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Zwitterionic Acetylated Cellulose Nanofibrils
A strategy is devised to synthesize zwitterionic acetylated cellulose nanofibrils (CNF). The strategy included acetylation, periodate oxidation, Schiff base reaction, borohydride reduction, and a quaternary ammonium reaction. Acetylation was performed in glacial acetic acid with a short reaction tim...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749602/ https://www.ncbi.nlm.nih.gov/pubmed/31470598 http://dx.doi.org/10.3390/molecules24173147 |
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author | Rostami, Jowan Mathew, Aji P. Edlund, Ulrica |
author_facet | Rostami, Jowan Mathew, Aji P. Edlund, Ulrica |
author_sort | Rostami, Jowan |
collection | PubMed |
description | A strategy is devised to synthesize zwitterionic acetylated cellulose nanofibrils (CNF). The strategy included acetylation, periodate oxidation, Schiff base reaction, borohydride reduction, and a quaternary ammonium reaction. Acetylation was performed in glacial acetic acid with a short reaction time of 90 min, yielding, on average, mono-acetylated CNF with hydroxyl groups available for further modification. The products from each step were characterized by FTIR spectroscopy, ζ-potential, SEM-EDS, AFM, and titration to track and verify the structural changes along the sequential modification route. |
format | Online Article Text |
id | pubmed-6749602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67496022019-09-27 Zwitterionic Acetylated Cellulose Nanofibrils Rostami, Jowan Mathew, Aji P. Edlund, Ulrica Molecules Article A strategy is devised to synthesize zwitterionic acetylated cellulose nanofibrils (CNF). The strategy included acetylation, periodate oxidation, Schiff base reaction, borohydride reduction, and a quaternary ammonium reaction. Acetylation was performed in glacial acetic acid with a short reaction time of 90 min, yielding, on average, mono-acetylated CNF with hydroxyl groups available for further modification. The products from each step were characterized by FTIR spectroscopy, ζ-potential, SEM-EDS, AFM, and titration to track and verify the structural changes along the sequential modification route. MDPI 2019-08-29 /pmc/articles/PMC6749602/ /pubmed/31470598 http://dx.doi.org/10.3390/molecules24173147 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rostami, Jowan Mathew, Aji P. Edlund, Ulrica Zwitterionic Acetylated Cellulose Nanofibrils |
title | Zwitterionic Acetylated Cellulose Nanofibrils |
title_full | Zwitterionic Acetylated Cellulose Nanofibrils |
title_fullStr | Zwitterionic Acetylated Cellulose Nanofibrils |
title_full_unstemmed | Zwitterionic Acetylated Cellulose Nanofibrils |
title_short | Zwitterionic Acetylated Cellulose Nanofibrils |
title_sort | zwitterionic acetylated cellulose nanofibrils |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749602/ https://www.ncbi.nlm.nih.gov/pubmed/31470598 http://dx.doi.org/10.3390/molecules24173147 |
work_keys_str_mv | AT rostamijowan zwitterionicacetylatedcellulosenanofibrils AT mathewajip zwitterionicacetylatedcellulosenanofibrils AT edlundulrica zwitterionicacetylatedcellulosenanofibrils |