Content area

Abstract

Oil wettability in the water-oil-rock systems is very sensitive to the evolution of surface charges on the rock surfaces induced by the adsorption of ions and other chemical agents in water flooding. Through a set of large-scale molecular dynamics simulations, we reveal the effects of surface charge on the oil contact angles in an ideal water-decane-silicon dioxide system. The results show that the contact angles of oil nano-droplets have a great dependence on the surface charges. As the surface charge density exceeds a critical value of 0.992 e/nm2, the contact angle reaches up to 78.8° and the water-wet state is very apparent. The variation of contact angles can be confirmed from the number density distributions of oil molecules. With increasing the surface charge density, the adsorption of oil molecules weakens and the contact areas between nano-droplets and silicon dioxide surface are reduced. In addition, the number density distributions, RDF distributions, and molecular orientations indicate that the oil molecules are adsorbed on the silicon dioxide surface layer-by-layer with an orientation parallel to the surface. However, the layered structure of oil molecules near the silicon dioxide surface becomes more and more obscure at higher surface charge densities.

Details

Title
Oil Contact Angles in a Water-Decane-Silicon Dioxide System: Effects of Surface Charge
Author
Xu, Shijing 1 ; Wang, Jingyao 1 ; Wu, Jiazhong 1 ; Liu, Qingjie 1 ; Sun, Chengzhen 2   VIAFID ORCID Logo  ; Bai, Bofeng 2 

 State Key Laboratory of Enhanced Oil Recovery, Research Institute of Petroleum Exploration and Development of PetroChina, Beijing, China 
 State Key Laboratory of Multiphase Flow in Power Engineering, Xi’an Jiaotong University, Xi’an, China 
Pages
1-9
Publication year
2018
Publication date
Apr 2018
Publisher
Springer Nature B.V.
ISSN
19317573
e-ISSN
1556276X
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2027460991
Copyright
Nanoscale Research Letters is a copyright of Springer, (2018). All Rights Reserved.