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Strong promoted catalytic ozonation of atrazine at low temperature using tourmaline as catalyst: Influencing factors, reaction mechanisms and pathways.

Authors :
Wang, Da
Xu, Haodan
Ma, Jun
Lu, Xiaohui
Qi, Jingyao
Song, Shuang
Source :
Chemical Engineering Journal. Dec2018, Vol. 354, p113-125. 13p.
Publication Year :
2018

Abstract

Graphical abstract Highlights • Catalytic ozonation of atrazine on tourmaline was studied. • Tourmaline exhibited superior catalytic performance even in low temperature (278 K). • Surface properties of tourmaline was characterized in detail. • 31 kinds of intermediates were identified and the degradation pathways of atrazine were proposed. Abstract Tourmaline, an economical and eco-friendly natural mineral, has been widely used during the water treatment processes. In this investigation, the raw tourmaline has been found to be effective as a catalyst for ozonation in the degradation of atrazine (ATZ) under low temperature (278 K). Within typical experimental conditions (tourmaline dosage = 1 g L−1, [ATZ] 0 = 5 μM, [O 3 ] 0 = 3 mg L−1, at pH 7.0 and 278 K), the removal efficiency of ATZ in catalytic ozonation was 98% after 10 min, compared with only 27% ATZ removal in the absence of catalyst. Surface properties and components of tourmaline were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectra (FTIR), pyridine-FTIR and energy dispersive X-ray (EDX). The characterization studies showed that metal attached hydroxyl groups (M OH, M = Fe, Al and Si) were the main active sites for ozone adsorption and decomposition. The formation of hydroxyl radicals (OH) as well as hydrogen peroxide (H 2 O 2) led to fast ATZ degradation and 31 kinds of intermediates; meanwhile, possible degradation pathways of ATZ were detected and proposed. The mechanisms of reaction were proposed for tourmaline-catalyzed ozonation based on all the experimental results and material characterizations. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13858947
Volume :
354
Database :
Academic Search Index
Journal :
Chemical Engineering Journal
Publication Type :
Academic Journal
Accession number :
131847731
Full Text :
https://doi.org/10.1016/j.cej.2018.07.032