Cyclomatrix Phosphazene Polymers via Alder-ene Reactions

2002 ◽  
Vol 10 (6) ◽  
pp. 457-466 ◽  
Author(s):  
C.P. Reghunadhan Nair ◽  
M. Sunitha ◽  
K. N. Ninan
Keyword(s):  
Thermal Stability ◽  
Slow Rate ◽  
Mechanical Analysis ◽  
Char Residue ◽  
Scanning Calorimetry ◽  
Sequential Reaction ◽  
Ene Reactions ◽  
Ene Reaction ◽  
Good Thermal Stability ◽  
Sodium Phenolate

Cyclomatrix phosphazene polymers were synthesized by the Alder-ene reaction between tris(2-allylphenoxy)triphenoxy cyclotriphosphazene (APCP) and bis(4-maleimido phenyl) methane (BMM). APCP was synthesized from hexachlorocyclotriphosphazene by sequential reaction with sodium phenolate and sodium (2-allylphenolate). It was co-cured in various stoichiometric ratios with BMM. The cure of the APCP/BMM blend was characterized by differential scanning calorimetry, dynamic mechanical analysis, and rheometry. The polymers exhibited good thermal stability and anaerobic char yield. Although allylphenoxy phosphazene led to early initiation of thermal decomposition, it was conducive to a slow rate of thermal erosion and higher char residue. The cured polymers showed a Tg in the range of 240-250°C. They formed good uni-directional composites with glass fibres, although the phosphazene was found to marginally decrease the inter-phase bonding.

Thermal properties of a series of tetrafunctional fluorene-based oxazines/P-a blends

2016 ◽  
Vol 29 (10) ◽  
pp. 1139-1147 ◽  
Author(s):  
Zi Sang ◽  
Tiantian Feng ◽  
Wenbin Liu ◽  
Jun Wang ◽  
Mehdi Derradji
Keyword(s):  
Thermal Stability ◽  
Differential Scanning Calorimetry ◽  
Thermal Properties ◽  
Mechanical Analysis ◽  
Proton Nuclear Magnetic Resonance ◽  
Primary Amines ◽  
Resonance Spectroscopy ◽  
High Glass Transition Temperature ◽  
Scanning Calorimetry ◽  
Good Thermal Stability

A new series of aniline and aniline-mixed tetrafunctional fluorene-based oxazine monomers were synthesized using 2,7-hydroxy-9,9-bis-(4-hydroxyphenyl) fluorene, paraformaldehyde, and primary amines (including aniline or aniline mixed with n-butylamine or n-octylamine composition). Fourier transform infrared spectroscopy and proton nuclear magnetic resonance spectroscopy were used to characterize the structure of the monomers. The copolymers were obtained by adding the monomers into a typical monofunctional polybenzoxazine (phenol-aniline-based benzoxazine). Differential scanning calorimetry, thermogravimetric analysis, and dynamic mechanical analysis were performed to study the thermal properties of the copolymers. The copolymers exhibited high glass transition temperature values (164–201°C). A good thermal stability was also obtained with a 5% weight loss temperature over 355°C and high char yields at 800°C (42–50%).

Dynamic Mechanical Properties of Epoxy Resin with Multifunctional Polyamine Curing Agent

2015 ◽  
Vol 744-746 ◽  
pp. 1374-1377
Author(s):  
Xi Wang
Keyword(s):  
Thermal Stability ◽  
Dynamic Mechanical Properties ◽  
Mechanical Analysis ◽  
Diglycidyl Ether ◽  
Curing Agent ◽  
Scanning Calorimetry ◽  
Good Thermal Stability ◽  
Dynamic Mechanical ◽  
Glass Relaxation ◽  
Thermal Stability Of

A nonlinear multifunctional polyamine N,N,N’,N’-tetra (3-aminopropyl)-1,6-diamino-hexane (TADH), was prepared and employed as a novel hardener for diglycidyl ether of bisphenol A (DGEBA). Nonisothermal reactions of DGEBA/TADH were systematically investigated with differential scanning calorimetry (DSC). In addition, analysis of thermal stability of the cured DGEBA/TADH with thermogravimetric analysis (TGA) revealed that it possessed quite good thermal stability and increased residual char content at 600◦C in nitrogen. Furthermore, dynamic mechanical analysis (DMA) of the DGEBA/TADH network showed its relaxations were characterized by localized motions of hydroxyl ether segments and cooperative motions of whole network chains (glass relaxation) at different temperature regions.

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 Electrospun Silk-Boron Nitride Nanofibers with Tunable Structure and Properties

Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1093
Author(s):  
Ye Xue ◽  
Xiao Hu
Keyword(s):  
Thermal Stability ◽  
Boron Nitride ◽  
Hexagonal Boron Nitride ◽  
Environmental Research ◽  
Strong Interactions ◽  
Helical Structures ◽  
Scanning Calorimetry ◽  
Modulated Differential Scanning Calorimetry ◽  
Good Thermal Stability ◽  
Thermal Stability Of

In this study, hexagonal boron nitride (h-BN) nanosheets and Bombyx mori silk fibroin (SF) proteins were combined and electrospun into BNSF nanofibers with different ratios. It was found that the surface morphology and crosslinking density of the nanofibers can be tuned through the mixing ratios. Fourier transform infrared spectroscopy study showed that pure SF electrospun fibers were dominated by random coils and they gradually became α-helical structures with increasing h-BN nanosheet content, which indicates that the structure of the nanofiber material is tunable. Thermal stability of electrospun BNSF nanofibers were largely improved by the good thermal stability of BN, and the strong interactions between BN and SF molecules were revealed by temperature modulated differential scanning calorimetry (TMDSC). With the addition of BN, the boundary water content also decreased, which may be due to the high hydrophobicity of BN. These results indicate that silk-based BN composite nanofibers can be potentially used in biomedical fields or green environmental research.

scholarly journals Thermal characterization of novel aliphatic polyesters with ether and thioether linkages

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
M. Soccio ◽  
N. Lotti ◽  
L. Finelli ◽  
A. Munari
Keyword(s):  
Thermal Stability ◽  
Molecular Weight ◽  
Chemical Structure ◽  
Room Temperature ◽  
Crystallization Rate ◽  
Thermal Characterization ◽  
Scanning Calorimetry ◽  
Aliphatic Polyesters ◽  
Good Thermal Stability

AbstractSeveral novel ether or thioether linkage containing aliphatic polyesters and poly(alkylene dicarboxylate)s were synthesized for comparison and characterized in terms of chemical structure and molecular weight. The thermal behavior was examined by thermogravimetric analysis and differential scanning calorimetry. All the polymers showed a good thermal stability, even though lower for the ether or thioether linkage-containing polyesters. The decrement of the thermal stability appears to be more relevant in the case of the presence of sulphur atoms. At room temperature the samples appeared semicrystalline, except PTTDG and PDEDG, which were viscous oils; the effect of the introduction of ether or thioether group was an increment of the Tgvalue, a decrement of the melting temperature and a significant decrease of the crystallization rate. The entity of the variations was found to be affected by the kind of group introduced, and the trend observed can be explained on the basis of atom electronegativity and dimensions

Heat-resistant and photoluminescent indole-based poly(ether sulfone)s

2017 ◽  
Vol 30 (4) ◽  
pp. 475-479 ◽  
Author(s):  
Wenxuan Wei ◽  
Li Yang ◽  
Guanjun Chang
Keyword(s):  
Thermal Stability ◽  
High Performance ◽  
Proton Nuclear Magnetic Resonance ◽  
Resonance Spectroscopy ◽  
Condensation Polymerization ◽  
High Glass Transition Temperature ◽  
Scanning Calorimetry ◽  
Good Thermal Stability ◽  
High Performance Polymers ◽  
Good Agreement

Indole-based poly(ether sulfone)s (PINESs), as novel high-performance polymers, have been obtained by the condensation polymerization of 4-hydroxyindole and hydroquinone with activated difluoro monomers via a catalyst-free nucleophilic substitution reaction. The structures of the polymers are characterized by means of Fourier transform infrared and proton nuclear magnetic resonance spectroscopy, and the results show good agreement with the proposed structures. Differential scanning calorimetry and thermogravimetric analysis measurements exhibit that polymers possess high glass transition temperature ( Tgs > 245°C) and good thermal stability with high decomposition temperatures ( Tds > 440°C). In addition, due to their special structure, PINESs are endowed with significantly strong photonic luminescence in N, N-dimethylformamide.

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.

Novel polyimides based on diamine containing thiazole units with thioether linkage and pyridine as pendent group

2017 ◽  
Vol 30 (7) ◽  
pp. 840-846 ◽  
Author(s):  
Jafar Rezania ◽  
Abbas Shockravi ◽  
Morteza Ehsani ◽  
Vahid Vatanpour
Keyword(s):  
Thermal Stability ◽  
Differential Scanning Calorimetry ◽  
Pyridine Ring ◽  
Polar Solvent ◽  
Nitrogen Atmosphere ◽  
Scanning Calorimetry ◽  
Glass Transition Temperatures ◽  
Good Thermal Stability ◽  
Pendent Group ◽  
High Yields

Three new organic-soluble polyimides (PIs) bearing flexible thioether linkages, thiazole, and pyridine ring units were synthesized from a novel thioether-bridged diamine monomer and commercially available aromatic dianhydrides (1–3) via chemical imidization method. The resulting polymers were obtained in high yields and possessed inherent viscosities in the range of 0.67–0.89. The PIs are characterized by Fourier-transform infrared (FTIR), nuclear magnetic resonance (NMR), differential scanning calorimetry, and thermogravimetric analysis (TGA). All of the PIs exhibited excellent solubility in polar solvent. The polymers showed good thermal stability with glass transition temperatures ( Tgs) in the range of 194–244°C, and decomposition temperatures ( T5%) exceeding 300°C were observed using TGA in nitrogen atmosphere for the current polymers.

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