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Decolorization and partial mineralization of a polyazo dye by Bacillus firmus immobilized within tubular polymeric gel
The degradation of C.I. Direct red 80, a polyazo dye, was investigated using Bacillus firmus immobilized by entrapment in tubular polymeric gel. This bacterial strain was able to completely decolorize 50 mg/L of C.I. Direct red 80 under anoxic conditions within 12 h and also degrade the reaction int...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339580/ https://www.ncbi.nlm.nih.gov/pubmed/22582158 http://dx.doi.org/10.1007/s13205-011-0035-3 |
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author | Ogugbue, Chimezie Jason Morad, Norhashimah Sawidis, Thomas Oranusi, Nathaniel A. |
author_facet | Ogugbue, Chimezie Jason Morad, Norhashimah Sawidis, Thomas Oranusi, Nathaniel A. |
author_sort | Ogugbue, Chimezie Jason |
collection | PubMed |
description | The degradation of C.I. Direct red 80, a polyazo dye, was investigated using Bacillus firmus immobilized by entrapment in tubular polymeric gel. This bacterial strain was able to completely decolorize 50 mg/L of C.I. Direct red 80 under anoxic conditions within 12 h and also degrade the reaction intermediates (aromatic amines) during the subsequent 12 h under aerobic conditions. The tubular gel harboring the immobilized cells consisted of anoxic and aerobic regions integrated in a single unit which was ideal for azo dye degradation studies. Results obtained show that effective dye decolorization (97.8%), chemical oxygen demand (COD) reduction (91.7%) and total aromatic amines removal were obtained in 15 h with the immobilized bacterial cell system whereas for the free cells, a hydraulic residence time of 24 h was required for an equivalent performance in a sequential anoxic and aerobic process. Repeated-batch experiments indicate the immobilized cells could decolorize C.I. Direct red 80 and reduce medium COD in five successive batch runs with enhanced activity obtained after each consecutive run, thus suggesting its stability and potential for repeated use in wastewater treatment. UV–visible spectrophotometry and HPLC analysis were used to confirm the partial mineralization of the dye. Data from this study could be used as a reference for the development of effective industrial scale biotechnological process for the removal of dyes and their metabolites in textile wastewater. |
format | Online Article Text |
id | pubmed-3339580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-33395802012-05-09 Decolorization and partial mineralization of a polyazo dye by Bacillus firmus immobilized within tubular polymeric gel Ogugbue, Chimezie Jason Morad, Norhashimah Sawidis, Thomas Oranusi, Nathaniel A. 3 Biotech Original Article The degradation of C.I. Direct red 80, a polyazo dye, was investigated using Bacillus firmus immobilized by entrapment in tubular polymeric gel. This bacterial strain was able to completely decolorize 50 mg/L of C.I. Direct red 80 under anoxic conditions within 12 h and also degrade the reaction intermediates (aromatic amines) during the subsequent 12 h under aerobic conditions. The tubular gel harboring the immobilized cells consisted of anoxic and aerobic regions integrated in a single unit which was ideal for azo dye degradation studies. Results obtained show that effective dye decolorization (97.8%), chemical oxygen demand (COD) reduction (91.7%) and total aromatic amines removal were obtained in 15 h with the immobilized bacterial cell system whereas for the free cells, a hydraulic residence time of 24 h was required for an equivalent performance in a sequential anoxic and aerobic process. Repeated-batch experiments indicate the immobilized cells could decolorize C.I. Direct red 80 and reduce medium COD in five successive batch runs with enhanced activity obtained after each consecutive run, thus suggesting its stability and potential for repeated use in wastewater treatment. UV–visible spectrophotometry and HPLC analysis were used to confirm the partial mineralization of the dye. Data from this study could be used as a reference for the development of effective industrial scale biotechnological process for the removal of dyes and their metabolites in textile wastewater. Springer Berlin Heidelberg 2011-11-05 2012-03 /pmc/articles/PMC3339580/ /pubmed/22582158 http://dx.doi.org/10.1007/s13205-011-0035-3 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by/4.0/ This article is published under license to BioMed Central Ltd. Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Article Ogugbue, Chimezie Jason Morad, Norhashimah Sawidis, Thomas Oranusi, Nathaniel A. Decolorization and partial mineralization of a polyazo dye by Bacillus firmus immobilized within tubular polymeric gel |
title | Decolorization and partial mineralization of a polyazo dye by Bacillus firmus immobilized within tubular polymeric gel |
title_full | Decolorization and partial mineralization of a polyazo dye by Bacillus firmus immobilized within tubular polymeric gel |
title_fullStr | Decolorization and partial mineralization of a polyazo dye by Bacillus firmus immobilized within tubular polymeric gel |
title_full_unstemmed | Decolorization and partial mineralization of a polyazo dye by Bacillus firmus immobilized within tubular polymeric gel |
title_short | Decolorization and partial mineralization of a polyazo dye by Bacillus firmus immobilized within tubular polymeric gel |
title_sort | decolorization and partial mineralization of a polyazo dye by bacillus firmus immobilized within tubular polymeric gel |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339580/ https://www.ncbi.nlm.nih.gov/pubmed/22582158 http://dx.doi.org/10.1007/s13205-011-0035-3 |
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