Field-deployable method for iron analysis using a simple preconcentration procedure and a 3D portable spectrophotometric system

2021 ◽  
pp. 106774
Author(s):  
M.A. Vargas-Muñoz ◽  
Kaewta Danchana ◽  
Víctor Cerdà ◽  
Edwin Palacio
2018 ◽  
Author(s):  
Hattie Ring ◽  
Zhe Gao ◽  
Nathan D. Klein ◽  
Michael Garwood ◽  
John C. Bischof ◽  
...  

The Ferrozinen assay is applied as an accurate and rapid method to quantify the iron content of iron oxide nanoparticles (IONPs) and can be used in biological matrices. The addition of ascorbic aqcid accelerates the digestion process and can penetrate an IONP core within a mesoporous and solid silica shell. This new digestion protocol avoids the need for hydrofluoric acid to digest the surrounding silica shell and provides and accessible alternative to inductively coupled plasma methods. With the updated digestion protocol, the quantitative range of the Ferrozine assay is 1 - 14 ppm. <br>


2018 ◽  
Author(s):  
Hattie Ring ◽  
Zhe Gao ◽  
Nathan D. Klein ◽  
Michael Garwood ◽  
John C. Bischof ◽  
...  

The Ferrozinen assay is applied as an accurate and rapid method to quantify the iron content of iron oxide nanoparticles (IONPs) and can be used in biological matrices. The addition of ascorbic aqcid accelerates the digestion process and can penetrate an IONP core within a mesoporous and solid silica shell. This new digestion protocol avoids the need for hydrofluoric acid to digest the surrounding silica shell and provides and accessible alternative to inductively coupled plasma methods. With the updated digestion protocol, the quantitative range of the Ferrozine assay is 1 - 14 ppm. <br>


1992 ◽  
Vol 57 (7) ◽  
pp. 1393-1404 ◽  
Author(s):  
Ladislav Svoboda ◽  
Jan Uhlíř ◽  
Zdeněk Uhlíř

The properties of Ostsorb DETA, a selective ion exchanger based on modified bead cellulose with chemically bonded diethylenetriamine functional groups, were studied, and its applicability to the preconcentration of trace amounts of lead from aqueous solutions was verified. The conditions of the preconcentration procedure in the column and batch modes were optimized for this purpose. The results obtained were applied to the determination of lead in phosphoric acid.


2010 ◽  
Vol 48 (2) ◽  
pp. 482-489 ◽  
Author(s):  
A. Shokrolahi ◽  
M. Ghaedi ◽  
R. Shabani ◽  
M. Montazerozohori ◽  
F. Chehreh ◽  
...  

2007 ◽  
Vol 443 (1-2) ◽  
pp. 16-24 ◽  
Author(s):  
John C. Ulicny ◽  
Michael P. Balogh ◽  
Noel M. Potter ◽  
Richard A. Waldo

1897 ◽  
Vol 19 (2) ◽  
pp. 177-178
Author(s):  
Edward K. Landis
Keyword(s):  

2002 ◽  
Vol 78 (4) ◽  
pp. 505-510 ◽  
Author(s):  
Ginevra Lombardi-Boccia ◽  
Beatriz Martı́nez-Domı́nguez ◽  
Altero Aguzzi ◽  
Francisco Rincón-León
Keyword(s):  
Red Meat ◽  

2011 ◽  
Vol 94 (4) ◽  
pp. 1304-1309 ◽  
Author(s):  
Regina Terumi Yamaki ◽  
Luana Sena Nunes ◽  
Hygor Rodrigues De Oliveira ◽  
André S Araújo ◽  
Marcos Almeida Bezerra ◽  
...  

Abstract The synthesis and characterization of the reagent 2-(5-bromothiazolylazo)-4-chlorophenol and its application in the development of a preconcentration procedure for cobalt determination using flame atomic absorption spectrometry after cloud point extraction is presented. This procedure is based on cobalt complexing and entrapment of the metal chelates into micelles of a surfactant-rich phase of Triton X-114. The preconcentration procedure was optimized by using a response surface methodology through the application of the Box-Behnken matrix. Under optimum conditions, the procedure determined the presence of cobalt with an LOD of 2.8 μg/L and LOQ of 9.3 μg/L. The enrichment factor obtained was 25. The precision was evaluated as the RSD, which was 5.5% for 10 μg/L cobalt and 6.9% for 30 μg/L. The accuracy of the procedure was assessed by comparing the results with those found using inductively coupled plasma-optical emission spectrometry. After validation, the procedure was applied to the determination of cobalt in pharmaceutical preparation samples containing cobalamin (vitamin B12).


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