{"title":"The dependence of the double-layer charge on the platinum hydrogen electrode surface upon the potential","authors":"A. Frumkin, O. Petry, R. Marvet","doi":"10.1016/0022-0728(66)80128-6","DOIUrl":"10.1016/0022-0728(66)80128-6","url":null,"abstract":"","PeriodicalId":100778,"journal":{"name":"Journal of Electroanalytical Chemistry (1959)","volume":"12 5","pages":"Pages 504-515"},"PeriodicalIF":0.0,"publicationDate":"1966-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0022-0728(66)80128-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"53134329","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Diffusion-limited adsorption at spherical electrodes","authors":"Sidney L. Philips","doi":"10.1016/S0022-0728(96)80004-0","DOIUrl":"10.1016/S0022-0728(96)80004-0","url":null,"abstract":"<div><p>Both the diffusion coefficient and maximum surface concentration of a surfactant may be calculated from potentiostatic current.time curves obtained using spherical electrodes. The theoretically-derived relation between the maximum surface concentration, diffusion coefficient, and time at which maximum surface coverage is attained was tested by adding tetrabutylammonium ion to a solution of Cd(II) in 0.1 <em>M</em> perchloric acid.</p></div>","PeriodicalId":100778,"journal":{"name":"Journal of Electroanalytical Chemistry (1959)","volume":"12 4","pages":"Pages 294-299"},"PeriodicalIF":0.0,"publicationDate":"1966-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-0728(96)80004-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"55558244","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"New indicating system: twin electrodes, at zero current","authors":"E. Kirowa-Eisner, M. Ariel","doi":"10.1016/S0022-0728(96)80003-9","DOIUrl":"10.1016/S0022-0728(96)80003-9","url":null,"abstract":"<div><p>A mechanism for the new indicating system “twin electrodes, at zero current”, is proposed. In the titration cell, even with efficient stirring, regions of different liquid velocity arise, resulting in different thicknesses of the diffusion layers at the electrodes placed in the solution. This causes the electrodes to respond at different rates to changes in the solution during the titration. The potential change of each electrode is given by an “S”-shaped curve. Owing to the small difference in their rates of response, a sharp peak is obtained when their potential difference is recorded throughout the titration.</p></div>","PeriodicalId":100778,"journal":{"name":"Journal of Electroanalytical Chemistry (1959)","volume":"12 4","pages":"Pages 286-293"},"PeriodicalIF":0.0,"publicationDate":"1966-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-0728(96)80003-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"55558232","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Potential sweep chronoamperometry in dimethyl sulfoxide at the hanging mercury drop electrode","authors":"Jerry L. Jones, Herbert A. Fritsche Jr.","doi":"10.1016/S0022-0728(96)80007-6","DOIUrl":"10.1016/S0022-0728(96)80007-6","url":null,"abstract":"<div><p>Electroanalytical studies in dimethyl sulfoxide have been extended to the hanging mercury drop electrode. Potential sweep chronoamperometry was utilized with potentiostatic control of the working electrode. Several ions have been examined for diffusion control in this system by means of the Randies-Sevčik equation. Halfwave potentials of selected depolarizers and polarization limits of several carrier electrolytes have been measured.</p></div>","PeriodicalId":100778,"journal":{"name":"Journal of Electroanalytical Chemistry (1959)","volume":"12 4","pages":"Pages 334-340"},"PeriodicalIF":0.0,"publicationDate":"1966-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-0728(96)80007-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"55558294","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Determination polarographique de la nitrohydroxylamine","authors":"A. Cǎlusaru","doi":"10.1016/S0022-0728(96)80008-8","DOIUrl":"10.1016/S0022-0728(96)80008-8","url":null,"abstract":"<div><p>The catalytic wave of nitrohydroxylamine in the presence of divalent cobalt can be used for the polarographic determination of this substance. The catalytic waves are well-developed in the following supporting electrolyte solution: NH<sub>4</sub>Cl, 0.05 <em>M</em>; NH<sub>4</sub>OH, 0.025 <em>M</em>; gelatine, 0.02%. The cobalt concentration should be about 10<sup>−3</sup><em>M</em> for 10<sup>−4</sup>–10<sup>−5</sup><em>M</em> N<sub>2</sub>O<sub>3</sub><sup>2−</sup> and 2.5 × 10<sup>−5</sup><em>M</em> for 10<sup>−6</sup>–10<sup>−</sup><em>M</em>N<sub>2</sub>O<sub>3</sub><sup>2−</sup>. The other nitrogen-containing compounds present such as nitrate, nitrite, hyponitrite and nitramide have little or no effect on the catalytic wave of nitrohydroxylamine. Only hydroxylamine interferes with the determination.</p></div>","PeriodicalId":100778,"journal":{"name":"Journal of Electroanalytical Chemistry (1959)","volume":"12 4","pages":"Pages 341-346"},"PeriodicalIF":0.0,"publicationDate":"1966-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-0728(96)80008-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"55558305","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Chronoamperometrische untersuchung metallischer monoschichten","authors":"E. Schmidt, H.R. Gygax","doi":"10.1016/S0022-0728(96)80005-2","DOIUrl":"10.1016/S0022-0728(96)80005-2","url":null,"abstract":"<div><p>The reduction of metals from aqueous solutions on the surface of solid electrodes is performed chronoamperometrically to study monolayer effects using chamber type indicator electrodes. A metallic monolayer is defined as a layer of electrically neutral foreign metal atoms at the electrode-electrolyte interface, the deposit having the approximate thickness of one atomic diameter.</p><p>The shape of current-time curve depends upon the structure of the activity isotherm within the region of unsaturated (submonoatomic) surface coverage of the electrode. A single current peak is observed during the deposition of Sn on Bi, Tl on Sn, and Cd on Bi, Pb and Sn. The reduction of Tl on Au, Ag and Cu, of Pb on Ag and Cu, and of Bi on Ag, however, leads to the splitting of the current transient into a so-called main peak with unit activity of the electrodeposited depolarizer, and a less negative prewave region, within which the activity of the reduced metal is less than unity.</p><p>The current balance of the electrode reaction is verified by coulometric evaluation of the chronoamperograms.</p></div>","PeriodicalId":100778,"journal":{"name":"Journal of Electroanalytical Chemistry (1959)","volume":"12 4","pages":"Pages 300-319"},"PeriodicalIF":0.0,"publicationDate":"1966-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-0728(96)80005-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"55558251","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Application of mercury-plated graphite electrodes to voltammetry and chronopotentiometry","authors":"S.P. Perone, K.K. Davenport","doi":"10.1016/S0022-0728(96)80001-5","DOIUrl":"10.1016/S0022-0728(96)80001-5","url":null,"abstract":"<div><p>The preparation and application of mercury-plated, graphite electrodes has been discussed. The electrodes were prepared by controlled.potentialelectrodeposition on the exposed planar surface of a wax.impregnated graphite electrode. The mercury-plated electrodes were evaluated by voltammetric and chronopotentiometric applications to various reversible and irreversible systems. Experimental data were compared to rigorous voltammetric theory. Theory for chronopotentiometric curves at thin-film electrodes with amalgam-forming substances was developed, and experimental correlations with the Cd(II) system were made. In each case correlations were good.</p></div>","PeriodicalId":100778,"journal":{"name":"Journal of Electroanalytical Chemistry (1959)","volume":"12 4","pages":"Pages 269-276"},"PeriodicalIF":0.0,"publicationDate":"1966-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-0728(96)80001-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"55558210","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Conductometric study on the quantitative precipitation of lanthanum and neodymium as normal tellurites","authors":"Sarju Prasad, K.C. Pathak","doi":"10.1016/S0022-0728(96)80011-8","DOIUrl":"10.1016/S0022-0728(96)80011-8","url":null,"abstract":"","PeriodicalId":100778,"journal":{"name":"Journal of Electroanalytical Chemistry (1959)","volume":"12 4","pages":"Pages 360-362"},"PeriodicalIF":0.0,"publicationDate":"1966-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-0728(96)80011-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"55557846","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Utilisation de l'tmpedance operationnelle pour la determination des coefficients de diffusions1","authors":"Eugéne Levart, Emmanuel Poirier, D'angÉ D'orsay","doi":"10.1016/S0022-0728(96)80002-7","DOIUrl":"10.1016/S0022-0728(96)80002-7","url":null,"abstract":"<div><p>Analytical expressions for the operational impedance, <em>Zs</em>, valid for all relaxation methods, are proposed for various types of electrode reactions.</p><p>Used experimentally, they enable kinetic parameters, and, more particularly, diffusion coefficients of reacting species to be determined.</p><p>The experimental part of the work is concerned with measurements made under galvanostatic pulse conditions for the Hg/Hg<sub>2</sub><sup>2+</sup> system in HClO<sub>4</sub> media at 30°. The results, stated in terms of the Laplace operator function, <em>s</em>, have shown that the diffusion coefficient of mercury ion is approximately constant at supporting electrolyte concentrations between 0.1 and 2 <em>M</em>.</p><p>The merits of the proposed, procedure are compared, with those of other electrochemical methods for the determination of diffusion coefficients.</p></div>","PeriodicalId":100778,"journal":{"name":"Journal of Electroanalytical Chemistry (1959)","volume":"12 4","pages":"Pages 277-285"},"PeriodicalIF":0.0,"publicationDate":"1966-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-0728(96)80002-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"55558221","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}