Hydrogen association-dissociation

Hydrogen adsorbs dissociatively on almost all metals. At 500 K the H atoms diffuse freely over the surface. Desorption occurs associatively by recombination of two H atoms, while desorption of atomic hydrogen can be ignored. 

Just as in the case of (16), an equation of the form (20) applies to any other association-dissociation reaction in which one of the dissociated species is mobile, the other fixed. When the two species are distinct but both mobile, as for hydrogen combining with, say, an interstitial silicon, a similar line of reasoning, whose details we omit, leads to equations of the same form as (16) and (20) but with D+ replaced by the sum of the diffusion coefficients of the two species. When the two mobile species are the same, as for the reaction H° + H° 5H2, it turns out that nA and n+ should each be replaced by the monatomic density n, D+ by the monatomic diffusion coefficient, and 4ir by 8tt in (16) but not in (20). 

Ethylenediaminetetraacetic acid is frequently symbolized H4Y, and the disodium salt, Na2H2Y. The hydrogens in these formulas are the acidic hydrogens associated with the carboxyl groups, as in any weak organic carboxylic acid they dissociate from the EDTA ion in a series of equilibrium steps ... 

Various types of possible interactions between reactions are discussed. Some of them are united by the general idea of chemical reaction interference. The ideas on conjugated reactions are broadened and the determinant formula is deduced the coherence condition for chemical interference is formulated and associated phase shifts are determined. It is shown how interaction between reactions may be qualitatively and quantitatively assessed and kinetic analysis of complex reactions with under-researched mechanisms may be performed with simultaneous consideration of the stationary concentration method. Using particular examples, interference of hydrogen peroxide dissociation and oxidation of substrates is considered. 

In the framework of the theory of elementary open catalytic system self-development suggested by Rudenko [59] evolutionary changes in homogeneous catalytic systems based on hydrogen peroxide dissociation are indicated [60], Hence, it is suggested that formation of amino acids, for example, is associated with the transformation of components in the... 

Increasing the CO partial pressure decreases the hydro-formylation reaction rate and the amount of alkene isomerization side reactions (see Hydrogenation Isomerization ofAlkenes), while increasing the aldehyde linear to branched product ratio. Pino proposed that the apparent marked difference between HCo(CO)4-catalyzed hydroformylation at low and high CO partial pressures was due to the existence of two active catalyst species, HCo(CO)4 and HCo(CO)3, formed from the CO association/dissociation equilibrium shown in... 

If a titratable group on a protein molecule can combine with substances, other than hydrogen ions, which may be present in a protein solution, then its titration properties will be altered. If the combining substance is present at a thermodynamic activity an, and if it combines with the basic form of the titratable group only, the equilibrium constant for association being ku, then the apparent hydrogen ion dissociation constant Xapp of the group becomes... 

Some key adsorbates and reaction intermediates relevant to fuel-cell anodes are H2 as the fuel, CO and CO2 as poisons in hydrogen reformate feeds, and water as a co-adsorbate and potential oxidant. In the case of the cathode, oxygen is clearly the most important reactant. In the case of a number of these molecules, such as H2, O2, and H2O, not only is the molecular adsorption important on platinum (or promoted platinum catalysts), but the dissociative adsorption of the molecules is important as well. With this in mind, some details concerning the dynamics of adsorption of these molecules, the associated dissociation barriers, molecular degrees of freedom, and energy partition are important to the overall catalytic processes. In addition to the... 

COX, B.G., PRUDEN, B.B., JEJE, A.A., Ceramic Reactor/Exchanger for H2S Dissociation, (Proc. 7th Canadian Hydrogen Workshop, 1995, Quebec City), MEHTA, S.K., BOSE, T.K. (Ed.), Canadian Hydrogen Association (1995) 329-352. 

The experiments described above have led to the conclusion that the chiral-induced equilibrium shift could be induced in the lanthanide (III) complex by a combination of electrostatic and hydrophobic interactions. Hydrogen bonding effects appear to be less important as suggested by experiments carried out under variable pH, temperature, concentration, solvent type, and solution dielectric constant conditions. By analogy to the associated/dissociated equilibrium shift models of Schipper (1978) in which the source of the equilibrium perturbation is attributed to a free energy of mixing, Brittain (1981) and Wu et al. (1989) attempted to ascertain the complex mechanism responsible for this type of Pfeiffer effect. However, their conclusions were opposite as they concluded that the [Tb(DPA)3] complex interacted with the... 

Physical cross-linking is easily incorporated into the structures of supramolecular side-chain polymers by using bi- or multifunctional molecules [9,31,93]. The complexation of the functionalized polyacrylates, a stilbazole, and bipyridine molecules form supramolecular side-chain cross-linked polymer 37 (Figure 27) [31,93]. Bis-imidazolyl compounds are also used for such cross-linking [105]. Reversible association-dissociation of the hydrogen bonding leads to the reversible thermal order-disorder transitions, which is an important feature of supramolecular materials. Liquid-crystalline main-chain supramolecular networks have been prepared from multifunctional components [32,123-126], which will be described in Section IV. 

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