Fabrication and properties of tree-branched cellulose nanofibers (CNFs) via acid hydrolysis assisted with pre-disintegration treatment

In this paper, the novel morphology of cellulose nanofibers (CNFs) with a unique tree-branched structure was discovered by using acid hydrolysis assisted with pre-disintegration treatment from wood pulps. For comparison, the pulps derived from both softwood and hardwood were utilized to extract nano...

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Main Authors: Li, Jun, Liu, Dongyan, Li, Junsheng, Yang, Fei, Sui, Guoxin, Dong, Roger
Format: Journal Article
Language:English
Published: MDPI AG 2022
Subjects:
Online Access:http://hdl.handle.net/20.500.11937/88759
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author Li, Jun
Liu, Dongyan
Li, Junsheng
Yang, Fei
Sui, Guoxin
Dong, Roger
author_facet Li, Jun
Liu, Dongyan
Li, Junsheng
Yang, Fei
Sui, Guoxin
Dong, Roger
author_sort Li, Jun
building Curtin Institutional Repository
collection Online Access
description In this paper, the novel morphology of cellulose nanofibers (CNFs) with a unique tree-branched structure was discovered by using acid hydrolysis assisted with pre-disintegration treatment from wood pulps. For comparison, the pulps derived from both softwood and hardwood were utilized to extract nanocellulose in order to validate the feasibility of proposed material fabrication technique. The morphology, crystalline structures, chemical structures, and thermal stability of nanocellulose were characterized by means of transmission electron microscopy (TEM), X-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR), as well as thermogravimetric analysis (TGA). Prior to acid hydrolysis, softwood and hardwood pulps underwent the disintegration treatment in the fiber dissociator. It has been found that nanocellulose derived from disintegrated pulps possesses much longer fiber length (approximately 5–6 μm) and more evident tree-branched structures along with lower degree of crystallinity when compared with those untreated counterparts. The maximum mass loss rate of CNFs takes place at the temperature level of approximately 225 °C, and appears to be higher than that of cellulose nanowhiskers (CNWs), which might be attributed to an induced impact of amorphous content. On the other hand, disintegration treatment is quite beneficial to the enhancement of tensile strength of nanocellulose films. This study elaborates a new route of material fabrication toward the development of well-tailored tree-branched CNFs in order to broaden the potential widespread applications of nanocellulose with diverse morphological structures.
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institution Curtin University Malaysia
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spelling curtin-20.500.11937-887592022-06-27T06:00:11Z Fabrication and properties of tree-branched cellulose nanofibers (CNFs) via acid hydrolysis assisted with pre-disintegration treatment Li, Jun Liu, Dongyan Li, Junsheng Yang, Fei Sui, Guoxin Dong, Roger nanocellulose tree-branched cellulose nanofibers (CNFs) acid hydrolysis wood pulps disintegration treatment In this paper, the novel morphology of cellulose nanofibers (CNFs) with a unique tree-branched structure was discovered by using acid hydrolysis assisted with pre-disintegration treatment from wood pulps. For comparison, the pulps derived from both softwood and hardwood were utilized to extract nanocellulose in order to validate the feasibility of proposed material fabrication technique. The morphology, crystalline structures, chemical structures, and thermal stability of nanocellulose were characterized by means of transmission electron microscopy (TEM), X-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR), as well as thermogravimetric analysis (TGA). Prior to acid hydrolysis, softwood and hardwood pulps underwent the disintegration treatment in the fiber dissociator. It has been found that nanocellulose derived from disintegrated pulps possesses much longer fiber length (approximately 5–6 μm) and more evident tree-branched structures along with lower degree of crystallinity when compared with those untreated counterparts. The maximum mass loss rate of CNFs takes place at the temperature level of approximately 225 °C, and appears to be higher than that of cellulose nanowhiskers (CNWs), which might be attributed to an induced impact of amorphous content. On the other hand, disintegration treatment is quite beneficial to the enhancement of tensile strength of nanocellulose films. This study elaborates a new route of material fabrication toward the development of well-tailored tree-branched CNFs in order to broaden the potential widespread applications of nanocellulose with diverse morphological structures. 2022 Journal Article http://hdl.handle.net/20.500.11937/88759 10.3390/nano12122089 English http://creativecommons.org/licenses/by/4.0/ MDPI AG fulltext
spellingShingle nanocellulose
tree-branched cellulose nanofibers (CNFs)
acid hydrolysis
wood pulps
disintegration treatment
Li, Jun
Liu, Dongyan
Li, Junsheng
Yang, Fei
Sui, Guoxin
Dong, Roger
Fabrication and properties of tree-branched cellulose nanofibers (CNFs) via acid hydrolysis assisted with pre-disintegration treatment
title Fabrication and properties of tree-branched cellulose nanofibers (CNFs) via acid hydrolysis assisted with pre-disintegration treatment
title_full Fabrication and properties of tree-branched cellulose nanofibers (CNFs) via acid hydrolysis assisted with pre-disintegration treatment
title_fullStr Fabrication and properties of tree-branched cellulose nanofibers (CNFs) via acid hydrolysis assisted with pre-disintegration treatment
title_full_unstemmed Fabrication and properties of tree-branched cellulose nanofibers (CNFs) via acid hydrolysis assisted with pre-disintegration treatment
title_short Fabrication and properties of tree-branched cellulose nanofibers (CNFs) via acid hydrolysis assisted with pre-disintegration treatment
title_sort fabrication and properties of tree-branched cellulose nanofibers (cnfs) via acid hydrolysis assisted with pre-disintegration treatment
topic nanocellulose
tree-branched cellulose nanofibers (CNFs)
acid hydrolysis
wood pulps
disintegration treatment
url http://hdl.handle.net/20.500.11937/88759