Kinetic Control by Chemical Step at an Adsorption-Blocked Electrode Surface

1965 ◽  
Vol 37 (13) ◽  
pp. 1638-1643 ◽  
Author(s):  
Mutsuo. Kodama ◽  
Royce W. Murray
Keyword(s):  
Electrode Surface ◽  
Kinetic Control ◽  
Blocked Electrode

Kinetics of compact layer formation and growth of 1,10-phenanthroline at the electrode surface

1990 ◽  
Vol 87 ◽  
pp. 1597-1607 ◽  
Author(s):  
L Benedetti ◽  
M Borsari ◽  
C Fontanesi ◽  
G Battistuzzi Gavioli
Keyword(s):  
Electrode Surface ◽  
Layer Formation ◽  
Compact Layer ◽  
Kinetics Of

A Photo-ionization VOCs Sensor Developed the Resistance to Contamination of Electrode Surface

2011 ◽  
Vol 131 (2) ◽  
pp. 88-89
Author(s):  
Yasuyuki Hirano ◽  
Elito Kazawa ◽  
Yoshiaki Haramoto ◽  
Hiromichi Yoshida
Keyword(s):  
Electrode Surface ◽  
Photo Ionization

Bio-Inspired Submicron Electrodes

2003 ◽  
Vol 775 ◽  
Author(s):  
Ivan Stanish ◽  
Daniel A. Lowy ◽  
Alok Singh
Keyword(s):  
Electrode Surface ◽  
Structural Integrity ◽  
Electron Flow ◽  
Charge Storage ◽  
Electroactive Material ◽  
Electron Coupling ◽  
Strong Potential ◽  
Electrical Potentials ◽  
Submicron Scale ◽  
Potential Gradients

AbstractImmobilized polymerized electroactive vesicles (IPEVs) are submicron biocapsules capable of storing charge in confined environments and chemisorbing on surfaces. Methods to immobilize stable submicron sized electroactive vesicles and the means to measure electroactivity of IPEVs at nanolevels have been demonstrated. IPEVs can withstand steep potential gradients applied across their membrane, maintain their structural integrity against surfaces poised at high/low electrical potentials, retain electroactive material over several days, and reversibly mediate (within the membrane) electron flow between the electrode surface and vesicle interior. IPEVs have strong potential to be used for charge storage and electron coupling applications that operate on the submicron scale and smaller.

In Operando Detection of the Physical Properties Change of the Interfacial Electrolyte during Li-Metal Electrode Reaction by Atomic Force Microscopy

2020 ◽  
Author(s):  
Mitsunori Kitta
Keyword(s):  
Atomic Force Microscopy ◽  
Energy Dissipation ◽  
Physical Properties ◽  
Electrode Surface ◽  
Electrode Reaction ◽  
Metal Electrode ◽  
Ion Concentration ◽  
Force Microscopy ◽  
Atomic Force ◽  
Discharge Reaction

This manuscript propose the operando detection technique of the physical properties change of electrolyte during Li-metal battery operation.The physical properties of electrolyte solution such as viscosity (η) and mass densities (ρ) highly affect the feature of electrochemical Li-metal deposition on the Li-metal electrode surface. Therefore, the operando technique for detection these properties change near the electrode surface is highly needed to investigate the true reaction of Li-metal electrode. Here, this study proved that one of the atomic force microscopy based analysis, energy dissipation analysis of cantilever during force curve motion, was really promising for the direct investigation of that. The solution drag of electrolyte, which is controlled by the physical properties, is directly concern the energy dissipation of cantilever motion. In the experiment, increasing the energy dissipation was really observed during the Li-metal dissolution (discharge) reaction, understanding as the increment of η and ρ of electrolyte via increasing of Li-ion concentration. Further, the dissipation energy change was well synchronized to the charge-discharge reaction of Li-metal electrode.This study is the first report for direct observation of the physical properties change of electrolyte on Li-metal electrode reaction, and proposed technique should be widely interesting to the basic interfacial electrochemistry, fundamental researches of solid-liquid interface, as well as the battery researches.

Titration of sulphates and lead using lead ion selective electrode

1981 ◽  
Vol 46 (2) ◽  
pp. 368-376 ◽  
Author(s):  
Josef Veselý
Keyword(s):  
Ionic Strength ◽  
Electrode Surface ◽  
Salt Content ◽  
Ion Selective Electrode ◽  
Lead Ion ◽  
Selective Electrode ◽  
Limit Of Determination ◽  
Total Salt Content ◽  
Automatic Titration

Titration of sulphates with lead perchlorate employing lead ion selective electrode indication was studied using additions of various organic solvents at different pH' and ionic strength values. As the optimum emerged systems with 60-70% 1,4-dioxane, pH' 5.3-5.6. After dehydration with sodium hydroxide, dioxane must be freed from the electrode surface-oxidizing impurities by their reduction with sodium metal and subsequent distillation. The method was applied to determination of sulphates in mountain spring waters. Units of ppm can be determined; the limit of determination, however, depends considerably on the content of dioxane, total salt content in the sample, and speed of the semi-automatic titration. Lead can be determined with EDTA in concentrations down to c(Pb2+) = 5 . 10-6 mol l-1.

Galvanostatic dissolution of mercury from the surface of glassy carbon into thiocyanate solution

1980 ◽  
Vol 45 (1) ◽  
pp. 169-178 ◽  
Author(s):  
František Opekar ◽  
Karel Holub
Keyword(s):  
Glassy Carbon ◽  
Electrode Surface ◽  
High Current Density ◽  
High Current ◽  
Nernst Equation ◽  
Potential Oscillations ◽  
Thiocyanate Solution ◽  
Theoretical Assumptions ◽  
Solution Proceeds ◽  
Dissolution Current

The galvanostatic dissolution of mercury from the surface of glassy carbon into a thiocyanate solution proceeds in accord with theoretical assumptions, as manifested by the constant product of the dissolution current and transition time. Under certain relations between the amount of oxidised mercury and concentration of thiocyanate at the electrode surface, however, a small part of the mercury dissolves at more positive potentials than correspond to the Nernst equation. This dissolution can be accompanied by potential oscillations. The anomalous behaviour is elucidated by the concept about coverage of a certain part of mercury with a film of sparingly soluble compounds of SCN- ions with mercury. This film is formed at the end of the galvanostatic dissolution on certain places of the electrode surface covered with mercury droplets, where SCN- ions are much exhausted as a result of a high current density.

Electroreduction of Cr(VI) from solutions of bifunctional alcohols

1989 ◽  
Vol 54 (10) ◽  
pp. 2638-2643
Author(s):  
David I. Balanchivadze ◽  
Tamara R. Chelidze ◽  
Jondo J. Japaridze
Keyword(s):  
Activation Energy ◽  
Ethylene Glycol ◽  
Electrode Surface ◽  
Frequency Factor ◽  
Limiting Current ◽  
Factor Log ◽  
Standard Rate ◽  
Standard Rate Constant ◽  
Chromate Ion ◽  
Activation Energy Of Diffusion

The effect of bifunctional alcohols ethylene glycol (EG) and 1,2-propylene glycol (1,2 PG) on the kinetic parameters for the irreversible chromate ion reduction were investigated by polarographic and coulometric methods of analysis. The electroreduction of chromate ion in neutral bifunctional alcohol solutions proceeds according to the scheme: Cr(VI)–Cr(III)–Cr(II) and the values of the standard rate constant k*0 decrease in the order H2O > EG > 1,2 PG. The values of real activation energy, Q, activation energy of diffusion, QD, and frequency factor log A° have been calculated. The obtained values of QD as well as Q proved the diffusion nature of limiting current. The values of the frequency factor log A° decrease in the order H2O > EG > 1,2 PG, which points to a less favourable orientation of the electroactive ions at the electrode surface in glycols.

Trypsin entrapped within liposomes. Partition of a low-molecular-mass substrate as the main factor in kinetic control of hydrolysis

1991 ◽  
Vol 56 (3) ◽  
pp. 712-717 ◽  
Author(s):  
Jana Formelová ◽  
Albert Breier ◽  
Peter Gemeiner ◽  
Lubica Kurillová
Keyword(s):  
Molecular Mass ◽  
Egg Yolk ◽  
Kinetic Control ◽  
Hydrolysis Kinetics ◽  
Liposomal Membrane ◽  
Kinetics Of ◽  
Main Factor

Trypsin has been entrapped within liposomes prepared from egg yolk phospholipides by the method of controlled dialysis, and the hydrolysis kinetics of Nα-benzoyl-DL-arginine p-nitroaniline catalyzed by the liposome-entrapped trypsin has been studied by monitoring the flux of substrate and product across the liposomal membrane. The partitioning of the substrate and product between liposomal and extraliposomal environment has been found to represent the main factor in the kinetic control of the hydrolysis.

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