Comparative Study of Hydrogen Electrooxidation on Gold and Platinum in Solutions Containing Perchlorate Ion

The electrooxidation of hydrogen on platinum and gold electrodes is comparatively described in this paper. The reaction is faster on platinum than on the gold surface, because the reactive diffuses inside of the gold metal. This process is complicated with the lift of surface reconstruction of the (100) plane, which allows the fast penetration of the H atoms through the more open surface. The diffusion limiting current is then discontinued and the current falls. On platinum, the current fall occurs simultaneously with the metal oxide formation. It is assumed that the hydrogen helps the adsorbed OH group formation, which is the first step of metal oxidation, and it has been called “incipient hydrous oxide” (IHO). Current begins to fall slowly at the (IHO) potential. At higher potential the current falls abruptly.Instituto de Investigaciones Fisicoquímicas Teóricas y AplicadasFacultad de Ciencias Exacta

Comparative Study of Hydrogen Electrooxidation on Gold and Platinum in Solutions Containing Perchlorate Ion

The electrooxidation of hydrogen on platinum and gold electrodes is comparatively described in this paper. The reaction is faster on platinum than on the gold surface, because the reactive diffuses inside of the gold metal. This process is complicated with the lift of surface reconstruction of the (100) plane, which allows the fast penetration of the H atoms through the more open surface. The diffusion limiting current is then discontinued and the current falls. On platinum, the current fall occurs simultaneously with the metal oxide formation. It is assumed that the hydrogen helps the adsorbed OH group formation, which is the first step of metal oxidation, and it has been called “incipient hydrous oxide” (IHO). Current begins to fall slowly at the (IHO) potential. At higher potential the current falls abruptly.Instituto de Investigaciones Fisicoquímicas Teóricas y AplicadasFacultad de Ciencias Exacta

Electrochromism and Swelling of Polypyrrole Membranes: An Electrochemical and Ellipsometric Study

The growth of polypyrrole (Ppy) layers on gold electrodes in nearly neutral pH solutions is analysed using “in situ” voltametric and ellipsometric techniques. Different film structures are obtained depending on the potentiodynamic programme and the composition of the electrolyte. More compact dodecylsulphate-(DS) doped Ppy layers were grown at 1.2 V versus RHE than those obtained by applying a higher potential. The more compact layers correspond to the growth of an oxidised Ppy/DS layer that shows low pseudo capacity behaviour. After dipping, the doped Ppy/DS film in KCl solution-significant variations in optical indices and thickness are detected as a function of the applied potential. Higher electrochromism as well as decrease in film thickness after cathodisation is achieved. The optical indices and the thickness of the Ppy layer formed under different applied potential/time programmes are estimated.Instituto de Investigaciones Fisicoquímicas Teóricas y AplicadasDepartamento de Matemátic

Comparative Study of Hydrogen Electrooxidation on Gold and Platinum in Solutions Containing Perchlorate Ion

The electrooxidation of hydrogen on platinum and gold electrodes is comparatively described in this paper. The reaction is faster on platinum than on the gold surface, because the reactive diffuses inside of the gold metal. This process is complicated with the lift of surface reconstruction of the (100) plane, which allows the fast penetration of the H atoms through the more open surface. The diffusion limiting current is then discontinued and the current falls. On platinum, the current fall occurs simultaneously with the metal oxide formation. It is assumed that the hydrogen helps the adsorbed OH group formation, which is the first step of metal oxidation, and it has been called “incipient hydrous oxide” (IHO). Current begins to fall slowly at the (IHO) potential. At higher potential the current falls abruptly.Instituto de Investigaciones Fisicoquímicas Teóricas y AplicadasFacultad de Ciencias Exacta

Electrochemical and optical study of the confined aqueous layer adsorbed on gold electrodes cycled in phosphate and dodecylsulphate solutions

The properties of the confined aqueous layer potentiodynamically formed on polycrystalline gold in aqueous phosphate and sodium dodecylsulphate solutions were studied using voltammetry, ellipsometry, and contact angle measurements. The nature of the incipient oxide layer was analyzed as a function of the cycling time in the double layer-oxide monolayer potential region. The replacement of the electrolyte by hexane allows the increase of the optical signal. Different potential cycling conditions change the homogeneity of the confined aqueous incipient oxide layer leading to different structural characteristics.Instituto de Investigaciones Fisicoquímicas Teóricas y AplicadasFacultad de Ciencias Exacta

Evaluating susceptibility of karst dolines (sinkholes) for collapse in Sango, Tennessee, USA

Dolines or sinkholes are earth depressions that develop in soluble rocks complexes such as limestone, dolomite, gypsum, anhydrite, and halite; dolines appear in a variety of shapes from nearly circular to complex structures with highly curved perimeters. The occurrence of dolines in the studied karst area is not random; they are the results of geomorphic, hydrologic and chemical processes that have caused partial subsidence, even total collapse of the land surface, when voids and caves are present in the bedrock and the regolith arch overbridging these voids is unstable. In the study area, the majority of collapses occur in the regolith (bedrock cover) that bridges voids in the bedrock. Because these collapsing dolines can damage property and cause even the loss of lives, there is a need to develop methods for evaluating karst hazards; such methods can be used by planners and practitioners for urban and economic development, especially in regions with a growing population. The purpose of this project is threefold: 1) to develop a karst feature database, 2) to investigate critical indicators associated with doline collapse, and 3) to design a doline susceptibility model for potential doline collapse based on external morphometric data. The study revealed the presence of short range spatial dependence in the distribution of the dolines’ morphometric parameters such as circularity, geographic orientation of the main doline axes and the length-to-width doline ratios; therefore, geostatistics can be used to spatially evaluate the susceptibility of the karst area for doline collapse using the probability of occurrence of these critical parameters. The partial susceptibility estimates were combined into final spatial probabilities enabling the identification of areas where undetected dolines may cause significant hazards

Electrochromism and Swelling of Polypyrrole Membranes: An Electrochemical and Ellipsometric Study

The growth of polypyrrole (Ppy) layers on gold electrodes in nearly neutral pH solutions is analysed using “in situ” voltametric and ellipsometric techniques. Different film structures are obtained depending on the potentiodynamic programme and the composition of the electrolyte. More compact dodecylsulphate-(DS) doped Ppy layers were grown at 1.2 V versus RHE than those obtained by applying a higher potential. The more compact layers correspond to the growth of an oxidised Ppy/DS layer that shows low pseudo capacity behaviour. After dipping, the doped Ppy/DS film in KCl solution-significant variations in optical indices and thickness are detected as a function of the applied potential. Higher electrochromism as well as decrease in film thickness after cathodisation is achieved. The optical indices and the thickness of the Ppy layer formed under different applied potential/time programmes are estimated

WATER ADSORPTION AND DESORPTION ISOTHERMS ON MILK POWDER: II. WHOLE MILK

The aim of this research was the determination of adsorption and desorption isotherms of cow whole milk powder. The experiments have been carried out at 15, 25 and 40 ºC, in ranges of moisture and water activity characteristic of normal conditions in which the processes of drying, packaging and storage are developed. By studying the influence of the temperature on the experimental plots, the isosteric adsorption heat was determined. Experimental data were correlated to the referential model of Guggenheim, Anderson and Boer (GAB). For both, adsorption and desorption, a good model fit was observed. The isotherms showed very similar shapes between them and, by comparing adsorption and desorption isotherms, the phenomenon of hysteresis was confirmed

Oxidación de Hidrógeno sobre Electrodos de Oro

The Hydrogen oxidation on gold electrodes in sulphuric acid solution is studied. The reaction is irreversible, since atomic H, which appears as reaction intermediate, diffuses inside of the metal. The reactive is introduced in two ways: by electrolysis at a cathodic potential during different times and saturating the solution with the gaseous reactive. During the electrolysis the different crystalline planes reconstruct and the reaction kinetics is not the same on the reconstructed plane than on the unreconstructed one. The catalytic influence of the incipient hydrous gold oxide is shown. The presence of sulfate ions leads to a characteristic profile at the double layer charge potential region, in which faradic currents can be distinguished from those capacitive contributions. During the metal treatment a surface compound is formed. An attempt has been done to characterize it by FTIRSe estudia la oxidación de Hidrógeno sobre electrodos de oro, en una solución de ácido sulfúrico. La reacción es irreversible pues el H atómico, que aparece como intermediario de la reacción, difunde hacia el interior del metal. El reactivo se introduce de dos maneras distintas: mediante electrólisis a un potencial catódico durante tiempos diferentes y saturando la solución con el reactivo gaseoso. Durante la electrólisis los distintos planos cristalinos se reconstruyen y este hecho tiene influencia sobre la cinética de la reacción. Se muestra la influencia catalítica del óxido incipiente hidratado sobre la velocidad de la reacción. La presencia de iones sulfato conduce a un perfil voltamperométrico característico en la región de carga de doble capa. En ésta también se encuentran contribuciones farádicas que pueden distinguirse de aquéllas capacitivas. Durante el tratamiento del metal, se forma un compuesto superficial y se realiza un intento de caracterizarlo mediante FTI