Polymer composites with inorganic fillers of different nature, concentration, particle size and shape were studied by optical spectroscopy (UV, visible, and IR ranges), optical and electron microscopy, and dynamic light scattering. An experiment to determine the size of the filler particles in aqueous suspension in the polymer matrix of a composite and directly in powders was conducted. It was shown that with increasing concentration aggregation of particles on drying an aqueous slurry occurs to a greater extent than for the filler in the polymer composite. It was demonstrated by examples that the optical spectroscopy can be successfully used for the analysis of sub-micron and micron sized filler particles in a polymer matrix or suspension. 相似文献
The combination of organophillised montmorillonite (MMT), synthetic hydromagnesite and aluminium hydroxide (ATH) as flame retardant system for polyethylene-based materials was studied and compared with a similar system with magnesium hydroxide, ATH and MMT. The thermal stability and the flame retardant properties were evaluated by thermogravimetric analysis (TGA), differential thermal analysis (DTA), limiting oxygen index (LOI) and cone calorimeter tests. The results indicated that the addition of montmorillonite makes it possible to reduce the total filler content to achieve the flame retardant requirements. The thermal stability of filled LDPE/EVA blends increases to a higher extent for the samples containing MMT. In the cone calorimeter tests we observed a reduction of the peak heat release rate for the sample containing montmorillonite in comparison with a sample with higher filler loading without this nanoclay. An increase of the stability of the char formed could be responsible for this favourable behaviour when montmorillonite is added.In addition, mechanical properties significantly improved for the composites containing montmorillonite both for the filler loading reduction and the reinforcement effect of the nanoclay. 相似文献
The fabrication of nanocomposites of low‐density polyethylene (LDPE), one of the world's most widely used polymers, and cellulose nanocrystals (CNCs), which represent the world's most abundant bio‐based nanofiller, is reported. While the hydrophobic polymer and the hydrophilic filler seem to be intrinsically incompatible, this article shows that it is possible to kinetically trap homogeneous nanocomposites by a templating approach. An organogel is first prepared by exchanging the solvent of an aqueous CNC dispersion against acetone, impregnating the resulting organogel, in which the CNCs form a percolating network with a hot LDPE solution in toluene, and compression‐molding the resulting materials into thin films. At a filler content of 7.6% v/v, the resulting materials display a three‐ to four‐fold increase in strength and stiffness compared with the neat LDPE, which confirms that the CNC network could be largely maintained. It is also possible to reprocess these nanocomposites and dilute them with LDPE using conventional melt‐processing techniques.
The effect of time of soaking on bulk density and dielectric constant has been measured on pure and niobium-doped barium titanate pyroelectric specimens. The temperature dependence of the dielectric constant for both pure and niobium-doped barium titanate samples has been investigated before and after poling. The percentage dielectric anisotropy and ferroelectricity was also calculated for various pure and modified barium titanate pyroelectric materials. Our results can be explained in terms of the redistribution of the barium titanate lattice in a different crystallographic orientation, polarization, as well as the existence of lattice imperfection accompanying temperature, poling and niobium doping. The obtained results were in good conformity, and correlated with the increased proportion of the remnant 90° domains (induced electrically charged vacancies as a result of Nb3+ substitution of Ti4+ in octahedral lattice sites). It was concluded that poling of Nb-doped barium titanate samples produces the best quality ceramic pyroelectrics. 相似文献
Flame retardant-modified sepiolite nanofiber (PSPHD-SEP) was fabricated through chemical grafting by introducing intumescent flame retardant oligomer (PSPHD) onto the surface of sepiolite fiber. Various sepiolite/low-density polyethylene (SEP/LDPE) composites have been prepared successfully via melt blending. The dispersion of various SEPs in LDPE matrix was observed by scanning electron microscope and transmission electron microscope. The thermal degradation behaviors of various SEP/LDPE composites with 3 mass% acid-modified sepiolite fiber (a-SEP) or PSPHD-SEP have been investigated employing thermogravimetric analysis/derivative thermogravimetry. The thermal degradation kinetics of neat LDPE, a-SEP/LDPE and PSPHD-SEP/LDPE systems was comparatively analyzed by means of Friedman and Flynn–Wall–Ozawa methods to further comprehend the effect of a-SEP and PSPHD-SEP on the thermal stability of LDPE. Due to the addition of PSPHD-SEP, the limiting oxygen index value of PSPHD-SEP/LDPE composite can reach 21.3%, and the UL-94V-2 rating is obtained. The cone calorimetry (CONE) tests showed that a reduced peak heat release rate can be achieved for PSPHD-SEP/LDPE composite accompanying with gas-phase fire retardant action.
Effect of various antioxidants on the thermal oxidation stability of LDPE and X-LDPE has been investigated. To achieve this purpose, miscellaneous commercial grade antioxidants such as Irganox 1010, Irganox1076, Irgafos168, Irganox B225, and Chimassorb 944 were selected. Then, formulations based on different content of antioxidant were prepared. The samples were crosslinked by exposure to electron beam irradiation. To assess the thermal oxidation stability of samples, oxidation induction time (OIT) test was accomplished on both the irradiated and unirradiated specimens. Ageing tests were carried out in order to evaluate the thermal oxidation stability of irradiated X-LDPE. The results indicate that Irganox 1010 is the most effective antioxidant amongst the selected ones, concerning thermal oxidation stability of LDPE, before and after aging test. 相似文献
LDPE films have been exposed to abiotic and biotic environments. The films were UV irradiated for periods of 0, 7, 14, 26 and 42 days before being mixed with water and soil.Degraded LDPE films were examined by infra-red spectroscopy. The carbonyl peak increased with time in the abiotic environment and the oxidative degradation reported in our earlier works was confirmed.In the presence of a biotic atmosphere, however, this peak decreased. At the same time there was an increase in double bonds which was related to weight loss. An explanation of this behavior is presented as a proposed mechanism for the biodegradation of polyethylene.This mechanism is compared, on the one hand, with abiotic photooxidation, Norrish type I and II degradation, and, on the other, with the biotic paraffin degradation. Abiotic, as well as biotic, ester formation mechanisms are also presented.An ESR spectrum confirms the presence of radicals on the polyethylene samples.At the beginning of the degradation the main agents seem to be UV light and/or oxidizing agents. When carbonyl groups have been produced, these are attacked by microorganisms which degrade the shorter segments of polyethylene chains and form carbon dioxide and water as end products.There is a synergistic effect between photooxidative degradation and biodegradation. The biodegradation of polyethylene can be compared with the biodegradation of paraffin. 相似文献
