Big Chemical Encyclopedia

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

Articles Figures Tables About

SPECIFIC METALS

Shannon and Prewitt base their effective ionic radii on the assumption that the ionic radius of (CN 6) is 140 pm and that of (CN 6) is 133 pm. Also taken into consideration is the coordination number (CN) and electronic spin state (HS and LS, high spin and low spin) of first-row transition metal ions. These radii are empirical and include effects of covalence in specific metal-oxygen or metal-fiuorine bonds. Older crystal ionic radii were based on the radius of (CN 6) equal to 119 pm these radii are 14-18 percent larger than the effective ionic radii. [Pg.310]

The active site on the surface of selective propylene ammoxidation catalyst contains three critical functionalities associated with the specific metal components of the catalyst (37—39) an a-H abstraction component such as Sb ", or Te" " an olefin chemisorption and oxygen or nitrogen insertion component such as Mo " or and a redox couple such as Fe " /Fe " or Ce " /Ce" " to enhance transfer of lattice oxygen between the bulk and surface... [Pg.183]

Hydrometallurgical Flow Sheets. The various hydrometallurgy operations can be combined in many ways to design processes appropriate for specific metals. [Pg.172]

Other methods of metal powder manufacture are also employed for specific metals. Selective corrosion of carbide-rich grain boundaries in stainless steel, a process called intergranular corrosion, also yields a powder. [Pg.182]

The limit of 1 ppm mercury placed on colors intended for use in foods was estabUshed by a letter from the Acting Director of the Division of Colors and Cosmetics to the certified color manufacturers in 1970. This action was the first step taken to replace the somewhat nebulous heavy metals specifications previously used with concrete limits for specific metals. [Pg.442]

Ideally, to ensure the complete removal of the metal ions from the aqueous phase, the complexant and the metal complex should remain in the hydrophobic phase. Thus, the challenges for separations include the identification of extractants that quantitatively partition into the IL phase and can still readily complex target metal ions, and also the identification of conditions under which specific metal ion species can be selectively extracted from aqueous streams containing inorganic complexing ions. [Pg.73]

The shortcomings of such a code are mainly attributable to the limited number of environments considered because specific behaviour is generally related to specific metal/electrolyte behaviour which can result in substantial potential changes or even polarity reversals. A polarity reversal implies a large potential at one or both metal electrodes and may be attributed to two main factors ... [Pg.461]

In a very few cases there are inhibitors that have been developed for the protection of specific metals, e.g. sodium mercaptobenzothiazole and benzotriazole for preventing the corrosion of copper. [Pg.779]

In acid-base titrations the end point is generally detected by a pH-sensitive indicator. In the EDTA titration a metal ion-sensitive indicator (abbreviated, to metal indicator or metal-ion indicator) is often employed to detect changes of pM. Such indicators (which contain types of chelate groupings and generally possess resonance systems typical of dyestuffs) form complexes with specific metal ions, which differ in colour from the free indicator and produce a sudden colour change at the equivalence point. The end point of the titration can also be evaluated by other methods including potentiometric, amperometric, and spectrophotometric techniques. [Pg.311]

Dyestuffs which form complexes with specific metal cations can serve as indicators of pM values 1 1-complexes (metal dyestuff = 1 1) are common, but l 2-complexes and 2 1-complexes also occur. The metal ion indicators, like EDTA itself, are chelating agents this implies that the dyestuff molecule possesses several ligand atoms suitably disposed for coordination with a metal atom. They can, of course, equally take up protons, which also produces a colour change metal ion indicators are therefore not only pM but also pH indicators. [Pg.315]

Entries where the oxidation state of a metal has been specified occur after all the entries for the unspecified oxidation state, and the same or similar entries may occur under both types of heading. Thus cyanide appears under Chromium complexes, Chromium(O) complexes, Chromium(I) complexes, etc. More specific entries, such as Chromium, hexacyano-, may also occur. Similar ligands may also occur in different entries. Thus a carboxylic acid-metal complex may occur under Carboxylic acid complexes, under entries for specific carboxylic acids, and under the specific metal. Coordination complexes may also be listed in the Cumulative Formula Index. [Pg.73]

The most appropriate experimental procedure is to treat the metal in UHV, controlling the state of the surface with spectroscopic techniques (low-energy electron diffraction, LEED atomic emission spectroscopy, AES), followed by rapid and protected transfer into the electrochemical cell. This assemblage is definitely appropriate for comparing UHV and electrochemical experiments. However, the effect of the contact with the solution must always be checked, possibly with a backward transfer. These aspects are discussed in further detail for specific metals later on. [Pg.21]

The formation of alkali-metal borides by direct synthesis requires temperatures of 750-1200°C, depending on the variety of boron utilized and the specific metal. This leads to two important consequences ... [Pg.261]

Figure 3.16 Volcano plot for the hydrogen evolution reaction (HER) for various pure metals and metal overlayers. Values are calculated at 1 barof H2 (298K) and at a surface hydrogen coverage of either 0.25 or 0.33 ML. The two curved lines correspond to the model (3.24), (3.25) transfer coefficients (not included in the indicated equations) of 0.5 and 1.0, respectively, have also been added to the model predictions in the figure. The current values for specific metals are taken from experimental data on polycrystalline pure metals, single-crystal pure metals, and single-crystal Pd overlayers on various substrates. Adapted from [Greeley et al., 2006a] see this reference for more details. Figure 3.16 Volcano plot for the hydrogen evolution reaction (HER) for various pure metals and metal overlayers. Values are calculated at 1 barof H2 (298K) and at a surface hydrogen coverage of either 0.25 or 0.33 ML. The two curved lines correspond to the model (3.24), (3.25) transfer coefficients (not included in the indicated equations) of 0.5 and 1.0, respectively, have also been added to the model predictions in the figure. The current values for specific metals are taken from experimental data on polycrystalline pure metals, single-crystal pure metals, and single-crystal Pd overlayers on various substrates. Adapted from [Greeley et al., 2006a] see this reference for more details.
Electrolytic cells are constructed of materials that can withstand the action of the electrolytes and of the electrode products. The cell may be of the open type or may be partially or fully closed, depending on the requirement of handling the electrode products. Some of these cells will be described while dealing with the production of specific metals. Very stringent requirements are imposed when considering the design of electrolytic cells for the deposition of refractory and reactive metals. Most of such metals are produced by using molten salt electrolytes. These metals are prone to atmospheric contamination at the electrolysis temperature, and it is thus necessary to operate the cell under an inert atmosphere. [Pg.702]

A series of amine-tethered nucleobases such as 8 has also been developed. These ligand systems have allowed the interaction of d-block metal ions with the N3pUrine site to be probed and an indication of base-specific metal-ion binding has begun to emerge (55-58). [Pg.102]

Tables 15 and 16 show the absorption maxima of some metal complexes of benzothiazolyl-substituted formazans 230 and 231.283 The wavelengths are metal ion dependent, making formazans useful reagents for the identification of specific metal ions or the simultaneous determination of two ions. The wavelengths are much longer than those of the formazan anion (Table 14). The general trend for electron-rich substituents is toward a larger shift this is to be expected as it tends to enhance the aromatic character of the ring and increase the covalent character of the metal — nitrogen bond. The sharpness of the absorption band has been attributed to coordination to the heterocyclic nitrogen as in 232.57S... Tables 15 and 16 show the absorption maxima of some metal complexes of benzothiazolyl-substituted formazans 230 and 231.283 The wavelengths are metal ion dependent, making formazans useful reagents for the identification of specific metal ions or the simultaneous determination of two ions. The wavelengths are much longer than those of the formazan anion (Table 14). The general trend for electron-rich substituents is toward a larger shift this is to be expected as it tends to enhance the aromatic character of the ring and increase the covalent character of the metal — nitrogen bond. The sharpness of the absorption band has been attributed to coordination to the heterocyclic nitrogen as in 232.57S...
Table 4.4 presents wastewater flow characterization for the foundry industry by casting metals. Also presented in this table is the level of process water recycle, and the number of plants surveyed with central wastewater treatment facilities for all of the processes at that plant. The discharge flow represents all processes within the specific metal casting facilities. [Pg.163]

Specific Metal, mg/L Manufacturers Guarantee Plant 19066 Plant 31022 Predicted Performance... [Pg.289]

Current reviews on biosorption are related to general approaches90-93 to diverse types of biomass such as microbial biomass, plant wastes, and agro-based waste materials, or to a specific metal.4-94-98 However, a review on metal biosorption using macrophytes biomass is not available. In this chapter, a review on the current knowledge of biosorption using preferentially nonliving biomass from aquatic plants is presented. [Pg.397]

Thus, most of the color in glass is produced by metallic ions derived from minerals, usually in relatively small amounts within the glass structure. Already in antiquity there was awareness of the effects of some other metals on the color of glass. It was known then, for example, that even relatively small amounts of specific metals, included as minerals in the components of a glass melt, could produce colored glass particular metalliferous minerals were therefore added to glass melts so as to produce special and... [Pg.146]

Fig. 8. Site-specific metal complexing dendrimers reported by Newkome et al. Fig. 8. Site-specific metal complexing dendrimers reported by Newkome et al.

See other pages where SPECIFIC METALS is mentioned: [Pg.44]    [Pg.343]    [Pg.233]    [Pg.53]    [Pg.528]    [Pg.220]    [Pg.1500]    [Pg.495]    [Pg.391]    [Pg.412]    [Pg.964]    [Pg.82]    [Pg.300]    [Pg.319]    [Pg.63]    [Pg.456]    [Pg.1]    [Pg.85]    [Pg.377]    [Pg.382]    [Pg.402]    [Pg.123]    [Pg.610]    [Pg.386]    [Pg.58]    [Pg.288]    [Pg.296]    [Pg.189]    [Pg.234]   


SEARCH



2,2 :6 ,2”-Terpyridine specific metals

Carbon monoxide adsorption specific metals

Corrosion Specifics at the Metal-Polymer Interface

Cytochrome bci Metal Cofactor Specifics

Formation of Specific Metal Complexes in Nanometric Zeolite Pores

Heavy metals specific substances

Hydride complexes specific metals

METAL-ORGANIC FRAMEWORKS specificity

Metal Cofactor Specifics

Metal cation specific

Metal cation specific carriers

Metal interaction chromatography amino acid specificity

Metal specific sequestering agents

Metal specificity

Metal specificity

Metal specifity

Metal specifity

Metal-carbonyl clusters specific metals

Metal-support interaction specific catalysts

Metals specific gravities

Metals specific heat Table

Metals specific heat values

Metals specific heats 157 spontaneous ignition

Metals, heavy specific compound

Organometallic compounds specific metals

Properties of Specific Metals

Rare earth metal specific

Site-Specific Internal Functionalization of Nucleic Acids with Transition-Metal Ligands and Other Moieties

Specific Insight for Removal of Mixed Heavy Metals, Including Cr, As, and Hg

Specific Material Considerations—Metals

Specific Metal Coatings

Specific acid catalysis of acetals, metals and glycosides

Specific aspects of metals

Specific heat metals

Specific heat of metals

Specific heat simple metals

Specific heat transition metals

Specific heat transitional metals

Specifications chemicals/metals

Specificity of metal ions

Specifics of Actinide Metal Preparation

Supported metals, small particles specific catalysts

Supported transition metal complex catalysts specificity

The General, Selective, and Specific Formation of Complexes by Metallic

Transition metal clusters specific types

Transition metal ions specific element

Transition metals specific element

Transition metals specificity

Trefoil Knots as Transition Metal Ligands - Specific Kinetic, Electrochemical, and Photochemical Properties

Trifluoroacetate compounds Metal trifluoroacetates, specific

© 2024 chempedia.info