scholarly journals Non-Isothermal Crystallisation Kinetics of Carbon Black- Graphene-Based Multimodal-Polyethylene Nanocomposites

Nanomaterials ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 110 ◽  
Author(s):  
Ibrahim Ahmad ◽  
Hyun-Kyung Kim ◽  
Suleyman Deveci ◽  
R. Kumar

The effect of carbon black (CB) and microwave-induced plasma graphene (g) on the crystallisation kinetics of the multimodal high-density polyethylene was studied under non-isothermal conditions. The non-isothermal crystallisation behaviour of the multimodal-high-density polyethylene (HDPE), containing up to 5 wt.% graphene, was compared with that of neat multimodal-HDPE and its carbon black based nanocomposites. The results suggested that the non-isothermal crystallisation behaviour of polyethylene (PE)-g nanocomposites relied significantly on both the graphene content and the cooling rate. The addition of graphene caused a change in the mechanism of the nucleation and the crystal growth of the multimodal-HDPE, while carbon black was shown to have little effect. Combined Avrami and Ozawa equations were shown to be effective in describing the non-isothermal crystallisation behaviour of the neat multimodal-HDPE and its nanocomposites. The mean activation energy barrier (ΔE), required for the transportation of the molecular chains from the melt state to the growing crystal surface, gradually diminished as the graphene content increased, which is attributable to the nucleating agent effect of graphene platelets. On the contrary, the synergistic effect resulting from the PE-CB nanocomposite decreased the ΔE of the neat multimodal-HDPE significantly at the lowest carbon black content.

Nanomaterials ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 392 ◽  
Author(s):  
Ibrahim Ahmad ◽  
Hyun-Kyung Kim ◽  
Suleyman Deveci ◽  
R. Kumar

In the published paper [1], there was a typo error mistake in Equation (5), which was supposed to be expressed as “ log Z t + n log t = log K T − m log Φ ” instead of “log Zt + n log t = log KT − ml” [...]


2014 ◽  
Vol 97 ◽  
pp. 34-40 ◽  
Author(s):  
Shaodi Zheng ◽  
Jie Deng ◽  
Luqiong Yang ◽  
Danqi Ren ◽  
Shinlin Huang ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 3396
Author(s):  
Luboš Běhálek ◽  
Jan Novák ◽  
Pavel Brdlík ◽  
Martin Borůvka ◽  
Jiří Habr ◽  
...  

The physical properties and non-isothermal melt- and cold-crystallisation kinetics of poly (l-lactic acid) (PLLA) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) biobased polymers reprocessed by mechanical milling of moulded specimens and followed injection moulding with up to seven recycling cycles are investigated. Non-isothermal crystallisation kinetics are evaluated by the half-time of crystallisation and a procedure based on the mathematical treatment of DSC cumulative crystallisation curves at their inflection point (Kratochvil-Kelnar method). Thermomechanical recycling of PLLA raised structural changes that resulted in an increase in melt flow properties by up to six times, a decrease in the thermal stability by up to 80 °C, a reduction in the melt half-time crystallisation by up to about 40%, an increase in the melt crystallisation start temperature, and an increase in the maximum melt crystallisation rate (up to 2.7 times). Furthermore, reprocessing after the first recycling cycle caused the elimination of cold crystallisation when cooling at a slow rate. These structural changes also lowered the cold crystallisation temperature without impacting the maximum cold crystallisation rate. The structural changes of reprocessed PHBV had no significant effect on the non-isothermal crystallisation kinetics of this material. Additionally, the thermomechanical behaviour of reprocessed PHBV indicates that the technological waste of this biopolymer is suitable for recycling as a reusable additive to the virgin polymer matrix. In the case of reprocessed PLLA, on the other hand, a significant decrease in tensile and flexural strength (by 22% and 46%, respectively) was detected, which reflected changes within the biobased polymer structure. Apart from the elastic modulus, all the other thermomechanical properties of PLLA dropped down with an increasing level of recycling.


2020 ◽  
Vol 869 ◽  
pp. 229-233
Author(s):  
Timur A. Borukaev ◽  
Abubekir Kh. Shaov ◽  
Raisa D. Archakova ◽  
Zakhirat Kh. Sultigova

The influence of carbon black on the deformation-strength properties of high density polyethylene is considered. It was found that the deformation-strength properties of the polymer matrix change over the entire range of the filler content. The amount of carbon black that can be introduced into high-density polyethylene and obtained a composite material with the optimal combination of stiffness, strength and ductility is established. It was shown that the change in the deformation-strength properties of composites is due to the behavior and influence of carbon black particles on the structure of the polymer matrix.


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