Published September 30, 2009 | Version v1
Journal article

Photocatalytic decolorization and degradation of Congo Red on innovative crosslinked chitosan/nano-CdS composite catalyst under visible light irradiation

  • 1. Department of Environmental Engineering, Taizhou University, Linhai 317000 (China) and College of Resource and Environmental Science, Wuhan University, Wuhan 430072 (China)
  • 2. Department of Environmental Engineering, Taizhou University, Linhai 317000 (China) and College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China)
  • 3. College of Resource and Environmental Science, Wuhan University, Wuhan 430072 (China)
  • 4. Department of Environmental Engineering, Taizhou University, Linhai 317000 (China)
  • 5. College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China)

Description

The crosslinked chitosan/nano-CdS (CS/n-CdS) composite catalyst prepared by simulating bio-mineralization process was extensively characterized by FT-IR spectra, XRD, SEM, TEM and TGA. An azo dye, Congo Red (CR), was used as model pollutant to study its photocatalytic activity under visible light irradiation. The influences of catalyst amount, initial CR concentrations, pH of the reaction solution and different anions on CR decolorization and degradation reaction kinetics were investigated. Results of characterization indicated the successful formation of hexagonal phase of CdS on raw chitosan under mild conditions. The photocatalytic degradation was found to follow a pseudo-first-order kinetics according to Langmuir-Hinshelwood (L-H) model. The dye could be decolorized more efficiently in acidic media than alkaline media. The presence of NO3- accelerated evidently the degradation of CR, while the other chosen anions (Br-, SO42- and Cl-) had an inhibitory effect on the decolorization of CR, of which the inhibitory effect of Cl- was the most pronounced. UV-vis spectra were analyzed to indicate that degradation of CR in the solution was the break up of the N=N bonds and degradation of aromatic fragment in this reaction system. The recycling experiments confirmed the relative stability of the catalyst.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jhazmat.2009.04.037

Additional details

Identifiers

DOI
10.1016/j.jhazmat.2009.04.037;
PII
S0304-3894(09)00608-6;

Publishing Information

Journal Title
Journal of Hazardous Materials
Journal Volume
169
Journal Issue
1-3
Journal Page Range
p. 933-940
ISSN
0304-3894
CODEN
JHMAD9

Optional Information

Copyright
Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.