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Rapid RAFT Polymerization of Acrylamide with High Conversion

Rapid RAFT polymerization can significantly improve production efficiency of PAM with designed molecular structure. This study shows that ideal Reversible Addition–Fragmentation Chain Transfer (RAFT) polymerization of acrylamide is achieved in dimethyl sulfoxide (DMSO) solution at 70 °C. The key to...

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Detalles Bibliográficos
Autores principales: Liu, Xuejing, Sun, Qiang, Zhang, Yan, Feng, Yujun, Su, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057598/
https://www.ncbi.nlm.nih.gov/pubmed/36985559
http://dx.doi.org/10.3390/molecules28062588
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author Liu, Xuejing
Sun, Qiang
Zhang, Yan
Feng, Yujun
Su, Xin
author_facet Liu, Xuejing
Sun, Qiang
Zhang, Yan
Feng, Yujun
Su, Xin
author_sort Liu, Xuejing
collection PubMed
description Rapid RAFT polymerization can significantly improve production efficiency of PAM with designed molecular structure. This study shows that ideal Reversible Addition–Fragmentation Chain Transfer (RAFT) polymerization of acrylamide is achieved in dimethyl sulfoxide (DMSO) solution at 70 °C. The key to success is the appropriate choice of both a suitable RAFT chain transfer agent (CTA) and initiating species. It is illustrated that dodecyl trithiodimethyl propionic acid (DMPA) is a suitable trithiocarbonate RAFT CTA and is synthesized more easily than other CTAs. Compared to other RAFT processes of polymers, the reaction system shortens reaction time, enhances conversion, and bears all the characteristics of a controlled radical polymerization. The calculation result shows that high concentrations can reduce high conversions, accelerate the reaction rate, and widen molecular weight distributions slightly. This work proposes an excellent approach for rapid synthesis of PAMs with a restricted molecular weight distribution.
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spelling pubmed-100575982023-03-30 Rapid RAFT Polymerization of Acrylamide with High Conversion Liu, Xuejing Sun, Qiang Zhang, Yan Feng, Yujun Su, Xin Molecules Article Rapid RAFT polymerization can significantly improve production efficiency of PAM with designed molecular structure. This study shows that ideal Reversible Addition–Fragmentation Chain Transfer (RAFT) polymerization of acrylamide is achieved in dimethyl sulfoxide (DMSO) solution at 70 °C. The key to success is the appropriate choice of both a suitable RAFT chain transfer agent (CTA) and initiating species. It is illustrated that dodecyl trithiodimethyl propionic acid (DMPA) is a suitable trithiocarbonate RAFT CTA and is synthesized more easily than other CTAs. Compared to other RAFT processes of polymers, the reaction system shortens reaction time, enhances conversion, and bears all the characteristics of a controlled radical polymerization. The calculation result shows that high concentrations can reduce high conversions, accelerate the reaction rate, and widen molecular weight distributions slightly. This work proposes an excellent approach for rapid synthesis of PAMs with a restricted molecular weight distribution. MDPI 2023-03-13 /pmc/articles/PMC10057598/ /pubmed/36985559 http://dx.doi.org/10.3390/molecules28062588 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Xuejing
Sun, Qiang
Zhang, Yan
Feng, Yujun
Su, Xin
Rapid RAFT Polymerization of Acrylamide with High Conversion
title Rapid RAFT Polymerization of Acrylamide with High Conversion
title_full Rapid RAFT Polymerization of Acrylamide with High Conversion
title_fullStr Rapid RAFT Polymerization of Acrylamide with High Conversion
title_full_unstemmed Rapid RAFT Polymerization of Acrylamide with High Conversion
title_short Rapid RAFT Polymerization of Acrylamide with High Conversion
title_sort rapid raft polymerization of acrylamide with high conversion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057598/
https://www.ncbi.nlm.nih.gov/pubmed/36985559
http://dx.doi.org/10.3390/molecules28062588
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