Abstract:Abstract. Three techniques including acid hydrolysis (AH), 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO)-mediated oxidation (TMO) and ultrasonication (US) were introduced to isolate nanocellulose from microcrystalline cellulose, in order to reinforce poly(vinyl alcohol) (PVA) films. Important differences were noticed in fiber quality of nanocellulose and film properties of PVA nanocomposite films. The TMO treatment was more efficient in nanocellulose isolation with higher aspect ratio, surface charge (-… Show more
“…This result is similar to those reported for palm tree cellulose (84%) ) and microcrystalline cellulose (86%) hydrolyzed by FeCl3 in HCl acidic medium but under higher temperature (91 to 98 o C) and longer hydrolysis duration (4 to 6 h) at optimum hydrolysis conditions. However, all the nanocellulose yields prepared via Cr(III)-and Mn(II)-catalyzed hydrolysis under mild reaction were much more higher than the value reported for the hydrolysis of cellulosic materials including rice straw cellulose (16.9%) (Jiang and Hsieh 2013), microcrystalline cellulose (28.6%) (Zhou 2012), and bamboo bleached fiber (30%) (Brito et al 2012) via H2SO4 (~65 wt.%) hydrolysis procedure. A recent study (Tang et al 2015) conducted by Tang's group found that the yield of nanocellulose produced via phosphoric acid hydrolysis followed by enzymatic hydrolysis was only able to achieve a yield of 23.98% with a crystallinity of 57.8%.…”
Section: Fig 2 Xrd Patterns Of Native Cellulose Mn(ii)- and Cr(iimentioning
confidence: 71%
“…An absolute value lying within 0 to ± 15 mV reflects the onset flocculation and agglomeration of nanocellulose (Zhou 2012), whereas the values greater (or lower) than ± 25 mV were generally considered to be relatively stable for mutual repulsion to form a good stability colloidal suspension . In this study, the zeta potential for Mn(II)-and Cr(III)-treated nanocellulose was about ─42.5 and ─44.9 mV, respectively in the aqueous suspensions, thus indicative of the possibility to produce rather stable colloidal suspensions due to sufficient repulsive force.…”
Section: Particle Size Analysis (Dls) and Zeta Potential Analysismentioning
Nanostructured cellulose was successfully prepared from native cellulose using a homogeneous catalytic H2SO4 hydrolysis pathway in the presence of Cr(III)-and Mn(II)-transition metal salts as the co-catalyst. The effect of transition metal salts with different valence states (Cr 3+ and Mn
2+) on the physicochemical properties (chemical characteristics, crystallinity index, nano-structure, thermal stability, and morphology) of prepared nanocellulose was investigated. Interestingly, TEM micrographs showed that the Cr(III)-treated and Mn(II)-treated nanocellulose exhibited a weblike nanostructured-surface with average diameters of 44.7 ± 13.2 nm and 58.4 ± 15.3 nm, respectively. XRD study revealed that the crystallinity of nanocellulose was increased because the catalytic degradation of the less crystalline regions of cellulose occurred at a faster rate than its crystalline phases. Cr(III)-treated nanocellulose was capable of rendering a higher crystallinity index (75.6 ± 0.1%) compared with Mn(II)-treated nanocellulose (72.3 ± 0.4%). Furthermore, a dynamic light scattering (DLS) study revealed that Cr(III)-treated nanocellulose showed a smaller distribution range (92% at 14 to 135 nm) compared with Mn(II)-treated nanocellulose (92% at 607 nm). A higher valence state for the Cr(III)-cation, with a trivalent state (+3), rendered a more effective hydrolysis reaction compared with the Mn(II)-cation, with a divalent state (+2), for preparing the nanocellulose.
“…This result is similar to those reported for palm tree cellulose (84%) ) and microcrystalline cellulose (86%) hydrolyzed by FeCl3 in HCl acidic medium but under higher temperature (91 to 98 o C) and longer hydrolysis duration (4 to 6 h) at optimum hydrolysis conditions. However, all the nanocellulose yields prepared via Cr(III)-and Mn(II)-catalyzed hydrolysis under mild reaction were much more higher than the value reported for the hydrolysis of cellulosic materials including rice straw cellulose (16.9%) (Jiang and Hsieh 2013), microcrystalline cellulose (28.6%) (Zhou 2012), and bamboo bleached fiber (30%) (Brito et al 2012) via H2SO4 (~65 wt.%) hydrolysis procedure. A recent study (Tang et al 2015) conducted by Tang's group found that the yield of nanocellulose produced via phosphoric acid hydrolysis followed by enzymatic hydrolysis was only able to achieve a yield of 23.98% with a crystallinity of 57.8%.…”
Section: Fig 2 Xrd Patterns Of Native Cellulose Mn(ii)- and Cr(iimentioning
confidence: 71%
“…An absolute value lying within 0 to ± 15 mV reflects the onset flocculation and agglomeration of nanocellulose (Zhou 2012), whereas the values greater (or lower) than ± 25 mV were generally considered to be relatively stable for mutual repulsion to form a good stability colloidal suspension . In this study, the zeta potential for Mn(II)-and Cr(III)-treated nanocellulose was about ─42.5 and ─44.9 mV, respectively in the aqueous suspensions, thus indicative of the possibility to produce rather stable colloidal suspensions due to sufficient repulsive force.…”
Section: Particle Size Analysis (Dls) and Zeta Potential Analysismentioning
Nanostructured cellulose was successfully prepared from native cellulose using a homogeneous catalytic H2SO4 hydrolysis pathway in the presence of Cr(III)-and Mn(II)-transition metal salts as the co-catalyst. The effect of transition metal salts with different valence states (Cr 3+ and Mn
2+) on the physicochemical properties (chemical characteristics, crystallinity index, nano-structure, thermal stability, and morphology) of prepared nanocellulose was investigated. Interestingly, TEM micrographs showed that the Cr(III)-treated and Mn(II)-treated nanocellulose exhibited a weblike nanostructured-surface with average diameters of 44.7 ± 13.2 nm and 58.4 ± 15.3 nm, respectively. XRD study revealed that the crystallinity of nanocellulose was increased because the catalytic degradation of the less crystalline regions of cellulose occurred at a faster rate than its crystalline phases. Cr(III)-treated nanocellulose was capable of rendering a higher crystallinity index (75.6 ± 0.1%) compared with Mn(II)-treated nanocellulose (72.3 ± 0.4%). Furthermore, a dynamic light scattering (DLS) study revealed that Cr(III)-treated nanocellulose showed a smaller distribution range (92% at 14 to 135 nm) compared with Mn(II)-treated nanocellulose (92% at 607 nm). A higher valence state for the Cr(III)-cation, with a trivalent state (+3), rendered a more effective hydrolysis reaction compared with the Mn(II)-cation, with a divalent state (+2), for preparing the nanocellulose.
“…Another drawback using nanocellulose fibers is the difficulty to disperse them uniformly in non-polar medium because of their polar surface (Oksman et al 2006). So, most researchers are focused on a water-soluble polymeric matrix, considering the hydrophilic character of cellulose for the easier dispersion of cellulose (Oksman et al 2006;Bondeson and Oksman 2007;Chen et al 2009;Alain Dufresne 2010;Lemahieu et al 2011;Zhou et al 2012;Tang et al 2015;Pracella et al 2014;Trifol et al 2016;Haafiz et al 2016;Ivdre et al 2016;Khoo et al 2016;Sethi et al 2017).…”
A new kind of thermoplastic elastomer nanocomposite reinforced with cellulose nanofibers has been reported. The aim of this investigation was to study the interaction and dispersion of cellulose nanofibers into the Pebax matrix. These copolymers are considered as polyether-b-amide thermoplastic elastomers. They are from renewable resources, and their hydrophilic character allows them to interact with nanocellulose. The interaction and reinforcement effect of nanocellulose at 3 levels of nanocellulose, (1%, 3%, and 5%), were examined by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and other mechanical tests. The results achieved from these tests indicated appropriate effects of cellulose nanofibers for the strong interaction and close contact with the polyamide phase of the Pebax polymer via strong hydrogen bonding.
“…The CNCs were isolated from the cotton linters through acid hydrolysis as previously mentioned (Zhou et al 2012). The cotton linters were immersed in 64 wt.% sulfuric acid solution with a ratio of 1 g/mL to 8.75 g/mL at 45 °C under strong continuous stirring for 1.5 h. The obtained hydrolyzed cellulose was repeatedly washed, via centrifugation (10000 rpm, 10 min) at least 3 ×, and dialyzed against deionized water until the pH of the suspension was near neutral.…”
Section: Preparation Of Cncmentioning
confidence: 99%
“…The heating rate of the films was fairly fast, and the ∆T reached an equilibrium state within 20 s. The temperature equilibrium of AuNPs in the matrix is dominated by the thermodynamic equilibrium process, including a heat-absorbing process caused by the photothermal effect of AuNPs and a heat-losing process such as convection, conduction, etc. (Zhou et al 2012). When the two processes are unbalanced, the ∆T presents either increases or decreases.…”
Cellulose, an abundant natural polysaccharide, can be applied to immobilize particles on the surface due to the presence of ample hydroxyl groups. A series of different sizes and contents of gold nanoparticles (AuNP) were prepared on cellulose nanocrystal (CNC). The obtained AuNP/CNC nanocomposites were then blended with shape-memory polyurethane (SMP) to prepare light-triggered AuNP/CNC/SMP nanocomposites through solvent conversion and a solution casting method. The nanocomposite films were endowed with higher mechanical properties and striking remote-control light-triggered shape-memory properties. Moreover, the CNC in the composites also enhanced the photothermal effect of AuNPs by preventing the aggregation of AuNPs. At the same time, the content of AuNPs with existing CNC had a stronger effect on the elevated temperature (∆T) and the shape-memory properties of films in comparison to the size of the AuNPs.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.