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Graphite catalytic activity

Solid Superacids. Most large-scale petrochemical and chemical industrial processes ate preferably done, whenever possible, over soHd catalysts. SoHd acid systems have been developed with considerably higher acidity than those of acidic oxides. Graphite-intercalated AlCl is an effective sohd Friedel-Crafts catalyst but loses catalytic activity because of partial hydrolysis and leaching of the Lewis acid halide from the graphite. Aluminum chloride can also be complexed to sulfonate polystyrene resins but again the stabiUty of the catalyst is limited. [Pg.565]

In this contribution it is shown that local density functional (LDF) theory accurately predicts structural and electronic properties of metallic systems (such as W and its (001) surface) and covalently bonded systems (such as graphite and the ethylene and fluorine molecules). Furthermore, electron density related quantities such as the spin density compare excellently with experiment as illustrated for the di-phenyl-picryl-hydrazyl (DPPH) radical. Finally, the capabilities of this approach are demonstrated for the bonding of Cu and Ag on a Si(lll) surface as related to their catalytic activities. Thus, LDF theory provides a unified approach to the electronic structures of metals, covalendy bonded molecules, as well as semiconductor surfaces. [Pg.49]

From these results there is evidence that it is possible to vise well-defined graphite intercalates as precursors for deliberate deintercalation, yielding a multiphasic supported material which is catalytically active. [Pg.483]

The first catalysts reported for the electroreduction of C02 were metallophthalocyanines (M-Pc).126 In aqueous solutions of tetraalkylammonium salts, current-potential curves at a cobalt phthalocyanine (Co-Pc)-coated graphite electrode showed a reduction current peak whose height was proportional to the C02 concentration and to the square root of the potential sweep rate at a given C02 concentration. On electrolysis, oxalic acid and glycolic acid were detected, but formic acid was not. Mn and Pd phthalocyanines were inactive, while Cu and Fe phthalocyanines were slightly active. At the potentials used for C02 reduction, M-Pc catalysts would be in their dinegative state, and the occupied dz2 orbital of the metal ion in the metallophthalocyanine was suggested to play an important role in the catalytic activity. [Pg.368]

It has been recently demonstrated that the simplest of the cobalt porphyrins (Co porphine) adsorbed on a pyrolytic graphite electrode is also an efficient electrocatalyst for reduction of 02 into 1120.376 The catalytic activity was attributed to the spontaneous aggregation of the complex on the electrode surface to produce a structure in which the cobalt-cobalt separation is small enough to bridge and activate 02 molecules. The stability of the catalyst is quite poor and largely improved by using porphyrin rings with mew-substitu-tion.377-380 Flowever, as the size of the mew-substituents increases the four-electron reduction efficiency decreases. [Pg.494]

A similar catalytic activity with a monomeric porphyrin of iridium has been observed when adsorbed on a graphite electrode.381-383 It is believed that the active catalyst on the surface is a dimeric species formed by electrochemical oxidation at the beginning of the cathodic scan, since cofacial bisporphyrins of iridium are known to be efficient electrocatalysts for the tetraelectronic reduction of 02. In addition, some polymeric porphyrin coatings on electrode surfaces have been also reported to be active electroactive catalysts for H20 production, especially with adequately thick films or with a polypyrrole matrix.384-387... [Pg.494]

The mechanisms and reasons of catalytic activity of polyaniline (PANI)-type conducting polymers toward oxygen reduction in acidic and saline solutions are investigated by electrochemical and quantum-chemical methods. The PANI/thermally expanded graphite compositions were developed for realization of fully functional air gas-diffusion electrodes. Principally new concept for creation of rechargeable metal-air batteries with such type of catalysts is proposed. The mockups of primary and rechargeable metal-air batteries with new type of polymer composite catalysts were developed and tested. [Pg.110]

Conducting polymers, polyaniline, catalytic activity, PANI/expanded graphite composites, metal-air batteries, primary rechargeable cells. [Pg.110]

Analysis of data presented clearly suggests that a sharp increase of catalytic activity takes place in relatively thin layer of PANI, which corresponds to the mass of about 0.6...0.9 mg (or Q=108...164 mC) per geometric surface of electrode (0.5 cm2). Further increase of PANI thickness (or mass) cannot increase enough the catalytic activity of porous electrode. That is the reason why the developed by us PANI/graphite composites have relatively high content of graphite (Table 4). [Pg.117]

If graphite A has catalytic activity in these reactions, the amount of graphite could be reduced, and 0.5 g (instead of 5 g) of graphite A was, indeed, sufficient to promote these reactions (Tab. 7.8) [66]. In the process in which a small amount of graphite was used ... [Pg.238]

For example, Asuri and his co-workers (Asuri et al., 2007) reported that the proteases attached to the surface of SWCNTs can create self-cleaning surfaces that resist protein adsorption. This kind of SWCNT-enzyme composite exhibited 30 times higher overall catalytic activity than control composites where the proteases were conjugated to a non-nanoscale graphite support. Importantly, the enzymes preserved more than 90% of their initial activity over 30% days in the liquid buffer, with only negligible amounts of enzymes leaching out. The result demonstrates that the nanocomposites of SWCNTs and polymers can act as hosts for enzymes and can prevent protein contamination on the surface of medical devices. We consider that SWCNTs may have the function as biocatalyst to improve the enzyme activity attached to the surface of CNTs. Our previous work also indirectly hints that CNTs could improve the bioactivity of enzymes such as Taq enzyme Cui et al. (2004). However, there are also adverse reports. CNTs can... [Pg.187]

Many noble metal nanoparticles (with Ru, Au, Pd, Pt, Os, Ag, Ir, Rh) have been deposited on CNTs and their catalytic activity towards a set of different reactions explored, showing the benefit of the presence of the graphitic support for catalysis. [Pg.62]

Nitrogen doping has repeatedly been reported to increase the basic nature [182, 183] and catalytic activity [184,185] of the graphitic carbon which is attributed to the... [Pg.379]


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See also in sourсe #XX -- [ Pg.417 , Pg.437 , Pg.441 ]




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Catalytic graphitization

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