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A (29)Si, (1)H, and (13)C Solid-State NMR Study on the Surface Species of Various Depolymerized Organosiloxanes at Silica Surface
ABSTRACT: Three poly(organosiloxanes) (hydromethyl-, dimethyl-, and epoxymethylsiloxane) of different chain lengths and pendant groups and their mixtures of dimethyl (DMC) or diethyl carbonates (DEC) were applied in the modification of fumed silica nanoparticles (FSNs). The resulting modified silica...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517472/ https://www.ncbi.nlm.nih.gov/pubmed/31089904 http://dx.doi.org/10.1186/s11671-019-2982-2 |
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author | Protsak, Iryna S. Morozov, Yevhenii M. Dong, Wen Le, Zichun Zhang, Dong Henderson, Ian M. |
author_facet | Protsak, Iryna S. Morozov, Yevhenii M. Dong, Wen Le, Zichun Zhang, Dong Henderson, Ian M. |
author_sort | Protsak, Iryna S. |
collection | PubMed |
description | ABSTRACT: Three poly(organosiloxanes) (hydromethyl-, dimethyl-, and epoxymethylsiloxane) of different chain lengths and pendant groups and their mixtures of dimethyl (DMC) or diethyl carbonates (DEC) were applied in the modification of fumed silica nanoparticles (FSNs). The resulting modified silicas were studied in depth using (29)Si, (1)H, and (13)C solid-state NMR spectroscopy, elemental analysis, and nitrogen adsorption-desorption (BET) analysis. The obtained results reveal that the type of grafting, grafting density, and structure of the grafted species at the silica surface depend strongly on the length of organosiloxane polymer and on the nature of the “green” additive, DMC or DEC. The spectral changes observed by solid-state NMR spectroscopy suggest that the major products of the reaction of various organosiloxanes and their DMC or DEC mixtures with the surface are D (RR’Si(O(0.5))(2)) and T (RSi(O(0.5))(3)) organosiloxane units. It was found that shorter methylhydro (PMHS) and dimethylsiloxane (PDMS) and their mixtures with DMC or DEC form a denser coverage at the silica surface since S(BET) diminution is larger and grafting density is higher than the longest epoxymethylsiloxane (CPDMS) used for FSNs modification. Additionally, for FSNs modified with short organosiloxane PMHS/DEC and also medium organosiloxane PDMS/DMC, the dense coverage formation is accompanied by a greater reduction of isolated silanols, as shown by solid-state (29)Si NMR spectroscopy, in contrast to reactions with neat organosiloxanes. The surface coverage at FSNs with the longest siloxane (CPDMS) greatly improves with the addition of DMC or DEC. The data on grafting density suggest that molecules in the attached layers of FSNs modified with short PMHS and its mixture of DMC or DEC and medium PDMS and its mixture of DMC form a “vertical” orientation of the grafted methylhydrosiloxane and dimethylsiloxane chains, in contrast to the reaction with PDMS/DEC and epoxide methylsiloxane in the presence of DMC or DEC, which indicates a “horizontal” chain orientation of the grafted methyl and epoxysiloxane molecules. This study highlights the major role of solid-state NMR spectroscopy for comprehensive characterization of solid surfaces. GRAPHICAL ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-019-2982-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6517472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-65174722019-05-29 A (29)Si, (1)H, and (13)C Solid-State NMR Study on the Surface Species of Various Depolymerized Organosiloxanes at Silica Surface Protsak, Iryna S. Morozov, Yevhenii M. Dong, Wen Le, Zichun Zhang, Dong Henderson, Ian M. Nanoscale Res Lett Nano Express ABSTRACT: Three poly(organosiloxanes) (hydromethyl-, dimethyl-, and epoxymethylsiloxane) of different chain lengths and pendant groups and their mixtures of dimethyl (DMC) or diethyl carbonates (DEC) were applied in the modification of fumed silica nanoparticles (FSNs). The resulting modified silicas were studied in depth using (29)Si, (1)H, and (13)C solid-state NMR spectroscopy, elemental analysis, and nitrogen adsorption-desorption (BET) analysis. The obtained results reveal that the type of grafting, grafting density, and structure of the grafted species at the silica surface depend strongly on the length of organosiloxane polymer and on the nature of the “green” additive, DMC or DEC. The spectral changes observed by solid-state NMR spectroscopy suggest that the major products of the reaction of various organosiloxanes and their DMC or DEC mixtures with the surface are D (RR’Si(O(0.5))(2)) and T (RSi(O(0.5))(3)) organosiloxane units. It was found that shorter methylhydro (PMHS) and dimethylsiloxane (PDMS) and their mixtures with DMC or DEC form a denser coverage at the silica surface since S(BET) diminution is larger and grafting density is higher than the longest epoxymethylsiloxane (CPDMS) used for FSNs modification. Additionally, for FSNs modified with short organosiloxane PMHS/DEC and also medium organosiloxane PDMS/DMC, the dense coverage formation is accompanied by a greater reduction of isolated silanols, as shown by solid-state (29)Si NMR spectroscopy, in contrast to reactions with neat organosiloxanes. The surface coverage at FSNs with the longest siloxane (CPDMS) greatly improves with the addition of DMC or DEC. The data on grafting density suggest that molecules in the attached layers of FSNs modified with short PMHS and its mixture of DMC or DEC and medium PDMS and its mixture of DMC form a “vertical” orientation of the grafted methylhydrosiloxane and dimethylsiloxane chains, in contrast to the reaction with PDMS/DEC and epoxide methylsiloxane in the presence of DMC or DEC, which indicates a “horizontal” chain orientation of the grafted methyl and epoxysiloxane molecules. This study highlights the major role of solid-state NMR spectroscopy for comprehensive characterization of solid surfaces. GRAPHICAL ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-019-2982-2) contains supplementary material, which is available to authorized users. Springer US 2019-05-14 /pmc/articles/PMC6517472/ /pubmed/31089904 http://dx.doi.org/10.1186/s11671-019-2982-2 Text en © The Author(s). 2019 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 | Nano Express Protsak, Iryna S. Morozov, Yevhenii M. Dong, Wen Le, Zichun Zhang, Dong Henderson, Ian M. A (29)Si, (1)H, and (13)C Solid-State NMR Study on the Surface Species of Various Depolymerized Organosiloxanes at Silica Surface |
title | A (29)Si, (1)H, and (13)C Solid-State NMR Study on the Surface Species of Various Depolymerized Organosiloxanes at Silica Surface |
title_full | A (29)Si, (1)H, and (13)C Solid-State NMR Study on the Surface Species of Various Depolymerized Organosiloxanes at Silica Surface |
title_fullStr | A (29)Si, (1)H, and (13)C Solid-State NMR Study on the Surface Species of Various Depolymerized Organosiloxanes at Silica Surface |
title_full_unstemmed | A (29)Si, (1)H, and (13)C Solid-State NMR Study on the Surface Species of Various Depolymerized Organosiloxanes at Silica Surface |
title_short | A (29)Si, (1)H, and (13)C Solid-State NMR Study on the Surface Species of Various Depolymerized Organosiloxanes at Silica Surface |
title_sort | (29)si, (1)h, and (13)c solid-state nmr study on the surface species of various depolymerized organosiloxanes at silica surface |
topic | Nano Express |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517472/ https://www.ncbi.nlm.nih.gov/pubmed/31089904 http://dx.doi.org/10.1186/s11671-019-2982-2 |
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