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Evaluating the efficiency of enzyme accelerated CO(2) capture: chemical kinetics modelling for interpreting measurement results

In this paper, the efficiency of the carbonic anhydrase (CA) enzyme in accelerating the hydration of CO(2) is evaluated using a measurement system which consists of a vessel in which a gaseous flow of mixtures of nitrogen and CO(2) is bubbled into water or water solutions containing a known quantity...

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Detalles Bibliográficos
Autores principales: Parri, Lorenzo, Fort, Ada, Lo Grasso, Anna, Mugnaini, Marco, Vignoli, Valerio, Capasso, Clemente, Del Prete, Sonia, Romanelli, Maria Novella, Supuran, Claudiu T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831361/
https://www.ncbi.nlm.nih.gov/pubmed/33430654
http://dx.doi.org/10.1080/14756366.2020.1864631
Descripción
Sumario:In this paper, the efficiency of the carbonic anhydrase (CA) enzyme in accelerating the hydration of CO(2) is evaluated using a measurement system which consists of a vessel in which a gaseous flow of mixtures of nitrogen and CO(2) is bubbled into water or water solutions containing a known quantity of CA enzyme. The pH value of the solution and the CO(2) concentration at the measurement system gas exhaust are continuously monitored. The measured CO(2) level allows for assessing the quantity of CO(2), which, subtracted from the gaseous phase, is dissolved into the liquid phase and/or hydrated to bicarbonate. The measurement procedure consists of inducing a transient and observing and modelling the different kinetics involved in the steady-state recovery with and without CA. The main contribution of this work is exploiting dynamical system theory and chemical kinetics modelling for interpreting measurement results for characterising the activity of CA enzymes. The data for model fitting are obtained from a standard bioreactor, in principle equal to standard two-phase bioreactors described in the literature, in which two different techniques can be used to move the process itself away from the steady-state, inducing transients.