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沥青质在预吸附水存在下对石英砂的吸附。

Asphaltene adsorption on quartz sand in the presence of pre-adsorbed water.

机构信息

Centre for Petroleum and Surface Chemistry, Department of Chemistry, University of Surrey, Guildford, Surrey GU2 7XH, UK.

Centre for Petroleum and Surface Chemistry, Department of Chemistry, University of Surrey, Guildford, Surrey GU2 7XH, UK.

出版信息

J Colloid Interface Sci. 2016 Oct 15;480:137-145. doi: 10.1016/j.jcis.2016.07.014. Epub 2016 Jul 9.

Abstract

BACKGROUND AND HYPOTHESIS

In the oil industry, asphaltenes are known for their tendency to aggregate in solution and to deposit on surfaces, with both properties being connected with operational problems associated with recovery, production and refining. Interactions involving asphaltenes and other crude oil components have been a major aspect of investigation in attempting to understand the full nature of these problems. Water is implicated in asphaltene behavior in solution, for example, where it has been found to delay the deposition of asphaltene aggregates. At interfaces, there is evidence that water-in-crude oil emulsion stability is enhanced through asphaltene-water interactions, and there have been a few reports that asphaltene adsorption on mineral surfaces is reduced in the presence of water. We consider the latter aspect, because the instances of reduced adsorption to date have not attempted to quantify the effect. Previous studies showed that vapor-phase adsorption of organic molecules is reduced in the presence of pre-adsorbed water and we were interested to determine whether the same is true for liquid-phase adsorption of asphaltenes.

EXPERIMENTS

The surface of quartz sand was controlled by pre-adsorption of water from different relative humidity (RH) environments as the water adsorption isotherm is known from previous studies. These pre-conditioned sand samples were used as substrates for the adsorption from toluene solutions of n-heptane-precipitated asphaltenes (C7A) from an Athabasca oil sands bitumen. To supplement the adsorption behavior, atomic force microscopy (AFM) images were taken of the resultant sand grains at 0 and 80% RH, and low-field NMR was used to estimate the sand wettability.

FINDINGS

Asphaltene adsorption on sand is sensitive to surface-adsorbed water, with ∼4-fold reduction in adsorption when increasing the RH from 0 to 100%. This is in general agreement with previous vapor-phase adsorption of small organic molecules, and is therefore believed to be the first demonstration of the effect of pre-adsorbed water on adsorption from solution. Asphaltene adsorption as a function of RH is the converse of literature water adsorption isotherm data. Three asphaltene adsorption regions have been tentatively identified based on water adsorption behavior and the literature interpretation of water structure on quartz: the highest asphaltene adsorption occurs at very low RH, decreasing to a near-constant value in the range ∼40-80% RH, followed by a rapid decrease beyond 80% RH. Further analysis strongly suggests that asphaltene adsorption decreases linearly with the thickness of the adsorbed water film. The effects of RH on asphaltene adsorption are also reflected in AFM images and NMR wettability results.

摘要

背景和假设

在石油工业中,沥青质以其在溶液中聚集和在表面沉积的倾向而闻名,这两种性质都与与回收、生产和精炼相关的操作问题有关。涉及沥青质和其他原油成分的相互作用一直是试图理解这些问题的全部性质的一个主要方面。例如,水在沥青质在溶液中的行为中起作用,在溶液中发现水会延迟沥青质聚集体的沉积。在界面上,有证据表明,通过沥青质-水相互作用,水-原油乳状液的稳定性得到增强,并且有一些报道称,在存在水的情况下,沥青质在矿物表面的吸附减少。我们考虑后一个方面,因为到目前为止,减少吸附的实例并没有试图量化这种效果。先前的研究表明,有机分子的气相吸附在预吸附水的存在下减少,我们有兴趣确定对于沥青质的液相吸附是否也是如此。

实验

石英砂的表面通过预吸附不同相对湿度(RH)环境中的水来控制,因为水吸附等温线是以前的研究已知的。这些经过预处理的砂样被用作从甲苯溶液中吸附正庚烷沉淀沥青质(C7A)的基质,正庚烷沉淀沥青质是从阿萨巴斯卡油砂沥青中得到的。为了补充吸附行为,在 0 和 80%RH 下对所得砂粒进行原子力显微镜(AFM)成像,并使用低场 NMR 估计砂的润湿性。

发现

沥青质在砂上的吸附对表面吸附水敏感,当 RH 从 0 增加到 100%时,吸附减少约 4 倍。这与以前的小有机分子气相吸附大致一致,因此被认为是首次证明预吸附水对溶液中吸附的影响。根据 RH 对沥青质吸附的影响与文献中水吸附等温线数据相反。根据水吸附行为和文献中对石英上水结构的解释,基于水吸附行为,已初步确定了三个沥青质吸附区:在非常低的 RH 下发生最高的沥青质吸附,在约 40-80%RH 的范围内降低到接近恒定的值,然后在 RH 超过 80%后迅速降低。进一步的分析强烈表明,沥青质吸附与吸附水膜的厚度呈线性下降。RH 对沥青质吸附的影响也反映在 AFM 图像和 NMR 润湿性结果中。

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