blend nanocomposites
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Author(s):  
Aswathi Madathinal Kunjappan ◽  
Arunima Reghunadhan ◽  
Ajitha A. Ramachandran ◽  
Lovely Mathew ◽  
Moothetty Padmanabhan ◽  
...  

Author(s):  
Srinivas Yekkala ◽  
Madhukar Katakam ◽  
Ramesh Suramoni ◽  
Mohan Babu Nandru

2021 ◽  
pp. 089270572110462
Author(s):  
MT Ramesan ◽  
M Subburaj ◽  
G Mathew ◽  
BK Bahuleyan

This work focused on the preparation of biopolymer blend nanocomposites from chitin (CT) and cashew tree gum (CTG) with different contents of copper sulphide nanoparticles (CuS) by solution casting method. The formation of nanocomposites have been characterized by FT infrared (FTIR), UV spectroscopy, X-ray diffraction (XRD), scanning electron microscope (SEM), high-resolution transmission electron microscope (HRTEM), thermogravimetry (TGA), differential scanning calorimetry (DSC) and impedance analysis. The characteristic absorption of nanoparticles in the FTIR spectra and shift in UV spectra of blend composites revealed the strong interaction between CuS nanoparticles and the polar segments of CT/CTG blend. With the increase in dosage of nanoparticles, a decrease in amorphous domains has been noted in the XRD scans. The uniform distribution of nanoparticles in CT/CTG network has been confirmed by the SEM analysis. HRTEM of the blend composites reveals the formation of hemispherical nanoparticles with a diameter of 15–30 nm. The glass transition temperature of blend composites increased with the addition of nano-CuS in the polymer matrix. Compared to the pure CT/CTG blend, the prepared nanocomposite showed higher thermal stability. Mechanical properties such as tensile strength and hardness of the blend nanocomposites were greatly enhanced by the reinforcement of CuS into the CT/CTG matrix. The AC conductivity and dielectric properties of the nanocomposites increased with the concentration of fillers and the magnitude of these properties was higher than the pure polymer blend.


2021 ◽  
Vol 63 (5) ◽  
pp. 598-605
Author(s):  
Sohini Chakraborty ◽  
Mekha Mariam Mathew ◽  
Remya Simon ◽  
Nisha George ◽  
Anoop Vadakkekara ◽  
...  

Author(s):  
Alif Walong ◽  
Bencha Thongnuanchan ◽  
Nattapon Uthaipan ◽  
Tadamoto Sakai ◽  
Natinee Lopattananon

Flame retardant rubber foams of ethylene vinyl acetate (EVA)/natural rubber (NR)/layered silicate blends filled with silicon dioxide (SiO2) were prepared by using azodicarbonamide (ADC) as a blowing agent. Specifically, SiO2 was added in EVA/NR blend nanocomposites to produce good flame retardant foams. The properties of EVA/NR blend nanocomposite foams with different SiO2 loading (0, 20, 30, 40 parts per hundred rubber, phr) were investigated through transmission electron microscopy (TEM), scanning electron microscopy (SEM), rheological property test, mechanical property measurement, flammability tests, thermogravimetry analysis (TGA) and pyrolysis-gas chromatography-mass spectrometry (Pyrolysis-GC-MS). Compared with the simple EVA/NR blend nanocomposite, the added SiO2 increased the blend compatibility between EVA and NR phases and melt strength/viscosity of the EVA/NR blend nanocomposites, thus promoting cellular structure of the EVA/NR nanocomposite foams. Increasing SiO2 loading resulted in higher cell density, smaller cell size, and lower volume of void. These improvements caused higher strength and elastomeric recovery. The LOI test results showed that flame retardancy of the EVA/NR blend nanocomposite foams increased at higher SiO2 loading as a result of formation of insulation silicon dioxide-based char. TGA and pyrolysis-GC-MS analyses also validated the finding that the silicon dioxide-based char in the foamed samples containing higher SiO2 loading was more effective on improving thermal stability, which was responsible for lower material combustibility and better flame retardancy. Based on our finding, it was concluded that a good flame retardant EVA/NR blend nanocomposite foam with the best improvement in strength and elastomeric recovery was achieved when combined with 40 phr SiO2.


Materials ◽  
2021 ◽  
Vol 14 (17) ◽  
pp. 4813
Author(s):  
Lilian Azubuike ◽  
Uttandaraman Sundararaj

The process of strengthening interfaces in polymer blend nanocomposites (PBNs) has been studied extensively, however a corresponding significant enhancement in the electrical and rheological properties is not always achieved. In this work, we exploit the chemical reaction between polystyrene maleic anhydride and the amine group in nylon (polyamide) to achieve an in-situ compatibilization during melt processing. Herein, nanocomposites were made by systematically adding polystyrene maleic anhydride (PSMA) at different compositions (1–10 vol%) in a two-step mixing sequence to a Polystyrene (PS)/Polyamide (aPA) blend with constant composition ratio of 25:75 (PS + PSMA:aPA) and 1.5 vol% carbon nanotube (CNT) loading. The order of addition of the individual components was varied in two-step mixing procedure to investigate the effect of mixing order on morphology and consequently, on the final properties. The electrical and rheological properties of these multiphase nanocomposite materials were investigated. The optical microscope images show that for PS/aPA systems, CNTs preferred the matrix phase aPA, which is the thermodynamically favorable phase according to the wettability parameter calculated using Young’s equation. However, aPA’s great affinity for CNT adversely influenced the electrical properties of our blend. Adding PSMA to PS/aPA changed the structure of the droplet phase significantly. At 1.5 vol% CNT, a more regular and even distribution of the droplet domains was observed, and this produced a better framework to create more CNT networks in the matrix, resulting in a higher conductivity. For example, with only 1.5 vol% CNT in the PBN, at 3 vol% PSMA, the conductivity was 7.4 × 10−2 S/m, which was three and a half orders of magnitude higher than that seen for non-reactive PS/aPA/CNT PBN. The mechanism for the enhanced conductive network formation is delineated and the improved rheological properties due to the interfacial reaction is presented.


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