scholarly journals Interfacing a microchip-based capillary electrophoresis system with a microwave induced plasma spectrometry for copper speciation

2011 ◽  
Vol 9 (5) ◽  
pp. 896-903 ◽  
Author(s):  
Henryk Matusiewicz ◽  
Mariusz Ślachciński

AbstractA microchip-based capillary electrophoresis (µCE) system was interfaced with a microwave induced plasma optical emission spectrometry (MIP-OES) to provide copper species separation capabilities. This system uses an extremely low flow demountable direct injection high efficiency nebulizer (D-DIHEN) sited directly at the liquid exit of the chip. A supplementary flow of buffer solution at the channel exit was used to improve nebulization efficiency. A small evaporation chamber has been incorporated into the interface in order to prevent the losses associated with traditional spray chambers, allowing the entire aerosol sample to enter the plasma. Syringe pumps were used to manipulate the flow rate and flow direction of the sample, buffer, and supplementary buffer solution. Sample volumes of 25 nL can be analyzed. With application of an electric field up to 500 V cm−1, species such as Cu(II) and Cu(EDTA)2− were separated in acidic solution within 90 s using a 26 mm long separation channel etched in a glass base. Resolution of the Cu(II) and Cu(EDTA)2− peaks was 1.1 using the chip-based µCE-MIP-OES system.

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.


1985 ◽  
Vol 39 (6) ◽  
pp. 935-942 ◽  
Author(s):  
Mark L. Bruce ◽  
John M. Workman ◽  
Joseph A. Caruso ◽  
Daniel J. Lahti

The use of the microwave-induced plasma with a new low-flow plasma centering torch has been evaluated. Data were collected through a computer-controlled, background-correcting polychromator system with two versions of the newly developed laminar flow torch. It showed sensitivities slightly better than the 0.5-mm-i.d. capillary quartz open tube torch. Detection limits were between 8 and 60 pg/s for carbon, hydrogen, bromine, chlorine, and fluorine—a considerably improved performance over the tangential flow torch. Torch lifetime and plasma stability are comparable to or better than the high-flow tangential flow torch with three-hour and three-day RSDs of 2% and 6%. Centered plasmas may be sustained with flow rates as low as 5 mL/min.


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.


Author(s):  
Alicia Mollo ◽  
Alexandra Sixto ◽  
Florencia Cora Jofre ◽  
Mariela Pistón ◽  
Marianela Savio

A hydride generation nitrogen microwave induced plasma optical emission spectrometry (HG – MIP OES) system was developed for lead determination. Plumbane chemical generation was performed using 0.045 mol L-1 K3Fe(CN)6...


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