Published May 15, 2010 | Version v1
Journal article

Desorption behavior of methylene blue on pyromellitic dianhydride modified biosorbent by a novel eluent: Acid TiO2 hydrosol

  • 1. Hubei Novel Reactor and Green Chemical Technology Key Laboratory, Key Laboratory for Green Chemical Process of Ministry of Education, School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, Wuhan 430074 (China)

Description

In this study, waste beer yeast powder was modified by pyromellitic dianhydride to improve its adsorption capacities for cationic dye: methylene blue (MB). According to the Langmuir equation, the maximum uptake capacities (qm) of the modified biomass for MB was 830.8 mg g-1, which was about five times than that obtained on the unmodified biomass. Adsorption mechanism was investigated by FTIR. Desorption kinetics of methylene blue in six solvents: HCl (0.1 mol L-1), ethanol, mixtures of HCl (0.1 mol L-1) and ethanol with different volume ratio and a self-clean eluent: acid TiO2 were studied in details. Results showed that desorption kinetics curve fit the two-step kinetic model, and methylene blue release process was distinctly divided into two steps: rapid and slow desorption steps. 52.2% of the methylene blue could be desorbed into TiO2 hydrosol after 30 h desorption at the first desorption cycle, and the desorbed dye in TiO2 hydrosol could be degrade completely under sunlight irradiation. After three desorption-photodegradation cycles, 80.0% of the absorbed dyes could be desorbed from the surface of the modified biomass. Although there was much work to do, the self-clean eluent: TiO2 hydrosol had great potential in practical use.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jhazmat.2009.12.021

Additional details

Identifiers

DOI
10.1016/j.jhazmat.2009.12.021;
PII
S0304-3894(09)01992-X;

Publishing Information

Journal Title
Journal of Hazardous Materials
Journal Volume
177
Journal Issue
1-3
Journal Page Range
p. 222-227
ISSN
0304-3894
CODEN
JHMAD9

Optional Information

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