scholarly journals Thermomechanical and Morphological Studies of CFRP Tested in Different Environmental Conditions

Materials ◽  
2018 ◽  
Vol 12 (1) ◽  
pp. 63 ◽  
Author(s):  
Claudia Barile ◽  
Caterina Casavola ◽  
Paramsamy Vimalathithan ◽  
Marco Pugliese ◽  
Vincenzo Maiorano
Keyword(s):  
Activation Energy ◽  
Thermal Degradation ◽  
Mass Loss ◽  
Environmental Conditions ◽  
Degradation Kinetics ◽  
Fiber Reinforced Polymers ◽  
Thermal Degradation Kinetics ◽  
Morphological Studies ◽  
Significant Difference ◽  
Kinetics Of

The present work describes the mechanical characterization combined with the thermal degradation kinetics of Carbon Fiber Reinforced Polymers (CFRP). The thermal degradation kinetics of CFRP have never been studied in the past. In that regard, the present work focuses on studying the thermal degradation kinetics of CFRP tested mechanically at different environmental conditions. Tensile tests were performed on the specimens with different lay-ups at room temperature, elevated temperature (71 °C), and cryogenic conditions (−54 °C), and the same specimens were used for thermal degradation kinetic studies. Mechanical tests show different responses respect to the different environmental conditions and different fibers orientation. On the other hand, the thermogravimetric results, mass loss, and derivative mass loss, show no significant difference in the degradation of CFRP tested at different temperatures. However, the thermal degradation kinetics shows more insight into the degradation pattern of the materials. The activation energy of degradation shows that the degradation of materials subjected to elevated conditions increases rapidly in the later stages of degradation, suggesting the formation of high char yield. The varying activation energy has been related to different degradation mechanisms. Lastly, the morphology of the materials was studied under SEM to understand the structural change in the material after tested in different weather conditions.

Non-isothermal crystallization and thermal degradation kinetics of MXene/linear low-density polyethylene nanocomposites

e-Polymers ◽  
2017 ◽  
Vol 17 (5) ◽  
pp. 373-381 ◽  
Author(s):  
Xinxin Cao ◽  
Mengqi Wu ◽  
Aiguo Zhou ◽  
You Wang ◽  
Xiaofang He ◽  
...  
Keyword(s):  
Activation Energy ◽  
Thermal Stability ◽  
Thermal Degradation ◽  
Isothermal Crystallization ◽  
Degradation Kinetics ◽  
Thermal Degradation Kinetics ◽  
Low Density Polyethylene ◽  
Low Density ◽  
Linear Low Density Polyethylene ◽  
Kinetics Of

AbstractA novel two-dimensional material MXene was used to synthesize nanocomposites with linear low-density polyethylene (LLDPE). The influence of MXene on crystallization and thermal degradation kinetics of LLDPE was investigated. Non-isothermal crystallization kinetics was investigated by using differential scanning calorimetry (DSC). The experimental data was analyzed by Jeziorny theory and the Mo method. It is found that MXene acted as a nucleating agent during the non-isothermal crystallization process, and 2 wt% MXene incorporated in the nanocomposites could accelerate the crystallization rate. Findings from activation energy calculation for non-isothermal crystallization came to the same conclusion. Thermal gravity (TG) analysis of MXene/LLDPE nanocomposites was conducted at different heating rates, and the TG thermograms suggested the nanocomposites showed an improvement in thermal stability. Apparent activation energy (Ea) of thermal degradation was calculated by the Kissinger method, and Ea values of nanocomposites were higher than that of pure LLDPE. The existence of MXene seems to lead to better thermal stability in composites.

Effect of Pd Nanoparticle on the Thermal Degradation Kinetics of Nylon 6/Pd Nanocomposite Prepared by a Dry Process

2012 ◽  
Vol 486 ◽  
pp. 27-33 ◽  
Author(s):  
Jae Young Lee ◽  
Sung Wan Hong ◽  
Kyeong Sik Han ◽  
Taeck Hong Lee ◽  
Hong Ki Lee
Keyword(s):  
Activation Energy ◽  
Thermal Degradation ◽  
Degradation Kinetics ◽  
Pd Nanoparticles ◽  
Nylon 6 ◽  
Thermal Degradation Kinetics ◽  
Heating Rates ◽  
Dry Process ◽  
Effect Of Pd ◽  
Kinetics Of

Palladium (Pd) nanoparticles were incorporated into a nylon 6 film via a dry process which consisted of simultaneous vaporization, penetration and reduction processes of palladium (II) bis (acetylacetonate, Pd (acac)2) at 180°C for various exposure time. The even dispersion of the generated Pd nanoparticles were observed by transmission electron microscope (TEM) and the Pd loading weight of about 15~43 wt% was measured by thermogravimetric analysis (TGA). In order to study the catalytic effect of Pd nanoparticles on the thermal degradation kinetics of nylon 6, TGA data at various heating rates were introduced to Flynn & Wall equation. The thermal degradation activation energy for neat nylon 6 was ca. 162~178 kJ/mol over the thermal degradation fraction of 0.05~0.40 while that of the nylon 6/Pd (26.5 wt%) nanocomposite was ca. 110~169 kJ/mol over the same fraction range. It meant the Pd nanoparticles were acted as a catalyst on the depolymerization of amide group in nylon 6. It was also found that the activation energy decreased slightly with the increasing Pd loading weight.

Thermal degradation kinetics of oxo-degradable PP/PLA blends

2018 ◽  
Vol 39 (1) ◽  
pp. 58-67 ◽  
Author(s):  
Dev K. Mandal ◽  
Haripada Bhunia ◽  
Pramod K. Bajpai
Keyword(s):  
Activation Energy ◽  
Thermal Stability ◽  
Thermogravimetric Analysis ◽  
Thermal Degradation ◽  
Kinetic Parameters ◽  
Degradation Kinetics ◽  
Nitrogen Atmosphere ◽  
Thermal Degradation Kinetics ◽  
Heating Rates ◽  
Kinetics Of

AbstractIn this article, the influence of polylactide and pro-oxidant on the thermal stability, degradation kinetics, and lifetime of polypropylene has been investigated using thermogravimetric analysis under nitrogen atmosphere at four different heating rates (i.e. 5, 10, 15, and 20°C/min). The kinetic parameters of degradation were studied over a temperature range of 30–550°C. The derivative thermogravimetric curves have indicated single stage and two stage degradation processes. The activation energy was evaluated by using the Kissinger, Kim-Park, and Flynn-Wall methods under the nitrogen atmosphere. The activation energy value of polypropylene was much higher than that of polylactide. Addition of polylactide and pro-oxidant in polypropylene decreased the activation energy. The lifetime of polypropylene has also decreased with the addition of polylactide and pro-oxidant.

Thermal Degradation Kinetics of Poly (vinyl chloride)

2010 ◽  
Vol 96 ◽  
pp. 245-249 ◽  
Author(s):  
Bin Han ◽  
Yu Long Wu ◽  
Guo Rui ◽  
Wei Feng ◽  
Zhen Chen ◽  
...  
Keyword(s):  
Activation Energy ◽  
Thermal Degradation ◽  
Degradation Kinetics ◽  
Mass Conservation ◽  
Thermal Degradation Kinetics ◽  
Pyrolysis Mechanism ◽  
Second Stage ◽  
Volatile Products ◽  
Infrared Spectrometer ◽  
Kinetics Of

The thermal degradation of PVC resin was examined by the thermogravimetric analysis (TGA). The pyrolysis volatile products were analyzed by Fourier transform infrared spectrometer synchronized with TG test (TG-FTIR). Based on the TG results, the kinetics of thermal degradation was studied by Friedman method. The pyrolysis mechanism was discussed also. The results indicate that the pyrolysis process of PVC can be divided into two main stages: 220°C - 380°C and 380°C - 560°C. By the calculation of mass conservation and TG-FTIR results, it can be supposed that not only HCl, but also some unsubstituted aromatics such as benzene were released during the first stage. The comparison of activation energy shows that the second stage exhibited higher activation energy than the first stage. Two activation energy values in the first stage confirm that there arose two reactions in the first stage.

Estimation of Cure and Thermal Degradation Kinetics of Epoxy/Organoclay Nanocomposite

2010 ◽  
Vol 123-125 ◽  
pp. 667-670 ◽  
Author(s):  
Jae Young Lee ◽  
Bum Choul Choi ◽  
Hong Ki Lee
Keyword(s):  
Activation Energy ◽  
Thermal Degradation ◽  
Epoxy Matrix ◽  
Degradation Kinetics ◽  
Cure Kinetics ◽  
Diglycidyl Ether ◽  
Thermal Degradation Kinetics ◽  
Heating Rates ◽  
Scanning Calorimetry ◽  
Kinetics Of

Polymer nanocomposite was synthesized through the intercalation and exfoliation of organoclay in an epoxy matrix. The epoxy matrix was composed of diglycidyl ether of bisphenol A (DGEBA, epoxy base resin), 4,4'-methylene dianiline (MDA, curing agent) and malononitrile (MN, chain extender) and organoclay was prepared by treating the montmorillonite with octadecyltrimethylammonium bromide (ODTMA). The intercalation of the organoclay was estimated by wide angle X-ray diffraction (WAXD) and transmission electron microscope (TEM) analyses. In order to measure the cure rate of DGEBA/MDA (30 phr)/MN (5 phr)/Organoclay (5 phr), differential scanning calorimetry (DSC) analysis were performed at the heating rates of 5, 10, 15 and 20 oC/min, and the data was interpreted by Kissinger equation. Thermal degradation kinetics of the epoxy nanocomposite was also studied by thermogravimetric analysis (TGA). The epoxy sample was decomposed in the TGA furnace at the heating rates of 5, 10, 15 and 20 oC/min with nitrogen atmosphere of 50 ml/min. The TGA data was introduced to the Ozawa equation and the degradation activation energy was calculated according to the degradation ratio. The activation energy for cure kinetics was 43.3 kJ/mol and that for thermal degradation was 171.5 kJ/mol.

scholarly journals Thermal-Resistant Polyurethane/Nanoclay Powder Coatings: Degradation Kinetics Study

Coatings ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 871
Author(s):  
Maryam Jouyandeh ◽  
Behzad Shirkavand Hadavand ◽  
Farimah Tikhani ◽  
Reza Khalili ◽  
Babak Bagheri ◽  
...  
Keyword(s):  
Activation Energy ◽  
Thermal Degradation ◽  
Degradation Kinetics ◽  
Decomposition Reaction ◽  
Thermal Degradation Kinetics ◽  
Powder Coatings ◽  
Heating Rates ◽  
Uniform Dispersion ◽  
Nano Clay ◽  
Kinetics Of

In the present study, thermal degradation kinetics of polyurethane (PU) powder coatings reinforced with organo-modified montmorillonite (OMMT) was investigated. PU nanocomposites were prepared in different concentrations of 1, 3, and 5 wt.% of OMMT via the extrusion method. The microstructure of the nanocomposites was observed by scanning electron microscope (SEM) illustrating uniform dispersion of OMMT nano-clay platelets in the PU matrix except for the sample containing 5 wt.% nano-palates. Thermal degradation kinetics of the PU nanocomposite was investigated using thermogravimetric analysis (TGA) at different heating rates of 5, 10, and 20 °C/min. The results showed that the initial decomposition temperatures were shifted toward higher values (more than 40 °C for T5% and up to 20 °C for T10%) by introducing the nano-clay to the PU matrix. Friedman, Kissinger–Akahira–Sunose (KAS), Flynn–Wall–Ozawa (FWO), and modified Coats-Redfern iso-conversional methods were applied to model the decomposition reaction and the activation energy of the nanocomposite powder coatings. Overall, the presence of nano-clay increased the activation energy of the PU degradation up to 45 kJ/mol, when compared to the blank PU, which suggests very high thermal stability of nanocomposites. The Sestak-Berggren approach proposed a good approximation for the reaction model, especially at low temperatures. Thus, PU decomposition was detected as an autocatalytic reaction, which was suppressed by the barrier effect of OMMT nano-palates intercalated with polymer chains.

Thermal degradation kinetics of a lignin particle-reinforced phenolic foam

2020 ◽  
pp. 0021955X2093288
Author(s):  
Juan Carlos Domínguez ◽  
Belén Del Saz-Orozco ◽  
Mercedes Oliet ◽  
M Virginia Alonso ◽  
Francisco Rodriguez
Keyword(s):  
Activation Energy ◽  
Thermal Degradation ◽  
Kinetic Parameters ◽  
Degradation Kinetics ◽  
Degradation Process ◽  
Activation Energies ◽  
Thermal Degradation Kinetics ◽  
Model Free ◽  
Predicted Values ◽  
Kinetics Of

In the present work, the thermal degradation kinetics of a phenolic (PF) and lignin particle-reinforced phenolic (LRPF) foam and the lignin used as the reinforcement (LR) were studied. The activation energies of the degradation processes were obtained using a discrete distributed activation energy model (discrete DAEM) and the Vyazovkin model-free kinetic (MFK) method. The discrete DAEM was validated by comparing the predicted values with the data obtained at 8 °C min−1. Heating ramps of 6 and 12 °C min−1 were used to calculate the kinetic parameters through the model. The effect of the reinforcement on the kinetics of the LRPF was studied by comparison with the results obtained for the PF. For reactions with non-zero mass fractions, the activation energies of the PF were in the range between 79.9 and 177.6 kJ mol−1, and the activation energy for the LRPF ranged from 91 to 187 kJ mol−1. For the LR, the activation energy values were in a narrower range than for the foams: 150–187 kJ mol−1. The degradation process of the LRPF was modified due to the use of LR: the range of activation energy for LRPF was between the ranges for the PF and LR. The activation energy dependence on conversion was also calculated using the Vyazovkin method and compared with the DAEM results; no compensation effect for the kinetic parameters was found.

Study on the Thermal Degradation Kinetics of Modified Chloroprene Rubber Adhesive Dedicated to Bonding UHMWPE and 45# Steel

2011 ◽  
Vol 399-401 ◽  
pp. 2125-2129
Author(s):  
Ping Hu ◽  
Qin Qin Luo ◽  
Meng Pan
Keyword(s):  
Activation Energy ◽  
Thermal Degradation ◽  
Mass Loss ◽  
Chemical Reaction ◽  
Degradation Kinetics ◽  
Degradation Process ◽  
Thermal Degradation Kinetics ◽  
Exponential Factor ◽  
Average Activation Energy ◽  
Order Chemical Reaction

Modified neoprene adhesive dedicated to bonding UHMWPE and 45# steel was prepared. Thermal analysis with TG-DTG curve was determined and its thermal decomposition kinetics was studied. The result show that the thermal degradation process of CR/MMA/CPE/MgO adhesive is a three-step reaction and the its thermal degradation starting temperature is 200°C and complete decomposition temperature is 570°C. The first mass loss stage is 0.6 order chemical reaction and its average activation energy E is 19.21kJ/mol and pre-exponential factor A is 3.68×102. The second mass loss stage is 3 order chemical reaction and its average activation energy E is 82.14kJ/mol and its pre-exponential factor A is 1.52×108. The third mass loss stage is 3 order chemical reaction and its average activation energy E is 55.07kJ/mol and pre-exponential factor A is 1.33×105.

Thermal Degradation Kinetics of Poly(Arylene Ether Nitrile) and its Crosslinked Polymer

2011 ◽  
Vol 284-286 ◽  
pp. 1917-1924 ◽  
Author(s):  
Jia Chun Zhong ◽  
Jian Yang ◽  
Hai Long Tang ◽  
Xiao Bo Liu
Keyword(s):  
Activation Energy ◽  
Thermal Degradation ◽  
Degradation Kinetics ◽  
Decomposition Temperature ◽  
Thermal Degradation Kinetics ◽  
Ozawa Method ◽  
Initial Decomposition Temperature ◽  
Solid State Decomposition ◽  
Friedman Method ◽  
Kinetics Of

The kinetics of the thermal degradation of Polyarylene ether natriles (PEN) (crosslinked and uncrosslinked) were investigated by thermogravimetric analysis (TGA). The corresponding kinetic parameters of PEN were determined using Flynn–Wall–Ozawa method and Friedman method, respectively. Satava method was also used to discuss the probable degradation mechanisms of PEN. The results showed that the activation energy obtained from Flynn–Wall–Ozawa method was in good agreement with the value obtained from Friedman method. The solid-state decomposition mechanisms of PEN and crosslinked PEN were A2 type (nucleation and growth) and R2 type (phase boundary controlled reaction), respectively. The activation energy and initial decomposition temperature of crosslinked PEN were higher than that of PEN, which indicates that crosslinking treatment is effective to enhance the thermal stability of PEN.

scholarly journals Thermal Degradation Kinetics and Modeling Study of Ultra High Molecular Weight Polyethylene (UHMWP)/Graphene Nanocomposite

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1597
Author(s):  
Iman Jafari ◽  
Mohamadreza Shakiba ◽  
Fatemeh Khosravi ◽  
Seeram Ramakrishna ◽  
Ehsan Abasi ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Molecular Weight ◽  
Thermal Degradation ◽  
High Molecular Weight ◽  
Degradation Kinetics ◽  
Graphene Nanosheets ◽  
Thermal Degradation Kinetics ◽  
Graphene Nanocomposites ◽  
Kinetics Of ◽  
Ultra High Molecular Weight

The incorporation of nanofillers such as graphene into polymers has shown significant improvements in mechanical characteristics, thermal stability, and conductivity of resulting polymeric nanocomposites. To this aim, the influence of incorporation of graphene nanosheets into ultra-high molecular weight polyethylene (UHMWPE) on the thermal behavior and degradation kinetics of UHMWPE/graphene nanocomposites was investigated. Scanning electron microscopy (SEM) analysis revealed that graphene nanosheets were uniformly spread throughout the UHMWPE’s molecular chains. X-Ray Diffraction (XRD) data posited that the morphology of dispersed graphene sheets in UHMWPE was exfoliated. Non-isothermal differential scanning calorimetry (DSC) studies identified a more pronounced increase in melting temperatures and latent heat of fusions in nanocomposites compared to UHMWPE at lower concentrations of graphene. Thermogravimetric analysis (TGA) and derivative thermogravimetric (DTG) revealed that UHMWPE’s thermal stability has been improved via incorporating graphene nanosheets. Further, degradation kinetics of neat polymer and nanocomposites have been modeled using equations such as Friedman, Ozawa–Flynn–Wall (OFW), Kissinger, and Augis and Bennett’s. The "Model-Fitting Method” showed that the auto-catalytic nth-order mechanism provided a highly consistent and appropriate fit to describe the degradation mechanism of UHMWPE and its graphene nanocomposites. In addition, the calculated activation energy (Ea) of thermal degradation was enhanced by an increase in graphene concentration up to 2.1 wt.%, followed by a decrease in higher graphene content.

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