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Electrolyte solutes

Pickling—a form of chemical and electrolytic removal of mill scale and corrosion products from the surfaces of metals in an acidic solution. Electrolytic pickling may be anodic or cathodic, depending on the polarization of the metal in the solution. [Pg.49]

An alternative ambient temperature design based on sodium ion reaction refers to the domain of the so-calledbatteries. The polysulfide bromide cell (PSB) provides a reversible electrochemical reaction between two salt solution electrolytes (sodium bromide and sodium polysulfide), according to the scheme... [Pg.333]

Large-volume parenterals designed to provide fluid (water), calories (dextrose solutions), electrolytes (saline solutions), or combinations of these materials have been described. Several other specialized LVP and sterile solutions are also used in medicine and will be described here, even though two product classes (peritoneal dialysis and irrigating solutions) are not parenteral products. [Pg.388]

Bv employing a soluble cationic polymer as the solution electrolyte polymer films can be sterical ly blocked from reducing beyond the formal zero valent form. In the zero-valent form the polymer is an ohmic conductor both in solution and dry. A model has been proposed which describes the conductivity of the polymer and in part accounts for its ohmic nature and semi conductor-1 ike temperature dependence. [Pg.428]

Aqueous solutions Electrolytic gradients Plastics Lipids... [Pg.79]

Pig. 7-1. (a) Cathodic reaction and (b) anodic reaction M = metal electrode S = aqueous solution (electrolyte Mm = metal ion in metallic bonding state M., = metal ion in hydrated state Om = electron in metals. [Pg.214]

Chapter 2 discussed the various forms of interaction between solute and the solvent molecules (see section 2.3), which leads to a certain solubility of the solute in the solvent phase. It was also described how the ratio of the solubility of the solute between two immiscible solvents could be used to estimate distribution ratios (or constants) for the solute in the particular system (see section 2.4). It was also pointed out that in the case of aqueous solute electrolytes, specific consideration had to be applied to the activity of the solute in the aqueous phase, a consideration that also was extended to solutes in organic solvents. [Pg.89]

Chlorine is produced commercially by the electrolysis of a liquid solution of sodium chloride (or seawater), through which process an electric current is passed though the solution (electrolyte). [Pg.250]

During anodization of titanium foil in a 2.5% HNO3 plus 1% HF water solution electrolyte, with or without addition of boric acid, the applied anodic potential was initially ramped from 0 to 20 V at a rate of 6 V/min the anodization potential was then held constant at 20 V for 4 h [102,103]. An initial ramp of the voltage was used because... [Pg.273]

Electrically switchable rear-view mirrors for cars and trucks have been in commercial production since the early 1990s, the leading company being the Gentex Corporation. The Gentex mirror consists of an ITO-glass surface, with the conductive side inwards, and a reflective metallic surface, spaced less than a millimetre apart. In the gap between these two electrodes is the solution electrolyte that is coloured at the anode by formation of the stable radical cation, similar to Wurster s... [Pg.61]

Current flows when the electron/hole pair is prevented from recombining directly via percolation of the photogenerated electron to the ITO electrode and by scavenging of the hole by the solution electrolyte. The circuit is completed by reduction of the oxidized electrolyte species (S042- or S20(,2 ) at the platinum electrode. [Pg.272]

Figure 7.5 Schematic representation of an n-type semiconductor-solution electrolyte junction showing the formation of depletion layer, band bending and Helmholtz layer (a) before immersion and (b) after immersion in solution. Figure 7.5 Schematic representation of an n-type semiconductor-solution electrolyte junction showing the formation of depletion layer, band bending and Helmholtz layer (a) before immersion and (b) after immersion in solution.
The solute (electrolyte, dissolved reactant) must be analytical grade. [Pg.376]

PLASMA. The portion of the blood remaining after removal of the white and red cells and the platelets it differs from serum in that it contains fibrinogen, which induces clotting by conversion into fibrin by activity of the enzyme thrombin. Plasma is made up of more than 40 proteins and also contains acids, lipids, and metal ions. It is an amber, opalescent solution in which the proteins are in colloidal suspension and the solutes (electrolytes and nonelectrolytes) are either emulsified or in true solution. The proteins can be separated from each other and from the other solutes by nltrafiltration, nltracentrifugation, electrophoresis, and immuno-chemical techniques. See also Blood. [Pg.1314]

While on the one hand the examples mentioned above suggest the persistence of elements of water structure in the presence of solutes (electrolytes), other evidence points to a significant interaction between a small uncharged molecule (or atom) and water. While we postpone... [Pg.106]

In the previous chapter, we described the thermodynamic properties of nonelectrolyte solutions. In this chapter, we focus on electrolytes as solutes. Electrolytes behave quite differently in solution than do nonelectrolytes. In Chapter 11, we described the strong electrolyte standard state and summarized relationships between the activity of the solute ai, the mean activity coefficient 7 , and the molality m in Table 11.3. [Pg.309]

Electrostatic binding [11] may provide another very useful approach to preconcentration analysis. Enhancement of the redox ion concentration in the ion-exchange polymer volume should permit very sensitive analysis when combined with an appropriate electroanalyti-cal method [12,13]. However, the sensitivity of the ion-exchange equilibrium to the sample solution electrolyte composition and concentration and the necessity of having a multiply charged analyte ion may limit the usefulness of the electrostatic binding approach. [Pg.251]

Vqq, of adsorbed carbon monoxide against electrode potential at gold electrodes, for CO-saturated (ca. ImM) solutions. Electrolytes were ( , ) 0.1 M HCIO, ( ) 0.1 M NaClO, and (A) 0.1 M KF. The arrowed dashed curves represent the sequential peak frequencies obtained upon potential excursions from 100 mV to 500 mV and return, into the region where CO electrooxidation, occurs. The solid straight line, drawn through the points obtained at potentials (< 100 mV) where adsorbed CO is stable towards electrooxidation, has a slope of about 50 cm l V. ... [Pg.146]

Polystyrene latexes have been prepared using persulfate initiator for many years, but only recently have methods been developed to determine the number and loci of the sulfate surface groups. To determine these surface groups, the latex is cleaned to remove the adsorbed emulsifier and solute electrolyte, then the surface sulfate groups in the H+ form are titrated conductometrically with base. The latexes can be cleaned effectively by ion exchange (2-5) or serum replacement (6) dialysis is not effective in removing the adsorbed emulsifier and solute electrolyte (3,5,6). +... [Pg.68]

For serum replacement (6), the latex is confined in a cell with a uniform-pore-size Nuclepore filtration membrane. Distilled, deionized water is pumped through the latex until the conductance of the effluent stream is about the same as that of the distilled, deionized water. This serum replacement removes the adsorbed emulsifier and solute electrolyte quantitatively and allows recovery of the serum in a form suitable for further analysis however, it does not+replace the Na+ and K counterions of the surface groups with Vl ions. To do this, dilute hydrochloric acid (ca. 10 N) is pumped through the latex, followed by distilled, deionized water to remove the excess acid. The latex is then titrated conductometrically to determine the surface charge. [Pg.71]

Krumgalz BS, Pogorelsky R, Pitzer KS (1995) Ion interaction approach to calculations of volumetric properties of aqueous multiple-solute electrolyte solutions. J Soln Chem 24 1025-1038... [Pg.234]

On the basis of your observations, are sucrose solutions electrolytes or nonelectrolytes ... [Pg.182]

Fig. 8.7 ICE values during the electrolysis at a BDD electrode of anionic and cationic surfactant solution. Electrolyte 0.0615 mM sodium dodecylbenzenesulfonate solution 0.07 mM hexade-cyltrimethyl ammonium chloride solution, i = 4mAcm 2 (Lissens et al. 2003)... Fig. 8.7 ICE values during the electrolysis at a BDD electrode of anionic and cationic surfactant solution. Electrolyte 0.0615 mM sodium dodecylbenzenesulfonate solution 0.07 mM hexade-cyltrimethyl ammonium chloride solution, i = 4mAcm 2 (Lissens et al. 2003)...
Dynamic characteristics of -> phase transitions upon intercalation after application of an infinitely small potential step may include a slow process of -> nucleation and the growth of primary droplets of a new phase (more concentrated with the inserted ions) at the boundary with the solution electrolyte. After that, a continuous boundary of the new phase is formed, which moves into the host s interior in a diffusion-like manner. This process can be formally described in terms of a moving... [Pg.354]

Nonaqueous electrochemical systems are used when (i) the electrode under consideration chemically reacts with water, (ii) the required electrolytic salt and/or the active solution species under study is not soluble in water, and (iii) when a wider electrochemical window of the solution electrolyte is required than that of aqueous solutions. [Pg.453]

Perbromates are obtained by oxidation of bromates in aqueous solution. Electrolytic oxidation, the best method of preparing perchlorates and periodates, is not very satisfactory in the case of perbromates. The most practical synthesis involves oxidation with elemental fluorine in sodium hydroxide solution. The procedure is somewhat hazardous, and the experimenter should familiarize himself with the precautions necessary for safely handling fluorine before undertaking the synthesis.1... [Pg.2]

FIGURE 4.8 Charge balance test for a kaolinitic soil in LiCl solutions. Electrolyte concentration circles, 0.001 M triangles, 0.005 M and squares, 0.001 M. Error bars are only given for 0.001-M electrolyte. Bars are similar in the other two cases. Data provided by J. Chorover. [Pg.105]


See other pages where Electrolyte solutes is mentioned: [Pg.215]    [Pg.197]    [Pg.364]    [Pg.74]    [Pg.131]    [Pg.584]    [Pg.717]    [Pg.421]    [Pg.176]    [Pg.283]    [Pg.293]    [Pg.40]    [Pg.584]    [Pg.265]    [Pg.93]    [Pg.279]    [Pg.87]    [Pg.88]    [Pg.162]    [Pg.88]   
See also in sourсe #XX -- [ Pg.383 , Pg.384 , Pg.418 ]

See also in sourсe #XX -- [ Pg.153 ]




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Electrolyte solutions

Electrolytic solution

Solution electrolyte solutes

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