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Operational parameters and their influence on particle-side mass transfer resistance in a packed bed bioreactor

The influence of internal mass transfer on productivity as well as the performance of packed bed bioreactor was determined by varying a number of parameters; chitosan coating, flow rate, glucose concentration and particle size. Saccharomyces cerevisiae cells were immobilized in chitosan and non-chit...

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Autores principales: Hussain, Amir, Kangwa, Martin, Yumnam, Nivedita, Fernandez-Lahore, Marcelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536250/
https://www.ncbi.nlm.nih.gov/pubmed/26272478
http://dx.doi.org/10.1186/s13568-015-0138-z
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author Hussain, Amir
Kangwa, Martin
Yumnam, Nivedita
Fernandez-Lahore, Marcelo
author_facet Hussain, Amir
Kangwa, Martin
Yumnam, Nivedita
Fernandez-Lahore, Marcelo
author_sort Hussain, Amir
collection PubMed
description The influence of internal mass transfer on productivity as well as the performance of packed bed bioreactor was determined by varying a number of parameters; chitosan coating, flow rate, glucose concentration and particle size. Saccharomyces cerevisiae cells were immobilized in chitosan and non-chitosan coated alginate beads to demonstrate the effect on particle side mass transfer on substrate consumption time, lag phase and ethanol production. The results indicate that chitosan coating, beads size, glucose concentration and flow rate have a significant effect on lag phase duration. The duration of lag phase for different size of beads (0.8, 2 and 4 mm) decreases by increasing flow rate and by decreasing the size of beads. Moreover, longer lag phase were found at higher glucose medium concentration and also with chitosan coated beads. It was observed that by increasing flow rates; lag phase and glucose consumption time decreased. The reason is due to the reduction of external (fluid side) mass transfer as a result of increase in flow rate as glucose is easily transported to the surface of the beads. Varying the size of beads is an additional factor: as it reduces the internal (particle side) mass transfer by reducing the size of beads. The reason behind this is the distance for reactants to reach active site of catalyst (cells) and the thickness of fluid created layer around alginate beads is reduced. The optimum combination of parameters consisting of smaller beads size (0.8 mm), higher flow rate of 90 ml/min and glucose concentration of 10 g/l were found to be the maximum condition for ethanol production.
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spelling pubmed-45362502015-08-21 Operational parameters and their influence on particle-side mass transfer resistance in a packed bed bioreactor Hussain, Amir Kangwa, Martin Yumnam, Nivedita Fernandez-Lahore, Marcelo AMB Express Original Article The influence of internal mass transfer on productivity as well as the performance of packed bed bioreactor was determined by varying a number of parameters; chitosan coating, flow rate, glucose concentration and particle size. Saccharomyces cerevisiae cells were immobilized in chitosan and non-chitosan coated alginate beads to demonstrate the effect on particle side mass transfer on substrate consumption time, lag phase and ethanol production. The results indicate that chitosan coating, beads size, glucose concentration and flow rate have a significant effect on lag phase duration. The duration of lag phase for different size of beads (0.8, 2 and 4 mm) decreases by increasing flow rate and by decreasing the size of beads. Moreover, longer lag phase were found at higher glucose medium concentration and also with chitosan coated beads. It was observed that by increasing flow rates; lag phase and glucose consumption time decreased. The reason is due to the reduction of external (fluid side) mass transfer as a result of increase in flow rate as glucose is easily transported to the surface of the beads. Varying the size of beads is an additional factor: as it reduces the internal (particle side) mass transfer by reducing the size of beads. The reason behind this is the distance for reactants to reach active site of catalyst (cells) and the thickness of fluid created layer around alginate beads is reduced. The optimum combination of parameters consisting of smaller beads size (0.8 mm), higher flow rate of 90 ml/min and glucose concentration of 10 g/l were found to be the maximum condition for ethanol production. Springer Berlin Heidelberg 2015-08-14 /pmc/articles/PMC4536250/ /pubmed/26272478 http://dx.doi.org/10.1186/s13568-015-0138-z Text en © Hussain et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Hussain, Amir
Kangwa, Martin
Yumnam, Nivedita
Fernandez-Lahore, Marcelo
Operational parameters and their influence on particle-side mass transfer resistance in a packed bed bioreactor
title Operational parameters and their influence on particle-side mass transfer resistance in a packed bed bioreactor
title_full Operational parameters and their influence on particle-side mass transfer resistance in a packed bed bioreactor
title_fullStr Operational parameters and their influence on particle-side mass transfer resistance in a packed bed bioreactor
title_full_unstemmed Operational parameters and their influence on particle-side mass transfer resistance in a packed bed bioreactor
title_short Operational parameters and their influence on particle-side mass transfer resistance in a packed bed bioreactor
title_sort operational parameters and their influence on particle-side mass transfer resistance in a packed bed bioreactor
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536250/
https://www.ncbi.nlm.nih.gov/pubmed/26272478
http://dx.doi.org/10.1186/s13568-015-0138-z
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