The composite polymer films of polyvinyl alcohol/polypyrrole/chloral hydrate (PVA-PPy-CH) had been prepared. Effects of J-rays on the electrical conductivity of the composite polymer films had
been investigated by using Inductance Capacitance Resistance meter (LCR) meter at a frequency
ranging from 20 Hz to 1 MHz. With the incorporation of chloral hydrate in the polymer sample, the conductivity increased indicates that it is capable to be used as dopant for polymerizing conjugated polymer. The electrical conductivity obtained increased as the dose increased, which is in the order of 10-5Scm-1 indicates that J-rays is capable to enhance the electrical conductivity of the composite polymer films. The parameter of s is in the range of 0.31 d s d 0.49 and obeyed simple power law dispersion Zs. The Scanning Electron Microscopy (SEM) micrographs reveal the formation of polypyrrole globules in polyvinyl alcohol matrix which increased as the irradiation dose was increased.
Production of carbon dioxide from degraded woods especially Karas or Aquilariella Malaccensis using integrated pyrolysis-combustion is important for radiocarbon dating application. The effects of pyrolysis temperatures (300-400 0 C), retention times (20-35 minutes) and flow rates of argon (400- 1000 ml/min) on the production of carbon dioxide were studied. The experiments were arranged according to a 2 3 response surface central composite statistical design (CSD). This response surface methodology (RSM) was used to assess factor interactions and empirical models regarding carbon dioxide yield. The optimized yield of carbon dioxide was 82.57% for Karas and the optimum reaction conditions are 300 0 C of pyrolysis temperature, 20 minutes retention time and 982ml/min flow rates of argon. Scanning electron microscope (SEM) and X-ray Diffraction (XRD) were conducted to assess the morphological characteristics of the woods and to look at the potential crystalline structure produced after the process took place, respectively.
The effect of sample density in the determination of radionuclides by gamma spectrometry was studied using two multinuclide standard sources of different densities. The self absorption corrections due to differences in sample matrix densities were estimated. The corrections were used in the analysis food and soil samples having packing densities between 0.2 – 1.6g/ml.
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.
The composite polymer films of polyvinyl alcohol/polypyrrole/chloral hydrate (PVA-PPy-CH) had been prepared. Effects of γ-rays on the electrical conductivity of the composite polymer films had been investigated by using Inductance Capacitance Resistance meter (LCR) meter at a frequency ranging from 20 Hz to 1 MHz. With the incorporation of chloral hydrate in the polymer sample, the conductivity increased indicates that it is capable to be used as dopant for polymerizing conjugated polymer. The electrical conductivity obtained increased as the dose increased, which is in the order of 10-5 Scm-1 indicates that γ-rays is capable to enhance the electrical conductivity of the composite polymer films. The parameter of s is in the range of 0.31 d s d 0.49 and obeyed simple power law dispersion ωs. The Scanning Electron Microscopy (SEM) micrographs reveal the formation of polypyrrole globules in polyvinyl alcohol matrix which increased as the irradiation dose was increased.
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.
A co-deposition of nickel-phosphorus-alumina (NiPA) composite coatings were obtained from an ordinary sulphate-based plating bath consisting of 5 g/l alumina (Al2O3) particles. The particles were dispersed by using mechanical agitation at 125 rpm. The presence of Ni3P and Al2O3 phases in the coatings was confirmed by XRD analysis. SEM/EDX results indicated that a smooth Ni3P coating was obtained and Al2O3 particles were embedded into the coating. Microscopic observation showed that the bonding between the Ni3P metal matrix and the Al2O3 ceramic particles was compact.
Electrodeposition of white copper-tin alloys (including white miralloys) has been done onto planar mild steel substrates from alkaline cyanide solutions at 65 0 C. The chemical composition of the coating is influenced by plating bath composition and current density. White miralloy can be produced from the test solution containing 10 g/l CuCN2 - , 45 g/l Na2SnO3, 25 g/l NaCN, and 12 g/l NaOH at current density about 5 mA/cm 2 . The local compositions of the coating cross section were analyzed using EDX installed in a FESEM operated at an accelerating voltage of 20 kV. The phases formed during co-deposition process were identified using XRD at 25 mA current and 35 kV voltage.
An instrumental neutron activation analytical (INAA) technique is used for the determination of thirty elements in five coal samples collected from Kapar power station, imported from Indonesia and Australia. Analyses of the samples are being associated with standards. All irradiations were performed in the nuclear reactor of Malaysia Nuclear Agency (MNA). Samples were counted by Hyper Pure Germanium (HPGe) detector for short period irradiations at MNA, while for the long period irradiations the samples were counted at Universiti Kebangsaan Malaysia (UKM). The concentrations of thirty elements have been determined: The major components are Cl, Ca, Mg, K, Fe, Ti and Na with the mean concentrations in the range between 70±69 ppm- 6100±1639 ppm; and the trace elements are Zr, V, Mn , Sc, Cr, Co, As ,Br ,Rb ,Sb ,Ba , La, Ce, Nd, Sm, Eu, Tb, Yb, Lu, Hf, Th, U and Ta with the mean concentrations in the range between 0.1381±0.0202 - 69.0±2.8 ppm. The results have been compared to the reported data of eight coal samples from the United States and the reported data of Australian bituminous coal.
In Malaysia, mineral processing plant is one of the Naturally Occurring Radioactive Material (NORM) processing industries controlled by the Atomic Energy Licensing Board (AELB) through the enforcement of Atomic Energy Licensing Act 1984 (Act 304). The activities generated waste which is called as TENORM wastes. TENORM wastes are mainly found in thorium hydroxide from the processing of xenotime and monazite, and iron oxide and red gypsum from the processing of ilmenite. Other TENORM wastes are scales and sludge from the oil and gas industries, tin slag produced from the smelting of tin, and ilmenite, zircon,
and monazite produced from the processing of tin tailing (amang). The environmental and radiological monitoring program is needed to ensure that the TENORM wastes did not caused any contamination to the environment. The wastes vary in the types of samples, parameters of analysis as well as the frequency of monitoring based on license’s conditions issued by the AELB. The main objective of this study is to assess the suitability of license’s condition and the monitoring program required in oil and gas, and mineral processing
industries. Study was done by assessing the data submitted to the AELB in order to comply with the licensing requirement. This study had found out that there are a few of license’s conditions that need to be reviewed accordingly based on the processing activity.
The indoor and outdoor radon/thoron progenies concentrations and natural background radiation levels throughout Sarawak and Sabah were measured. The measurements were carried out at 234 locations in 40 towns in Sarawak and Sabah. The mean indoor and outdoor radon equilibrium equivalent concentrations (EEC) in Sarawak were found to be 1.2 Bqm-3 and 1.5 Bqm-3 respectively. In Sabah, the mean indoor and outdoor radon equilibrium equivalent concentrations were 1.7 Bqm-3. The mean indoor and outdoor thoron equilibrium equivalent concentrations of 0.4 Bqm-3 and 0.3Bqm-3 respectively, were the same for Sarawak and Sabah. The mean indoor and outdoor radiation levels of 46 nGyh-1 and 42 nGyh-1 in Sarawak were slightly lower than the respective values in Sabah, i.e. 53 nGyh-1 and 46 nGy h-1.
Many attempts have been focused in the past on preparing of synthetic E-tricalcium (E-TCP), which being employed as bone substitute due to its biocompatibility and resorbability. Low temperature synthesize such as sol-gel method become popular due to the high product purity and homogenous composition. Sol-gel method is less economical towards commercialization because the cost of raw materials and the yield of the product that can be achieved. This paper describes the synthesis of ETCP via mixing of CaCO3 and H3PO4 followed by calcinations process at 750qC – 1050qC. X-ray diffraction (XRD), scanning electron microscopy (SEM), differential scanning calorimeter (DSC), fourier transformation infra-red (FTIR) were used for characterization and evaluation of the phase composition, morphology, particle size and thermal behavior of the product. E-TCP phase start to occur after calcinations at 750qC.
Radiotherapy has become the most important modality in treating cancer with approximately 50% of
cancer patient undergo the treatment. However, more improvement to the radiotherapy treatment
efficacy is required to deprive cancer. Assessment of tumor progress during treatment is important, to
accommodate the changes that occur during the fractionation course. The objective of this study is to
assess tumor cell damage after external beam radiotherapy by using technetium-99m
pertechnetate (99mTcOf) as a tracer. In this study, HeLa cells were irradiated with 6 MVphoton beam
with different radiation dose ranging from 0.5 Gy to 10 Gy. The irradiated cells were recultured in 6-
well plates and incubated for 10 days. After that, 2 mCi of 99mTcOf were prescribed to each cell
colonies. The viable cells were separated from the rest, and measured for 99mTcOf uptake using singlehead
gamma camera with LEHR collimation. As results, the cells survival, fractions clearly indicate
diminishing effect, to the cells at, higher dose of irradiation. Good correlation were observed between
mmTcGi uptake and survival, fraction for cells irradiated at, lower dose and less significant, correlation
were indicated at higher dose. In conclusion, there is potential for the efficacy of external beam
radiotherapy in treating cancer to be assessed by using radioisotope as a non-invasive tracer. In this
case, technetium-99m, pertechnetate (99mTcOjt) could be attached to the specific antibody so that, better
correlation, between, the cells uptake and possible cell damages could be observed.
L18 orthogonal array in mix level of Taguchi robust design method was carried out to optimize experimental conditions for the preparation of polymer blend composite. Tensile strength and neutron absorption of the composite were the properties of interest. Filler size, filler loading, ball mixing time and dispersion agent concentration were selected as parameters or factors which are expected to affect the composite properties. As a result of Taguchi analysis, filler loading was the most influencing parameter on the tensile strength and neutron absorption. The least influencing was ball-mixing time. The optimal conditions were determined by using mix-level Taguchi robust design method and a polymer composite with tensile strength of 6.33 MPa was successfully prepared. The composite was found to fully absorb thermal neutron flux of 1.04 x 105n/cm2/s with only 2 mm in thickness. In addition, the filler was also characterized by scanning electron microscopy (SEM) and elemental analysis (EDX).
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.
Feasibility studies on the vitrification of spent ion exchange resins combined with glass cullet powder have been conducted using a High Temperature Test Furnace. Bottle glass cullet powder was used as matrix material to convert the ash of the spent resins into a glass. Vitrificat ion of spent ion exchange resins presents a reasonable disposal alternative, because of its inherent organic destruction capabilities, the volume reduction levels obtainable, and the durable product that it yields. In this study, the spent ion exchange resin from the PUSPATI TRIGA reactor of Nuclear Malaysia was combusted in a lab scale combustor and the resulting ash was vitrified together with glass cullet powder in a high temperature furnace to produce a stable spent resin ash embedded in glass. The factors affecting this immobilized waste, such as thermal stability, radiological stability and leachability have all been investigated. However, the outcome of these tests, which include the radionuclide activity concentration in the slag, the optimum conditioning temperature - in relation with volume reduction during vitrification - and the volume mixing ratio of matrix material were reported. It was found that the radionuclides present in spent resins were 54 Mn, 60 Co and 152Eu. The elementary chemical composition (carbon, hydrogen, nitrogen and sulphur) of spent resins was 27.6% C, 5.68% H, 2.04% N and 4.20% S, respectively. The maximum calorific value of spent resins was 1735 kJ/kg. The average activity concentrations of 54 Mn and 60Co in ash at 200oC were 9,411 ± 243 Bq/Kg and 12,637± 201 Bq/Kg. flue gases containing CO2, CO, SO2 and NO started to be emitted above 200oC. The optimum conditioning temperature was also the highest tested, i.e. 900oC in 45 minutes, and the best mixing ratio ash to matrix material was also the highest, ie 1:9. Finally, the leaching analysis of slag at 900oC in 45 minutes showed that the leaching activity of 60Co was below 0.5 Bq/mL.
Ficus deltoidea or locally known as Mas cotek is one of the common medicinal plants used in
Malaysia. Our previous studies showed that this plant have blood glucose lowering effect. Glucose
uptake into muscle and adipocytes cells is one of the known mechanisms of blood glucose lowering
effect. This study was performed to evaluate the effect of Ficus deltoidea on glucose uptake activity
into muscle cells. The cells were incubated with Ficus deltoidea extracts either a,lone or combination
with insulin. Amount of glucose uptake by L6 myotubes was determined using glucose tracer, 2-deoxy-
[l-:-Hj-glucose. The results showed that Ficus deltoidea extracts at particular doses enhanced basal or
insulin-mediated glucose uptake into muscle cells significantly. Hot aqueous extract enhanced glucose
uptake at the low concentration (10 pg/ml) whereas methanolic extract enhanced basal glucose uptake
at high concentrations (500 and 1000 fig/ml). Meanwhile, ethanolic extract enhanced glucose uptake at
low and high concentrations. Methanolic extract also mimicked insulin activity during enhancing
glucose uptake into L6 muscle cells. Glucose uptake activity of Ficus deltoidea could be attributed by
the phenolic compounds presence in the plant. This study had shown that Ficus deltoidea has the
ability to enhance glucose uptake into muscle cells which is partly contributed the antidiabetic activity
of this plant.
An experimental study of the field emission from nitrogen doped Diamond-Like-Carbon (DLC) thin films prepared by plasma Chemical Vapor Deposition (CVD) was carried out for the purpose of investigating the characteristic of field electron emission from the surface of nitrogen doped DLC thin film. Thin DLC film was deposited on silicon using the plasma CVD method, from a mixture of Methane (CH4), Helium (He) and Nitrogen (N2) at room temperature. Emission current was measured while high volume of voltage was applied between the cathode-anode diode structures. Barrier height was obtained by current density-electric field (J-E) characteristic in the relation of Fowler-Nordheim equation. The value of barrier height in range of 0.03eV to 0.06eV was obtained and considered as low barrier.
One-dimensional nanostructure materials are very attractive because of their electronic and optical properties depending on their size. It is well known that properties of material can be tuned by reducing size to nanoscale because at the small sizes, that they behave differently with its bulk materials and the band gap will control by the size. The tunability of the band gap makes nanostructured materials useful for many applications. As one of the wide band gaps semiconductor compounds, zinc selenide (ZnSe) nanostructures (nanoparticles, nanowires, nanorods) have received much attention for the application in optoelectronic devices, such as blue laser diode, light emitting diodes, solar cells and IR optical windows. In this study, ZnSe nanostructures have been synthesized by reduction process of zinc selenate using hydrazine hydrate (N2H4.2H2O). The reductive agent of hydrazine hydrate was added to the starting materials of zinc selenate were heat treated at 500 o C for 1 hour under argon flow to form onedimensional nanostructures. The SEM and TEM images show the formation of nanocompositelike structures, which some small nanobars and nanopellets stick to the rod. The x-ray diffraction and elemental composition analysis confirm the formation of mixture zinc oxide and zinc selenide phases.
An air fin cooler system consists of a tube bundle that is used to cool the various processing fluids in process industries that utilizes air as a cooling medium. The said tubes failed when exposed to corrosive environment(s). Tubes located at the bottom row of the air fin cooler were corroded as a result of exposure to rain water, brought in by induced air when the wind blows. The tube material is A179 Carbon steel. Two tubes, namely Tube A and Tube B along with an aluminum fin in each tube were investigated. A leak was observed on tube A, probably due to Corrosion Under Deposit mechanism. A general corrosion attack was observed at tube B, and macroscopic analysis showed that the corrosion occurred along the grain boundaries, which consist of ferrite and pearlite. Microanalysis showed that the corrosion product on the outer surface of the tube consists of Fe, O, S and Cl elements. It is concluded that the humid environment contains corrosive elements such as S and Cl. EDAX analysis on the fin showed that the material is pure aluminum. However, the aluminum was corroded by galvanized corrosion and produced brittle Al2O3 as a result.