At present, research in composite materials is being directed at using natural fibres instead of synthetic fibres. Kenaf which is extensively grown in the Far East including Malaysia, has been identified as a bast (stem) fibre with significant market potential. In this work, long and random kenaf fibres (non-woven mat form) were used in the as-received condition and alkalized with a 0.06M NaOH solution. They were combined with polypropylene thin sheets, sandwiched between layers of kenaf fibres and hot-pressed to form natural fibre composites. The mechanical properties of the composites were investigated to observe the effect of fibre alignment, fibre treatment and pre-irradiation method used. A general trend was observed whereby alkalized and long fibre composites gave higher flexural modulus and flexural strength compared with random mat and untreated fibres. The long fibre composites also gave a higher work of fracture. However, the correlation between fibre surface treatment and the work of fracture was less clear. Pre-irradiation on the polypropylene pellets and fibres before the composite is manufactured showed significant improvement on the flexural modulus and flexural strength. The bond performance test performed on the treated composites demonstrated good bonding and interfacial adhesion between the fibre and matrix. However, the method of moulding used need to be improved to optimize the performance of the composites.
Ni–SiC composite coatings were electrodeposited from a Watts-type bath containing 5 g/l SiC particles in suspension. The particles were dispersed with the aid of mechanical agitation at 75 rpm and 150 rpm. EDX analysis confirmed the existence of Ni and SiC in the coatings. The effects of agitation speed on hardness properties of the coatings were investigated. SEM results showed that lower agitation speed could improve the amount of co-deposited SiC particles and increase the hardness of the composite coatings. The bonding between the Ni metal matrix and the SiC ceramic particles was compact.
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 purpose of this study was to determine the adsorption coefficient (Koc) of chlorpyrifos in clay soil by measuring the Freundlich adsorption coefficient (Kads(f)) and desorption coefficient (1/n value) of chlorpyrifos. It was found that the Freundlich adsorption coefficient (Kads(f)) and the linear regression (r 2 ) of the Freundlich adsorption isotherm for chlorpyrifos in the clay soil were 52.6 L/kg and 0.5344, respectively. Adsoprtion equilibrium time was achieved within 24 hours for clay soil. This adsoprtion equilibrium time was used to determine the effect of concentration on adsorption. The adsorption coefficient (Koc) of clay soil was found to be 2783 L/kg with an initial concentration solution of 1 µg/g, soil-solution ratio (1:5) at 30 o C when the equilibrium between the soil matrix and solution was 24 hours. The Kdes decreased over four repetitions of the desorption process. The chlorpyrifos residues may be strongly adsorbed onto the surface of clay.
There is a growing interest from, newcomer countries to utilise nuclear energy for electricity
generation. The International Atomic. Energy Agency (IAEA) has developed two methodologies,
namely, the IAEA Milestone Approach and the International Project on Innovative Nuclear Reactors
and Fuel Cycles (INPRO) Methodology to help its Member States in assessing the viability of nuclear
power programme (NPP) and nuclear energy system. This paper highlights important features of both
methodologies in supporting deployment of nuclear power programme for a newcomer country. In
summary, the IAEA Milestone Approach focuses for near term while the INPRO Methodology focuses
for long term assessment to support the deployment of first NPP in newcomer countries. Depending
on newcomer country's priority and resources, both methodologies can be performed either separately
or in-parallel.
Texture evolution of NiO formed during oxidation of polycrystalline single oriented (100) Ni-Cr was investigated. This foil was also termed rolling assisted biaxially textured substrate (RABiTS). X-ray diffractograms of oxidized Ni-Cr RABiTS foil showed the existence of mostly (200) NiO indicating (100)-type NiO formed exclusively on (100) singly oriented Ni-Cr grains. Epitaxial relationship between the two layers is observed. However the dual-in-plane texture was recorded.
The in-plane texture was assessed by conducting phi scan and plotting series of pole figures measured at (111) NiO peak. The mechanism of the oxides formation was proposed to take into account the formation of (100)-type NiO. Cross section morphology of the oxidised foils reveals two oxidation layers; fast growing external layer consisting of the (100)-type NiO and an internal layer consisted of mostly Cr2O3 and maybe NiCr2O4. The thickness of NiO was ~ 10Pm. Cr2O3 formed as needle-like oxides embedded in a matrix of Ni foil. Inward diffusion of oxygen is believed to have caused this to happen. The external NiO layer was consisted of duplex microstructure characterised by columnar layer growing vertical on the surface of the metal and a few micron thick of equiaxed NiO. Delamination of the outer NiO layer often occurred at the columnarequiaxed interface which could be cured by CeO2 deposition on the foil prior to the oxidation process. CeO2 was deposited by conversion immersion using Ce(NO3)3.6H2O solution. (200) NiO formed on this coated sample as well.
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.
Sodium silicate was used to synthesize silica fine particles at room temperature using non-ionic surfactant of triethanolamine (TEA), dissolution salt and precipitating agent. The experiments were conducted by different composition of precursor material, nonionic surfactant and dissolution salt concentrations through the sol-gel process. Various particle sizes in the range 100-300nm were synthesized. The particle size of silica powders were analyzed via Field Emission Scanning Electron Microscope (FESEM), Energy Dispersive X-ray Analysis (EDAX), X-Ray Fluorescence (XRF), and Fourier Transformation Infrared (FTIR). The result has demonstrated that the particle size can be controlled by changing the ratio of non-ionic surfactant and dissolution salt or the sodium silicate concentration.
UV-curable hyperbranched urethane acrylate (HBPUA) from oleic acid of palm oil has been synthesized through a medium aided by p-toluene sulfonic acid as a catalyst. This mixture was then used as the core (HBP) and reacted with palm oil oleic acid to form the hyperbranched polyol (HBP-1). HBPUA was prepared by reacting HBP-1 resin with diisocyanate and hydroxyl-containing acrylate monomer with the presence of 0.1-2 wt% dibutyltin dilaurate as a catalyst. The reaction was confirmed by several analytical data i.e. hydroxyl value (OHV), Fourier Transform infrared (FTIR) spectroscopy, gel permeation chromatography (GPC) and nuclear magnetic resonance (NMR) spectroscopy analyses. The HBPUA was easily curable when subjected to ultraviolet (UV) radiation.
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.
Chitosan was chemically modified with bulky structure, cis-5-norbornene-2, 3-dicarboxylic anhydride and the characteristic of this modified chitosan was studied. The resulting material was analyzed by FTIR, TGA, DSC, XRD and SEM to study the effect of N-acylation to the polysaccharide structure. FTIR results show that the anhydride monomer was successfully bound to amine group of chitosan. Thermal analysis of the modified structure provides the chitosan fibers with thermal stability while XRD and SEM show the lost of crystallinity of modified chitosan. XRD of modified chitosan shows broader peak pattern and a considerable increase in a dimension while SEM of chitosan presented the single particle morphology while norbornene-chitosan shows aggromolarate behaviour due to the hydrophobic nature of norbornene pendant group which induced aggromolaration of the particles in modified structure.
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.
In order to prepare Malaysia to be nuclear ready, the Malaysian 1 MW TRIGA MARK II research
reactor (RTP) located at the Malaysian Nuclear Agency was premeditated with the aim to effectually
actualize the multitude areas of basic nuclear research, labor training and education. To meet the
modern safety standards, analyses of a strong interaction between the thermal-hydraulic system
behavior and the space-dependent neutron kinetics are needed as mere thermal-hydraulics codes are
said to be incapable to succeed the present safety standards. This could be achieved through the
coupling of neutronic and thermal-hydraulic codes of the reactor. Previous studies had shown that the
coupled codes are able to successfully be employed for the correlation between thermal-hydraulic
analysis and neutron kinetics at transient and steady state. In this study, the coupling was achieved
through MCNP and TRIGLAV codes for neutronic and thermal-hydraulic respectively. Core-15 of
RTP was modeled for both of the codes; hence calculating the criticality, analysis of power and
neutron flux distribution. The consistency and accuracy of the developed Core-15 MCNP model was
established by comparing calculations to the experimental results and TRIGLAV code. The criticality
predictions for both codes are in very good agreement with the experimental results. The core reached
its criticality after 66 fuels. The highest hot rod power peaking factor was found to be 1.28. The
results are conservative and can be applied to show the reliability of MCNP and TRIGLAV codes.
Radon-222 emanation from selected locally produced samples of building materials, used in Malaysia were measured using the Professional Continuous Radon Monitor Model 1027, which is a patented electronic detecting-junction photodiode sensor to measure the concentration of radon gas. Each sample was placed for 72 hours inside a 3.11 x 10 -2 m 3 sealed container. It was found that the average radon concentration Bqm -3 of air for concrete bricks, concrete brick with cemented coatings, concrete brick with cemented coatings and paint samples were, 303.7 Bq/m 3, 436.6 Bqm -3, and 410.7 Bqm -3, respectively. (Bqm -3 ) for brown clay brick, brown clay brick with cemented coatings, brown clay brick with cemented coatings and paint were 166.5 Bqm -3, 166.5 Bqm -3, and 148 Bqm -3, respectively. (Bqm -3 ) for sample of compact ceramic tile was 0 Bqm -3. The findings show that concrete brick samples are important source of radon emanation, while brown clay brick have been accepted as the recommendation of the U.S. Environmental Protection Agency (EPA), and ceramic tiles had no emanation of radon gas due to their compact surface, or the glazed layer created on the tile surface during the manufacturing process, which blocks radon emanation. A positive correlation between radon emanation and radium content has been observed for both brown clay brick and concrete brick samples whereas a negative correlation for ceramic tile has been observed. Consequently from the findings, in order to reduce radon emanation and radon exposure in house dwellings and in addition to EPA recommendation of sealed cracks and established good ventilation, we recommend concrete walls to be painted and concrete floors to be paved with ceramic tiles.
There are many essential and non-essential elements including metals and radionuclides present in vegetables. Howeve r, the accumulation of the several metals and radionuclides might cause the contamination to vegetables itself. Green m ustard (Brasissca rapa var. Parachinesis L.) was selected to represent the vegetable in this study. Objectives of this stud y are to determine the concentration of metals and radionuclides in the samples and to calculate the enrichment factor ( EF) and also to estimate the uptake, base on biological accumulation coefficient (BAC), for the various parts of selecte d vegetables. Three farmlands in the Cameron Highlands were studied namely Bharat, Kg Raja and Bertam area. The g reen mustard and soil samples were collected during the harvest season. Samples were dried, ground and sieved prior t o analysis. Analyses for both samples were done by using X-rays Fluorescence Spectroscopy (XRF) to measure the conc entration of Fe, Zn, Hg, U and Th. The concentration of all elements in the soils is lower than their concentration in the control soil, except for Zn, U and Th. The concentration of all elements in Green Mustard is lower than their concentrat ion in the soil where it was grown. The EF values in the Brasissca rapa var. Parachinesis L are lower than 2 except for U and Th, indicating some degree of contamination due to anthropogenic activities or naturally origin. The BAC values show that Zn and Hg were accumulated in the green mustard, depending on where the plant grows.
The purpose of this study is to measure and monitor the radon concentration from fabricated foamed light concrete, made of Portland cement, mine sand and granite. The concentration of radon released was measured using Radon Monitor Model 1027 from Sun Nuclear. The results of this research showed that the avearge radon concentration from foamed light concrete was 2.2 pCiL-1 L. Higher radon concentrations were detected after three days of measurements. Environment Protection Agency stated in its guidelines that radon concentration must lower than 4 pCiL-1 for a healthy environment. Thus, the use of foamed light concrete can be one of the alternatives to reduce radon concentration levels in human environment.
We put attention on Intrinsic Josephson Junction (IJJ) to study the fundamental physic for device applications. Convenient self-flux method was used to grow BSCCO single crystals. We investigated the lid effect to examine the single crystal growth of high TC (Critical Temperature). We found that for the crystal growth with no lid, two stage transitions of TC ≅ 61 K and 77 K were observed. While for the crystal growth with lid, the BSCCO has TC ≅ 80K, ΔTC = 10K and approximately average size5x2mm 2 . When we increased weight of lid, the single crystal have increased to TC =80K, ΔTC = 4K and the typical size was ≅7x3mm 2 . TC and the crystal growth show a tendency to increase by the effect of the lid. From observed quasi-particle characteristics, c-axis direction changed from semiconductor to intrinsic Josephson characteristic with decreasing temperature.
A study of wear behaviour on anodised PM aluminium matrix composites (AMC) reinforced with Saffil™ alumina short fibres was done. AMC was fabricated by powder metallurgy methods (PM) with using Al flake powders and Saffil™ alumina short fibres. AMC reinforced with 15 wt % Saffil¥ alumina short fibre was selected because it showed optimum mechanical and physical properties. Sulphuric acid anodising process was performed and the objective is to obtain suitable parameters of sulphuric acid concentration, anodising voltage and anodising time on MMC. The study of anodising process was carried out with various sulphuric acid concentrations (from 0 to 20 % volume), anodising voltage (10 V to 20 V) and anodising time (from 0 to 60 minutes) at room temperature. Scanning electron microscope (SEM) was used to investigate coating morphology and thickness. From the research, anodising voltage of 18 V and 15 % vol H2SO4 in anodising time of 60 minutes were suitable parameters for sulphuric acid anodising of this AMC. SEM showed the coating thickness around 20 Pm. From the reserch, it was found that H2SO4 anodising was able to give good coating to MMC.
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.
Barium strontium titanate (Ba0.7Sr0.3TiO3) powder was processed at temperature 80 o C by reacting titania sol in aqueous solutions that contained BaCl2, SrCl2 and NaOH at atmospheric pressure.
The structural characteristic of the powder and sintered pellet were studied using Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD) whereas the electrical characteristic was determined via Impedance Spectroscopy (IS) and LCR meter. The synthesized powder was found to have a tetragonal phase after heating at 1300 o C. XRD pattern also showed the presence of secondary phase BaTi2O5 (BT2). The SEM results shows the fine grain size was in the range of 0.2 Pm to 0.4 Pm whereas the large ones are approximately 0.8 Pm to 1.2 Pm The ac response of sample sintered at 1300 o C indicated that three electrically different regions. Element 1 can be assigned as a ferroelectric grain boundary region and it is actually BT2, element 2 as a ferroelectric bulk region and the third element is a conductive core which has a low resistance (200 :) and capacitance value.