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Ion-specific

These effects can be illustrated more quantitatively. The drop in the magnitude of the potential of mica with increasing salt is illustrated in Fig. V-7 here yp is reduced in the immobile layer by ion adsorption and specific ion effects are evident. In Fig. V-8, the pH is potential determining and alters the electrophoretic mobility. Carbon blacks are industrially important materials having various acid-base surface impurities depending on their source and heat treatment. [Pg.190]

Figure V-8 illustrates that there can be a pH of zero potential interpreted as the point of zero charge at the shear plane this is called the isoelectric point (iep). Because of specific ion and Stem layer adsorption, the iep is not necessarily the point of zero surface charge (pzc) at the particle surface. An example of this occurs in a recent study of zircon (ZrSi04), where the pzc measured by titration of natural zircon is 5.9 0.1... Figure V-8 illustrates that there can be a pH of zero potential interpreted as the point of zero charge at the shear plane this is called the isoelectric point (iep). Because of specific ion and Stem layer adsorption, the iep is not necessarily the point of zero surface charge (pzc) at the particle surface. An example of this occurs in a recent study of zircon (ZrSi04), where the pzc measured by titration of natural zircon is 5.9 0.1...
Specific breakage rate Specific conductivity Specific ion electrode Specific properties... [Pg.919]

The JnitedSfates Pharmacopeia (76) specifications for sodium monofluorophosphate require a minimum of 12.1% fluoride as PO F (theoretical 13.2%) and a maximum of 1.2% fluoride ion reflecting unreacted sodium fluoride. Analysis for PO F is by difference between total fluoride ia the product less fluoride ion as determined by a specific ion electrode. The oral LD q of sodium monofluorophosphate ia rats is 888 mg/kg. [Pg.226]

A number of simple, standard methods have been developed for the analysis of ammonium compounds, several of which have been adapted to automated or instmmental methods. Ammonium content is most easily deterrnined by adding excess sodium hydroxide to a solution of the salt. Liberated ammonia is then distilled into standard sulfuric acid and the excess acid titrated. Other methods include colorimetry (2) and the use of a specific ion electrode (3). [Pg.362]

Important to environmental analysis is the ability to automate the injection, as weU as the identification and quantitation of large numbers of samples. Gc/ms systems having automatic injectors and computerized controllers have this capabiUty, even producing a final report in an unattended manner. Confirmation and quantitation are accompHshed by extracting a specific ion for each of the target compounds. Further confirmation can be obtained by examining the full scan mass spectmm. [Pg.402]

Specific-Ion Electrodes In addition to the pH glass electrode specific for hydrogen ions, a number of electrodes that are selective for the measurement of other ions have been developed. This selectivity is obtained through the composition of the electrode membrane (glass, polymer, or liquid-liquid) and the composition of the elec trode. Tbese electrodes are subject to interference from other ions, and the response is a function of the total ionic strength of the solution. However, electrodes have been designed to be highly selective for specific ions, and when properly used, these provide valuable process measurements. [Pg.765]

Membrane Efficiency The permselectivity of an ion-exchange membrane is the ratio of the transport of electric charge through the membrane by specific ions to the total transport of electrons. Membranes are not strictly semipermeable, for coions are not completely excluded, particularly at higher feed concentrations. For example, the Donnan eqmlibrium for a univalent salt in dilute solution is ... [Pg.2030]

Ion probes. Determining the level of ions in solution also helps to control corrosion. An increase in concentration of specific ions can contribute to scale formation, which can lead to a corrosion-related failure. Ion-selective elec trode measurements can be included, just as pH measurements can, along with other more typical corrosion measurements. Especially in a complete monitoring system, this can add information about the effect of these ions on the material of interest at the process plant conditions. [Pg.2440]

Another area where probes can be used effectively is in monitoring of deposits such as scale. One method of measurement is detecting specific ions that contribute to scale buildup or fouling another is measuring the ac tual layers. Scale and fouling often devastate the corrosion resistance of a system, leading to a costly corrosion-related plant shutdown. [Pg.2440]

Corrosion of industrial alloys in alkaline waters is not as common or as severe as attack associated with acidic conditions. Caustic solutions produce little corrosion on steel, stainless steel, cast iron, nickel, and nickel alloys under most cooling water conditions. Ammonia produces wastage and cracking mainly on copper and copper alloys. Most other alloys are not attacked at cooling water temperatures. This is at least in part explained by inherent alloy corrosion behavior and the interaction of specific ions on the metal surface. Further, many dissolved minerals have normal pH solubility and thus deposit at faster rates when pH increases. Precipitated minerals such as phosphates, carbonates, and silicates, for example, tend to reduce corrosion on many alloys. [Pg.185]

There are five major methods for the determination of fluonde ions m aqueous solution (1) volumetric, (2) gravimetnc, (3) null pointpotentiometry, (4) fluonde lon-selecti ve electrode (also known as specific ion electrode), and (5) ion chromatography... [Pg.1026]

Similar to the pH meter, gas meters employ specific ion electrodes. The electrodes generate a potential proportional to the activity of a specific ion in solution. The calibration is achieved in standard solution and results read in mV or concentration in mg/L or ppm on the meter. The water can be adapted to monitor the concentration of carbon dioxide, hydrogen sulfide, ammonia, chloride, calcium, potassium and sodium to name a few. [Pg.1317]

Pitting of passive metals such as the stainless steels, aluminium alloys, etc., in the presence of specific ions, e.g. Ci ions Dezincification deaiuminification graphitisation... [Pg.12]

Specific ion electrodes, similar in design to the glass electrode, have been developed to analyze for a variety of cations and anions. One of the first to be used extensively was a fluoride ion electrode that is sensitive to F- at concentrations as low as 0.1 part per million and hence is ideal for monitoring fluoridated water supplies. An electrode that is specific for Cl- ions is used to diagnose cystic fibrosis. Attached directly to the skin, it detects the abnormally high concentrations of sodium chloride in sweat that are a characteristic symptom of this disorder. Diagnoses that used to require an hour or more can now be carried out in a few minutes as a result, large numbers of children can be screened rapidly and routinely. [Pg.495]

The general approach illustrated by Example 18.7 is widely used to determine equilibrium constants for solution reactions. The pH meter in particular can be used to determine acid or base equilibrium constants by measuring the pH of solutions containing known concentrations of weak acids or bases. Specific ion electrodes are readily adapted to the determination of solubility product constants. For example, a chloride ion electrode can be used to find [Cl-] in equilibrium with AgCl(s) and a known [Ag+]. From that information, Ksp of AgCl can be calculated. [Pg.495]

In contrast to bilateral triple-ion formation, unilateral triple-ion formation may also occur in solvents of high permittivity, when ion-pair association is increased by noncoulombic specific ion-ion interactions in solvents of low basicity such as PC or AN. Exclusive formation of anionic tripleions [A-C+A-] ", is observed in these solvents when large organic molecular anions A interact with small cations such as Li + or H+. For example, in contrast to lithium acetate in DMSO [97], where ion association is moderate, ion association as well as unilateral triple-ion formation is observed in the solvent PC [105] due to the much lower basicity of this solvent, (see Table 2)... [Pg.468]

With few exceptions, information on the anticonvulsant pharmacology of specific ion channel subunits analyzed in expression systems is scarce. Hitherto, a first understanding of the mechanism of action of most antiepileptic dtugs has evolved from analyses of somatic ion channel pharmacology either in isolated neurons from human or rodent neurons, or cell culture models. [Pg.127]

NOTE The moisture content of steam can be measured by means of a throttling calorimeter or by analysis of the sodium content in a sample of condensed steam, using perhaps a specific ion electrode or flame photometer. [Pg.9]

Imposing maximum limitations on TDS and certain specific ions or salts (such as hydroxyl ions or chlorides)... [Pg.242]

Systemic and coronary arteries are influenced by movement of calcium across cell membranes of vascular smooth muscle. The contractions of cardiac and vascular smooth muscle depend on movement of extracellular calcium ions into these walls through specific ion channels. Calcium channel blockers, such as amlodipine (Norvasc), diltiazem (Cardizem), nicardipine (Cardene), nifedipine (Procardia), and verapamil (Calan), inhibit die movement of calcium ions across cell membranes. This results in less calcium available for the transmission of nerve impulses (Fig. 41-1). This drug action of the calcium channel blockers (also known as slow channel blockers) has several effects on die heart, including an effect on die smooth muscle of arteries and arterioles. These drug dilate coronary arteries and arterioles, which in turn deliver more oxygen to cardiac muscle. Dilation of peripheral arteries reduces die workload of die heart. The end effect of these drug is the same as that of die nitrates. [Pg.381]

Studies of ligands which might provide specificity in binding to various oxidation states of plutonium seems a particularly promising area for futher research. If specific ion electrodes could be developed for the other oxidation states, study of redox reactions would be much facilitated. Fast separation schemes which do not change the redox equilibria and function at neutral pH values would be helpful in studies of behavior of tracer levels of plutonium in environmental conditions. A particularly important question in this area is the role of PuOj which has been reported to be the dominant soluble form of plutonium in some studies of natural waters (3,14). [Pg.230]

In an ionic solid, the coordination number means the number of ions of opposite charge immediately surrounding a specific ion. In the rock-salt structure, the coordination numbers of the cations and the anions are both 6, and the structure overall is described as having (6,6)-coordination. In this notation, the first number is the cation coordination number and the second is that of the anion. The rock-salt structure is found for a number of other minerals having ions of the same charge number, including KBr, Rbl, MgO, CaO, and AgCl. It is common whenever the cations and anions have very different radii, in which case the smaller cations can fit into the octahedral holes in a face-centered cubic array of anions. The radius ratio, p (rho), which is defined as... [Pg.321]

MS-MS is a term that covers a number of techniques in which two stages of mass spectrometry are used to investigate the relationship between ions found in a mass spectrum. In particular, the product-ion scan is used to derive structural information from a molecular ion generated by a soft ionization technique such as electrospray and, as such, is an alternative to CVF. The advantage of the product-ion scan over CVF is that it allows a specific ion to be selected and its fragmentation to be studied in isolation, while CVF bring about the fragmentation of all species in the ion source and this may hinder interpretation of the data obtained. [Pg.208]


See other pages where Ion-specific is mentioned: [Pg.718]    [Pg.1112]    [Pg.377]    [Pg.516]    [Pg.384]    [Pg.2203]    [Pg.143]    [Pg.541]    [Pg.277]    [Pg.100]    [Pg.1317]    [Pg.310]    [Pg.157]    [Pg.185]    [Pg.826]    [Pg.1191]    [Pg.250]    [Pg.948]    [Pg.370]    [Pg.214]    [Pg.230]    [Pg.476]    [Pg.170]    [Pg.155]    [Pg.244]    [Pg.140]    [Pg.177]   
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See also in sourсe #XX -- [ Pg.497 ]

See also in sourсe #XX -- [ Pg.587 ]




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Adsorbed ions, specific

Boron specific ion-exchange resin

Double layer specifically adsorbed ions

Electrostatic Aspects on Ion Binding Specificity

Ion channels specificity

Ion specific adsorption

Ion specifications

Ion specifications

Ion specificity

Ion-specific carriers

Ion-specific electrode

Ion-specific parameters

Ions, specific interactions between

Ions, specifically bound

Permselectivity for specific ions

Permselectivity of Specific Ions through the Ion Exchange Membrane in Electrodialysis

Properties of Specific Ions

Specific Adsorption of Ions and Effect on Double-Layer

Specific Ion Effect on the Growth of PEMs

Specific Ion Interaction Theory

Specific Ion Interaction Theory (SIT

Specific Radical Ions

Specific adsorption of ions

Specific effects of flocculating ions

Specific hydrogen ion catalysed

Specific hydrogen ion catalysis

Specific hydroxide ion catalysis

Specific hydroxyl ion catalysis

Specific ion effects

Specific ion exchange resins

Specific ion exchangers

Specific ion interaction

Specific ion interaction model

Specific ion sequences

Specifically adsorbed ions

Specificity of metal ions

Strength specific ions

The Specific Adsorption of Ions

The specific ion interaction equations

Transition metal ions specific element

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