Determination of elemental bioavailability in soils and sediments by microwave induced plasma optical emission spectrometry (MIP-OES): Matrix effects and calibration strategies

Talanta ◽  
2021 ◽  
pp. 123166
Author(s):  
Raquel Serrano ◽  
Enriqueta Anticó ◽  
Guillermo Grindlay ◽  
Luis Gras ◽  
Clàudia Fontàs
2020 ◽  
Vol 12 (20) ◽  
pp. 2638-2644 ◽  
Author(s):  
Alexandre Müller ◽  
Dirce Pozebon ◽  
Anderson Schwingel Ribeiro

Microwave-induced plasma optical emission spectrometry (MIP OES) allowed the determination of 19 elements in a complex sample matrix. Spectral lines and sample preparation procedures were investigated.


2020 ◽  
Vol 35 (7) ◽  
pp. 1389-1394 ◽  
Author(s):  
Oleg V. Pelipasov ◽  
Evgeniya V. Polyakova

The matrix effects in MIP OES arising in the presence of elements with Eion 5.13–9.39 eV (Na, Cu, Pb, Cd, Zn) depending on the concentration, nebulization flow rate, and plasma power were studied.


2020 ◽  
Vol 35 (10) ◽  
pp. 2113-2131 ◽  
Author(s):  
Alexandre Müller ◽  
Dirce Pozebon ◽  
Valderi L. Dressler

The N2-sustained microwave-induced plasma optical emission spectrometry (N2-MIP OES) has been increasingly applied for metals and non-metals determination in different fields.


2017 ◽  
Vol 71 (12) ◽  
pp. 2692-2698 ◽  
Author(s):  
Amanda G. Althoff ◽  
Charles B. Williams ◽  
Tina McSweeney ◽  
Daniel A. Gonçalves ◽  
George L. Donati

In this work, we evaluate the application of microwave-induced plasma optical emission spectrometry (MIP OES) to determine of Al, Cr, Co, Cu, Fe, Mn, Ni and Zn in children’s cough syrup, eye drops, and oral antiseptic using standard dilution analysis (SDA). The SDA method is simple, with only two calibration solutions prepared per sample. The first solution (S1), composed of 50% sample +50% of a standard solution, is introduced into the plasma and the analytical signals are monitored in a time-resolved fashion. Then, the second solution (S2), composed of 50% sample +50% blank, is poured into the vial containing S1. As the solutions mix, the analytical signals gradually drop to a stable baseline. The calibration curve is computed by plotting the ratio of the analyte signal (SA) over the internal standard signal (which is also part of S1) (SIS) on the y-axis, versus the inverse of the IS concentration on the x-axis (i.e., SA/SIS versus 1/CIS). In this study, SDA results were compared with values obtained with the traditional methods of external calibration (EC), internal standardization (IS), and standard additions (SA) in MIP OES determinations. The precision (represented as percent RSD) for SDA showed values in the range of 2.50–8.00% for all samples, while conventional calibration methods showed RSDs in the range of 6.40–32.50% for EC, 8.30–21.80% for IS, and 5.20–17.40% for SA. The LODs calculated for SDA are below the maximum limits allowed by the major pharmaceutical regulatory agencies, and presents superior precision and accuracy compared to the traditional calibration methods. Considering its simplicity and efficiency, SDA is an important new tool for accurate analyses of pharmaceuticals.


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