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Partitioning of surfactants between the water and oil phases and relations to enhanced oil recovery methods

机译:表面活性剂在水和油相之间的分配及其与强化采油方法的关系

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摘要

The focus in this master thesis has been to investigate how a varying Ca2+/Na+ mole fraction affects the interfacial tension of a surfactant/brine - dodecane/toluene interface. It has also been investigated how the same systems are affected by a varying oil phase composition, stretching from pure- dodecane to toluene. Measurements regarding the pure dodecane phase have been performed during the project thesis in the autumn of 2013.Series in which model oil composition was richest in dodecane start off with high IFT values at lower calcium content and experience a decrease followed by a rise, as calcium content increases. IFT for systems where toluene was the most abundant component in the oil phase rose as calcium fraction in the system was increased. Series with equally mixed oil phases or 75/25 wt. % in favor of either dodecane or toluene showed IFT values that were clearly influenced by both components. Experiments proved that an increase of dodecane fraction relative to toluene in the model oil phase moved the minimum IFT point(s) towards higher calcium mole fractions. This behavior was expected from the EACN theory. Some values in the series conducted proved hard to measure, therefore a decrease in overall ionic strength proved useful in terms of finding the minimal interfacial tension for some of the dodecane/toluene series.The IFT value of the dodecane/brine and toluene/brine systems showed not to be affected by an increasing calcium mole fraction when surfactant was removed from the aqueous solution. This indicates that the observed changes in IFT in systems where surfactant is used, is clearly an effect of interactions between surfactants and cations. The optimal outcome has been to get a more mechanistic understanding of the oil-water interface, and the results can be used to model how a varying Ca2+/Na+ mole fraction affects the interfacial tension of an aqueous-oil system. Experimental results match exceptionally well with what is expected behavior from the EACN theory, and can be of high interest to further research related to combined surfactant- and low salinity flooding in relation to EOR.
机译:本硕士论文的重点是研究变化的Ca2 + / Na +摩尔分数如何影响表面活性剂/盐水-十二烷/甲苯界面的界面张力。还研究了相同的系统如何受到从纯十二烷到甲苯的不同油相组成的影响。在2013年秋季的项目论文中进行了有关纯十二烷相的测量。其中十二烷中模型油成分最丰富的系列以较高的IFT值(较低的钙含量)开始,然后随着钙的增加而下降,然后上升内容增加。随着系统中钙含量的增加,甲苯在油相中含量最高的系统的IFT升高。混合油相相同或75/25 wt。赞成十二烷或甲苯的%表明其IFT值明显受到两种组分的影响。实验证明,在模型油相中,十二烷分数相对于甲苯的增加将最小IFT点移向较高的钙摩尔分数。此行为是EACN理论所预期的。已证明该系列中的一些值难以测量,因此总离子强度的降低被证明有助于找到某些十二烷/甲苯系列的最小界面张力。十二烷/盐水和甲苯/盐水系统的IFT值当从水溶液中除去表面活性剂时,显示出不受增加的钙摩尔分数的影响。这表明在使用表面活性剂的系统中观察到的IFT变化显然是表面活性剂和阳离子之间相互作用的影响。最佳结果是获得对油水界面的更多机械理解,并且该结果可用于模拟变化的Ca2 + / Na +摩尔分数如何影响水油系统的界面张力。实验结果与EACN理论的预期行为异常吻合,对于与EOR有关的表面活性剂和低盐度联合驱油技术的进一步研究具有很高的兴趣。

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    Teigen Erlend;

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  • 年度 2014
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