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Silver monovalent

Departures from the ideal behavior expressed by equation 7 usually are found in alkaline solutions containing alkaH metal ions in appreciable concentration, and often in solutions of strong acids. The supposition that the alkaline error is associated with the development of an imperfect response to alkaH metal ions is substantiated by the successhil design of cation-sensitive electrodes that are used to determine sodium, silver, and other monovalent cations (3). [Pg.466]

Tetrasilver tetroxide is a powerful oxidizer for sanitizing swimming pools, hot tubs, and industrial cooling system waters (see Water, treatment of SWIMMINGPOOLS, SPAS, AND HOT tubs). This oxide is slightly soluble and its dissociation into silver ions is enhanced by the addition of the oxidizer KgSgOg. Bivalent and trivalent silver disinfectants have been shown to be from 50 to 200 times more effective as sanitizers than monovalent silver compounds. [Pg.82]

The overlap between 5- and p-bands also occurs for the alkali metals and for the monovalent noble metals copper, silver, and gold, which have face-centered cubic structures. The noble metals differ from the alkalis because of the filled d-shell just below the 5-shell in energy the d-band and the 5-band overlap in the solid. [Pg.29]

Silver occurs naturally in several oxidation states, the most common being elemental silver (Ag°) and the monovalent ion (Ag+). Soluble silver salts are, in general, more toxic than insoluble salts. In natural waters, the soluble monovalent species is the form of environmental concern. Sorption is the dominant process that controls silver partitioning in water and its movements in soils and sediments. As discussed later, silver enters the animal body through inhalation, ingestion, mucous membranes, and broken skin. The interspecies differences in the ability of animals to accumulate, retain, and eliminate silver are large. Almost all of the total silver intake is usually... [Pg.534]

It is important that the copper is in the monovalent state and incorporated into the silver hahde crystals as an impurity. Because the Cu+ has the same valence as the Ag+, some Cu+ will replace Ag+ in the AgX crystal, to form a dilute solid solution Cu Agi- X (Fig. 2.6d). The defects in this material are substitutional CuAg point defects and cation Frenkel defects. These crystallites are precipitated in the complete absence of light, after which a finished glass blank will look clear because the silver hahde grains are so small that they do not scatter light. [Pg.63]

Cu2+ and Hg2+ are perhaps the most obvious targets for reaction-based signaling systems. However, this approach has also been realized for monovalent Ag+. Here, again a rhodamine derivative (rhodamine B spirolactam 48, Fig. 18) allows the highly selective detection of Ag+ with a detection limit of 14 ppb in water containing 20% ethanol. Silver nanoparticles, a topical analyte today, can also be detected, after oxidation of the particles with H2O2/H3PO4 [141]. The selectivity was tested with Ca2+, Ba2+, Mg2+, Cr2+, Mn2+, Fe3+, Co2+, Ni2+, Cu+, Cu2+, Zn2+, Pd2+, Cd2+, Hg+, and Hg2+ and no interference was found. [Pg.67]

The pH dependence of the rate of development by hydroxylamine indicates that the monovalent ion is the active species. The rate varies as about the 0.65 power of the hydroxylamine concentration at pH 12.7 and the 0.75 power at pH 10.8. These results suggest adsorption of the hydroxylamine ion, and are in complete agreement with previous findings for the catalyzed reduction of silver chloride precipitates. [Pg.134]

Although the acidic antibiotics do not show the high selectivity characteristic of the neutral ones, there is still some preference, a strong one for monovalent as compared with divalent cations, and within the monovalent cations a variation from one acid to another. Monensin prefers sodium to potassium. The larger nigeridn, (X7), prefers potassium to sodium its silver, potassium, and sodium salts are isomorphous and anhydrous. Crystal structure determinations on the silver salt were carried out independently by workers in the U.S.A. (78) and in Japan... [Pg.94]

The spectra of silver and gold nanoclusters are intense and distinct (Table 4). They are thus particularly suitable to detect the evolution of a cluster composition during the construction of a bimetallic cluster in mixed solution. The system studied by pulse radiolysis was the radiolytic reduction of a mixed solution of two monovalent ions, the cyano-silver and the cyano-gold ions Ag(CN)2 and Au(CN)2 (Fig- 7) [66]. Actually, the time-resolved observation demonstrated a two-step process. First, the atoms Ag and Au are readily formed after the pulse and coalesce into an alloyed oligomer. However, due to... [Pg.589]

Gold has a more marked tendency to form complex salts than either copper or silver, but the ammines of gold arc somewhat unstable. Gold forms two series of salts where the metal is monovalent or divalent respectively from both series of salts ammines have been obtained. [Pg.39]

Results with Sr ] in Mice. While the results with Ag cryp-tate were encouraging, we sought further preliminary evidence of the potential value of labeled cryptates as blood-flow radiopharmaceuticals. There were several reasons for these studies the monovalent silver ion is very polarizable and thus may not be a general model for monovalent cations (5,17). In contrast, divalent cations form stronger inclusive cryptates than monovalent cations of the same ionic radii. On the other hand, the added charge of the divalent ion would require that the cryptand shield more charge if it is to result in an equally lipophilic complex. [Pg.208]

Class I and/or II MTs have been described in all animals examined. Mammalian MTs have been some of the most extensively studied of the 61 or 62 amino acids, 20 are cysteine residues. Metal ions are bound to the MT exclusively through thiolate bonds involving all 20 cysteines (see Hamer, 1986). They associate with a wide range of metals in vitro, 18 different metals in the case of rat liver MT (Nielson etal., 1985). Divalent and trivalent metals exhibit saturation binding at 7 mole equivalents forming M7-MT, whereas copper (Cu(I)) and silver (Ag(I)) bind as monovalent ions forming M12-MT. The structure of these molecules is such that two metal-binding domains are formed an a-cluster from the carboxy-terminal portion of the protein, contains 11 cysteines which bind either 4 divalent or 6 monovalent ions the (3-cluster, the amino-terminal... [Pg.3]

Silver is a rare element, which occurs naturally in its pure form as a white, ductile metal, and in ores. It has an average abundance of about 0.1 ppm in the earth s crust and about 0.3 ppm in soils. There are four oxidation states (0, 1 +, 2+, and 3+) the 0 and 1 + forms are much more common than the 2+ and 3+ forms. Silver occurs primarily as sulfides, in association with iron (pyrite), lead (galena), and tellurides, and with gold. Silver is found in surface waters in various forms (1) as the monovalent ion (e.g., sulphide, bicarbonate, or sulfate salts) (2) as part of more complex ions with chlorides and sulfates and (3) adsorbed onto particulate matter. [Pg.99]


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See also in sourсe #XX -- [ Pg.1087 , Pg.1088 , Pg.1089 , Pg.1090 , Pg.1091 , Pg.1092 , Pg.1093 ]




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