Sensitivity of cationic surfactant templates to specific anions in liquid interface crystallization

被引:2
|
作者
Sanstead, Paul J. [1 ]
Florio, Nick [1 ]
Giusto, Kiersten [1 ]
Morris, Catherine [1 ]
Lee, Sunghee [1 ]
机构
[1] Iona Coll, Dept Chem, New Rochelle, NY 10801 USA
基金
美国国家科学基金会;
关键词
Potassium sulfate; Templated crystallization; Specific anion effect; Microdroplet crystallization; Liquid interface; Surfactant; DIOCTADECYLDIMETHYLAMMONIUM BROMIDE; POTASSIUM-SULFATE; AQUEOUS MIXTURES; PHASE-BEHAVIOR; COUNTERION; MONOLAYERS; NUCLEATION; ADSORPTION; SHAPE; IONS;
D O I
10.1016/j.jcis.2012.02.067
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
We investigated the specific effects of potassium salts of various anions upon the interfacially templated crystal nucleation of K2SO4. Previously, we have shown that the presence of several salts at low concentrations could induce changes in important crystallization characteristics templated by 1-octadecylamine at the liquid-liquid interface, and that these changes depended greatly on the specific identity of the salt. In this work we extend our surfactant monolayers to include dimethyldioctadecylammonium bromide (DODAB) and hexadecyltrimethylammonium bromide (CTAB). Addition of 10 mM of various potassium salts results in a diminution in efficiency of the templating capability of CTAB monolayer, as evidenced by higher C-onset values and polycrystalline habit. The ability of the anions to perturb these values varied in a manner consistent with a Hofmeister series. However, DODAB maintained its templating effectiveness regardless of the nature of the salt or concentration. DODAB and CTAB are likely to be undergoing different reordering effects in the monolayer upon binding with chaotropic anions: a combined reduction in surface charge with different monolayer ordering results in a differing template ability. These studies have provided significant insights into the understanding of the interaction of ordered surfactant arrays with salts, and provide exciting possibilities for crystal engineering and materials design. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:152 / 159
页数:8
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