Amphiphilicity evolution in self-assembled carbon-based nanostructures for stabilizing different types of Pickering emulsions

被引:0
作者
Wang, Baichen [1 ,2 ]
Liao, Xiaolin [1 ]
Gao, Yu [1 ]
Li, Wei [1 ]
机构
[1] Shenyang Aerosp Univ, Sch Mat Sci & Engn, Liaoning Key Lab Adv Polymer Matrix Composites, Shenyang, Peoples R China
[2] Shenyang Aerosp Univ, Sch Mat Sci & Engn, Liaoning Key Lab Adv Polymer Matrix Composites, Shenyang 110136, Peoples R China
基金
中国国家自然科学基金;
关键词
Pickering emulsion; carbon nanostructures; amphiphilicity; self-assembly; catalytic reduction; GRAPHENE OXIDE; SELECTIVE OXIDATION; NANOTUBES; IMIDAZOLE; FOAMS; PERFORMANCE; REDUCTION; MECHANISM; CATALYSIS;
D O I
10.1080/1539445X.2023.2283881
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Carbon-based nanostructures have been firmly established as highly scalable and versatile platforms, which have found extensive applications in several fields of multifunctional nanocomposites, energy storage, environment protection, and electronics device. Pickering emulsion template method is one of the efficient strategies for assembling metastable carbon nanomaterials into stable macroarchitectures. Here, the combination of graphene oxide (GO) and carbon nanotubes (CNTs) was chemically and continuously treated with 2-ethyl-4-methylimidazole (EMI) to acquire tunable wettability. The hybridization of CNTs and reduction of GO can make the as-synthesized carbon nanohybrids be capable of stabilizing oil-in-water (O/W) and water-in-oil (W/O) Pickering emulsions, respectively. The major shift in the type of Pickering emulsion is conveniently implemented through the catalytic reduction of GO by EMI. The sp2-hybridized carbon networks self-assembled with CNTs and reduced graphene oxide (RGO) are intentionally located at the biphasic liquid interface of different types of Pickering emulsions, which can endow the architecture elaborated from Pickering emulsion strategy with multiple functionalities.
引用
收藏
页码:13 / 21
页数:9
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