Dynamic crystallization behavior of PA-12/PP-MWCNT nanocomposites: non-isothermal kinetics approach

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Sucharita Sethy ◽  
Saroj Kumar Samantaray ◽  
Bhabani K. Satapathy
Keyword(s):  
Crystallization Behavior ◽  
Crystallization Rate ◽  
Isothermal Kinetics ◽  
Scanning Calorimetry ◽  
Relative Crystallinity ◽  
Mwcnt Content ◽  
Polyamide 12 ◽  
Multi Walled Carbon Nanotubes ◽  
Walled Carbon Nanotubes ◽  
Mwcnt Loading

Abstract The effect of multi-walled carbon nanotubes (MWCNT) loading on the crystallization behavior of matrix polyamide 12 (PA-12), in PA-12/polypropylene-MWCNT (PP-MWCNT)-based nanocomposites were analyzed for their non-isothermal crystallization behavior at various cooling rates of 2.5–20 °C/min in differential scanning calorimetry (DSC). Several kinetic models such as Jeziorny (modified-Avrami), Mo and Tobin models were employed to analyze the crystallization behavioral trend with respect to time and temperature of the nanocomposites. The crystallization rate increased half-time of crystallization with MWCNT content as estimated from the Jeziorny theory. The linear agreement between Jeziorny model and experimental relative crystallinity outperforms the Tobin analysis where the coefficient of linear regression was found to be considerably trailing behind and off the satisfactory mark. The Mo model accounts for the percentage crystallinity and thereby successfully explained the crystallization behavior of PA-12 where the kinetic parameters increased with crystallinity indicating higher cooling rate for higher crystallinity. The MWCNT induced crystallization (nucleation activity) values were close to zero irrespective of MWCNT loading which reiterates the enhanced crystallization (rate) of PA-12 in the nanocomposites. Estimations based on Friedman approach showed inter-relationship between activation energy and crystallinity where the later was found to be governed by major (matrix) PA-12 phase.

Functionalization of Multiwalled Carbon Nanotubes by Poly (Ethlylene Glycol) and Non-Isothermal Crystallization Kinetic Study

2011 ◽  
Vol 688 ◽  
pp. 127-134
Author(s):  
Song Gao ◽  
Kun Yan Sui ◽  
Zhi Ming Wu ◽  
Wen Wen Wu ◽  
Yan Zhi Xia
Keyword(s):  
Carbon Nanotubes ◽  
Crystallization Behavior ◽  
Crystallization Kinetic ◽  
Crystallization Rate ◽  
Avrami Equation ◽  
Nonisothermal Crystallization ◽  
Multiwalled Carbon ◽  
Multi Walled Carbon Nanotubes ◽  
Walled Carbon Nanotubes ◽  
Kinetics Of

Multi-walled carbon nanotubes (MWNT) were successfully chemically modified (MWNT-COOH) and reacted with polyethylene glycol (PEG) to prepare nanocomposites. As- prepared kinds of functionalized MWNT (MWNT-g-PEG) were characterized with FTIR, TGA and TEM. Nonisothermal crystallization kinetics of MWNT-g-PEG composites was investigated by differential scanning calorimeter (DSC). The kinetics was analyzed using the Ozawa and Avrami equation modified by Jeziorny. The results showed that the Ozawa approach failed to describe the crystallization behavior of nanocomposites, whereas the modified Avrami analysis could explain the behavior of MWNT-g-PEG nanocomposite only. It is observed that the presence of MWNT hindered the mobility of PEG chains and decreased the overall crystallization rate. It was found that the crystallization behavior of MWNT-g-PEG nanocomposite was strongly affected by the incorporation of MWNT. The data for the nonisothermal crystallization could be analyzed properly by the Avrami equation modified by Jeziorny. The results showed that the presence of MWNT decreased the overall nonisothermal crystallization rate of the PEG chains which were grafted onto the MWNT due to MWNT might act as physical hindrances retarding the mobility of PEG chains and decreased the crystallinity.

Cure and Dynamic-Mechanical Behaviors of Vinyl Ester Resinfilled with Multi-Walled Carbon Nanotubes

2010 ◽  
Vol 150-151 ◽  
pp. 1413-1416 ◽  
Author(s):  
Hong Yan Chen ◽  
Zhen Xing Kong ◽  
Ji Hui Wang
Keyword(s):  
Carbon Nanotubes ◽  
Vinyl Ester ◽  
Mechanical Response ◽  
Cure Kinetics ◽  
Crosslinking Density ◽  
Vinyl Ester Resin ◽  
Scanning Calorimetry ◽  
Dynamic Mechanical ◽  
Multi Walled Carbon Nanotubes ◽  
Walled Carbon Nanotubes

The cure kinetics of Derakane 411-350, a kind of vinyl ester resin, and its suspensions containing multi-walled carbon nanotubes( MWCNTs) were investigated via non-isothermal dynamic scanning calorimetry (DSC) measurements. The results showed that incorporation of MWCNTs into vinyl ester resin excessively reduces polymerization degree and crosslinking density of vinyl ester resin. For suppressing the negative effect caused by nanotubes, the higher temperature initiator combined with the initiator MEKP was used. Dynamic-mechanical Behavior testing was then carried out on the cured sample in order to relate the curing behavior of MWCNTs modified resin suspensions to mechanical response of their resulting nanocomposites. It was revealed that nanocomposites containing MWCNTs possessed larger storage modulus values as well as higher glass transition temperatures (Tg) as compared to those without MWCNTs after using mixed intiators system to improve the degree of cure.

Experimental Investigation of Morphological and Electrical Characteristics of PS/MWCNT Nanocomposite Films

2018 ◽  
Vol 915 ◽  
pp. 104-109
Author(s):  
Barış Demirbay ◽  
Şaziye Uğur
Keyword(s):  
Annealed Film ◽  
Nanocomposite Films ◽  
Electrical Characteristics ◽  
Liquid Form ◽  
Mwcnt Content ◽  
Electrical Percolation ◽  
Glass Substrates ◽  
Multi Walled Carbon Nanotubes ◽  
Electrical Percolation Threshold ◽  
Walled Carbon Nanotubes

Electrical characteristics and morphology of nanocomposite films composed of two different polystyrene (PS) latexes impregnated with multi-walled carbon nanotubes (MWCNT) in the range between 0 wt% and 20 wt% were assessed by considering photon transmission (UV-Vis) technique and electrical conductivity measurements. Emulsion polymerization technique was employed both to synthesize very fine PS particles dispersed in water and to tailor the sizes of the PS particles as 382 nm and 560 nm, respectively. PS/MWCNT nanocomposite films were obtained from the liquid form on glass substrates via drop-casting method and all they dried at 40 QUOTE C. Each dried sample was then annealed at varying temperatures between 100 QUOTE C and 250 QUOTE C for 10 min. The surface conductivity QUOTE of each annealed film at 250 QUOTE C was measured and was found to increase dramatically above a certain mass fraction of MWCNT content, QUOTE . Each set of PS/MWCNT nanocomposite film had a similar electrical percolation threshold of QUOTE =1.5 wt% as the MWCNT content and critical exponents of QUOTE were found to be 2.64 and 1.19 for 382 nm and 560 nm PS latex systems, respectively.

The non-isothermal crystallization behavior of polyamide 6 and polyamide 6/HDPE/MAH/L-101 composites

2019 ◽  
Vol 39 (2) ◽  
pp. 124-133 ◽  
Author(s):  
Bingxiao Liu ◽  
Guosheng Hu ◽  
Jingting Zhang ◽  
Zhongqiang Wang
Keyword(s):  
Crystallization Kinetics ◽  
Isothermal Crystallization ◽  
Crystallization Behavior ◽  
Isothermal Condition ◽  
Crystallization Rate ◽  
Polyamide 6 ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Analysis And Design ◽  
Processing Techniques

AbstractStudy of the crystallization kinetics is particularly necessary for the analysis and design of processing operations, especially the non-isothermal crystallization behavior, which is due to the fact that most practical processing techniques are carried out under non-isothermal conditions. The non-isothermal crystallization behaviors of polyamide 6 (PA6) and PA6/high-density polyethylene/maleic anhydride/2,5-dimethyl-2,5-di(tert-butylperoxy)hexane (PA6/HDPE/MAH/L-101) composites were investigated by differential scanning calorimetry (DSC). The crystallization kinetics under non-isothermal condition was analyzed by the Jeziorny and Mo equations, and the activation energy was determined by the Kissinger and Takhor methods. The crystal structure and morphology were analyzed by wide-angle X-ray diffraction (WXRD) and polarized optical microscopy (POM). The results indicate that PA6/HDPE/MAH/L-101 has higher crystallization temperature and crystallization rate, which is explained as due to its heterogeneous nuclei.

Role of interfacial interaction on the crystallization behavior and melting characteristics of PP/Nano-CaCO3 composites modified with different compatibilizers

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Yuhai Wang ◽  
Hao Shen ◽  
Gu Li ◽  
Kancheng Mai
Keyword(s):  
Synergistic Effect ◽  
Heterogeneous Nucleation ◽  
Crystallization Temperature ◽  
Crystallization Behavior ◽  
Crystallization Rate ◽  
Interfacial Interaction ◽  
Scanning Calorimetry ◽  
Polar Groups ◽  
Melting Characteristics

AbstractPP/nano-CaCO3 composites with different interfacial interaction were prepared by addition of compatibilizers with the same polar groups but different backbones. The non-isothermal and isothermal crystallization behavior of PP/nano- CaCO3 composites was investigated using differential scanning calorimetry (DSC). The results indicated that the interfacial interaction between PP and nano-CaCO3 increased the crystallization temperature and crystallization rate of PP due to the heterogeneous nucleation of nano-CaCO3. The interfacial interaction between nano- CaCO3 and compatibilizer further increased the crystallization temperature and crystallization rate of PP and induced the formation of β-crystal of PP due to the synergistic effect of heterogeneous nucleation between nano-CaCO3 and compatibilizer. This synergistic effect of heterogeneous nucleation between nano- CaCO3 and compatibilizer depended on the interfacial interaction between compatibilizer and PP matrix. The increased compatibility between compatibilizer and PP matrix favoured the heterogeneous nucleation between nano-CaCO3 and compatibilizer

Compression Moulding of Thermoplastic Nanocomposites Filled with MWCNT

2017 ◽  
Vol 25 (8) ◽  
pp. 611-620 ◽  
Author(s):  
Fabrizio Quadrini ◽  
Denise Bellisario ◽  
Loredana Santo ◽  
Felicia Stan ◽  
Fetecau Catalin
Keyword(s):  
Carbon Nanotubes ◽  
Differential Scanning Calorimetry ◽  
Filler Content ◽  
Thermoplastic Polyurethane ◽  
Mechanical Tests ◽  
Compression Moulding ◽  
Scanning Calorimetry ◽  
Melt Mixing ◽  
Multi Walled Carbon Nanotubes ◽  
Walled Carbon Nanotubes

Multi-walled carbon-nanotubes (MWCNTs) were melt-mixed with three different thermoplastic matrices (polypropylene, PP, polycarbonate, PC, and thermoplastic polyurethane, TPU) to produce nanocomposites with three different filler contents (1, 3, and 5 wt.%). Initial nanocomposite blends (in the shape of pellets) were tested under differential scanning calorimetry to evaluate the effect of the melt mixing stage. Nanocomposite samples were produced by compression moulding in a laboratory-scale system, and were tested with quasi-static (bending, indentation), and dynamic mechanical tests as well as with friction tests. The results showed the effect of the filler content on the mechanical and functional properties of the nanocomposites. Compression moulding appeared to be a valuable solution to manufacture thermoplastic nanocomposites when injection moulding leads to loss of performance. MWCNT-filled thermoplastics could be used also for structural and functional uses despite, the present predominance of electrical applications.

Nucleating effect of surface modified MWNTs on crystallization of MWNTs/PA6 composites

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Juan Li ◽  
Qun Gu ◽  
Xinyu Fan ◽  
Zhenghong Guo ◽  
Zhengping Fang
Keyword(s):  
Polyamide 6 ◽  
Surface Characteristic ◽  
Crystalline Form ◽  
Scanning Calorimetry ◽  
Amino Functionalization ◽  
Before And After ◽  
Multi Walled Carbon Nanotubes ◽  
Surface Modified ◽  
Walled Carbon Nanotubes ◽  
Nucleating Effect

AbstractThe surface characteristic of multi-walled carbon nanotubes (MWNTs) plays an important role in the crystallization of polyamide 6 (PA6). In this paper, 1,6-hexamethylenediamine(HMD) are grafted on MWNTs. The MWNTs before and after modification are used to fabricate PA6 composites through melt-blending. The nucleating effect of MWNTs with different surface characteristic is investigated by differential scanning calorimetry (DSC), polarized optical microscopy (POM) and Xray diffraction (XRD).The heterogeneous nucleating ability of MWNTs determined by the Dobreva method are higher for pristine than amine-functionalized MWNTs/PA6 composites with 1.0 wt% MWNTs. Addition of MWNTs induce more heterogeneous nucleation and retards the crystal growth of PA6. The presence of MWNTs facilitates the formation of α crystalline form, while amino-functionalization weakens this trend. MWNTs act as effective nucleation agents for PA6, resulting in the increased number and decreased size of spherulites. MWNTs facilitate the formation of α crystalline form of PA6. Amino-functionalization decreases the crystallization and nucleating effect of MWNTs on PA6

Non-isothermal crystallization behavior of polypropylene/zinc oxide composites

2016 ◽  
Vol 23 (5) ◽  
pp. 505-510 ◽  
Author(s):  
Jianqiang Fang ◽  
Minghua Lang ◽  
Xuchu Ye ◽  
Wei Zhang ◽  
Kongjun Zhu
Keyword(s):  
Activation Energy ◽  
Zinc Oxide ◽  
Isothermal Crystallization ◽  
Crystallization Behavior ◽  
Crystallization Kinetic ◽  
Exothermic Peak ◽  
Crystallization Time ◽  
Scanning Calorimetry ◽  
Relative Crystallinity ◽  
Oxide Composites

AbstractThe non-isothermal crystallization behavior of polypropylene (PP)/zinc oxide composites with various mass ratios was investigated by differential scanning calorimetry. The Jeziorny and Mo models were applied to calculate the non-isothermal crystallization kinetic parameters of the composites. During non-isothermal crystallization, the width of the exothermic peak increased from 7°C to 12°C with increasing cooling rate. The exothermic peak position at 10°C shifted to a lower temperature, and the half crystallization time t1/2 decreased from 2.86 min to 0.51 min. The Friedman model was used to determine the variation of activation energy at each stage of crystallization. The crystallization activation energies obtained varied significantly at each stage of crystallization. The crystallization activation energy of PP was -126.8 kJ/mol at 70% relative crystallinity but reached -232.8 kJ/mol at 10% relative crystallinity.

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