Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive Effects

Detalhes bibliográficos
Autor(a) principal: Gonçalves, Rui A.
Data de Publicação: 2021
Outros Autores: Lam, Yeng-Ming, Lindman, Björn
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/95676
https://doi.org/10.3390/molecules26133946
Resumo: Double-chain amphiphilic compounds, including surfactants and lipids, have broad significance in applications like personal care and biology. A study on the phase structures and their transitions focusing on dioctadecyldimethylammonium chloride (DODAC), used inter alia in hair conditioners, is presented. The phase behaviour is dominated by two bilayer lamellar phases, Lβ and Lα, with "solid" and "melted" alkyl chains, respectively. In particular, the study is focused on the effect of additives of different polarity on the phase transitions and structures. The main techniques used for investigation were differential scanning calorimetry (DSC) and small- and wide-angle X-ray scattering (SAXS and WAXS). From the WAXS reflections, the distance between the alkyl chains in the bilayers was obtained, and from SAXS, the thicknesses of the surfactant and water layers. The Lα phase was found to have a bilayer structure, generally found for most surfactants; a Lβ phase made up of bilayers with considerable chain tilting and interdigitation was also identified. Depending mainly on the polarity of the additives, their effects on the phase stabilities and structure vary. Compounds like urea have no significant effect, while fatty acids and fatty alcohols have significant effects, but which are quite different depending on the nonpolar part. In most cases, Lβ and Lα phases exist over wide composition ranges; certain additives induce transitions to other phases, which include cubic, reversed hexagonal liquid crystals and bicontinuous liquid phases. For a system containing additives, which induce a significant lowering of the Lβ-Lα transition, we identified the possibility of a triggered phase transition via dilution with water.
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spelling Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive EffectsAdditive effectsDouble-chain surfactantHair conditionerLamellar gelLamellar liquid crystaSurfactant packingDouble-chain amphiphilic compounds, including surfactants and lipids, have broad significance in applications like personal care and biology. A study on the phase structures and their transitions focusing on dioctadecyldimethylammonium chloride (DODAC), used inter alia in hair conditioners, is presented. The phase behaviour is dominated by two bilayer lamellar phases, Lβ and Lα, with "solid" and "melted" alkyl chains, respectively. In particular, the study is focused on the effect of additives of different polarity on the phase transitions and structures. The main techniques used for investigation were differential scanning calorimetry (DSC) and small- and wide-angle X-ray scattering (SAXS and WAXS). From the WAXS reflections, the distance between the alkyl chains in the bilayers was obtained, and from SAXS, the thicknesses of the surfactant and water layers. The Lα phase was found to have a bilayer structure, generally found for most surfactants; a Lβ phase made up of bilayers with considerable chain tilting and interdigitation was also identified. Depending mainly on the polarity of the additives, their effects on the phase stabilities and structure vary. Compounds like urea have no significant effect, while fatty acids and fatty alcohols have significant effects, but which are quite different depending on the nonpolar part. In most cases, Lβ and Lα phases exist over wide composition ranges; certain additives induce transitions to other phases, which include cubic, reversed hexagonal liquid crystals and bicontinuous liquid phases. For a system containing additives, which induce a significant lowering of the Lβ-Lα transition, we identified the possibility of a triggered phase transition via dilution with water.This research was funded by Procter & Gamble and Agency for Science, Technology and Research (A*STAR), Singapore (APG2013/016), Singapore Ministry of Education Academic Research Fund Tier 1 (2019-T1-002-35) and FCT.MDPI2021-06-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/95676http://hdl.handle.net/10316/95676https://doi.org/10.3390/molecules26133946eng1420-3049Gonçalves, Rui A.Lam, Yeng-MingLindman, Björninfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-05-25T03:06:51Zoai:estudogeral.uc.pt:10316/95676Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:14:06.119210Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive Effects
title Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive Effects
spellingShingle Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive Effects
Gonçalves, Rui A.
Additive effects
Double-chain surfactant
Hair conditioner
Lamellar gel
Lamellar liquid crysta
Surfactant packing
title_short Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive Effects
title_full Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive Effects
title_fullStr Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive Effects
title_full_unstemmed Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive Effects
title_sort Double-Chain Cationic Surfactants: Swelling, Structure, Phase Transitions and Additive Effects
author Gonçalves, Rui A.
author_facet Gonçalves, Rui A.
Lam, Yeng-Ming
Lindman, Björn
author_role author
author2 Lam, Yeng-Ming
Lindman, Björn
author2_role author
author
dc.contributor.author.fl_str_mv Gonçalves, Rui A.
Lam, Yeng-Ming
Lindman, Björn
dc.subject.por.fl_str_mv Additive effects
Double-chain surfactant
Hair conditioner
Lamellar gel
Lamellar liquid crysta
Surfactant packing
topic Additive effects
Double-chain surfactant
Hair conditioner
Lamellar gel
Lamellar liquid crysta
Surfactant packing
description Double-chain amphiphilic compounds, including surfactants and lipids, have broad significance in applications like personal care and biology. A study on the phase structures and their transitions focusing on dioctadecyldimethylammonium chloride (DODAC), used inter alia in hair conditioners, is presented. The phase behaviour is dominated by two bilayer lamellar phases, Lβ and Lα, with "solid" and "melted" alkyl chains, respectively. In particular, the study is focused on the effect of additives of different polarity on the phase transitions and structures. The main techniques used for investigation were differential scanning calorimetry (DSC) and small- and wide-angle X-ray scattering (SAXS and WAXS). From the WAXS reflections, the distance between the alkyl chains in the bilayers was obtained, and from SAXS, the thicknesses of the surfactant and water layers. The Lα phase was found to have a bilayer structure, generally found for most surfactants; a Lβ phase made up of bilayers with considerable chain tilting and interdigitation was also identified. Depending mainly on the polarity of the additives, their effects on the phase stabilities and structure vary. Compounds like urea have no significant effect, while fatty acids and fatty alcohols have significant effects, but which are quite different depending on the nonpolar part. In most cases, Lβ and Lα phases exist over wide composition ranges; certain additives induce transitions to other phases, which include cubic, reversed hexagonal liquid crystals and bicontinuous liquid phases. For a system containing additives, which induce a significant lowering of the Lβ-Lα transition, we identified the possibility of a triggered phase transition via dilution with water.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-28
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/95676
http://hdl.handle.net/10316/95676
https://doi.org/10.3390/molecules26133946
url http://hdl.handle.net/10316/95676
https://doi.org/10.3390/molecules26133946
dc.language.iso.fl_str_mv eng
language eng
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dc.publisher.none.fl_str_mv MDPI
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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