Use of Graphite Furnace Television in Electrothermal Atomization Atomic Absorption Spectrometry
β Scribed by G. Donati; M. Ottaviani; E. Veschetti
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 245 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0026-265X
No coin nor oath required. For personal study only.
β¦ Synopsis
The determination of metals in traces by means of electrothermal atomization atomic absorption spectrometry (ETA-AAS) presents analytical difficulties for complex matrixes such as seawater or brines. Some of them can be overcome with sample pretreatment or through the use of matrix modifiers at the moment of the instrumental analysis. These operations require a preliminary study of the working conditions, the effect of which is evaluated through the trend of the background signal, the signal-to-noise ratio, and the recovery of analytes after a given pretreatment. The optimization of the first two aspects is generally achieved for attempts through monitoring of the signals produced by the photomultiplier in correspondence of the total and aspecific absorptions. To this purpose the use of a solid state CCD camera like an ancillary device was applied to the development of the thermal program. The television camera was temporarily lined with the furnace during the drying and ashing phases. Detailed images of the phenomena related to the phase transitions occurring in graphite furnace prior to atomization were thus obtained.
π SIMILAR VOLUMES
A graphite furnace atomic absorption spectrometry method with Zeeman background correction for the direct determination of cadmium in grape wines is described. Use of ammonium dihydrogen phosphate, magnesium nitrate, and palladium nitrate as matrix modifiers was investigated. Palladium nitrate with
A procedure was developed for the quanhficatlon of thalbum at the ultratrace level (ng g-l) m geoloacal matenals The sample 1s dissolved m 3 M H2S04 to which IS added KI and K,HP04 The thalhum IS then extracted as its mdo complex mto methyhsobutyl ketone (MIBK), leavmg behind most of the n-on The re
Palladium was determined in pharmaceuticals by direct graphite furnace atomic absorption spectrometry (GFAAS) method. The detection limit was 0.1 mg/g in 5% solution; the recovery of 0.5-2.0 mg/g Pd spike was close to 100%. The flow injection GFAAS method was worked out using oxime and iminodiacetic