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C surfaces

Example of copredpitation (a) schematic of a chemically adsorbed inclusion or a physically adsorbed occlusion in a crystal lattice, where C and A represent the cation-anion pair comprising the analyte and the precipitant, and 0 is the impurity (b) schematic of an occlusion by entrapment of supernatant solution (c) surface adsorption of excess C. [Pg.239]

Magnesia Calcination temperature, °C Surface area, m /g CrystaUite size, p.m Porosity, %... [Pg.353]

Fig. 1. (a) Particle and examples of equivalent spherical diameters (b) volume, (c) surface, and (d) settling. [Pg.126]

Hot-Water Process. The hot-water process is the only successflil commercial process to be appHed to bitumen recovery from mined tar sands in North America as of 1997 (2). The process utilizes linear and nonlinear variations of bitumen density and water density, respectively, with temperature so that the bitumen that is heavier than water at room temperature becomes lighter than water at 80°C. Surface-active materials in tar sand also contribute to the process (2). The essentials of the hot-water process involve conditioning, separation, and scavenging (Fig. 9). [Pg.358]

Fig. 2. Measuring static charge, (a) Field voltage measurement (b) Faraday cage (c) surface resistivity measurement and (d) static decay test. Fig. 2. Measuring static charge, (a) Field voltage measurement (b) Faraday cage (c) surface resistivity measurement and (d) static decay test.
C—Surface Coil Type Condenser, Intercondenser and Aftercondenser N—Signifies no condenser in the series. [Pg.350]

P5. Povinelli, L. A., and Ciepluch, C. C., Surface phenomena in solid propellant combustion, presented at JANAFjARPAjNASA Solid-Propellant Group Meeting, Pittsburgh, Pennsylvania, 1962. [Pg.69]

Luo, J. B. and Yang, M. C., Surface Modification of Computer Magnetic Head, Sino-German Symposium on Micro Systems and Nano Technology, 7-9 Sept., Braunschweig, Germany, 2001. [Pg.234]

Figure 5. XPS C(ls) core level after a) trimethylbenzene and b) methylacetylene adsorption at 265 K on the 575 K annealed surface c) surface in b) flashed to 575 K. Figure 5. XPS C(ls) core level after a) trimethylbenzene and b) methylacetylene adsorption at 265 K on the 575 K annealed surface c) surface in b) flashed to 575 K.
Figure 8. Reflection infrared spectra (ATR-IR) of polypropylene film surface before (A) and after grafting with methacrylic acid (MAA) measured at the top (B) and the bottom (C) surface. Figure 8. Reflection infrared spectra (ATR-IR) of polypropylene film surface before (A) and after grafting with methacrylic acid (MAA) measured at the top (B) and the bottom (C) surface.
Fig. 12. SEM photographs of CoP and CoP/C surfaces after 24 hrs exposure to Cl2 and 70% RH at RT. Mag 1200X [125]. (Reprinted by permission of The Electrochemical Society). Fig. 12. SEM photographs of CoP and CoP/C surfaces after 24 hrs exposure to Cl2 and 70% RH at RT. Mag 1200X [125]. (Reprinted by permission of The Electrochemical Society).
Basset, J. M., Gates, B. C., Candy, J. P., Choplin, A., Leconte, M., Quignard, E, and Santini, C. C., Surface Organometallic Chemistry Molecular Approaches to Surface Catalysis, NATO ASI Series, Kluwer, Dordrecht, 1988. [Pg.285]

Figure 8.28. Demonstration of a CDF. Data recorded during non-isothermal oriented crystallization of polyethylene at 117°C. Surface plots show the same CDF (a) Linear scale viewed from the top. (b) Linear scale viewed from the bottom, (c) Viewed from the top, logarithmic scale. Indicated are the determination of the most probable layer thickness, lt, and of the maximum layer extension, le. (d) Viewed from the bottom, logarithmic scale. The IDF in fiber direction is indicated by a light line in (a) and (b) (Source [56])... Figure 8.28. Demonstration of a CDF. Data recorded during non-isothermal oriented crystallization of polyethylene at 117°C. Surface plots show the same CDF (a) Linear scale viewed from the top. (b) Linear scale viewed from the bottom, (c) Viewed from the top, logarithmic scale. Indicated are the determination of the most probable layer thickness, lt, and of the maximum layer extension, le. (d) Viewed from the bottom, logarithmic scale. The IDF in fiber direction is indicated by a light line in (a) and (b) (Source [56])...
Temperature plays an important role in determining the amount and type of the carbon deposit. Generally during FTS at higher temperatures the amount of carbon deposited will tend to increase,30-31 but the case is often not so straightforward. An example of temperature dependence on the rate of carbon deposition and deactivation is the case of nickel CO hydrogenation catalysts, as studied by Bartholomew.56 At temperatures below 325°C the rate of surface carbidic carbon removal by hydrogenation exceeds that of its formation, so no carbon is deposited. However, above 325°C, surface carbidic carbon accumulates on the surface... [Pg.56]


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