A new class of amide-based organogels: from oil spill recovery to self-assembly structure analysis

被引:3
|
作者
Yang, Dongdong [1 ,2 ]
Xia, Shuwei [1 ,2 ]
Bao, Mutai [1 ,2 ]
Chen, Xiuping [1 ,2 ]
Kang, Hu [1 ,2 ]
Zhao, Haosen [1 ,2 ]
Li, Yiming [1 ,2 ]
机构
[1] Ocean Univ China, Frontiers Sci Ctr Deep Ocean Multispheres & Earth, Key Lab Marine Chem Theory & Technol, Minist Educ, Qingdao 266100, Peoples R China
[2] Ocean Univ China, Coll Chem & Chem Engn, Qingdao 266100, Peoples R China
基金
中国国家自然科学基金;
关键词
DENSITY FUNCTIONALS; SELECTIVE GELATION; FUTURE; ATOMS; FIELD; GELS;
D O I
10.1039/d2ta10000b
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
Frequent oil spill accidents not only cause a great loss of energy but also bring about severe ecological risks. Phase-selective organogelators (PSOGs) can selectively solidify oil from oil-water mixtures through the formation of organogels and then the oil can be removed with mechanical tools conveniently. However, the efficient gelation of PSOGs, microscopic self-assembly mechanism of PSOGs in organic solvents and their structure-property relationship are still confusing. In this work, we synthesized three new aromatic amide PSOGs (A(18), B-18 and A(16)) with different molecular structures and investigated their gelling ability for various organic solvents using rheological tests and SEM images. Importantly, the monomer and dimer structures of the three PSOGs were analyzed using Gaussian 09. Multiwfn and Visual Molecular Dynamics (VMD) were used to obtain their electrostatic potential (ESP) graph. The difference in the properties of A(18), B-18 and A(16) may be determined by FT-IR and XRD. In addition, we know through calculation that A(18) and A(16) form H-aggregates, while B-18 forms J-aggregates, which also reflected the better nature of B-18. These results of theoretical calculations are well consistent with our experimental results and can help us to understand deeply the structure-property relationship of PSOGs.
引用
收藏
页码:6181 / 6190
页数:10
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