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Rheology and Catastrophic Phase Inversion of Emulsions in the Presence of Starch Nanoparticles

机译:淀粉纳米粒子存在下乳液的流变学和灾难性相位反转

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Emulsionsstabilizedbysolidnanoparticles, referredtoasPickeringemulsions, are becomingincreasingly important in applications as they are free of surfactants. However, the bulk propertiesand stability of Pickering emulsions are far from being well understood. In this work, the rheologicalbehavior and catastrophic phase inversion of emulsions in the presence of starch nanoparticles werestudied using in-situ measurements of viscosity and electrical conductivity. The aqueous phaseconsisting of starch nanoparticles was added sequentially in increments of 5% vol. to the oil phaseunderagitationconditiontopreparetheemulsions. Theemulsionswerewater-in-oil(W/O)typeatlowto moderate concentrations of aqueous phase. At a certain critical volume fraction of aqueous phase,catastrophic phase inversion of W/O emulsion to oil-in-water (O/W) emulsion took place accompanieda sharp jump in the electrical conductivity and a sharp drop in the emulsion viscosity. The W/Oemulsions were nearly Newtonian at low concentrations of aqueous phase. At high concentrations ofaqueous phase, prior to phase inversion, the W/O emulsions exhibited a shear-thickening behavior.The O/W emulsions produced after phase inversion were shear-thinning in nature. The comparison ofthe experimental viscosity data with the predictions of emulsion viscosity model revealed only partialcoverage of droplet surfaces with nanoparticles. With the increase in the concentration of starchnanoparticles (SNPs) in the aqueous phase of the emulsions, the phase inversion of W/O emulsion toO/W emulsion was delayed to higher volume fraction of aqueous phase. Thus SNPs imparted somestability to W/O emulsions against coalescence and phase inversion.
机译:乳液溶解玻璃甘露尼铵,参考酵母乳液,在施用中被释放,因为它们没有表面活性剂。然而,油脂乳液的散装性能和稳定性远远不易理解。在这项工作中,使用原位测量粘度和导电性的淀粉纳米颗粒存在下乳液的流变衰老和灾难性相位反转。淀粉纳米颗粒的水性相逐次以5%Vol的增量依次加入。到oil pumpaceundagitionconditiontopereteMetemulsions。脱乳液(W / O)碎片(W / O)碎片中等浓度的水相。在水相的某种临界体积分数下,W / O乳液的灾难性相位反转在水 - 水中(O / W)乳液进行伴随在电导率下伴随着急剧跳跃,乳液粘度急剧下降。在低浓度的水相时,W / Oem乳液几乎是牛顿。在高浓度的α水相,在相倒置之前,W / O乳液表现出剪切增稠行为。在相倒反应后产生的O / W乳液在自然界中剪切稀释。实验粘度数据与乳液粘度模型预测的比较仅揭示了纳米颗粒的液滴表面的部分粘合剂。随着乳液的水相中浓度的浓度(SNP)的浓度增加,W / O乳液的相转移延迟至较高体积水相的水相。因此,SNP赋予W / O乳液对聚结和相位倒置的可定性。

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