Nucleating Effect of Carbon Nanoparticles and Their Influence on the Thermal and Chemical Stability of Polypropylene

The effect of carbon nanofibers (CNFs) and carbon nanotubes (CNTs) on the thermal and chemical stability of polypropylene (PP) when subjected to oxidation in a strong acid medium was studied. The effect of CNFs and CNTs on the crystalline morphology and the melting and crystallization temperatures was also studied. The thermal stability increased markedly; the decomposition temperature, for example, increased from 293∘C for pure PP to 312 and 320∘C for PP with CNFs and CNTs, respectively. The crystallization temperature increased perceptibly with the addition of CNTs or CNFs, from 107∘C for pure PP to 112 and 114∘C for PP with CNFs and CNTs, respectively. The oxidative degradation with nitric acid produced a reduction in molecular weight; however, this negative effect was less pronounced in the PP compositions with carbon nanoparticles. After 8 hours in nitric acid, this reduction was from 141,000 to 68,000 (for pure PP), to 75,000 (for PP-CNFs), and 79,500 (for PP-CNTs). X-ray diffraction showed that the alpha type crystallinity remains, irrespective of the nucleating agent. Finally, the intensity ratio between the (040) (at 16.7∘) and the (110) (at 13.9∘) reflections increased, which was taken as an indication of an increasing nucleating efficiency

Nucleating Effect of Carbon Nanoparticles and Their Influence on the Thermal and Chemical Stability of Polypropylene

The effect of carbon nanofibers (CNFs) and carbon nanotubes (CNTs) on the thermal and chemical stability of polypropylene (PP) when subjected to oxidation in a strong acid medium was studied. The effect of CNFs and CNTs on the crystalline morphology and the melting and crystallization temperatures was also studied. The thermal stability increased markedly; the decomposition temperature, for example, increased from 293 • C for pure PP to 312 and 320 • C for PP with CNFs and CNTs, respectively. The crystallization temperature increased perceptibly with the addition of CNTs or CNFs, from 107 • C for pure PP to 112 and 114 • C for PP with CNFs and CNTs, respectively. The oxidative degradation with nitric acid produced a reduction in molecular weight; however, this negative effect was less pronounced in the PP compositions with carbon nanoparticles. After 8 hours in nitric acid, this reduction was from 141,000 to 68,000 (for pure PP), to 75,000 (for PP-CNFs), and 79,500 (for PP-CNTs). X-ray diffraction showed that the alpha type crystallinity remains, irrespective of the nucleating agent. Finally, the intensity ratio between the (040) (at 16.7 • ) and the (110) (at 13.9 • ) reflections increased, which was taken as an indication of an increasing nucleating efficiency

Effect of Nanometric Metallic Hydroxides on the Flame Retardant Properties of HDPE Composites

The effect of nanometric magnesium and aluminum hydroxides on the flame retardancy of high density polyethylene was studied. Additionally, the effect of maleic anhydride grafted polyethylene (PEgMA) and methyl acrylate grafted polyethylene (EMA) compatibilizers, on the tensile properties, was also studied. Morphological characterization of nanocomposites was carried out by means of scanning transmission electron microscopy (STEM). Flame retardant properties of nanocomposites were evaluated by the UL-94 horizontal and vertical tests as well as by cone calorimeter tests. Thermal degradation behavior was analyzed with a thermogravimetric analyzer (TGA). Tensile tests were carried out according to ASTM D 638-03 in an Instron 4301 tensile testing machine. From STEM images, a good dispersion of flame retardants (MH and ATH) in the polymer matrix was observed, which was reflected in the flame retardant properties. Results showed that the combination of nanometric MH and ATH produced excellent flame retardant properties, achieving a classification of V0 in the UL-94-V test and producing the lowest peak of heat release rate (PHRR) and the lowest total heat released (THR) in the cone calorimeter test. Finally, the addition of compatibilizer, especially PEgMA, resulted in much better tensile properties as compared to the noncompatibilized composition, maintaining the flame retardant properties