The University of Southampton
University of Southampton Institutional Repository

Kinetic modelling of the hydrolysis, acidogenic and methanogenic steps in the anaerobic digestion of two-phase olive pomace (TPOP)

Kinetic modelling of the hydrolysis, acidogenic and methanogenic steps in the anaerobic digestion of two-phase olive pomace (TPOP)
Kinetic modelling of the hydrolysis, acidogenic and methanogenic steps in the anaerobic digestion of two-phase olive pomace (TPOP)
A simplified kinetic model for studying the hydrolysis, acidogenic and methanogenic steps of the anaerobic digestion process of two-phase olive pomace (TPOP) was proposed on the basis of the experimental results obtained. The process was conducted in a laboratory-scale completely stirred tank reactor at mesophilic temperature (35 °C) operating at hydraulic retention times (HRT) in the range of 10–50 days. Hydrolysis and acidogenic steps prevailed at HRTs lower than 20 days, while the methanogenic step prevailed at higher HRT values. Four differential equations described the overall process. A first-order kinetics for hydrolysis of non-soluble organic matter and a Michaelis–Menten equation type for soluble organic matter decomposition, total volatile acids consumption and methane production. The following kinetic constants with their standard deviations were obtained for the above-mentioned anaerobic stages: (a) hydrolysis and solubilization of organic matter: k1 (kinetic constant for non-soluble organic matter degradation): 0.054 ± 0.003 day?1; k2 (maximum rate of soluble organic matter production): 4.2 ± 0.3 g soluble chemical oxygen demand (SCOD)/l day; k3 (saturation constant): 9.8 ± 0.5 g SCOD/l; (b) acidogenesis: k4 (maximum rate of soluble organic matter degradation): 3.6 ± 0.2 g SCOD/l day; k5 (saturation constant): 10.2 ± 0.5 g SCOD/l; and (c) methanogenesis: k6 (maximum rate of total volatile acids (TVA) consumption): 4.3 ± 0.2 g TVA-COD/l day; and k7 (saturation constant): 3.1 ± 0.2 g TVA-COD/l. The kinetic constants obtained and the proposed equations were used to simulate the different steps of the anaerobic digestion process of TPOP and to obtain the theoretical values of non-soluble and soluble CODs, TVA and methane production. The small deviations obtained (equal or lower than 10%) between the theoretical and experimental values suggest that the parameters obtained represent and predict the activity of the different microorganism types involved in the overall anaerobic digestion process of this waste.
kinetic modelling, anaerobic digestion, hydrolysis, acidogenic and methanogenic steps, two-phase olive pomace
1359-5113
1841-1847
Borja, R.
ed513484-04ff-4424-ab79-dc715ca63146
Martin, A.
169f0afa-12fc-43b5-a72d-7bfc493aa170
Sánchez, E.
cf73c967-6a9b-4a5e-8e99-26198ecc3d6c
Rincón, B.
d8fe6652-8ff6-4662-bfb7-3b231d140957
Raposo, F.
47104451-511a-4b03-aaa9-67348da4567d
Borja, R.
ed513484-04ff-4424-ab79-dc715ca63146
Martin, A.
169f0afa-12fc-43b5-a72d-7bfc493aa170
Sánchez, E.
cf73c967-6a9b-4a5e-8e99-26198ecc3d6c
Rincón, B.
d8fe6652-8ff6-4662-bfb7-3b231d140957
Raposo, F.
47104451-511a-4b03-aaa9-67348da4567d

Borja, R., Martin, A., Sánchez, E., Rincón, B. and Raposo, F. (2005) Kinetic modelling of the hydrolysis, acidogenic and methanogenic steps in the anaerobic digestion of two-phase olive pomace (TPOP). Process Biochemistry, 40 (5), 1841-1847. (doi:10.1016/j.procbio.2004.06.026).

Record type: Article

Abstract

A simplified kinetic model for studying the hydrolysis, acidogenic and methanogenic steps of the anaerobic digestion process of two-phase olive pomace (TPOP) was proposed on the basis of the experimental results obtained. The process was conducted in a laboratory-scale completely stirred tank reactor at mesophilic temperature (35 °C) operating at hydraulic retention times (HRT) in the range of 10–50 days. Hydrolysis and acidogenic steps prevailed at HRTs lower than 20 days, while the methanogenic step prevailed at higher HRT values. Four differential equations described the overall process. A first-order kinetics for hydrolysis of non-soluble organic matter and a Michaelis–Menten equation type for soluble organic matter decomposition, total volatile acids consumption and methane production. The following kinetic constants with their standard deviations were obtained for the above-mentioned anaerobic stages: (a) hydrolysis and solubilization of organic matter: k1 (kinetic constant for non-soluble organic matter degradation): 0.054 ± 0.003 day?1; k2 (maximum rate of soluble organic matter production): 4.2 ± 0.3 g soluble chemical oxygen demand (SCOD)/l day; k3 (saturation constant): 9.8 ± 0.5 g SCOD/l; (b) acidogenesis: k4 (maximum rate of soluble organic matter degradation): 3.6 ± 0.2 g SCOD/l day; k5 (saturation constant): 10.2 ± 0.5 g SCOD/l; and (c) methanogenesis: k6 (maximum rate of total volatile acids (TVA) consumption): 4.3 ± 0.2 g TVA-COD/l day; and k7 (saturation constant): 3.1 ± 0.2 g TVA-COD/l. The kinetic constants obtained and the proposed equations were used to simulate the different steps of the anaerobic digestion process of TPOP and to obtain the theoretical values of non-soluble and soluble CODs, TVA and methane production. The small deviations obtained (equal or lower than 10%) between the theoretical and experimental values suggest that the parameters obtained represent and predict the activity of the different microorganism types involved in the overall anaerobic digestion process of this waste.

This record has no associated files available for download.

More information

Published date: April 2005
Keywords: kinetic modelling, anaerobic digestion, hydrolysis, acidogenic and methanogenic steps, two-phase olive pomace

Identifiers

Local EPrints ID: 53027
URI: http://eprints.soton.ac.uk/id/eprint/53027
ISSN: 1359-5113
PURE UUID: 7069fb26-747c-4b7e-9d34-b856cdca3559

Catalogue record

Date deposited: 18 Jul 2008
Last modified: 11 Nov 2024 19:38

Export record

Altmetrics

Contributors

Author: R. Borja
Author: A. Martin
Author: E. Sánchez
Author: B. Rincón
Author: F. Raposo

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×