How multiple noncovalent interactions regulate the aggregation behavior of amphiphilic triblock copolymer/surface-active ionic liquid mixtures
文献类型：期刊论文
| 作者 | Luo, Haiyan1; Jiang, Kun2; Wang, Xiaotian1; Yao, Haoyu3; Liang, Xiangfeng3; Li, Yingbo1,4; Liu, Huizhou1,3,4 |
| 刊名 | JOURNAL OF MOLECULAR LIQUIDS
 |
| 出版日期 | 2022-10-01 |
| 卷号 | 363页码:12 |
| ISSN号 | 0167-7322 |
| 关键词 | Noncovalent interactions Block copolymers Ionic liquids Aggregation behavior Structural evolution |
| DOI | 10.1016/j.molliq.2022.119856 |
| 英文摘要 | Amphiphilic block copolymers/ionic liquids mixtures have been emerging as a new class of "chemical entity' with numerous advanced applications. However, interaction mechanism governing the aggregation and the microstructure of aggregates are still far from full understanding. Herein, the role of noncovalent interactions in regulation of aggregation behaviors of mixtures of Pluronic F127 and surface-active ionic liquids, i.e. C(n)mimBr, CnPyBr and CnMPB is investigated by DLS, cryo-TEM, NMR and molecular dynamics simulation. The interaction modes between F127 and SAILs are remarkably dependent on the concentration and cationic headgroup of SAIL. At low SAIL concentration (< CMC), mixed micelles mainly composed of F127 with some SAIL cations embedded into micelles are formed, which was primarily driven by hydrophobic interaction. However, the residence of C(n)mimBr cations in micelles is quite different from that of CnPyBr and CnMPB cations due to its distinctive hydrogen bonding with PEO segment of F127. Upon further addition of SAILs (C-SAILs > CMC), gradual disintegration of F127-rich micelles was observed due to the enhanced repulsive electrostatic force at micellar core-corona interface, accompanying with the re-formation of two types of micelles: one consisting of pure SAILs and one that SAIL micelles bound with F127 monomers via hydrogen bonding and/or hydrophobic interactions. This work provides new insight into the aggregation mechanism of these complex systems and will be helpful to rational tailoring innovative copolymers /IL-based system for specific applications. (C) 2022 Elsevier B.V. All rights reserved. |
| WOS关键词 | AQUEOUS-SOLUTION ; BLOCK-COPOLYMERS ; LIGHT-SCATTERING ; ELECTROMOTIVE-FORCE ; MICELLIZATION ; SURFACTANTS ; MICELLES ; NMR ; SANS ; SIZE |
| 资助项目 | National Natural Science Foundation of China[U20A20142] ; National Natural Science Foundation of China[21676283] ; National Natural Science Foundation of China[21506221] ; Shandong Energy Institute[SEI I202133] ; Postdoctoral Research Foundation of China[2021M703238] |
| WOS研究方向 | Chemistry ; Physics |
| 语种 | 英语 |
| 出版者 | ELSEVIER |
| WOS记录号 | WOS:000831781400007 |
| 资助机构 | National Natural Science Foundation of China ; Shandong Energy Institute ; Postdoctoral Research Foundation of China |
| 源URL | [http://ir.ipe.ac.cn/handle/122111/54250]  |
| 专题 | 中国科学院过程工程研究所 |
| 通讯作者 | Li, Yingbo; Liu, Huizhou |
| 作者单位 | 1.Chinese Acad Sci, Inst Proc Engn, CAS Key Lab Green Proc & Engn, Beijing 100190, Peoples R China 2.Qingdao Univ, Sch Chem & Chem Engn, Qingdao 266071, Shandong, Peoples R China 3.Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, CAS Key Lab Biobased Mat, Qingdao 266061, Peoples R China 4.Chinese Acad Sci, Inst Proc Engn, PO 353, Beijing 100190, Peoples R China |
| 推荐引用方式 GB/T 7714 | Luo, Haiyan,Jiang, Kun,Wang, Xiaotian,et al. How multiple noncovalent interactions regulate the aggregation behavior of amphiphilic triblock copolymer/surface-active ionic liquid mixtures[J]. JOURNAL OF MOLECULAR LIQUIDS,2022,363:12. |
| APA | Luo, Haiyan.,Jiang, Kun.,Wang, Xiaotian.,Yao, Haoyu.,Liang, Xiangfeng.,...&Liu, Huizhou.(2022).How multiple noncovalent interactions regulate the aggregation behavior of amphiphilic triblock copolymer/surface-active ionic liquid mixtures.JOURNAL OF MOLECULAR LIQUIDS,363,12. |
| MLA | Luo, Haiyan,et al."How multiple noncovalent interactions regulate the aggregation behavior of amphiphilic triblock copolymer/surface-active ionic liquid mixtures".JOURNAL OF MOLECULAR LIQUIDS 363(2022):12. |
入库方式： OAI收割
来源：过程工程研究所
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