Showing 4 results for Hydrothermal
F. Asjadi , S. Khatiboleslam Sadrnezhad,
Volume 31, Issue 1 (6-2012)
Abstract
In this paper, VO2 nanorods were produced by hydrothermal assisted synthesis of equimolar aqueous NH4Cl and NaVO3 solution. Effect of time and the amount of ethylenediaminetetracetic acid (EDTA) additive on morphology and composition of the final product was determined. The optimum concentration of EDTA was determined to be 0.007 gm/cm3 and the optimum time of the synthesis was 24 h.
R. Nayerhoda, F. Asjadi, P. Seifi, M. Salimi,
Volume 34, Issue 1 (5-2015)
Abstract
In the present investigation, spherical nanoparticles of nickel ferrite with uniform structure were successfully produced by hydrothermal method in the presence of polyethylene glycol (PEG) as a polymeric surfactant at 180°C for 12 hour aging time and the effects of the synthesis time, temperature and surfactant were investigated. According to the X-ray analysis, conversion of nickel oxide and hematite to nickel ferrite was a way to produce NiFe2O4. At 140°C, agglomerated particles without specific shape were formed, but at 180°C particles were homogenous with spherical shape. Saturation magnetization increased by increasing the hydrothermal process aging time.
P. Razmjouee, S. M. Mirkazemi,
Volume 34, Issue 1 (5-2015)
Abstract
In this investigation, the effect of Polyvinylpyrrolidone (PVP) additive on microstructure, morphology and magnetic properties of cobalt ferrite nanoparticles prepared by hydrothermal method was studied. X-ray diffraction (XRD) studies in different synthesis conditions showed the formation of cobalt ferrite and cobalt oxide. Comparing IR spectrum of PVP additive, sol prepared before hydrothermal process and C-0.1PVP3, 190 obtained by FTIR spectroscopy indicated the formation of bond between PVP and surface of metallic hydroxide and cobalt ferrite particles, which prevented them from growing and coarsening. Scanning electron microscope (SEM) was used to study the morphology of samples. According to vibration sample magnetometer (VSM) results, as PVP amount increases from 0.1 to 0.3 volume percent, coercive field increases from 298 to 684 Oe and saturation magnetization decreases from 58 to 51 emu/g.
S. Daneshvar E Asl, S. Kh. Sadrnezhaad,
Volume 37, Issue 2 (9-2018)
Abstract
Rutile-phase titanium dioxide nanorod arrays were prepared by the hydrothermal method. Then, anatase-phase nanoleaves were successfully synthesized on the nanorod arrays via mild aqueous chemistry. Nanorod arrays scanning electron microscopy revealed that the thin film is uniform and crack free and the average diameter and height of the nanorods are 90 nm and 2 µm, respectively. Furthermore, nanorods are vertical to the substrate surface and have desired coverage density due to the predeposition of TiO2 seed layer which leaded to decrease the surface roughness of the substrate. Nanoleafed nanorods scanning electron microscopy indicated that the nanoleaves were grown uniformly on the entire surface of nanorods and the specific surface area and roughness factor of those are significantly improved. Energy dispersive spectrums suggested that F- and Cl- ions are partially doped into TiO2 crystals. Raman and X-ray spectra confirmed the formation of anatase-phase nanoleaves on the rutile-phase nanorods. X-ray diffraction also indicated that the nanorod arrays are highly oriented with respect to the substrate surface. The diffused reflectancetransmittance data revealed the incident light was more efficiently harvested by the nanoleafed nanorod thin film and the values of energy gap are 2.78 and 2.82 eV for rutile TiO2 nanorod and rutile+anatase TiO2 nanoleafed nanorod thin films, respectively. Synthesized nanostructure, having improved charge separation and transfer (due to the presence of the surface anatase/rutile junctions), high specific surface area and light harvesting (due to the presence of the nanoleaves) and low band gap energy (due to the nonmetallic elements doping), is viable alternative to traditional single crystalline TiO2 nanorods for highly efficient photoelectrochemical applications.
