TY - JOUR
T1 - Reduction of hexavalent chromium and degradation of tetracycline using a novel indium-doped Mn2O3 nanorod photocatalyst
AU - Abinaya, Manickavasagan
AU - Govindan, Kadarkarai
AU - Kalpana, Murugesan
AU - Saravanakumar, Karunamoorthy
AU - Prabavathi, Seenivasan Laskhmi
AU - Muthuraj, Velluchamy
AU - Jang, Am
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2020/10/5
Y1 - 2020/10/5
N2 - This study investigates the photocatalytic reduction of hexavalent chromium (Cr(VI)) and degradation of tetracycline (TC) via visible-light-active In-doped Mn2O3 photocatalysis. Mn2O3 photocatalysts loaded with different In doses are prepared using a simple hydrothermal method, and the results indicate the formation of Mn2O3 nanorod-like structures with good crystallinity. The most significant photocatalytic parameters, namely the catalyst and substrate concentrations, pH, and co-existing ions for the Cr(VI) reduction and TC degradation reactions are systematically examined. Result demonstrates that the Cr(VI) reduction and TC mineralization efficiencies of 52% and 40%, respectively are achieved at the optimum pH of 7, undoped Mn2O3 (10 mg/L), and Cr(VI) or TC concentration of 50 mg/L. However, these efficiencies are remarkably increased to 95% and 93%, respectively, when 10 mg/L of 5% In-doped Mn2O3 is used as the photocatalyst under the same reaction conditions. Moreover, the co-existing HCO3− anions and Ca2+ and Mg2+ divalent cations considerably deteriorate the performance of the In-doped photocatalysts compared with the SO42− and Cl− anions and Na+ and K+ monovalent cations. Liquid chromatography–mass spectrometry analysis reveals that the photodegradation of TC is mainly driven by the elimination of the −CH3 group followed by the subsequent cleavage of the primary –NHCH3 group.
AB - This study investigates the photocatalytic reduction of hexavalent chromium (Cr(VI)) and degradation of tetracycline (TC) via visible-light-active In-doped Mn2O3 photocatalysis. Mn2O3 photocatalysts loaded with different In doses are prepared using a simple hydrothermal method, and the results indicate the formation of Mn2O3 nanorod-like structures with good crystallinity. The most significant photocatalytic parameters, namely the catalyst and substrate concentrations, pH, and co-existing ions for the Cr(VI) reduction and TC degradation reactions are systematically examined. Result demonstrates that the Cr(VI) reduction and TC mineralization efficiencies of 52% and 40%, respectively are achieved at the optimum pH of 7, undoped Mn2O3 (10 mg/L), and Cr(VI) or TC concentration of 50 mg/L. However, these efficiencies are remarkably increased to 95% and 93%, respectively, when 10 mg/L of 5% In-doped Mn2O3 is used as the photocatalyst under the same reaction conditions. Moreover, the co-existing HCO3− anions and Ca2+ and Mg2+ divalent cations considerably deteriorate the performance of the In-doped photocatalysts compared with the SO42− and Cl− anions and Na+ and K+ monovalent cations. Liquid chromatography–mass spectrometry analysis reveals that the photodegradation of TC is mainly driven by the elimination of the −CH3 group followed by the subsequent cleavage of the primary –NHCH3 group.
KW - Co-existing anions
KW - Cr(VI) reduction
KW - Degradation mechanism
KW - In-doped MnOphotocatalysis
KW - Tetracycline degradation
UR - https://www.scopus.com/pages/publications/85084863256
U2 - 10.1016/j.jhazmat.2020.122885
DO - 10.1016/j.jhazmat.2020.122885
M3 - Article
C2 - 32446140
AN - SCOPUS:85084863256
SN - 0304-3894
VL - 397
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
M1 - 122885
ER -