THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION
Autor(a) principal: | |
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Data de Publicação: | 2024 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Cerne (Online) |
Texto Completo: | https://cerne.ufla.br/site/index.php/CERNE/article/view/3320 |
Resumo: | Background: The restricted dispersibility of cellulose in water has grown to be a significant problem which is a key step in making cellulose soluble in water and common solvent. To overcome the obstacle, cellulose structure is being modified to improve the surface properties and the utilization of the cellulose itself. In this study, cellulose I and cellulose II were examined after treated with water-soluble 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO). The hydrogen bond between chains and the crystallinity of the cotton linter (cellulose I) was first broken by NaOH/urea treatment. Then, cellulose I and NaOH/urea-treated cellulose (cellulose II) were oxidized with sodium chlorite, sodium bromide, and TEMPO in a catalytic amount. Results: The success of oxidation is revealed when both cellulose I and II treated with TEMPO had preferentially converted the hydroxyl groups to carboxylate groups through Fourier Transform Infrared Spectrometer (FTIR). Besides, through X-ray diffraction analysis, cellulose I and II exhibited a decreased in the crystallinity. All samples were examined by thermogravimetric analysis, dispersion analysis, and field emission scanning electron microscopy. Conclusion: The result showed, cellulose has been successfully modified using TEMPO-mediated oxidation with improved dispersion properties. The scattered structure revealed through morphology analysis proved that cellulose treated with TEMPO had resulted in a more dispersed and separated cellulose fibre structure. High cellulose dispersion ability will allow the manufacturing process of hydrogel, film and fibre to be much easier and faster. This is necessary for creating novel, environmentally friendly materials for various applications across numerous industries and future research anticipated to increase. |
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THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION2,2,6,6-tetramethylpiperidine-1-oxyl radicalBioresource based productsCarboxyl groupsCellulose solubilityCrystallinityDissolutionBackground: The restricted dispersibility of cellulose in water has grown to be a significant problem which is a key step in making cellulose soluble in water and common solvent. To overcome the obstacle, cellulose structure is being modified to improve the surface properties and the utilization of the cellulose itself. In this study, cellulose I and cellulose II were examined after treated with water-soluble 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO). The hydrogen bond between chains and the crystallinity of the cotton linter (cellulose I) was first broken by NaOH/urea treatment. Then, cellulose I and NaOH/urea-treated cellulose (cellulose II) were oxidized with sodium chlorite, sodium bromide, and TEMPO in a catalytic amount. Results: The success of oxidation is revealed when both cellulose I and II treated with TEMPO had preferentially converted the hydroxyl groups to carboxylate groups through Fourier Transform Infrared Spectrometer (FTIR). Besides, through X-ray diffraction analysis, cellulose I and II exhibited a decreased in the crystallinity. All samples were examined by thermogravimetric analysis, dispersion analysis, and field emission scanning electron microscopy. Conclusion: The result showed, cellulose has been successfully modified using TEMPO-mediated oxidation with improved dispersion properties. The scattered structure revealed through morphology analysis proved that cellulose treated with TEMPO had resulted in a more dispersed and separated cellulose fibre structure. High cellulose dispersion ability will allow the manufacturing process of hydrogel, film and fibre to be much easier and faster. This is necessary for creating novel, environmentally friendly materials for various applications across numerous industries and future research anticipated to increase. CERNECERNE2024-04-22info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://cerne.ufla.br/site/index.php/CERNE/article/view/3320CERNE; Vol. 30 No. 1 (2024): ; E-103320CERNE; v. 30 n. 1 (2024): ; E-1033202317-63420104-7760reponame:Cerne (Online)instname:Universidade Federal de Lavras (UFLA)instacron:UFLAenghttps://cerne.ufla.br/site/index.php/CERNE/article/view/3320/1365Copyright (c) 2024 CERNEhttp://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessAhmad Ghazali, NursyamimiMohd Salleh, KushairiJafri, Nur FathihahMohamad Khalid, Khairunnisa AtiqahZakaria , SaraniAb Halim, Nurul Husna2024-05-07T17:38:27Zoai:cerne.ufla.br:article/3320Revistahttps://cerne.ufla.br/site/index.php/CERNEPUBhttps://cerne.ufla.br/site/index.php/CERNE/oaicerne@dcf.ufla.br||cerne@dcf.ufla.br2317-63420104-7760opendoar:2024-05-21T19:54:52.681066Cerne (Online) - Universidade Federal de Lavras (UFLA)true |
dc.title.none.fl_str_mv |
THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION |
title |
THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION |
spellingShingle |
THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION Ahmad Ghazali, Nursyamimi 2,2,6,6-tetramethylpiperidine-1-oxyl radical Bioresource based products Carboxyl groups Cellulose solubility Crystallinity Dissolution |
title_short |
THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION |
title_full |
THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION |
title_fullStr |
THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION |
title_full_unstemmed |
THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION |
title_sort |
THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION |
author |
Ahmad Ghazali, Nursyamimi |
author_facet |
Ahmad Ghazali, Nursyamimi Mohd Salleh, Kushairi Jafri, Nur Fathihah Mohamad Khalid, Khairunnisa Atiqah Zakaria , Sarani Ab Halim, Nurul Husna |
author_role |
author |
author2 |
Mohd Salleh, Kushairi Jafri, Nur Fathihah Mohamad Khalid, Khairunnisa Atiqah Zakaria , Sarani Ab Halim, Nurul Husna |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Ahmad Ghazali, Nursyamimi Mohd Salleh, Kushairi Jafri, Nur Fathihah Mohamad Khalid, Khairunnisa Atiqah Zakaria , Sarani Ab Halim, Nurul Husna |
dc.subject.por.fl_str_mv |
2,2,6,6-tetramethylpiperidine-1-oxyl radical Bioresource based products Carboxyl groups Cellulose solubility Crystallinity Dissolution |
topic |
2,2,6,6-tetramethylpiperidine-1-oxyl radical Bioresource based products Carboxyl groups Cellulose solubility Crystallinity Dissolution |
description |
Background: The restricted dispersibility of cellulose in water has grown to be a significant problem which is a key step in making cellulose soluble in water and common solvent. To overcome the obstacle, cellulose structure is being modified to improve the surface properties and the utilization of the cellulose itself. In this study, cellulose I and cellulose II were examined after treated with water-soluble 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO). The hydrogen bond between chains and the crystallinity of the cotton linter (cellulose I) was first broken by NaOH/urea treatment. Then, cellulose I and NaOH/urea-treated cellulose (cellulose II) were oxidized with sodium chlorite, sodium bromide, and TEMPO in a catalytic amount. Results: The success of oxidation is revealed when both cellulose I and II treated with TEMPO had preferentially converted the hydroxyl groups to carboxylate groups through Fourier Transform Infrared Spectrometer (FTIR). Besides, through X-ray diffraction analysis, cellulose I and II exhibited a decreased in the crystallinity. All samples were examined by thermogravimetric analysis, dispersion analysis, and field emission scanning electron microscopy. Conclusion: The result showed, cellulose has been successfully modified using TEMPO-mediated oxidation with improved dispersion properties. The scattered structure revealed through morphology analysis proved that cellulose treated with TEMPO had resulted in a more dispersed and separated cellulose fibre structure. High cellulose dispersion ability will allow the manufacturing process of hydrogel, film and fibre to be much easier and faster. This is necessary for creating novel, environmentally friendly materials for various applications across numerous industries and future research anticipated to increase. |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-04-22 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://cerne.ufla.br/site/index.php/CERNE/article/view/3320 |
url |
https://cerne.ufla.br/site/index.php/CERNE/article/view/3320 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://cerne.ufla.br/site/index.php/CERNE/article/view/3320/1365 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2024 CERNE http://creativecommons.org/licenses/by/4.0/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2024 CERNE http://creativecommons.org/licenses/by/4.0/ |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
CERNE CERNE |
publisher.none.fl_str_mv |
CERNE CERNE |
dc.source.none.fl_str_mv |
CERNE; Vol. 30 No. 1 (2024): ; E-103320 CERNE; v. 30 n. 1 (2024): ; E-103320 2317-6342 0104-7760 reponame:Cerne (Online) instname:Universidade Federal de Lavras (UFLA) instacron:UFLA |
instname_str |
Universidade Federal de Lavras (UFLA) |
instacron_str |
UFLA |
institution |
UFLA |
reponame_str |
Cerne (Online) |
collection |
Cerne (Online) |
repository.name.fl_str_mv |
Cerne (Online) - Universidade Federal de Lavras (UFLA) |
repository.mail.fl_str_mv |
cerne@dcf.ufla.br||cerne@dcf.ufla.br |
_version_ |
1799874944613482496 |