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Intercalation of hydrogen

A mathematical model describing the processes of AC charging-discharge with account for EDL charging, intercalation of hydrogen into carbon, and its nonsteady-state solid-phase diffusion, electrode kinetics, ion transport over the electrode thickness, and characteristics of its porous structure was developed and confirmed experimentally. It is shown that the maximum path of diffusion of hydrogen atoms all other conditions being equal is inversely proportional to the hydrophilic specific surface area of the electrode. [Pg.289]

A wider application of ruthenium oxide capacitors is hindered by the high cost of ruthenium oxide. Attempts have been reported, therefore, to substitute ruthenium oxide with other, cheaper materials capable of intercalation and deintercalation of hydrogen and/or other ions. Promising results with pseudocapacities of about 100 F/g have been obtained with the mixed oxides of ruthenium and vanadium and also with mixed oxides on the basis of manganese oxide. [Pg.373]

Ihmels H, Otto D (2005) Intercalation of Organic Dye Molecules into Double-Stranded DNA - General Principles and Recent Developments. 258 161-204 Iida H, Krische MJ (2007) Catalytic Reductive Coupling of Alkenes and Alkynes to Carbonyl Compounds and Imines Mediated by Hydrogen. 279 77-104 Imai H (2007) Self-Organized Formation of Hierarchical Structures. 270 43-72 Indelli MT, see Chiorboli C (2005) 257 63-102 Inoue Y, see Borovkov VV (2006) 265 89-146 Ishii A, Nakayama J (2005) Carbodithioic Acid Esters. 251 181-225 Ishii A, Nakayama J (2005) Carboselenothioic and Carbodiselenoic Acid Derivatives and Related Compounds. 251 227-246... [Pg.260]

Furthermore, it is often possible to extract from the structural analysis of solid solvates a significant information on solvation patterns and their relation to induced structural polymorphism. An interesting illustration has been provided by crystal structure determinations of solvated 2,4-dichloro-5-carboxy-benzsulfonimide (5)35). This compound contains a large number of polar functions and potential donors and acceptors of hydrogen bonds and appears to have only a few conformational degrees of freedom associated with soft modes of torsional isomerism. It co-crystallizes with a variety of solvents in different structural forms. The observed modes of crystallization and molecular conformation of the host compound were found to be primarily dependent on the nature of the solvent environment. Thus, from protic media such as water and wet acetic acid layered structures were formed which resemble intercalation type compounds. [Pg.16]

The intercalated catalysts can often be regarded as biomimetic oxidation catalysts. The intercalation of cationic metal complexes in the interlamellar space of clays often leads to increased catalytic activity and selectivity, due to the limited orientations by which the molecules are forced to accommodate themselves between sheets. The clays have electrostatic fields in their interlayer therefore, the intercalated metal complexes are more positively charged. Such complexes may show different behavior. For example, cationic Rh complexes catalyze the regioselective hydrogenation of carbonyl groups, whereas neutral complexes are not active.149 Cis-Alkenes are hydrogenated preferentially on bipyridyl-Pd(II) acetate intercalated in montmorillonite.150 The same catalyst was also used for the reduction of nitrobenzene.151... [Pg.258]

Fullerene showed antibacterial activity, which can be attributed to different interactions of C60 with biomolecules (Da Ros et al., 1996). In fact, there is a possibility to induce cell membrane disruption. The fullerene sphere seems not really adaptable to planar cellular surface, but for sure the hydrophobic surface can easily interact with membrane lipids and intercalate into them. However, it has been demonstrated that fullerene derivatives can inhibit bacterial growth by unpairing the respiratory chain. There is, first, a decrease of oxygen uptake at low fullerene derivative concentration, and then an increase of oxygen uptake, which is followed by an enhancement of hydrogen peroxide production. The higher concentration of C60 seems to produce an electron leak from the bacterial respiratory chain (Mashino et al., 2003). [Pg.10]


See other pages where Intercalation of hydrogen is mentioned: [Pg.86]    [Pg.351]    [Pg.417]    [Pg.503]    [Pg.202]    [Pg.213]    [Pg.12]    [Pg.289]    [Pg.1568]    [Pg.86]    [Pg.203]    [Pg.92]    [Pg.86]    [Pg.351]    [Pg.417]    [Pg.503]    [Pg.202]    [Pg.213]    [Pg.12]    [Pg.289]    [Pg.1568]    [Pg.86]    [Pg.203]    [Pg.92]    [Pg.308]    [Pg.160]    [Pg.967]    [Pg.400]    [Pg.403]    [Pg.316]    [Pg.201]    [Pg.443]    [Pg.468]    [Pg.819]    [Pg.194]    [Pg.332]    [Pg.115]    [Pg.1219]    [Pg.258]    [Pg.447]    [Pg.392]    [Pg.396]    [Pg.433]    [Pg.261]    [Pg.277]    [Pg.456]    [Pg.534]    [Pg.362]    [Pg.421]    [Pg.41]    [Pg.195]    [Pg.196]    [Pg.330]    [Pg.508]    [Pg.56]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.3 , Pg.4 , Pg.6 , Pg.10 ]

See also in sourсe #XX -- [ Pg.12 , Pg.288 ]




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Hydrogen intercalation

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