scholarly journals Voltammetric Determination of Pd(II) Using 5-Hydroxyimino-4-imino-1,3-thiazolidin-2-one after a Thermal Activation of the Interaction

2021 ◽  
Vol 15 (3) ◽  
pp. 324-329
Author(s):  
Petro Rydchuk ◽  
◽  
Oksana Labyk ◽  
Lesya Oleksiv ◽  
Oleksandr Tymoshuk ◽  
...  
Keyword(s):  
Thermal Activation ◽  
Limit Of Detection ◽  
Supporting Electrolyte ◽  
Voltammetric Determination ◽  
Real Sample ◽  
Optimal Conditions ◽  
Voltammetric Method ◽  
The Real ◽  
Ph Range

The interaction of Pd(II) with 5-hydroxyimino-4-imino-1,3-thiazolidin-2-one (HITO) was investigated over the pH range of 1.0–10.0. Optimal conditions for the voltammetric determination of Pd(II) were established. A new voltammetric method of Pd(II) determination by the peak of complex using NaCl as a supporting electrolyte at pH 2.0 was developed with the limit of detection 2.0∙10-7 M. The study of the method’s selectivity was presented in the work. The correctness of the method was confirmed by the analysis of model solutions and the real sample (resistor SP5-35B).

scholarly journals Fast and Sensitive Voltammetric Method for the Determination of Rifampicin on Renewable Amalgam Film Electrode

Sensors ◽  
2021 ◽  
Vol 21 (17) ◽  
pp. 5792
Author(s):  
Marek Szlósarczyk ◽  
Robert Piech ◽  
Anna Milc ◽  
Urszula Hubicka
Keyword(s):  
Supporting Electrolyte ◽  
Pulse Height ◽  
Pharmaceutical Formulations ◽  
Pharmaceutical Products ◽  
Film Electrode ◽  
Optimal Conditions ◽  
Step Potential ◽  
Voltammetric Method ◽  
Deposition Step

In this work, a new sensitive voltammetric method for the determination of rifampicin without time-consuming preconcentration is presented. The objective was to develop a simple, fast and sensitive voltammetric procedure for the analysis of rifampicin in pharmaceutical products. The cyclic renewable mercury film silver-based electrode (Hg(Ag)FE) was applied as a working electrode for this purpose. The optimal conditions for the determination of rifampicin were defined, in terms of the composition of supporting electrolyte (including pH) and instrumental parameters (potential and time of deposition, step potential, pulse height). The method was validated resulting in a satisfactory linearity range of 0.4–250.0 µgmL−1; the limits of detection and quantification are 0.12 µgmL−1 and 0.4 µgmL−1, respectively; and the repeatability of the method expressed as RSD is 4.1% (n = 6) with a surface area of 10.9 mm2. The proposed method was successfully applied in the analysis of rifampicin in simple and composed pharmaceutical formulations.

scholarly journals Voltammetric Determination Of Pt(IV) Using 5-Hydroxyimino-4- Imino-1,3-Thiazolidine-2-One

2019 ◽  
Vol 14 (3) ◽  
pp. 130-139
Author(s):  
P.V. Rydchuk ◽  
O.S. Tymoshuk ◽  
L.V. Oleksiv ◽  
T.I. Chaban ◽  
V.S. Matiychuk
Keyword(s):  
Background Electrolyte ◽  
Organic Reagent ◽  
Voltammetric Determination ◽  
Real Sample ◽  
Optimal Conditions ◽  
Exhaust Gases ◽  
Model Solutions ◽  
Catalytic Hydrogen ◽  
Sensitive Method

5-Hydroxyimino-4-imino-1,3-thiazolidine-2-one has been suggested as a new organic reagent for the voltammetric determination of platinum. The optimal conditions of Pt(IV) voltammetric determination using 5-hydroxyimino-4- imino-1,3-thiazolidine-2-one on the peak of catalytic hydrogen currents have been determined: the background electrolyte is 0.3 M NaCl, pH of the solution is 2.0, 50-fold concentration excess of organic reagent. The sensitive method of Pt(IV) voltammetric determination was developed (LOD = 4.1·10-9 М). The range of determinable contents covers two concentration orders. The selectivity of the developed methods have been studied towards concomitant metals ions. The accuracy of the developed method has been tested on model solutions using “added-found” method. The method has been approved during the analysis of a real sample, viz. the catalyst for oxidation of exhaust gases of the car “Chevrolet”.

scholarly journals Voltammetric determination of imidacloprid and thiamethoxam

2005 ◽  
Vol 70 (5) ◽  
pp. 735-743 ◽  
Author(s):  
Valeria Guzsvány ◽  
Ferenc Gaál ◽  
Luka Bjelica ◽  
Silvija Ökrész
Keyword(s):  
Glassy Carbon ◽  
Electrode Surface ◽  
Limit Of Detection ◽  
Voltammetric Determination ◽  
Polarization Mode ◽  
Voltammetric Method ◽  
Surface Pretreatment ◽  
Working Electrode ◽  
Limit Of Quantitation

A simple voltammetric method using a glassy carbon working electrode was developed for the determination of two members from the neonicotinoid group of insecticides: imidacloprid and thiamethoxam. The experiments showed that the voltammetric response depends on the mode of electrode surface pretreatment and the polarization mode. The response appeared to be linear in the range from 0.028 to 0.50 mg/cm3 for both analyses. The limit of detection was 0.0077 mg/cm3 for imidacloprid and 0.0085 mg/cm3 for thiamethoxam, the limit of quantitation was 0.026 mg/cm3 and 0.028 mg/cm3, respectively. The developed method was applied for the determination of these insecticides in potato samples sprayed with Confidor 200-SL or Actara 25-WG as well as commercial formulations of imidacloprid and thiamethoxam. A recovery trial was performed to assess the accuracy of the results, the recovery values being between 95?102 % for both of neonicotinoids.

Novel palladium(II) selective membrane electrode based on 4-[(5-mercapto-1,3,4-thiadiazol-2-ylimino)methyl]benzene-1,3-diol

2010 ◽  
Vol 75 (5) ◽  
pp. 563-575 ◽  
Author(s):  
Moslem Mohammadi ◽  
Mehdi Khodadadian ◽  
Mohammad K. Rofouei
Keyword(s):  
Limit Of Detection ◽  
Membrane Electrode ◽  
Aqueous Samples ◽  
Selective Determination ◽  
Poly Vinyl Chloride ◽  
Selective Membrane ◽  
Ph Range ◽  
Palladium Content ◽  
Methyl Benzene

A plasticized poly(vinyl chloride) membrane electrode based on 4-[(5-mercapto-1,3,4-thiadiazol-2-ylimino)methyl]benzene-1,3-diol (L) for highly selective determination of palladium(II) (in PdCl42– form) is developed. The electrode showed a good Nernstian response (29.6 ± 0.4 mV per decade) over a wide concentration range (3.1 × 10–7 to 1.0 × 10–2 mol l–1). The limit of detection was 1.5 × 10–7 mol l–1. The electrode has a response time of about 20 s, and it can be used for at least 2 months without observing any considerable deviation from Nernstian response. The proposed electrode could be used in the pH range of 2.5–5.5. The practical utility of the electrode has been demonstrated by its use for the estimation of palladium content in aqueous samples.

scholarly journals Surface-Enhanced Oxidation and Determination of Isothipendyl Hydrochloride at an Electrochemical Sensing Film Constructed by Multiwalled Carbon Nanotubes

2012 ◽  
Vol 2012 ◽  
pp. 1-6
Author(s):  
S. N. Prashanth ◽  
Shankara S. Kalanur ◽  
Nagappa L. Teradal ◽  
J. Seetharamappa
Keyword(s):  
Limit Of Detection ◽  
Biological Fluids ◽  
Differential Pulse ◽  
Electrochemical Sensing ◽  
Good Precision ◽  
Multiwalled Carbon ◽  
Limit Of Quantification ◽  
Surface Enhanced ◽  
Ph Range

The electrochemical behavior of isothipendyl hydrochloride (IPH) was investigated at bare and multiwalled-carbon-nanotube modified glassy carbon electrode (MWCNT-GCE). IPH (55 μM) showed two oxidation peaks in Britton-Robinson (BR) buffer of pH 7.0. The oxidation process of IPH was observed to be irreversible over the pH range of 2.5–9.0. The influence of pH, scan rate, and concentration of the drug on anodic peak was studied. A differential pulse voltammetric method with good precision and accuracy was developed for the determination of IPH in pure and biological fluids. The peak current was found to be linearly dependent on the concentration of IPH in the range of 1.25–55 μM. The values of limit of detection and limit of quantification were noticed to be 0.284 and 0.949 μM, respectively.

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.

scholarly journals Microfabricated Au-Film Sensors for the Voltammetric Determination of Hg(II)

Proceedings ◽  
2018 ◽  
Vol 2 (13) ◽  
pp. 1518
Author(s):  
Maria Tsetsoni ◽  
Eleni Roditi ◽  
Christos Kokkinos ◽  
Anastasios Economou
Keyword(s):  
Electrode Surface ◽  
Limit Of Detection ◽  
Anodic Stripping Voltammetry ◽  
Stripping Voltammetry ◽  
Voltammetric Determination ◽  
Film Sensor ◽  
Au Film ◽  
Working Electrode ◽  
Anodic Stripping

In this work, a microfabricated Au-film sensor was designed and fabricated for thevoltammmetric determination of Hg(II). The electrode was fabricated on a silicon chip with astandard microengineering approach utilizing photolithography for patterning the electrode shapeand sputtering for deposition of thin Cr and Au films on the surface of the sensors. The sensorswere used for the determination of trace Hg(II) with anodic stripping voltammetry (ASV): initiallyHg(II) in the sample was accumulated on the Au working electrode surface by reduction andformation of an Au(Hg) amalgam followed by oxidation of the preconcentrated metallic Hg using asquare wave voltammetric scan. The limit of detection was 1.5μgL−1 and the coefficient of variationof 10 consecutive measurements was 3.1%.

scholarly journals A novel catalytic adsorptive stripping voltammetric method for the determination of germanium ultratraces in the presence of chloranilic acid and the V(IV)·HEDTA complex

2020 ◽  
Vol 24 (11-12) ◽  
pp. 2891-2899
Author(s):  
Jerzy Zarębski ◽  
Andrzej Bobrowski ◽  
Agnieszka Królicka ◽  
Julia Gonciarczyk ◽  
Vasiliki Manolopoulou ◽  
...  
Keyword(s):  
Limit Of Detection ◽  
Electrolyte Composition ◽  
Hanging Mercury Drop Electrode ◽  
Film Electrode ◽  
Optimal Conditions ◽  
Subsequent Reduction ◽  
Adsorbed State ◽  
Chloranilic Acid ◽  
Effects Of Ph

Abstract A novel, sensitive catalytic adsorptive stripping voltammetric procedure which can be used to determine trace amounts of germanium is described. The method is based on the interfacial accumulation of the complex formed by Ge(IV) and the product of the reduction of chloranilic acid on the hanging mercury drop electrode or the renewable silver amalgam film electrode, and its subsequent reduction from the adsorbed state followed by the catalytic action of the V(IV)·HEDTA complex. The presence of V(IV)·HEDTA greatly enhances the adsorptive stripping response of Ge. The reduction of the Ge(IV) in the presence of chloranilic acid and V(IV)·HEDTA was investigated in detail and the effects of pH, electrolyte composition, and instrumental parameters were studied. Under optimal conditions, the catalytic peak current of germanium exhibited good linearity for Ge(IV) concentrations in the range of 0.75–60 nM (for 60 s of accumulation at −0.1 V, r2 = 0.995) and a low limit of detection (LOD = 0.085 nM). The procedure was successfully applied to determine Ge in water samples.

scholarly journals Glassy carbon and boron doped glassy carbon electrodes for voltammetric determination of linuron herbicide in the selected samples

2012 ◽  
Vol 10 (4) ◽  
pp. 1271-1279 ◽  
Author(s):  
Jelena Đorđević ◽  
Ana Kalijadis ◽  
Ksenija Kumrić ◽  
Zoran Jovanović ◽  
Zoran Laušević ◽  
...  
Keyword(s):  
Glassy Carbon Electrode ◽  
Glassy Carbon ◽  
Supporting Electrolyte ◽  
Electrochemical Determination ◽  
Temperature Treatment ◽  
Voltammetric Determination ◽  
Carbon Electrode ◽  
Glassy Carbon Electrodes ◽  
Boron Doped

AbstractIn this study the application of home-made unmodified (GC) and bulk modified boron doped glassy carbon (GCB) electrodes for the voltammetric determination of the linuron was investigated. The electrodes were synthesized with a moderate temperature treatment (1000°C). Obtained results were compared with the electrochemical determination of the linuron using a commercial glassy carbon electrode (GC-Metrohm). The peak potential (E p ) of linuron oxidation in 0.1 mol dm−3 H2SO4 as electrolyte was similar for all applied electrodes: 1.31, 1.34 and 1.28 V for GCB, GC and GC-Metrohm electrodes, respectively. Potential of linuron oxidation and current density depend on the pH of supporting electrolyte. Applying GCB and GC-Metrohm electrodes the most intensive electrochemical response for linuron was obtained in strongly acidic solution (0.1 mol dm−3 H2SO4). Applying the boron doped glassy carbon electrode the broadest linear range (0.005–0.1 µmol cm−3) for the linuron determination was obtained. The results of voltammetric determination of the linuron in spiked water samples showed good correlation between added and found amounts of linuron and also are in good agreement with the results obtained by HPLC-UV method. This appears to be the first application of a boron doped glassy carbon electrode for voltammetric determination of the environmental important compounds.

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