Big Chemical Encyclopedia

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

Articles Figures Tables About

Role of the surface

Discuss the role of the surface free-energy in phenomena such as alloy segregation, surface reconstruction, faceting and sintering of small particles. How does a gas environment (air, vacuum) affect the surface composition of alloys ... [Pg.406]

In order to clarify the role of the surface field strength, we have plotted the values of Aq against E [see Fig. 4(A) [29]]. Surprisingly, all the data lie on a straight line despite the large differences in sizes, charges, and even structures, as seen in the figure. A similar linear plot was also obtained for the polyanion transfer at the 1,2-DCE/W interface [30]. [Pg.44]

Monitoring and controlling pesticides in water (the way it was done in Russia and all other countries) does not give a true picture of the danger of pesticides in bodies of water, since it does not take into account the distribution of pesticides within the water mass layers [1,3]. The concentration of pesticides in the thin layer of water near the surface can be hundreds ( ) of times higher than in the rest of the water mass. The role of the surface layer is exceptionally important, not only for substance exchange between the atmosphere and the water, but also for the lives of many hydro organisms. [Pg.34]

This mechanism is based on the known importance of hydroxides in other deposition reactions, such as the anomalous codeposition of ferrous metal alloys [38-39], Salvago and Cavallotti claim an analogy with the mechanism of Ni2 + reduction from colloids in support of their proposed mechanism. There is no direct evidence for the hydrolyzed species, however. Furthermore, the mechanism does not explain two experimentally observed facts Ni deposition will proceed if the Ni2 + and the reducing agent are in separate compartments of a cell [36, 37] and P is not deposited in the absence of Ni2 +. The chemical mechanism does not take adequate account of the role of the surface state in catalysis of the reaction. It has no doubt been the extreme oversimplification, by some, of the electrochemical mechanism that has led other investigators to reject it. [Pg.256]

Adsorption may influence precipitation by means other than the processes mentioned above. Davies (Chapter 23) discusses the role of the surface as a catalyst for oxidation of adsorbed Mnz+. Redox reactions may contribute substantially to the formation of manganese oxide coatings on mineral surfaces in soils and sediments. [Pg.13]

DMFC modeling thus aims to provide a useful tool for the basic understanding of transport and electrochemical phenomena in DMFC and for the optimization of cell design and operating conditions. This modeling is challenging in that it entails the two-phase treatment for both anode and cathode and that both the exact role of the surface treatment in backing layers and the physical processes which control liquid-phase transport are unknown. [Pg.517]

Notably, the role of the surface of the metal oxide is not merely that of another reaction medium but also that of allowing a specific reactivity, including yields and in particular selectivity. [Pg.17]

Augustynski J (1993) The role of the surface intermediates in the photoelectrochemical behavior of anatase and rutile Ti02. Electochim Acta 38 43-46... [Pg.247]

Role of the surface free energy or surface tension 381... [Pg.379]

It is noteworthy that recent advances in the electrochemistry of silver are related more to the role of the surface of Ag electrodes, than to the investigations of Ag compounds in solutions. [Pg.914]

With respect to the catalytic phenomena, it is hoped that an insight in the role of the surface at the first steps of activation of a reacting mole-... [Pg.81]

A catalytic reaction is in general composed of a series of elementary processes, and the surface atoms are necessarily involved in making intermediates and/or activated complexes, as well as in the adsorption of reactant and product molecules. For this reason, the participation of surface atoms is indispensable in all of the elementary processes accomplishing the catalysis, but the kinetics are mainly influenced by the manner of the participation of surface atoms in the rate-determining steps. Accordingly, in order to make clear the roles of the surface atoms in catalysis, it should be clarified how the surface atoms participate in the rate-determining steps as well as in the other elementary processes. [Pg.99]

Hydrogenation of olefins is a good example for demonstrating the roles of the surface atoms in catalysis. The orbital symmetry rule in chemical reactions suggests that the highest occupied molecular orbital (HOMO) of one reaction partner and the lowest unoccupied molecular orbital (LUMO) of the other should meet the symmetry requirements. In this respect, a concerted addition of an H2 molecule to the double bond of an olefin, that is, a molecular addition reaction, is a forbidden process. Adsorption of olefin on transition metal surfaces undoubtedly changes the population of electrons in the HOMO (7tu) and the LUMO (re ) as shown schematically in Fig. 1. In spite of such perturbation of the electron densities of the HOMO and the... [Pg.99]

Jan, K.-M. Role of the Surface Charge in Red Blood Cell Interactions ... [Pg.43]

Investigations on single crystal faces are obviously not of direct interest in technology, but they are essential to again insight into the role of the surface structure. In... [Pg.26]

Surface films appear to play a major role in the initiation of SCC and may also contribute to hydrogen embrittlement effects. It is assumed that the main role of the surface film is to localize the damage inflicted on the material by the environment. This can be caused by mechanical breakdown of the protective film by slip step or electromechanical breakdown of the passive film.95 SCC may be related to the nature of the surface film. It has been observed that the SCC of C-Steels is related to the presence of magnetite in several low -temperature environments (around 90°C), except... [Pg.442]

To understand the role of the surface silanols and their contribution to retention, these compounds were separated on a column that was purposely coated to half of the Cjg level of the original Clg (Fig. 5-21b) (coated column had approximately 50% silanol content). If peak tailing is due solely to the silanol interaction, the peak symmetry should be worse than on the fully coated column. But there was no decrease in peak symmetry. In fact, retention of the tetracaine (peak 4) increased slightly while the peak symmetry improved. Thus, it appears that silanols do contribute to retention but the amount of silanols is not the main cause of peak asymmetry. The logical extension of this approach is to separate the compounds on unbonded silica gel, as shown in Figure 5-27c. In this situation, peak symmetry is quite good and retention is decreased. [Pg.165]

It seems quite possible to use some theoretical parameters, e.g. Cc or C for detecting transitions between the different phase states of the foam bilayers. Comparing these transitions with the corresponding phase transitions in bulk surfactant solutions would allow a deeper insight into the molecular interactions in biostructures and into the role of the surface forces in biomembrane formation, stability and fusion. Foam bilayers could also be used as a model for the investigation of reverse micelles and enzyme-substrate interactions which are top problems in biology. [Pg.262]

Koebnik, R. (1999). Structural and functional roles of the surface-exposed loops of the /3-barrel membrane protein OmpA from Escherichia coli.J. Baderiol. 181, 3688-3694. [Pg.67]

Thus, the proposed method for analyzing the kinetics of defect formation, based on the quasi-epitaxy model, clearly demonstrates the role of the surface in the ADC equilibrium and allows one to assess the effects of temperature and Jb of the equilibration of defect concentrations. Computer simulations of defect formation kinetics in II-VI crystal non-equilibrium chalcogen vapor systems indicate that steady state defect concentrations in the surface layer are reached very rapidly and, accordingly, are not... [Pg.35]

The role of the surface oxide was mainly in influencing the accessibility of the metal to the molybdenum disulphide. With copper, for example, the oxygen is not strongly bonded to the metal and can be displaced. On the other hand, with titanium the oxide is strongly held, but lattice vacancies are present which expose titanium metal to the molybdenum disulphide. [Pg.73]

In these studies the role of the surface, the sample temperature and the sample structure (defects, voids and crystallinity) appear to be important but require further study. As mentioned earlier, void formation has been imaged when ice is placed in an electron microscope. However, the relationship between the formation of interior surfaces and O2 production has not been studied, although it appears that O2 may be formed more efficiently at a surface. [Pg.405]


See other pages where Role of the surface is mentioned: [Pg.176]    [Pg.360]    [Pg.227]    [Pg.699]    [Pg.515]    [Pg.517]    [Pg.577]    [Pg.588]    [Pg.590]    [Pg.652]    [Pg.200]    [Pg.98]    [Pg.279]    [Pg.259]    [Pg.268]    [Pg.23]    [Pg.205]    [Pg.245]    [Pg.12]    [Pg.510]    [Pg.512]    [Pg.388]    [Pg.205]    [Pg.147]    [Pg.33]    [Pg.519]    [Pg.609]    [Pg.1563]   
See also in sourсe #XX -- [ Pg.151 ]




SEARCH



© 2024 chempedia.info