Synthesis of amphiphilic silicon quantum dots and its application in high efficiency imbibition oil recovery in low permeability reservoirs

被引:0
|
作者
Zhao, Mingwei [1 ,2 ]
Li, Ying [1 ,2 ]
Dai, Caili [1 ,2 ]
Chen, Yingpeng [3 ]
Sun, Xin [1 ,2 ]
Ge, Xinyu [1 ,2 ]
Ma, Shixu [1 ,2 ]
机构
[1] China Univ Petr East China, State Key Lab Deep Oil & Gas, Qingdao 266580, Peoples R China
[2] China Univ Petr East China, Sch Petr Engn, Shandong Key Lab Oilfield Chem, Qingdao 266580, Peoples R China
[3] Univ Alberta, Dept Chem & Mat Engn, Edmonton, AB T6G 1H9, Canada
基金
中国国家自然科学基金;
关键词
Amphiphilic silicon quantum dots; Low permeability; Spontaneous imbibition; Enhanced oil recovery; NANOFLUIDS; EMULSION;
D O I
10.1016/j.colsurfa.2024.134917
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, a novel three-step method was used to modify the surface of silicon quantum dots to synthesize amphiphilic silicon quantum dots (A-SiQDs) with higher interfacial activity. The particle size of A-SiQDs was only 3.5 nm. By adding a small amount of dodecyl dimethyl betaine (BS-12), the performance of A-SiQDs was further improved. Through particle size and zeta potential testing, it can be seen that the mixed system of ASiQDs and BS-12 had good temperature and salinity resistance, and can be stable at 120 degrees C and 50,000 mg/L NaCl. Meanwhile, the mixed system exhibited superior interfacial activity compared with individual A-SiQDs and BS-12. The mixed system can lower the interfacial tension from 32.15 mN/m to 1.82 mN/m and transform the rock surface from an oil-wet to a strong water-wet state. This ensured the excellent imbibition ability of the mixed system, which can increase the oil recovery to 35.7 %. Finally, from the perspective of force, the influence of nanofluids on oil stripping and migration was analyzed to reveal the imbibition mechanism. This paper proposes a facile three-step method for synthesizing A-SiQDs, and also provides a novel nanomaterial for high efficiency imbibition in low-permeability reservoirs.
引用
收藏
页数:8
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