Direct determination of metals associated with airborne particulates using a graphite probe collection technique and graphite probe atomic absorption spectrometric analysis

1987 ◽  
Vol 42 (11-12) ◽  
pp. 1227-1233 ◽  
Author(s):  
C.L. Chakrabarti ◽  
He Xiuren ◽  
Wu Shaole ◽  
W.H. Schroeder
2010 ◽  
Vol 7 (s1) ◽  
pp. S433-S441
Author(s):  
Ameen W. Qasim ◽  
Zuhair A. A. Khammas

A new application of an indirect atomic absorption spectrometric (AAS) method was offered for the assay of low concentration of trifluoperazine hydrochloride (TFPH) in pure and pharmaceutical dosage form with good accuracy and precision. The method is depended on the formation of metal complex between the drug (TFPH) and palladium(II) to form orange-yellowish product extractable in organic solvent prior to its aspiration into an air-acetylene flame and indirectly determined by AAS. Using AA responses, all experimental parameters such as, pH, concentration of palladium, reaction time, extraction time and phase ratio which affect the complexation and extraction of TFPH-Pd(II), have been investigated. Under optimized conditions, linearity was observed in the range of 0.5-17 μg mL-1with detection limit (S/N) of 0.038 μg mL-1, precision in range of 1.18-1.92%, accuracy as the %Erelof 2.4% and recoveries ranged from 101.7 to 104% with mean value of 102.4±0.135. The proposed method was applied for the determination of TFPH in the drug stelazine by both direct calibration and standard additions procedures and found to be 4.88 and 4.87 mg per unite, respectively compared with the stated value of 5 mg per unite. This method is also compared statistically with direct determination by using UV-Vis spectrophotometric technique which is preformed in our laboratory and found to be insignificant at 95% confidence level. All statistical calculations were implemented via the chemsoftware Minitab version 11.


1985 ◽  
Vol 322 (7) ◽  
pp. 743-746 ◽  
Author(s):  
Robert F. M. Herber ◽  
Annie M. Roelofsen ◽  
Winifred Hazelhoff Roelfzema ◽  
Jenny H. J. Copius Peereboom-Stegeman

2010 ◽  
Vol 1 (2) ◽  
pp. 111-119
Author(s):  
Narsito Narsito

In the present work, some fundamental aspects of the formation of gaseous lead hydride from aqueous solutions containing divalent lead ions (Pb2+) and its application in the atomic absorption spectrometric analysis lead has been investigated. By utilizing a peristaltic pump, an acidic solution of Pb2+ was first oxidized with ammonium peroxodisulphate, NH4S2O8, and followed by reduction with sodium tetrahydroborate, NaBH4. After a gas-liquid separation, the gaseous lead hydride produced was directly swept into an electrically heated open ended quartz tube, located at the light path of an atomic absorption spectrometer in order to have possibilities for specific atomic absorption spectroscopic measurements. The absorbance signals caused by lead atomic absorption could be used proportionally to estimate the density of atomic lead vapor produced in the thermal decomposition under investigation. Results showed that on-line pre-oxidation of the analyte is very important and crucial step in the gaseous hydride generation of lead, and no lead hydride was produced without the involvement of this step. Moreover, it was observed that the use of low major gas flows cannot be applied in quantitative atomic absorption spectrometric determination of lead by this technique. This condition may result in possible losses of the analyte atomic vapor due to metallic condensation.


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