Steric Stabilization of “Charge-Free” Cellulose Nanowhiskers by Grafting of Poly(ethylene glycol)

A sterically stabilized aqueous suspension of “charge-free” cellulose nanowhiskers was prepared by hydrochloric acid hydrolysis of cotton powders and subsequent surface grafting of monomethoxy poly(ethylene glycol) (mPEG). The preparation scheme included carboxylation of the terminal hydroxyl groups...

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Main Authors: Jun Araki, Shiho Mishima
Format: Article
Language:English
Published: MDPI AG 2014-12-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/20/1/169
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spelling doaj-07fe88b88449402896160d50200ef8182020-11-24T23:28:26ZengMDPI AGMolecules1420-30492014-12-0120116918410.3390/molecules20010169molecules20010169Steric Stabilization of “Charge-Free” Cellulose Nanowhiskers by Grafting of Poly(ethylene glycol)Jun Araki0Shiho Mishima1Faculty of Textile Science and Technology, Shinshu University, Tokida 3-15-1, Ueda, Nagano Prefecture 386-8567, JapanGraduate School of Science and Technology, Shinshu University, Tokida 3-15-1, Ueda, Nagano Prefecture, 386-8567, JapanA sterically stabilized aqueous suspension of “charge-free” cellulose nanowhiskers was prepared by hydrochloric acid hydrolysis of cotton powders and subsequent surface grafting of monomethoxy poly(ethylene glycol) (mPEG). The preparation scheme included carboxylation of the terminal hydroxyl groups in mPEG via oxidation with silica gel particles carrying 2,2,6,6-tetramethyl-1-pyperidinyloxyl (TEMPO) moieties and subsequent esterification between terminal carboxyls in mPEG and surface hydroxyl groups of cellulose nanowhiskers, mediated by 1,1'-carbonyldiimidazole (CDI) in dimethyl sulfoxide or dimethylacetamide. Some of the prepared PEG-grafted samples showed remarkable flow birefringence and enhanced stability after 24 h, even in 0.1 M NaCl, suggesting successful steric stabilization by efficient mPEG grafting. Actual PEG grafting via ester linkages was confirmed by attenuated total reflectance-Fourier transform infrared spectrometry. In a typical example, the amount of grafted mPEG was estimated as ca. 0.3 g/g cellulose by two measurements, i.e., weight increase after grafting and weight loss after alkali cleavage of ester linkages. Transmission electron microscopy indicated unchanged nanowhisker morphology after mPEG grafting.http://www.mdpi.com/1420-3049/20/1/169steric stabilizationcellulose nanowhiskerspoly(ethylene glycol)1,1'-carbonyldiimidazole (CDI)dispersion stability
collection DOAJ
language English
format Article
sources DOAJ
author Jun Araki
Shiho Mishima
spellingShingle Jun Araki
Shiho Mishima
Steric Stabilization of “Charge-Free” Cellulose Nanowhiskers by Grafting of Poly(ethylene glycol)
Molecules
steric stabilization
cellulose nanowhiskers
poly(ethylene glycol)
1,1'-carbonyldiimidazole (CDI)
dispersion stability
author_facet Jun Araki
Shiho Mishima
author_sort Jun Araki
title Steric Stabilization of “Charge-Free” Cellulose Nanowhiskers by Grafting of Poly(ethylene glycol)
title_short Steric Stabilization of “Charge-Free” Cellulose Nanowhiskers by Grafting of Poly(ethylene glycol)
title_full Steric Stabilization of “Charge-Free” Cellulose Nanowhiskers by Grafting of Poly(ethylene glycol)
title_fullStr Steric Stabilization of “Charge-Free” Cellulose Nanowhiskers by Grafting of Poly(ethylene glycol)
title_full_unstemmed Steric Stabilization of “Charge-Free” Cellulose Nanowhiskers by Grafting of Poly(ethylene glycol)
title_sort steric stabilization of “charge-free” cellulose nanowhiskers by grafting of poly(ethylene glycol)
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2014-12-01
description A sterically stabilized aqueous suspension of “charge-free” cellulose nanowhiskers was prepared by hydrochloric acid hydrolysis of cotton powders and subsequent surface grafting of monomethoxy poly(ethylene glycol) (mPEG). The preparation scheme included carboxylation of the terminal hydroxyl groups in mPEG via oxidation with silica gel particles carrying 2,2,6,6-tetramethyl-1-pyperidinyloxyl (TEMPO) moieties and subsequent esterification between terminal carboxyls in mPEG and surface hydroxyl groups of cellulose nanowhiskers, mediated by 1,1'-carbonyldiimidazole (CDI) in dimethyl sulfoxide or dimethylacetamide. Some of the prepared PEG-grafted samples showed remarkable flow birefringence and enhanced stability after 24 h, even in 0.1 M NaCl, suggesting successful steric stabilization by efficient mPEG grafting. Actual PEG grafting via ester linkages was confirmed by attenuated total reflectance-Fourier transform infrared spectrometry. In a typical example, the amount of grafted mPEG was estimated as ca. 0.3 g/g cellulose by two measurements, i.e., weight increase after grafting and weight loss after alkali cleavage of ester linkages. Transmission electron microscopy indicated unchanged nanowhisker morphology after mPEG grafting.
topic steric stabilization
cellulose nanowhiskers
poly(ethylene glycol)
1,1'-carbonyldiimidazole (CDI)
dispersion stability
url http://www.mdpi.com/1420-3049/20/1/169
work_keys_str_mv AT junaraki stericstabilizationofchargefreecellulosenanowhiskersbygraftingofpolyethyleneglycol
AT shihomishima stericstabilizationofchargefreecellulosenanowhiskersbygraftingofpolyethyleneglycol
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