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Effect of sugars on the phase behaviour, flow and interfacial properties of protein/polysaccharide aqueous two-phase systems

机译:糖对蛋白质/多糖水性两相系统的相行为,流动和界面性能的影响

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The paper reviews the phase behaviour, microstructure, flow behaviour and interfacial properties of four sodium caseinate (NaCAS)/galactomannan (GM) model systems with sugar (i.e. glucose, fructose, sucrose and trehalose) dissolved in citrate buffer (pH 5.8) at 20°C. The established phase diagrams showed that sugar type and sugar concentration affect the phase behaviour of all systems. Below 15 wt% sugar, the miscibility of biopolymers improved and the increment of the sugar concentration decreased the miscibility. Glucose, fructose and sucrose improved the compatibility of the biopolymers, whereas trehalose had the opposite effect. Galactomannans with a mannose-to-galactose ratio < 2 (i.e. guar gum (GG) and fenugreek gum (FG)) were more miscible than galactomannans with a mannoseto- galactose ratio > 2 (i.e. locust bean gum (LBG) and tara gum (TG)). The effect was pronounced only in systems with the sugar present. Quiescent microstructure and flow were largely unaffected by sugar type, but changed with its concentration. Sugar increased the overall viscosity and enhanced the non-Newtonian behaviour of the model systems. Phase sense (for blends of < 20 wt% sugar) depended on the volume fraction of each phase and the applied shear rate. Under quiescent conditions, phase-inversion took place for equal phase volumes. However, at higher shear regimes phase-inversion was observed for the initially polysaccharide-continuous blends. In the presence of > 20 wt% sugar, phase sense depended on the volume fraction only; no shear-induced phaseinversion was observed. Similarly, the interfacial properties of the systems were also affected by sugar type and concentration and correlated well with their position in the phase diagram. The closer the systems were to the critical point, the shorter the tile-line length they were positioned on, and the lower their interfacial tension was. The lowest interfacial tension was measured for the systems with 30 wt% sugar (disaccharides especially).
机译:本文综述了溶解在柠檬酸盐缓冲液(pH 5.8)中的糖(即葡萄糖,果糖,蔗糖和海藻糖)四钠酪蛋白(NACAS)/半乳蛋白酶(GM)模型系统的相位行为,微观结构,流动性和界面性质。 °C。建立的相图显示糖型和糖浓度影响所有系统的相行为。低于15wt%的糖,生物聚合物的混溶性改善,糖浓度的增量降低了混溶性。葡萄糖,果糖和蔗糖改善了生物聚合物的相容性,而海藻糖具有相反的效果。具有甘露聚糖的半乳甘露聚糖比(即瓜尔胶(GG)和Fenugreek Gum(FG))比具有甘露聚糖的半乳糖甘露聚糖比例更混溶> 2(即尖锐豆胶(LBG)和塔拉胶( TG))。效果仅在具有糖目前的系统中发音。静态微观结构和流动大大不受糖型的影响,但随着其浓度而变化。糖增加了整体粘度并增强了模型系统的非牛顿行为。相位感(对于<20wt%糖的共混物)依赖于每相的体积分数和施加的剪切速率。在静态条件下,发生相位卷的阶段反转。然而,在较高的剪切制度下,观察到最初多糖连续共混物的相位倒置。在存在> 20wt%糖的情况下,相位感依赖于体积分数;未观察到剪切诱导的嘌呤转化。类似地,系统的界面性质也受糖型和浓度的影响,并且在相图中的位置良好地相关。系统越接近临界点,瓦片线长度越短,它们的界面张力越低。测量最低界面张力,用于具有30wt%糖(特别是二糖)的系统。

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