Unifying nucleation and crystal growth mechanisms in membrane crystallisation

dc.contributor.authorMapetere, A.
dc.contributor.authorDi Profio, Gianluca
dc.contributor.authorCurcio, Efrem
dc.contributor.authorCampo Moreno, Pablo
dc.contributor.authorMcAdam, Ewan J.
dc.date.accessioned2025-04-28T14:05:42Z
dc.date.available2025-04-28T14:05:42Z
dc.date.freetoread2025-04-28
dc.date.issued2025-05-01
dc.date.pubOnline2025-03-29
dc.description.abstractWhile several mechanisms have been proposed to describe crystallisation processes in membrane distillation, it has not been possible to provide a definitive description since the nucleation kinetics are difficult to measure. This study therefore introduced non-invasive techniques to measure induction time within two discrete domains (the membrane surface and bulk solution) and was complemented by the introduction of a modified power law relation between supersaturation and induction time, that enables mass and heat transfer processes in the boundary layer to be directly related to classical nucleation theory (CNT). Temperature (T, 45–60 °C) and temperature difference (ΔT, 15–30 °C) were used to adjust boundary layer properties, which established a log-linear relation between the nucleation rate and the supersaturation level in the boundary layer at induction, which is characteristic of CNT. Crystal size distribution analysis demonstrated how nucleation rate and crystal growth rate could be adjusted using ΔT and T respectively. Consequently, ΔT and T can be used collectively to fix the supersaturation set point within the boundary layer to achieve the preferred crystal morphology. However, at higher supersaturation levels, scaling was observed. Discrimination of the primary nucleation mechanisms, using measured induction times, revealed scaling to be formed homogeneously, which indicates exposure of the pores to extremely high supersaturation levels. Morphological analysis of scaling indicated growth to be dominated by secondary nucleation mechanisms, that resulted in a habit that is distinctive from the crystal phase formed in the bulk solution. From this analysis, a critical supersaturation threshold was identified, below which kinetically controlled scaling can be ‘switched-off’, leaving crystals to form solely in the bulk solution comprising the preferred cubic morphology. This study serves to unify understanding on nucleation and growth mechanisms to enhance control over crystallisation in membrane systems.
dc.description.journalNameJournal of Membrane Science
dc.description.sponsorshipThis research was financially supported by European Research Council Starting Grant 714080, ‘Sustainable chemical alternatives for reuse in the circular economy’ (SCARCE).
dc.identifier.citationMapetere A, Di Profio G, Curcio E, et al., (2025) Unifying nucleation and crystal growth mechanisms in membrane crystallisation. Journal of Membrane Science, Volume 725, May 2025, Article number 124021
dc.identifier.eissn1873-3123
dc.identifier.elementsID672809
dc.identifier.issn0376-7388
dc.identifier.paperNo124021
dc.identifier.urihttps://doi.org/10.1016/j.memsci.2025.124021
dc.identifier.urihttps://dspace.lib.cranfield.ac.uk/handle/1826/23819
dc.identifier.volumeNo725
dc.languageEnglish
dc.language.isoen
dc.publisherElsevier
dc.publisher.urihttps://www.sciencedirect.com/science/article/pii/S0376738825003345?via%3Dihub
dc.relation.isreferencedbyhttps://doi.org/10.57996/cran.ceres-2747
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectMetastable zone
dc.subjectTemperature and temperature difference
dc.subjectZero liquid discharge
dc.subjectBrine
dc.subjectDistillation
dc.subject40 Engineering
dc.subjectChemical Engineering
dc.subject34 Chemical sciences
dc.titleUnifying nucleation and crystal growth mechanisms in membrane crystallisation
dc.typeArticle
dc.type.subtypeJournal Article
dcterms.dateAccepted2025-03-22

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