4.7 Article

Immobilization of chitosan-templated MnO2 nanoparticles onto filter paper by redox method as a retrievable Fenton-like dip catalyst

期刊

CHEMOSPHERE
卷 268, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2020.128835

关键词

Manganese dioxide; Biopolymer; Dip catalyst; Redox precipitation; Fenton-like

资金

  1. National Natural Science Foundation of China [22002078]
  2. Scientific Research Foundation of Shaanxi University of Science Technology [2015BJ-27]

向作者/读者索取更多资源

An efficient and retrievable dip catalyst MnO2/CH-FP was designed for Fenton-like degradation of methylene blue over a wide pH range. The catalyst showed superior degradation efficiency and stability compared to bare MnO2, thanks to its larger surface area and more accessible active sites.
By exploiting the hydrophilicity of cellulose filter paper (FP) and the excellent chelating property of chitosan (CH) for Mn2+, we have designed an efficient and retrievable dip catalyst MnO2/CH-FP for Fenton-like degradation of methylene blue (MB) over a wide pH range from 2.8 to 11.2. The MnO2 nanoparticles were uniformly immobilized in the CH-FP matrix by in-situ redox precipitation method where Mn(NO3)(2) was treated with KMnO4 at mild conditions. A series of MnO2/CH-FP hybrids with different MnO2 loading were fabricated via varying concentration of Mn(NO3)(2) solution, and their structure-function relationships were discussed based on detailed characterization. The optimal catalyst 1.0MnO(2)/CH-FP could cooperate with multiple low-concentration dosages of H2O2 to efficiently degrade 95.6% MB in 90 min (50 mg L-1 MB, 1 g L-1 catalyst, 30 mg L-1 H2O2, pH 7). It is also shown that 1.0MnO(2)/CH-FP could still keep 83.3% degradation efficiency of MB after six cycles. Moreover, the activity of this composite greatly surpassed that of bare MnO2 for nearly 50%, owing to its larger surface area and more accessible active sites. This method for preparing MnO2/CH-FP could effectively avoid the agglomeration of MnO2 nanoparticles and make the reaction turn on/off almost instantaneously by mere insertion/removal. (C) 2020 Elsevier Ltd. All rights reserved.

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