Solvothermal synthesis of multiwall carbon nanotubes/BiOI photocatalysts for the efficient degradation of antipyrine under visible light.

Abstract:

:Antipyrine (ANT), as a widely used relieve headache, fever anti-inflammatory pharmaceutical in medical treatment, is difficult to be removed completely in water. The application of photocatalytic removal of ANT is restricted to UV light irradiation (<5% of solar energy), and the degradation pathways of ANT require more theoretical evidence. In this study, a series of three dimensions (3D) hierarchical structure multiwall carbon nanotubes/bismuth oxyiodide (MWCNTs/BiOI) photocatalysts were systematically designed and firstly applied to remove ANT through visible light (>43% of solar energy) induced photodegradation. Consequently, the as-prepared MWCNTs/BiOI photocatalysts presented superior photocatalytic activities on ANT degradation with respect to that of BiOI under 60 min visible light irradiation (100% vs 82.2%). Especially, the enhanced photocatalytic mechanism on ANT was analyzed by morphology, optical and photo-electrochemical properties. Results revealed that the designed 3D micro-mesoporous structure could promote the diffusion of photogenerated electron-hole pairs, and the utilization of photoelectrons could be efficiently improved by MWCNTs (1.5 times). Furthermore, based on radicals scavenging experiments, the photogenerated hole (h+) and superoxide radical (O2-) were demonstrated as the dominant active species in ANT photocatalytic oxidation process. The photodegradation pathways of ANT were proposed with the calculation of frontier electron densities (FEDs) and the analysis of LC-MS/MS. This study presents a feasible approach for the high efficiency removal of trace pharmaceuticals under visible light photocatalytic process.

journal_name

Environ Res

journal_title

Environmental research

authors

Gao P,Yin Z,Feng L,Liu Y,Du Z,Duan Z,Zhang L

doi

10.1016/j.envres.2020.109468

subject

Has Abstract

pub_date

2020-06-01 00:00:00

pages

109468

eissn

0013-9351

issn

1096-0953

pii

S0013-9351(20)30361-3

journal_volume

185

pub_type

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