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71.
The redistribution of impurity in alite during recrystallization has been confirmed by means of the electron probe microanalysis. Each of the main impurity components shows a significant decrease in content during recrystallization. This demonstrates that the growth velocity of alite exerts influence on the amount of the impurity taken up in alite in solid solution from the interstitial melt. Whether M3 or M1 occurs at ambient temperature depends on the cooling rate of clinker as well as the chemical composition of alite. 相似文献
72.
A unique class of conjugated compounds composed of the derivative of condensed polycyclic aromatic compound with the phenyl group and diphenyldiacetylene oligomer was synthesized by annealing of diphenyldiacetylene under elevated pressure. The effect of annealing pressure on the conductivity of the compounds was studied. The total conductivity of the compound decreased with a decrease of frequency, approaching a constant value (dc conductivity: Cdc). The dc conductivity of the compound increased from below 10?15 to 10 S cm?1 with increasing annealing pressure. The dc conductivity of the oligomer was below 10?15 S cm?1 and that of the derivative increased from 10?8 to 10 S cm?1 with decreasing H/C (H/C:0.45–0.04). The conduction of the conjugated compound was electronic. The temperature coefficient of those dc conductivities was positive, with an approximately linear relation between In (CdcT0.5) and (1/T)0.25, where T is the temperature. The ac conductivities Cac were proportional to temperature and frequency f and had the following equation Cac = TfS, S = 0.67–0.75. These results showed that the conduction mechanism can be explained by the hopping in a manifold of states at the Fermi level. © 1994 John Wiley & Sons, Inc. 相似文献
73.
74.
Motoi Takahashi Toshiyuki Mori Fei Ye Ajayan Vinu Hidehiko Kobayashi John Drennan 《Journal of the American Ceramic Society》2007,90(4):1291-1294
A Pt on nano-sized CeO2 particles that in turn are supported on carbon black (CB) was synthesized using the co-impregnation method. This potential anode material for fuel cell applications was synthesized in a stepwise process. The pure CeO2 was synthesized using an ammonium carbonate precipitation method, and the Pt particles dispersed on the CeO2 in such a way that a uniform dispersion with the CB was obtained (Pt–CeO2 /CB). The electrochemical activity of the methanol (CH3 OH) oxidation reaction on the Pt–CeO2 /CB was investigated using cyclic voltammetry and chronoamperometry experimentation. The onset potential of CH3 OH oxidation reaction on the Pt–CeO2 /CB anode was shifted to a lower potential as compared with that on commercially available Pt–Ru/carbon (C) alloy anode. In addition, the activation energy of the Pt–CeO2 /CB anode was much lower than that of the Pt–Ru/C alloy anode. Moreover, the current density of the Pt–CeO2 /CB anode was much higher than that of the Pt–Ru/C alloy anode at temperatures between 28° and 60°C. These results suggest that the anode performance of the Pt–CeO2 /CB anode at the operating temperature of typical fuel cells (80°C) is superior to that of the more usual Pt–Ru/C alloy anode. Importantly, the rare metal, Ru, is not required in the present anode material and the amount of Pt required is also significantly reduced. As a consequence, we report a promising candidate Pt–CeO2 /CB composite anode for application in the development of direct methanol fuel cells. 相似文献
75.
The interface area between the bubble and emulsion phases in a fluidized catalyst bed is one of the important parameters used to analyze and design the fluidized bed reactor. We used a fast‐scanning X‐ray CT system to observe the bubble shape and structure. We then obtained the transient 2‐dimensional cross sectional gas‐phase distribution in a fluidized catalyst bed. Using image‐processing techniques, pseudo 3‐dimensional images of the bubbles were reconstructed. The bubble structure was studied based on the 3‐dimensional images and the previously obtained results in a 2‐dimensional fluidized bed. It was found that the bubble shape was not spherical but complicated, and that the bubbles ascending in a fluidized catalyst bed consisted of some smaller bubbles. 相似文献
76.
Photon rupture with a focused single pulse of pulsed YAG-laser irradiation was used to fabricate an aluminum electrochemical micro-reactor. Porous type anodic oxide film formed on aluminum specimens was irradiated in solutions with a pulsed Nd-YAG laser beam through a convex lens to fabricate micro-channels, micro-electrode, and through holes (for reference electrode, solution inlet, and outlet). During irradiation, specimens were moved by a computer controlled XYZ stage. After irradiation, the surface of the micro-channel and through hole were again treated to form anodic oxide film and the surface of the micro-electrode was treated electrochemically to provide an Au layer. The calculated volume of the micro-reactor including micro-channel and through holes is about 1.5 μl. The cyclic voltammogram of the micro-electrochemical cell was measured in K3Fe(CN)6/K4Fe(CN)6 with both static and flowing solution at different scanning rates. The anodic and cathodic peak currents were measured and the values depended on scanning rate and ion concentration when the solution was static. With the flowing solution, limiting currents were observed and the anodic limiting current was increased with the cubic root of the solution flow rate. 相似文献
77.
NO
x
reduction with a combination of catalysts, Pd catalyst, NO
x
storage reduction (NSR) catalyst and Cu/ZSM-5 in turn, was investigated to elucidate for the high NO
x
reduction activity of this catalyst combination under oxidative atmosphere with periodic deep rich operation. The catalytic
activity was evaluated using the simulated exhaust gases with periodically fluctuation between oxidative and reductive atmospheres,
and it was found that the NO
x
reduction activity with this catalyst combination was apparently higher than that of the solely accumulation of these individual
activities, which was caused by the additional synergic effect by this combination. The Pd catalyst upstream of the NSR catalyst
improved NO
x
storage ability by NO2 formation under oxidative atmosphere. The stored NO
x
was reduced to NH3 on the NSR catalyst, and the generated NH3 was adsorbed on Cu/ZSM-5 downstream of the NSR catalyst under the reductive atmosphere, and subsequently reacted with NO
x
on the Cu/ZSM-5 under the oxidative atmosphere. 相似文献
78.
The performance of an experimental pilot-scale electrochemical reactor using a rotating cylindrical electrode equipped with wiper blades is described. Data obtained from monopolar depositing and bipolar stripping—depositing of copper from dilute aqueous electrolytes are presented and certain economic aspects of metal recovery are discussed. 相似文献
79.
The ionic conduction in sintered Bi2O2-Y2O3 was investigated by measuring the conductivity and the emf of an oxygen concentration cell using the specimen tablet as electrolyte. The face centred cubic phase in this system was found to show high oxide ion conduction accompanied by a little electronic conduction when exposed to air. This phase was stable with a composition of 25 ~ 43 mol % Y2O3 over a wide range of temperatures, and the oxide ion conductivity increased with decrease in Y2O3. The conductivities of (Bi2O3)0.75 (Y2O3)0.25 were 1.6×10?1 Ω?1 cm?1 at 700°C and 1.2×10?2 Ω?1 cm?1 at 500°C values which are many times higher than those of stabilized zirconia (ZrO2)0.90(Y2O3)0.10 at corresponding temperatures. Specimens containing less than 25 mol % Y2O3 showed a phase transition at 700 ~ 580°C and the conductivities decreased remarkably below these temperatures. High oxide ion conduction in the fcc phase is attributed to the migration of oxide ion vacancies which were present in an appreciable amount. 相似文献
80.
Masaru Takahashi Tetsu Nakatani Shinji Iwamoto Tsunenori Watanabe Masashi Inoue 《Applied catalysis. B, Environmental》2007,70(1-4):73-79
The solvothermal reaction of mixtures of aluminum isopropoxide (AIP) and gallium acetylacetonate (Ga(acac)3) directly yielded the mixed oxides of γ-Ga2O3-Al2O3. In the solvothermal synthesis, the crystal structure of mixed oxides was controlled by the initial formation of γ-Ga2O3 nuclei. The mixed oxides prepared in diethylenetriamine have extremely high activities for selective catalytic reduction (SCR) of NO with methane as a reducing agent. With increasing crystallite size of the spinel structure, the catalytic activity increased. The ratio of the amount of methane consumed by combustion to total methane conversion was proportional to the density of acid sites on the surface of the mixed oxides. The mixed oxide catalysts prepared in diethylenetriamine had lower densities of acid sites and showed a higher methane-efficiency for CH4-SCR than those prepared in other solvents. These catalysts maintained their high activity even when the reaction was carried out under the severe conditions (i.e., high space velocity and low NO concentration). 相似文献