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沥青质在油水界面的长期吸附动力学:随机序列吸附视角

Long-term adsorption kinetics of asphaltenes at the oil-water interface: a random sequential adsorption perspective.

作者信息

Pauchard Vincent, Rane Jayant P, Zarkar Sharli, Couzis Alexander, Banerjee Sanjoy

机构信息

Energy Institute, City College of New York , New York, New York 10031, United States.

出版信息

Langmuir. 2014 Jul 22;30(28):8381-90. doi: 10.1021/la500384r. Epub 2014 Jul 7.

Abstract

Previous studies indicated that asphaltenes adsorbed as monomers on oil-water interfaces and the early stage kinetics of the process was controlled by diffusion and hence dependent on oil viscosity. By measuring interfacial tension (IFT) as a function of surface coverage during droplet expansions in pendant drop experiments, it was also concluded that the IFT data could be interpreted with a Langmuir equation of state (EoS), which was independent of oil viscosity, time of adsorption, and bulk asphaltenes concentration. The surface excess coverage was calculated to be ∼0.3 nm(2)/molecule, which suggested adsorption in face-on configuration of asphaltenes monomers at the interface and average PAH core per molecule of about 6 for the asphaltenes investigated, consistent with the Yen-Mullins model. The current study focuses on the kinetics of asphaltenes adsorption at longer times and higher interfacial coverage. Long-term IFT data have been measured by the pendant drop method for different asphaltenes concentrations and for different bulk viscosities of the oil phase (0.5-28 cP). The data indicate that when coverage reaches 35-40%, the adsorption rates slow down considerably compared to the diffusion-controlled rates at the very early stages. The surface pressure increase rate (or IFT decrease rate) at these higher coverages is now independent of oil viscosity but dependent upon both surface pressure itself and asphaltene monomer concentration. The long-term asymptotic behavior of surface coverage is found to be consistent with the predictions from surface diffusion-mediated random sequential adsorption (RSA) theory which indicates a linear dependency of surface coverage on 1/√t and an asymptotic limit very close to 2D random close packing of polydispersed disks (85%). From these observations RSA theory parameters were extracted that enabled description of adsorption kinetics for the range of conditions above surface coverage of 35%.

摘要

先前的研究表明,沥青质以单体形式吸附在油水界面上,该过程的早期动力学受扩散控制,因此取决于油的粘度。通过在悬滴实验中测量液滴膨胀过程中界面张力(IFT)随表面覆盖率的变化,还得出结论,IFT数据可以用状态方程(EoS)的朗缪尔方程来解释,该方程与油的粘度、吸附时间和本体沥青质浓度无关。计算得出表面过量覆盖率约为0.3 nm²/分子,这表明在界面处沥青质单体以面朝上的构型吸附,对于所研究的沥青质,每个分子的平均多环芳烃核心约为6,这与Yen-Mullins模型一致。当前的研究集中在较长时间和较高界面覆盖率下沥青质的吸附动力学。通过悬滴法测量了不同沥青质浓度和不同油相本体粘度(0.5 - 28 cP)下的长期IFT数据。数据表明,当覆盖率达到35 - 40%时,与非常早期阶段受扩散控制的速率相比,吸附速率显著减慢。在这些较高覆盖率下,表面压力增加速率(或IFT降低速率)现在与油的粘度无关,但取决于表面压力本身和沥青质单体浓度。发现表面覆盖率的长期渐近行为与表面扩散介导的随机顺序吸附(RSA)理论的预测一致,该理论表明表面覆盖率与1/√t呈线性关系,并且渐近极限非常接近多分散圆盘的二维随机密堆积(85%)。从这些观察结果中提取了RSA理论参数,这些参数能够描述表面覆盖率高于35%的条件范围内的吸附动力学。

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