Girard Henri-Louis, Bourrianne Philippe, Chen Dayong, Jaishankar Aditya, Vreeland Jessica L, Cohen Robert E, Varanasi Kripa K, McKinley Gareth H
Department of Mechanical Engineering, MIT, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Department of Chemical Engineering, MIT, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Langmuir. 2020 Apr 14;36(14):3894-3902. doi: 10.1021/acs.langmuir.0c00029. Epub 2020 Apr 2.
Asphaltenes, heavy aromatic components of crude oil, are known to adsorb on surfaces and can lead to pipe clogging or hinder oil recovery. Because of their multicomponent structure, the details of their interactions with surfaces are complex. We investigate the effect of the physicochemical properties of the substrate on the extent and mechanism of this adsorption. Using wetting measurements, we relate the initial kinetics of deposition to the interfacial energy of the surface. We then quantify the long-term adsorption dynamics using a quartz crystal microbalance and ellipsometry. Finally, we investigate the mechanism and morphology of adsorption with force spectroscopy measurements as a function of surface chemistry. We determine different adsorption regimes differing in orientation, packing density, and initial kinetics on different substrate functionalizations. Specifically, we find that alkane substrates delay the initial monolayer formation, fluorinated surfaces exhibit fast adsorption but low bonding strength, and hydroxyl substrates lead to a different adsorption orientation and a high packing density of the asphaltene layer.
沥青质是原油中的重质芳香族成分,已知其会吸附在表面,可能导致管道堵塞或阻碍石油开采。由于其多组分结构,它们与表面相互作用的细节很复杂。我们研究了基底的物理化学性质对这种吸附程度和机理的影响。通过润湿性测量,我们将沉积的初始动力学与表面的界面能联系起来。然后,我们使用石英晶体微天平椭圆偏振仪量化长期吸附动力学。最后,我们通过力谱测量研究吸附的机理和形态,作为表面化学的函数。我们确定了在不同基底功能化上,吸附取向、堆积密度和初始动力学不同的不同吸附状态。具体而言,我们发现烷烃基底会延迟初始单层的形成,氟化表面表现出快速吸附但结合强度低,而羟基基底会导致不同的吸附取向和沥青质层的高堆积密度。