Bovinille Anye Cho , George Mbella Teke , Godfrey K. Gakingo , Robert William McClelland Pott , Dongda Zhang
{"title":"微型生物反应器混合动力学与过渡流态光生物反应动力学的 CFD 预测模拟","authors":"Bovinille Anye Cho , George Mbella Teke , Godfrey K. Gakingo , Robert William McClelland Pott , Dongda Zhang","doi":"10.1016/j.bej.2024.109585","DOIUrl":null,"url":null,"abstract":"<div><div>High-throughput systems using miniaturised stirred bioreactors accelerate bioprocess development due to their simplicity and low cost. However, fluctuating hydrodynamics pose numerical challenges for coupling (bio)reaction kinetics, critical for optimisation and scale-up/down in chemical and bioprocess industries. To address this, hydrodynamic convergence was achieved by time-averaging instantaneous RANS solutions of the <em>transitional</em> SST model over a sufficiently long period to achieve statistical significance in step one. Subsequently, photo-bioreaction transport models, accounting for the photobioreactor’s directional illumination and curvature, were solved based on these converged fields, overcoming two-step coupling challenges in an approach not previously reported. Applied to a 0.7 L Schott bottle photobioreactor mechanically mixed by a magnetic stirrer (100–500 rpm), the model accurately predicted swirly vortex fields at 500 rpm, with a 7 % error margin for simulated tracer diffusion, and aligned biomass growth profiles with literature data on <em>Rhodopseudomonas palustris</em>. However, parallel computing efficiency did not scale linearly with processor count, making time-averaging computationally expensive. Also, improved bioreactor mixing enhanced biomass productivity, but rpms over 300 required increased incident light intensity (>100 Wm<sup>−2</sup>) due to observed light limitation. Hence, this model facilitates optimising stirring speeds and refining operational parameters for scale-up and scale-down processes.</div></div>","PeriodicalId":8766,"journal":{"name":"Biochemical Engineering Journal","volume":"214 ","pages":"Article 109585"},"PeriodicalIF":3.7000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CFD predictive simulations of miniature bioreactor mixing dynamics coupled with photo-bioreaction kinetics in transitional flow regime\",\"authors\":\"Bovinille Anye Cho , George Mbella Teke , Godfrey K. Gakingo , Robert William McClelland Pott , Dongda Zhang\",\"doi\":\"10.1016/j.bej.2024.109585\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>High-throughput systems using miniaturised stirred bioreactors accelerate bioprocess development due to their simplicity and low cost. However, fluctuating hydrodynamics pose numerical challenges for coupling (bio)reaction kinetics, critical for optimisation and scale-up/down in chemical and bioprocess industries. To address this, hydrodynamic convergence was achieved by time-averaging instantaneous RANS solutions of the <em>transitional</em> SST model over a sufficiently long period to achieve statistical significance in step one. Subsequently, photo-bioreaction transport models, accounting for the photobioreactor’s directional illumination and curvature, were solved based on these converged fields, overcoming two-step coupling challenges in an approach not previously reported. Applied to a 0.7 L Schott bottle photobioreactor mechanically mixed by a magnetic stirrer (100–500 rpm), the model accurately predicted swirly vortex fields at 500 rpm, with a 7 % error margin for simulated tracer diffusion, and aligned biomass growth profiles with literature data on <em>Rhodopseudomonas palustris</em>. However, parallel computing efficiency did not scale linearly with processor count, making time-averaging computationally expensive. Also, improved bioreactor mixing enhanced biomass productivity, but rpms over 300 required increased incident light intensity (>100 Wm<sup>−2</sup>) due to observed light limitation. Hence, this model facilitates optimising stirring speeds and refining operational parameters for scale-up and scale-down processes.</div></div>\",\"PeriodicalId\":8766,\"journal\":{\"name\":\"Biochemical Engineering Journal\",\"volume\":\"214 \",\"pages\":\"Article 109585\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2024-11-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemical Engineering Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1369703X24003723\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1369703X24003723","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
CFD predictive simulations of miniature bioreactor mixing dynamics coupled with photo-bioreaction kinetics in transitional flow regime
High-throughput systems using miniaturised stirred bioreactors accelerate bioprocess development due to their simplicity and low cost. However, fluctuating hydrodynamics pose numerical challenges for coupling (bio)reaction kinetics, critical for optimisation and scale-up/down in chemical and bioprocess industries. To address this, hydrodynamic convergence was achieved by time-averaging instantaneous RANS solutions of the transitional SST model over a sufficiently long period to achieve statistical significance in step one. Subsequently, photo-bioreaction transport models, accounting for the photobioreactor’s directional illumination and curvature, were solved based on these converged fields, overcoming two-step coupling challenges in an approach not previously reported. Applied to a 0.7 L Schott bottle photobioreactor mechanically mixed by a magnetic stirrer (100–500 rpm), the model accurately predicted swirly vortex fields at 500 rpm, with a 7 % error margin for simulated tracer diffusion, and aligned biomass growth profiles with literature data on Rhodopseudomonas palustris. However, parallel computing efficiency did not scale linearly with processor count, making time-averaging computationally expensive. Also, improved bioreactor mixing enhanced biomass productivity, but rpms over 300 required increased incident light intensity (>100 Wm−2) due to observed light limitation. Hence, this model facilitates optimising stirring speeds and refining operational parameters for scale-up and scale-down processes.
期刊介绍:
The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology.
The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields:
Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics
Biosensors and Biodevices including biofabrication and novel fuel cell development
Bioseparations including scale-up and protein refolding/renaturation
Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells
Bioreactor Systems including characterization, optimization and scale-up
Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization
Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals
Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release
Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites
Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation
Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis
Protein Engineering including enzyme engineering and directed evolution.