TY - JOUR
T1 - The case for the photocatalytic spinning disc reactor as a process intensification technology
T2 - Comparison to an annular reactor for the degradation of methylene blue
AU - Boiarkina, Irina
AU - Norris, Stuart
AU - Patterson, Darrell
PY - 2013/6/1
Y1 - 2013/6/1
N2 - A spinning disc reactor was investigated as a process intensification technology for photocatalysis and compared with a conventional annular reactor. It was found that the average photonic efficiency achieved in the SDR was three times larger than the maximum photonic efficiency achieved in the annular reactor, 0.19 ±0.08% versus 0.062 ± 0.009%, indicating that the SDR is significantly more efficient at utilising the incoming light. Similarly, the average volumetric rate of reaction for the SDR was an order of magnitude larger than that of the annular reactor, 3.6±1.5×10-43.6±1.5×10-4 mol.m−3.s−1 versus 0.13±0.02×10-40.13±0.02×10-4 mol.m−3.s−1, due to the significantly smaller volume in the SDR. However, the average surface rate of reaction is more useful for comparison in an immobilised catalyst system. In the SDR, the initial surface rate of reaction was approximately the same (within the margin of error) as the photocatalytic reaction in the annular reactor. This suggests that both reactors exhibit the same rate limiting step. Given the significantly higher mass transfer rate in the SDR over the annular reactor, it is likely that the rate limiting step is either the adsorption of oxygen onto the catalyst or the electron transfer from the catalyst to the oxygen, often found to be the rate limiting step in photocatalytic reactions. However, the maximum surface rate of reaction achieved in the SDR (at a flow rate of 15mL.s−1) was two times larger than the maximum reaction achieved in the annular reactor-this suggests that at this condition the rate limiting step is being overcome, and that when operated at this condition the photocatalytic SDR is performing as a process intensification technology.
AB - A spinning disc reactor was investigated as a process intensification technology for photocatalysis and compared with a conventional annular reactor. It was found that the average photonic efficiency achieved in the SDR was three times larger than the maximum photonic efficiency achieved in the annular reactor, 0.19 ±0.08% versus 0.062 ± 0.009%, indicating that the SDR is significantly more efficient at utilising the incoming light. Similarly, the average volumetric rate of reaction for the SDR was an order of magnitude larger than that of the annular reactor, 3.6±1.5×10-43.6±1.5×10-4 mol.m−3.s−1 versus 0.13±0.02×10-40.13±0.02×10-4 mol.m−3.s−1, due to the significantly smaller volume in the SDR. However, the average surface rate of reaction is more useful for comparison in an immobilised catalyst system. In the SDR, the initial surface rate of reaction was approximately the same (within the margin of error) as the photocatalytic reaction in the annular reactor. This suggests that both reactors exhibit the same rate limiting step. Given the significantly higher mass transfer rate in the SDR over the annular reactor, it is likely that the rate limiting step is either the adsorption of oxygen onto the catalyst or the electron transfer from the catalyst to the oxygen, often found to be the rate limiting step in photocatalytic reactions. However, the maximum surface rate of reaction achieved in the SDR (at a flow rate of 15mL.s−1) was two times larger than the maximum reaction achieved in the annular reactor-this suggests that at this condition the rate limiting step is being overcome, and that when operated at this condition the photocatalytic SDR is performing as a process intensification technology.
KW - spinning disc reactor
KW - Photocatalysis
KW - Process intensification
KW - Annular reactor
KW - Reactor comparison
UR - http://www.scopus.com/inward/record.url?scp=84877342044&partnerID=8YFLogxK
UR - http://www.sciencedirect.com/science/article/pii/S1385894713004610
UR - http://dx.doi.org/10.1016/j.cej.2013.03.125
U2 - 10.1016/j.cej.2013.03.125
DO - 10.1016/j.cej.2013.03.125
M3 - Article
SN - 1385-8947
VL - 225
SP - 752
EP - 765
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -