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Efficient adsorption and sustainable degradation of gaseous acetaldehyde and o-xylene using rGO-TiO2 photocatalyst
Ist Teil von
Chemical engineering journal (Lausanne, Switzerland : 1996), 2018-10, Vol.349, p.708-718
Ort / Verlag
Elsevier B.V
Erscheinungsjahr
2018
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
As-prepared rGO-TiO2 nanocomposites exhibited superior adsorptivity and photodegradation ability in the degradation of acetaldehyde and o-xylene. Furthermore, this work firstly revealed the different roles of free radicals in the degradation of the two types of VOCs. O2− and OH played similar roles in the photocatalytic degradation process of o-xylene, while O2− was predominant radical in the degradation of acetaldehyde.
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•rGO-TiO2 for the photodegradation of two types of gaseous pollutants.•The different adsorption and photodegradation mechanism of acetaldehyde and o-xylene.•Different roles of O2− and OH in the process of photodegradation.•Sustainable photodegradation of gaseous VOCs in a wide range of flow rates.
Two types of volatile organic chemicals (VOCs), acetaldehyde and o-xylene, were selected to probe the different adsorption and photodegradation mechanism of gaseous photocatalysis. Reduced graphene oxide (rGO)-TiO2 nanocomposites were prepared by facile solvothermal process to perform the photocatalytic reactions. In the experiments, the removal efficiencies of the acetaldehyde and o-xylene at 80 mL·min−1 flow rate were only 15% and 12% when P25 was applied, while the efficiencies were sharply increased to 42% and 54% by using 0.5 wt% rGO-TiO2 as the photocatalyst, respectively. Interestingly, it is notable that the removal efficiency of o-xylene was higher than that of acetaldehyde with identical rGO-TiO2 photocatalyst. Experiments suggested that there were possibly two reasons. Firstly, the adsorbance of o-xylene was more than that of acetaldehyde owing to the π-π conjugation between rGO and aromatic compounds, which was proved by adsorption equilibrium and TPD tests. ESR tests proved that rGO can promote the generation of surface OH radicals and depress the O2− radicals formation. Compared with the dominant role played by O2− radicals in the degradation of acetaldehyde, an almost equal position of O2− and OH radicals was observed in the degradation of o-xylene according to the subsequent radical scavenger experiments. Moreover, the optimized rGO-TiO2 exhibited sustainable photocatalytic activity at 40–120 mL·min−1 flow rate through 160 min tests, while P25 was deactivate only after 25 min. This work demonstrated the different adsorption and degradation characteristics of two types of VOCs, which could propel the target orientation design of photocatalyst in VOCs removal applications.