Gräbner D., Matsuo T., Hoinkis E., Thunig C., Hoffmann H.
Lehrstuhl für Physikalische Chemie I, Universität Bayreuth, Bayreuth, D-95440, Germany
J Colloid Interface Sci. 2001 Apr 1;236(1):1-13. doi: 10.1006/jcis.2000.7388.
A new anionic surfactant (M-LAMS) that is capable of forming intermolecular hydrogen bonds was investigated. Inverse solubilities of Na and Ca salts were found. Critical micelle concentration and aggregation behavior were determined by surface tension, light scattering, electric birefringence, and SANS measurements. It is found that the Na salt forms globular micelles while the Ca salt forms rodlike micelles. The phase behavior of the micellar solutions with increasing cosurfactant concentration was also studied. It is observed that 100 mM Na-LAMS solutions in the presence of 100 mM CaCl(2) undergo several phase transformations with increasing n-hexanol concentration. We found not only the expected micellar L(1) phase and a lamellar phase at concentrations quite low for this kind of system, but also a novel phase: At a cosurfactant/surfactant ratio x(C) of 1.2 a white precipitate is formed at the bottom of the sample. With increasing ratio x(C) the precipitate dissolves into a liquid crystalline L(alpha) phase that at x(C)=3.2 is transformed into an L(3) or sponge phase. Investigation by FF-TEM, light microscopy, and SANS shows that the precipitate consists of agglomerated polydisperse multilamellar vesicles. The vesicles consist of densely packed bilayers that contain little water. The bilayer thickness is about 20 Å and independent of its composition whereas the interlamellar distance is strikingly linked to concentrations of cosurfactant (surfactant/cosurfactant ratio) and electrolyte. With increasing cosurfactant content, the bilayers become less rigid and resulting thermal undulations force the membranes apart and weaken their interactions until a common L(alpha) phase is formed. This transition is an example of a bonding-nonbonding transition of membranes. Copyright 2001 Academic Press.
研究了一种能够形成分子间氢键的新型阴离子表面活性剂(M-LAMS)。发现了钠和钙盐的反常溶解度。通过表面张力、光散射、电双折射和小角中子散射测量确定了临界胶束浓度和聚集行为。发现钠盐形成球状胶束,而钙盐形成棒状胶束。还研究了胶束溶液随助表面活性剂浓度增加的相行为。观察到,在100 mM氯化钙存在下,100 mM Na-LAMS溶液随着正己醇浓度的增加会发生几次相变。我们不仅发现了这种体系在相当低浓度下预期的胶束L(1)相和层状相,还发现了一种新型相:在助表面活性剂/表面活性剂比率x(C)为1.2时,样品底部形成白色沉淀。随着比率x(C)的增加,沉淀溶解成液晶L(α)相,在x(C)=3.2时转变为L(3)或海绵相。通过快速冷冻透射电子显微镜、光学显微镜和小角中子散射研究表明,沉淀由聚集的多分散多层囊泡组成。囊泡由紧密堆积的双层组成,几乎不含水。双层厚度约为20 Å,与其组成无关,而层间距离与助表面活性剂浓度(表面活性剂/助表面活性剂比率)和电解质显著相关。随着助表面活性剂含量的增加,双层变得不那么刚性,产生的热起伏迫使膜分开并削弱它们的相互作用,直到形成共同的L(α)相。这种转变是膜的键合-非键合转变的一个例子。版权所有2001年学术出版社。