Literature DB >> 24555861

Self-aggregation of new alkylcarboxylate-based anionic surface active ionic liquids: experimental and theoretical investigations.

Ni Cheng1, Pengming Yu, Tao Wang, Xiang Sheng, Yanhui Bi, Yanjun Gong, Li Yu.   

Abstract

Halogen-free and low-cost alkylcarboxylate-based anionic surface active ionic liquids (SAILs), namely, 1-butyl-3-methylimidazolium alkylcarboxylates ([C4mim][C(n)H(2n-1)O2], n = 8, 10, 12), were first synthesized through the neutralization of imidazolium hydroxide by alkylcarboxylic acids. A systematic study of their self-aggregation behavior in water was investigated by surface tension, electrical conductivity, steady-state fluorescence quenching, and (1)H NMR. The micellar properties of this series of SAILs in ethylammonium nitrate (EAN) were also studied by surface tensiometry for comparison. A set of surface active parameters and thermodynamic parameters of these compounds in water and EAN was obtained. Surface tension results show that the surface activity of [C4mim][C(n)H(2n-1)O2] in EAN is inferior to that in water. They exhibit a higher ability to aggregate in water than the traditional anionic surfactants, sodium alkylcarboxylates (SAC), and anionic SAILs, 1-butyl-3-methylimidazolium alkylsulfates ([C4mim][C(n)H(2n+1)SO4]) with the same hydrocarbon chain length. This demonstrates that the incorporation of carboxylate group and [C4mim](+) cation favors micelle formation. To understand the discrepancy in the surface activity of alkylsulfate- and alkylcarboxylate-based SAILs, theoretical calculations were performed to give electrostatic potential of the corresponding anions. The higher surface activity of [C4mim][C12H23O2] mainly originates from the lower electronegativity of its anion. Density functional theory (DFT) calculations manifest that the interaction energy of binary combination SAILs-EAN is larger than that of SAILs-H2O, implying the stronger interaction of the former. Consequently, it is more difficult for [C4mim][C(n)H(2n-1)O2] to self-aggregate in EAN than in H2O. This work is expected to be of practical value for the environmentally friendly alkylcarboxylate-based SAILs in some potential applications, including nanomaterials synthesis and phase separation, among others.

Entities:  

Year:  2014        PMID: 24555861     DOI: 10.1021/jp4124056

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  2 in total

1.  Synthesis, Self-Aggregation, Surface Characteristics, Electrochemical Property, Micelle Size, and Antimicrobial Activity of a Halogen-Free Picoline-Based Surface-Active Ionic Liquid.

Authors:  Nidhi N Patel; Saurabh S Soni; Niraj Patel; Kiran Patel; Vaibhav K Patel; Deep Sharma; Sanjay H Panjabi
Journal:  ACS Omega       Date:  2022-08-15

2.  The Formation of pH-Sensitive Wormlike Micelles in Ionic Liquids Driven by the Binding Ability of Anthranilic Acid.

Authors:  Qing You; Yan Zhang; Huan Wang; Hongfu Fan; Jianping Guo; Ming Li
Journal:  Int J Mol Sci       Date:  2015-11-26       Impact factor: 5.923

  2 in total

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