Evidence map›Paper›PMID 42570107›Full record

ArticleBioprocess and biosystems engineering2026

Simulating large-scale biotech bubble columns: challenges and insights from the parcel approach.

Carolin Link, Lars Puiman, Ralf Takors

Abstract read
In one paragraph

Article in Bioprocess and biosystems engineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Carolin LinkInstitute of Biochemical Engineering, University of Stuttgart, Allmandring 31, 70569, Stuttgart, Germany.
Lars PuimanAustralian Institute for Bioengineering and Nanotechnology, The University of Queensland, Corner Cooper Rd & College Rd, St. Lucia, Brisbane, QLD, 4072, Australia.
Ralf TakorsInstitute of Biochemical Engineering, University of Stuttgart, Allmandring 31, 70569, Stuttgart, Germany. takors@ibvt.uni-stuttgart.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The growing industrial demand for economically attractive large-scale bioprocesses has increased the need for reliable and computationally feasible modelling approaches. Gas fermentation plays a particular role as the targeted commodities ask for large-scale solutions using bubble-column type bioreactors that allow them to benefit from the economy-of-scale. To reduce development efforts, large-scale designs increasingly build on computational fluid dynamics (CFD) simulations. State-of-the-art approaches employ finite-volume Reynolds-averaged Navier-Stokes (FV-RANS) methods that require enormous computational efforts. In contrast, Euler-Lagrange (E-L) approaches offer detailed local resolution as a prerequisite for optimum bioreactor design. By tracking individual bubbles, they predict bubble population dynamics while computations are parallelized. However, to cope with realistic bubble numbers, large-scale simulations typically make use of the so-called 'parcel size' approach, i.e. multiple bubbles are represented by a single computational particle. This study applies Lattice Boltzmann large eddy simulations (LB-LES) to illustrate the observed consequences: Swarm-like bubble behavior is found that results in inhomogeneous bubble distributions. As a consequence, the volumetric mass transfer coefficient k

Indexed as

BioreactorsBiotechnologyComputer SimulationHydrodynamicsGasesGasesCFDEuler-LagrangeLattice BoltzmannParcel approach

Identifiers

PMID42570107
PMCPMC13582231

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.