2021
DOI: 10.1007/978-1-0716-1826-4_15
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Chemical Reaction Engineering to Understand Applied Kinetics in Free Enzyme Homogeneous Reactors

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Cited by 4 publications
(6 citation statements)
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“…Under these conditions, the conversion of the reactor would decrease. 86,490 On the contrary, if the enzyme loading is too high, the volumetric activity would also be high, and the contact time (residence time) between the catalyst and the reaction medium might be too short. This might generate high superficial velocities that increase pressure drop over the bed and result in preferential channels through the reactor (so-called channeling), and also decreasing the effectiveness of enzyme use.…”
Section: From Batch To Continuous Reactors and Process Intensificationmentioning
confidence: 99%
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“…Under these conditions, the conversion of the reactor would decrease. 86,490 On the contrary, if the enzyme loading is too high, the volumetric activity would also be high, and the contact time (residence time) between the catalyst and the reaction medium might be too short. This might generate high superficial velocities that increase pressure drop over the bed and result in preferential channels through the reactor (so-called channeling), and also decreasing the effectiveness of enzyme use.…”
Section: From Batch To Continuous Reactors and Process Intensificationmentioning
confidence: 99%
“…However, for process implementation kinetic stability is more relevant. 4,89,382,490,494,495 Still the researcher must decide about the amount of information acquired in the context of catalyst development. While analysis under real operational conditions would require extremely long experiments that would slowdown the immobilization development process, a first screening for stabilization consists in the selection of denaturing conditions where the reference catalyst is inactivated in the timeframe of minutes or hours.…”
Section: From Batch To Continuous Reactors and Process Intensificationmentioning
confidence: 99%
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“…The time interval was 20 s and the mean [O 2 ] from the interval was used. Reaction rates dependent on [O 2 ] are thus calculated (Lorente‐Arevalo et al, 2021a, 2022).…”
Section: Methodsmentioning
confidence: 99%