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Carbon as a function of temperature

With the help of corresponding data, i.e., the standard values and the corresponding temperature coefficients from Sect. A.2.1 in the Appendix, the p(T) curve can be determined (Fig. 5.13). This curve gives the decomposition pressure of calcium carbonate as a function of temperature ... [Pg.152]

Figure 6.6. Variations in the properties of vitreous carbon as a function of temperature,... Figure 6.6. Variations in the properties of vitreous carbon as a function of temperature,...
These models were generated to study self-diffusion of fluids within microporous carbons as a function of temperature and porosity. However, their immediate application to microporosity of activated carbons from traditional sources is not that obvious. From this point of... [Pg.104]

Fluorine can be handled using a variety of materials (100—103). Table 4 shows the corrosion rates of some of these as a function of temperature. System cleanliness and passivation ate critical to success. Materials such as nickel, Monel, aluminum, magnesium, copper, brass, stainless steel, and carbon steel ate commonly used. Mote information is available in the Hterature (20,104). [Pg.129]

Stmctures that form as a function of temperature and time on cooling for a steel of a given composition are usually represented graphically by continuous-cooling and isothermal-transformation diagrams. Another constituent that sometimes forms at temperatures below that for peadite is bainite, which consists of ferrite and Fe C, but in a less well-defined arrangement than peadite. There is not sufficient temperature and time for carbon atoms to diffuse long distances, and a rather poody defined acicular or feathery stmcture results. [Pg.237]

Values for the free energy and enthalpy of formation, entropy, and ideal gas heat capacity of carbon monoxide as a function of temperature are listed in Table 2 (1). Thermodynamic properties have been reported from 70—300 K at pressures from 0.1—30 MPa (1—300 atm) (8,9) and from 0.1—120 MPa (1—1200 atm) (10). [Pg.48]

Table 6. Flammability Limits of Carbon Monoxide in Dry Air as a Function of Temperature at Atmospheric Pressure ... Table 6. Flammability Limits of Carbon Monoxide in Dry Air as a Function of Temperature at Atmospheric Pressure ...
Figure 5.2. (a) Arrangement of a Snoek pendulum, (b) Internal friction as a function of temperature, at different pendulum frequencies, for a solution of carbon in iron, (c) Diffusion of carbon in iron over 14 decades, using the Snoek effect (-30-200°C) and conventional radioisotope... [Pg.194]

Basically there are two approaches to predicting the occurrence of erosion corrosion. Practical or experience based methods typified by Keller s approach for carbon steels in wet steam. Keller developed an equation that related the erosion corrosion rate as a function of temperature, steam quality, velocity and geometric factor. In recent years this approach has... [Pg.301]

The preceeding discussion was confined mostly to the carbon deposition curves as a function of temperature, pressure, and initial composition. Also of interest, especially for methane synthesis, is the composition and heating value of the equilibrium gas mixture. It is desirable to produce a gas with a high heating value which implies a high concentration of CH4 and low concentrations of the other species. Of particular interest are the concentrations of H2 and CO since these are generally the valuable raw materials. Also, by custom it is desirable to maintain a CO concentration of less than 0.1%. The calculated heating values are reported as is customary in the gas industry on the basis of one cubic foot at 30 in. Hg and 15.6°C (60°F) when saturated with water vapor (II). Furthermore, calculations are made and reported for a C02- and H20-free gas since these components may be removed from the mixture after the final chemical reaction. Concentrations of CH4, CO, and H2 are also reported on a C02 and H20-free basis. [Pg.49]

Figure 2.27. Temperature programmed desorption (TPD) spectra of carbon monoxide (measured by Ap) as a function of temperature from nickel surfaces (a) Ni(l 11), (b) Ni(l 11) when the initially dosed surface has been subjected to an electron beam (150 pA for 10 minutes over an area of 1 mm2) and (c) a cleaved nickel surface.85 Reprinted with permission from Elsevier Science. Figure 2.27. Temperature programmed desorption (TPD) spectra of carbon monoxide (measured by Ap) as a function of temperature from nickel surfaces (a) Ni(l 11), (b) Ni(l 11) when the initially dosed surface has been subjected to an electron beam (150 pA for 10 minutes over an area of 1 mm2) and (c) a cleaved nickel surface.85 Reprinted with permission from Elsevier Science.
Figure 8. Rate of carbon monoxide oxidation on calcined Pt cube monolayer as a function of temperature [27]. The square root of the SFG intensity as a function of time was fit with a first-order decay function to determine the rate of CO oxidation. Inset is an Arrhenius plot for the determination of the apparent activation energy by both SFG and gas chromatography. Reaction conditions were preadsorbed and 76 Torr O2 (flowing). (Reprinted from Ref. [27], 2006, with permission from American Chemical Society.)... Figure 8. Rate of carbon monoxide oxidation on calcined Pt cube monolayer as a function of temperature [27]. The square root of the SFG intensity as a function of time was fit with a first-order decay function to determine the rate of CO oxidation. Inset is an Arrhenius plot for the determination of the apparent activation energy by both SFG and gas chromatography. Reaction conditions were preadsorbed and 76 Torr O2 (flowing). (Reprinted from Ref. [27], 2006, with permission from American Chemical Society.)...
Figure 6.4 On the left is a phase diagram for carbon dioxide. Broken lines indicate isotherm crossing at either constant pressure or density. On the right is illustrated the change in solubility of naphthalene as a function of temperature and pressure. Figure 6.4 On the left is a phase diagram for carbon dioxide. Broken lines indicate isotherm crossing at either constant pressure or density. On the right is illustrated the change in solubility of naphthalene as a function of temperature and pressure.
When heated, many solids evolve a gas. For example, most carbonates lose carbon dioxide when heated. Because there is a mass loss, it is possible to determine the extent of the reaction by following the mass of the sample. The technique of thermogravimetric analysis involves heating the sample in a pan surrounded by a furnace. The sample pan is suspended from a microbalance so its mass can be monitored continuously as the temperature is raised (usually as a linear function of time). A recorder provides a graph showing the mass as a function of temperature. From the mass loss, it is often possible to establish the stoichiometry of the reaction. Because the extent of the reaction can be followed, kinetic analysis of the data can be performed. Because mass is the property measured, TGA is useful for... [Pg.266]

Fig. 7-5. Outgoing long-wave planetary radiation as a function of temperature, comparing clear and cloudy skies for carbon dioxide partial pressure equal to one and four times the current level. Fig. 7-5. Outgoing long-wave planetary radiation as a function of temperature, comparing clear and cloudy skies for carbon dioxide partial pressure equal to one and four times the current level.
Fig. 4.5 Detergency of C12E4 and C12E5 against hexadecane as a function of temperature (left side) and the corresponding three-phase ranges for these surfactants as a function of the number n of carbon atoms of alkanes [46],... Fig. 4.5 Detergency of C12E4 and C12E5 against hexadecane as a function of temperature (left side) and the corresponding three-phase ranges for these surfactants as a function of the number n of carbon atoms of alkanes [46],...
Figures 7-9 show the fractional conversion of methanol in the pulse as a function of temperature for the three catalysts and the three methanol feeds. Evidently the kinetic isotope effect is present on all three catalysts and over the complete temperature range, indicating that the rate limiting step is the breaking of a carbon-hydrogen bond under all conditions. From these experiments, the effect cannot be determined quantitatively as in the case of the continuous flow experiments, but to obtain the same conversion of CD,0D, the temperature needs to be 50-60° higher. This corresponds to a factor of about three in reaction rate. The difference in activity between PfoCL and Fe.(MoO.), is larger in the pulse experiments compared to tHe steady stateJ results. Figures 7-9 show the fractional conversion of methanol in the pulse as a function of temperature for the three catalysts and the three methanol feeds. Evidently the kinetic isotope effect is present on all three catalysts and over the complete temperature range, indicating that the rate limiting step is the breaking of a carbon-hydrogen bond under all conditions. From these experiments, the effect cannot be determined quantitatively as in the case of the continuous flow experiments, but to obtain the same conversion of CD,0D, the temperature needs to be 50-60° higher. This corresponds to a factor of about three in reaction rate. The difference in activity between PfoCL and Fe.(MoO.), is larger in the pulse experiments compared to tHe steady stateJ results.
Figure 2.8 shows a Boyle s-law plot of pressure p (as y) against volume V (as x) for carbon dioxide. The figure is drawn as a function of temperature. Each line on the graph represents data obtained at a single, constant temperature, and helps explain why we call each line an isotherm. The uppermost isotherm represents data collected at 31.5 °C. Its shape is essentially straightforward, although it clearly shows distortion. The middle trace (at... [Pg.50]

The present paper focuses on the interactions between iron and titania for samples prepared via the thermal decomposition of iron pentacarbonyl. (The results of ammonia synthesis studies over these samples have been reported elsewhere (4).) Since it has been reported that standard impregnation techniques cannot be used to prepare highly dispersed iron on titania (4), the use of iron carbonyl decomposition provides a potentially important catalyst preparation route. Studies of the decomposition process as a function of temperature are pertinent to the genesis of such Fe/Ti02 catalysts. For example, these studies are necessary to determine the state and dispersion of iron after the various activation or pretreatment steps. Moreover, such studies are required to understand the catalytic and adsorptive properties of these materials after partial decomposition, complete decarbonylation or hydrogen reduction. In short, Mossbauer spectroscopy was used in this study to monitor the state of iron in catalysts prepared by the decomposition of iron carbonyl. Complementary information about the amount of carbon monoxide associated with iron was provided by volumetric measurements. [Pg.10]

It is found that the relaxation parameter T p as a function of temperature does not follow an increase with chain length, as the square of the number of methylene carbons. Nor is it linear with N, the number of methylene carbons, which should be true if relaxation to the lattice were rate controlling. Rather, it shows a temperature-induced increase of the minimum value of Tjp with about the 1.6 of N. So, both spin diffusion and spin lattice coupling are reflected. For a spin diffusion coefficient D of approximately 2 x 10 12 cm.2/sec., the mean square distance for diffusion of spin energy in a time t is the ft1 = 200/T A, or about 15A on a Tjp time scale. [Pg.181]


See other pages where Carbon as a function of temperature is mentioned: [Pg.140]    [Pg.187]    [Pg.416]    [Pg.140]    [Pg.187]    [Pg.416]    [Pg.151]    [Pg.254]    [Pg.391]    [Pg.443]    [Pg.1061]    [Pg.51]    [Pg.806]    [Pg.422]    [Pg.153]    [Pg.779]    [Pg.346]    [Pg.85]    [Pg.196]    [Pg.196]    [Pg.515]    [Pg.726]    [Pg.11]    [Pg.279]    [Pg.115]    [Pg.111]    [Pg.247]    [Pg.134]    [Pg.250]    [Pg.6]   
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As a function of temperature

Carbon function

Carbon functionalization

Carbon functionalized

Carbon functionalizing

Carbon temperature

Carbonate functionality

Function of temperature

Temperature as a function

Temperature of carbonization

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