We report the growth of carbon nanofibers (CNFs) from carbon particles by chemical vapor deposition (CVD) with ultrasonic neblizer using ethanol as carbon source. Dense CNFs having diameters of several tens of nanometers have been successfully synthesized by the CVD without using any metal catalysts. The carbon particles formed from decompostion of fullerene were found to be suitable for the synthesis of CNFs. Details of the optimum conditions for producing CNFs and the expected growth mechanism are also described.

Carbon nanotubes (CNTs) have generated great interest within the many areas of nanotechnology due to their superior and outstanding physical properties. However effective dispersion in many solvents has imposed limitations upon the use of CNTs in a number of novel applications. Functionalization presents a solution for CNTs to be more soluble which make them integrate well into any organic, inorganic or biological systems. CNTs can be easily functionalized using cyclodextrin (CD) treatment. The CD modification of carbon nanotubes is both simple and effective. It requires no prolonged heating, filtration and washing which can severely damage the small diameter nanotubes. The formation of surface functional groups and changes of nanotubes structures of functionalized carbon nanotubes (f-CNTs) were monitored by Fourier transform infrared spectroscopy (FTIR), Thermo gravimetric analysis (TGA) and field emission scanning electron microscopy (FESEM), respectively. From the TGA results, the amount of weight loss of the f-CNTs in varying ratios indicated the amount of CD that was functionalized. It was also noted that the FTIR spectra showed the presence of functional groups associated with CD in the f-CNTs. As a result, the cyclodextrin groups were found to be possibly adsorbed at the surface of the nanotubes walls. The f-CNTs showed substantial solubility in N-methyl-2-pyrrolidone (NMP) which helps in a better distribution of the CNTs in the mixed matrix membrane (MMM) prepared. Hence, the influence of the f-CNTs in the polymer matrix will give rise to enhanced physical properties of the MMM suitable for applications in gas separations.

Alumina supported cobalt-ferrum catalysts were prepared using wet impregnation method by applying 3 different conditions, namely hotplate (A), sonication (B) and soaking (C). The alumina supported cobalt-ferrum catalysts were applied in the synthesis of multi-walled carbon nanotubes (MWNTs) using catalytic chemical vapour deposition (CCVD) technique. The morphology and particle size of the cobalt-ferrum catalysts and the MWNTs yield were examined by field emission-scanning electron microscopy (FE-SEM) while the surface elemental composition of the samples was obtained by energy dispersive X-ray analysis (EDX). The morphology of catalysts A, B and C were found to be different, the particle sizes were ranged from 20-40 nm. The diameters of the MWNTs yield from samples A, B and C were found to be related to the catalyst particle size, thus the smaller the catalyst particle, the thinner the MWNTs obtained. The MWNTs with smaller diameter were obtained with higher purity and quality becuase the nanotube surface are free from amorphous carbon. Therefore, different catalyst preparation methods resulted in different sizes of the catalyst particle in order to synthesize MWNTs with desired diameter.

Ge surfaces were irradiated by Ar+ ions at 600 eV with and without simultaneous supply of Ge or Al at room temperature. The surfaces ion-irradiated without any simultaneous metal supply were characterized by densely distributed conical protrusions. By contrast, various kinds of nanostructures were formed on the Ge surfaces ion-irradiated with a simultaneous metal supply. They featured cones and nanobelts with a flattened top for Ge supply cases, whereas they were characterized by the nanorods, nanobelts and nanowalls for Al supply cases. Very interestingly, most of the nanorods and nanobelts formed with an Al supply possessed a bottleneck structure. Thus, the Ge nanostructures were controllable in morphology by species and amount of simultaneously supplied metals.

Carbon nanofibers (CNFs) were fabricated on graphite plates using "Ar+ ion sputtering method" in large amount at room temperature. The morphology of CNFs was controlled by a simultaneous carbon supply during ion sputtering. CNF-tipped cones were formed on graphite plate surfaces without carbon supply whereas those with a simultaneous carbon supply featured mainly needle-like protrusions of large size. The field electron emission (FE) properties, measured using parallel plate configurations in 10-4 Pa range, showed the threshold fields of 4.4 and 5.2 V/µm with a current density of 1 µA/cm2 for CNF-tipped cones and needle-like protrusion, respectively. Reliability test results indicated that CNF-tipped cones were more stable than needle-like protrusion. The morphological change after reliability test showed a so-called "self-regenerative" process and structure damage for CNF-tipped cones and needle-like protrusions, respectively.