似文献   

2.
水中痕量汞的测定目前多采用冷原子吸收法。而借助原子吸收分光光度计的标尺扩展功能较一般测汞仪具有更好的灵敏度。本文利用废旧F732测汞仪的薄膜泵和石英管吸收池作为汞的原子化装置,使汞在普通原子吸收分光光度计上的测定变得简便、易行。用于水中痕量汞的测定,得到满意的效果。  相似文献   

3.
介绍了原子吸收分光光度计日常维护注意事项及常见故障排除方法.  相似文献   

4.
介绍了WFX - 1E型原子吸收分光光度计的故障与修理情况  相似文献   

5.
介绍原子吸收分光光度计检定最佳测试条件的选择技巧。  相似文献   

6.
原子吸收分光光度计上采用连续光源用于光度分析的研究   总被引:7,自引:1,他引:6  
探讨了应用连续光源和双光束原子吸收分光光度计用于光度分析的可行性。  相似文献   

7.
介绍了WFX-1E型原子吸收分光光度计的故障与修理情况。  相似文献   

8.
对原子吸收分光光度计计量检定中的几个问题作了一些探讨,并提出了相应的改进措施。  相似文献   

9.
谭业辉 《化学计量》1995,4(1):12-13,29
对原子吸收分光光度计计量检定中的几个问题作了一些问题,并提出了相应的改进措施。  相似文献   

10.
原子吸收分光光度计用于分子吸收分析测定磷的研究   总被引:21,自引:0,他引:21  
应用钙元素空心阴极灯中钙元素的422.7nm谱线和原子吸收分光光度计,对磷钒钼黄体系进行了研究,并对生铁样品中磷的含量进行了测定,获得满意的结果。  相似文献   

11.
原子吸收分光光度计中光栅的设计及选择   总被引:1,自引:0,他引:1  
简单论述了光栅在原子吸收分光光度计(AAS)中的作用;提出了一般AAS中不需要使用1800条/mm光栅的理由;同时,对有关问题进行了讨论. 可供AAS的设计者、使用者们参考.  相似文献   

12.
An analytical exercise between two laboratories was performed in order to compare the elemental composition of a water sample. The metal concentration of Cr, Cu, Fe, Mn, Ni, Pb, and Zn in the water sample was analyzed by Total Reflection X-Ray Fluorescence and Atomic Absorption Spectrometry. The analysis by Total Reflection X-Ray Spectrometry was realized by an Ital Structures TX-2000 and the analysis by Atomic Absorption Spectrometry was made by a Perkin Elmer Spectrophotometer Model 3110. Results show a good agreement in the metal concentrations obtained by both techniques. The variation coefficient between the results with both techniques was less than 14%. Therefore, it is possible to conclude that both techniques are reliable and adequate for the determination of these elements in environmental water samples.  相似文献   

13.
《Analytical letters》2012,45(11):817-830
Abstract

Simultaneous determination of calcium and magnesium content in human blood serum has been reported as a routine clinical laboratory method, which is rapid, simple, and requires 50 δ of serum for complete analysis with triplicate runs. This is accomplished using a Model 1250 Varian Techtron Atomic Absorption Spectrophotometer with the stoichiometric nitrous oxide-acetylene flame of 0.2 cm red-cone height. Calcium and magnesium standards and also the serum specimens are prepared in aqueous medium containing 2000 ppm potassium chloride. Serum specimens are ultimately diluted to 1:100 fold. About 40–50 samples can be analyzed per hour of instrument operation, if standard solutions and diluted serum specimens are readily available.  相似文献   

14.
This study examines the synthesis of SBA-15 with tailored pore sizes through controlled thermal treatment for the adsorption of Pb and Cd ions. The aim is to produce a material that can adsorb heavy metals at both high and low concentrations. The materials were characterised by means of N(2) physisorption, powder X-ray diffraction (PXRD), diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), microanalysis and transmission electron microscopy (TEM). The surface areas ranged from 410 to 871 m(2)g(-1), and pore diameter was increased from 5.9 to 10.8 nm. This method allows for maximum adsorption of metal ions at very low concentrations. Metal ion adsorption was determined using an Atomic Absorption Spectrophotometer. The effects of pH were found to play a major role in the precipitation and, therefore, adsorption of metal ions. This method proved to be efficient at adsorbing large quantities of both metals (39 and 41 mg g(-1) for Pb and Cd, respectively).  相似文献   

15.
Liquid phase benzylation of benzene with benzyl chloride was investigated over different compositions of cobalt zinc ferrite (CoxZn1-xFe2O4, x-0.0, 0.25, 0.5, 0.75, 1.0) nano composites, synthesized by sol–gel method. The un-substituted cobalt ferrite catalyst exhibited excellent activity among the series effecting complete conversion of benzyl chloride in 60?min at 90?°C with 100% selectivity for diphenyl methane. The effect of various reaction parameters on the reaction was studied. Higher benzylation activity of cobalt ferrite nanocomposite is attributed to the presence of higher quantities of moderately acidic sites and a good correlation was observed between surface acidity and benzylation activity of catalysts. The catalysts are reusable without any significant structural change as indicated by X-ray Diffraction (XRD) and Atomic Absorption Spectrophotometer (AAS).  相似文献   

16.
Trace level of selenium and mercury in photographic emulsion are used to improve photographic properties. The presence of silver halide in photographic emulsion does not allow the application of the most common analytical methods such as Hydride Generation Atomic Absorption Spectrometry (HG-AAS) and cold vapour Atomic Absorption Spectrometry (CV-AAS). Besides, silver removal was not quantitative, leading to a significant loss of the analytes and low reproducibility. The present work suggest the use of inductively coupled plasma Atomic Emission Spectrometry (ICP-AES) equipped with Ultrasonic Nebulizer (USN) for direct aqueous samples analysis at microgram l-1 level (d.l. 5.1 ppb for Hg and 6.1 ppb for Se).  相似文献   

17.
 Methods for metal preconcentration are often described in the literature. However, purposes are often different, depending on whether the methods are applied in environmental, clinical or technological fields. The respective method needs to be efficient, give high sensitivity, and ideally also is selective which is useful when used in combination with atomic spectroscopy. This review presents the actual tendencies in metal preconcentration using techniques such as Flame Atomic Absorption Spectrometry (FAAS), Electrothermal Atomic Absorption Spectrometry (ETAAS), Hydride Generation Atomic Absorption Spectrometry (HGAAS), Inductively Coupled Plasma Optical Emission Spectrometry (ICP OES) and Inductively Coupled Plasma Mass Spectrometry (ICP-MS). Procedures based on related to electrochemical, coprecipitation/precipitation, liquid–liquid and solid–liquid extraction and atom trapping mechanisms are presented. Correspondence: Department of Analytical Chemistry, Universidade Estadual de Campinas – UNICAMP, P.O. Box 6154, 13083-970 Campinas, Brazil. e-mail: zezzi@iqm.unicamp.br Received December 20, 2001; accepted October 11, 2002  相似文献   

18.
在对原子吸收光谱仪石墨炉电源电路板测绘的基础上,分析了该电源主电路的故障原因,并给出了维修过程。  相似文献   

19.
I. Lavilla 《Talanta》2009,80(1):109-116
In this work, ultrasound-assisted emulsification with a probe system is proposed as a rapid and simple sample treatment for atomic spectrometric determinations (Electrothermal Atomic Absorption Spectrometry, Inductively Coupled Plasma Optical Emission Spectrometry, Flame Atomic Absorption Spectrometry and Cold Vapour Atomic Absorption Spectrometry) of trace elements (As, Cd, Cr, Cu, Hg, Mg, Mn, Ni, Sr and Zn) in cosmetic samples such as shampoos, gel (hair gel), crèmes (body milk, hair conditioner) and oil (body oil). The type of dispersion medium, the sample mass-to-dispersion medium volume ratio, as well as the parameters related to the ultrasound-assisted emulsification (sonication amplitude and treatment time) were exhaustively studied. Only 1 min of ultrasonic shaking and a dispersion medium containing 0.5% (w/v) of SDS + 3% (v/v) of HNO3 or HCl allows obtaining a stable emulsion at least for 3 months. Thermal programs, nebulization of emulsions, speed of pumps and concentration of reagents used in cold vapour generation were optimized. Calibration using aqueous standards was feasible in all cases. Calibration by the standard addition method and recovery studies was also applied for validation. Microwave-assisted digestion and Inductively Coupled Plasma Mass Spectrometry were used for comparison purposes. Relative standard deviations from analysis of five independent emulsions were less than 9% in all cases.  相似文献   

20.
The applicability of GDMS, SIMS, SSMS, NAA and TMS with AAS, ICP-OES and ICP-MS end determination for routine bulk ultratrace analysis of high purity refractory metals was investigated. Due to the heterogeneous distribution of trace elements in the sub-ppm range, sample consumption and analysis time have a tremendous influence on quantification with procedures of low sample consumption. As an example, GDMS, which is commonly used for ultrapure material certification by most of the manufacturers in Europe and the USA, exhibits discrepancies by more than one order of magnitude for repetitive analyses of a series of trace components in the same sample. Furthermore, results of different laboratories using the same instrument are frequently not comparable. Due to easy standardization and large sample consumption TMS procedures combined with FAAS, GFAAS, ICP-AES and ICP-MS as methods of end determination exhibit better precision and accuracy than GDMS and SIMS. Detection limits are comparably low or even better in case of ICP-MS end determination. TMS procedures are less expensive and less time consuming than highly sophisticated analytical techniques like GDMS, SIMS or NAA. Additionally, they can be easily applied by experienced personnel in a well equipped industrial analytical laboratory.List of Acronyms Used AAS Atomic Absorption Spectrometry - FAAS Flame Atomic Absorption Spectrometry - GDMB Gesellschaft Deutscher Metallhütten- und Bergleute - GDMS Glow Discharge Mass Spectrometry - GFAAS Graphite Furnace Atomic Absorption Spectrometry - ICP-AES Inductively Coupled Plasma Atomic Emission Spectrometry - ICP-MS Inductively Coupled Plasma Mass Spectrometry - IDMS Isotope Dilution Mass Spectrometry - NAA Neutron Activation Analysis - SIMS Secondary Ion Mass Spectrometry - SSMS Spark Source Mass Spectrometry - TMS Trace-Matrix Separation - VLSI Very Large Scale Integration - XRFS X-Ray fluorescence Spectroscopy Dedicated to Professor Günther Tölg on the occasion of his 60th birthday  相似文献   

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