Surface alumina

Surface heterogeneity may be inferred from emission studies such as those studies by de Schrijver and co-workers on P and on R adsorbed on clay minerals [197,198]. In the case of adsorbed pyrene and its derivatives, there is considerable evidence for surface mobility (on clays, metal oxides, sulfides), as from the work of Thomas [199], de Mayo and co-workers [200], Singer [201] and Stahlberg et al. [202]. There has also been evidence for ground-state bimolecular association of adsorbed pyrene [66,203]. The sensitivity of pyrene to the polarity of its environment allows its use as a probe of surface polarity [204,205]. Pyrene or ofter emitters may be used as probes to study the structure of an adsorbate film, as in the case of Triton X-100 on silica [206], sodium dodecyl sulfate at the alumina surface [207] and hexadecyltrimethylammonium chloride adsorbed onto silver electrodes from water and dimethylformamide [208]. In all cases progressive structural changes were concluded to occur with increasing surfactant adsorption. 

Tonck A, Georges J M and Loubet J L 1988 Measurements of intermoiecuiar forces and the rheology of dodecane between alumina surfaces J. Coiioid interface Sc/. 126 150-5... 

They represent an improvement over earlier platinum on alumina catalysts in their abiHty to resist coke fouling when operated at low pressures. Dehydrogenation and hydrogenation occur on the active metal sites isomerization takes place on the acidic alumina surface. 

A. Tonck, J. M. Georges, J. L. Loubet. Measurements of intermolecular forces and the rheology of dodecane between alumina surfaces. J Colloid Interface Sci 72(5 150-163, 1988. 

There is little data available to quantify these factors. The loss of catalyst surface area with high temperatures is well-known (136). One hundred hours of dry heat at 900°C are usually sufficient to reduce alumina surface area from 120 to 40 m2/g. Platinum crystallites can grow from 30 A to 600 A in diameter, and metal surface area declines from 20 m2/g to 1 m2/g. Crystal growth and microstructure changes are thermodynamically favored (137). Alumina can react with copper oxide and nickel oxide to form aluminates, with great loss of surface area and catalytic activity. The loss of metals by carbonyl formation and the loss of ruthenium by oxide formation have been mentioned before. 

Intermolecular Forces and the Rheology of Dodecane Between Alumina Surfaces, J. Colloid Interface Sci., Vol. 126, No. 1, 1988, pp. 150-163. 

Having calculated the force for a particular event the slip is calculated using the bush model and hence the energy dissipation is obtained. Using the factors of the abrasion equation, determined with the LAT 100 on an alumina surface the abrasion loss for each event is calculated. The forces are different for a driven and a nondriven axle and accordingly different abrasion rates will result. 

Lanthanum oxide is valence invariant, and does not exhibit any oxygen storage capacity, but it effectively stabilizes 5/-AI2O3. It spreads over the alumina surface and provides a barrier against dissolution of rhodium in the support. 

The carbonate can also be compared with adsorbed formate species prepared by reacting methanol with the alumina surface at 350 C ( ). The spectrum for adsorbed formate. Figure 4d, shows the asymmetric carboxylate stretches at 1565 and 1440 cm l respectively, the CH stretch at 2832 cm , and the CH bending mode at 1505 cm . The Al-OC stretching mode is seen at 1060 cm", and the out-of-plane deformation at 750 cm . The signal to noise ratio in the low frequency end of the spectrum is insufficient to see the planar deformation, which should occur around 630 cm . It should be noted that the carbonate and formate species are very similar, the main distinction being the vibrations associated with the CH bond. 

This interpretation of the experimental data is supported by the differences observed in the deactivation patterns and carbon contents after test, since one notorious effect of Hjp is the capacity to diminish the deactivation caused by coke deposition on the active sites [21,22]. This is supposed to be due to a reaction with the coke precursors, very likely a hydrogenolysis. In pure silica-aluminas, where no source of spillover is present, no special protection against deactivation should be observed. Indeed, the silica-aluminas lose most of their activity (about 80%) before reaching the steady-state and present the highest carbon contents after catalytic test. On the other hand, in the case of the mechanical mixtures, where spillover hydrogen is continuously produced by the CoMo/Si02 phase and can migrate to the silica-alumina surface, the predicted protection effect is noticed. The relative losses of activity are much lower... 

Modification of Y-AI2O3 by K cation was shown to form a potassium oxides layer. This layer blocks the alumina surface and decreases drastically (> 99%) the catalytic activity with respect to pure Y-AI2O3... 

Metal Carbonyls on a Well Defined Alumina Surface. 119... 

We start the di.scussion by an analysis of the processes occurring in wet impregnation of alumina using a solution of H2PtCI(,. The alumina surface interacts with HiPtCUby adsorption of PtCle ... 

Alumina is not widely used in modem HPLC [48]. Porous gamma alumina is prepared by dehydration and thermal treatment of crystalline bayerite [8,49]. It is available in several types with pore diameters from 6-lS nm, surface areas 70-250 m /g and pore volumes 0.2-0.3 ml/g. After conditioning with acid or base its apparent surface pH can be adjusted between pH 3-9. The alumina surface is more heterogeneous than silica containing both hydroxyl... 

The mechanism is thought to involve an interaction of the silica or alumina surface with HC1 that facilitates proton transfer. 

Fig. 3.5.7 NMR image of imbibed c-C4Fg gas in a 35 and 40% porosity Y-TZP ceramic, containing an alumina surface treatment. Adapted from Ref. [20].

Catalysts with Sn-alumina interaction were prepared by the reaction of the lithiated alumina surface and SnCl4 (Scheme 7.14).243... 

Konovalova, T. A., J. Krzystek et al. (1999). 95-670GHz EPR studies of canthaxanthin radical cation stabilized on a silica-alumina surface. J. Phys. Chem. B 103 5782-5786. 

Okitsu K, Nagaoka S, Tanabe S, Matsumoto H, Mizukoshi Y, Nagata Y (1999) Sonochemical preparation of size-controlled palladium nanoparticles on alumina surface. Chem Lett 28 271-272... 

Another approach to cyclic nitronates has been developed by Rosini et al. in which nitro-aldol and subsequent cyclization is used as a key step. For example, 2,3-epoxy aldehydes react with ethyl nitroacetate on alumina surface in the absence of solvent to give 4-hydroxyisoxazoline 2-oxides in good yields (Eq. 8.80).130... 

It is also possible to form radical cations and radical anions on the same alumina or silica-alumina surface (88). One of the more interesting observations was that a marked enhancement of the radical anion spectrum for trinitrobenzene results when perylene is adsorbed on an alumina surface, and similarly the radical cation signal is reenforced by adsorption of trinitrobenzene. The linewidths of the spectra confirm that the radical ions are separated by a distance greater than 10 A. This means that the electron must be transfered through the lattice or that the ions separate after the transfer step, which seems unlikely. Oxygen was still required for the formation of the radical cation. 

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