2019
DOI: 10.1007/s10973-019-09109-4
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Surface modification effects on the thermal stability of cellulose nanostructures obtained from lignocellulosic residues

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Cited by 17 publications
(7 citation statements)
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“…One possible explanation is that the polymer chains create a uniform layer that acts as a protective shield on the nanocellulose surface [153]. Recently published works show that increasing the lignin content [154], doping with melamine-grafted nano SiO 2 [155], absorption of surfactants [156] all have a beneficial effect on the thermal stability of cellulose nanomaterials. Methods like these provide opportunities to overcome stability and extraction challenges in these biobased materials, which are important issues to consider for scale-up to industrial production of biobased packaging materials.…”
Section: Discussionmentioning
confidence: 99%
“…One possible explanation is that the polymer chains create a uniform layer that acts as a protective shield on the nanocellulose surface [153]. Recently published works show that increasing the lignin content [154], doping with melamine-grafted nano SiO 2 [155], absorption of surfactants [156] all have a beneficial effect on the thermal stability of cellulose nanomaterials. Methods like these provide opportunities to overcome stability and extraction challenges in these biobased materials, which are important issues to consider for scale-up to industrial production of biobased packaging materials.…”
Section: Discussionmentioning
confidence: 99%
“…According to our previous works, cellulose nanocrystals (CNC) were prepared and characterized [26,27]. CNCs had an average length of 2.0 ± 0.8 µm and mean diameter of 131.1 ± 29.6 nm (L/D = 15), and ζ potential of −33.0 ± 1.0 mV [28]. Cellulose nanofibrils (CNF) were kindly provided by Suzano Papel e Celulose (Suzano, São Paulo, Brazil).…”
Section: Methodsmentioning
confidence: 99%
“…At low shear rates, oil droplets are held together due to insufficient hydrodynamic forces to break system bonds, resulting in high viscosity. As the shear rate increases, hydrodynamic forces break the bonds and deform the CNF network and oil droplets, resulting in lower viscosity [28,29]. This behavior is directly related to the chemical bonds present between the emulsion components.…”
Section: Rheologymentioning
confidence: 99%
“…The presence of sodium carboxylate (COONa) and carboxylic acid (-COOH) groups was identified by the peak at 1570 cm −1 . [43] The peak at 1390 cm −1 was attributed to hydroxyl (-OH) from the carboxylate groups. The peak at 1050 cm −1 corresponded to the C-O vibrations of primary and secondary alcohols and the angular deformation of the C-O-C groups of the carbohydrate rings present in the polymer structures and in the lateral groups.…”
Section: Ftir Spectroscopymentioning
confidence: 99%
“…The peak at 1050 cm −1 corresponded to the C-O vibrations of primary and secondary alcohols and the angular deformation of the C-O-C groups of the carbohydrate rings present in the polymer structures and in the lateral groups. [43] The -COOH groups can form hydrogen bonds that hold the CMC chains together, whereas the -COONa groups increase the hydrophilicity and give the CMC hydrogel a transparent appearance. [44] According to Lima et al, [33] therefore, citric acid is a good crosslinker for CMC, a highly hydrophilic crosslinked gel.…”
Section: Ftir Spectroscopymentioning
confidence: 99%