TY - JOUR
T1 - Vibrofluidized- and fixed-bed photocatalytic reactors
T2 - Case of gaseous acetone photooxidation
AU - Vorontsov, Alexander V.
AU - Savinov, Evgueni E.
AU - Smirniotis, Panagiotis G.
N1 - Funding Information:
This project has been funded in part by the National Research Council under the Collaboration in Basic Science and Engineering Program (COBASE). The content of this publication do not necessarily reflect the views or policies of the NRC, nor does mention of trade names, commercial products, or organizations imply endorsement by the NRC.
PY - 2000/11
Y1 - 2000/11
N2 - Vibrofluidized- and multiple fixed-bed photoreactors were compared under identical operating conditions. The comparison was based on the quantum efficiency for the gas-phase photocatalytic oxidation of acetone using TiO2 (Hombikat UV 100). Multiple fixed-bed reactor configurations were used, along with a vibrofluidized-bed configuration. Quantum efficiency decreased in the following order: vibrofluidized bed (8.7%) > fixed-bed granules (6.9%) > fixed film bed (5.9%) ~ fixed powdered bed (5.8%). The increased activity of the vibrofluidized-bed could not be attributed to enhanced external mass transport, as all reactor systems used in the present study demonstrated negligible external mass transfer resistances. Instead, the increased activity is most likely credited to the effect of periodic illumination phenomenon taking place because of the random motion of catalyst granules in the fluidized-bed and higher light absorption of scattered light. The enhanced activity observed for the granular fixed bed could be related to mechanical activation of TiO2 during the preparation of granules, as well as to increased light absorption. A maximum of acetone oxidation rate with respect to humidity level was observed. Even at high humidity levels, ultrasound did not affect the rate of gas-phase acetone oxidation. A model has been developed to quantify the absorption of light in a fluidized-bed photoreactor. The model takes into account absorption and single-light scattering and accuratetly describes the dependence of acetone oxidation rate on the quantity of TiO2 granules in the vibrofluidized bed. (C) 2000 Elsevier Science Ltd. All rights reserved.
AB - Vibrofluidized- and multiple fixed-bed photoreactors were compared under identical operating conditions. The comparison was based on the quantum efficiency for the gas-phase photocatalytic oxidation of acetone using TiO2 (Hombikat UV 100). Multiple fixed-bed reactor configurations were used, along with a vibrofluidized-bed configuration. Quantum efficiency decreased in the following order: vibrofluidized bed (8.7%) > fixed-bed granules (6.9%) > fixed film bed (5.9%) ~ fixed powdered bed (5.8%). The increased activity of the vibrofluidized-bed could not be attributed to enhanced external mass transport, as all reactor systems used in the present study demonstrated negligible external mass transfer resistances. Instead, the increased activity is most likely credited to the effect of periodic illumination phenomenon taking place because of the random motion of catalyst granules in the fluidized-bed and higher light absorption of scattered light. The enhanced activity observed for the granular fixed bed could be related to mechanical activation of TiO2 during the preparation of granules, as well as to increased light absorption. A maximum of acetone oxidation rate with respect to humidity level was observed. Even at high humidity levels, ultrasound did not affect the rate of gas-phase acetone oxidation. A model has been developed to quantify the absorption of light in a fluidized-bed photoreactor. The model takes into account absorption and single-light scattering and accuratetly describes the dependence of acetone oxidation rate on the quantity of TiO2 granules in the vibrofluidized bed. (C) 2000 Elsevier Science Ltd. All rights reserved.
KW - Acetone
KW - Hombikat UV 100
KW - Light scattering
KW - Mechanical activation
KW - Photocatalytic oxidation
KW - Vibrofluidized-bed photoreactor
UR - http://www.scopus.com/inward/record.url?scp=0034327278&partnerID=8YFLogxK
U2 - 10.1016/S0009-2509(00)00115-9
DO - 10.1016/S0009-2509(00)00115-9
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AN - SCOPUS:0034327278
SN - 0009-2509
VL - 55
SP - 5089
EP - 5098
JO - Chemical Engineering Science
JF - Chemical Engineering Science
IS - 21
ER -