scholarly journals Conversion of a sequential inductively coupled plasma emission spectrometer into a multichannel simultaneous system using a photodiode array detector

1998 ◽  
Vol 20 (3) ◽  
pp. 69-75 ◽  
Author(s):  
Maria Fernanda Pimentel ◽  
Mário César Ugulino Araújo ◽  
Benício de Barros Neto ◽  
Célio Pasquini

A monochannel plasma emission spectrometer was converted to a multichannel instrument by the introduction of a detection system based on an array of 1024 photodiodes and a low-resolution dispersion device. The new, relatively inexpensive equipment, features both the high speed typical of simultaneous instruments and the versatility of scanning systems. This paper reports on an evaluation of the modified equipment for quantitative analysis with the simultaneous determination of Al, Mn, Mg, Ca, Fe and Cu in a natural water matrix. An average relative prediction error of 2.4% was found which is the same as the error obtained with the conventional analytical method. Data acquisition with the modified instrument is up to 40 times faster.

1992 ◽  
Vol 46 (6) ◽  
pp. 1025-1031 ◽  
Author(s):  
Wing-Tat Chan ◽  
X. L. Mao ◽  
Richard E. Russo

Nanosecond and picosecond pulsed laser ablated materials from Bi-Sr-Ca-Cu-O superconducting targets are monitored by inductively coupled plasma-atomic emission spectrometry with a photodiode array detector. Differential vaporization was observed; elements of the lower-melting-point oxides (Bi2O3, and CuO) are enriched in the vapor phase, indicating a thermal vaporization mechanism. Melted droplets observed with SEM and enriched Ca and Sr content in the ablation crater measured with EDX support the hypothesis. A steady-state mass ablation composition after prolonged laser sampling is also observed; the ratios of intensity for Bi, Ca, and Sr to Cu are constant for power density 0.1 to 3.0 GW/cm2.


2017 ◽  
Vol 100 (3) ◽  
pp. 796-803 ◽  
Author(s):  
Gagan Jyot ◽  
Balwinder Singh

Abstract An easy and simple analytical method was standardized and validated for the estimation of residues of thiamethoxam and its metabolites in cotton. The samples were extracted with acetonitrile, water, and methanol; diluted with brine solution;partitioned into dichloromethane and ethyl acetate; dried over anhydrous sodium sulfate; and cleaned up by glass column chromatography. Final clear extracts were concentrated under vacuum and reconstituted into HPLC grade acetonitrile, and residues were estimated using an HPLC instrument equipped with a C18 column and photodiode array detector system. Acetonitrile–1% formic acid in HPLC grade water (30 + 70) was used as mobile phase at 0.2 mL/min. Consistent recoveries ranging from 82 to 97% for thiamethoxam and its metabolites were observed when samples were spiked at 0.05–1.0 mg/kg levels. The LOQ of the method was determined to be 0.05mg/kg. The analytical method was validated in terms of the selectivity, linearity, precision, and accuracy of the detection system.


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