Physical properties, thermal stability, and glass transition temperature of multi-walled carbon nanotube/polypyrrole nanocomposites

2014 ◽  
Vol 21 (8) ◽  
pp. 737-747 ◽  
Author(s):  
Mansoor Farbod ◽  
Nooshin Mobini
Keyword(s):  
Thermal Stability ◽  
Glass Transition ◽  
Carbon Nanotube ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Physical Properties ◽  
Multi Walled Carbon Nanotube

Free, partial, and fully constrained recovery analysis of cold-programmed shape memory epoxy/carbon nanotube nanocomposites: Experiments and predictions

2018 ◽  
Vol 29 (10) ◽  
pp. 2164-2176 ◽  
Author(s):  
R Abishera ◽  
R Velmurugan ◽  
KV Nagendra Gopal
Keyword(s):  
Glass Transition ◽  
Carbon Nanotube ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Shape Memory ◽  
Thermally Activated ◽  
Large Structures ◽  
Multi Walled Carbon Nanotube ◽  
Optical Strain Measurement ◽  
Optical Strain

Thermally activated shape memory polymers are typically programmed by initially heating the material above the glass transition temperature ( Tg), deforming to the desired shape, cooling below Tg, and unloading to fix the temporary shape. This process of deforming at high temperatures becomes a time-, labor-, and energy-expensive process while applying to large structures. Alternatively, materials with reversible plasticity shape memory property can be programmed at temperatures well below the glass transition temperature which offers several advantages over conventional programming. Here, the free, partial, and fully constrained recovery analysis of cold-programmed multi-walled carbon nanotube–reinforced epoxy nanocomposites is presented. The free recovery analysis involves heating the temporary shape above Tg without any constraints (zero stress), and for fully constrained recovery analysis, the temporary shape is held constant while heating. The partially constrained recovery behavior is studied by applying a constant stress of 10%, 25%, and 50% of the maximum recovery stress obtained from the completely constrained recovery analysis. The samples are also characterized for their thermal, morphological, and mechanical properties. A non-contact optical strain measurement method is used to measure the strains during cold-programming and shape recovery. The different recovery behaviors are analyzed by using a thermo-viscoelastic–viscoplastic model, and the predictions are compared with the experimental results.

Investigating the role of GeO2 in enhancing the thermal stability and proton mobility of proton-conducting phosphate glasses

2021 ◽  
Author(s):  
Takahisa Omata ◽  
Aman Sharma ◽  
Takuya Kinoshita ◽  
Issei Suzuki ◽  
Tomohiro Ishiyama ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Phosphate Glasses ◽  
Proton Mobility ◽  
Proton Conducting

In this study, the effect of GeO2 on the thermal stability and proton mobility (μH) of proton-conducting phosphate glasses was experimentally investigated using 22HO1/2−3NaO1/2−(12−x)LaO3/2−xGeO2−63PO5/2 glasses. Increasing glass transition temperature (Tg)...

Influence of Carbon Nanotube Aspect Ratio on Glass Transition Temperature of Polymers: A Molecular Dynamics Simulation Study

2015 ◽  
Vol 817 ◽  
pp. 797-802 ◽  
Author(s):  
Cai Jiang ◽  
Jian Wei Zhang ◽  
Shao Feng Lin ◽  
Su Ju ◽  
Da Zhi Jiang
Keyword(s):  
Molecular Dynamics ◽  
Glass Transition ◽  
Carbon Nanotube ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Aspect Ratio ◽  
Epoxy Resin ◽  
Md Simulations ◽  
Diglycidyl Ether ◽  
Dynamics Simulation

Molecular dynamics (MD) simulations on three single walled carbon nanotube (SWCNT) reinforced epoxy resin composites were conducted to study the influence of SWCNT type on the glass transition temperature (Tg) of the composites. The composite matrix is cross-linked epoxy resin based on the epoxy monomers bisphenol A diglycidyl ether (DGEBA) cured by diaminodiphenylmethane (DDM). MD simulations of NPT (constant number of particles, constant pressure and constant temperature) dynamics were carried out to obtain density as a function of temperature for each composite system. The Tg was determined as the temperature corresponding to the discontinuity of plot slopes of the densityvsthe temperature. In order to understand the motion of polymer chain segments above and below the Tg, various energy components and the MSD at various temperatures of the composites were investigated and their roles played in the glass transition process were analyzed. The results show that the Tg of the composites increases with increasing aspect ratio of the embedded SWCNT

Nanocomposite Epoxy Resin for SiC Module

2011 ◽  
Vol 2011 (HITEN) ◽  
pp. 000196-000200 ◽  
Author(s):  
Kenji Okamoto ◽  
Yuji Takematsu ◽  
Miyako Hitomi ◽  
Yoshinari Ikeda ◽  
Yoshikazu Takahashi
Keyword(s):  
Thermal Stability ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Epoxy Resin ◽  
Molecular Motion ◽  
Experimental Results ◽  
Power Module ◽  
Operation Temperature ◽  
Thermal Stability Of

There is a demand to improve the thermal stability of epoxy molding resins used in the power module of SiC power chips operating at temperatures of 200°C or more. This paper describes a technique for increasing the thermal stability of the resin by decreasing molecular motion through the addition of nanofiller. The experimental results showed that the glass transition temperature (Tg) of the epoxy resin increased by approximately 30°C when the silica nanofiller was added. The epoxy resin added nanofiller was investigated in order to achieve the operation temperature 200°C of power module.

scholarly journals Melt Stable Functionalized Organosolv and Kraft Lignin Thermoplastic

Processes ◽  
2020 ◽  
Vol 8 (9) ◽  
pp. 1108
Author(s):  
Shubhankar Bhattacharyya ◽  
Leonidas Matsakas ◽  
Ulrika Rova ◽  
Paul Christakopoulos
Keyword(s):  
Thermal Stability ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Kraft Lignin ◽  
Added Value ◽  
Lignin Valorization ◽  
1H Nuclear Magnetic Resonance ◽  
Ft Ir ◽  
Viable Biomass

A shift towards an economically viable biomass biorefinery concept requires the use of all biomass fractions (cellulose, hemicellulose, and lignin) for the production of high added-value products. As lignin is often underutilized, the establishment of lignin valorization routes is highly important. In-house produced organosolv as well as commercial Kraft lignin were used in this study. The aim of the current work was to make a comparative study of thermoplastic biomaterials from two different types of lignins. Native lignins were alkylate with two different alkyl iodides to produce ether-functionalized lignins. Successful etherification was verified by FT-IR spectroscopy, changes in the molecular weight of lignin, as well as 13C and 1H Nuclear Magnetic Resonance (NMR). The thermal stability of etherified lignin samples was considerably improved with the T2% of organosolv to increase from 143 °C to up to 213 °C and of Kraft lignin from 133 °C to up to 168 °C, and glass transition temperature was observed. The present study shows that etherification of both organosolv and Kraft lignin with alkyl halides can produce lignin thermoplastic biomaterials with low glass transition temperature. The length of the alkyl chain affects thermal stability as well as other thermal properties.

Poly(Binaphthalenevinylene-alt-Phenylenevinylene) Derivatives: Novel Luminescent Polymers for Light-Emitting Devices

1999 ◽  
Vol 598 ◽  
Author(s):  
Lixin Zheng ◽  
Xuezhong Jiang ◽  
Michelle S. Liu ◽  
Alex K-Y. Jen
Keyword(s):  
Thermal Stability ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Model Compound ◽  
Condensation Reaction ◽  
Spectral Characteristics ◽  
Light Emitting ◽  
Light Emitting Devices ◽  
Luminescent Polymers

ABSTRACTNovel conjugated light-emitting polymers were synthesized via a Wittig-Horner condensation reaction between a binaphthyl dicarbaldehyde and a series of electron-rich or electron-deficient aryl diphosphonates. After comparing these materials with the model compound, 4c, it was revealed that the introduction of a twisted, non-coplanar binaphthyl structure provided an effective approach for tailoring the spectral characteristics of the polymers and improving their solubility and thermal stability (glass transition temperature, Tg, 200°C). Furthermore, the band structures of the polymers could be fine-tuned by changing the electronic properties of the bridging aromatic units. The electroluninescence (EL) and device characteristics were also reported in this paper.

Sign in / Sign up

Export Citation Format

Share Document