Issue 41, 2020

Synthesizing C–N–P-tridoped TiO2 in a Salix psammophila-activated carbon body to enhance its regeneration performance

Abstract

Based on the natural interconnected pore networks of Salix psammophila (SP), TiO2 was synthesized in an SP-based activated carbon (AC) body through a series of facile processes including impregnation, calcination, and activation. Compared with the traditional surface modification, TiO2/AC (TiO2 and AC composite) in this study exhibited better durability and higher regeneration performance under visible-light irradiation. There were five reasons: (1) the binding force between TiO2 and AC was significantly enhanced, and methylene blue removal ratio only decreased by 11% after three trials; (2) C, N, and P atoms were spontaneously incorporated into the TiO2 lattice during the synthesis processes, which observably extended the TiO2's visible-light response; (3) the anatase/rutile mixed phase and greater surface hydroxyl concentration elevated TiO2 photodegradation; (4) AC being close to TiO2 was able to trap electrons, further increasing the TiO2's photocatalytic activity; (5) the synergistic effect of adsorption and photodegradation was enhanced. With increasing TiO2 content, TiO2/AC regeneration performance was improved initially and then became weak; TiO2/AC2 : 1 (2 : 1 is the mass ratio of tetrabutyl titanate and ethanol) exhibited the highest regeneration performance: 55% methylene blue was removed by the saturated AC after 2 h visible-light irradiation, which was almost double that of the traditional surface-modified sample.

Graphical abstract: Synthesizing C–N–P-tridoped TiO2 in a Salix psammophila-activated carbon body to enhance its regeneration performance

Article information

Article type
Paper
Submitted
29 Jul 2020
Accepted
21 Sep 2020
First published
21 Sep 2020

New J. Chem., 2020,44, 17871-17881

Synthesizing C–N–P-tridoped TiO2 in a Salix psammophila-activated carbon body to enhance its regeneration performance

W. Liu, B. Wang and M. Zhang, New J. Chem., 2020, 44, 17871 DOI: 10.1039/D0NJ03816D

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