The effects of basic fibre-forming parameters on the thermal properties and flammability of fibres from polyimidoamide (PIA)
nanocomposite have examined. The comparative analysis of the properties of fibres from modified PIA and PIA nanocomposite
has been conducted.
The multi-functional fibres prepared from PIA nanocomposite show increased porosity and sorption properties as well as a high
thermal stability and reduced flammability in comparison with fibres without MMT. 相似文献
Thermal properties of sodium alginate and calcium alginate fibres containing nanoadditives were analysed. Thermal decomposition
of fibres based on sodium alginate, both pure and containing nanoadditive, produces sodium carbonate (for fibres without nanoadditive)
or, for modified fibres, a mixture of sodium carbonate with the corresponding nanoadditive, which does not undergo any changes
within the range of measured temperatures. The chief gaseous products accompanying the decomposition are carbon (IV) oxide
and water. The shape of the DTG curves and values of the *T50 coefficient indicate an improvement in the thermal properties of the fibres when ceramic nanoadditives (SiO2 and HAp) are introduced, as compared with pure sodium alginate fibres. When ceramic nanoadditives (MMT, SiO2, bioglass) are added to the material of calcium alginate fibres the nature of the thermal processes is not affected. However,
similarly as for sodium alginate fibres modified with nanoadditive, here also it was note the effect on the value of the *T50 coefficient. The greatest thermal stability, expressed by the value of *T50, was observed when SiO2, HAp and bioglass were used as nanoadditives. Considering that the porosity, sorption properties and cross section were similar
for all fibres, it can be suggested that in all cases the structure of the fibres has a lesser effect than the type of nanoadditive
on the thermal properties of the investigated fibres. The effect of the chemical structure of the material was reflected in
the higher decomposition temperature of calcium alginate nanocomposite fibres compared with sodium alginate fibres. This also
applies to fibres without any nanoadditive. 相似文献
A polystyrene‐modified epoxidized novolac resin/montmorillonite nanocomposite was fabricated and characterized successfully. For this purpose, novolac resin (NR) was epoxidized through the reaction of phenolic hydroxyl group with epichlorohydrin in super basic medium to produce epoxidized novolac resin (ENR). Afterward, a polystyrene was synthesized by atom transfer radical polymerization (ATRP) technique, and then brominated at the benzylic positions using N‐bromosuccinimide (NBS). The brominated polystyrene (PSt‐Br) was reacted with ethanolamine in basic medium in order to afford an amine‐functionalized polystyrene (PSt‐NH2). An organo‐modified montmorillonite (O‐MMT) was synthesized through the treatment of MMT with hexadecyl trimethyl ammonium chloride salt. Finally, ENR‐PSt/MMT nanocomposite was fabricated through curing a mixture of ENR (70 wt.%) and O‐MMT (5 wt.%) with PSt‐NH2 (25 wt.%). Transition electron microscopy (TEM) and powder X‐ray diffraction (XRD) analysis revealed that the fabricated nanocomposite has an exfoliated structure. Thermal property studies using thermogravimetric analysis (TGA) showed that the curing of ENR by PSt‐NH2, as well as incorporation of a small amount of MMT have synergistic effect on the thermal stability of the ENR resin. 相似文献
Styrene and montmorillonite organically modified with imidazolium surfactants (MMT) at various alkyl chain lengths (C12, C16 and C18) were used to prepare the corresponding PS/MMT/C12, PS/MMT/C16 and PS/MMT/C18 nanocomposites by in situ polymerization. XRD and TEM analyses evidenced the formation of both intercalated and exfoliated structures. The glass transition
temperatures (Tg) of nanocomposites, as well as that of neat PS, were obtained by DSC measurements. The thermal degradations were carried
out in the scanning mode, in both inert and oxidative environments, and the initial temperatures of decomposition (Ti) and the apparent activation energies of degradation (Ea) were determined. Due to an oxidative degradation mechanism, the Ti and Ea values in air atmosphere were lower than those under nitrogen.
The results indicated that nanocomposites are more thermally stable than polystyrene, and suggested an increasing degree of
exfoliation as a function of alkyl chain length of surfactant, associated with enhancing thermal stability. 相似文献
The thermal, morphological and optical studies of BaSO4 and MMT (nanoclay) embedded in PVDF were investigated. Nanocomposites samples of PVDF–BaSO4–MMT were prepared by varying the loadings (1–4 mass%) in case of BaSO4 and MMT nanomaterials, respectively. Polyvinylidene fluoride–barium sulfate-montmorillonite (PVDF–BaSO4–MMT) nanocomposites were prepared by solvent-mixing technique. Nanoparticles were synthesized by in situ deposition technique with the help of nonionic polymeric surfactant, and the particle size of nanoparticles was recognized by scanning electron microscopy (SEM) analysis which confirms that the particle has diameter of 80–90 nm. As prepared, nanocomposites films (thickness, 25 μm) were characterized by Fourier transform infrared microscopy (FTIR), SEM and electron diffraction spectroscopy (EDS). FTIR shows that all the chemical constituents were present in the nanocomposites, whereas SEM analysis suggested that the nanofillers dispersed well in polymer matrix and EDS showed the elemental composition of nanocomposite samples. Thermal properties of nanocomposites were studied by using TG/DTA/DTG. TG/DTA studies showed decomposition temperature of pure PVDF is 473.5 °C. The decomposition temperature (Td) of nanocomposites was increased by 93 °C in case of nanocomposites with addition of both BaSO4 and MMT nanomaterials. The difference in the thermal degradation temperature was found to be 1.2% higher in case of addition of BaSO4 nanoparticle as compared to nanoclay. The obtained transparent nanocomposite films were characterized by using UV–Vis spectrophotometer which shows that transparencies of nanocomposites are maintained in visible region, the intensity of absorption band in UV region is increased with the addition of BaSO4 nanoparticles, while in case of addition of nanoclay the UV region does not show drastic changes. Addition of both nanoparticle and nanoclay shows higher absorption in comparison with the individual samples. But further, doubling the amount of nanoparticle and nanoclay shows decrease in UV absorption. Overall, the results of thermal studies show that the incorporation of BaSO4 and MMT could significantly improve the thermal properties of nanocomposites. 相似文献
Summary: Exfoliated and intercalated polyethylene/montmorillonite (PE/MMT) nanocomposites with high MMT content were prepared by in situ polymerization. The isothermal crystallization kinetics of the nanocomposites were analyzed with Lauritzen–Hoffman regime theory. Regime III crystallization, which is difficult to observe in linear polyethylene, appears in the PE/MMT nanocomposites. The broader temperature range of regime III crystallization in PE/MMT nanocomposites shows that the mobility and reptation ability of the PE chains are greatly reduced by the MMT, especially in the intercalated nanocomposite.
Plots of ln K/n + U*/R(Tc − T0) against 1/Tc(ΔT)f for the intercalated and exfoliated PE/MMT nanocomposites. 相似文献
Polycarbonate was melt blended with solid bisphenol A bis(diphenyl phosphate), and a series of organoclays. Effects of the organoclay modifiers on the flammability, thermal and mechanical properties of the nanocomposites were studied by limiting oxygen index, UL-94 burning test, thermogravimetric analysis, differential scanning calorimetry, tensile test and dynamic mechanical analysis. Although all the nanocomposites exhibit an intercalated-exfoliated morphology, they vary in the magnitude of intercalation revealed by X-ray diffraction and transmission electron microscopy. Flammability of the nanocomposites is strongly related to the thermal stability rather than the morphology. Glass transition temperature (Tg) and mechanical properties are controlled by both the morphology and the affinity of the organoclays with the matrix. The modifier containing hydroxyl moiety has stronger interactions with the matrix but it can promote its degradation, thus the corresponding nanocomposite exhibits a better intercalated morphology, higher Tg, superior strength and modulus however a worse thermal stability and flame retardancy. An additional silane within the organoclays would make the organoclays more compatible with the matrix but be a steric obstacle to the intercalation of the matrix chains; however, flame retardancy of the corresponding nanocomposite is enhanced due to the flame retardant nature of the silane. Similarly, the modifier bearing two long alkyl tails shows stronger affinity with the matrix than the one bearing a single tail, but it would hinder the intercalation due to the steric effect. These establishments between organoclay modifiers and the properties of nanocomposites might be guidance for developing materials with practical applications. 相似文献
Summary: Poly(propylene)/monoalkylimidazolium‐modified montmorillonite (PP/IMMT) nanocomposites were prepared by in situ intercalative polymerization of propylene with TiCl4/MgCl2/MMT catalyst. The PP synthesized possessed high isotacticity and molecular weight. Both wide‐angle X‐ray diffraction (XRD) and transmission electron microscopy (TEM) examinations evidenced the nanocomposite formation with exfoliated MMT homogeneously distributed in the PP matrix. A thermal stability study revealed that the nanocomposites possess good thermal stability.
X‐ray diffraction patterns of PP/IMMT (MMT = 2.2 wt.‐%) nanocomposite before and after processing. 相似文献
Polyurethane (PU) has been prepared by using polyether polyol (jagropol oil) and 1,6- hexamethylene diisocyanate (HMDI) as a cross-linker. The organically modified montmorillonite clay (MMT) is well-dispersed into urethane matrix by an in situ polymerization method. A series of PU/MMT nanocomposites have been prepared by incorporating varying amounts of nanoclay viz., 1, 3, 5 and 6 wt %. Thermogravimetric analysis (TGA) of the PU/MMT nanocomposites has been performed in order to establish the thermal stability and their mode of thermal degradation. The TGA thermograms exhibited the fact that nanocomposites have a higher decomposition temperature in comparison with the pristine PU. It was found that the thermal degradation of all PU nanocomposites takes place in three steps. All the nanocomposites were stable up to 205°C. Degradation kinetic parameters of the composites have been calculated for each step of the thermal degradation processes using three mathematical models namely, Horowitz–Metzger, Coats–Redfern and Broido's methods. 相似文献
Poly(vinyl chloride) (PVC) nanocomposites with sodium montmorillonite (Na-MMT) and organically modified MMT (O-MMT) have been prepared by melt processing using mixing and extrusion techniques. The differential scanning calorimetry (DSC) with stochastic temperature modulation (TOPEM?) results show that the glass transition temperature (Tg) of PVC is slightly higher than Tg of PVC/Na-MMT and PVC/O-MMT which would indicate that MMT plays a role of an internal plasticizer that increases the distance between the PVC macrochains. The DSC TOPEM non-reversing heat flow profiles show enthalpy relaxation effects, and the lowest value has been found for pristine PVC—the presence of MMT (both Na+ and ammonium salt modified) may generate a certain orientation level of PVC macrochains during the extrusion process. Specific heat vs temperature dependencies at different frequencies revealed that the best fit to the single profile was found for PVC/Na-MMT nanocomposite, and this observation may be related to internal stability of the composite material as confirmed by analysis of the change in the specific heat (Δcp). 相似文献
Poly(ε-caprolactone) (PCL) masterbatches with the intercalated and the exfoliated morphology were prepared by ring opening polymerization of ε-caprolactone in the presence of organomodified montmorillonite (MMT) Cloisite 30B. Poly(l-lactide) (PLLA) nanocomposites with Cloisite 30B or PCL masterbatches were prepared by melt blending. The effects of the silicate type, MMT content and the nanocomposite morphology on thermal and mechanical properties of PLLA nanocomposites were examined. The montmorillonite particles in PLLA/Cloisite 30B and PLLA/intercalated masterbatch nanocomposites were intercalated. In contrary to expectations, the exfoliated silicate layers of exfoliated masterbatch were not transferred into the PLLA matrix. Due to a low miscibility of PCL and PLLA, MMT remained in the phase-separated masterbatch domains. The stress-strain characteristics of PLLA nanocomposites, Young modulus E, yield stress σy and yield strain εy, decreased with increasing MMT concentration, which is associated with the increase in PCL content. The expected stiffening effect of MMT was low due to a low aspect ratio of its particles and was obscured by both plastifying effects of PCL and low PLLA crystallinity. Interestingly, in contrast to the neat PLLA, ductility was enhanced in all PLLA/Cloisite 30B materials and in PLLA/masterbatch nanocomposites with low MMT concentrations. 相似文献
The thermal expansion coefficients of glass fiber–polymer composites were calculated applying the solid cylindrical model taking into account the interaction effects among the glass fibers. The stress and displacement in the composite model were determined as functions of the thermal stress. It was found theoretically that the deviation of the thermal expansion coefficient from the linear mixture relationship based on volume additivity appeared at around Tg + 20 K upon cooling. The thermal expansion coefficient of the composite was also found to be markedly dependent on the dispersion state of the glass fibers. An expression for the difference in the Tg of the matrix resin in the composite from that in the unloaded resin was obtained on the assumption that the volume change of the matrix resin caused by mixing was compensated by free volume expansion. The experimental results obtained by differential scanning calorimetry (DSC) measurements were found to agree well with the theoretically predicted ones. 相似文献