scholarly journals Thermal and Flammability Characteristics of Blended Jatropha Bio-Epoxy as Matrix in Carbon Fiber–Reinforced Polymer

2019 ◽  
Vol 3 (1) ◽  
pp. 6 ◽  
Author(s):  
Mohd Radzi Mohd Hafiezal ◽  
Abdan Khalina ◽  
Zainal Abidin Zurina ◽  
Md Deros Mohd Azaman ◽  
Zin Mohd Hanafee
Keyword(s):  
Thermal Stability ◽  
Carbon Fiber ◽  
Composite Structure ◽  
Mechanical Analysis ◽  
Scanning Calorimetry ◽  
Flammability Characteristics ◽  
The Matrix ◽  
Potential Alternative ◽  
Ft Ir ◽  
The Difference

This purpose of this paper was to reveal characteristics of a composite structure containing carbon fiber as a reinforcement and blended synthetic epoxy/bio-epoxy derived from crude jatropha oil as resin and compared with fully synthetic epoxy. The composite structure was prepared by the vacuum-assisted resin transfer molding technique and was left to cure for 24 h at room temperature. Both were characterized for their thermal, chemical, and flammable characteristics. The incorporation of jatropha bio-epoxy into the matrix significantly improved the thermal stability between 288–365 °C as obtained by thermogravimetric analysis (TGA) test. Dynamic mechanical analysis (DMA) curves showed slight diminution of performances and Tg from DMA tests confirmed well with the trend of Tg obtain by differential scanning calorimetry (DSC) curves. On the other hand, the flammability property was rated horizontal burning (HB) which was the same as the fully synthetic composite, but the duration to self-extinguish was halved for the composite with jatropha bio-epoxy. Fourier transform infrared attenuated total reflectance (FT-IR/ATR) was conducted to determine the difference of functional groups’ spectrum due to bonding type existing on both specimens. Overall, the composite specimen with blended bio-epoxy exhibited better thermal stability, comparable flammability characteristics, and performances. The aim of this paper was to introduce bio-based epoxy as a potential alternative epoxy and to compete with synthetic epoxy so as to minimize the footprint of non-renewable composite.

scholarly journals Preparation, Thermal, and Thermo-Mechanical Characterization of Polymeric Blends Based on Di(meth)acrylate Monomers

Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 878
Author(s):  
Krystyna Wnuczek ◽  
Andrzej Puszka ◽  
Łukasz Klapiszewski ◽  
Beata Podkościelna
Keyword(s):  
Mechanical Analysis ◽  
Attenuated Total Reflection ◽  
Scanning Calorimetry ◽  
Force Microscopy ◽  
Chemical Structures ◽  
Atomic Force ◽  
Polymeric Blends ◽  
Ft Ir ◽  
Acrylate Monomers ◽  
Synthesized Materials

This study presents the preparation and the thermo-mechanical characteristics of polymeric blends based on di(meth)acrylates monomers. Bisphenol A glycerolate diacrylate (BPA.GDA) or ethylene glycol dimethacrylate (EGDMA) were used as crosslinking monomers. Methyl methacrylate (MMA) was used as an active solvent in both copolymerization approaches. Commercial polycarbonate (PC) was used as a modifying soluble additive. The preparation of blends and method of polymerization by using UV initiator (Irqacure® 651) was proposed. Two parallel sets of MMA-based materials were obtained. The first included more harmless linear hydrocarbons (EGDMA + MMA), whereas the second included the usually used aromatic copolymers (BPA.GDA + MMA). The influence of different amounts of PC on the physicochemical properties was discussed in detail. Chemical structures of the copolymers were confirmed by attenuated total reflection–Fourier transform infrared (ATR/FT-IR) spectroscopy. Thermo-mechanical properties of the synthesized materials were investigated by means of differential scanning calorimetry (DSC), thermogravimetric (TG/DTG) analyses, and dynamic mechanical analysis (DMA). The hardness of the obtained materials was also tested. In order to evaluate the surface of the materials, their images were obtained with the use of atomic force microscopy (AFM).

scholarly journals Biocomposites from Rice Straw Nanofibers: Morphology, Thermal and Mechanical Properties

Materials ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2138 ◽  
Author(s):  
José Carlos Alcántara ◽  
Israel González ◽  
M. Mercè Pareta ◽  
Fabiola Vilaseca
Keyword(s):  
Rice Straw ◽  
Mechanical Performance ◽  
Cellulose Nanofibers ◽  
Nucleating Agent ◽  
Mechanical Analysis ◽  
Nanocomposite Films ◽  
Chemical Extraction ◽  
Poly Vinyl Alcohol ◽  
Scanning Calorimetry ◽  
The Matrix

Agricultural residues are major potential resources for biomass and for material production. In this work, rice straw residues were used to isolate cellulose nanofibers of different degree of oxidation. Firstly, bleached rice fibers were produced from the rice straw residues following chemical extraction and bleaching processes. Oxidation of rice fibers mediated by radical 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO) at pH 10 was then applied to extract rice cellulose nanofibers, with diameters of 3–11 nm from morphological analysis. The strengthening capacity of rice nanofibers was tested by casting nanocomposite films with poly(vinyl alcohol) polymer. The same formulations with eucalyptus nanofibers were produced as comparison. Their thermal and mechanical performance was evaluated using thermogravimetry, differential scanning calorimetry, dynamic mechanical analysis and tensile testing. The glass transition of nanocomposites was shifted to higher temperatures with respect to the pure polymer by the addition of rice cellulose nanofibers. Rice nanofibers also acted as a nucleating agent for the polymer matrix. More flexible eucalyptus nanofibers did not show these two phenomena on the matrix. Instead, both types of nanofibers gave similar stiffening (as Young’s modulus) to the matrix reinforced up to 5 wt.%. The ultimate tensile strength of nanocomposite films revealed significant enhancing capacity for rice nanofibers, although this effect was somehow higher for eucalyptus nanofibers.

Influence of different surface-coated carbon fibers on the properties of the poly(phenylene sulfide) composites

2018 ◽  
Vol 53 (8) ◽  
pp. 1123-1132 ◽  
Author(s):  
Bedriye Ucpinar ◽  
Ayse Aytac
Keyword(s):  
Differential Scanning Calorimetry ◽  
Carbon Fiber ◽  
Carbon Fibers ◽  
Mechanical Analysis ◽  
Fiber Reinforced ◽  
Scanning Calorimetry ◽  
Carbon Fiber Reinforced ◽  
Coated Carbon ◽  
Scanning Electron ◽  
Phenylene Sulfide

This paper aims to study the effect of different surface coatings of carbon fiber on the thermal, mechanical, and morphological properties of carbon fiber reinforced poly(phenylene sulfide) composites. To this end, unsized and different surface-coated carbon fibers were used. Prepared poly(phenylene sulfide)/carbon fiber composites were characterized by using Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, tensile test, dynamic mechanical analysis, and scanning electron microscopy. Tensile strength values of the surfaced-coated carbon fibers reinforced poly(phenylene sulfide) composites are higher than the unsized carbon fiber reinforced poly(phenylene sulfide) composite. The highest tensile strength and modulus values were observed for the polyurethane-coated carbon fiber reinforcement. Dynamic mechanical analysis studies indicated that polyurethane-coated carbon fiber reinforced composite exhibited higher storage modulus and better adhesion than the others. Differential scanning calorimetry results show that melting and glass transition temperature of the composites did not change significantly. Scanning electron microscopic studies showed that polyurethane and epoxy-coated carbon fibers exhibited better adhesion with poly(phenylene sulfide).

scholarly journals Examining the Influence of Re–Used Nanofiller—Pyrolyzed Montmorillonite, on the Thermal Properties of Polypropylene–Based Engineering Nanocomposites

Materials ◽  
2019 ◽  
Vol 12 (16) ◽  
pp. 2636
Author(s):  
Tomasz M. Majka ◽  
Oskar Bartyzel ◽  
Konstantinos N. Raftopoulos ◽  
Joanna Pagacz ◽  
Krzysztof Pielichowski
Keyword(s):  
Thermal Stability ◽  
Differential Scanning Calorimetry ◽  
Thermal Properties ◽  
Thermogravimetric Analysis ◽  
Control Sample ◽  
Mechanical Analysis ◽  
Scanning Calorimetry ◽  
Stabilization Effect ◽  
Polypropylene Melt ◽  
Better Than

Pyrolysis of the polypropylene/montmorillonite (PP/OMMT) nanocomposites allows for recovery of the filler that can be then re–used to produce PP/pyrolyzed MMT (PMMT) nanostructured composites. In this work, we discuss the thermal properties of PP/PMMT composites investigated by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). It has been found that effect of PMMT (5 wt. % and 10 wt. %) on matrix thermal stability occurs at temperatures above 300 °C. Addition of 5 wt. % and 10 wt. % of PMMT into polypropylene system gave good stabilization effect, as confirmed by the overall stabilization effect (OSE) values, which increased by 4% and 7%, respectively, compared to the control sample (PP). Interestingly, the presence of 1 wt. % and 3 wt. % of pyrolyzed clay stabilizes the system better than the same concentrations of organoclay added into polypropylene melt. DSC data revealed that pyrolyzed clay has still the same tendency as organoclay to enhance formation of the α and β crystalline PP phases only. The pyrolyzed MMT causes an improvement of the modulus in the glassy as well as rubbery regions, as confirmed by DMA results.

Thermal stability and dynamic mechanical behavior of functional multiphase boride ceramics/epoxy composites

2019 ◽  
Vol 39 (6) ◽  
pp. 508-514
Author(s):  
Yannan He ◽  
Zhiqiang Yu
Keyword(s):  
Mechanical Properties ◽  
Thermal Stability ◽  
Loss Modulus ◽  
Dynamic Mechanical Properties ◽  
Mechanical Analysis ◽  
Epoxy Composites ◽  
Scanning Calorimetry ◽  
Element Analysis ◽  
Reaction Heat ◽  
Dynamic Mechanical

Abstract The thermal and dynamic mechanical properties of epoxy composites filled with zirconium diboride/nano-alumina (ZrB2/Al2O3) multiphase particles were investigated by means of differential scanning calorimetry, dynamic thermo-mechanical analysis, and numerical simulation. ZrB2/Al2O3 particles were surface organic functional modified by γ-glycidoxypropyltrimethoxysilane for the improvement of their dispersity in epoxy matrix. The results indicated that the curing exotherm of epoxy resin decreased significantly due to the addition of ZrB2/Al2O3 multiphase particles. In comparison to the composites filled with unmodified particles, the modified multiphase particles made the corresponding filling composites exhibit lower curing reaction heat, lower loss modulus, and higher storage modulus. Generally speaking, the composites filled with 5 wt% modified multiphase particles presented the best thermal stability and thermo-mechanical properties due to the better filler-matrix interfacial compatibility and the uniform dispersity of modified particles. Finite element analysis also suggested that the introduction of modified ZrB2/Al2O3 multiphase particles increased the stiffness of the corresponding composites.

scholarly journals Effect of Compatibilizer on the Interface Bonding of Graphene Oxide/Polypropylene Composite Fibers

Polymers ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 1283 ◽  
Author(s):  
Miao Miao ◽  
Chunyan Wei ◽  
Ying Wang ◽  
Yongfang Qian
Keyword(s):  
Thermal Stability ◽  
Graphene Oxide ◽  
Loss Modulus ◽  
Composite Fiber ◽  
Mechanical Analysis ◽  
Interfacial Bonding ◽  
Composite Fibers ◽  
Scanning Calorimetry ◽  
Blending Method ◽  
Thermal Stability Of

To improve the interfacial bonding and thermal stability of graphene oxide (GO)/polypropylene (PP) composite fibers, a composite fiber with PP as the matrix, GO as reinforcement and maleic anhydride-grafted PP (PP-g-MAH) as a compatibilizer was prepared by a simple and efficient melt-blending method. The GO content was 0.0–5.0 wt %. According to the Fourier Transform Infrared (FT-IR) spectroscopy results, the interfacial bonding in the PP/MAH/GO composite fibers was improved. The Dynamic Mechanical Analysis (DMA) results show that the addition of GO resulted in better interfacial adhesion and higher storage modulus (E′). The loss modulus (E′′) of the PP/MAH/GO-x composite fibers increased with increasing amount of added GO, whereas the loss factor (tan δ) decreased. GO and PP-g-MAH were analyzed by Thermogravimetric Analysis (TGA). The thermal stability of the composite fibers was improved compared to PP. Differential Scanning Calorimetry (DSC) analysis showed that the addition of PP-g-MAH to the composite fiber improved the interfacial bonding of GO in the PP matrix. Thus, compatibility between the two components was obtained. Based on the Scanning Electron Microscopy (SEM) results, the PP fibers exhibited relative orientation due to the strong crystalline morphology. The rough section, PP/GO blend fiber exhibits a very clear phase separation morphology due to the incompatibility between the two and the compatibility of GO and PP in PP/MAH/GO-3 composite fiber is improved, resulting in the interface between the two has improved.

scholarly journals Multifunctional PLA Blends Containing Chitosan Mediated Silver Nanoparticles: Thermal, Mechanical, Antibacterial, and Degradation Properties

Nanomaterials ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 22 ◽  
Author(s):  
Agueda Sonseca ◽  
Salim Madani ◽  
Gema Rodríguez ◽  
Víctor Hevilla ◽  
Coro Echeverría ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Silver Nanoparticles ◽  
Lactic Acid ◽  
Food Packaging ◽  
Synthesis Method ◽  
Crystallization Rate ◽  
Poly Lactic Acid ◽  
Scanning Calorimetry ◽  
The Matrix ◽  
Degradation Properties

Poly(lactic acid) (PLA) is one of the most commonly employed synthetic biopolymers for facing plastic waste problems. Despite its numerous strengths, its inherent brittleness, low toughness, and thermal stability, as well as a relatively slow crystallization rate represent some limiting properties when packaging is its final intended application. In the present work, silver nanoparticles obtained from a facile and green synthesis method, mediated with chitosan as a reducing and stabilizing agent, have been introduced in the oligomeric lactic acid (OLA) plasticized PLA in order to obtain nanocomposites with enhanced properties to find potential application as antibacterial food packaging materials. In this way, the green character of the matrix and plasticizer was preserved by using an eco-friendly synthesis protocol of the nanofiller. The X-ray diffraction (XRD) and differential scanning calorimetry (DSC) results proved the modification of the crystalline structure as well as the crystallinity of the pristine matrix when chitosan mediated silver nanoparticles (AgCH-NPs) were present. The final effect over the thermal stability, mechanical properties, degradation under composting conditions, and antimicrobial behavior when AgCH-NPs were added to the neat plasticized PLA matrix was also investigated. The obtained results revealed interesting properties of the final nanocomposites to be applied as materials for the targeted application.

Thermal and Mechanical Properties of Cyclized Polybutadiene Dielectrics

1986 ◽  
Vol 76 ◽  
Author(s):  
C. W. Wilkins ◽  
H. E. Bair ◽  
M. G. Chan ◽  
R. S. Hutton
Keyword(s):  
Mechanical Properties ◽  
Differential Scanning Calorimetry ◽  
Physical And Mechanical Properties ◽  
Mechanical Analysis ◽  
Infrared Analysis ◽  
Thermal And Mechanical Properties ◽  
Scanning Calorimetry ◽  
The Difference ◽  
Thermal Mechanical Analysis ◽  
Lower Glass Transition Temperature

ABSTRACTWe have studied some of the physical and mechanical properties of cyclized polybutadiene (CBR) dielectrics by dynamic mechanical analysis, thermal mechanical analysis, thermogravimetry, infrared analysis, and differential scanning calorimetry. Of interest is the difference in properties between thin (<30 μm) films which have been cured under vacuum and those which have been cured in air. Our results indicate that curing under vacuum prevents oxidation and reduces crosslinking. Vacuum cured films have 20% smaller moduli and 200 lower glass transition temperature than do films produced in air.

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.

Preparation and Properties of Silane-Terminated Poly(urethane-Imide)

2013 ◽  
Vol 690-693 ◽  
pp. 1577-1580
Author(s):  
Xiao Xi Hu ◽  
Yun Wang
Keyword(s):  
Thermal Stability ◽  
Water Resistance ◽  
Tensile Tests ◽  
Mechanical Analysis ◽  
Gravimetric Analysis ◽  
Thermal Gravimetric ◽  
Silane Coupling ◽  
Ft Ir ◽  
And Storage ◽  
Thermal Stability Of

A serious of silane-terminated poly (urethane-imide) (Si-PUI) was synthesized via prepolymer method using polycarbonatediols (PCDL), 2,4-tolylene diisocyanate (TDI), 4,4'-Oxydiphthalic Anhydride (ODPA) and silane coupling agent KH-550. The structure of the products was characterized by FT-IR. The thermal properties were measured by thermal gravimetric analysis (TGA). The thermal mechanical behavior was investigated by dynamic mechanical analysis (DMA).The mechanical characteristic was measured by tensile tests. The water absorption (Wa) was also been tested. With the imide content increasing, the thermal stability, tensile strength and storage modulus of poly (urethane-imide) improve significantly, and the glass transition temperature rises. The introduction of silanes improves the water resistance and further enhances the thermal stability of poly (urethane-imide).

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