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Graphite porous

The present review discusses the results of the H NMR spectroscopy for a wide range of carbonaceous materials (heat-treated and nongraphitizable activated carbons, carbon blacks, exfoliated and oxidized graphites, porous and amorphous carbonized silicas). This technique made it possible to determine the spectral characteristics of organic molecules with diverse chemical properties, as well as of water molecules adsorbed on the surface. These characteristics are compared with the structural properties of the materials under consideration. The calculations done for the majority of the subjects of inquiry gave the values of their free surface energies in an aqueous medium as well as the characteristics of bound water layers of various types. [Pg.70]

Carbon/graphite nanofibers (Fig. 2.14) are made by carbonization/ grapbitization of their precursors of electrospun pol nner nanofibers (e.g., PAN nanofibers). Two types of carbon/graphite nanofibers can be developed, (type 1) continuous, nanoscaled carbon fibers with superior mechanical strength and (type 2) highly graphitic, porous graphite nanofibers with specific surface areas of up to 2500 m /g. [Pg.65]

Besides amorphous carbons, graphitic porous carbons are also widely investigated and may be valuable for figuring out the CO2 capture behavior due to its... [Pg.46]

Fig. 5.10. Chlorine evolution overpotential at a graphite porous electrode at 25 C 2.9M NaCl + 1.5M HCl. The dotted curve corresponds to calculations for 6 =. ... Fig. 5.10. Chlorine evolution overpotential at a graphite porous electrode at 25 C 2.9M NaCl + 1.5M HCl. The dotted curve corresponds to calculations for 6 =. ...
The above methods for obtaining D, as well as other ones, are reviewed in Refs. 3-12, and Refs. 7-9 give tables of D values for various adsorbents. For example, D is close to 3 for the highly porous silica gels and close to 2 for nonporous fumed silica and for graphitized carbon black coconut charcoal and alumina were found to have D values of 2.67 and 2.79, respectively [7]. [Pg.575]

Fig. 4.25 Adsorption isotherms showing low-pressure hysteresis, (a) Carbon tetrachloride at 20°C on unactivated polyacrylonitrile carbon Curves A and B are the desorption branches of the isotherms of the sample after heat treatment at 900°C and 2700°C respectively Curve C is the common adsorption branch (b) water at 22°C on stannic oxide gel heated to SOO C (c) krypton at 77-4 K on exfoliated graphite (d) ethyl chloride at 6°C on porous glass. (Redrawn from the diagrams in the original papers, with omission of experimental points.)... Fig. 4.25 Adsorption isotherms showing low-pressure hysteresis, (a) Carbon tetrachloride at 20°C on unactivated polyacrylonitrile carbon Curves A and B are the desorption branches of the isotherms of the sample after heat treatment at 900°C and 2700°C respectively Curve C is the common adsorption branch (b) water at 22°C on stannic oxide gel heated to SOO C (c) krypton at 77-4 K on exfoliated graphite (d) ethyl chloride at 6°C on porous glass. (Redrawn from the diagrams in the original papers, with omission of experimental points.)...
Porous bron2e and iron, a variety of plastics, carbon—graphite, wood, and mbber are widely used in dry sliding or under conditions of sparse lubrication. These materials have commonly allowed design simplifications, freedom from regular maintenance, reduced sensitivity to contamination, and good performance at low speeds and with intermittent lubrication. Although these materials are often used dry or with sparse lubrication, performance normally improves the closer the approach to full-film lubrication. [Pg.5]

As a generahty, porous metal sleeve bearings tolerate Pp levels up to 1.8 MN/(m-s) (50, 000 psift/min). Pp levels for thmst bearings should not exceed about 20% of the sleeve bearing limit. Variations of oil viscosity, oil content, graphite content, and other material and property details also influence the approximate operating limits given in Table 7. [Pg.6]

Porous Graphite. Several grades of low density, porous carbon and graphite are commercially available. A controlled combination of high... [Pg.515]

Porous carbon and graphite are used ia filtration of hydrogen fluoride streams, caustic solutions, and molten sodium cyanide ia diffusion of chlorine iato molten aluminum to produce aluminum chloride and ia aeration of waste sulfite Hquors from pulp and paper manufacture and sewage streams. [Pg.516]

Pyrolytic graphite was first produced in the late 1800s for lamp filaments. Today, it is produced in massive shapes, used for missile components, rocket nozzles, and aircraft brakes for advanced high performance aircraft. Pyrolytic graphite coated on surfaces or infiltrated into porous materials is also used in other appHcations, such as nuclear fuel particles, prosthetic devices, and high temperature thermal insulators. [Pg.527]

Rigid Porous Media These are available in sheets or plates and tubes. Materials used include sintered stainless steel and other metals, graphite, aluminum oxide, silica, porcelain, and some plastics—a gamut that allows a wide range of chemical and temperature resistance. Most applications are for clarification. [Pg.1707]

When the layer of graphite and corrosion products is impervious to the solution, corrosion wdl cease or slow down. If the layer is porous, corrosion will progress by galvanic behavior between graphite and iron. The rate of this attack will be approximately that for the maximum penetration of steel by pitting. The layer of graphite formed may also be effective in reducing the g vanic action between cast iron and more noble alloys such as bronze used for valve trim and impellers in pumps. [Pg.2420]

Figure 17.10 shows metal loss on the throat of the pump housing. External pump housing surfaces were also affected (Fig. 17.11). Note the large tubercles. (Tubercles are knoblike mounds of corrosion products. They typically have a hard, black outer shell enclosing porous reddish-brown or black iron oxides) (see Chap. 3, Tuberculation ). The metal surface beneath these tubercles had sustained graphitic corrosion, in some cases to a depth of Vi in. (0.6 cm) (Fig. 17.12). Figure 17.10 shows metal loss on the throat of the pump housing. External pump housing surfaces were also affected (Fig. 17.11). Note the large tubercles. (Tubercles are knoblike mounds of corrosion products. They typically have a hard, black outer shell enclosing porous reddish-brown or black iron oxides) (see Chap. 3, Tuberculation ). The metal surface beneath these tubercles had sustained graphitic corrosion, in some cases to a depth of Vi in. (0.6 cm) (Fig. 17.12).
All VGCF was graphitized prior to composite consolidation. Composites were molded in steel molds lined with fiberglass reinforced, non-porous Teflon release sheets. The finished composite panels were trimmed of resin flash and weighed to determine the fiber fraction. Thermal conductivity and thermal expansion measurements of the various polymer matrix composites are given in Table 6. Table 7 gives results from mechanical property measurements. [Pg.151]

Impregnated carbon and grapliite can be used up to I80°C, and porous graphite can be used up to 400°C in oxidizing environments and 3000°C in a reducing atmosphere. Carbon and graphite bricks and tiles are used for... [Pg.101]

This Fmoc analog is prepared from the chloroformate, O-succinimide, or p-nitrophenyl carbonate and is cleaved with 10% piperidine in 1 1 6M guanidine/IPA. It was designed to interact strongly on a column of porous graphitized carbon so as to aid in the purification of peptides after cleavage from the resin. [Pg.508]

Zebiihr et al. (29) developed an automated system for determining PAHs, PCBs and PCDD/Fs by using an aminopropyl silica column coupled to a porous graphitic carbon column. This method gives five fractions, i.e. aliphatic and monoaromatic hydrocarbons, polycyclic aromatic hydrocarbons, PCBs with two or more ortho-chlorines, mono-ort/io PCBs, and non-ortho PCBs and PCDD/Fs. This method employed five switching valves and was successfully used with extracts of sediments, biological samples and electrostatic filter precipitates. [Pg.343]

A CSP based on the adsorption of a chiral anthrylamine on porous graphitic carbon successfully resolved the enantiomers of tropic acid derivatives and anti-inflammatory agents in SFC [65]. The carbon-based CSP produced superior results when compared to an analogous silica-based CSP. Occasional washing of the column was necessary to remove highly retained substances. [Pg.310]

Graphite is a denser crystalline form of carbon. Graphite anodes are prepared by heating calcined petroleum coke particles with a coal tar pitch binder. The mix is then shaped as required and heated to approximately 2 800°C to convert the amorphous carbon to graphite. Graphite has now superseded amorphous carbon as a less porous and more reliable anode material, particularly in saline conditions. [Pg.184]

Jorne et al. [36] investigated the reactivity of graphites in acidic solutions that are typically used for Zn/Cl2 cells. The degradation of porous graphite is attributed to oxidation to C02. The rate of C02 evolution gradually decreased with oxidation time until a steady state was reached. The decline in the C02 evolution rate is attributed to the formation of surface oxides on the active sites. [Pg.241]


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Column packings porous graphitic carbon

Electrode porous graphite

Packed columns porous graphitic carbon

Packing material porous graphitic carbon

Packings porous graphitized carbon

Porous graphite carbon

Porous graphitic carbon

Porous graphitic carbon HPLC

Porous graphitic carbon HPLC chromatography

Porous graphitic carbon stationary phases

Porous graphitized carbon

Stationary phases porous graphitized carbon

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