TY - JOUR
T1 - Sonocatalytic degradation of oxalic acid in the presence of oxygenand Pt/TiO2
AU - Chave, Tony
AU - Navarro, Nathalie M.
AU - Pochon, Patrick
AU - Perkas, Nina
AU - Gedanken, Aharon
AU - Nikitenko, Sergey I.
N1 - Publisher Copyright:
© 2014 Elsevier B.V.
PY - 2015/3/1
Y1 - 2015/3/1
N2 - In order to treat aqueous effluents containing organic pollutants, several techniques can be considereddepending on the organic compound concentration. Sonochemistry appears to be a promising solutionto answer water remediation issue. In fact, when submitted into a liquid, ultrasound can induce thenucleation, growth, and violent collapse of vapor/gas filled bubbles. However, despite the extreme localconditions observed during acoustic cavitation, using ultrasound alone is efficient only at low concentration in organic pollutants. In the present study, 0.05 M oxalic acid degradation kinetics were followed at40°C under various conditions, in presence or not of Pt/TiO2 catalyst under silent conditions or ultrasoundat 20 and 360 kHz. Experiments were achieved under controlled atmosphere and comparison betweenargon, Ar/O2(20 vol% O2) and pure O2 conditions was performed. Oxidation rate increase of oxalic acidwas measured under Ar/O2 atmosphere in presence of Pt/TiO2 catalyst due to strong dispersion effectof both low and high ultrasonic frequency and formation of chemically active species by sonolysis. Highfrequency ultrasonic irradiation under Ar/O2 atmosphere gives the highest kinetic increase compared tosilent conditions with oxalic acid degradation rate around 13 μmol min-1 at 40°C with 2 g L-1 of 3 wt%Pt on P25 TiO2 catalyst.
AB - In order to treat aqueous effluents containing organic pollutants, several techniques can be considereddepending on the organic compound concentration. Sonochemistry appears to be a promising solutionto answer water remediation issue. In fact, when submitted into a liquid, ultrasound can induce thenucleation, growth, and violent collapse of vapor/gas filled bubbles. However, despite the extreme localconditions observed during acoustic cavitation, using ultrasound alone is efficient only at low concentration in organic pollutants. In the present study, 0.05 M oxalic acid degradation kinetics were followed at40°C under various conditions, in presence or not of Pt/TiO2 catalyst under silent conditions or ultrasoundat 20 and 360 kHz. Experiments were achieved under controlled atmosphere and comparison betweenargon, Ar/O2(20 vol% O2) and pure O2 conditions was performed. Oxidation rate increase of oxalic acidwas measured under Ar/O2 atmosphere in presence of Pt/TiO2 catalyst due to strong dispersion effectof both low and high ultrasonic frequency and formation of chemically active species by sonolysis. Highfrequency ultrasonic irradiation under Ar/O2 atmosphere gives the highest kinetic increase compared tosilent conditions with oxalic acid degradation rate around 13 μmol min-1 at 40°C with 2 g L-1 of 3 wt%Pt on P25 TiO2 catalyst.
KW - Catalysis-Ultrasound
KW - Oxalic acid
KW - Oxygen
KW - Sonocatalysis
KW - Sonochemistry
UR - http://www.scopus.com/inward/record.url?scp=85027919589&partnerID=8YFLogxK
U2 - 10.1016/j.cattod.2014.07.040
DO - 10.1016/j.cattod.2014.07.040
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AN - SCOPUS:85027919589
SN - 0920-5861
VL - 241
SP - 55
EP - 62
JO - Catalysis Today
JF - Catalysis Today
IS - PA
ER -