TY - JOUR
T1 - Effect of aqueous matrix species on synergistic removal of bisphenol-A under solar irradiation using nitrogen-doped TiO2/AC composite
AU - Yap, Pow Seng
AU - Lim, Teik Thye
N1 - Funding Information:
The research group acknowledges the financial support provided by the National Research Foundation (NRF) , Singapore through project EWI RFP 0802-11. P.-S. Yap thanks Nanyang Technological University (NTU) for the award of a PhD research scholarship.
PY - 2011/1/14
Y1 - 2011/1/14
N2 - A bi-functional composite, namely nitrogen-doped titanium dioxide anchored on activated carbon (N-TiO2/AC) was synthesized using the sol-gel method with two-stage calcination procedure. Bisphenol-A (BPA) was used as a model contaminant. The effects of co-existing aqueous species viz. prevalent inorganic anions (Cl-, NO3-, SO42-, HCO3-, H2PO4- and silica), organic anion (C2O42-), photocatalysis inhibitor (CH3OH) and oxidant (H2O2) were comprehensively studied using the best performing composite, i.e. N-TiO2/AC (400M-700T). Introduction of H2PO4- (0.01-0.1mM) led to a slight enhancement in the photocatalytic degradation (PCD) efficiency for BPA removal. Provision of AC support for N-TiO2 abated the inhibitory effect induced by SO42- at high concentration (up to 100mM). Decreased BPA photodegradation was observed with increasing concentrations of C2O42-, thus suggesting that direct hole (h+) oxidation occurred. Variation of pH (from 4 to 10) in the presence of 0.1mM of silica induced little effect on BPA photodegradation. Addition of H2O2 into N-TiO2/AC system apparently resulted in decreased BPA removal because some adsorbed BPA was released from surface-degraded AC.
AB - A bi-functional composite, namely nitrogen-doped titanium dioxide anchored on activated carbon (N-TiO2/AC) was synthesized using the sol-gel method with two-stage calcination procedure. Bisphenol-A (BPA) was used as a model contaminant. The effects of co-existing aqueous species viz. prevalent inorganic anions (Cl-, NO3-, SO42-, HCO3-, H2PO4- and silica), organic anion (C2O42-), photocatalysis inhibitor (CH3OH) and oxidant (H2O2) were comprehensively studied using the best performing composite, i.e. N-TiO2/AC (400M-700T). Introduction of H2PO4- (0.01-0.1mM) led to a slight enhancement in the photocatalytic degradation (PCD) efficiency for BPA removal. Provision of AC support for N-TiO2 abated the inhibitory effect induced by SO42- at high concentration (up to 100mM). Decreased BPA photodegradation was observed with increasing concentrations of C2O42-, thus suggesting that direct hole (h+) oxidation occurred. Variation of pH (from 4 to 10) in the presence of 0.1mM of silica induced little effect on BPA photodegradation. Addition of H2O2 into N-TiO2/AC system apparently resulted in decreased BPA removal because some adsorbed BPA was released from surface-degraded AC.
KW - Activated carbon
KW - Anions
KW - Aqueous matrix species
KW - Nitrogen doping
KW - Solar photocatalysis
KW - Titanium dioxide
UR - http://www.scopus.com/inward/record.url?scp=78650303503&partnerID=8YFLogxK
U2 - 10.1016/j.apcatb.2010.11.013
DO - 10.1016/j.apcatb.2010.11.013
M3 - Article
AN - SCOPUS:78650303503
SN - 0926-3373
VL - 101
SP - 709
EP - 717
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
IS - 3-4
ER -