Abstract

In this work, Ag nano-particles deposited and N-doped TiO2 nanosheets grown on the Ti mesh (Ag/N-TiO2/Ti mesh) were synthesized through combination of a hydrothermal process and a photo-reduction deposition strategy, and then applied to photocatalytic (PC) degradation of bisphenol A (BPA). The physicochemical performances of Ag/N-TiO2/Ti mesh were investigated by a series of characterizations. Results showed that N doping promoted the formation of rutile, and increased the thickness of TiO2 nanosheets (30 nm–40 nm). Furthermore, N element was existed in the form of substitutional nitrogen state (O-Ti-N) in the lattice of TiO2, generating N2p doping energy level. The Ag nanoparticles were deposited on the surface of N-TiO2 in the form of Ag0. The PC removal efficiency of BPA by Ag/N-TiO2/Ti mesh was 90.5% within 60 min, much higher than that of N-TiO2/Ti mesh (78.0%) and TiO2/Ti mesh (59.5%). The N adulteration and surfaceplasmaresonance of Ag0 significantly enhanced the visible-light absorbance and photo-excited electrons-holes separation, which accounted for the improved PC degradation of BPA. By using the light transmittance performance of Ti mesh to stack three Ag/N-TiO2/Ti mesh (named 3-Ag/N-TiO2/Ti mesh) in a distance interval of 0.5 cm constructed a new reaction system, and it removed over 99.99% of BPA within 30 min, which was significantly higher than that of Ag/N-TiO2/Ti mesh system (59.5%). This was mainly ascribed to the effective optical energy utilization and the enhanced mass transfer. This study not only indicated that Ag/N-TiO2/Ti mesh was a promising photocatalyst, but also offered useful information for designing specific reactor in practical application (such as amplified cylindrical reactor).

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.