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Interfacial Rheology and Heterogeneity of Aging Asphaltene Layers at the Water-Oil Interface
被引:71
|作者:
Chang, Chih-Cheng
[1
]
Nowbahar, Arash
[1
]
Mansard, Vincent
[1
,2
]
Williams, Ian
[1
]
Mecca, Jodi
[3
]
Schmitt, Adam K.
[3
]
Kalantar, Tom H.
[3
]
Kuo, Tzu-Chi
[3
]
Squires, Todd M.
[1
]
机构:
[1] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[2] Lab Anal & Architecture Syst, F-31031 Toulouse, France
[3] Dow Chem Co USA, Midland, MI 48640 USA
来源:
关键词:
MODEL EMULSION COALESCENCE;
DILUTED-BITUMEN EMULSIONS;
STABILITY;
MICROSCOPY;
MONOLAYERS;
SURFACE;
FILMS;
DEMULSIFICATION;
MICRORHEOLOGY;
LANGMUIR;
D O I:
10.1021/acs.langmuir.8b00176
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Surface-active asphaltene molecules are naturally found in crude oil, causing serious problems in the petroleum industry by stabilizing emulsion drops, thus hindering the separation of water and oil. Asphaltenes can adsorb at water-oil interfaces to form viscoelastic interfacial films that retard or prevent coalescence. Here, we measure the evolving interfacial shear rheology of water-oil interfaces as asphaltenes adsorb. Generally, interfaces stiffen with time, and the response crosses over from viscous-dominated to elastic dominated. However, significant variations in the stiffness evolution are observed in putatively identical experiments. Direct visualization of the interfacial strain field reveals significant heterogeneities within each evolving film, which appear to be an inherent feature of the asphaltene interfaces. Our results reveal the adsorption process and aged interfacial structure to be more complex than that previously described. The complexities likely impact the coalescence of asphaltene-stabilized droplets, and suggest new challenges in destabilizing crude oil emulsions.
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页码:5409 / 5415
页数:7
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