The storage of oil sludge at refineries is a major problem to the petroleum industry. Oil sludge treatments such as by using sludge farming, incineration, physical and chemical techniques have been applied to separate the hydrocarbon from the solid sediment. The paper relates a characteristic study performed on solid sediment from a local oil sludge sample for making sintered brick. The study includes the used of XRD, XRF, digital microscopy and particle size analyzer. The result shows that the sample highly contains quartz minerals with particle size ranging from 0.5 – 200 ȝm. The chemical phosphorous from the surfactant can be removed by washing to make this solid sediment to be used as a material in the brick making.
Template-assisted growth is an important nanoelectrochemical deposition technique for synthesizing one-dimensional (1-D) nanostructures with uniformly well-controlled shapes and sizes. A good template with well-defined dimensions is imperative for realizing this task. Porous anodic alumina (PAA) has been a favorable candidate for this purpose as it can be tailor-made with precise pore geometries, such as pore length and diameter as well as inter-pore distances, via the anodisation of pure aluminium. This paper reports the fabrication of PAA templates and electrochemical synthesis of functional nanostructures in the form of nanowires using PAA templates as scaffolds. Axial heterostructured and homogeneous nanowires formed by engineering materials configuration via composition and/or layer thickness variations were fabricated for different functionalities. X-ray diffraction and imaging techniques were used to elucidate the microstructures, morphologies and chemical compositions of the nanowires produced. Due to their large surface area-to-volume ratios, and therefore high sensitivities, these functional nanostructures have useful applications as critical components in nanosensor devices and various areas of nanotechnology. Potential applications include as hydrogen gas sensors in nuclear power plant for monitoring structural integrity of reactor components and containment building, as well as environmental monitoring of air pollution and leakages of toxic gases and chemicals.
Thermoelectric nanostructures hold great promise for capturing and directly converting into electricity some vast amount of low-grade waste heats now being lost to the environment (e.g. from nuclear power plant, fossil fuel burning, automotives and household appliances). In this study, large-area vertically-aligned silicon nanowire (SiNW) arrays were synthesized in an aqueous solution containing AgN•i and HF on p-type Si (100) substrate by self-selective electroless etching process. The etching conditions were systematically varied in order to achieve different stages of nanowire formation. Diameters of the SiNWs obtained varied from approximately 50 to 200 nm and their lengths ranged from several to a few tens of um. Te/Bi2Tex.Si thermoelectric core-shell nanostructures were subsequently obtained via galvanic displacement of SiNWs in acidic HF electrolytes containing HTe02+ and 139' /HTe02+ ions. The reactions were basically a nano-electrochemical process due to the difference in redox potentials between the materials. The surface-modified SiNWs of core-shell structures had roughened surface morphologies and, therefore, higher surface-to-bulk ratios compared to unmodified SiNWs. They have potential applications in sensors, photovoltaic and thermoelectric nanodevices. Growth study on the SiNWs and core-shell nanostructures produced is presented using various microscopy, diffraction and probe-based techniques for microstructural, morphological and chemical characterizations.
Structural and dielectric properties of barium strontium, titanate (Ba(ÿ)SrxTiO$) ceramics with x—
0.25, 0.5 and 0.75 were investigated. The Ba(i-xjSrxTiOs ceramics were synthesised by solid state
reaction method. Microstructure, surface morphology and dielectric properties of the synthesised
ceramics were examined using XRD, SEM and Impedance Spectroscopy respectively. XRD results
revealed that all samples contained BaTiOg as primary phase with tetragonal perovskite crystal
structure. The crystallite size slightly increased with the increasing of Sr contents. SEM micrographs
showed that the microstructure become denser when Sr contents increased. Impedance spectroscopy
showed dielectric constant for all samples were decreased with increasing temperature up to 200°C.
The capability of zinc oxide (ZnO) as a hydrogen sensing element has been pushed to its limits. Different methods have been explored to extend its sensing capability. In this paper, we report a novel approach which significantly improves the hydrogen sensing capability of zinc oxide by applying a bias voltage to ZnO nanorods as the sensing elements. Zinc oxide in the form of aligned nanorods was first synthesized on an Au-coated Si(111) substrate using a facile method via the galvanic-assisted chemical process. The sensing performance of the zinc oxide nanorods was investigated in response to the applied biasing voltage. It was found that the sensitivity, response time and detection limit of the ZnO sensing elements were dramatically improved with increasing bias voltage. A 100% increment in sensing response was achieved for the detection of 2000 ppm hydrogen gas when the bias voltage was increased from -2 to -6 V with 70% reduction in response and recovery times. This remarkable sensing performance is attributed to the reaction of hydrogen with chemisorbed oxygen ions on the surface of the ZnO nanorods that served as the electron donors to increase the sensor conductance. Higher reverse bias voltages sweep the electrons faster across the electrodes. This shortened the response time and, at the same time, depleted the electrons in the sensor elements and weakens oxygen adsorption. The oxygen ions could then be readily removed by hydrogen, leading to a higher sensitivity of the sensors. This, therefore, envisages a way for high-speed hydrogen gas sensing with high detection sensitivities.
Grog is an additive material that plays important roles in ceramic making. It improves the fabrication process of green bodies as well as the physical properties of fired bodies. Few low-cost materials and wastes have found their application as grog in recent years, thus encouraging the replacement of commercial grogs with cost-saving materials. Coal fly ash, a combustion waste produced by coal-fired power plant, has the potential to be converted into grog owing to its small particle sizes and high content of silica and alumina. In this study, grog was derived from coal fly ash and mixed with kaolin clay to produce ceramics. Effects of the grog addition on the resultant ceramics were investigated. It was found that, to a certain extent, the grog addition reduced the firing shrinkage and increased the total porosity of the ceramics. The dimensional stability of the ceramics at a firing temperature of 1200 °C was also not noticeably affected by the grog. However, the grog addition in general had negative effects on the biaxial flexural strength and refractoriness of the ceramics.