In situ crystallization and transformation kinetics of polymorphic forms of saturated-unsaturated-unsaturated triacylglycerols: 1-palmitoyl-2,3-dioleoyl glycerol, 1-stearoyl-2,3-dioleoyl glycerol, and 1-palmitoyl-2-oleoyl-3-linoleoyl glycerol

dc.contributor.authorBayés-García, Laura
dc.contributor.authorCalvet Pallàs, Maria Teresa
dc.contributor.authorCuevas Diarte, Miguel Ángel
dc.contributor.authorUeno, S.
dc.date.accessioned2020-05-15T15:29:08Z
dc.date.available2020-05-15T15:29:08Z
dc.date.issued2016-07
dc.date.updated2020-05-15T15:29:09Z
dc.description.abstractWe examined the influence of dynamic thermal treatment (variation of cooling/heating rates) on the polymorphic crystallization and transformation pathways of 1-palmitoyl-2,3-dioleoyl glycerol (POO), 1-stearoyl-2,3-dioleoyl glycerol (SOO), and 1-palmitoyl-2-oleoyl-3-linoleoyl glycerol (POL), which are major saturated-unsaturated-unsaturated (SUU) triacylglycerols (TAGs) of vegetable oils and animal fats (e.g., palm oil, olive oil, and Iberian ham fat). Using mainly a combination of differential scanning calorimetry (DSC) and synchrotron radiation X-ray diffraction (SR-XRD), we analyzed the polymorphic behavior of TAGs when high (15 °C min− 1), intermediate (2 °C min− 1), and low (0.5 °C min− 1) cooling and heating rates were applied. Multiple polymorphic forms were detected in POO, SOO, and POL (sub-α, α, β'2, and β'1). Transient disordered phases, defined as kinetic liquid crystal (KLC) phases, were determined in POO and SOO for the first time. The results demonstrated that more stable forms were directly obtained from the melt by decreasing the cooling rates, whereas less stable forms predominated at high cooling rates, as confirmed in our previous work. Regarding heating rate variation, we confirmed that the nature of the polymorphic transformations observed (solid-state, transformation through KLC phase, or melt-mediation) depended largely on the heating rate. These results were discussed considering the activation energies involved in each process and compared with previous studies on TAGs with different saturated-unsaturated structures (1,3-dioleoyl-2-palmitoylglycerol, 1,3-dipalmitoyl-2-oleoyl-glycerol, trioleoyl glycerol, and 1,2-dioleoyl-3-linoleoyl glycerol).
dc.format.extent57 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec669002
dc.identifier.issn0963-9969
dc.identifier.urihttps://hdl.handle.net/2445/160578
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.foodres.2016.05.011
dc.relation.ispartofFood Research International, 2016, vol. 85, p. 244-258
dc.relation.urihttps://doi.org/10.1016/j.foodres.2016.05.011
dc.rightscc-by-nc-nd (c) Elsevier B.V., 2016
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.sourceArticles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada)
dc.subject.classificationCristal·lografia
dc.subject.classificationPolimorfisme (Cristal·lografia)
dc.subject.classificationLípids
dc.subject.classificationTriglicèrids
dc.subject.otherCrystallography
dc.subject.otherPolymorphism (Crystallography)
dc.subject.otherLipids
dc.subject.otherTriglycerides
dc.titleIn situ crystallization and transformation kinetics of polymorphic forms of saturated-unsaturated-unsaturated triacylglycerols: 1-palmitoyl-2,3-dioleoyl glycerol, 1-stearoyl-2,3-dioleoyl glycerol, and 1-palmitoyl-2-oleoyl-3-linoleoyl glycerol
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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