Porous structure carbon

Puziy AM, Poddubnaya OI, Martmez-Alonso A, Suarez-Garcfa F, and Tascon JMD. Synthetic carbons activated with phosphoric acid-II. Porous structure. Carbon, 2002 40(9) 1507-1519. 

In general, the presence of impurities determines the extent of the rate of desorption of adsorbed peroxide, although the catalytic peroxide ehmination effect decreases during the electrode operation. For porous structured carbons this effect can be due to the buildup of a substantial amount of peroxide in the solution within pores. Furthermore, the high peroxide concentration contributes to increasing the 2 radical ion and OH radical concentration within the pores via the following equilibrium ... 

Daley, M. A., Tandon, D., Economy, J. and Hippo, E. J., Elucidating the porous structure of activated carbon fibers using direct and indirect methods. Carbon, 1996,34(10), 1191 1200. 

Adsorbents, and activated carbon in particular, are typically characterized by a highly porous structure. Adsorbents with the highest adsorption capacity for gasoline or fuel vapors have a large pore volume associated with pore diameters on the order of 50 Angstroms or less. When adsorption occurs in these pores, the process is comparable to condensation in which the pores become filled with hquid adsorbate. Fig. 5 depicts the adsorption process, including transfer of adsorbate molecules through the bulk gas phase to the surface of the solid, and diffusion onto internal surfaces of the adsorbent and into the pores. 

Structural carbon shapes fabricated by heating coke with a mixture of tar and pitches are porous and are made impermeable by impregnation with a resin (usually a phenolic resin). Cashew nut shell liquid resin is used when resistance to alkalis and acids is required. 

A similar, but highly porous, vitreous carbon material—reticulated vitreous carbon (RVC)—has found widespread application for flow analysis and spectro-electrochemistry (25). As shown in Figure 4-10, RVC is an open-pore ( spongelike ) material such a network combines the electrochemical properties of glassy carbon with many structural and hydrodynamic advantages. These include a very high surface area ( 66 cm2 cm-3 for the 100-ppi grade), 90-97% void volume, and a low resistance to fluid flow. 

Thermal-Gradient Infiltration. The principle of thermal-gradient infiltration is illustrated in Fig. 5.15b. The porous structure is heated on one side only. The gaseous reactants diffuse from the cold side and deposition occurs only in the hot zone. Infiltration then proceeds from the hot surface toward the cold surface. There is no need to machine any skin and densification can be almost complete. Although the process is slow since diffusion is the controlling factor, it has been used extensively for the fabrication of carbon-carbon composites, including large reentry nose cones. 

Pego AP, Siebum SB, Luyn MJAV, et al. Preparation of degradable porous structures based on 1,3-trimethylene carbonate and D,L-lactide(co)polymers for heart tissue engineering. Tissue Eng, 2003, 9, 981 994. 

The above brief analysis underlines that the porous structure of the carbon substrate and the presence of an ionomer impose limitations on the application of porous and thin-layer RDEs to studies of the size effect. Unless measurements are carried out at very low currents, corrections for mass transport and ohmic limitations within the CL [Gloaguen et ah, 1998 Antoine et ah, 1998] must be performed, otherwise evaluation of kinetic parameters may be erroneous. This is relevant for the ORR, and even more so for the much faster HOR, especially if the measurements are performed at high overpotentials and with relatively thick CLs. Impurities, which are often present in technical carbons, must also be considered, given the high purity requirements in electrocatalytic measurements in aqueous electrolytes at room temperature and for samples with small surface area. 

Figure 28. Distribution of sulfur and carbon in anodic aluminas corresponding to the different stages of porous structure growth, as determined by Auger spectroscopy.160...

Different types of activated carbon are among the most suitable materials for this purpose. For this reason specialists, involved in development of active materials for EC try to increase carbon s specific surface as much as possible and to optimize the internal structure of the carbon porous structure. 

Figures 1-3 demonstrate the effect of KOH/precursor ratio, reaction temperature and reaction time, respectively, on porous structure parameters of carbon produced by KOH activation. While the presented relationships concern mostly carbonaceous mesophase, basically they are typical of all coal and pitch-derived materials of the study.

Tamon H, Ishizaka H, Mikami M, Okazaki M. Porous structure of organic and carbone aerogels synthesized by sol-gel polycondensation of resorcinol with formaldehyde. Carbon 1997 35 791-6... 

The nitrogen-containing carbonaceous replicas of siliceous materials were prepared and studied with the nitrogen adsorption, TEM, TGA, XPS, and EDX methods. The carbons obtained using SBA-15 as a matrix exhibited well-developed and highly ordered porous structures. Those from the MLV material showed lower sorption capacities and 3-D structures less ordered as in the case of the SBA-15 replicas. 

From the beginning of 14C studies, bone was burdened with a marginal status as a sample type. It was missing from the list of sample materials which Libby initially recommended [10]. He and other researchers discouraged its use for the reason that the carbon content and specifically the organic carbon content, was low even in relatively recent bone and because it was a very porous structure potentially subject to chemical alteration and presumably to contamination. It was concluded that bone would systematically violate the third assumption of the 14C method as listed in Table 1. (It should be noted that "burned bone" was highly recommended. However, the sample material was the carbonized hair, skin, and other tissue rather than the bone matrix itself.)... 

An active, catalytic layer, comprising a three-dimensional porous structure composed of a mixture of hydrophilic carbon particles (Vulcan XC-72) supporting a finely dispersed catalyst, and a hydrophobic binder (PTFE). This layer faces the liquid side and can be visualised as being formed from many hydro-phobic channels (the route of the oxygen supply) and hydrophilic channels, required for the rapid removal of caustic released into the gap between the membrane and GDE. 

After the description of chemical structure and control of meso-architecture and surface area, selected applications of such carbon materials as battery electrodes, supercapacitors, and in the design of controlled hybrid heterojunctions were presented. In the Li battery, coating or hybridization with hydrothermal carbon brought excellent capacities at simultaneous excellent stabilities and rate performances. This was exemplified by hybridization with Si, Sn02 (both anode materials) as well as LiFeP04 (a cathode material). In the design of supercapacitors, porous HTC carbons could easily reach the benchmark of optimized activated traditional carbons, with better stability and rate performance. 

CNTs have a different porous structure than activated carbon. The specific surface area of CNTs can range from 50 m2/g (multi-walled CNTs with 50 graphene walls) to 1315 m2/g (single-walled CNTs). Theoretically, the porous structure of CNTs is identical to the tubular structure of CNTs and the pore sizes of CNTs correspond to the inner diameters of opened CNTs and should have a narrow distribution. Activated carbons usually have a broad pore distribution covering micropore, meso-pore and macropore ... 

In MCFCs, which operate at relatively high temperature, no materials are known that wet-proof a porous structure against ingress by molten carbonates. Consequently, the technology used to obtain a stable three-phase interface in MCFC porous electrodes is different from that used in PAFCs. In the MCFC, the stable interface is achieved in the electrodes by carefully tailoring the pore structures of the electrodes and the electrolyte matrix (LiA102) so that the capillary forces establish a dynamic equilibrium in the different porous structures. Pigeaud et al. (4) provide a discussion of porous electrodes for MCFCs. 

The porous electrodes used in PAFCs are described extensively in the patent literature (6) see also the review by Kordesch (5). These electrodes contain a mixture of the electrocatalyst supported on carbon black and a polymeric binder, usually PTFE (about 30 to 50 wt%). The PTFE binds the carbon black particles together to form an integral (but porous) structure, which is supported on a porous carbon paper substrate. The carbon paper serves as a structural support for the electrocatalyst layer, as well as the current collector. A typical carbon paper used in PAFCs has an... 

Two main types of catalyst layers are used in PEM fuel cells polyfefrafluo-roethylene (PTFE)-bound catalyst layers and thin-film catalyst layers [3]. The PTFE-bound CL is the earlier version, used mainly before 1990. If confains two components hydrophobic PTFE and Pt black catalyst or carbon-supported Pt catalyst. The PTFE acts as a binder holding the catalyst together to form a hydrophobic and structured porous matrix catalyst layer. This porous structure can simultaneously provide passages for reacfanf gas fransport to the catalyst surface and for wafer removal from fhe cafalysf layer. In fhe CL, the catalyst acts as both the reaction site and a medium for electron conduction. In the case of carbon-supported Pt catalysts, both carbon support and catalyst can act as electron conductors, but only Pt acts as the reaction site. 

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