Neutron aperture is one of the collimator components in a neutron radiography facility. The optimum design of neutron aperture is very importance in order to obtain largest L/D ratio with highest thermal neutron flux and low gamma-rays at the image plane. In this study, the optimization of neutron aperture parameters were done using Monte Carlo N-Particle Transport Code, version five (MCNP5). This code has a capability to simulate the neutron, photon, and electron or coupled of neutron/photon/electron transport, including the capability to calculate eigen values for critical system. The aperture parameters concerned in this study are the selection of best aperture material, aperture thickness, aperture position and aperture center hole diameter. In these simulations, vacuum beam port medium was applied.
MeSH terms: Electron Transport; Electrons; Gamma Rays; Monte Carlo Method; Neutrons; Vacuum; Photons
Electrical capacitance tomography (ECT) velocimetry technique was utilized in this study to quantify the flow structure of gas-liquid based on the ECT images. A new 8 electrodes sensor ECT has been successfully developed to provide 2D images in a cross section of pipeline. The ECT has been attentively applied in the test section of the flow rig for imaging the gas-liquid distribution. The inside diameter of ECT pipeline sensor is 100mm. Meanwhile, the flow rig consists of close loop of “CPVC” pipes that includes a pipe test section, two tanks of oil and water respectively and allows the working pressure up to 5 bars. Transparent pipe is used for visual monitoring. A portable Doppler flow meter that utilizes the ultrasonic signal has also been placed at the test section to measure the velocity. The images obtained by ECT show that the different flow patterns have been observed in the horizontal pipe during the experiment. The technique enables realization of the time and position at which particle density fluctuations with respect to dominant time-space levels pass through the pipeline.
The blooming use of ionizing radiation in industry, research, agriculture, medicine and nuclear industry increases the risk of overexposure for radiation workers as well as members of the public. Ionizing radiation is a strong clastogen, causing chromosome breakage, and resulting in cytogenetic aberrations in exposed cells. Cytogenetic analysis of human blood lymphocytes has been widely used as the biological technique for quantifying radiation dose in man. In the investigation of radiation accident, it is important to estimate the dose absorbed by the exposed person in order for the attending medical doctor to plan for their therapy. This paper reviews the current status on cytogenetic biodosimetry methods for radiation dose assessment.
The objective of this study was to compare the acquired image of teflon, human bone equivalent material on a Positron Emission Tomography/Computed Tomography (PET/CT) scanner with Monte Carlo simulation (MCNP). The cylindrical shape teflon phantom with dimensions of 19.5 cm length and 5.0 cm diameter was used for imaging with different settings of kilovolts (kV) and milliamperes (mA) of PET/CT. In this simulation, the photon flux in each pixel was accumulated by the Flux Image Radiograph (FIR) tally as flux image detectors and the image was plotted using Microsoft Office Excel. Results show that MCNP image was comparable with that of CT image and the obtained MCNP image depends on pixels size of the FIR tally.
MeSH terms: Humans; Monte Carlo Method; Polytetrafluoroethylene; Tomography, X-Ray Computed; Photons; Phantoms, Imaging; Positron-Emission Tomography; Multimodal Imaging
New solid acid catalyst consisting of zirconium sulfate (ZS) supported on a pure-HMS hexagonal mesoporous material (HMS) have been prepared and characterized. This heterogeneous catalyst is able to make a contribution to the field of acid catalyst involving bulky organic molecules. XRD analysis shows that ZS is intact after impregnated on HMS surface and formed finely dispersed species. No ZS crystal phase was developed even at ZS loadings as high as 40 wt %. The occurrence of chemical interaction between ZS and HMS was observed by XPS analysis. Further, XRF results demonstrated that there is no leaching of ZS elements after impregnation. This study shows that ZS can be impregnated on HMS and would be a promising solid acid catalyst for acid-type reactions espcially invovling bulky organic molecuels.
Chemical composition of fine (PM2.5) aerosol samples collected for the 5 years period (2001- 2005) using Gent Stacked filter unit sampler at Klang Valley (3 o 10 ’ 30 ’’ N, 101 o 43 ’ 24 ’’ E) were analysed using Neutron Activation Analysis (NAA) and Proton Induced X-ray Emission (PIXE). Results of the study show that the major component of the fine aerosol was black carbon and sulfur with the mass concentration ranged from 4.4 - 6.7µg m -3 and 1.2 - 1.9µg m -3 , respectively. The total fine aerosol mass concentration were in the ranged of 25 - 31µg m -3 with the reconstructed mass was about 50% as relative to the gravimetric mass. Statistical method, factor analysis with varimax approach has been applied to the aerosol composition data for the fingerprint identification. The analysis produces five identified fingerprint represent soil, industry, motor vehicles/biomass burning and Pb and Zn sources. There is also an unidentified source that could be related to unknown industrial activities.
The paper describes the uses of microfocus XRF to identify infected Basal Stem Rot (BSR) disease in Malaysian palm oil plants. Among symptoms of BSR are wilting of the leaves and plant malnutrition. The study involves determining the inorganic element content of normal and infected leaves. Si, Mo, Cl, K, Ca and Mn had been identified as the major elements. Their distribution was determined by constructing an elemental map of each of this element on the leaves. Line scan was also performed to look into changes on the element composition on a defined region. Quantitative analysis of Cl, Ca and K on the normal and infected leaves show that the infected leaves have lower Cl content and a higher Ca/K ratio than the normal leaves.
Ultrasound technology progressed through the 1960’s from simple A-mode and B-mode scans to today’s M-mode and Doppler two dimensional (2-D) and even three dimensional (3-D) systems. Modern ultrasound imaging has its roots in sonar technology after it was first described by Lord John Rayleigh over 100 years ago on the interaction of acoustic waves with media. Tomography technique was developed as a diagnostic tool in the medical area since the early of 1970’s. This research initially focused on how to retrieve a cross sectional images from living or non-living things. After a decade, the application of tomography systems span into the industrial area. However, the long exposure time of medical radiation-based method cannot tolerate the dynamic changes in industrial process two phase liquid/gas flow system.. An alternative system such as a process tomography system, can give information on the nature of the flow regime characteristic. The overall aim of this paper is to investigate the use of a small scale ultrasonic tomography method based on ultrasonic transmission mode tomography for online monitoring of liquid/gas flow in pipe/vessel system through ultrasonic transceivers application. This non-invasive technique applied sixteen transceivers as the sensing elements to cover the pipe/vessel cross section. The paper also details the transceivers selection criteria, hardware setup, the electronic measurement circuit and also the image reconstruction algorithm applied. The system was found capable of visualizing the internal characteristics and provides the concentration profile for the corresponding liquid and gas phases.
Fine grinding of high purity talc in jet mill at low grinding pressure was carried out by varying the feed rate and classifier rotational speed. These ground particles were sonicated in laboratory ultrasonic bath by varying the soniction period at five levels. The ground and sonicated particles were characterized in terms of particle size and particle size distribution. Mechanochemical and sonochemical effect of talc was determine via X-ray diffraction. Particle shape and surface texture of the ground and sonicated product was determined via scanning electron microscope and transmission electron microscope. The ground particle size exhibited particle size below 10 µm with narrow size distribution. The reduction of peak intensity in (002) plane indicated the layered structure has been distorted. The sonicated talc shows that the thickness of the talc particles after the sonication process is 20 nm but the lateral particle size still remains in micron range. The reduction of the XRD peak intensity for (002) plane and thickness of sonicated talc as shown in SEM and TEM micrographs proves that fine grinding and sonication process produces talc nanosheets.
In these studies, cordierite was mechanically synthesized after a sol-gel process. The effect of milling time of cordierite was investigated. Aluminium nitrate nonahydrate, magnesium nitrate hexahydrate and tetraethylorthosilicate (TEOS) were used as starting materials. Gels obtained were mechanically activated in planetary ball mill by at 300rpm grinding speed and grinding time (15min, 30min, 45min and 60min). Powders produced were characterized by X-Ray Diffraction (XRD) and Field Emission Scanning Electron Microscope (FESEM) and Energy Dispersive X-Ray (EDX). XRD analysis proved that α-cordierite was formed at lower temperature (1200°C) as compliment to without grinding, whereby it is formed at1300°C. FESEM analysis shows the size of the cordierite were in submicron scale. EDX analysis proved that magnesium, aluminium, silicon and oxygen are elements existed in cordierite.
α Cordierite is very important phase in MgO-Al2O3-SiO2 system because of their very outstanding thermal, chemical and electrical properties. In this presents study nonstoichiometry cordierite (MgO:Al2O3:SiO2 = 3:1.5:5) using 2 different initial raw materials ( (i)mixture of pure oxide, and ii) mainly mixture of minerals) were fabricated and compared in terms of phase transformation and physical properties. Cordierite was prepared by glass method at low melting temperature (1350°C). Low melting temperature has resulted in partly crystalline glass which has possesses higher hardness, required longer milling time and result in contamination from grinding media. However, α-cordierite has successfully crystallized and fully densified at 850°C/2h. Activation energy for densification was investigated from thermal expansion coefficient (TCE) results. Other properties that were discussed included thermal properties using DTA/TGA.
MeSH terms: Ceramics; Glass; Hardness; Oxides; Silicon Dioxide; Temperature
Being an imperative material for man either used as building materials, pottery or as components in material industry and technology, knowledge of clays elemental contents is important. In the present study ten clay samples obtained from various locations in North-West Peninsular Malaysia were used. Majority of the clays were economically manufactured to be used as building materials or pottery. The objective of study was to determine the main elemental contents of the samples, and relate the results to the types of minerals, as well as to compare them with clays from other studies. In the study X-ray Fluorescence (XRF) coupled to samples dilution method and standard calibration samples was used. The elements detected in the study were Si, Al, Fe, Ti, K and Ca. Depending on locations, the percentage concentration ranged between 24.8 – 32.4 for Si, 10.8 – 19.0 for Al, 0.09 – 2.12 for Fe, 0.08 – 1.13 for Ti, 0.45 – 3.39 for K and trace amount of Ca and P. However, Mg that normally found in typical clay was not found in the studied samples. Comparing the oxide of the major elements with other studies, it was found that the clay samples contained mixtures of kaolinite (two-layered structure) and illite (three-layered structure).
The hardcoat anodising process was done by using different concentration of H2SO4 from 0% to 20%. The 90 volt of anodising process was applied by using Al foil as cathode materials. The surface changes on PM Al-Mg resulted by hardcoat anodising was characterised by XRD measured. Surface hardness was measured by Micro-Vickers hardness machine. The experiment found different XRD pattern between anodised PM Al-Mg samples. The study was found by that the optimum value for H2SO4 concentration was 15 % H2SO4 and result 26 μm thickness, 5.07% of mass changes and HVN 105.4 hardness. The hardcoat anodising was affected to the XRD pattern for PM Al-Mg.
Silicon nanostructures have successfully been synthesized by thermal evaporation technique using nickel catalyst. Silicon powder served as starting source material was evaporated at high temperature (900-1100°C) in inert carrier gas. The grown silicon nanostructures were collected on (111) silicon substrate surface that positioned at varied location from source material. By controlling heating rate, gas flow rate, growth temperature and time, substrate position and location; to the optimum condition produced the best quality at silicon nanostructures. In this work, the best parameter to produce silicon nanostructures is system ramping up 1000°C at 20°C/min heating rate, N2 flow at 100ml/min; silicon needle-like one dimensional silicon nanostructures growth on vertically-positioned substrate located at 12cm from source material for 1 hour growth time. The effects of these parameters on the structures and physical of nanostructures were characterized by field emission scanning electron microscope and x-ray diffraction.
Phase composition of calcium phosphate ceramic is a characteristic directly related to the biological response of implants due to the differences in mechanical and biochemical properties of these compounds. The biodegradation rate of biphasic calcium phosphate (BCP) can be controlled by altering the HA to β-TCP ratios. In this study the crystalline phase evolution of BCP synthesized via precipitation from aqueous solution of (NH4)2PO4 titrated into heated solution of Ca (NO3)2 was evaluated. The resulting powder was fabricated into porous scaffold using polyurethane foam method. Bulk powders were sintered from 700 - 1400°C to determine the most significant sintering temperature to obtain a stable and well crystallize BCP phases. The porous scaffolds were then sintered at selected temperature and the effects of various sintering times from 5,7,9,11,13 and 15 h were investigated. Bulk powders were characterized by dilatometer, IR analysis and XRD and porous scaffolds were analyzed by XRD and SEMEdx. RIR method was performed to show that the HA to β-TCP ratios were increased with increasing of sintering time and reached the maximum HA value at 11h. It is found that, the possibilities to manipulate the HA to β-TCP ratios in BCP porous scaffold by just controlling the sintering time of the scaffold without controlling the starting powder characteristics.
MeSH terms: Calcium Phosphates; Ceramics; Hydroxyapatites; Polyurethanes; Powders; Temperature
Ceramic materials play key role in several biomedical applications. One of them is bone graft which is use in treating bone defect which caused by injury or osteoporosis. Calcium phosphates based ceramic are preferred as bone grafts in hard tissue engineering because of their chemical compositions are similar to the composition of human bone, superior bioresorbable and bioactivity. In this study, β-tricalcium phosphate (β-TCP) ceramic was synthesized by using sol-gel method. Phosphorous pentoxide (P2O5) and calcium nitrate tetrahydrate (Ca(NO3)2.4H2O) were used as calcium and phosphate precursors. The effects of calcination temperature on the synthesis powder were studied using the XRD, SEM-EDS and FTIR techniques. It was found that calcination temperature greatly influence the purity of the synthesized powders. The β-TCP was the dominant phase with the formation of α-TCP at calcination temperature from 600 to 800°C. Pure β-TCP was obtained at calcination of 900°C. As the temperature increased to 1000°C, the β-TCP was decomposed to for calcium phosphate oxide (CPO). The sol-gel method has some advantages over other methods, mainly its simplicity and ability to produce pure β-TCP at lower calcination temperature.
Monodispersed and size-tunable nanocrystalline cobalt (Co) particles in the range of 100 to 400 nm are prepared by the reduction of Co(II) species in propylene glycol. Control of the particle size is achieved by varying the initial Co(II) species concentration and by the addition of nucleating agents. Smaller Co particles are produced with increasing amounts of Co(II) species and in the presence of nucleating agents. X-ray diffraction analysis (XRD) shows that the Co particles are predominantly face-centered cubic crystals of about 8-14 nm. The Co particles are also ferromagnetic at room temperature.
Thin films of cerium oxide (CeO2) were prepared on silicon (Si) substrate by metal organic decomposition route. 0.25 M of cerium (III) acetylacetonate (acac) was used as starting materials with the addition of methanol and acetic acid as solvents. Oxide conversion of the film by thermal treatment was conducted at temperature ranging from 400 o C to 1000 o C for 15 min in argon ambient. X-ray diffraction (XRD) analysis utilizing Cukα radiation (Model Brukker’s Diffrac Plus ), Filmetrics system measurement, field emission scanning electron microscope (FE-SEM) (Model Zeiss Supra 35VP FE-SEM) and atomic force microscopy (AFM) (Model SII Nanonavi) were employed to characterize the phase formed and morphologies of the film produced.
In this study, natural Hydroxyapatite (HA) was extracted from clean cow bone by treatment with NaOH and heating at high temperature before ground into fine powder. The HA powder were than mixed together with binder for several hours. Dense HA were formed in die steel mould by using uniaxially pressing method. Sample was sintered at different temperature 1150, 1200, 1250 and 1300°C for several hours. The phases of specimen were identified using X-ray diffraction (XRD). The mechanical properties were analyzed using three-point bending testing and the microstructure was observed by scanning electron microscopy. From XRD results, natural HA shows phase of pure HA up to 1250 o C and fracture strength results indicated that the mechanical properties of specimen increase as temperature increase. From microstructure observation using SEM, HA specimen shows initial stages of sintering process at temperature 1150°C and show changes in microstructure evolution as temperature increase up to 1300°C.
MeSH terms: Animals; Bone and Bones; Cattle; Female; Hot Temperature; Heating; Microscopy, Electron, Scanning; Powders; Pressure; Steel; Temperature; X-Ray Diffraction; Durapatite
The microstructural evolution of Sn-40Pb/Cu joints has been investigated under 125 o C thermal exposure conditions using single shear lap joints. A scanning electron microscope (SEM) was used to observe the morphology of the phases and energy dispersive x-ray (EDX) was used to estimate the elemental compositions of the phases. A double layer of Cu6Sn5 and Cu3Sn were observed. The Cu6Sn5 developed with a scalloped morphology, while the Cu3Sn always grew as a somewhat undulated planar layer in phase with the Cu6Sn5. The Cu6Sn5 layer began to transform from scallop shape to planar type after aging for 375 hours due to reduction in the interfacial energy. The intermetallic layers showed a linear dependence on the square root of aging time. The growth rate constant of the intermetallic compounds are estimated as 15.2 x 10 - 14 and 0.152 x 10 -14 cm 2 /s for Cu6Sn5 and Cu3Sn intermetallic, respectively.