Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES): a Powerful Analytical Technique for Elemental Analysis

Author(s):  
Sharib Raza Khan ◽  
Babita Sharma ◽  
Pooja A. Chawla ◽  
Rohit Bhatia
1978 ◽  
Vol 32 (4) ◽  
pp. 366-371 ◽  
Author(s):  
David L. Windsor ◽  
M. Bonner Denton

The application of inductively coupled plasma optical emission spectrometry (ICP-OES) to the elemental analysis of organic compounds is evaluated successfully for seven nonmetallic elements. A comparison of this method with previously reported microwave techniques shows that, while both methods are sensitive (detection limits in the low nanogram region), ICP-OES has fewer complications and appears to be less prone to interferences than the analogous microwave techniques. The results of these studies suggest that ICP-OES should be applicable to the simultaneous multielement analysis of the gaseous effluents from a gas chromatograph.


2014 ◽  
Vol 97 (3) ◽  
pp. 687-699 ◽  
Author(s):  
James M Bartos ◽  
Barton L Boggs ◽  
J Harold Falls ◽  
Sanford A Siegel

Abstract A two-part single-laboratory validation study was conducted for determination of the P and K content in commercial fertilizer materials by inductively coupled plasma-optical emission spectrometry (ICP- OES). While several methods exist for determination of P and K in fertilizer products, the main focus of this study was on ICP-OES determination, which offers several unique advantages. Fertilizer samples with consensus P and K values from the Magruder and Association of Fertilizer and Phosphate Chemists (AFPC) check sample programs were selected for this study. Validation materials ranging from 4.4 to 52.4% P2O5 (1.7 to 22.7% P) and 3 to 62% K2O (2.5 to 51.5% K) were utilized. Because all P and K compounds contained in fertilizer materials are not "available" for plants to use, this study was conducted in two parts. Part A focused on ammonium citrate–disodium EDTA as the extraction solvent, as it estimates the pool of fertilizer P and K that is considered available to plants. Part B focused on hydrochloric acid as the digestion solvent, as it estimates the total P and K content of the fertilizer product. Selectivity studies indicated that this method can have a high bias for fertilizer products containing sources of phosphite or organic P compared to gravimetric or colorimetric methods that measure just orthophosphate. Provided the analytical challenges outlined in this study are addressed, this method offers the potential for a quick, accurate, and safe alternative for determining the P and K content of commercial inorganic fertilizer materials.


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