Effective degradation of tetracycline by organic-inorganic hybrid materials induced by triethylenediamine
As an important advanced oxidation technology for environmental purification, photocatalytic degradation has received extensive attention. Designing and synthesizing a catalyst with high-intensity photocatalytic performance is a very challenging subject. Herein, one polydentate cation was synthesize...
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Published in | Environmental research Vol. 198; p. 111253 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Inc
01.07.2021
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Subjects | |
Online Access | Get full text |
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Summary: | As an important advanced oxidation technology for environmental purification, photocatalytic degradation has received extensive attention. Designing and synthesizing a catalyst with high-intensity photocatalytic performance is a very challenging subject. Herein, one polydentate cation was synthesized by 1,4-diazabicyclo[2.2.2]octane (DABCO) and 1, 4-bis (bromomethyl) benzene. Inorganic-organic hybrid compounds 1, 2 were synthesized by hydrothermal and room temperature volatilization with inorganic metal salts, namely, {[L1]0.5·[Cu2Br4]0.5}n (1), {[L1]·[Cu2I4]·CH3CN}n (2). Under visible light, compounds 1 and 2 were investigated for their degradation effects on tetracycline (TC) in water. The experimental results showed that compounds 1 and 2 with appropriate concentration of H2O2 had obvious photocatalytic degradation effect on TC. In addition, the influencing factors of photocatalysis such as the amount of adsorbent, the initial concentration of TC and the different pH value were investigated. The photocatalyst exhibits good stability and cyclability.
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•Cation induced self-assembly for the synthesis of two MOF-based hybrid materials.•MOF-based hybrid materials have high efficiency for photodegradation of TC.•The stability of catalysts was demonstrated through TC degrading cycling experiments. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0013-9351 1096-0953 1096-0953 |
DOI: | 10.1016/j.envres.2021.111253 |