Preparation and characterization of carbon fiber/polylactic acid/thermoplastic polyurethane (CF/PLA/TPU) composites prepared by a vane mixer

2017 ◽  
Vol 37 (4) ◽  
pp. 355-364 ◽  
Author(s):  
Xiaochun Yin ◽  
Liang Wang ◽  
Sai Li ◽  
Guangjian He ◽  
Zhitao Yang ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Polylactic Acid ◽  
Storage Modulus ◽  
Mixing Time ◽  
Thermoplastic Polyurethane ◽  
Complex Viscosity ◽  
Melting Behavior ◽  
Scanning Calorimetry ◽  
Crystallization And Melting Behavior ◽  
Thermal Stability Of

Abstract Various quantities of carbon fibers (CFs) (from 5% to 20% in weight) were added to matrix by melt blending to produce polylactic acid (PLA)/thermoplastic polyurethane (TPU)/CF composites. Differential scanning calorimetry measurements revealed that the CF content and mixing time had little influence on the crystallization and melting behavior of PLA. Thermogravimetric analysis showed that the introduction of CFs tended to decrease the thermal stability of PLA/TPU/CF composites, and the increase of mixing time tended to increase the thermal stability of PLA/TPU/CF composites when the mixing time is <5 min. Rheological results showed that all the samples exhibited non-Newtonian and shear thinning characteristics. The storage modulus and complex viscosity both increased with the increase of the CF content. It also showed that the increase of mixing time tended to increase the storage modulus and complex viscosity of PLA/TPU/CF composites when the mixing time is <5 min. Scanning electron microscopy images showed that the TPU/PLA blends contain a continuous PLA phase with evenly distributed TPU particles in the size range of 0.25–3 μm, and the blends are immiscible at the micron scale. Mechanical properties showed that the addition of proper CF content could lead to an obvious increase (about 11.43%) in tensile strength.

Thermal and Thermomechanical Properties of Poly(butylene succinate) Nanocomposites

2008 ◽  
Vol 8 (4) ◽  
pp. 1679-1689 ◽  
Author(s):  
Mamookho E. Makhatha ◽  
Suprakas Sinha Ray ◽  
Joseph Hato ◽  
Adriaan S. Luyt
Keyword(s):  
Thermal Stability ◽  
Tensile Modulus ◽  
Melting Behavior ◽  
Mechanical Analysis ◽  
Thermomechanical Properties ◽  
Scanning Calorimetry ◽  
Melt Mixing ◽  
Butylene Succinate ◽  
Modulated Differential Scanning Calorimetry ◽  
Thermal Stability Of

This article describes the thermal and thermomechanical properties of poly(butylene succinate) (PBS) and its nanocomposites. PBS nanocomposites with three different weight ratios of organically modified synthetic fluorine mica (OMSFM) have been prepared by melt-mixing in a batch mixer at 140 °C. The structure and morphology of the nanocomposites were characterized by X-ray diffraction (XRD) analyses and transmission electron microscopy (TEM) observations that reveal the homogeneous dispersion of the intercalated silicate layers into the PBS matrix. The thermal properties of pure PBS and the nanocomposite samples were studied by both conventional and temperature modulated differential scanning calorimetry (DSC) analyses, which show multiple melting behavior of the PBS matrix. The investigation of the thermomechanical properties was performed by dynamic mechanical analysis. Results reveal significant improvement in the storage modulus of neat PBS upon addition of OMSFM. The tensile modulus of neat PBS is also increased substantially with the addition of OMSFM, however, the strength at yield and elongation at break of neat PBS systematically decreases with the loading of OMSFM. The thermal stability of the nanocomposites compared to that of the pure polymer sample was examined under both pyrolytic and thermooxidative environments. It is shown that the thermal stability of PBS is increased moderately in the presence of 3 wt% of OMSFM, but there is no significant effect on further silicate loading in the oxidative environment. In the nitrogen environment, however, the thermal stability systematically decreases with increasing clay loading.

scholarly journals Exploring the Effects of MXene on Nonisothermal Crystallization and Melting Behavior of β-Nucleated Isotactic Polypropylene

Polymers ◽  
2021 ◽  
Vol 13 (21) ◽  
pp. 3815
Author(s):  
Wanxin Peng ◽  
Furui Sun ◽  
Yuke Liang ◽  
Jian Kang ◽  
Jinyao Chen ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Isotactic Polypropylene ◽  
Isothermal Crystallization ◽  
Polarized Light ◽  
Thermal Conditions ◽  
Melting Behavior ◽  
Polymorphic Behavior ◽  
Scanning Calorimetry ◽  
Cooling Rates ◽  
Thermal Stability Of

In this study, one of the commonly used MXene (Ti3C2Tx) and β nucleated isotactic polypropylene (β-iPP)/MXene composites of different compositions were fabricated. The effects of MXene on non-isothermal crystallization and polymorphic behavior of β-iPP/MXene composites were comparatively studied. The non-isothermal crystallization kinetics indicates that for all samples, the lower cooling rates promote composites to crystallize at higher temperatures. When MXene and β-Nucleating agent (β-NA) are added separately, the crystallization temperature of composites shifts towards higher temperatures at all cooling rates. When MXene and β-NA are added simultaneously, the composite shows different cooling rate dependence, and the effects of improving crystallization temperatures is more obvious under rapid cooling. The activation energy of four samples iPP, iPP/MXene, iPP/β-NA, and iPP/MXene/β-NA were −167.5, −185.5, −233.8, and −218.1 kJ/mol respectively, which agree with the variation tendency of crystallization temperatures. The polymorphic behavior analysis obtained from Differential Scanning calorimetry (DSC) is affected by two factors: the ability to form β-crystals and the thermal stability of β-crystals. Because β-crystals tend to recrystallize to α-crystals below a critical temperature, to eliminate the effect of β-α recrystallization, the melting curves at end temperatures Tend = 50 °C and Tend = 100 °C are comparatively studied. The results show that more thermally unstable β-crystals would participate in β-α recrystallization with higher cooling rates. Moreover, thermal stability of β-crystals is improved by adding MXene. To further verify these findings, samples of three different thermal conditions were synthesized and analyzed by DSC, X-Ray Diffraction (XRD), and Polarized Light Optical Microscopy (PLOM), and the results were consistent with the above findings. New understandings of synthesizing β-iPP/MXene composites with adjustable morphologies and polymorphic behavior were proposed.

scholarly journals Investigating Physio-Thermo-Mechanical Properties of Polyurethane and Thermoplastics Nanocomposite in Various Applications

Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2467
Author(s):  
Tyser Allami ◽  
Ahmed Alamiery ◽  
Mohamed H. Nassir ◽  
Amir H. Kadhum
Keyword(s):  
Thermal Stability ◽  
Electrical Properties ◽  
Hard Segment ◽  
Soft Segment ◽  
Thermoplastic Polyurethane ◽  
Tensile Modulus ◽  
Scanning Calorimetry ◽  
Strain Behavior ◽  
Phase Separation Kinetics ◽  
Thermal Stability Of

The effect of the soft and hard polyurethane (PU) segments caused by the hydrogen link in phase-separation kinetics was studied to investigate the morphological annealing of PU and thermoplastic polyurethane (TPU). The significance of the segmented PUs is to achieve enough stability for further applications in biomedical and environmental fields. In addition, other research focuses on widening the plastic features and adjusting the PU–polyimide ratio to create elastomer of the poly(urethane-imide). Regarding TPU- and PU-nanocomposite, numerous studies investigated the incorporation of inorganic nanofillers such as carbon or clay to incorporating TPU-nanocomposite in several applications. Additionally, the complete exfoliation was observed up to 5% and 3% of TPU–clay modified with 12 amino lauric acid and benzidine, respectively. PU-nanocomposite of 5 wt.% Cloisite®30B showed an increase in modulus and tensile strength by 110% and 160%, respectively. However, the nanocomposite PU-0.5 wt.% Carbone Nanotubes (CNTs) show an increase in the tensile modulus by 30% to 90% for blown and flat films, respectively. Coating PU influences stress-strain behavior because of the interaction between the soft segment and physical crosslinkers. The thermophysical properties of the TPU matrix have shown two glass transition temperatures (Tg’s) corresponding to the soft and the hard segment. Adding a small amount of tethered clay shifts Tg for both segments by 44 °C and 13 °C, respectively, while adding clay from 1 to 5 wt.% results in increasing the thermal stability of TPU composite from 12 to 34 °C, respectively. The differential scanning calorimetry (DSC) was used to investigate the phase structure of PU dispersion, showing an increase in thermal stability, solubility, and flexibility. Regarding the electrical properties, the maximum piezoresistivity (10 S/m) of 7.4 wt.% MWCNT was enhanced by 92.92%. The chemical structure of the PU–CNT composite has shown a degree of agglomeration under disruption of the sp2 carbon structure. However, with extended graphene loading to 5.7 wt.%, piezoresistivity could hit 10-1 S/m, less than 100 times that of PU. In addition to electrical properties, the acoustic behavior of MWCNT (0.35 wt.%)/SiO2 (0.2 wt.%)/PU has shown sound absorption of 80 dB compared to the PU foam sample. Other nanofillers, such as SiO2, TiO2, ZnO, Al2O3, were studied showing an improvement in the thermal stability of the polymer and enhancing scratch and abrasion resistance.

Ultrasound-assisted melt mixing for the preparation of UHMWPE/OMMT nanocomposites

2017 ◽  
Vol 31 (6) ◽  
pp. 784-802 ◽  
Author(s):  
Wang Liang ◽  
Yin Xiaochun ◽  
He Guangjian ◽  
Feng Yanhong ◽  
Qu Jinping
Keyword(s):  
Storage Modulus ◽  
Treatment Time ◽  
Mixing Time ◽  
Ultrahigh Molecular Weight Polyethylene ◽  
Complex Viscosity ◽  
Onset Temperature ◽  
Scanning Calorimetry ◽  
Melt Mixing ◽  
Extensional Deformation ◽  
X Ray

Ultrahigh molecular weight polyethylene (UHMWPE)/organic montmorillonite (OMMT) nanocomposites were prepared via a self-made vane mixer which could supply a synergy of ultrasound and extensional deformation. Structure and working principle of this novel mixer were illustrated in detail. Effects of the OMMT content, mixing time, and ultrasound treat time on composites’ morphology, rheological properties, and thermal properties were reported in terms of transmission electron microscopy (TEM), wide-angle X-ray scattering, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). X-ray diffraction (XRD) and TEM showed that the OMMT lay spacing increased from 2.82 nm to 3.29 nm and OMMT dispersed evenly in the matrix using this novel melt mixing equipment. It certified that the melt mixing procedure synergized by ultrasound and extensional deformation was very effective in the exfoliation of silicate layers and also the filler distribution and dispersion. DSC measurements revealed that the crystallization temperature ( Tc) had no visible change with increasing the OMMT content and the melting temperature ( Tm) and melting enthalpy crystallinity ( Xc) increased with the proper OMMT content. The higher Tm and Xc showed with the proper ultrasound treatment time, however, the Tc had no visible change. TGA showed that the onset temperature at which 20% weight loss of the material increased markedly in the case of UHMWPE/OMMT-1 wt% nanocomposite. The onset temperature slightly decreased with the use of ultrasound. Rheological analyses showed that all the samples exhibited non-Newtonian and shear thinning characteristics. Both the storage modulus and complex viscosity increased with continuous addition of the OMMT layers. It also indicated that the introduction of ultrasound tended to decrease the storage modulus and complex viscosity. Universal tensile test indicated that superior tensile strength occurred in samples containing OMMT layers.

scholarly journals The Influence of Mercerised Kenaf Fibres Reinforced Polylactic Acid Composites on Dynamic Mechanical Analysis

2011 ◽  
Vol 471-472 ◽  
pp. 815-820 ◽  
Author(s):  
Rosnita A. Talib ◽  
Intan Syafinaz Mohamed Amin Tawakkal ◽  
Abdan Khalina
Keyword(s):  
Thermal Stability ◽  
Polylactic Acid ◽  
Storage Modulus ◽  
Loss Modulus ◽  
Dry Weight ◽  
Compression Moulding ◽  
Melt Mixing ◽  
Dynamic Mechanical ◽  
Thermal Stability Of ◽  
Kenaf Fibres

The potential of using cellulose to reinforce the thermal stability of kenaf derived cellulose (KDC)/polylactic acid (PLA) composite was investigated in this study. The cellulose was derived from kenaf bast fibre which was chemically treated via chlorination and mercerisation processes. The composites with various loadings of cellulose (dry weight basis) ranging from 0% to 60% were produced by melt mixing and compression moulding. Dynamic mechanical properties namely storage modulus (E’), loss modulus (E”) and tan δ of the KDC/PLA composites and the commercial PLA were analysed and compared as a function of temperature. ESEM micrographs demonstrated that the mercerisation of kenaf fibres have successfully removed the lignin and hemicellulose, thus producing cellulose which can be observed by its rougher surface and greater size reduction than the raw fibre. The DMA results demonstrated that the storage modulus of 60% KDC/PLA composite is twice higher than the commercial PLA and the rest of the composites within a high temperature range (above 80°C). The glass transition temperatures (Tg) generated from the loss modulus curves exhibit that the peak of the loss modulus was shifted to higher temperature as the percentage of the cellulose loading was increased. These results show a better thermal stability of the composites when incorporated with the cellulose.

Thermal Analysis of Chitosan-Lactate and Chitosan-Aluminum Monostearate Composite System

2012 ◽  
Vol 506 ◽  
pp. 278-281 ◽  
Author(s):  
Kotchamon Yodkhum ◽  
T. Phaechamud
Keyword(s):  
Thermal Stability ◽  
Thermal Analysis ◽  
Thermal Degradation ◽  
Chitosan Solution ◽  
Melting Behavior ◽  
Degradation Behavior ◽  
Scanning Calorimetry ◽  
Chitosan Derivatives ◽  
Thermal Degradation Behavior ◽  
Thermal Stability Of

Chitosan possess many attractive properties for applying as biomaterials. For some application, biomaterial devices have to be sterilized using high temperature, e.g. stream sterilizing process. However, thermal degradation behavior of chitosan has been reported previously. Many researchers have attempted to improve thermal degradation behavior of chitosan by synthesize chitosan derivatives or blending chitosan with other polymers or additives. However, chitosan derivatives found to be less thermal stability than chitosan itself. On the contrary, adding some lipid additive could improve thermal stability of chitosan. In this study, protecting effect of aluminum monostearate (Alst) on thermal stability of chitosan was investigated employing thermal analysis techniques, e.g. thermogravimetry (TG), differential scanning calorimetry (DSC) and hot-stage microscope. Lactic acid solution (2% w/v) was used as solvent for dissolving chitosan. Chitosan solution, named as chtiosan-lactate (CL) and chitosan solution contained 2.5% w/w Alst (CLAlst) were prepared and fabricated into sponges using freeze drying technique. Degradation temperature of CLAlst system investigated from TG was shifted to the higher temperature comparing that of CL which indicated that Alst could improve thermal stability of chitosan after processed as biomaterial. From DSC result, small endothermic peak was observed around 60-70°C for CLAlst whereas that of CL did not exhibit any peak. Melting behavior of the sponges observed under hot-stage microscope was demonstrated that chitosan was decomposed whereas Alst dispersed in chitosan backbone was gradually melted.

Thermal Stability of N-Heterocycle-Stabilized Iodanes – A Systematic Investigation

2019 ◽  
Author(s):  
Andreas Boelke ◽  
Yulia A. Vlasenko ◽  
Mekhman S. Yusubov ◽  
Boris Nachtsheim ◽  
Pavel Postnikov
Keyword(s):  
Thermal Stability ◽  
Differential Scanning Calorimetry ◽  
Thermogravimetric Analysis ◽  
Systematic Investigation ◽  
Scanning Calorimetry ◽  
Thermal Stability Of

<p>The thermal stability of pseudocyclic and cyclic <i>N</i>-heterocycle-stabilized (hydroxy)aryl- and mesityl(aryl)-l<sup>3</sup>-iodanes (NHIs) through thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) is investigated. NHIs bearing <i>N</i>-heterocycles with a high N/C-ratio such as triazoles show among the lowest descomposition temperatures and the highest decomposition energies. A comparison of NHIs with known (pseudo)cyclic benziodoxolones is made and we further correlated their thermal stability with reactivity in a model oxygenation. </p>

Influence of trisilanol isooctyl POSS content on the structure, morphology and rheological properties of thermoplastic polyurethane (TPU)

2020 ◽  
Vol 40 (9) ◽  
pp. 727-735
Author(s):  
Rudinei Fiorio ◽  
Chaitanya Danda ◽  
João Maia
Keyword(s):  
Thermal Stability ◽  
Rheological Properties ◽  
Thermoplastic Polyurethane ◽  
Reactive Extrusion ◽  
Strain Rates ◽  
Force Microscopy ◽  
Atomic Force ◽  
Extensional Strain ◽  
Oligomeric Silsesquioxane ◽  
Thermal Stability Of

AbstractIn this study, thermoplastic polyurethanes (TPUs) containing trisilanol isooctyl polyhedral oligomeric silsesquioxane (POSS), a reactive nanofiller, were synthesized and characterized rheologically and morphologically, and the effects of POSS content on the melt thermal stability of the TPUs are investigated. Samples containing 0, 0.23, 0.57, 1.14, and 2.23% (w/w) POSS were synthesized by reactive extrusion and characterized by Fourier transform infrared spectroscopy (FTIR), oscillatory and extensional rheometry, atomic force microscopy (AFM), and small- and wide-angle X-ray scattering (SAXS and WAXS, respectively). The rheological properties of molten TPU are time-dependent and the melt thermal stability of the TPU is maximal at 1.14% of POSS. The addition of 0.23 and 0.57% POSS promotes strain-hardening at low extensional strain rates (0.01 and 0.10 s−1), not affecting the extensional characteristics at higher strain rates. The addition of increasing amounts of POSS leads to the formation of POSS-rich clusters well dispersed in the TPU matrix. SAXS and WAXS results show that the POSS domains are amorphous and that POSS does not modify the crystalline structure of TPU. Therefore, this work indicates that synthesizing TPU in the presence of trisilanol isooctyl POSS can increase the melt thermal stability of the polymer, facilitating its processing.

scholarly journals A Characteristic Study of Polylactic Acid/Organic Modified Montmorillonite (PLA/OMMT) Nanocomposite Materials after Hydrolyzing

Crystals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 376
Author(s):  
Su-Mei Huang ◽  
Jiunn-Jer Hwang ◽  
Hsin-Jiant Liu ◽  
An-Miao Zheng
Keyword(s):  
Thermal Stability ◽  
Polylactic Acid ◽  
Decomposition Temperature ◽  
Material Strength ◽  
Scanning Calorimetry ◽  
Hydrolysis Process ◽  
Twin Screw ◽  
Thermal Pressing ◽  
Organophilic Clay ◽  
Mmt Clay

In this study, the montmorillonite (MMT) clay was modified with NH4Cl, and then the structures were exfoliated or intercalated in a polylactic acid (PLA) matrix by a torque rheometer in the ratio of 0.5, 3.0, 5.0 and 8.0 wt%. X-ray diffraction (XRD) revealed that the organic modified-MMT(OMMT) was distributed successfully in the PLA matrix. After thermal pressing, the thermal stability of the mixed composites was measured by a TGA. The mixed composites were also blended with OMMT by a co-rotating twin screw extruder palletizing system, and then injected for the ASTM-D638 standard specimen by an injection machine for measuring the material strength by MTS. The experimental results showed that the mixture of organophilic clay and PLA would enhance the thermal stability. In the PLA mixed with 3 wt% OMMT nanocomposite, the TGA maximum decomposition temperature (Tmax) rose from 336.84 °C to 339.08 °C. In the PLA mixed with 5 wt% OMMT nanocomposite, the loss of temperature rose from 325.14 °C to 326.48 °C. In addition, the elongation rate increased from 4.46% to 10.19% with the maximum loading of 58 MPa. After the vibrating hydrolysis process, the PLA/OMMT nanocomposite was degraded through the measurement of differential scanning calorimetry (DSC) and its Tg, Tc, and Tm1 declined.

scholarly journals Isothermal Vulcanization and Non-Isothermal Degradation Kinetics of XNBR/Epoxy/XNBR-g-Halloysite Nanotubes (HNT) Nanocomposites

Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2872
Author(s):  
Seyed Mohamad Reza Paran ◽  
Ghasem Naderi ◽  
Elnaz Movahedifar ◽  
Maryam Jouyandeh ◽  
Krzysztof Formela ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Degradation Kinetics ◽  
Halloysite Nanotubes ◽  
Butadiene Rubber ◽  
Order Model ◽  
Scanning Calorimetry ◽  
Theoretical Methods ◽  
Vulcanization Kinetics ◽  
Kinetics Of ◽  
Thermal Stability Of

The effect of several concentrations of carboxylated nitrile butadiene rubber (XNBR) functionalized halloysite nanotubes (XHNTs) on the vulcanization and degradation kinetics of XNBR/epoxy compounds were evaluated using experimental and theoretical methods. The isothermal vulcanization kinetics were studied at various temperatures by rheometry and differential scanning calorimetry (DSC). The results obtained indicated that the nth order model could not accurately predict the curing performance. However, the autocatalytic approach can be used to estimate the vulcanization reaction mechanism of XNBR/epoxy/XHNTs nanocomposites. The kinetic parameters related to the degradation of XNBR/epoxy/XHNTs nanocomposites were also assessed using thermogravimetric analysis (TGA). TGA measurements suggested that the grafted nanotubes strongly enhanced the thermal stability of the nanocomposite.

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