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Mean gas holdup, lateral distribution of gas holdup and axial mixing of gas and liquid were measured in bubble columns of 12 and 19cm i.d. The lateral distribution of gas holdup was strongly dependent on the flow regimes in the column. The axial mixing of liquid in the homogeneous bubble flow regime was much smaller than that in the heterogeneous bubble flow regime, and was not expressed by existing correlations. The axial mixing of liquid in the homogeneous bubble flow and the intermediate flow regime was simulated with a flow model based on the lateral distribution of buoyancy force and the effective viscosity. The axial mixing of gas was larger than that of liquid.  相似文献   
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In fluidized beds of 0.052 and 0.12 m i.d. air, water and aqueous solutions of carboxymethyl cellulose (viscosity = 9.0 X 10-4- 52 X 10-2 Pa s), and glass beads were used as gas, liquid and solid phase, respectively. The diameters of the glass beads were 4.2 X 10-4 6.6 X 10-4 1.2 X l0-3, and 2.2 X 10-3 m.The liquid holdup in the gas-liquid-solid fluidized bed was well correlated by modifying the Garside and Al-Dibouni's equation with the gas phase Froude number.The wall heat transfer coefficient of the gas-liquid-solid fluidized beds in the range of stable fluidization state runs correlated as a function of modified Nusselt number, modified Reynolds number and gas phase Froude number.  相似文献   
3.
Amorphous polymer/crystalline polymer blends can be prepared via the simultaneous polymerization of polymethacrylate/polyurethane combinations. The relationship between higher order structures and fracture mechanisms in these blends must be uncovered to elucidate the source of the increased fracture toughness of such materials. The present work involves the production of blended polymethacrylate/polyurethane and assess the internal structures of these specimens using optical and electron microscopy. These observations reveal the presence of both spherulites and elastomeric phases. The spherulites consisting of the polyurethane and are several micrometers in diameter whereas the phase-separated polyurethane elastomeric domains are approximately 100 nm in size. Multiple cracks, crack bridging and plastic deformation around the precrack tips of loaded specimens are evidently responsible for the increased toughness of these blends. The former two phenomena are attributed to the presence of spherulites while the plastic deformation of the methacrylate matrix is ascribed to cavitation of the polyurethane elastomeric phases in response to loading.  相似文献   
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