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Rheology of α-Gel Formed by Amino Acid-Based Surfactant with Long-Chain Alcohol: Effects of Inorganic Salt Concentration
[Image: see text] Mixtures of surfactants, long-chain alcohols, and water sometimes yield lamellar gels with hexagonally packed alkyl chains. This assembly is called “α-gel” or “α-form hydrated crystal.” In this study, we characterized the rheological properties of α-gel prepared using disodium N-do...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280742/ https://www.ncbi.nlm.nih.gov/pubmed/34082534 http://dx.doi.org/10.1021/acs.langmuir.1c00626 |
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author | Ichihara, Kumika Sugahara, Tadashi Akamatsu, Masaaki Sakai, Kenichi Sakai, Hideki |
author_facet | Ichihara, Kumika Sugahara, Tadashi Akamatsu, Masaaki Sakai, Kenichi Sakai, Hideki |
author_sort | Ichihara, Kumika |
collection | PubMed |
description | [Image: see text] Mixtures of surfactants, long-chain alcohols, and water sometimes yield lamellar gels with hexagonally packed alkyl chains. This assembly is called “α-gel” or “α-form hydrated crystal.” In this study, we characterized the rheological properties of α-gel prepared using disodium N-dodecanoylglutamate (C12Glu-2Na), 1-hexadecanol (C16OH), and water at different NaCl concentrations. The α-gel structure was assessed using small- and wide-angle X-ray scattering (SWAXS). The SWAXS measurements revealed that an increased NaCl concentration (0–200 mmol dm(–3)) resulted in a decreased d-spacing caused by the screening of electrostatic repulsion between lamellar bilayers. This led to an increased amount of excess water (i.e., the water present between the α-gel domains), and hence, the viscosity of the α-gel decreased in the range of the NaCl concentration. A further increase in the NaCl concentration (200–1000 mmol dm(–3)) resulted in decreased electrostatic repulsion between the α-gel domains and/or an increased number of α-gel domains (multilamellar vesicles). These effects increased the domain-to-domain interactions, leading to increased viscosity. Therefore, we concluded that the viscosity of the α-gel was controlled by the amount of excess water and the domain-to-domain interactions. Once the network structure collapsed under the strain, it was difficult to recover the original network structure. The low recoverability resulted from increased cohesion between the domains at high NaCl concentrations. |
format | Online Article Text |
id | pubmed-8280742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82807422021-07-16 Rheology of α-Gel Formed by Amino Acid-Based Surfactant with Long-Chain Alcohol: Effects of Inorganic Salt Concentration Ichihara, Kumika Sugahara, Tadashi Akamatsu, Masaaki Sakai, Kenichi Sakai, Hideki Langmuir [Image: see text] Mixtures of surfactants, long-chain alcohols, and water sometimes yield lamellar gels with hexagonally packed alkyl chains. This assembly is called “α-gel” or “α-form hydrated crystal.” In this study, we characterized the rheological properties of α-gel prepared using disodium N-dodecanoylglutamate (C12Glu-2Na), 1-hexadecanol (C16OH), and water at different NaCl concentrations. The α-gel structure was assessed using small- and wide-angle X-ray scattering (SWAXS). The SWAXS measurements revealed that an increased NaCl concentration (0–200 mmol dm(–3)) resulted in a decreased d-spacing caused by the screening of electrostatic repulsion between lamellar bilayers. This led to an increased amount of excess water (i.e., the water present between the α-gel domains), and hence, the viscosity of the α-gel decreased in the range of the NaCl concentration. A further increase in the NaCl concentration (200–1000 mmol dm(–3)) resulted in decreased electrostatic repulsion between the α-gel domains and/or an increased number of α-gel domains (multilamellar vesicles). These effects increased the domain-to-domain interactions, leading to increased viscosity. Therefore, we concluded that the viscosity of the α-gel was controlled by the amount of excess water and the domain-to-domain interactions. Once the network structure collapsed under the strain, it was difficult to recover the original network structure. The low recoverability resulted from increased cohesion between the domains at high NaCl concentrations. American Chemical Society 2021-06-03 2021-06-15 /pmc/articles/PMC8280742/ /pubmed/34082534 http://dx.doi.org/10.1021/acs.langmuir.1c00626 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Ichihara, Kumika Sugahara, Tadashi Akamatsu, Masaaki Sakai, Kenichi Sakai, Hideki Rheology of α-Gel Formed by Amino Acid-Based Surfactant with Long-Chain Alcohol: Effects of Inorganic Salt Concentration |
title | Rheology of α-Gel Formed by Amino Acid-Based
Surfactant with Long-Chain Alcohol: Effects of Inorganic Salt Concentration |
title_full | Rheology of α-Gel Formed by Amino Acid-Based
Surfactant with Long-Chain Alcohol: Effects of Inorganic Salt Concentration |
title_fullStr | Rheology of α-Gel Formed by Amino Acid-Based
Surfactant with Long-Chain Alcohol: Effects of Inorganic Salt Concentration |
title_full_unstemmed | Rheology of α-Gel Formed by Amino Acid-Based
Surfactant with Long-Chain Alcohol: Effects of Inorganic Salt Concentration |
title_short | Rheology of α-Gel Formed by Amino Acid-Based
Surfactant with Long-Chain Alcohol: Effects of Inorganic Salt Concentration |
title_sort | rheology of α-gel formed by amino acid-based
surfactant with long-chain alcohol: effects of inorganic salt concentration |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280742/ https://www.ncbi.nlm.nih.gov/pubmed/34082534 http://dx.doi.org/10.1021/acs.langmuir.1c00626 |
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