An investigation of anthraquinone dye biodegradation by immobilized Aspergillus flavus in fluidized bed bioreactor
Autor: | Saadia Andleeb, Naima Atiq, Safia Ahmed, Geoff D. Robson |
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Rok vydání: | 2011 |
Předmět: |
Biochemical oxygen demand
Vinyl Compounds Hydraulic retention time Health Toxicology and Mutagenesis Molecular Sequence Data Catechols Phthalic Acids Anthraquinones Waste Disposal Fluid Anthraquinone chemistry.chemical_compound Bioreactors Toxicity Tests Lolium Bioreactor Environmental Chemistry Coloring Agents Effluent Chromatography High Pressure Liquid Phylogeny Biological Oxygen Demand Analysis Chromatography Chemical oxygen demand Equipment Design General Medicine Benzoic Acid Cells Immobilized Biodegradation Pollution Phthalic acid Pyrimidines chemistry Textile Industry Aspergillus flavus |
Zdroj: | Environmental Science and Pollution Research. 19:1728-1737 |
ISSN: | 1614-7499 0944-1344 |
Popis: | Biodegradation and biodecolorization of Drimarene blue K(2)RL (anthraquinone) dye by a fungal isolate Aspergillus flavus SA2 was studied in lab-scale immobilized fluidized bed bioreactor (FBR) system.Fungus was immobilized on 0.2-mm sand particles. The reactor operation was carried out at room temperature and pH 5.0 in continuous flow mode with increasing concentrations (50, 100, 150, 200, 300, 500 mg l(-1)) of dye in simulated textile effluent on the 1st, 2nd, 5th, 8th, 11th, and 14th days. The reactors were run on fill, react, settle, and draw mode, with hydraulic retention time (HRT) of 24-72 h. Total run time for reactor operation was 17 days.The average overall biological oxygen demand (BOD), chemical oxygen demand (COD), and color removal in the FBR system were up to 85.57%, 84.70%, and 71.3%, respectively, with 50-mg l(-1) initial dye concentration and HRT of 24 h. Reductions in BOD and COD levels along with color removal proved that the mechanism of biodecolorization and biodegradation occurred simultaneously. HPLC and LC-MS analysis identified phthalic acid, benzoic acid, 1, 4-dihydroxyanthraquinone, 2,3-dihydro-9,10-dihydroxy-1,4-anthracenedione, and catechol as degradation products of Drimarene blue K(2)RL dye. Phytotoxicity analysis of bioreactor treatments provided evidence for the production of less toxic metabolites in comparison to the parent dye.The present fluidized bed bioreactor setup with indigenously isolated fungal strain in its immobilized form is efficiently able to convert the parent toxic dye into less toxic by-products. |
Databáze: | OpenAIRE |
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