Molecular design and applications of a nanostructure green Tripodal surface active ionic liquid in enhanced oil recovery: Interfacial tension reduction, wettability alteration, and emulsification

被引:16
|
作者
Kharazi, Mona [1 ]
Saien, Javad [1 ]
Torabi, Morteza [1 ]
Zol, Mohammad Ali [1 ]
机构
[1] Bu Ali Sina Univ, Fac Chem & Petr Sci, Hamadan 6517838695, Iran
基金
美国国家科学基金会;
关键词
Tripodal ionic liquids; Green materials; Enhanced oil recovery; Interfacial tension; Wettability; Emulsification; ADSORPTION; NANO; TOXICITY; BEHAVIOR; FAMILY;
D O I
10.1016/j.petsci.2023.07.010
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Surface active ionic liquids (SAILs) are considered as prominent materials in enhanced oil recovery thanks to their high interfacial activity. This study reports the preparation and applications of a nano-structure Tripodal imidazolium SAIL as an environmentally-friendly substitute to the conventional sur-factants. The product has a star-like molecular structure centered by a triazine spacer, namely [(C4im)3TA][Cl3], prepared by a one-step synthesis method and characterized with FT-IR, NMR, XRD, and SEM analysis methods. The interfacial tension of the system was decreased to about 78% at critical micelle concentration of less than 0.08 mol$dm = 3. Increasing temperature, from 298.2 to 323.2 K, improved this capability. The solid surface wettability was changed from oil-wet to water-wet and 80% and 77% stable emulsions of crude oil-aqueous solutions were created after one day and one week, respectively. Compared to the Gemini kind homologous SAILs, the superior effects of the Tripodal SAIL were revealed and attributed to the strong hydrophobic branches in the molecule. The Frumkin adsorption isotherm precisely reproduced the generated IFT data, and accordingly, the adsorption and thermodynamic parameters were determined.(c) 2023 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/ 4.0/).
引用
收藏
页码:3530 / 3539
页数:10
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