Comparison of electrophoretic methods for determination of critical micelle concentration of anionic alkylsulfate surfactants in water/organic environment
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F19%3A39912862" target="_blank" >RIV/00216275:25310/19:39912862 - isvavai.cz</a>
Výsledek na webu
<a href="https://link.springer.com/article/10.1007/s10337-018-3664-4" target="_blank" >https://link.springer.com/article/10.1007/s10337-018-3664-4</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s10337-018-3664-4" target="_blank" >10.1007/s10337-018-3664-4</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Comparison of electrophoretic methods for determination of critical micelle concentration of anionic alkylsulfate surfactants in water/organic environment
Popis výsledku v původním jazyce
The methods for determination of critical micelle concentration of anionic surfactants using capillary electrophoresis instrumentation were compared in this work. We have focused on the determination of critical micelle concentration of homological series of n-alkyl sulfates using four different methods: the electrical current-based method, and method using migration times, retention factors and effective mobilities of n-alkylbenzenes as probe molecules. We have studied the effects of operation conditions (capillary dimensions, applied voltage) and composition of probe samples on the values of critical micelle concentration. The values of critical micelle concentration determined in water and in 25 mmol L−1 borate buffer pH 8.5 without and with addition of 20% (v/v) of acetonitrile ranged from 60 mmol L−1 for sodium nonyl sulfate to 6.1 mmol L−1 for sodium tridecyl sulfate, with higher values for electrolyte containing acetonitrile. The concentration and solvent of probe molecules have significant effect on the determined value of critical micelle concentration. We have studied in detail critical micelle concentration of sodium dodecyl sulfate in mixtures with low concentration of acetonitrile up to the 6% (v/v). In this region, higher uncertainty of determination of critical micelle concentration was experienced.
Název v anglickém jazyce
Comparison of electrophoretic methods for determination of critical micelle concentration of anionic alkylsulfate surfactants in water/organic environment
Popis výsledku anglicky
The methods for determination of critical micelle concentration of anionic surfactants using capillary electrophoresis instrumentation were compared in this work. We have focused on the determination of critical micelle concentration of homological series of n-alkyl sulfates using four different methods: the electrical current-based method, and method using migration times, retention factors and effective mobilities of n-alkylbenzenes as probe molecules. We have studied the effects of operation conditions (capillary dimensions, applied voltage) and composition of probe samples on the values of critical micelle concentration. The values of critical micelle concentration determined in water and in 25 mmol L−1 borate buffer pH 8.5 without and with addition of 20% (v/v) of acetonitrile ranged from 60 mmol L−1 for sodium nonyl sulfate to 6.1 mmol L−1 for sodium tridecyl sulfate, with higher values for electrolyte containing acetonitrile. The concentration and solvent of probe molecules have significant effect on the determined value of critical micelle concentration. We have studied in detail critical micelle concentration of sodium dodecyl sulfate in mixtures with low concentration of acetonitrile up to the 6% (v/v). In this region, higher uncertainty of determination of critical micelle concentration was experienced.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10406 - Analytical chemistry
Návaznosti výsledku
Projekt
<a href="/cs/project/GA18-14893S" target="_blank" >GA18-14893S: Fokusující efekty ve vícerozměrných separacích v kapalné fázi</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Chromatographia
ISSN
0009-5893
e-ISSN
—
Svazek periodika
82
Číslo periodika v rámci svazku
1
Stát vydavatele periodika
DE - Spolková republika Německo
Počet stran výsledku
7
Strana od-do
733-739
Kód UT WoS článku
000464854300003
EID výsledku v databázi Scopus
—