Crystallization and transformation of polymorphic forms of trioleoyl glycerol (OOO) and 1,2-dioleoyl-3-rac-linoleoyl glycerol (OOL)

This study examined the influence of different thermal treatments on the crystallization and transformation of trioleoyl glycerol (OOO) and 1,2-dioleoyl-3-rac-linoleoyl glycerol (OOL). Two triacylglycerol (TAG) samples were cooled at 0.5-15 °C·min-1 and heated at 2 and 15 °C·min-1. The polymorphic c...

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Detalhes bibliográficos
Autores: Bayés-García, Laura, Calvet Pallàs, Maria Teresa, Cuevas Diarte, Miguel Ángel, Ueno, S., Sato, Kiyotaka
Formato: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2013
País:España
Recursos:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/160809
Acesso em linha:https://hdl.handle.net/2445/160809
Access Level:acceso abierto
Palavra-chave:Cristal·lografia
Polimorfisme (Cristal·lografia)
Triglicèrids
Crystallography
Polymorphism (Crystallography)
Triglycerides
Descrição
Resumo:This study examined the influence of different thermal treatments on the crystallization and transformation of trioleoyl glycerol (OOO) and 1,2-dioleoyl-3-rac-linoleoyl glycerol (OOL). Two triacylglycerol (TAG) samples were cooled at 0.5-15 °C·min-1 and heated at 2 and 15 °C·min-1. The polymorphic characteristics of the two TAGs were analyzed in situ using differential scanning calorimetry, Raman spectroscopy, and synchrotron radiation X-ray diffraction. Multiple polymorphic forms were identified in OOO (α, β′2, β′1, β2, and β1) and OOL (α, β′2, and β′1). Larger quantities of more stable forms (e.g., β2 and β1 of OOO and β′1 of OOL) were obtained when the samples were slowly cooled and heated. In contrast, less stable polymorphs were obtained with increased cooling and heating rates. Polymorphic transformations occurred in either solid-state or melt-mediation and were influenced by heating rates. The results were analyzed by considering the activation energies for crystallization and transformation of stable and less stable polymorphic forms in comparison with previous studies on 1,3-dipalmitoyl-2-oleoyl-glycerol and 1, 3-dioleoyl-2-palmitoyl-glycerol.