Tcacenco Celize M, Zana Raoul, Bales Barney L
Department of Physics and Astronomy, California State University at Northridge, Northridge, California 91330-8268, USA.
J Phys Chem B. 2005 Aug 25;109(33):15997-6004. doi: 10.1021/jp052544z.
Micelles formed in water from ammonium dodecyl sulfate (AmDS) are characterized using time-resolved fluorescence quenching (TRFQ), electron paramagnetic resonance (EPR), conductivity, Krafft temperature, and density measurements. TRFQ was used to measure the aggregation number, N, and the quenching rate constant of pyrene by dodecylpyridinium chloride, k(Q). N depends only on the concentration (C(aq)) of ammonium ions in the aqueous phase whether these counterions are derived from the surfactant alone or from the surfactant plus added ammonium chloride as follows: N = N0(C(aq)/cmc0)(gamma), where N0 is the aggregation number at the critical micelle concentration in the absence of added salt, cmc0, and is equal to 77, 70, and 61 at 16, 25, and 35 degrees C, respectively. The exponent gamma = 0.22 is independent of temperature in the range 16 to 35 degrees C. The fact that N depends only on C(aq) permits the determination of the micelle ionization degree (alpha) by employing various experimental approaches to exploit a recent suggestion (J. Phys. Chem. B 2001, 105, 6798) that N depends only on C(aq). Utilizing various combinations of salt and surfactant, values of alpha were obtained by finding common curves as a function of C(aq) of the following experimental results: the Krafft temperature, N, k(Q), the microviscosity of the Stern layer determined from the rotational correlation time of a spin probe, 5-doxyl stearic acid methyl ester, and the spin-probe sensed hydration of the micelle surface. The values of alpha, determined from applying the aggregation number-based definition of alpha to all of these quantities, were within experimental uncertainty of the values alpha = 0.19, 0.20, and 0.21 derived from conductivity measurements at 16, 25, and 35 degrees C, respectively. The volume fraction of the Stern layer occupied by water decreases as N increases. For AmDS micelles, both the hydration and its decrease are predicted by a simple theory of micelle hydration by fixing the parameters of the theory for sodium dodecyl sulfate and employing no further adjustable parameters. For a given value of N, the hydration decreases as the temperature increases.
使用时间分辨荧光猝灭(TRFQ)、电子顺磁共振(EPR)、电导率、克拉夫特温度和密度测量等方法对由十二烷基硫酸铵(AmDS)在水中形成的胶束进行了表征。TRFQ用于测量芘的聚集数N以及十二烷基吡啶氯化物对芘的猝灭速率常数k(Q)。N仅取决于水相中铵离子的浓度(C(aq)),无论这些抗衡离子是仅来自表面活性剂还是来自表面活性剂加添加的氯化铵,具体如下:N = N0(C(aq)/cmc0)(γ),其中N0是在没有添加盐的临界胶束浓度下的聚集数cmc0,在16、25和35℃时分别等于77、70和61。指数γ = 0.22在16至35℃范围内与温度无关。N仅取决于C(aq)这一事实使得可以通过采用各种实验方法来利用最近的一个建议(《物理化学杂志B》2001年,105卷,6798页)来确定胶束电离度(α),该建议认为N仅取决于C(aq)。利用盐和表面活性剂的各种组合,通过找到作为以下实验结果的C(aq)函数的公共曲线来获得α值:克拉夫特温度、N、k(Q)、由自旋探针5 - 二氧硬脂酸甲酯的旋转相关时间确定的斯特恩层微粘度以及自旋探针感知的胶束表面水合作用。将基于聚集数的α定义应用于所有这些量所确定的α值,在分别由16、25和35℃下的电导率测量得出的α = 0.19、0.20和0.21值的实验不确定度范围内。随着N的增加,斯特恩层被水占据的体积分数降低。对于AmDS胶束,通过固定十二烷基硫酸钠理论的参数且不使用进一步的可调参数,一种简单的胶束水合理论预测了水合作用及其降低情况。对于给定的N值,水合作用随温度升高而降低。