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首页> 外文期刊>Colloids and Surfaces, A. Physicochemical and Engineering Aspects >Vesicles in fatty acid salt-fatty acid stabilized o/w emulsion - emulsion structure and rheology
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Vesicles in fatty acid salt-fatty acid stabilized o/w emulsion - emulsion structure and rheology

机译:脂肪酸盐-脂肪酸稳定的O / W乳液中的囊泡-乳液的结构和流变性

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摘要

Texture and rheology properties of fatty acid salt-fatty acid mixture stabilized oil-water (o/w) emulsions are being explored. While NaOH solution was introduced as aqueous phase, oil phase contained in it dissolved lauric acid. When these oil and water phases are brought in contact, a portion of lauric acid transforms into sodium laurate in situ via acid-base reaction, the combination of which at a certain threshold concentration and above is believed to act as emulsifier in stabilizing the given o/w emulsion system. Light microscopy under cross polarizing conditions suggested that in addition to the formation of surfactant stabilized emulsion droplets, formation of molecular aggregates of vesicle type is imminent in these conditions, both the size and number density of which is found to be a function of emulsifier concentration ratio. The concentration of emulsifier (sodium laurate-lauric acid) is being assessed in this work indirectly as a function of NaOH concentration, due to the problem associated with its quantification. Non or a very small number of vesicles was observed at NaOH concentration below 0.4 M, whilst in the presence of 0.4-0.8 M NaOH the vesicle population increased substantially. While vesicle population density decreased past 0.8 M NaOH, their size increased with NaOH-concentration from 0.8 to 1 M. These observations suggested that sodium laurate-lauric acid concentration ratio that corresponds to 0.6-0.8 M NaOH is the optimum NaOH concentration at which maximum vesicle number density is observed. As far as theology properties are concerned, at any given gamma, in the absence of NaOH, the eta of the oil solubilized lauric acid was found to be much lower than the eta of corresponding sodium laurate-lauric acid stabilized o/w emulsion. Though eta(gamma) profiles of sodium laurate-lauric acid stabilized o/w emulsion was not a linear function under the given sets of experimental conditions, at all conditions eta strongly depended on sodium laurate-lauric acid concentrations (concentration of NaOH in this case). What more is that at any given gamma, the eta was observed to be maximum at sodium laurate-lauric acid concentration ratio that corresponded to 0.8 M NaOH, a situation which corresponds to the presence of the maximum vesicle number density. In addition to eta, in the presence of 0.8 M NaOH, higher values of sigma(gamma) was observed, implying that at this particular NaOH concentration these emulsions possessed greater degree of emulsion structuring compared to other NaOH concentrations. These observations lead to the conclusion that sodium laurate concentration plays a great role in the formation of fatty acid salt vesicles, that under the given set of conditions sodium laurate-lauric acid concentration corresponding to 0.8 M NaOH is the optimum concentration at which maximum number of vesicles are produced, and that theology property of these emulsions depend not only on emulsion droplets but also on the vesicle number density and size. Test on oscillatory shear mode also suggested that much like o/w emulsions stabilized with other type surfactant, the viscoelastic properties of these sodium laurate-lauric acid stabilized o/w emulsions depended highly on surfactant concentration. The fact that G" response was dominant over G' response at all measured frequency and sodium laurate-lauric acid concentration, it is evident that viscous property dominated over elastic property in these emulsion. The good news is that improved elastic property is observed at sodium laurate-lauric acid concentration that corresponded to 0.6-0.8 M NaOH. And not only, in the8 M NaOH, while G" response of these samples was dominant over G' response at low (ω) over bar domain, the dynamic moduli crossed-over at around 2 Hz, past which the G' response became dominant over G". This implies that, at this particular surfactant concentration, emulsions stabilized with sodium laurate-laurate mixture displays an excellent viscoel
机译:脂肪酸盐-脂肪酸混合物稳定的油-水(o / w)乳液的质构和流变性能正在研究中。当将NaOH溶液作为水相引入时,其中包含的油相溶解了月桂酸。当这些油相和水相接触时,一部分月桂酸会通过酸碱反应原位转化为月桂酸钠,在一定的阈值浓度或更高浓度下,月桂酸的组合可作为乳化剂来稳定给定的邻苯二甲酸盐。 / w乳液系统。交叉极化条件下的光学显微镜表明,除了形成表面活性剂稳定的乳液液滴外,在这些条件下还即将形成囊泡型分子聚集体,发现其大小和数量密度均是乳化剂浓度比的函数。 。由于与定量有关的问题,在这项工作中间接评估了乳化剂(月桂酸钠-月桂酸钠)的浓度与NaOH浓度的关系。在低于0.4 M的NaOH浓度下观察到无囊泡或极少数囊泡,而在存在0.4-0.8 M NaOH的情况下,囊泡数量显着增加。当囊泡密度降低至超过0.8 M NaOH时,其大小随NaOH浓度从0.8增至1 M而增加。这些观察结果表明,对应于0.6-0.8 M NaOH的月桂酸钠-月桂酸浓度比是最大的最佳NaOH浓度。观察到囊泡密度。就神学特性而言,在任何给定的伽马值下,在没有NaOH的情况下,发现油溶性月桂酸的eta值都远低于相应的月桂酸钠-月桂酸稳定的o / w乳剂的eta。尽管在给定的实验条件下,月桂酸钠-月桂酸稳定的o / w乳液的η(γ)曲线不是线性函数,但在所有条件下,eta强烈依赖于月桂酸钠-月桂酸的浓度(在这种情况下为NaOH的浓度) )。更重要的是,在任何给定的伽马值下,在对应于0.8 M NaOH的月桂酸钠-月桂酸浓度比处观察到eta值最大,这种情况对应于最大囊泡数密度的存在。除η外,在0.8 M NaOH的存在下,观察到更高的σ值,这意味着与其他NaOH浓度相比,在该特定NaOH浓度下,这些乳液具有更大程度的乳液结构化。这些观察结果得出以下结论:月桂酸钠浓度在脂肪酸盐小泡的形成中起着重要作用,在给定的条件下,对应于0.8 M NaOH的月桂酸钠-月桂酸浓度是最佳浓度,其中最大产生了囊泡,这些乳剂的神学特性不仅取决于乳剂液滴,还取决于囊泡数的密度和大小。对振荡剪切模式的测试还表明,与用其他类型的表面活性剂稳定的o / w乳液非常相似,这些月桂酸钠-月桂酸稳定的o / w乳液的粘弹性质在很大程度上取决于表面活性剂的浓度。在所有测得的频率和月桂酸钠-月桂酸浓度下,G“响应均高于G'响应这一事实,很明显,在这些乳液中,粘稠性高于弹性,这是一个好消息。月桂酸酯-月桂酸的浓度对应于0.6-0.8 M NaOH。不仅如此,在8 M NaOH中,尽管这些样品的G“响应高于bar域在低(ω)时的G'响应,但动态模量与在大约2 Hz时,G'响应超过G“占主导地位。这意味着在此特定的表面活性剂浓度下,用月桂酸钠-月桂酸酯混合物稳定的乳液显示出优异的粘滞性

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