Amphiphilic second-order phase transitions determined through NMR

被引:1
作者
Reilly, Teresa [1 ]
Mohamed, Mohamed I. H. [2 ]
Lehmann, Teresa E. [3 ]
Alvarado, Vladimir [1 ]
机构
[1] Univ Wyoming, Dept Chem Engn, Laramie, WY 82071 USA
[2] Univ Wyoming, Dept Petr Engn, Laramie, WY 82071 USA
[3] Univ Wyoming, Dept Chem, Laramie, WY 82071 USA
关键词
Surfactant; Phase transitions; Nuclear magnetic resonance; Dynamic light scattering; NUCLEAR-MAGNETIC-RESONANCE; FLUORESCENCE ANISOTROPY; SURFACTANT; WATER; VESICLES; BEHAVIOR; NANOAGGREGATION; SPECTROSCOPY; MICROSCOPY; INTERFACE;
D O I
10.1016/j.molliq.2018.07.066
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
In this work, nuclear magnetic resonance (NMR) spectroscopy is used to investigate surfactant phase behavior over a broad concentration region. This technique is an adaptation of a previously developed method applied to detect the critical micelle concentration (CMC) of surfactants. In this method, a surfactant concentration is correlated to the normalized intensity, or area, of the NMR signal for each surfactant. In this procedure a linear relationship develops on either side of the CMC, with a distinct change in slope where the primary phase change occurs. The research conducted herein investigates the NMR response at higher surfactant concentration, where the phase change consists of a change in micelle shape or other structural configurations. These secondary phase transitions can be expected from 10 to 90 wt.%, where the CMC measurements are conducted at concentrations <1 wt.%. The solutions were also analyzed with dynamic light scattering (DLS) and a cross-polarizer microscope to confirm suspected detected phase changes. Visible changes in the rheological response were observed and therefore carefully examined. In a large part, the results seen with all methods corresponded with visible differences in the surfactant solutions and detected changes in the NMR protocol. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:647 / 657
页数:11
相关论文
共 39 条
[1]  
AHMED MK, 1992, CHEM PHYS LIPIDS, V63, P139, DOI 10.1016/0009-3084(92)90030-S
[2]   THE USE OF DIFFERENTIAL SCANNING CALORIMETRY AS A TOOL TO CHARACTERIZE LIPOSOME PREPARATIONS [J].
BILTONEN, RL ;
LICHTENBERG, D .
CHEMISTRY AND PHYSICS OF LIPIDS, 1993, 64 (1-3) :129-142
[3]   Self-assembly and phase behaviour of PEI : cationic surfactant aqueous mixtures forming mesostructured films at the air/solution interface [J].
Comas-Rojas, Hansel ;
Enriquez-Victorero, Carlos ;
Roser, Stephen J. ;
Edler, Karen J. ;
Perez-Gramatges, Aurora .
SOFT MATTER, 2013, 9 (15) :4003-4014
[4]  
Davis H.T., 1987, PHYS AMPHIPHILIC LAY, P310
[5]  
Dierking I., 2003, TEXTURES LIQUID CRYS
[6]   Investigations into the phase behavior of nonionic ethoxylated surfactants using H-2 NMR spectroscopy [J].
Dimitrova, GT ;
Tadros, TF ;
Luckham, PF ;
Kipps, MR .
LANGMUIR, 1996, 12 (02) :315-318
[7]  
Ferguson J., 1991, APPL FLUID RHEOLOGY
[8]   CUBIC PHASES IN SURFACTANT AND SURFACTANT-LIKE LIPID SYSTEMS [J].
FONTELL, K .
COLLOID AND POLYMER SCIENCE, 1990, 268 (03) :264-285
[9]  
Franck A.J., 2004, Book ofTA instruments, P1
[10]   Physicochemical Constraints on Surfactant Blends under Harsh Conditions and Evaluation of a Proposed Solution [J].
Garcia-Olvera, Griselda ;
Reilly, Teresa M. ;
Lehmann, Teresa E. ;
Alvarado, Vladimir .
ENERGY & FUELS, 2017, 31 (01) :95-106