Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Electrolytes influenced

Electrolytes influence almost every facet of cavitation from nucleation to coalescence, to the conditions of the bubble interior which determine the nature and severity of inertial collapse. Burikin et al. [34] investigated optical cavitation and found that on both hydrophobic and hydrophilic surfaces the cavitation probability... [Pg.364]

Amokrane and Badiali proposed a semiempirical approach to the determination of the solvent contribution C, to the capacitance of the double layer in aqueous and nonaqueous " solutions. They used the relation C = Cf - C m, where Q is the experimentally determined capacity of the inner layer and Cm is the contribution of the metal. The plots ofC, vs. (Tm were presented for various solvents and correlated with their properties.However, the problem of the supporting electrolyte was entirely neglected in the quoted papers. It was shown recently that the height and position of the maximum on the C, vs. Gm plots depend on the type of the supporting electrolyte. Experimental differential capacity data obtained on the Hg electrode in methanol and ethanol containing various electrolytes with nonadsorbing anions (F , PFg, ClOi) indicate that the type as well as concentration of the electrolyte influences the position and the height of the maximum on the C, vs. plots (Fig. 13). [Pg.58]

The supporting electrolytes influence polarographic and voltammetric measurements in the manners as described below ... [Pg.306]

The thermodynamic equilibrium is calculated with the Henry coefficients corrected for the electrolyte influence. As nitric acid is a strong electrolyte, the solubilities of nitrogen oxides in water [81] must be recalculated according to [20] to account for the non-ideal electrolyte behavior. [Pg.285]

Ternary System Phase Diagram Determinations Concerning Potassium Electrolyte Influence on Aqueous Solutions of Dioxane or T etrahy drof uran... [Pg.182]

In an attempt to clarify the mechanism whereby electrolytes influence the solvency of water for a polymer, Garvey and Robb (1979) measured the heats of dilution of poly(vinyl pyrrolidone) in aqueous electrolyte solutions. The heat of dilution was found to be negative (i.e. mixing is favoured by the enthalpy changes) so that phase separation must inevitably be controlled by entropy effects. Thermodynamics demands that in the salting-out of a polymer by a second component, this component must be negatively adsorbed from the polymer. This can be expressed mathematically by... [Pg.141]

A knowledge of the electrolyte temperature is important in CE as temperature changes in the electrolyte influence precision, accuracy, separation efficiency, and method robustness [7,14,32], During the past two decades, a considerable amount of research has been conducted toward electrolyte temperature measurements in CE [1,14,19,21,32 2], Early methods have included using the variation of electroosmotic mobility (eieof), electrophoretic mobility (p-ep), and electrical conductivity (k) to measure temperature [38,39], More recently, techniques such as external thermocouples [21], Raman thermometry [19,40], NMR spectroscopy [32,35], thermochromic probes [41], and the variation in fluorescence response [42] have been used to measure temperatures. Most of these methods require the modiflcation of the existing instrument and/or the purchase of additional equipment. [Pg.555]

The variation of diffusion current and peak current with the pH of the supporting electrolyte, influences the diffusion coefficient values also to vary in the same manner. The reason for slight variations attributed in diffusion coefficient values with increase in pH may be due to the decrease in the availablity of protons with increase in pH. In general, forward rate constant values are noticed to decrease with increase in the pH of the solution. The values of heterogeneous forward rate constants obtained at DME are less when compared to those obtained at HMDE. This is probaply ascribed to the different electrolysis conditions existing at the two electrodes. The kinetic parameters are reported in Table 1 and 2. [Pg.342]

Reactivity is a property of the monomer but it is also influenced by the experimental conditions. Therefore, the further conditions should be considered such as the solvent and the composition of the electrolyte, influence of additives, and temperature. [Pg.345]

Chemical environment strongly influences transport. Adsorption and intercalation influence the potential distribution at the interface, affecting the tendency for electrons to accumulate in the film and the photovoltage. Composition of electrolyte influences rate of electron scavenging. Film history influences the density of traps and recombination centers. [Pg.468]

Liu, W. W., X. B. Yan, J. W. Lang, and Q. J. Xue. 2011. Electrochemical behavior of graphene nanosheets in alkylimidazolium tetrafluoroborate ionic liquid electrolytes Influences of organic solvents and the alkyl chains. Journal of Materials Chemistry 21 13205-13212. [Pg.238]

KCl and CaCl2. If k was not changed, k was decreased by these electrolytes. In the complex formation of (cationic) C4PVP and (neutral) L-tryptophan, the formation constant A was practically indifferent to addition of the electrolytes. Electrolyte influence on these three reactions indicates the importance of the electrostatic interactions... [Pg.90]

On single-crystal electrodes the UPD deposits often form well-defined, ordered monolayers. Hypothetical superlattice structures have been proposed, which rely on the charges determined for the various peaks observed in the cyclic voltam-mograms. The anions of the supporting electrolytes influence the shape and the position of the UPD peaks in the cyclic voltammograms, although the superlattice structures are not always affected by... [Pg.926]

It is well known that dissolved electrolytes influence the solubility of gases in aqueous solution. This is generally called the salting-out effect if the solubility of the gas is decreased relative to pure water as is most often the case. [Pg.927]

Reaction 4 attempts to recover the considerable influence of electrolytes in empirical kinetics, through its discharge on the polymer. The formed radical is immediately transferred to a monomer molecule. This indirect initiation can explain the behaviour of pyrrole electropolymerization at high potentials in water [51]. The other electrolyte influences act on the metal oxide production [49], by stabilization of the monomeric radical cations [130] and through polymer oxidation. [Pg.442]

In the first process, the Brownian motion velocity and presence of electrolytes influences the increase in viscosity of the immobilizing media, the coagulation velocity, the domain of attraction forces, and the concentration of colloidal solution. Consequently, from the Smoluchowski equation (Pomogailo and Kestelman 2005), the rate constant of particle coagulation, k, is inversely proportional to the viscosity of the media, r ... [Pg.322]

No-l Ni -0.86 96 H2 H2O EC Catalyst absorbed on Hg, Sensitive to pH. Support electrolytes influence selectivity. KNO3 and KCIO4 are the best [10]... [Pg.316]

Many ordered surface phases were found on electrodes by electrolytic metal deposition at underpotentials, often having different stractures than those observed by deposition from the gas phase. The reason is that the interactions of the substrate and the deposits with components of the electrolyte influence the forces of interaction between deposited atoms. This is demonstrated particularly well by the influence of anion adsorption on the potential and structure of underpotentially deposited metals. The stracture of the full monolayer is in some cases different from the bulk phase of the deposited metal. The monolayer stracture can be controlled by the stracture of the substrate, and such differences can extend even to the second layer. Three-dimensional nucleation, however, seems to play a minor role in the growth of the bulk phase on foreign substrates when imderpotential deposition takes place. ... [Pg.66]

Salis, A., Bilanicova, D., Ninham, B.W., and Monduzzi, M. (2007) Hofmeister effects in enzymatic activity weak and strong electrolyte influences on the... [Pg.547]


See other pages where Electrolytes influenced is mentioned: [Pg.227]    [Pg.222]    [Pg.68]    [Pg.265]    [Pg.155]    [Pg.157]    [Pg.233]    [Pg.215]    [Pg.248]    [Pg.382]    [Pg.460]    [Pg.320]    [Pg.129]    [Pg.3531]    [Pg.418]    [Pg.9]    [Pg.591]    [Pg.520]    [Pg.1636]    [Pg.311]    [Pg.61]    [Pg.85]    [Pg.50]    [Pg.311]   
See also in sourсe #XX -- [ Pg.211 ]




SEARCH



Electrolyte flow influence

Influence of LOI on Alumina Dissolution in Molten Aluminum Electrolyte

Potassium electrolyte influence

© 2024 chempedia.info