N-doped hierarchically porous carbon for highly efficient metal-free catalytic activation of peroxymonosulfate in water: A non-radical mechanism.

Abstract:

:Metal-free carbo-catalyst has recently emerged as a promising candidate as a substituent for tradition-metal based heterogeneous catalyst for catalytic activation of peroxymonosulfate (PMS). However, most reported carbo-catalysts suffer from low catalytic efficiency and poor stability, thus a high-performance catalyst is urgently desired. In this study, a novel carbo-catalyst (NHPC-800), prepared by using tannic acid and dicyandiamide as renewable carbon/nitrogen feedstocks via a simple pyrolysis route, is reported as an activator of PMS with highly efficient catalytic ability and stability. The as-prepared NHPC-800 possesses as high as 22.4 atom% of nitrogen dopants and a hierarchically porous structure with abundant meso/macropores, accompanied by the abundant edges and wrinkles, which supply sufficient exposed catalytically active centers and fast electrons/mass transportations. Using rhodamine B as a model pollutant, the NHPC-800 shows a highly efficient catalytic ability which is superior to most reported carbo-catalysts and even some state-of-the-art metal catalysts. Based on competitive quenching experiments and electron paramagnetic resonance (EPR) results, a non-radical pathway involving the generation of 1O2 is responsible for the degradation of pollutants. Given that the NHPC-800 shows good recycling performance and strong resistance to adventitious interference such as anions and natural organic matters, we believe NHPC-800 can be a promising candidate for practical applications, and this study can provide inspirations for the further development of highly efficient carbo-catalysts.

journal_name

Chemosphere

journal_title

Chemosphere

authors

Long Y,Bu S,Huang Y,Shao Y,Xiao L,Shi X

doi

10.1016/j.chemosphere.2018.10.175

subject

Has Abstract

pub_date

2019-02-01 00:00:00

pages

545-555

eissn

0045-6535

issn

1879-1298

pii

S0045-6535(18)32046-0

journal_volume

216

pub_type

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