Structure of the mixed cationic-non-ionic surfactant monolayer of hexadecyltrimethylammonium bromide and monododecyl hexaethylene glycol at the air/water interface

被引:23
作者
Penfold, J
Staples, E
Cummins, P
Tucker, I
Thomas, RK
Simister, EA
Lu, JR
机构
[1] UNILEVER RES,PORT SUNLIGHT LAB,WIRRAL,MERSEYSIDE,ENGLAND
[2] UNIV OXFORD,PHYS CHEM LAB,OXFORD OX1 3QZ,ENGLAND
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1996年 / 92卷 / 09期
关键词
D O I
10.1039/ft9969201549
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
Specular neutron reflection, together with isotopic substitution has been used to determine the structure of the mixed surfactant monolayer of hexadecyltrimethylammonium bromide (C-16,,TAB) and monododecyl hexaethylene glycol (C(12)E(6)) adsorbed at the air/water interface. The measurements have been made at a range of surfactant compositions and concentrations [both below and above the critical micellar concentration, (c.m.c.)] and at different temperatures, all in the presence of 0.1 mol l(-1) sodium bromide. The structure of the cationic surfactant in the mixed layer is similar to that of a pure C(16)TAB layer at an equivalent area per molecule. Whereas, although the alkyl chain extension of C(12)E(6) is similar in both pure and mixed monolayers, the molecule is more immersed in the solvent in the mixed monolayer. The midpoint of the alkyl chain distribution for the non-ionic surfactant is further from the solvent interface than that of the cationic surfactant. However, the midpoints of the distributions for the entire molecules coincide. Over the concentration range studied the structure is independent of composition and depends only on the amount adsorbed. Some differences in the structure with increasing temperature, associated with temperature driven dehydration of the surfactants, are observed.
引用
收藏
页码:1549 / 1554
页数:6
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