Photodegradation of 2-mercaptobenzothiazole in the γ-Fe2O3/oxalate suspension under UVA light irradiation
- 1. Guangdong Key Laboratory of Agricultural Environment Pollution Integrated Control, Guangdong Institute of Eco-Environment and Soil Science, Guangzhou 510650 (China)
- 2. College of Resources and Environmental Sciences, Northwest Agriculture and Forestry University, Yangling, Shanxi 712100 (China)
Description
The aim of this study is to investigate the effect of various factors on the photodegradation of organic pollutants in natural environment with co-existence of iron oxides and oxalic acid. 2-Mercaptobenzothiazole (MBT) was selected as a model pollutant, while γ-Fe2O3 was selected as iron oxide. The crystal structure and morphology of the prepared γ-Fe2O3 was determined by X-ray diffractograms (XRD) and scanning electron microscopy (SEM), respectively. The specific surface area was 14.36 m2/g by Brunauer-Emmett-Teller (BET) method. The adsorption behavior of γ-Fe2O3 was evaluated by Langmuir model. The effect of the dosage of iron oxide, initial concentration of oxalic acid (Cox0), initial pH value, the light intensity and additional transition metal cations on MBT photodegradation was investigated in the γ-Fe2O3/oxalate suspension under UVA light irradiation. The optimal γ-Fe2O3 dosage was 0.4 g/L and the optimal Cox0 was 0.8 mM with the UVA light intensity of 1800 mW/cm2. And the optimal dosage of γ-Fe2O3 and Cox0 for MBT degradation also depended strongly on the light intensity. The optimal γ-Fe2O3 dosage was 0.1, 0.25 and 0.4 g/L, and the optimal Cox0 was 1.0, 0.8, and 0.8 mM with the light intensity of 600, 1200 and 1800 mW/cm2, respectively. The optimal initial pH value was at 3.0. The additional transition metal cations including Cu2+, Ni2+ or Mn2+ could significantly accelerate MBT degradation. This investigation will give a new insight to understanding the MBT photodegradation in natural environment
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2007.08.072Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2007.08.072;
- PII
- S0304-3894(07)01246-0;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 153
- Journal Issue
- 1-2
- Journal Page Range
- p. 426-433
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 40036105
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- COPPER IONS; FERRITES; IRON OXIDES; IRRADIATION; MANGANESE IONS; NICKEL IONS; OXALATES; OXALIC ACID; PH VALUE; POLLUTANTS; POLLUTION CONTROL; SCANNING ELECTRON MICROSCOPY; SPECIFIC SURFACE AREA; TRANSITION ELEMENTS; X-RAY DIFFRACTION
- Descriptors DEC
- CARBOXYLIC ACID SALTS; CARBOXYLIC ACIDS; CHALCOGENIDES; CHARGED PARTICLES; COHERENT SCATTERING; CONTROL; DICARBOXYLIC ACIDS; DIFFRACTION; ELECTRON MICROSCOPY; ELEMENTS; FERRIMAGNETIC MATERIALS; IONS; IRON COMPOUNDS; MAGNETIC MATERIALS; MATERIALS; METALS; MICROSCOPY; ORGANIC ACIDS; ORGANIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PHYSICAL PROPERTIES; SCATTERING; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.