TY - JOUR
T1 - Inhibit the formation of toxic methylphenolic by-products in photo-decomposition of formaldehyde–toluene/xylene mixtures by Pd cocatalyst on TiO2
AU - Wu, Qiqi
AU - Ye, Jiani
AU - Qiao, Wei
AU - Li, Yongwang
AU - Niemantsverdriet, J. W.(Hans)
AU - Richards, Emma
AU - Pan, Feng
AU - Su, Ren
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/8/15
Y1 - 2021/8/15
N2 - Photocatalytic removal of single volatile organic compounds (VOCs) has been widely investigated; however, photodecomposition of VOC mixtures has been rarely addressed, which may bring safety doubts in indoor air purification due to possible formation of harmful compounds. Here we show that in photocatalytic oxidation of formaldehyde–toluene and formaldehyde–xylene mixtures, the introduction of Pd cocatalyst on TiO2 photocatalyst successfully inhibits the formation of toxic methylphenols, thus promoting the complete mineralization of VOC mixtures into CO2 via the harmless benzaldehyde intermediates. Mechanistic analysis reveals that the loading of Pd cocatalyst effectively removes the inherent surface −OH groups of TiO2, which significantly promotes the activation of O2 into [rad]OH radicals. The Pd cocatalyst also directs the [rad]OH radicals to attack the methyl group instead of the aromatic ring for the formation of benzaldehyde and its further oxidation to CO2, thus yielding a better overall photocatalytic performance.
AB - Photocatalytic removal of single volatile organic compounds (VOCs) has been widely investigated; however, photodecomposition of VOC mixtures has been rarely addressed, which may bring safety doubts in indoor air purification due to possible formation of harmful compounds. Here we show that in photocatalytic oxidation of formaldehyde–toluene and formaldehyde–xylene mixtures, the introduction of Pd cocatalyst on TiO2 photocatalyst successfully inhibits the formation of toxic methylphenols, thus promoting the complete mineralization of VOC mixtures into CO2 via the harmless benzaldehyde intermediates. Mechanistic analysis reveals that the loading of Pd cocatalyst effectively removes the inherent surface −OH groups of TiO2, which significantly promotes the activation of O2 into [rad]OH radicals. The Pd cocatalyst also directs the [rad]OH radicals to attack the methyl group instead of the aromatic ring for the formation of benzaldehyde and its further oxidation to CO2, thus yielding a better overall photocatalytic performance.
KW - Formaldehyde, toluene and xylenes
KW - Oxygen activation
KW - Pd cocatalyst
KW - Photo-oxidation of VOC mixtures
KW - Toxic intermediates
UR - https://www.scopus.com/pages/publications/85102579679
U2 - 10.1016/j.apcatb.2021.120118
DO - 10.1016/j.apcatb.2021.120118
M3 - 文章
AN - SCOPUS:85102579679
SN - 0926-3373
VL - 291
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
M1 - 120118
ER -