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首页> 外文期刊>Sciences des Aliments >Evolution of fat crystallinity in anhydrous milk fat-in-water emulsion, as studied by different physical combined techniques.
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Evolution of fat crystallinity in anhydrous milk fat-in-water emulsion, as studied by different physical combined techniques.

机译:通过不同的物理组合技术研究,无水牛奶水包脂肪乳液中脂肪结晶的演变。

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The structural characteristics of a same milk fat-in-water emulsion was determined using different physical techniques. The emulsion stability was monitored through determination of the fat droplet size distribution and proportion of adsorbed proteins at the fat droplet-water intersurface. Thermograms observed by differential scanning colorimetry (DSC) showed that Delta T (difference between temperature of initial crystallization and melting completion) was higher by approximately 10 degrees C in the emulsified milk fat than in the bulk fat sample. Moreover, isothermal treatment at 4 degrees C led to a peak time value (tmax=4 degrees C) which was ~12 min longer than in bulk fat. The evolution of viscoelastic properties under cooling and reheating reflected not only the contribution of crystalline fat in the emulsion during the ageing step at 4 degrees C but also the contribution of gelatin which was added for structuration of the aqueous continuous phase. The coupling with DSC of time-resolved synchotron X ray diffraction at both small and wide angles showed that fat crystallization behaved differently under cooling and reheating. Under cooling and reheating, (sub alpha ) -> alpha polymorphic transition and alpha -> beta ' were observed, respectively. Separation of proton relaxation between aqueous and fat phases observed by low field nuclear magnetic resonance showed that the crystalline fat formed at 4 degrees C was more affected by the presence of emulsifiers than by emulsification. The results obtained using different approaches were presented in regard to their potential of giving complementary information on emulsion structural properties..
机译:使用不同的物理技术确定相同的牛奶水包脂肪乳液的结构特征。通过测定脂肪滴-水界面处的脂肪滴尺寸分布和吸附蛋白的比例来监测乳液的稳定性。通过差示扫描比色法(DSC)观察到的热分析图显示,乳化的乳脂中的Delta T(初始结晶温度与熔融完成之间的差)比散装脂肪样品高约10摄氏度。此外,在4摄氏度下进行等温处理会导致峰值时间值(tmax = 4摄氏度),比峰值脂肪的峰值时间长约12分钟。冷却和再加热下粘弹性的演变不仅反映了乳液在4摄氏度老化过程中结晶脂肪的贡献,还反映了明胶的贡献,明胶的添加是为了使水连续相结构化。时间分辨的同步加速器X射线衍射在小角度和广角处与DSC耦合显示,脂肪结晶在冷却和再加热下表现不同。在冷却和再加热下,分别观察到(sub alpha)-> alpha多态性转变和alpha-> ​​beta'。通过低场核磁共振观察到的水相和脂肪相之间质子弛豫的分离表明,在4摄氏度形成的结晶脂肪受乳化剂的影响比受乳化作用的影响更大。提出了使用不同方法获得的有关乳剂结构特性补充信息潜力的结果。

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