Cellulose nanofibrils in bio-nanocomposite films and their applications

2021 ◽  
pp. 173-189
Author(s):  
Jonathan Orasugh ◽  
Swapan Ghosh ◽  
Dipankar Chattopadhyay
2015 ◽  
Vol 7 (45) ◽  
pp. 25464-25472 ◽  
Author(s):  
Hong Dong ◽  
Yelena R. Sliozberg ◽  
James F. Snyder ◽  
Joshua Steele ◽  
Tanya L. Chantawansri ◽  
...  

2013 ◽  
Vol 829 ◽  
pp. 534-538 ◽  
Author(s):  
Alireza Shakeri ◽  
Sattar Radmanesh

Cellulose nanofibrils ( NF ) have several advantages such as biodegradability and safety toward human health. Zein is a biodegradable polymer with potential use in food packaging applications. It appears that polymer nanocomposites are one of the most promising applications of zein films. Cellulose NF were prepared from starting material Microcrystalline cellulose (MCC) by an application of a high-pressure homogenizer at 20,000 psi and treatment consisting of 15 passes. Methods such as atomic force microscopy were used for confirmation of nanoscale size production of cellulose. The average diameter 45 nm were observed. Zeincellulose NF nanocomposite films were prepared by casting ethanol suspensions of Zein with different amounts of cellulose NF in the 0% to 5%wt. The nanocomposites were characterized by using Fourier transform infrared spectroscopy ( FTIR ), Atomic force microscopy ( AFM ) and X-ray diffraction ( XRD ) analysis. From the FTIR spectra the various groups present in the Zein blend were monitored. The homogeneity, morphology and crystallinity of the blends were ascertained from the AFM and XRD data, respectively. The thermal resistant of the zein nanocomposite films improved as the nanocellulose content increased. These obtained materials are transparent, flexible and present significantly better physical properties than the corresponding unfilled Zein films.


2021 ◽  
Author(s):  
Anna A. Luginina ◽  
Sergey V. Kuznetsov ◽  
Vladimir K. Ivanov ◽  
Valery V. Voronov ◽  
Alexey D. Yapryntsev ◽  
...  

Abstract Luminescent nanocomposite films, containing SrF 2 :Но up-conversion particles, were prepared by two different protocols from aqueous dispersions of TEMPO-oxidized cellulose nanofibrils (TOCNF) functionalized with 3-aminopropyltriethoxysilane (APS) without the use of organic solvents at pH = 4.0-4.5 and 9.0-9.5, respectively. Proposed synthetic protocols included formation of the films by drying the dispersions containing pre-hydrolyzed APS adsorbed onto TOCNF and SrF 2 :Но particles followed by heating at 105 °C. Hydrophobic (water contact angle 101 ± 2°), strong, and translucent TOCNF/SrF 2 :Но-APS films were prepared by casting from a solution at pH = 4.0-4.5. Scanning electron microscopy, energy-dispersive X-ray spectroscopy with element mapping, Fourier-transform infrared spectroscopy, X-ray diffraction methods confirmed homogeneous distribution of up-conversion particles in TOCNF matrices as well as the grafting of linear polysiloxanes via the condensation of silanol groups and OH-groups on the surface of TOCNF. Differential scanning calorimetry and thermogravimetry data confirmed an increase in thermal stability of the APS modified nanocomposite films obtained at pH = 4.0-4.5. Hydrophobic TOCNF/SrF 2 :Но-APS nanocomposite films exhibited an intense red luminescence in the visible spectrum range ( 5 I 7 level excitation of Ho 3+ ions with 1912 nm laser irradiation) as well as two-times higher laser damage threshold compared to unmodified TOCNF/SrF 2 :Но films. TOCNF/SrF 2 :Но films can be used for visualization 2 μm laser radiation in medicine and long-distance atmosphere monitoring.


2019 ◽  
Vol 20 (10) ◽  
pp. 2127-2139 ◽  
Author(s):  
Madhuri Lakhane ◽  
Megha Mahabole ◽  
Kashinath Bogle ◽  
Rajendra Khairnar ◽  
Vanja Kokol

2014 ◽  
Vol 104 ◽  
pp. 143-150 ◽  
Author(s):  
Jiangqi Zhao ◽  
Xu He ◽  
Yaru Wang ◽  
Wei Zhang ◽  
Xinxing Zhang ◽  
...  

Holzforschung ◽  
2016 ◽  
Vol 70 (12) ◽  
pp. 1125-1134 ◽  
Author(s):  
Vesna Žepič ◽  
Ida Poljanšek ◽  
Primož Oven ◽  
Matjaž Čop

Abstract Freeze dried nanofibrils were acetylated in a heterogeneous system with acetic anhydride, pyridine, and dimethylformamide and the obtained acetylated cellulose nanofibrils (CNFac) were combined with poly(lactic acid) (PLA) to a composite. CNFac with its partially hydrophobic surface showed a good compatibility with PLA resulting in composite films with improved properties. Tensile strength (TS), modulus of elasticity (MOE), and elongation at break (EB) of PLA/CNF increased significantly when 2–5% of CNFac was added to the PLA matrix, while the addition of 10% and higher amounts CNFac decreased the EB at a higher TS and MOE. Mechanical parameters did not improve in the case of unmodified CNF addition. The addition of CNFac maintained transparency and had absorbance values between those of pure PLA film and PLA film with 2% CNF, while films formed with the addition of 5 and 10% of CNF were less transparent. The addition of CNF did not essentially affect the thermal properties of nanocomposite films. The addition of 2–10% of CNFac increased the enthalpy and maximal temperature of cold crystallization as opposed to higher loading of CNFac. The results of differential scanning calorimetry (DSC) coincide with those of the mechanical properties. Tailoring properties of PLA/CNF are only reproducible in case of homogenously distributed CNF within the PLA matrix and by an improved interphase adhesion between PLA and CNFac.


Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1460
Author(s):  
Mohamad Ridzuan Amri ◽  
Chuah Teong Guan ◽  
Syeed Saifulazry Osman Al-Edrus ◽  
Faizah Md Yasin ◽  
Siti Fatahiyah Mohamad

The objective of this work was to study the influence of cellulose nanofibrils (CNF) on the physical, mechanical, and thermal properties of Jatropha oil-based waterborne polyurethane (WBPU) nanocomposite films. The polyol to produce polyurethane was synthesized from crude Jatropha oil through epoxidation and ring-opening method. The chain extender, 1,6-hexanediol, was used to improve film elasticity by 0.1, 0.25, and 0.5 wt.% of CNF loading was incorporated to enhance film performance. Mechanical performance was studied using a universal test machine as specified in ASTM D638-03 Type V and was achieved by 0.18 MPa at 0.5 wt.% of CNF. Thermal gravimetric analysis (TGA) was performed to measure the temperature of degradation and the chemical crosslinking and film morphology were studied using Fourier-transform infrared spectroscopy (FTIR) and field emission scanning electron microscopy (FESEM). The results showed that when the CNF was incorporated, it was found to enhance the nanocomposite film, in particular its mechanical and thermal properties supported by morphology. Nanocomposite film with 0.5 wt.% of CNF showed the highest improvement in terms of tensile strength, Young’s modulus, and thermal degradation. Although the contact angle decreases as the CNF content increases, the effect on the water absorption of the film was found to be relatively small (<3.5%). The difference between the neat WPBU and the highest CNF loading film was not more than 1%, even after 5 days of being immersed in water.


Nanomaterials ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 1121 ◽  
Author(s):  
Shuangxi Nie ◽  
Yuehua Zhang ◽  
Linmao Wang ◽  
Qin Wu ◽  
Shuangfei Wang

Nanocomposites consisting of cellulose nanofibrils (CNFs) and nano-aluminum nitride (AlN) were prepared using a simple vacuum-assisted filtration process. Bleached sugarcane bagasse pulp was treated with potassium hydroxide and sodium chlorite, and was subsequently ultra-finely ground and homogenized to obtain CNFs. Film nanocomposites were prepared by mixing CNFs with various AlN amounts (0–20 wt.%). X-ray diffraction revealed that the crystal form of CNF-AlN nanocomposites was different to those of pure CNFs and AlN. The mechanical performance and thermal stability of the CNF-AlN nanocomposites were evaluated through mechanical tests and thermogravimetric analysis, respectively. The results showed that the CNF-AlN nanocomposites exhibited excellent mechanical and thermal stability, and represented a green renewable substrate material. This type of nanocomposite could present great potential for replacing traditional polymer substrates, and could provide creative opportunities for designing and fabricating high-performance portable electronics in the near future.


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