Mechanical and thermal properties of nanocomposite films based on an aromatic polyimide and carbon nanocones

2011 ◽  
Vol 53 (7) ◽  
pp. 1509-1515 ◽  
Author(s):  
I. V. Gofman ◽  
I. V. Abalov ◽  
V. E. Yudin ◽  
V. G. Tiranov
2020 ◽  
Vol 41 (12) ◽  
pp. 5182-5194
Author(s):  
Xiaolong Lu ◽  
Pranjal Nautiyal ◽  
Jenniffer Bustillos ◽  
Archana Loganathan ◽  
Cheng Zhang ◽  
...  

2017 ◽  
Vol 27 (6) ◽  
pp. 1778-1786 ◽  
Author(s):  
Xiangwen Wang ◽  
Yong Fan ◽  
Hao Chen ◽  
Ruixiao Yang ◽  
Wei Zhao

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.


2020 ◽  
Vol 221 (12) ◽  
pp. 2000085 ◽  
Author(s):  
Zhigeng Chen ◽  
Sen Zhang ◽  
Qi Feng ◽  
Yancheng Wu ◽  
Shumei Liu ◽  
...  

KIMIKA ◽  
2016 ◽  
Vol 27 (1) ◽  
pp. 22-28
Author(s):  
David Jr. P. Penaloza

In this work, the mechanical and thermal properties of nanocomposite films prepared from the surface-initiated polymerization of norbornene mediated by a surface-bound ruthenium alkylidine catalyst were investigated. Thermal gravimetric and dynamic mechanical analyses revealed enhanced properties of the resulting nanocomposite films over that of the unfilled polymer.


2016 ◽  
Vol 12 (1) ◽  
pp. 37-48 ◽  
Author(s):  
Nooshin Noshirvani ◽  
Babak Ghanbarzadeh ◽  
Hadi Fasihi ◽  
Hadi Almasi

Abstract The goal of this work was to compare the barrier, mechanical, and thermal properties of two types of starch–polyvinyl alcohol (PVA) nanocomposites. Sodium montmorillonite (MMT) and nanocrystalline cellulose were chosen as nanoreinforcements. X-ray diffraction (XRD) test showed well-distributed MMT in the starch–PVA matrix, possibly implying that the clay nanolayers formed an exfoliated structure. The moisture sorption, solubility and water vapor permeability (WVP) studies revealed that the addition of MMT and nanocrystalline cellulose reduced the moisture affinity of starch–PVA biocomposite. At the level of 7 % MMT, the nanocomposite films showed the highest ultimate tensile strength (UTS) (4.93 MPa) and the lowest strain to break (SB) (57.65 %). The differential scanning calorimetry (DSC) results showed an improvement in thermal properties for the starch–PVA–MMT nanocomposites, but not for the starch–PVA–NCC nanocomposites. Results of this study demonstrated that the use of MMT in the fabrication of starch–PVA nanocomposites is more favorable than that of nanocrystalline cellulose to produce a desirable biodegradable film for food packaging applications.


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