Phenol Degradation Kinetics by Free and Immobilized <i>Pseudomonas putida</i> BCRC 14365 in Batch and Continuous-Flow Bioreactors

Phenol degradation by <i>Pseudomonas putida </i>BCRC 14365 was investigated at 30 °C and a pH of 5.0–9.0 in the batch tests. Experimental results for both free and immobilized cells demonstrated that a maximum phenol degradation rate occurred at an initial pH of 7. The peak value of phen...

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Main Authors: Yen-Hui Lin, Yu-Siang Cheng
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:Processes
Subjects:
Online Access:https://www.mdpi.com/2227-9717/8/6/721
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spelling doaj-ca4be77d614a459e80daff4eef7c9c5a2020-11-25T03:29:25ZengMDPI AGProcesses2227-97172020-06-01872172110.3390/pr8060721Phenol Degradation Kinetics by Free and Immobilized <i>Pseudomonas putida</i> BCRC 14365 in Batch and Continuous-Flow BioreactorsYen-Hui Lin0Yu-Siang Cheng1Department of Safety, Health and Environmental Engineering, Central Taiwan University of Science and Technology, 666, Bu-zih Road, Bei-tun District, Taichung 406053, TaiwanDepartment of Safety, Health and Environmental Engineering, Central Taiwan University of Science and Technology, 666, Bu-zih Road, Bei-tun District, Taichung 406053, TaiwanPhenol degradation by <i>Pseudomonas putida </i>BCRC 14365 was investigated at 30 °C and a pH of 5.0–9.0 in the batch tests. Experimental results for both free and immobilized cells demonstrated that a maximum phenol degradation rate occurred at an initial pH of 7. The peak value of phenol degradation rates by the free and immobilized cells were 2.84 and 2.64 mg/L-h, respectively. Considering the culture at 20 °C, there was a lag period of approximately 44 h prior to the start of the phenol degradation for both free and immobilized cells. At the temperatures ranging from 25 to 40 °C, the immobilized cells had a higher rate of phenol degradation compared to the free cells. Moreover, the removal efficiencies of phenol degradation at the final stage were 59.3–92% and 87.5–92%, for the free and immobilized cells, respectively. The optimal temperature was 30 °C for free and immobilized cells. In the batch experiments with various initial phenol concentrations of 68.3–563.4 mg/L, the lag phase was practically negligible, and a logarithmic growth phase of a particular duration was observed from the beginning of the culture. The specific growth rate (<i>μ</i>) in the exponential growth phase was 0.085–0.192 h<sup>−1</sup> at various initial phenol concentrations between 68.3 and 563.4 mg/L. Comparing experimental data with the Haldane kinetics, the biokinetic parameters, namely, maximum specific growth rate (<i>μ</i><sub>max</sub>), the phenol half-saturation constant (<i>K</i><sub>s</sub>) and the phenol inhibition constant (<i>K</i><sub>I</sub>), were determined to equal 0.31 h<sup>−1</sup>, 26.2 mg/L and 255.0 mg/L, respectively. The growth yield and decay coefficient of <i>P. putida </i>cells were 0.592 ± 4.995 × 10<sup>–3</sup> mg cell/mg phenol and 5.70 × 10<sup>–2</sup> ± 1.122 × 10<sup>–3</sup> day<sup>−1</sup>, respectively. A completely mixed and continuous-flow bioreactor with immobilized cells was set up to conduct the verification of the kinetic model system. The removal efficiency for phenol in the continuous-flow bioreactor was approximately 97.7% at a steady-state condition. The experimental and simulated methodology used in this work can be applied, in the design of an immobilized cell process, by various industries for phenol-containing wastewater treatment.https://www.mdpi.com/2227-9717/8/6/721phenol degradationkineticsPseudomonas putidabatch experimentscontinuous-flow bioreactor
collection DOAJ
language English
format Article
sources DOAJ
author Yen-Hui Lin
Yu-Siang Cheng
spellingShingle Yen-Hui Lin
Yu-Siang Cheng
Phenol Degradation Kinetics by Free and Immobilized <i>Pseudomonas putida</i> BCRC 14365 in Batch and Continuous-Flow Bioreactors
Processes
phenol degradation
kinetics
Pseudomonas putida
batch experiments
continuous-flow bioreactor
author_facet Yen-Hui Lin
Yu-Siang Cheng
author_sort Yen-Hui Lin
title Phenol Degradation Kinetics by Free and Immobilized <i>Pseudomonas putida</i> BCRC 14365 in Batch and Continuous-Flow Bioreactors
title_short Phenol Degradation Kinetics by Free and Immobilized <i>Pseudomonas putida</i> BCRC 14365 in Batch and Continuous-Flow Bioreactors
title_full Phenol Degradation Kinetics by Free and Immobilized <i>Pseudomonas putida</i> BCRC 14365 in Batch and Continuous-Flow Bioreactors
title_fullStr Phenol Degradation Kinetics by Free and Immobilized <i>Pseudomonas putida</i> BCRC 14365 in Batch and Continuous-Flow Bioreactors
title_full_unstemmed Phenol Degradation Kinetics by Free and Immobilized <i>Pseudomonas putida</i> BCRC 14365 in Batch and Continuous-Flow Bioreactors
title_sort phenol degradation kinetics by free and immobilized <i>pseudomonas putida</i> bcrc 14365 in batch and continuous-flow bioreactors
publisher MDPI AG
series Processes
issn 2227-9717
publishDate 2020-06-01
description Phenol degradation by <i>Pseudomonas putida </i>BCRC 14365 was investigated at 30 °C and a pH of 5.0–9.0 in the batch tests. Experimental results for both free and immobilized cells demonstrated that a maximum phenol degradation rate occurred at an initial pH of 7. The peak value of phenol degradation rates by the free and immobilized cells were 2.84 and 2.64 mg/L-h, respectively. Considering the culture at 20 °C, there was a lag period of approximately 44 h prior to the start of the phenol degradation for both free and immobilized cells. At the temperatures ranging from 25 to 40 °C, the immobilized cells had a higher rate of phenol degradation compared to the free cells. Moreover, the removal efficiencies of phenol degradation at the final stage were 59.3–92% and 87.5–92%, for the free and immobilized cells, respectively. The optimal temperature was 30 °C for free and immobilized cells. In the batch experiments with various initial phenol concentrations of 68.3–563.4 mg/L, the lag phase was practically negligible, and a logarithmic growth phase of a particular duration was observed from the beginning of the culture. The specific growth rate (<i>μ</i>) in the exponential growth phase was 0.085–0.192 h<sup>−1</sup> at various initial phenol concentrations between 68.3 and 563.4 mg/L. Comparing experimental data with the Haldane kinetics, the biokinetic parameters, namely, maximum specific growth rate (<i>μ</i><sub>max</sub>), the phenol half-saturation constant (<i>K</i><sub>s</sub>) and the phenol inhibition constant (<i>K</i><sub>I</sub>), were determined to equal 0.31 h<sup>−1</sup>, 26.2 mg/L and 255.0 mg/L, respectively. The growth yield and decay coefficient of <i>P. putida </i>cells were 0.592 ± 4.995 × 10<sup>–3</sup> mg cell/mg phenol and 5.70 × 10<sup>–2</sup> ± 1.122 × 10<sup>–3</sup> day<sup>−1</sup>, respectively. A completely mixed and continuous-flow bioreactor with immobilized cells was set up to conduct the verification of the kinetic model system. The removal efficiency for phenol in the continuous-flow bioreactor was approximately 97.7% at a steady-state condition. The experimental and simulated methodology used in this work can be applied, in the design of an immobilized cell process, by various industries for phenol-containing wastewater treatment.
topic phenol degradation
kinetics
Pseudomonas putida
batch experiments
continuous-flow bioreactor
url https://www.mdpi.com/2227-9717/8/6/721
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