The application of optical-fiber thermal wave cavity (OF-TWC) technique was investigated to measure the thermal diffusivity of Ag nanofluids. The thermal diffusivity was obtained by measuring the thermal wavelength of sample in a cavity scan mode. The spherical Ag nanoparticles samples were prepared at various sizes using the microwave method. Applying the thermal wavelength measurement in a flexible OF-TWC technique requires only two experimental data sets. It can be used to estimate thermal diffusivity of a small amount of liquid samples (0.3 ml) in a brief period. UV-Vis spectroscopy and transmission electron microscopy were used to measure the characterization of the Ag nanoparticles. The thermal diffusivity of distilled water, glycerol, and two different types of cooking oil was measured and has an excellent agreement with the reported results in the literature (difference of only 0.3%-2.4%). The nanofluids showed that the highest value of thermal diffusivity was achieved for smaller sized nanoparticles. The results of this method confirmed that the thermal wavelength measurement method using the OF-TWC technique had potential as a tool to measure the thermal diffusivity of nanofluids with different variables such as the size, shape, and concentration of the nanoparticles.
Two novel glycolipids have been synthesized and their phase behaviour studied. They have been characterized using FT-IR, FAB and 13C NMR and 1H NMR to ensure the purity of novel glycolipids. The two glycolipids are distinguished based on the head group of glycolipids (monosaccharide/glucose and disaccharide/maltose). These two novel glycolipids have been used as surfactant to perform two phase diagrams. Phase behaviours that have been investigated are 2-hexyldecyl-beta-D-glucopyranoside (2-HDG)/n-octane/water ternary system and 2-hexyldecyl-beta-D-maltoside (2-HDM)/n-octane/water ternary system. SAXS and polarizing optical microscope have been used to study the phase behaviours of these two surfactants in ternary phase diagram. Study of effect of the head group on branched-alkyl chain surfactants in ternary system is a strategy to derive the structure-property relationship. For comparison, 2-HDM and 2-HDG have been used as surfactant in the same ternary system. The phase diagram of 2-hexyldecyl-beta-D-maltoside/n-octane/water ternary system exhibited a Lalpha phase at a higher concentration regime, followed with two phases and a micellar solution region in a lower concentration regime. The phase diagram of 2-HDG/water/n-octane ternary system shows hexagonal phase, cubic phase, rectangular ribbon phase, lamellar phase, cubic phase as the surfactant concentration increase.
The phase behaviour of a system composed of amino acid-based surfactant (sodium N-lauroylsarcosinate hydrate), 1-decanol and deionised water was investigated for vesicle formation. Changing the molar ratio of the amphiphiles, two important aggregate structures were observed in the aqueous corner of the phase diagram. Two different sizes of microemulsions were found at two amphiphile-water boundaries. A stable single vesicle lobe was found for 1∶2 molar ratios in 92 wt% water with vesicles approximately 100 nm in size and with high zeta potential value. Structural variation arises due to the reduction of electrostatic repulsions among the ionic headgroups of the surfactants and the hydration forces due to adsorbed water onto monolayer's. The balance of these two forces determines the aggregate structures. Analysis was followed by the molecular geometrical structure. These findings may have implications for the development of drug delivery systems for cancer treatments, as well as cosmetic and food formulations.
For the first time, a sonochemical process has been used to synthesis cobalt oxide Co3O4nanoflowers and nanorods morphology in the presence of the ionic liquid 1-Ethyl-3-methylimidazolium tetrafluoroborate [EMIM][BF4] as reaction media and morphology template. Different sonication time periods and different molar ratios of the ionic liquid (IL) were used to investigate their effects on the structural, optical, chemical and magnetic properties of the produced Co3O4nanoparticles. During synthesis process brown powder contains cobalt hydroxide Co(OH)2and cobalt oxyhydroxide (Cobalt hydroxide oxide) CoO(OH) was formed, after calcination in air for 4h at 400°C a black powder of Co3O4nanoparticles was produced. The produced Co3O4nanoparticles properties were characterized by X-ray diffraction (XRD), Field Emission Scanning Electron Microscopy (FE-SEM), transmission electron microscopy (TEM), FTIR spectroscopy, UV-vis spectroscopy, and Vibrating Sample Magnetometer (VSM). To explain the formation mechanism of Co3O4NPs some investigations were carried on the brown powder before calcination.
Self-assembled nanocarriers attract increasing attention due to their wide application in various practical fields; among them, one of the most focused fields is drug delivery. Appropriate selection of surfactant is the basis for preparing a successful nanocarrier. Until now, from phospholipid to synthetic surfactants, many surfactants have been used to explore a suitable drug delivery vehicle for the complex in-vivo environment. Among all, bio surfactants are found to be more suitable due to their bio-origin, less-toxicity, biodegradability, cheaper rate and above all, their versatile molecular structures. This molecular property enables them to self assemble into fascinating structures. Moreover, binding DNA, enhancing pH sensitivity and stability allows novelty over their synthetic counterparts and phospholipid. This review paper focuses on the properties and applications of bio-nano-carriers for drug delivery. Micelle, microemulsion, and vesicle are the three nanocarriers which are discussed herein.
Gd2 O2 S:Eu3+ nanophosphors have been successfully synthesized using microwave irradiation and γ-irradiation methods with polyvinyl pyrrolidone as a stabilizer. The physical and luminescence spectra were compared. The morphologies of both Gd2 O2 S:Eu3+ nanophosphors were in the hexagonal phase and mainly consisted of spherical nanostructures with diameters of ~90 nm and ~50 nm for both microwave irradiation and γ-irradiation methods. Upon 325 nm of ultraviolet (UV) light excitation, strong red emissions (626 nm) were observed for both methods; these emissions corresponded to the 5 D0 →7 F2 transition of Eu3+ ions. However, Gd2 O2 S:Eu3+ nanophosphors following microwave treatment showed better luminescence intensity than Gd2 O2 S:Eu3+ nanophosphors treated with γ-irradiation. This difference was attributed to the crystallinity phase and surface quenching effects of Gd2 O2 S:Eu3+ nanophosphors. The reaction mechanisms of Gd2 O2 S:Eu3+ nanophosphors in both methods are discussed in detail.
Modulated continuous wave (CW) lasers cause photothermal effect that leads to rapid optical absorption and generation of thermal waves around the irradiated nanostructures. In this work, we examined the effect of modulated CW laser irradiation on the particle fragmentation process to enhance the thermal diffusivity of nanofluids. A facile and cost-effective diode laser was applied to reduce the agglomerated size of Al2O3 nanoparticles in deionized water. The thermal wave generation, which was determined by the modulated frequency of the laser beam and the optical and thermal properties of the nanofluid, is also briefly discussed and summarized. The influence of laser irradiation time on nanoparticle sizes and their size distribution was determined by dynamic light scattering and transmission electron microscopy. The thermal diffusivity of the nanofluid was measured using the photopyroelectric method. The data obtained showed that the modulated laser irradiation caused the partial fragmentation of some agglomerated particles in the colloids, with an average diameter close to the original particle size, as indicated by a narrow distribution size. The reduction in the agglomerated size of the particles also resulted in an enhancement of the thermal diffusivity values, from 1.444 × 10-3 to 1.498 × 10-3 cm2/s in 0 to 30 min of irradiation time. This work brings new possibilities and insight into the fragmentation of agglomerated nanomaterials based on the photothermal study.
Mesoporous TiO2 hollow spheres nanostructures with high surface areas were successfully prepared using a microwave method. The prepared hollow spheres have a size range between 200 and 500 nm. The spheres consisted of numerous smaller TiO2 nanoparticles with an average diameter of 8 nm. The particles had an essentially mesoporous structure with a pore size in the range of 2-50 nm. The results confirmed that the synthesised of anatase TiO2 nanoparticles with specific surface area approximately 172.3 m2/g. The effect of ultra violet and visible light irradiation and catalyst dosage on the TiO2 photocatalytic activity was studied by measuring the degradation rate of methylene blue. The maximum dye degradation performances with low amount catalyst loading (30 mg) were 99 % and 63.4 % using the same duration of ultra violet and visible light irradiation, respectively (120 min).
Recently, TiO2/multi-walled carbon nanotube (MWCNT) hybrid nanocatalysts have been a subject of high interest due to their excellent structures, large surface areas and peculiar optical properties, which enhance their photocatalytic performance. In this work, a modified microwave technique was used to rapidly synthesise a TiO2/MWCNT nanocatalyst with a large surface area. X-ray powder diffraction, field-emission scanning electron microscopy, transmission electron microscopy and Brunauer-Emmett-Teller measurements were used to characterise the structure, morphology and the surface area of the sample. The photocatalytic activity of the hybrid nanocatalysts was evaluated through a comparison of the degradation of methylene blue dye under irradiation with ultraviolet and visible light. The results showed that the TiO2/MWCNT hybrid nanocatalysts degraded 34.9% of the methylene blue (MB) under irradiation with ultraviolet light, whereas 96.3% of the MB was degraded under irradiation with visible light.
Silver nanoparticles were successfully prepared in two different solvents using a microwave heating technique, with various irradiation times. The silver nanoparticles were dispersed in polar liquids (distilled water and ethylene glycol) without any other reducing agent, in the presence of the stabilizer polyvinylpyrrolidone (PVP). The optical properties, thermal properties, and morphology of the synthesized silver particles were characterized using ultraviolet-visible spectroscopy, photopyroelectric technique, and transmission electron microscopy. It was found that for the both solvents, the effect of microwave irradiation was mainly on the particles distribution, rather than the size, which enabled to make stable and homogeneous silver nanofluids. The individual spherical nanostructure of self-assembled nanoparticles has been formed during microwave irradiation. Ethylene glycol solution, due to its special properties, such as high dielectric loss, high molecular weight, and high boiling point, can serve as a good solvent for microwave heating and is found to be a more suitable medium than the distilled water. A photopyroelectric technique was carried out to measure thermal diffusivity of the samples. The precision and accuracy of this technique was established by comparing the measured thermal diffusivity of the distilled water and ethylene glycol with values reported in the literature. The thermal diffusivity ratio of the silver nanofluids increased up to 1.15 and 1.25 for distilled water and ethylene glycol, respectively.
In this paper, we report how few layers graphene that can be produced in large quantity with low defect ratio from exfoliation of graphite by using a high intensity probe sonication in water containing liquid hand soap and PVP. It was founded that the graphene powder obtained by this simple exfoliation method after the heat treatment had an excellent exfoliation into a single or layered graphene sheets. The UV-visible spectroscopy, FESEM, TEM, X-ray powder diffraction and Raman spectroscopy was used to analyse the graphene product. The thermal diffusivity of the samples was analysed using a highly accurate thermal-wave cavity photothermal technique. The data obtained showed excellent enhancement in the thermal diffusivity of the graphene dispersion. This well-dispersed graphene was then used to fabricate an electrically conductive polymer-graphene film composite. The results demonstrated that this low cost and environmental friendly technique allowed to the production of high quality layered graphene sheets, improved the thermal and electrical properties. This may find use in the wide range of applications based on graphene.
High porous ZnO nanoflakes were successfully prepared using microwave assisted hydrothermal method. The presence of aluminum changes the environment of preparation reaction which controlled the crystallographic orientation. The unique morphology and properties of ZnO nanoflakes may due to the effect of microwave irradiation and the ambient condition. The approach is very simple and rapid that grows around 3 μm ZnO within 30 minutes. The mechanism of the construction of unique ZnO nanoflakes growth using the present approach will be proposed. Hence, the prospective performance of ethanol vapor sensing for the rapid growth of ZnO porous nanostructures was investigated.
Radiofrequency (RF) and microwave (MW) radiation exposures from the antennas of rooftop-mounted mobile telephone base stations have become a serious issue in recent years due to the rapidly evolving technologies in wireless telecommunication systems. In Malaysia, thousands of mobile telephone base stations have been erected all over the country, most of which are mounted on the rooftops. In view of public concerns, measurements of the RF/MW levels emitted by the base stations were carried out in this study. The values were compared with the exposure limits set by several organisations and countries. Measurements were performed at 200 sites around 47 mobile phone base stations. It was found that the RF/MW radiation from these base stations were well below the maximum exposure limits set by various agencies.