差示扫描量热法
结晶
吸热过程
同步加速器
材料科学
结晶学
亚稳态
Crystal(编程语言)
相(物质)
X射线晶体学
衍射
熔点
晶体结构
六方晶系
分析化学(期刊)
热力学
化学
物理化学
色谱法
物理
有机化学
吸附
计算机科学
核物理学
光学
复合材料
程序设计语言
作者
Luisa Barba,Gianmichele Arrighetti,Sonia Calligaris
标识
DOI:10.1002/ejlt.201200259
摘要
Abstract Crystallization and melting properties of triacylglycerols in extra virgin olive oil were studied by using synchrotron X‐ray diffraction (XRD) and differential scanning calorimetry (DSC). The phase transitions were monitored by cooling and heating the samples at 2°C/min from 60 to −60°C and vice versa. Upon cooling, a first DSC endothermic peak was recorded at −9.6°C followed by one at −33.5°C. These thermal events were associated to the formation of two different structures: a triple‐chain length (3L) having a c parameter of about 58.38 Å and a quadruple chain length structure (4L) with a c parameter of about 89.99 Å, respectively. Both structures evidenced a cell packing arrangement ascribable to a β′ form. During heating, part of the metastable β′ crystals rearranged into the more thermodynamically stable β form. Then, upon further heating, the sequential melting of the two crystal structures was observed. The melting was completed at 10.7°C. Beside this interpretation of XRD data, a model considering a cell with a c parameter of about 170 Å and a hexagonal crystal system was proposed. Even if more research is needed to validate this approach, it allowed all XRD events recorded during the experiments to be described. See commentary by Chiavaro [p. 267–269], http://dx.doi.org/10.1002/ejlt.201200415
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