RESUMO
The phenol-formaldehyde-carbon nanotube composites were characterized for their free volume properties and interfacial interactions between nanotubes and the polymer matrix. The base polymeric material was a novolac type phenol-formaldehyde (PF) condensation resin cross-linked with para-toluene sulfonic acid. Multi-wall carbon nanotubes (MWCNTs) were synthesized using a catalytical chemical vapor deposition method and characterized using high-resolution transmission electron microscopy. The PF resin-carbon nanotubes composites having 2, 5, 10 and 20% (w/w%) MWCNTs were prepared. The crystallinity and morphology of the samples were characterized using X-ray diffraction and scanning electron microscopy. The free volume size in the polymer nanocomposites was observed to increase with the increase in nanotube content. Positron age momentum correlation (AMOC) studies revealed the electronic environment around different positron annihilation sites. The studies showed that ortho-positronium principally annihilates from interfacial regions of polymer and nanotubes in the nanocomposite. The positron lifetime studies together with AMOC measurements indicate an increase in the free volumes at the interface of polymer and MWCNTs in the composite. The free positron intensities showed that the polymer and nanotubes are weakly interacting in this system.
RESUMO
We have studied various metallorganic and organometallic compounds by simultaneous nonisothermal thermogravimetric and differential thermogravimetric analyses to confirm their volatility and thermal stability. The equilibrium vapor pressures of the metallorganic and organometallic compounds were determined by horizontal dual arm single furnace thermoanalyzer as transpiration apparatus. Antoine coefficients were calculated from the temperature dependence equilibrium vapor pressure data. The model-fitting solid-state kinetic analyses of Al(acac)3, (acac = acetylacetonato), Cr(CO)6, Fe(Cp)2, (Cp-cyclopentadienyl), Ga(acac)3, Mn(tmhd)3, and Y(tmhd)3 (tmhd = 2,2,6,6,-tetramethyl-3,5-heptanedionato) revealed that the processes follow diffusion controlled, contracting area and zero order model sublimation or evaporation kinetics. The activation energy for the sublimation/evaporation processes were calculated by model-free kinetic methods. Thin films of nickel and lanthanum-strontium-manganite (LSM) are grown on silicon substrate at 573 K using selected metallorganic complexes of Ni[(acac)2en], La(tmhd)3, Sr(tmhd)2 and Mn(tmhd)3 as precursors by plasma assisted liquid injection chemical vapor deposition (PA-LICVD). The deposited films were characterized by scanning electron microscopy and energy dispersive X-ray analysis for their composition and morphology.
RESUMO
Multi-wall carbon nanotubes have been synthesized by catalytic chemical vapour deposition method. Attempts have been made to decorate the walls of these nanotubes with various metal nanoparticles (Ni, Cu and Fe) after functionalizing the nanotubes walls by wet chemical method. Small-Angle Neutron Scattering data reveals chain cluster type morphology of the carbon nanotubes. Transmission electron microscopy, Energy dispersive analysis of X-rays and Small-Angle Neutron Scattering measurements show that decoration of nanotube walls by metallic nano-particles could be realized for Ni and Cu nano-particles. Further, wall decoration by nano-particles of Fe could not be achieved by wet chemical method due to strong agglomeration behavior of Fe nano-particles.
RESUMO
In-line x-ray phase contrast is an emerging x-ray imaging technique that promises to improve the contrast in x-ray imaging process. This technique is most suited for x-ray imaging of soft materials, low atomic number elements such as carbon composite fibers, very thin coatings, etc. We have used this new emerging technique for visualization and characterization of the pyrocarbon coated materials using a combination of microfocus x-ray source and x-ray charge coupled device detector. These studies are important for characterization of coating and optimization of various process parameters during deposition. These experiments will help us to exploit the potential of this technique for studies in other areas of material science such as characterization of carbon fibered structures and detection of cracks and flaws in materials. The characterization of the imaging system and optimization of some process parameters for carbon deposition are also described in detail.