2001
DOI: 10.1039/b100754h
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Application of laser-induced breakdown spectrometry for direct determination of trace elements in starch-based flours

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Cited by 55 publications
(21 citation statements)
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“…Further experiments are necessary to determine the best approach. It is also worth noting that the scatter in the data observed here is significantly larger than that reported in previous studies [6,9,10], which may be related to the relatively weak laser pulse energy (10 mJ) employed in the present study compared to those used in other studies (100-350 mJ) [6,9,10]. Greater laser pulse energies consume more sample matter per laser pulse to somewhat mitigate microscale inhomogeneities in the sample and can also benefit from more stable plasma formation.…”
Section: Key Resultscontrasting
confidence: 54%
See 1 more Smart Citation
“…Further experiments are necessary to determine the best approach. It is also worth noting that the scatter in the data observed here is significantly larger than that reported in previous studies [6,9,10], which may be related to the relatively weak laser pulse energy (10 mJ) employed in the present study compared to those used in other studies (100-350 mJ) [6,9,10]. Greater laser pulse energies consume more sample matter per laser pulse to somewhat mitigate microscale inhomogeneities in the sample and can also benefit from more stable plasma formation.…”
Section: Key Resultscontrasting
confidence: 54%
“…It was found that a gate delay of 1 μs and an integration time of 10 μs provided the optimum signal to noise ratio and that the coefficient of variation of measurements was approximately 8-15%. Cho et al [6] mixed starch powder or NIES samples with 50% (w/w) to improve sample rigidity for optimal plasma formation and used the Mg line at 279.553 nm and the K line at 766.49 nm to determine concentrations of those elements with detection limits of 0.4 and 3 μg/g for Mg and K, respectively.…”
Section: Figure 1 Laser-induced Breakdown Spectroscopy (Libs) Measurmentioning
confidence: 99%
“…The effect of spot size, laser repetition rate, laser energy, number of laser pulses and delay time on the analytical results were checked by the monitoring of an integrated area of atomic/ionic emission peaks and the signal background ratio (SBR). Besides influence of vertical distance above sample surface and pressure of surrounding gas are also important instrumental parameters [15], the instrument used in this work does not allow their optimization. At least two emission wavelengths were evaluated for each element; however, as their behavior was similar, only K(I) 766.49 and Mg(II) 279.553 nm were used.…”
Section: Libs Instrumental Optimizationmentioning
confidence: 99%
“…In the absence of an internal standard, the ratios between slopes are close to 2, indicating that spiked filter paper or spiked babassu mesocarp cannot be used in wood analysis. Due to this kind of interference, most relevant papers [10,[15][16][17] have used the LIBS method of calibration using a sample matrix spiked with an increasing concentration of analytes or dilution using appropriate materials. These results are in accordance to Sun et al [18] which proposed the measurement of Mn, Zn, P, Fe and Cu in plant materials by LIBS.…”
Section: Calibration Of System Libsmentioning
confidence: 99%
“…LIBS is a method in which elemental analysis of any kind of sample (Rosenwasser et al 2001;Cho et al 2007;Samek et al 2000;Rai et al 2002) even having heterogeneous composition can be easily done with minimal disturbance. LIBS works by firing an intense pulse of laser light on the sample surface.…”
Section: Introductionmentioning
confidence: 99%