用流动电位法测定离子和非离子表面活性剂的临界胶束浓度。

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
ELECTROPHORESIS Pub Date : 2025-04-23 DOI:10.1002/elps.8145
Yuri Chenyakin, David Da Yong Chen
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引用次数: 0

摘要

采用毛细管电泳系统测定了阴离子、阳离子、两性和非离子表面活性剂的临界胶束浓度(CMC)。通过测定流动电位随表面活性剂浓度变化趋势的突变,测定阴离子表面活性剂十二烷基硫酸钠(SDS)、阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)、两性表面活性剂3-(3-胆酰胺丙基)二甲氨基)-1-丙磺酸(CHAPS)和非离子表面活性剂聚乙二醇对(1,1,3,3-四甲基丁基)-苯基醚(Triton X-100)在水或盐溶液中的CMC值。CMC值分别为8.23、0.93、5.80和0.16 mM。该方法还证明了SDS和CTAB的cmc随温度变化的不同。SDS的CMC从10°C到25°C下降,然后从25°C到40°C上升,而CTAB仅在10°C-40°C范围内线性上升。表面活性剂溶液中的毛细管壁zeta电位可以通过测量的流动电位、电导率和溶液粘度来计算。表面电荷密度用得到的zeta电位计算。在zeta电位为2 ~ 20 mM的SDS溶液中,SDS的表面电荷密度为5.6 ~ 0.8 C/m2。计算得到的zeta电位和表面电荷密度在8 mM左右达到平稳,这与本研究测定的SDS的CMC和文献值一致。通过流电位测量获得的CMC值与其他CMC测定技术(如表面张力和电导率测量)获得的值相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of Critical Micelle Concentration of Ionic and Non-Ionic Surfactants by Streaming Potential Measurements.

A capillary electrophoresis system capable of measuring streaming potentials was used for the determination of critical micelle concentration (CMC) of anionic, cationic, zwitterionic and non-ionic surfactants. The CMC values of anionic surfactant sodium dodecyl sulphate (SDS), cationic surfactant cetyltrimethylammonium bromide (CTAB), zwitterionic surfactant 3-((3-cholamidopropyl) dimethylammonio)-1-propanesulfonate (CHAPS) and non-ionic surfactant polyethylene glycol p-(1,1,3,3-tetramethylbutyl)-phenyl ether (Triton X-100) in water or salt solutions were determined by determining the abrupt change in the trend of streaming potential change with the surfactant concentration. The CMC values were 8.23, 0.93, 5.80 and 0.16 mM, respectively. This method was also used to demonstrate how the CMCs of SDS and CTAB change differently with temperature. The CMC of SDS decreased from 10°C to 25°C and then increased from 25°C to 40°C, whereas CTAB only increased linearly within 10°C-40°C. The capillary wall zeta potentials in surfactant solutions can be calculated from the measured streaming potential, conductivity and solution viscosity. Surface charge densities were calculated using the zeta potentials obtained. The surface charge densities of SDS were calculated to be 5.6-0.8 C/m2 when SDS solutions with concentrations of 2-20 mM zeta potentials were used. The calculated zeta potentials and surface charge densities reached a plateau at about 8 mM, which coincided with the CMC of SDS determined in the present study and the literature values. The CMC values obtained from streaming potential measurement are comparable to values obtained with other CMC determination techniques such as surface tension and conductometric measurements.

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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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