Design and evaluation of a novel-controlled periodic illumination reactor to study photocatalysis

Citation
Kj. Buechler et al., Design and evaluation of a novel-controlled periodic illumination reactor to study photocatalysis, IND ENG RES, 38(4), 1999, pp. 1258-1263
Citations number
24
Categorie Soggetti
Chemical Engineering
Journal title
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
ISSN journal
08885885 → ACNP
Volume
38
Issue
4
Year of publication
1999
Pages
1258 - 1263
Database
ISI
SICI code
0888-5885(199904)38:4<1258:DAEOAN>2.0.ZU;2-E
Abstract
A novel reactor designed to study the effects of continuous or controlled p eriodic illumination (CPI) on photocatalytic reactions was built and tested . The reactor uses immobilized films of TiO2 on the circular face of a disk . Rotating disk hydrodynamics provide uniform access to the catalyst surfac e. These coated disks rotate in a closed cell filled with the reagents at a ngular velocities ranging from 20 to 100 revolutions per minute (rev/min). A bank of black lamps provides uniform UV illumination to the disk surface. A mechanical shutter is used to provide the periodic illumination. This sh utter can provide light or dark times as short as 100 ms and as long as min utes. To evaluate the performance of this reactor, the oxidation of formate ion (HCOO-) to CO2 and H2O was studied at various light intensities and a single light and dark time. As the light intensity was increased from 0.05 to 5.5 mW/cm(2) the photoefficiency for continuous illumination experiments decreased from 80% to 5%. At a light time of 0.6 s and a dark time of 2.0 s and a light intensity of 5.5 mW/cm(2), the photoefficiency increased from 5% during the continuous illumination experiments to 20% with CPI. However , at low light; intensities (I < 0.5 mW/cm(2)), CPI did not effect the phot oefficiency. Analysis of the results indicates that the reactor is oxygen d iffusion-limited at light intensities above 0.5 mW/cm(2) when air is used a s the oxidant. At intensities below 0.3 mW/cm(2), the reaction is photon li mited and we are able to study the kinetics of the reaction. At light inten sities between 0.3 and 0.5 mW/cm(2), the reaction is controlled by both sur face kinetics and diffusion limitations.