Please use this identifier to cite or link to this item:
Title: Peroxymonosulfate activated by amorphous particulate MnO2 for mineralization of benzene gas : redox reaction, weighting analysis, and numerical modelling
Authors: Li, HW
Lee, SC 
Wang, ZW
Huang, Y
Ho, WK
Cui, L
Keywords: Amorphous particulate MnO2
Benzene gas
Numeric model
Weighting analysis
Issue Date: 2017
Publisher: Elsevier
Source: Chemical engineering journal, 2017, v. 316, p. 61-69 How to cite?
Journal: Chemical engineering journal 
Abstract: Amorphous particulate MnO2 (AMO) which features micro-nano hierarchical structure can be viewed as a favorable alternative to crystalline α-MnO2 for Peroxymonosulfate (PMS) activation. The former not only is comparatively simple to obtain but also has similar performance on powerful adsorption and catalytic capability. In this paper, the combined use of AMO and PMS oxidizing system showed the paralleled degradation efficiency of benzene gas with 50.5 ± 3.75%, which was just around 5 percentage points lower than that achieved in the α-MnO2&PMS system. Highly stable catalytic activity of the AMO&PMS system exhibited during an ensuing cyclic experiment, averaging at 63.08% for benzene mineralization. Additionally, a novel method of weighting analysis which evaluates the synergetic effects among operating parameters on benzene removal was firstly explored in the nanosized catalyst-based activation system. Through a novel specific reaction drag model for porous media, specific drag coefficients at various testing conditions, k2, in terms of pressure drop across microporous AMO, were held to establish the correlations between ideal mineralization efficiencies and optimal parameter combinations. A further comparison between laboratory data and model simulations confirmed that, regardless of pH variations, the mineralization rate can be enhanced to around 67.7% at a more higher temperature (45 °C) when the consumed ratio of AMO to PMS leveled off at 0.8, during which time much lower k2 of 0.24 Pa·min·m/mg would present.
EISSN: 1385-8947
DOI: 10.1016/j.cej.2017.01.070
Appears in Collections:Journal/Magazine Article

View full-text via PolyU eLinks SFX Query
Show full item record


Last Week
Last month
Citations as of Aug 12, 2018


Last Week
Last month
Citations as of Aug 18, 2018

Page view(s)

Last Week
Last month
Citations as of Aug 13, 2018

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.