Mixtures of n-dodecyl-β-D-maltoside and hexaoxyethylene dodecyl ether - Surface properties, bulk properties, foam films, and foams

被引:55
|
作者
Stubenrauch, C. [1 ,2 ]
Claesson, P. M. [3 ,4 ]
Rutland, M. [3 ,4 ]
Manev, E. [5 ]
Johansson, I. [6 ]
Pedersen, J. S. [7 ]
Langevin, D. [8 ]
Blunk, D. [9 ]
Bain, C. D. [10 ]
机构
[1] Univ Coll Dublin, Sch Chem & Bioproc Engn, Dublin 4, Ireland
[2] Univ Stuttgart, Inst Phys Chem, D-70569 Stuttgart, Germany
[3] Royal Inst Technol, Dept Chem Surface & Corros Sci, SE-10044 Stockholm, Sweden
[4] Inst Surface Chem, SE-11486 Stockholm, Sweden
[5] Univ Sofia St Kliment Ohridski, Dept Phys Chem, Sofia 1126, Bulgaria
[6] Akzo Nobel Surface Chem AB, S-44485 Stenungsund, Sweden
[7] Univ Aarhus, Dept Chem, DK-8000 Aarhus, Denmark
[8] Univ Paris 11, Phys Solides Lab, F-91405 Orsay, France
[9] Univ Cologne, Inst Organ Chem, D-50939 Cologne, Germany
[10] Univ Durham, Dept Chem, Durham DH1 3LE, England
关键词
Surfactant mixtures; Non-ionic surfactants; Surface properties; Phase diagrams; Foams; Foam films; NONIONIC SURFACTANTS; AQUEOUS-SOLUTIONS; OVERFLOWING CYLINDER; POLY(ETHYLENE OXIDE); CRITICAL THICKNESS; SUGAR SURFACTANTS; PHASE-BEHAVIOR; ADSORPTION; WATER; MICELLES;
D O I
10.1016/j.cis.2009.12.002
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
Mixtures of the two non-ionic surfactants hexaoxyethylene dodecyl ether (C12E6) and n-dodecyl-beta-D-maltoside (beta-C(12)G(2)) were studied with regard to surface properties, bulk properties, foam films, and foams. The reason for studying a mixture of an ethylene oxide (CiEj) and a sugar (C(n)G(m),) based surfactant is that despite being non-ionic, these two surfactants behave quite differently. Firstly, the physico-chemical properties of aqueous solutions of C(n)G(m) surfactants are less temperature-sensitive than those of CiEj solutions. Secondly, the surface charge density q(0) of foam films stabilized by C(n)G(m) surfactants is pH insensitive down to the so-called isoelectric point, while that of foam films stabilized by CiEj surfactants changes linearly with the pH. The third difference is related to interaction forces between solid surfaces. Under equilibrium conditions very high forces are needed to expel beta-C(12)G(2) from between thiolated gold surfaces, while for C12E6 low loads are sufficient. Fourthly, the adsorption of C12E6 and beta-C(12)G(2) on hydrophilic silica and titania, respectively, is inverted. While the surface excess of C12E6 is large on silica and negligible on titania, beta-C(12)G(2) adsorbs very little on silica but has a large surface excess on titania. What is the reason for this different behaviour? Under similar conditions and for comparable head group sizes, it was found that the hydration of CiEj surfactants is one order of magnitude higher but on average much weaker than that of C(n)G(m) surfactants. Moreover, C(n)G(m) surfactants possess a rigid maltoside unit, while CiEj surfactants have a very flexible hydrophilic part. Indeed, most of the different properties mentioned above can be explained by the different hydration and the head group flexibilities. The intriguing question of how mixtures of CiEj and C(n)G(m) surfactants would behave arises organically. Thus various properties of C12E6 + beta-C(12)G(2) mixtures in aqueous solution have been studied with a focus on the 1:1 mixture. The results are compared with those of the single surfactants and are discussed accordingly. (C) 2009 Elsevier B.V. All rights reserved.
引用
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页码:5 / 18
页数:14
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