István Endre Lukács

A comparative research on stability, viscosity (µ), and thermal conductivity (k) of carbon nanosphere (CNS) and carbon nanopowder (CNP) nanofluids was performed. CNS was synthesized by the hydrothermal method, while CNP was provided by the manufacturer. Stable nanofluids at high concentrations 0.5, 1.0, and 1.5 vol% were prepared successfully. The properties of CNS and CNP nanoparticles were analyzed with Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), specific surface area (S_BET), X-ray powder diffraction (XRD), thermogravimetry/differential thermal analysis (TG/DTA), and energy dispersive X-ray analysis (EDX). The CNP nanofluids have the highest k enhancement of 10.61% for 1.5 vol% concentration compared to the base fluid, while the CNS does not make the thermal conductivity of nanofluids (k_nf) significantly higher. The studied nanofluids were Newtonian. The relative µ of CNS and CNP nanofluids was 1.04 and 1.07 at 0.5 vol% concentration and 30 °C. These results can be explained by the different sizes and crystallinity of the used nanoparticles.

Extending the absorption range of TiO₂ nanofibers to visible light is a great improvement of the photocatalytic property of TiO₂. In this study, TiO₂/WO₃/C/N nanofibers were prepared by electrospinning using precursors soluble in water then annealing in argon. Titanium(IV) bis(ammonium lactato)dihydroxide (TiBALDH) and ammonium metatungstate (AMT) were used as the precursor for TiO₂ and WO₃ respectively. Different volume ratios of the precursors were added to a solution of PVP before electrospinning. The fibers were studied by XPS, SEM-EDX, TEM, FTIR, XRD, Raman spectroscopy and UV–VIS diffuse reflectance spectroscopy (DRS). The photocatalytic degradation of methylene blue by the fibers in visible light was investigated. The fibers had anatase TiO₂ and monoclinic WO₃. Based on UV–VIS DRS and Kubelka-Munk function the fibers could absorb visible light. Moreover, 100% TiBALDH had an indirect band gap of 2.9 eV, and the band gap decreased with increase in AMT, i.e., for 0% TiBALDH, band gap was 2.4 eV. The fibers degraded methylene blue dye in visible light, and 90% TiBALDH had the highest photocatalytic activity, i.e., it degraded 40% of the dye after 240 min.

Nanofluids obtained from halloysite and de-ionized water (DI) were prepared by using surfactants and changing pH for heat-transfer applications. The halloysite nanotubes (HNTs) nanofluids were studied for several volume fractions (0.5, 1.0, and 1.5 vol%) and temperatures (20, 30, 40, 50, and 60 °C). The properties of HNTs were studied with a scanning electron microscope (SEM), energy-dispersive X-ray analysis (EDX), Fourier-transform infrared (FT-IR) spectroscopy, X-ray powder diffraction (XRD), Raman spectroscopy and thermogravimetry/differential thermal analysis (TG/DTA). The stability of the nanofluids was proven by zeta potentials measurements and visual observation. With surfactants, the HNT nanofluids had the highest thermal conductivity increment of 18.30% for 1.5 vol% concentration in comparison with the base fluid. The thermal conductivity enhancement of nanofluids containing surfactant was slightly higher than nanofluids with pH = 12. The prepared nanofluids were Newtonian. The viscosity enhancements of the nanofluid were 11% and 12.8% at 30 °C for 0.5% volume concentration with surfactants and at pH = 12, respectively. Empirical correlations of viscosity and thermal conductivity for these nanofluids were proposed for practical applications.

Over many years, great efforts have been made to develop new fluids for heat transfer applications. In this paper, the thermal conductivity (TC) and viscosity of SiO₂–P25 TiO₂ (SiO₂–P25) hybrid nanofluids were investigated for different nanoparticle volume concentrations (0.5, 1.0 and 1.5 vol%) at five various temperatures (20, 30, 40, 50 and 60 °C). The mixture ratio (SiO₂:P25) in all prepared hybrid nanofluids was 1:1. Besides, pure SiO₂, P25 nanofluids were prepared with the same concentrations for comparison with the hybrid nanofluids. The base fluid used for the preparation of nanofluids was a mixture of deionized water and ethylene glycol at a ratio of 5:1. Before preparing the nanofluids, the nanoparticles were analyzed with energy-dispersive X-ray analysis, scanning electron microscope, X-ray powder diffraction, and Fourier transform infrared spectroscopy. The zeta potentials of the prepared nanofluids except SiO₂ nanofluids were above 30 mV. These nanofluids were visually observed for stability in many days. The TC enhancement of the hybrid nanofluid was higher than the pure nanofluid. In particular, with 1.0 vol% concentration, the maximum enhancement of SiO₂, P25 and SiO₂–P25 nanofluids were 7.5%, 9.9% and 10.5%, respectively. The rheology of the nanofluids was Newtonian. The viscosity increment of SiO₂, P25 and hybrid nanofluids were 19%, 32% and 24% with 0.5 vol% concentration. A new correlation was developed for the TC and dynamic viscosity of SiO₂–P25 hybrid nanofluid.

Effects of different reaction parameters in the hydrothermal synthesis of molybdenum oxides (MoO₃) were investigated and monoclinic (β-) MoO₃ was prepared hydrothermally for the first time. Various temperatures (90/210 °C, and as a novelty 240 °C) and durations (3/6 h) were used. At 240 °C, cetyltrimethylammonium bromide (CTAB) and CrCl₃ additives were also tested. Both the reaction temperatures and durations played a significant role in the formation of the products. At 90 °C, h-MoO₃ was obtained, while at 240 °C the orthorhombic (α-) MoO₃ formed with hexagonal rod-like and nanofibrous morphology, respectively. The phase transformation between these two phases was observed at 210 °C. At this temperature, the 3 h reaction time resulted in the mixture of h- and α-MoO₃, but 6 h led to pure α-MoO₃. With CTAB the product was bare o-MoO₃, however, when CrCl₃ was applied, pure metastable m-MoO₃ formed with the well-crystallized nanosheet morphology. The gas sensing of the MoO₃ polymorphs was tested to H₂, which was the first such gas sensing study in the case of m-WO₃. Monoclinic MoO₃ was found to be more sensitive in H₂ sensing than o-MoO₃. This initial gas sensing study indicates that m-MoO₃ has promising gas sensing properties and this MoO₃ polymorph is promising to be studied in detail in the future.

In this study, Bi₂WO₆ was prepared by the hydrothermal method. The effects of reaction temperature (150/170/200 °C) and reaction time (6/12/24 h) were investigated. The role of strongly acidic pH (1 >) and the full range between 0.3 and 13.5 were studied first. Every sample was studied by XRD and SEM; furthermore, the Bi₂WO₆ samples prepared at different temperatures were examined in detail by EDX and TEM, as well as FT-IR, Raman and UV-vis spectroscopies. It was found that changing the temperature and time slightly influenced the crystallinity and morphology of the products. The most crystallized product formed at 200 °C, 24 h. The pure, sheet-like Bi₂WO₆, prepared at 200 °C, 24 h, and 0.3 pH, gradually transformed into a mixture of Bi₂WO₆ and Bi_3.84W_0.16O_6.24 with increasing pH. The nanosheets turned into a morphology of mixed shapes in the acidic range (fibers, sheets, irregular forms), and became homogenous cube- and octahedral-like shapes in the alkaline range. Their band gaps were calculated and were found to vary between 2.66 and 2.59 eV as the temperature increased. The specific surface area measurements revealed that reducing the temperature favors the formation of a larger surface area (35.8/26/21.6 m²/g belonging to 150/170/200 °C, respectively).

Various methods are currently under development to enhance the biocompatibility of neural electrodes and to minimize the reactive gliosis around the implant surface. As cells in their native microenvironment interact with 3D nanoscale topographies of the extracellular matrix, physical modification of implant surfaces may provide an alternative solution to the negative tissue response by imitating the structure of the extracellular matrix, and therefore affecting the attachment and behavior of neurons and glial cells. The attachment of primary mouse astrocytes on nanostructured SU8 polymer surfaces fabricated by e-beam lithography was investigated in our study. We found that attachment of primary mouse astrocytes on silicon-SU8 surfaces is strongly influenced by the surface topography.