Research on Thermal Degradation Kinetics of Polyphenylene Sulfide Filter Media

2013 ◽  
Vol 300-301 ◽  
pp. 1171-1174 ◽  
Author(s):  
De Qiang Chang ◽  
Jing Xian Liu ◽  
Ning Mao ◽  
Bao Zhi Chen
Keyword(s):  
Thermal Stability ◽  
Thermal Degradation ◽  
Degradation Kinetics ◽  
Decomposition Temperature ◽  
Polyphenylene Sulfide ◽  
Thermal Degradation Kinetics ◽  
Filter Media ◽  
Initial Decomposition Temperature ◽  
Kinetics Of ◽  
Thermal Stability Of

In order to study the thermal stability of PPS (polyphenylene sulfide) filter media, by means of thermogravimetry(TG), thermal degradation kinetics behavior of two kinds of PPS filter media were analyzed. The kinetic parameters of PPS filter media were obtained according to Flynn-Wall-Ozawa method. Thermal stability of PPS filter media was discussed. It was found that the initial decomposition temperature and activation energy of N3 sample are all higher than B1 sample, the thermal stability of N3 sample is better than B1 sample, and kinetic analysis can be used as an important method to evaluate the thermal stability of filter media.

Study on the Thermal Stability of Polyphenylene Sulfide Filter Media by Non-Isothermal Thermogravimetry

2013 ◽  
Vol 663 ◽  
pp. 988-992 ◽  
Author(s):  
De Qiang Chang ◽  
Jing Xian Liu ◽  
Ning Mao ◽  
Bao Zhi Chen
Keyword(s):  
Thermal Stability ◽  
Degradation Kinetics ◽  
Decomposition Temperature ◽  
Polyphenylene Sulfide ◽  
Thermal Degradation Kinetics ◽  
Filter Media ◽  
Initial Decomposition Temperature ◽  
Isothermal Thermogravimetry ◽  
Thermal Stability Of ◽  
Better Than

In order to study the thermal stability of PPS (polyphenylene sulfide) filter media, by means of non- isothermal thermogravimetry, thermal degradation kinetics behavior of two kinds of PPS filter media were analyzed. The kinetic parameters of PPS filter media were obtained according to Friedman method. Thermal stability of PPS filter media was discussed. It was found that the initial decomposition temperature and activation energy of N3 sample are all higher than B1 sample, the thermal stability of N3 sample is better than B1 sample, and kinetic analysis can be used as an important method to evaluate the thermal stability of filter media.

Thermal Properties and Thermal Degradation Kinetics of Polypropylene/ Organomodified Ni-Al Layered Double Hydroxide (LDH) Nanocomposites Prepared by Melt Intercalation Technique

2011 ◽  
Vol 471-472 ◽  
pp. 209-214 ◽  
Author(s):  
Kaberi Kakati ◽  
Aditya Prakash ◽  
G. Pugazhenthi
Keyword(s):  
Thermal Stability ◽  
Thermal Degradation ◽  
Degradation Kinetics ◽  
Sodium Dodecyl ◽  
Decomposition Temperature ◽  
Thermal Degradation Kinetics ◽  
Precipitation Method ◽  
Melt Intercalation ◽  
Kinetics Of ◽  
Thermal Stability Of

The objective of this work is to investigate the influence of LDH loading on the thermal stability and thermal degradation kinetics of the PP/Ni-Al LDH nanocomposites using thermogravimetric analysis (TGA) and to compare the results with that of the neat PP. For this, Ni-Al LDH was first prepared by co-precipitation method at constant pH using their nitrate salts and subsequently organically modified using sodium dodecyl sulphate (SDS) by regeneration method. A series of novel PP/Ni-Al LDH nanocomposites was then prepared with various amounts of LDH by melt intercalation method. The XRD results confirm the formation of exfoliated PP/LDH nanocomposites. PP/LDH nanocomposites exhibit enhanced thermal stability relative to the neat PP due to the presence of barrier effect of LDH lamellar layers and the thermal stability of the nanocomposites also increases with increase in the LDH loading. When 10% weight loss is selected as a point of comparison, the decomposition temperature of PP/LDH (5 wt %) nanocomposite is 15 oC higher than that of neat PP. The thermal degradation activation energy of the nanocomposites is determined via Coats-Redfern method and compared with that of neat PP. The improvement of thermal stability of PP nanocomposites is also confirmed by increasing the activation energies (Ea) and the integral procedural decomposition temperature (IPDT) compared with neat PP. Criado method is finally used to determine the degradation reaction mechanism of various samples.

Influence of Organomodified Ni-Al Layered Double Hydroxide (LDH) Content on the Thermal Properties and Degradation Kinetics of Polystyrene (PS)/Ni-Al LDH Nanocomposites Prepared via Solvent Blending Method

2013 ◽  
Vol 747 ◽  
pp. 23-26 ◽  
Author(s):  
Manish Kumar Sinha ◽  
G. Pugazhenthi
Keyword(s):  
Thermal Stability ◽  
Thermal Properties ◽  
Degradation Kinetics ◽  
Decomposition Temperature ◽  
Thermal Degradation Kinetics ◽  
Blending Method ◽  
Friedman Method ◽  
Double Hydroxide ◽  
Kinetics Of ◽  
Thermal Stability Of

A series of polystyrene (PS) nanocomposites with various concentration of organomodified Ni-Al LDH (3, 7 wt%) were synthesized by solvent blending method and the effect of Ni-Al LDH content on the thermal properties and degradation kinetics of PS/ Ni-Al LDH nanocomposites was examined. Thermogravimetric analysis (TGA) was employed to evaluate the thermal properties of the prepared PS nanocomposites with various content of Ni-Al LDH. The obtained TGA results reveal that the PS/Ni-Al LDH nanocomposites exhibits enhanced thermal stability when compared with pure PS and the thermal stability of the nanocomposites increase with an increase in the LDH content from 3 to 7 wt%. When 15% weight loss is selected as a point of comparison, the thermal decomposition temperature of the PS/Ni-Al LDH nanocomposite containing 7 wt% of LDH is about 28°C higher than that of pure PS. The thermal degradation kinetics of the nanocomposite materials are investigated using two kinetic models such as Flynn-Wall-Ozawa method and Friedman method. The improvement of thermal stability of the nanocomposites with increasing LDH content is also validated by increasing the activation energies.

Thermal degradation kinetics of poly(arylene ether nitrile) and its cross-linked polymer

2016 ◽  
Vol 29 (2) ◽  
pp. 211-217 ◽  
Author(s):  
Jiachun Zhong ◽  
Heng Guo ◽  
Jian Yang ◽  
Xiaobo Liu
Keyword(s):  
Thermal Degradation ◽  
Degradation Kinetics ◽  
Decomposition Temperature ◽  
Thermal Degradation Kinetics ◽  
Initial Decomposition Temperature ◽  
Solid State Decomposition ◽  
Arylene Ether ◽  
Friedman Method ◽  
Kinetics Of ◽  
Good Agreement

The kinetics of the thermal degradation of poly(arylene ether nitrile) (PEN; cross-linked and uncross-linked) was investigated by thermogravimetric analysis. The corresponding kinetic parameters of PEN were determined using the Flynn–Wall–Ozawa and the Friedman method. The Satava method was also used to explore the probable degradation mechanisms of PEN. The results showed that the activation energy ( E) obtained from the Flynn–Wall–Ozawa method was in good agreement with the value obtained from the Friedman method. The solid-state decomposition mechanisms of uncross-linked and cross-linked PEN were A2 (nucleation and growth) and R2 type (phase boundary–controlled reaction), respectively. The E and initial decomposition temperature of cross-linked PEN were higher than those of uncross-linked PEN, which indicates that cross-linking treatment is effective in enhancing the thermal stability of PEN.

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.

Thermo-oxidative and thermal degradation kinetics of silica/polymethyl methacrylate composites with electrostatic interaction phase interfaces

2019 ◽  
Vol 39 (2) ◽  
pp. 105-116 ◽  
Author(s):  
Hongyan Li ◽  
Yongqiang Fu ◽  
Hongli Liu ◽  
Cong Sun ◽  
Ruyi Li ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Thermal Degradation ◽  
Polymethyl Methacrylate ◽  
Electrostatic Interaction ◽  
Degradation Kinetics ◽  
Thermal Degradation Kinetics ◽  
Degradation Kinetic ◽  
Further Development ◽  
Kinetics Of ◽  
Insulation Performance

AbstractThe thermo-oxidative and thermal degradation kinetic parameters of polymethyl methacrylate-methacryloxyethyltrimethyl ammonium chloride/silica aerogel composites (PMMA-MTC/SA) were investigated in this paper and were compared with the thermal stability and thermal conductivity of different types of composites. As a composite with electrostatic interaction, the thermo-oxidative and thermal degradation activation energies (E) of PMMA-MTC/SA were 173.97 and 188.05 kJ/mol, respectively. The results indicated that the electrostatic interaction could indeed enhance the thermal stability of silica/polymethyl methacrylate composites on the premise of good mechanical properties and heat insulation performance. It is of great significance for the further development of silica-based thermal insulation composites.

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.

Thermal properties and thermal degradation kinetics of phenolic and wood flour-reinforced phenolic foams

2016 ◽  
Vol 51 (1) ◽  
pp. 125-138 ◽  
Author(s):  
JC Domínguez ◽  
B del Saz-Orozco ◽  
M Oliet ◽  
MV Alonso ◽  
F Rodriguez
Keyword(s):  
Thermal Stability ◽  
Thermal Degradation ◽  
Degradation Kinetics ◽  
Wood Flour ◽  
Activation Energies ◽  
Thermal Degradation Kinetics ◽  
Kinetic Methods ◽  
Model Free ◽  
Phenolic Foam ◽  
Kinetics Of

In the present work, the thermal stability, changes in chemical structure during thermal degradation, and the kinetics of thermal degradation of a phenolic foam were studied. An 8.5 wt% of Pinus radiata wood flour reinforcement was added to the phenolic foam. A commercial phenolic resol was used as the matrix for the foam. The wood flour-reinforced foam showed a structure similar to the phenolic foam according to the Fourier transform infrared spectroscopy results. The wood flour increased the thermal stability of the phenolic foam in the first stage of thermal degradation ( T 5%), decreased it in the second step ( T 25%), and negligibly influenced the final stage. The activation energies of the degradation processes of the studied materials were obtained by the Kissinger-Akahira-Sunose and Flynn-Wall-Ozawa model-free kinetic methods and a 2-Gaussian distributed activation energy model. The values of the activation energies obtained by the model-free kinetic methods for the first degradation stage of the phenolic foams were in a range between 110 and 170 kJ mol−1, whereas for the wood flour it was 162 kJ mol−1 for almost all of the conversion range of its main degradation stage. The applied models showed good fits for all the materials, and the activation energies calculated were in agreement with the values found in the literature.

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