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Preparation of Colloidal Organosilica Spheres through Spontaneous Emulsification

[Image: see text] Colloidal particles of controlled size are promising building blocks for the self-assembly of functional materials. Here, we systematically study a method to synthesize monodisperse, micrometer-sized spheres from 3-(trimethoxysilyl)propyl methacrylate (TPM) in a benchtop experiment...

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Autores principales: van der Wel, Casper, Bhan, Rohit K., Verweij, Ruben W., Frijters, Hans C., Gong, Zhe, Hollingsworth, Andrew D., Sacanna, Stefano, Kraft, Daniela J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569361/
https://www.ncbi.nlm.nih.gov/pubmed/28731356
http://dx.doi.org/10.1021/acs.langmuir.7b01398
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author van der Wel, Casper
Bhan, Rohit K.
Verweij, Ruben W.
Frijters, Hans C.
Gong, Zhe
Hollingsworth, Andrew D.
Sacanna, Stefano
Kraft, Daniela J.
author_facet van der Wel, Casper
Bhan, Rohit K.
Verweij, Ruben W.
Frijters, Hans C.
Gong, Zhe
Hollingsworth, Andrew D.
Sacanna, Stefano
Kraft, Daniela J.
author_sort van der Wel, Casper
collection PubMed
description [Image: see text] Colloidal particles of controlled size are promising building blocks for the self-assembly of functional materials. Here, we systematically study a method to synthesize monodisperse, micrometer-sized spheres from 3-(trimethoxysilyl)propyl methacrylate (TPM) in a benchtop experiment. Their ease of preparation, smoothness, and physical properties provide distinct advantages over other widely employed materials such as silica, polystyrene, and poly(methyl methacrylate). We describe that the spontaneous emulsification of TPM droplets in water is caused by base-catalyzed hydrolysis, self-condensation, and the deprotonation of TPM. By studying the time-dependent size evolution, we find that the droplet size increases without any detectable secondary nucleation. Resulting TPM droplets are polymerized to form solid particles. The particle diameter can be controlled in the range of 0.4 to 2.8 μm by adjusting the volume fraction of added monomer and the pH of the solution. Droplets can be grown to diameters of up to 4 μm by adding TPM monomer after the initial emulsification. Additionally, we characterize various physical parameters of the TPM particles, and we describe methods to incorporate several fluorescent dyes.
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spelling pubmed-55693612017-08-27 Preparation of Colloidal Organosilica Spheres through Spontaneous Emulsification van der Wel, Casper Bhan, Rohit K. Verweij, Ruben W. Frijters, Hans C. Gong, Zhe Hollingsworth, Andrew D. Sacanna, Stefano Kraft, Daniela J. Langmuir [Image: see text] Colloidal particles of controlled size are promising building blocks for the self-assembly of functional materials. Here, we systematically study a method to synthesize monodisperse, micrometer-sized spheres from 3-(trimethoxysilyl)propyl methacrylate (TPM) in a benchtop experiment. Their ease of preparation, smoothness, and physical properties provide distinct advantages over other widely employed materials such as silica, polystyrene, and poly(methyl methacrylate). We describe that the spontaneous emulsification of TPM droplets in water is caused by base-catalyzed hydrolysis, self-condensation, and the deprotonation of TPM. By studying the time-dependent size evolution, we find that the droplet size increases without any detectable secondary nucleation. Resulting TPM droplets are polymerized to form solid particles. The particle diameter can be controlled in the range of 0.4 to 2.8 μm by adjusting the volume fraction of added monomer and the pH of the solution. Droplets can be grown to diameters of up to 4 μm by adding TPM monomer after the initial emulsification. Additionally, we characterize various physical parameters of the TPM particles, and we describe methods to incorporate several fluorescent dyes. American Chemical Society 2017-07-21 2017-08-22 /pmc/articles/PMC5569361/ /pubmed/28731356 http://dx.doi.org/10.1021/acs.langmuir.7b01398 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle van der Wel, Casper
Bhan, Rohit K.
Verweij, Ruben W.
Frijters, Hans C.
Gong, Zhe
Hollingsworth, Andrew D.
Sacanna, Stefano
Kraft, Daniela J.
Preparation of Colloidal Organosilica Spheres through Spontaneous Emulsification
title Preparation of Colloidal Organosilica Spheres through Spontaneous Emulsification
title_full Preparation of Colloidal Organosilica Spheres through Spontaneous Emulsification
title_fullStr Preparation of Colloidal Organosilica Spheres through Spontaneous Emulsification
title_full_unstemmed Preparation of Colloidal Organosilica Spheres through Spontaneous Emulsification
title_short Preparation of Colloidal Organosilica Spheres through Spontaneous Emulsification
title_sort preparation of colloidal organosilica spheres through spontaneous emulsification
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569361/
https://www.ncbi.nlm.nih.gov/pubmed/28731356
http://dx.doi.org/10.1021/acs.langmuir.7b01398
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