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The role of initiator on the dispersibility of polystyrene microgels in non-aqueous solvents
Non-aqueous microgel particles are commonly synthesised in water, dried, and then redispersed in non-aqueous solvents. An important factor to consider when synthesising such particles is the initiator, which can determine how well the particles disperse in solvents. Polystyrene microgel particles we...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321690/ https://www.ncbi.nlm.nih.gov/pubmed/28280286 http://dx.doi.org/10.1007/s00396-017-4023-y |
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author | Bonham, Jessica A. Waggett, Franceska Faers, Malcolm A. van Duijneveldt, Jeroen S. |
author_facet | Bonham, Jessica A. Waggett, Franceska Faers, Malcolm A. van Duijneveldt, Jeroen S. |
author_sort | Bonham, Jessica A. |
collection | PubMed |
description | Non-aqueous microgel particles are commonly synthesised in water, dried, and then redispersed in non-aqueous solvents. An important factor to consider when synthesising such particles is the initiator, which can determine how well the particles disperse in solvents. Polystyrene microgel particles were made with three different initiators. When a neutral, oil soluble initiator (azobisisobutyronitrile) was used the particles dispersed in toluene as well as cyclohexane and decalin. In contrast, anionic, water-soluble initiators (potassium persulfate or azobis(4-cyanovaleric acid)) created particles that only redispersed in toluene and not the other two solvents. Of the three considered, toluene is the best solvent for polystyrene and also has the highest polarizability, making it most effective at redispersing particles with polar or ionisable functional groups. Zeta potential and conductivity measurements, however, did not detect a direct relationship between particle charging and redispersibility. Oil soluble initiators result in “inside out” polymerisation where the initiator groups are buried inside the growing particle, whereas water-soluble initiators result in “outside in” polymerisation, with the polar initiator groups residing on the particle surface. By tailoring the ratio between water and oil soluble initiators, it may be possible to synthesise microgel particles with uniform or designed charge profiles from the core to the surface. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00396-017-4023-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5321690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-53216902017-03-07 The role of initiator on the dispersibility of polystyrene microgels in non-aqueous solvents Bonham, Jessica A. Waggett, Franceska Faers, Malcolm A. van Duijneveldt, Jeroen S. Colloid Polym Sci Original Contribution Non-aqueous microgel particles are commonly synthesised in water, dried, and then redispersed in non-aqueous solvents. An important factor to consider when synthesising such particles is the initiator, which can determine how well the particles disperse in solvents. Polystyrene microgel particles were made with three different initiators. When a neutral, oil soluble initiator (azobisisobutyronitrile) was used the particles dispersed in toluene as well as cyclohexane and decalin. In contrast, anionic, water-soluble initiators (potassium persulfate or azobis(4-cyanovaleric acid)) created particles that only redispersed in toluene and not the other two solvents. Of the three considered, toluene is the best solvent for polystyrene and also has the highest polarizability, making it most effective at redispersing particles with polar or ionisable functional groups. Zeta potential and conductivity measurements, however, did not detect a direct relationship between particle charging and redispersibility. Oil soluble initiators result in “inside out” polymerisation where the initiator groups are buried inside the growing particle, whereas water-soluble initiators result in “outside in” polymerisation, with the polar initiator groups residing on the particle surface. By tailoring the ratio between water and oil soluble initiators, it may be possible to synthesise microgel particles with uniform or designed charge profiles from the core to the surface. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00396-017-4023-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-02-07 2017 /pmc/articles/PMC5321690/ /pubmed/28280286 http://dx.doi.org/10.1007/s00396-017-4023-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Contribution Bonham, Jessica A. Waggett, Franceska Faers, Malcolm A. van Duijneveldt, Jeroen S. The role of initiator on the dispersibility of polystyrene microgels in non-aqueous solvents |
title | The role of initiator on the dispersibility of polystyrene microgels in non-aqueous solvents |
title_full | The role of initiator on the dispersibility of polystyrene microgels in non-aqueous solvents |
title_fullStr | The role of initiator on the dispersibility of polystyrene microgels in non-aqueous solvents |
title_full_unstemmed | The role of initiator on the dispersibility of polystyrene microgels in non-aqueous solvents |
title_short | The role of initiator on the dispersibility of polystyrene microgels in non-aqueous solvents |
title_sort | role of initiator on the dispersibility of polystyrene microgels in non-aqueous solvents |
topic | Original Contribution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321690/ https://www.ncbi.nlm.nih.gov/pubmed/28280286 http://dx.doi.org/10.1007/s00396-017-4023-y |
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