Graphene nanoplatelets (xGnP), expanded graphite (EG), multiwall carbon nanotubes (MWCNTs), and carbon black (CB) were dispersed in various amounts in a thermosetting polyurethane (PU) matrix derived from castor oil and composite plaques were obtained by compression molding. The electrical percolation threshold was found to be 0.1 vol% for MWCNT, 0.5 vol% for xGnP, 2.8 vol% for CB, and 2.7 vol% for EGfilled systems. The relation between electrical conductivity, morphology, and electromagnetic interference shielding effectiveness (EMI SE) of the resulting composites was studied to understand how the EMI SE is influenced by morphology and electrical conductivity of each filler. The composites display significantly distinct EMI SE values, depending on the type of carbon filler and its volume fraction. Composite based in PU/ EG and PU/xGnP exhibited the highest EMI SE values (70 and 47 2dB, respectively); however, PU/MWCNT composites showed higher EMI SE (24 2dB) value at the same filler content (3 vol%) than the other composite system. POLYM. COMPOS., 00:000-000,
The catalytic activity of cobalt and iron nanoparticles for the growth of carbon nanotubes (CNTs) was studied by a specific reproducible and up-scalable fabrication method. Co and Fe catalysts were deposited over SiO2 nanoparticles by a wet-impregnation method and two different annealing steps were applied for the catalyst formation/activation. The samples were calcined at an optimal temperature of 450 °C resulting in the formation of metal oxide nano-islands without the detection of silicates. Further reduction treatment (700 °C) under H2 successfully converted oxide nanoparticles to Co and Fe metallic species. Furthermore, the catalytic efficiency of both supported-metal nanoparticles at 2 and 5% in weight of silica was evaluated through the growth of CNTs. The CNT structure, morphology and size dispersion were tailored according to the metal catalyst concentration.
The fabrication of iron and iron carbide nanoparticles (NPs) for catalytic reactions such as the growth of carbon nanotubes (CNTs) compete with the challenge of covering a wide range of substrates with perfect control of the NP reactivity. We present in this work a novel atomic layer deposition (ALD) process to grow Fe/Fe3C thin films over silica flat substrates. The depositions were carried out exposing the surface through various number of ALD cycles, resulting in Fe-based films with thicknesses ranging from 4 nm to almost 40 nm. After a thermal treatment, the film dewetts into nanoparticles, where the efficiency to grow CNTs will depend on the average size distribution of the nanocatalyst. X-ray diffraction and x-ray photoelectron spectroscopy were used to track the elemental, phase, and shape (film to particles) transformation in order to identify the key features of the nanocatalyst, thereby controlling the CNT nucleation and growth. Thin film thickness of around 5 nm promotes the growth of a dense CNT forest. Furthermore, the metal–CNT films reveal optical properties that are totally tailored by the initial number of ALD cycles.
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