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Carbon phase

Activated carbons for use in Hquid-phase appHcations differ from gas-phase carbons primarily in pore size distribution. Liquid-phase carbons have significantly more pore volume in the macropore range, which permits Hquids to diffuse more rapidly into the mesopores and micropores (69). The larger pores also promote greater adsorption of large molecules, either impurities or products, in many Hquid-phase appHcations. Specific-grade choice is based on the isotherm (70,71) and, in some cases, bench or pilot scale evaluations of candidate carbons. [Pg.533]

The component reactions in eqn. (2) are very fast, and the system exists in equilibrium. Additional carbon dioxide entering the sea is thus quickly converted into anions, distributing carbon atoms between the dissolved gas phase, carbonate and bicarbonate ions. This storage capacity is clear when the apparent equilibrium constants for the two reactions in eqn. (2) are examined, namely... [Pg.19]

Tibbetts, G.G., Gorkiewicz, D.W., and Alig, R.A. A new reactor for growing carbon fibers from liquid- and vapor-phase hydrocarbons, Carbon, 993, 31(5), 809 814. Tibbetts, G.G., Bernardo, C.A., Gorkiewicz, D.W. and Alig R.L. Role of sulfur in the production of carbon fibers in the vapor phase. Carbon, 1994, 32(4), 569 576. [Pg.165]

The following are some of the typical industrial applications for liquid-phase carbon adsorption. Generally liquid-phase carbon adsorbents are used to decolorize or purify liquids, solutions, and liquefiable materials such as waxes. Specific industrial applications include the decolorization of sugar syrups the removal of sulfurous, phenolic, and hydrocarbon contaminants from wastewater the purification of various aqueous solutions of acids, alkalies, amines, glycols, salts, gelatin, vinegar, fruit juices, pectin, glycerol, and alcoholic spirits dechlorination the removal of... [Pg.279]

Figure 2.14. The molecular orbitals of gas phase carbon monoxide, (a) Energy diagram indicating how the molecular orbitals arise from the combination of atomic orbitals of carbon (C) and oxygen (O). Conventional arrows are used to indicate the spin orientations of electrons in the occupied orbitals. Asterisks denote antibonding molecular orbitals, (b) Spatial distributions of key orbitals involved in the chemisorption of carbon monoxide. Barring indicates empty orbitals.5 (c) Electronic configurations of CO and NO in vacuum as compared to the density of states of a Pt(lll) cluster.11 Reprinted from ref. 11 with permission from Elsevier Science. Figure 2.14. The molecular orbitals of gas phase carbon monoxide, (a) Energy diagram indicating how the molecular orbitals arise from the combination of atomic orbitals of carbon (C) and oxygen (O). Conventional arrows are used to indicate the spin orientations of electrons in the occupied orbitals. Asterisks denote antibonding molecular orbitals, (b) Spatial distributions of key orbitals involved in the chemisorption of carbon monoxide. Barring indicates empty orbitals.5 (c) Electronic configurations of CO and NO in vacuum as compared to the density of states of a Pt(lll) cluster.11 Reprinted from ref. 11 with permission from Elsevier Science.
Figure 6.3 Conparlson of the separation of the octylphenol poly(ethylene glycol) ether, Triton X-16S on a packed column, left, and an open tubular column, right, using UV detection. For the packed column separation al0cmx2mmI.D. column packed with Nucleosil C g, d. 3 micrometers, temperature > 170 C, and mobile phase carbon dioxide (2 ml/min] and methanol (0.15 nl/rnin). pressure programmed from 130 to 375 bar in 12 min were used. For the open tubular column separation a 10 m x 50 micrometers I.O., SB-Biphenyl-30, temperature = 175°C, mobile phase carbon dioxide (0.175 ml/min) and 2-propanol (0.0265 ml/min) pressure programmed, 125 bar for 5 min, then ramped from 125 to 380 bar over 19.5 min, and held at 380 bar for 15 min. were used. (Reproduced with permission from ref. 57. Copyright Preston Publications, Inc.) ... Figure 6.3 Conparlson of the separation of the octylphenol poly(ethylene glycol) ether, Triton X-16S on a packed column, left, and an open tubular column, right, using UV detection. For the packed column separation al0cmx2mmI.D. column packed with Nucleosil C g, d. 3 micrometers, temperature > 170 C, and mobile phase carbon dioxide (2 ml/min] and methanol (0.15 nl/rnin). pressure programmed from 130 to 375 bar in 12 min were used. For the open tubular column separation a 10 m x 50 micrometers I.O., SB-Biphenyl-30, temperature = 175°C, mobile phase carbon dioxide (0.175 ml/min) and 2-propanol (0.0265 ml/min) pressure programmed, 125 bar for 5 min, then ramped from 125 to 380 bar over 19.5 min, and held at 380 bar for 15 min. were used. (Reproduced with permission from ref. 57. Copyright Preston Publications, Inc.) ...
EFFICIENCY OF DIFFERENT OPEN TDBUALR COLUMNS OPERATED AT 10 u , FOR A SOLUTE WITH k - 3, DENSITY - 0.22 g/ l, TEMPERATURE = 40 C AND NOBILE PHASE CARBON DIOXIDE... [Pg.313]

For effective volatilization using an enclosed mechanical aeration system, contaminated soil is mixed in a pug mill or rotary drum. The gasoline components are released from the soil matrix by the churning action of the air/soil contact. The induced airflow within the chamber captures the gasoline emissions and passes them through an air pollution control device (e.g., a water scrubber or vapor-phase carbon adsorption system) before they are discharged through a properly sized stack. [Pg.736]

Above the eutectic temperature in the iron-FcsC system (1130°C)12, growth of large graphite plates and flakes occurs from the liquid phase. Carbon precipitates in the form of highly ordered graphite crystals from molten iron supersaturated with carbon. The Raman spectrum for chlorination at 1200°C is shown in Fig. 2c. A very strong and narrow... [Pg.414]

The first examples of microwave-mediated solid-phase carbon-nitrogen cross-coupling reactions were reported in 1999 by the group of Combs [16], using a boronic... [Pg.308]

To minimize coking, the reactor may be operated at short residence times, or hydrogen may be added to the process stream to convert gas-phase carbon into methane. It is also advantageous to minimize the temperature upstream of the catalyst bed, since gas-phase carbon is less readily formed at low temperatures. [Pg.215]

S. Buelow, P. Dell Orco, D. K Morita, D. Pesiri, E Bim-baum, S. L Borkowsky, G. H. Brown, S. Feng, L Luan, D. A. Morgenstern, W. Tumas, Recent Advances in Chemistry and Chemical Processing in Dense Phase Carbon Dioxide at Los Alamos , In Green Chemistry Frontiers in Benign Chemical Syntheses and Processes, (Eds. P. T. Anastas and T. C. Williamson), Oxford University Press, Oxford, 1998, pp. 265-285. [Pg.25]

R. Ciriminna, S. Campestrini and M. Pagliaro, Fluorinated Silica Gels Doped with TPAP as Effective Aerobic Oxidation Catalysts in Dense Phase Carbon Dioxide, Adv. Synth. Catal., 2004, 346, 231. [Pg.142]

Von Bavel et al. [55] used a solid phase carbon trap in conjunction with supercritical fluid chromatography for the simultaneous determination of polychlorobiphenyls, pesticides, polychlorodibenzo-p-dioxins and polychlorodibenzofurans in soils. [Pg.174]

Von Bavel et al. [55] have developed a solid phase carbon trap (PX-21 active carbon) for the simultaneous determination of polychlorodibenzo-p-dioxins and polychlorodibenzofurans also polychlorobiphenyls and chlorinated insecticides in soils using superfluid extraction liquid chromatography for the final determination. Supercritical fluid extraction with carbon dioxide has been applied to the determination of dioxins in soil [114],... [Pg.183]

The partition of different lipids between two immiscible solvents (countercurrent distribution) is useful for crude fractionation of lipid classes with greatly differing polarities. Repeated extractions in a carefully chosen solvent pair increase the effectiveness of the separation but in practice mixtures of lipids are still found in each fraction. A petroleum ether-ethanol-water system can be used to remove polar contaminants (into the alcoholic phase) when interest lies in the subsequent analysis of neutral glycerides, which may be recovered from the ether phase. Carbon... [Pg.429]

The most common partition coefficient encountered in environmental work (Sect. 2.1.4) is the octanol water partition coefficient (K0VI) and the solid phase carbon-water partition coefficient (Koc). A partition coefficient for dissolved organic matter-water (i. e., Kd ()M) or dissolved organic carbon-water (i. e., Kd oc) occasionally appears in the literature. In the case of PCBs, Boyd and Sun [378] defined a partition coefficient for residual transformer oil and water as Kd oil, while Sun and Boyd [379] defined a coefficient for PCB dielectric fluid-water as Kd pen-These authors [378,379] identified a total partition coefficient that com-... [Pg.278]


See other pages where Carbon phase is mentioned: [Pg.281]    [Pg.443]    [Pg.185]    [Pg.529]    [Pg.534]    [Pg.534]    [Pg.18]    [Pg.243]    [Pg.458]    [Pg.277]    [Pg.277]    [Pg.279]    [Pg.280]    [Pg.280]    [Pg.283]    [Pg.533]    [Pg.947]    [Pg.644]    [Pg.823]    [Pg.78]    [Pg.86]    [Pg.396]    [Pg.921]    [Pg.1010]    [Pg.288]    [Pg.39]    [Pg.186]    [Pg.226]    [Pg.264]    [Pg.479]    [Pg.70]   
See also in sourсe #XX -- [ Pg.269 ]




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Activated carbon solid-phase extraction

Active phase, catalysis carbon stabilization

Aqueous-phase chemistry carbon dioxide

Bonded phase Carbon content, determination

Bonded stationary phases porous carbon

Boron-carbon phase diagram

CARBON FIBERS FROM VAPOR-PHASE (CVD) REACTION

Carbon Dioxide in the Gas Phase

Carbon acidity, carbanion basicity condensed-phase measurements

Carbon black continuous liquid phase mixing

Carbon dioxide aqueous phase equilibria

Carbon dioxide liquid phase partial pressure

Carbon dioxide phase change

Carbon dioxide phase diagram, schematic

Carbon dioxide three phase pressure

Carbon dioxide, 68-71 phase diagram

Carbon dioxide, as mobile phase

Carbon dioxide, pressure-temperature phase

Carbon dioxide, pressure-temperature phase diagram

Carbon formation solid phase catalyst

Carbon monoxide phase diagram

Carbon nanotubes liquid-phase functionalization

Carbon phase diagram for

Carbon phase potential

Carbon phase transition

Carbon stationary phase

Carbon-based chiral stationary phases

Carbon-containing solid-phase

Carbon-containing solid-phase determinations

Carbon-dioxide mobile phase

Carbon-hydrogen bonds solid-phase reactions

Carbon-silica dual phase filler

Carbon-silica dual phase fillers (CSDPF

Carbon-silicon phase diagram

Carbonate phases

Carbonization liquid phase

Carbonization solid phase

Carbons vapour phase coatings

Dissolved organic carbon solid-phase extractions

Ettringite carbonated phase

Fluid phase carbonate-rich

Gas-phase acidities of carbon acids

Gas-phase oxidation of carbon

Gas-phase-grown carbon fibers

Graphitized (Graphite) Carbon Phases

Graphitized carbon phases

Graphitized carbon reversed-phase liquid

Iron-carbon phase

Iron-carbon phase diagram

Liquid phase carbon adsorption

Magnesium carbonates phase relations

Mixed metal amorphous and spinel phase oxidation catalysts derived from carbonates

Nickel-carbon phase diagram

Phase Behavior of Iron-Carbon Alloys

Phase Carbon Acidity Measurements

Phase Transition of Graphite to Concentric Shell Carbon

Phase diagram carbon

Phase diagram for carbon dioxide

Phase diagram for pure carbon dioxide

Phase diagram of carbon

Phase iron-carbon alloys

Phase near critical carbon dioxide

Phase rare earth-carbon

Phase supercritical carbon dioxide

Porous graphitic carbon stationary phases

Role of the Carbon Phase in Heterogeneous Photocatalysis

Solid phase organic carbon-water partition

Solid phase organic carbon-water partition phases

Solid-Phase Organic Radiosynthesis with Carbon

Solid-phase carbonization activated carbon from

Solid-phase extractions carbon-18 adsorbents

Stationary phase Carbon-based columns

Stationary phase Carbon-coated phases

Stationary phase graphitized carbons

Stationary phases porous graphitized carbon

The Carbon Phase Diagram

The Phase and Transition Diagram for Carbon

The carbonate phase

The iron-carbon phase diagram

Three dimensional carbon phases

Vapor phase carbon adsorption system

Yttrium-carbon phase diagram

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