Publication Cover
Ozone: Science & Engineering
The Journal of the International Ozone Association
Volume 35, 2013 - Issue 4
577
Views
35
CrossRef citations to date
0
Altmetric
Original Articles

Facile Synthesis of Activated Carbon-Supported Porous Manganese Oxide via in situ Reduction of Permanganate for Ozone Decomposition

, , , &
Pages 308-315 | Received 07 Feb 2013, Accepted 08 Mar 2013, Published online: 16 Jul 2013
 

Abstract

Lichen-like porous manganese oxides (MnOx) with birnessite-type structure, which were assembled with curled nanosheets (less than 10 nm in thickness), were deposited in situ on the surface of activated carbon (AC) via facile reduction of permanganate by AC, and were tested for the decomposition of ozone, a common air pollutant. Despite the low Mn loading (typically 0.04%–0.14%), the as-synthesized MnOx/AC catalysts exhibited high catalytic activity and stability for ozone decomposition at room temperature and high relative humidity, which can be attributed to the enrichment of the Mn element on the catalyst surface and a well-organized porous surface morphology of MnOx.

Acknowledgments

The work is funded by the National High Technology Research and Development Program of China (Grant No. 2012AA062701) and Tsinghua University Initiative Scientific Research Program.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 403.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.