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Influence of pH-Responsive Monomer Content on the Behavior of Di-Block Copolymers in Solution and as Stabilizers of Pickering Latex Particle Emulsifiers

In this study, diblock copolymers poly(methyl methacrylate)—block—poly (2-dimethylaminoethyl methacrylate) (pMMA-b-pDMAEMA) are investigated for the steric stabilization of latex particles and the subsequent use of these latex particles as Pickering emulsifiers. Solution properties of the diblock co...

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Autores principales: Manga, Mohamed S., Cayre, Olivier J., Biggs, Simon, Hunter, Timothy N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6062645/
https://www.ncbi.nlm.nih.gov/pubmed/30079336
http://dx.doi.org/10.3389/fchem.2018.00301
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author Manga, Mohamed S.
Cayre, Olivier J.
Biggs, Simon
Hunter, Timothy N.
author_facet Manga, Mohamed S.
Cayre, Olivier J.
Biggs, Simon
Hunter, Timothy N.
author_sort Manga, Mohamed S.
collection PubMed
description In this study, diblock copolymers poly(methyl methacrylate)—block—poly (2-dimethylaminoethyl methacrylate) (pMMA-b-pDMAEMA) are investigated for the steric stabilization of latex particles and the subsequent use of these latex particles as Pickering emulsifiers. Solution properties of the diblock copolymers highlight that the pDMAEMA block length influences the critical micelle concentration (CMC) and micelle hydrodynamic diameter in response to changes in pH and the pK(a). The block length can also be used as a way to control the particle size of sterically stabilized polystyrene latex particles prepared via emulsion polymerization. The suspension properties of these latex particles are also presented. Emulsion studies using these latex particles as emulsifiers show that both continuous phase pH and electrolyte concentration affect emulsion stability to coalescence. At high pH, stable emulsions are formed due to the affinity of the particles to the interface. At low pH, protonation of the amine groups reduces the affinity and thus droplet coalescence is observed. Increasing the electrolyte concentration improves emulsion stability, but causes an increase in droplet size due to adsorption of flocculated/aggregated particles. Finally, it is shown that these latex particles can be used in conjunction with membrane emulsification techniques to produce emulsions with low polydispersity.
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spelling pubmed-60626452018-08-03 Influence of pH-Responsive Monomer Content on the Behavior of Di-Block Copolymers in Solution and as Stabilizers of Pickering Latex Particle Emulsifiers Manga, Mohamed S. Cayre, Olivier J. Biggs, Simon Hunter, Timothy N. Front Chem Chemistry In this study, diblock copolymers poly(methyl methacrylate)—block—poly (2-dimethylaminoethyl methacrylate) (pMMA-b-pDMAEMA) are investigated for the steric stabilization of latex particles and the subsequent use of these latex particles as Pickering emulsifiers. Solution properties of the diblock copolymers highlight that the pDMAEMA block length influences the critical micelle concentration (CMC) and micelle hydrodynamic diameter in response to changes in pH and the pK(a). The block length can also be used as a way to control the particle size of sterically stabilized polystyrene latex particles prepared via emulsion polymerization. The suspension properties of these latex particles are also presented. Emulsion studies using these latex particles as emulsifiers show that both continuous phase pH and electrolyte concentration affect emulsion stability to coalescence. At high pH, stable emulsions are formed due to the affinity of the particles to the interface. At low pH, protonation of the amine groups reduces the affinity and thus droplet coalescence is observed. Increasing the electrolyte concentration improves emulsion stability, but causes an increase in droplet size due to adsorption of flocculated/aggregated particles. Finally, it is shown that these latex particles can be used in conjunction with membrane emulsification techniques to produce emulsions with low polydispersity. Frontiers Media S.A. 2018-07-20 /pmc/articles/PMC6062645/ /pubmed/30079336 http://dx.doi.org/10.3389/fchem.2018.00301 Text en Copyright © 2018 Manga, Cayre, Biggs and Hunter. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Manga, Mohamed S.
Cayre, Olivier J.
Biggs, Simon
Hunter, Timothy N.
Influence of pH-Responsive Monomer Content on the Behavior of Di-Block Copolymers in Solution and as Stabilizers of Pickering Latex Particle Emulsifiers
title Influence of pH-Responsive Monomer Content on the Behavior of Di-Block Copolymers in Solution and as Stabilizers of Pickering Latex Particle Emulsifiers
title_full Influence of pH-Responsive Monomer Content on the Behavior of Di-Block Copolymers in Solution and as Stabilizers of Pickering Latex Particle Emulsifiers
title_fullStr Influence of pH-Responsive Monomer Content on the Behavior of Di-Block Copolymers in Solution and as Stabilizers of Pickering Latex Particle Emulsifiers
title_full_unstemmed Influence of pH-Responsive Monomer Content on the Behavior of Di-Block Copolymers in Solution and as Stabilizers of Pickering Latex Particle Emulsifiers
title_short Influence of pH-Responsive Monomer Content on the Behavior of Di-Block Copolymers in Solution and as Stabilizers of Pickering Latex Particle Emulsifiers
title_sort influence of ph-responsive monomer content on the behavior of di-block copolymers in solution and as stabilizers of pickering latex particle emulsifiers
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6062645/
https://www.ncbi.nlm.nih.gov/pubmed/30079336
http://dx.doi.org/10.3389/fchem.2018.00301
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