Self-Assembly of Block Copolymers in Ionic Liquids

被引:0
|
作者
Xie, Ru [1 ]
Lopez-Barron, Carlos R. [2 ]
Wagner, Norman J. [1 ]
机构
[1] Univ Delaware, Dept Chem & Biomol Engn, Ctr Neutron Sci, 150 Acad St, Newark, DE 19716 USA
[2] ExxonMobil Chem Co, Adv Characterizat Dept, 5200 Bayway Dr, Baytown, TX 77520 USA
基金
美国国家科学基金会;
关键词
SOLUTION TEMPERATURE BEHAVIOR; GEL GATE DIELECTRICS; PEO-PPO-PEO; ETHYLAMMONIUM NITRATE; TRIBLOCK COPOLYMER; PHASE-BEHAVIOR; POLYMER ELECTROLYTES; MICELLE FORMATION; POLY(ETHYLENE OXIDE); DIBLOCK COPOLYMER;
D O I
暂无
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Self-assembly of amphiphilic block copolymers can impart desired discrete or continuous nanostructures, such as micelles utilized as drug delivery vehicles in aqueous solvents, or cross-linked micelles for stretchable electronics fabrications in ionic liquids. These appealing applications have motivated significant research efforts to understand the nano- and microstructure as well as the structure-property relationships underlying such self-assembled systems, with the ultimate goal being effective formulation. To take full advantage of the bottom-up self-assembly approach, a comprehensive understanding of the factors that govern the self-assembly behavior of dilute, concentrated and functionalized system of non-ionic block copolymers self-assembly in ionic liquids, as well as robust characterization methods for quantifying the microstructure and properties relationship must be reviewed. For each system, the most significant challenges are presented and discussed. In addition, current and potential applications of block copolymers/ionic liquid system are also discussed. This provides a measure of the current state of understanding, which motivates a brief look forward towards future directions in this field.
引用
收藏
页码:83 / 142
页数:60
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