2008
DOI: 10.1016/j.sab.2008.04.019
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Determination of manganese in diesel, gasoline and naphtha by graphite furnace atomic absorption spectrometry using microemulsion medium for sample stabilization

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Cited by 32 publications
(16 citation statements)
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“…A common solvent (co-solvent) was used to obtain a homogeneous mixture between the aqueous and the oily medium. The selected cosolvent was propan-1-ol and this choice was based on previous experiences in the preparation of microemulsions of petrol and diesel when determining trace metals using atomic spectrometry [10]. The kerosene content was fixed to 10% (in volume) and in order to try to obtain stable and homogeneous systems, the content of the aqueous phase was varied from 2.5 to 15% with final composition achieved with a complementary volume of the common solvent (propan-1-ol).…”
Section: Microemulsion Compositionmentioning
confidence: 99%
“…A common solvent (co-solvent) was used to obtain a homogeneous mixture between the aqueous and the oily medium. The selected cosolvent was propan-1-ol and this choice was based on previous experiences in the preparation of microemulsions of petrol and diesel when determining trace metals using atomic spectrometry [10]. The kerosene content was fixed to 10% (in volume) and in order to try to obtain stable and homogeneous systems, the content of the aqueous phase was varied from 2.5 to 15% with final composition achieved with a complementary volume of the common solvent (propan-1-ol).…”
Section: Microemulsion Compositionmentioning
confidence: 99%
“…A number of techniques such as inductively coupled plasma-mass spectrometry (ICP-MS) [8], anodic stripping voltammetry [9][10][11], atomic absorption spectroscopy (AAS) [12], X-ray fluorescence [13], ICP-AES, glassy carbon electrodes [14][15][16] and cathodic stripping voltammetry [17][18][19] are used for its determination. These techniques are sophisticated, time consuming and require large infrastructure back up and expertise and are therefore cumbersome for the analysis of Mn 2+ in large number of samples.…”
Section: Introductionmentioning
confidence: 99%
“…14,[30][31][32] Acid digestion is time consuming, presents risks of losses of analyte and sample contamination, and also requires the use of corrosive and hazardous reagents; thus it is the least suitable for routine work, although it allows instrument calibration with aqueous calibration solutions. Sample dilution with organic solvents offers speed and simplicity, but the toxicity of these solvents is an obstacle regarding its use, as well as the low stability of the analyte in these solutions, 6,[33][34][35][36] higher organic loads, difficulties in calibration and dilution are implicit to the procedure. Emulsion or microemulsion formation is also simple and quick; it provides greater analyte stability compared to organic solvent dilution and also allows, in some cases, calibration with aqueous calibration solutions.…”
Section: Introductionmentioning
confidence: 99%