scholarly journals Sequential determination of benserazide and levodopa by voltammetric method using chloranil as a mediator

2010 ◽  
Vol 21 (8) ◽  
pp. 1572-1580 ◽  
Author(s):  
Ali A. Ensafi ◽  
A. Arabzadeh ◽  
H. Karimi-Maleh
Keyword(s):  
Voltammetric Method ◽  
Sequential Determination

scholarly journals Sequential determination of chromium(VI) and chromium(III) by potentiometric flow-injection method.

2000 ◽  
Vol 49 (1) ◽  
pp. 59-64 ◽  
Author(s):  
Hiroki OHURA ◽  
Toshihiko IMATO ◽  
Ikuo MATSUO ◽  
Sumio YAMASAKI
Keyword(s):  
Flow Injection ◽  
Injection Method ◽  
Sequential Determination ◽  
Chromium Vi

scholarly journals Flow injection analysis of water. Part 1: Automatic preconcentration determination of sulphate, ammonia and iron(II)/iron(III)

1993 ◽  
Vol 15 (4) ◽  
pp. 141-146 ◽  
Author(s):  
J. S. Cosano ◽  
M. D. Luque de Castro ◽  
M. Valcárcel
Keyword(s):  
Flow Injection ◽  
Good Reproducibility ◽  
Chemical Systems ◽  
Sequential Determination ◽  
On Line ◽  
Exchange Material ◽  
Iron Complexation ◽  
Simple Flow ◽  
Ammonia Formation

This paper describes a simple flow-injection (FI) manifold for the determination of a variety of species in industrial water. The chemical systems involved in the determination of ammonia (formation of Indophenol Blue), sulfate (precipitation with Ba(II)), and iron (complexation with 1,10-phenanthroline with the help of a prior redox reaction for speciation) were selected so that a common manifold could be used for the sequential determination of batches of each analyte. A microcolumn of a suitable ion exchange material was used for on-line preconcentration of each analyte prior to injection; linear ranges for the determination of the analytes at the ng/ml levels were obtained with good reproducibility. The manifold and methods are ready for full automation.

Interference by Tin in AOAC Dry-Ash Voltammetric Method for Determination of Lead and Cadmium in Canned Foods

1988 ◽  
Vol 71 (4) ◽  
pp. 857-859
Author(s):  
Walter Holak ◽  
John J Specchio
Keyword(s):  
Tartaric Acid ◽  
False Positive ◽  
Supporting Electrolyte ◽  
Canned Food ◽  
Voltammetric Method ◽  
Lead And Cadmium ◽  
Anodic Stripping ◽  
Canned Foods ◽  
Positive Results

Abstract When lead and cadmium were determined in samples of canned food by the AOAC anodic stripping voltammetric method, an interference was observed which was believed to be tin(IV). This interference could cause false positive results for lead and cadmium. The electroactivity of tin(IV) was suppressed by increasing the concentration of tartaric acid in the supporting electrolyte from 0.005M to 0.1M after mixing with an equal volume of sample solution.

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