Formation of different products during photo-catalytic reaction on TiO2 suspension in water with and without 2-propanol under diverse ambient conditions

Formation of different products during photo-catalytic reaction on TiO2 suspension in water with... Studies on photo-catalytic reduction of CO2 using TiO2 photo-catalyst (0.1%, w/v) as a suspension in water was carried out at 350 nm light. CO2 from both commercially available source, as well as generated in situ through 2-propanol oxidation, was used for this study. The photolytic products such as hydrogen (H2), carbon monoxide (CO) andmethane (CH4) generated were monitored in TiO2 suspended aqueous solution with and without a hole scavenger, viz., 2-propanol. Similar photolytic experiments were also carried out with varying ambient such as air, O2, N2 and N2O. The yields of CO and CH4 in all these systems under the present experimental conditions were found to be increasing with light exposure time. H2 yield in N2-purged systems containing 2-propanol was found to be more as compared to the without 2-propanol system. The rate of H2 production in N2-purged aqueous solutions containing 0.1% TiO2 suspension were evaluated to be 0.226 and 5.8 μl/h, without and with 0.5 M 2-propanol, respectively. This confirmed that 2-propanol was an efficient hole scavenger and it scavenged photo-generated holes (h+), allowing its counter ion, viz., e−, to react with water molecule/H+ to yield more H2. The formation of both CO and CH4 in the photolysis of CO2-purged aqueous solutions containing suspended TiO2 in absence of 2-propanol reveal that the generation of CH4 is taking place mainly through CO intermediate. In presence of air/O2, the yield of H2 in the system without 2-propanol was observed to be negligible as compared to the system containing 2-propanol in which low yield of H2 was obtained with a formation rate of approx. 0.5 μl/h. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Formation of different products during photo-catalytic reaction on TiO2 suspension in water with and without 2-propanol under diverse ambient conditions

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Publisher
Springer Journals
Copyright
Copyright © 2007 by VSP
Subject
Chemistry; Catalysis; Physical Chemistry; Inorganic Chemistry
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1163/156856707781749883
Publisher site
See Article on Publisher Site

Abstract

Studies on photo-catalytic reduction of CO2 using TiO2 photo-catalyst (0.1%, w/v) as a suspension in water was carried out at 350 nm light. CO2 from both commercially available source, as well as generated in situ through 2-propanol oxidation, was used for this study. The photolytic products such as hydrogen (H2), carbon monoxide (CO) andmethane (CH4) generated were monitored in TiO2 suspended aqueous solution with and without a hole scavenger, viz., 2-propanol. Similar photolytic experiments were also carried out with varying ambient such as air, O2, N2 and N2O. The yields of CO and CH4 in all these systems under the present experimental conditions were found to be increasing with light exposure time. H2 yield in N2-purged systems containing 2-propanol was found to be more as compared to the without 2-propanol system. The rate of H2 production in N2-purged aqueous solutions containing 0.1% TiO2 suspension were evaluated to be 0.226 and 5.8 μl/h, without and with 0.5 M 2-propanol, respectively. This confirmed that 2-propanol was an efficient hole scavenger and it scavenged photo-generated holes (h+), allowing its counter ion, viz., e−, to react with water molecule/H+ to yield more H2. The formation of both CO and CH4 in the photolysis of CO2-purged aqueous solutions containing suspended TiO2 in absence of 2-propanol reveal that the generation of CH4 is taking place mainly through CO intermediate. In presence of air/O2, the yield of H2 in the system without 2-propanol was observed to be negligible as compared to the system containing 2-propanol in which low yield of H2 was obtained with a formation rate of approx. 0.5 μl/h.

Journal

Research on Chemical IntermediatesSpringer Journals

Published: Jan 1, 2007

References

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