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Carbon activation filaments

Busofit is a universal adsorbent, which is efficient to adsorb different gases (H2, N2, 02, CH4, and NH3). Figure 2 shows the texture of the active carbon fiber filament. The carbon fiber refers to microporous sorbents with a developed surface and a complicated bimodal structure. The material can be performed as a loose fibers bed or felt or as monolithic blocks with binder to have a good thermal conductivity along the filament. [Pg.635]

Various adsorbents are normally used for this process such as iron oxides, activated carbon and filamentous fungal biomass. During the last years, there was a growing interest in the use of biomaterials for the sorption and preconcentra-fion of heavy metals from water. Yeast biomass was tested for the speciation of methylmercury and Hg (II) [7]. Carbon nanotubes grown on granulated activated carbon (GAC) were applied since it is said to be a potential adsorbent for heavy metal removal in water treatment. [Pg.88]

Fig. 11. The loss of carbon rapidly increases with the increase of temperature. Heating of the catalysts in open air for 30 minutes at 973 K leads to the total elimination of carbon from the surface. The gasification of amorphous carbon proceeds more rapidly than that of filaments. The tubules obtained after oxidation of carbon-deposited catalysts during 30 minutes at 873 K are almost free from amorphous carbon. The process of gasification of nanotubules on the surface of the catalyst is easier in comparison with the oxidation of nanotubes containing soot obtained by the arc-discharge method[28, 29]. This can be easily explained, in agreement with Ref [30], by the surface activation of oxygen of the gaseous phase on Co-Si02 catalyst. Fig. 11. The loss of carbon rapidly increases with the increase of temperature. Heating of the catalysts in open air for 30 minutes at 973 K leads to the total elimination of carbon from the surface. The gasification of amorphous carbon proceeds more rapidly than that of filaments. The tubules obtained after oxidation of carbon-deposited catalysts during 30 minutes at 873 K are almost free from amorphous carbon. The process of gasification of nanotubules on the surface of the catalyst is easier in comparison with the oxidation of nanotubes containing soot obtained by the arc-discharge method[28, 29]. This can be easily explained, in agreement with Ref [30], by the surface activation of oxygen of the gaseous phase on Co-Si02 catalyst.
The activity and stability of catalysts for methane-carbon dioxide reforming depend subtly upon the support and the active metal. Methane decomposes to carbon and hydrogen, forming carbon on the oxide support and the metal. Carbon on the metal is reactive and can be oxidized to CO by oxygen from dissociatively adsorbed COj. For noble metals this reaction is fast, leading to low coke accumulation on the metal particles The rate of carbon formation on the support is proportional to the concentration of Lewis acid sites. This carbon is non reactive and may cover the Pt particles causing catalyst deactivation. Hence, the combination of Pt with a support low in acid sites, such as ZrO, is well suited for long term stable operation. For non-noble metals such as Ni, the rate of CH4 dissociation exceeds the rate of oxidation drastically and carbon forms rapidly on the metal in the form of filaments. The rate of carbon filament formation is proportional to the particle size of Ni Below a critical Ni particle size (d<2 nm), formation of carbon slowed down dramatically Well dispersed Ni supported on ZrO is thus a viable alternative to the noble metal based materials. [Pg.463]

In contrast to the Pt catalysts discussed above, Ni based catalysts (i.e., also when supported on ZrO usually form coke at such a rapid rate that most fixed bed reactors are completely blocked after a few minutes time on stream (see Fig. 8) [16], The coke formed with the Ni catalysts is filamentous. The Ni particle remaining at the tip of the filament hardly deactivates as the coke formed on its surface seems to be transported through the metal particle into the carbon fibre, but the drastic increase in volume causes reactor plugging and prevents use of the still active catalyst (see Fig. 8). The TEM photographs indicate that the carbon filaments have similar diameters to those of the Ni particles. [Pg.471]

On the surface of the Ni catalyst, carbon is normally produced in a whisker (or filamentous) form. According to Rostrup-Nielsen, carbon formation is avoided when the concentration of carbon dissolved in Ni crystal is smaller than that at the equilibrium. The steady-state activity is proportional to [C ], which can be expressed by the following equation ... [Pg.44]

At higher temperatures, out of the typical FT regime, carbon could encapsulate the active metal, thereby blocking access to reactants. In extreme cases carbon filaments can also be formed that can result in the breakup of catalyst particles.42... [Pg.53]

A critical factor for biotechnology application is the stability of the enzyme electrode. Hydrogenase immobilized into carbon filament material has high level of both operational and storage stability. Even after the half year of storage with periodical testing, the enzyme electrode preserved more than 50 % of its initial activity [9,10], Thus, it is possible to achieve appropriate stability of the enzyme electrode, suitable for hydrogen fuel cells development. [Pg.38]


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Activated carbon filaments

Filamentous carbon

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