Search results for "Polarography"

Simultaneous determination of 4-nitroanisole, 4-nitrophenol, and 4-nitrocatechol by phase-sensitive ac polarography.

1977

Abstract Phase‐sensitive ac polarography was applied to the simultaneous quantitative determination of 4‐nitroanisole, 4‐nitrophenol and 4‐nitrocatechol in alkaline solutions. Certain experimental precautions are necessary to determine each compound in the presence of the other two. Thus, 4‐nitrocatechol is determined indirectly by forming a yellow ratio chelate with cupric ions, whereas 4‐nitroanisole is determined directly by the reduction waves of the nitro group. For the determination of 4‐nitrophenol, the interference by the simultaneously present 4‐nitrocatechol must be eliminated by masking it by the addition of magnesium ions. The method described permits a qualitative and quantitat…

Electrochemical and spectroscopic investigations of selected N -heteroalkylaminomethylenebisphosphonic acids with Pb(II) ions

2016

Abstract The coordination properties of aminomethylenebisphosphonic acids towards various metal ions have been exploited during the last decade. These compounds are good chelators for biologically important metal ions, such as Cu(II), Fe(II), Zn(II), Ca(II), and Mg(II), as well as a toxic ion (i.e., Cd(II)). In this study, the interactions of five aminomethylenebisphosphonates with N-substituted heteroalkyl moieties (L1, L2 and L3) and their N-pyridyl (L4) and N-benzylpiperazine (L5) derivatives with Pb(II) ions were investigated. A wide range of analytical methods were employed, including potentiometry, pulse polarography (DPP), nuclear magnetic resonance (NMR) spectroscopy and electrospra…

Calculation of voltammetric peaks by the transformed Heyrovsky-Ilkovi? equation

1990

Calculating real polarographic or voltammetric peaks is rather difficult. A new possibility to compute such peaks is the use of the transformed Heyrovsky-Ilkovic equation. The calculation allows to simulate polarograms or voltammograms by computer. Furthermore, it is possible to smooth voltammetric peaks without loss of peak height or separation of overlapping peaks.

Electrochemical study of intramolecular charge transfer complexes derived from 1,4-naphthoquinone Part 1. Electroreduction

1995

Abstract Electrochemical investigations (polarography, cyclic voltammetry, rotating ring-disk electrode voltammetry) of intramolecular charge transfer complexes (AC) derived from 1,4-naphthoquinone were performed in acetonitrile. It is concluded that in the first one-electron stage of its electrochemical reduction the AC is in a complexed form. At the same time the amino moiety, which shows a marked inductive (−I) effect, acts as an electron donor in the donor-acceptor (D-A) interaction. Facilitation of the reduction of the quinone part by the aryl amine residue is compensated by the D-A interaction, which makes the electroreduction more difficult. By using ultramicroelectrodes it was shown…

Ascorbic Acid Stability in Ground Asparagus Samples and in Oxalic Acid Extracts

1995

To establish the storage conditions for asparagus preparation before ascorbic acid determination, samples were ground, the mass was divided into three aliquots that were, respectively, stored at 4°C, – 18°C, or extracted with 1% oxalic acid. The extract was further split into aliquots and stored at 25°, 4°, –18° and -75°C. Ascorbic acid content was measured at different times of storage by a polarographic method. The rate of degradation increased with storage temperature; the degradation rate was higher in ground samples than in extracts; no significant changes in ascorbic acid content were observed in extracts stored for 7 days at -18° or for 90 days at -75°C.

Constant-potential electrolysis: determination of diffusion coefficients of thallium by using a hanging mercury drop electrode.

1976

The technique of constant-potential electrolysis at a stationary spherical electrode (hanging mercury drop) was investigated for the determination of the diffusion coefficient of Tl(I) in sodium citrate-sodium hydroxide medium and of Tl in mercury. Current-time curves, at controlled potential, were obtained, covering periods from 1 to 25 sec after the start of the electrolysis. The influence of applied potential, time of electrolysis, convection and shielding of the electrode was studied.

Polarographic determination of glycine with a dropping copper amalgam electrode

1975

The anodic oxidation of a dropping copper amalgam electrode in presence of dilute solutions of glycine in 0.50 M NaClO4 has been studied. An anodic wave at −0.28V (SCE) is observed, yielded by diffusion of glycinate anion in the solution towards the electrode surface. The wave-heights increase with the glycinate concentration (function of glycine concentration and pH value) until the anodic oxidation is controlled by the metal diffusion into mercury. The effect of pH is interpreted by attributing it to the depolarizer effects at glycinate anion even though the zwitterion is present in much larger concentrations. The applicability of anodic oxidation of a dropping copper amalgam electrode in…

Interactions of N-heteroalkylaminomethylenebisphosphonic acids with Cd(II) ions: Electrochemical and spectroscopic investigations

2015

The aminomethylenebisphosphonates are known to be excellent chelators for many metal ions. In this work, the coordination properties of three different aminomethylenebisphosphonates with N-substituted heteroalkyl moieties (L1, L2 and L3) and their N-pyridyl derivative (L4) toward cadmium(II) ions are described. Due to their coordination abilities over a broad range of pH, the compounds of this group are good candidates for heavy metal detoxification. To determine the stability constants and the coordination mode of formed aminomethylenebisphosphonate-cadmium(II) complexes, four analytical methods were employed: potentiometry, pulse polarography (DPP), nuclear magnetic resonance spectroscopy…

Optimalization of the measuring technique in differential pulse polarography

1979

Differential Faradaic rectification polarography (DFRP)

1979

A new polarographic technique is described which is based on the determination of the Faradaic rectification effect. It will be of interest for analytical investigations and for electrode kinetics.