THE DISPERSIBILITY OF CELLULOSE I AND CELLULOSE II BY TEMPO-MEDIATED OXIDATION

Detalhes bibliográficos
Autor(a) principal: Ahmad Ghazali, Nursyamimi
Data de Publicação: 2024
Outros Autores: Mohd Salleh, Kushairi, Jafri, Nur Fathihah, Mohamad Khalid, Khairunnisa Atiqah, Zakaria , Sarani, Ab Halim, Nurul Husna
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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spelling 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
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