The amount of sugarcane bagasse and rice straw in the state of Perlis (Malaysia) is abundant while its utilization is still limited. One of the alternatives for the bagasse and straw utilization is as pulp raw material. This paper reviews on pulp from sugarcane bagasse and rice straw and its suitability for paper production. In this study, the pulp was extracted by the Soxhlet extraction method. The objective of this study was to investigate the cellulose, lignin and silica content of the pulp from sugarcane bagasse and rice straw. For rice straw, the presence of large amount of pentosanes in the pulp and black liquors, which also contain silica were decreased the using of straw in the paper industry. Therefore, formic acid pulping and NaOH treatment are studied to reduce or prevent silica. The isolated pulp samples were further characterized by Scanning Electron Microscope (SEM) to investigate their fiber dimensions.
Detection and analysis of resin is particularly significant since the commercial value of agarwood is related to the quantity of resins that are present. This article explores the potential of a scanning electron microscope in combination with new non-destructive 3D visualization technique, X-ray micro-computed tomography, as imaging tools to visualize micro-structure resin in agarwood. These techniques were used to compare two samples of agarwood chips: high grade and low grade. From the results, it can be concluded that a wood cell filled with resin deposit have a higher attenuation. It can be shown that the combination of scanning electron microscopy and micro-CT can offer high resolution images concerning the localization and structure of resin inside Agarwood. While the second allows the 3D investigation of internal structure of agarwood, the first technique can provide details 2D morphological information. These imaging techniques, although sophisticated can be used for standard development especially in grading of agarwoodlbr commercial activities.
Kenaf fibre that is known as Hibiscus cannabinus, L. family Malvaceae is an herbaceous plant that can be grown under a wide range of weather conditions. The uses of kenaf fibres as a reinforcement material in the polymeric matrix have been widely investigated. It is known that epoxy has a disadvantage of brittleness and exhibits low toughness. In this research, liquid epoxidized natural rubber (LENR) was introduced to the epoxy to increase its toughness. Kenaf fibres, with five different fibre loadings of 5%, 10%, 15%, 20% and 25% by weight, were used to reinforce the epoxy resins (with and without addition of epoxidized natural rubber) as the matrices. The flexural strength, flexural modulus and fracture toughness of the rubber toughened epoxy reinforced kenaf fibre composites were investigated. The results showed that the addition of liquid epoxidized natural rubber (LENR) had improved the flexural modulus, flexural strength and fracture toughness by 48%, 30%, and 1.15% respectively at 20% fibre loading. The fractured surfaces of these composites were investigated by using scanning electron microscopic (SEM) technique to determine the interfacial bonding between the matrix and the fibre reinforcement.
Heat treatment was introduced onto the aluminum coated low carbon steel to promote the formation of thin layer of oxide for enhancement of oxidation protection of steel. This process has transformed the existing intermetallic layer formed during hot dip aluminizing process. Experiment was conducted on the low carbon steel substrates with 10mm x 10mm x 2mm dimension. Hot dip aluminizing of low carbon steel was carried out at 750 ºC dipping temperature in a molten pure aluminum for 5 minutes. Aluminized samples were heat treated at 600 ºC, 700 ºC, 800 ºC, and 900 ºC for 1 hour. X-ray Diffraction (XRD), Scanning Electron Microscope (SEM) and EDAX were used in investigation. From the observation, it showed the intermetallic thickness increased with the increase in temperature. The result of EDAX analysis revealed the existence of oxide phase and the intermetallics. The XRD identified the intermetallics as Fe2Al5 and FeAl3.
With a view to understanding the effect of rare earth element (Ce, Pr, Nd, Sm and Gd) substitution for the La site in LaMnO3 (LMO), the samples were prepared via solid-state reaction. Structure investigation by X-ray diffraction (XRD) showed that structure transformation from trigonal (LMO) to orthorhombic (PMO, NMO, SMO and GMO) occurred when smaller trivalent rare earth element was replaced. The MnO6 octahedra were tilted and elongated or compressed, corresponding to the ionic radii of the rare earth inserted. Meanwhile, microstructure study using scanning electron microscopy (SEM) illustrated that La substitution by another rare earth element caused a reduction in grain size. This might due to the changes in enthalpy of fusion by other rare earth ions, where higher enthalpy of fusion favours formation of smaller grain size. However, CeMnO3 did not form under this preparation condition. The magnetic properties studied from the hysteresis plot taken at room temperature indicated that the substitution of La with other magnetic trivalent rare earth ions strongly weakened the magnetic strength of the system.
This study was conducted to prepare a mixed matrix membrane (MMM) and to test the performance of the prepared MMM for CO2 and CH4 gas separation. MMM containing polyethersulfone (PES) and multi-walled carbon nanotubes (MWCNTs) was prepared by a dry-wet phase inversion technique using a pneumatically-controlled membrane casting machine. The surface modification was performed on MWCNTs in order to enhance the selectivity of CO2/CH4. The surface modification of MWCNTs using chemical and physical approaches has been adopted. Mixed acid (HNO3/H2SO4) and β-CD were used for chemical and physical approaches, respectively. Effects of surface modification on MWCNTs/PES MMM were investigated. MWCNTs/PES MMMs were characterised using scanning electron microscopy (SEM), the Fourier Transform Infrared (FT-IR) spectroscopy and pure gas permeation test. The permeability and selectivity, which are the parameters describing membrane performance were calculated via the data obtained from pure gas permeation test with the feed pressure difference from 3 to 7 bars. In this study, surface modified MWCNTs/PES MMM using mixed acid and β-CD has successfully enhanced the CO2/CH4 selectivity by 40.6% compared to that of neat PES.
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.
Titanium alloy (e.g. Ti-6Al-4V) has an excellent combination of properties. However in many cases,
the application is limited because of the poor wear property. In this work, a surface modification
(plasma nitriding) is carried out to improve the surface properties of Ti-6Al-4V, as a treatment prior to a hardcoating deposition, leading to a duplex coating system. This is an effort to improve the surface and near surface property of Ti-6Al-4V. Plasma nitriding is performed utilizing microwave plasma method in 25% Ar- 75% N2 atmosphere at temperatures of 600°C and 700°C for different processing times (1, 3 and 5 hours). The phase and microstructure of plasma nitrided substrate were characterized by using X-ray diffraction (XRD) and Scanning electron microscopy (SEM). The plasma nitrided Ti-6Al-4V properties (surface roughness, surface hardness and case depth) were determined using profilometer and microhardness, respectively. Results obtained showed a significant increase on the surface hardness of Ti-6Al-4V. This is due to the formation of TiN and Ti2N phases in the form of compound layer. Besides, it shows that the diffusion of nitrogen into the Ti-6Al-4V substrate produces case depth up to 130 µm and this contributes to the improvement of the near surface hardness due to the changes in the microstructures. It was also found that the surface hardness and surface roughness increased with the increases in the process temperature and times.
The calcareous rings of two species of local sea cucumbers, Stichopus hermanni Semper and Holothuria atra Jaeger, were located, dissected, exposed and recorded. The calcareous rings of both species each composed of ten plates knit together by connective tissues. The radial plate of H. atra was a square with a notch at the anterior part whereas in S. hermanni it was squarish consisting of 4 ridges in the anterior part with a notch at the posterior part. The interradial plates of both species were smaller than the radial plates. A ridge was present at the anterior part of the interradial plate in H. atra. In S. hermanii, the ridge at the anterior part of the interradial was thin and prominent. Under the scanning electron microscope the calcareous rings from the two species exhibited a mosaic of small, numerous spicules bound to each other.
Researchers have developed and modified DNA biosensor techniques to provide a fast, simple and sensitive method for detection of human diseases, bacterial food contamination, forensic and environmental research. This study describes the physical characterization of screen-printed carbon electrodes using the scanning electron microscope.
Among the challenges for superconducting devices to be applied in industry are the need for high transport critical current density (Jr) and sustainability of the device in different environment. For superconducting material to maintain high 4, effective flux pinning centers are needed. The addition of small size MgO particles in bulk Bi2Sr2CaCu2O8 (Bi-2212) superconductor has been proven to enhance the effective flux pinning centers in the superconducting material. Nevertheless, the flux pinning properties of the superconducting materials may change if they are exposed to radioactive environment. Electron irradiation is one of the common techniques that can be used to study the impact of irradiation on superconducting materials. In this work, a small amount of nanosize MgO particles were used as the flux pinning centers for Bi-2212 superconducting material. The Bi-2212/MgO composite was heat treated and followed by partial melting and slow cooling. Some of the samples were subjected to electron irradiation using the facility at the Malaysian Nuclear Agency. Characterizations of non-irradiated and irradiated samples were performed via X-ray Diffraction Patterns (XRD), Scanning Electron Microscopy (SEM) and measurements of J, dependence on temperature in self-field. Higher J, indicates better flux pinning properties in irradiated superconductor composite. This is achieved if defects with larger radius with dimension comparable to the coherence length of the superconducting material were created. On the other hand, decreased in Je indicates ineffective flux pinning and this is attributed to the overlapping of defects that break the superconducting region. Our study showed that electron irradiation deteriorated the flux pinning properties of the Bi-2212/MgO superconductor composite.
Linear density polyethylene (LDPE)/thermoplastic sago starch (TPSS), blended with and without the addition of compatibilizer [Polyethylene-grafted-Maleic Anhydride, (PE-g-MA)] were prepared for soil burial test. The test was conducted in the natural soil environment for 3 and 6 months. Different loading of TPSS (10, 20, 30, 40, and 50 wt. %) were used in this study. After soil burial, the blends were evaluated for their tensile properties and scanning electron microscopy (SEM) to observe the surface morphology properties after the test. For LDPE/TPSS, it was observed that the tensile strength decreased with the increase of soil burial time, as well as Young modulus and elongation at break (EB). The LDPE/TPSS/PE-g-MA also showed the same trend for the tensile properties, but with higher properties as compared to uncompatibilized blends. The tensile properties also decreased with the increase in the TPSS loading for both the LDPE/TPSS and LDPE/TPSS/PE-g-MA. Meanwhile,
the scanning electron microscopy (SEM) on the blend surfaces after the soil burial test showed that degradability increased with the increase in the exposure time as well as the TPSS loading.
Silicon nanowires were synthesized on Si substrates (111) via thermal evaporation using AuPd thin layer catalyst. Pre cleaned of Si wafer was used as a substrate to assemble the nanostructure products. In this work, the effect of growth temperature that ranging from 800 to 1000°C on the formation of silicon nanowires studied extensively. X-ray diffraction and field emission scanning electron microscope were employed to characterize the structures and morphology of nanowires. Vertical aligned silicon nanowires have been successfully grown on Si substrates at 900 and 1000°C. At 1100°C, the high aspect ratio of silicon nanowires can be produced but the formation density is low. The presence of AuPd catalyst on the tip of nanowires, it is expected that VLS is the most suitable to explain the growth mechanism of obtained SiNWs. The crystalline structure of SiNWs was proved by XRD data.
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.
This paper examines the chemical elements used as colour additives in cosmetic coloured contact lenses (Cos-CCL) using Field Emission Scanning Electron Microscope equipped with Energy Dispersive X-ray Spectroscopy (FESEM-EDX) analysis. The samples comprised two different Cos-CCL brands and colours (sample A1-black iris colour & B1-gray iris colour) with their respective clear contact lens counterparts as controls (sample A2 & B2). The parameters of Cos-CCL were observed carefully so that they resembled their respective controls. All the samples were analysed for chemical element characterisation by using EDX spectroscopy surface mapping analysis on both front and back surfaces. EDX spectroscopy point analysis was done on cross-section surface of Cos-CCL when colour additive pattern could not be detected by FESEM on either surface. FESEM-EDX spectroscopy analysis has revealed iron element in the colour additives of the A1 sample and aluminium elements in the B2 sample. These two elements were not present in the respective control samples. It can be concluded that iron and aluminium elements are exclusively attributed to the colour additive in Cos-CCL samples. It is important for manufacturers of Cos-CCL to disclose information of their products and create greater awareness on the risks facing users.
Despite its large band gap, ZnO has wide applicability in many fields ranging from gas sensors to solar cells. ZnO was chosen over other materials because of its large exciton binding energy (60 meV) and its stability to high-energy radiation. In this study, ZnO nanorods were deposited on ITO glass via a simple dip coating followed by a hydrothermal growth. The morphological, structural and compositional characteristics of the prepared films were analyzed using X-ray diffractometry (XRD), field emission scanning electron microscopy (FESEM), and ultraviolet-visible spectroscopy (UV-Vis). Photoelectrochemical conversion efficiencies were evaluated via photocurrent measurements under calibrated halogen lamp illumination. Thin film prepared at 120 °C for 4 h of hydrothermal treatment possessed a hexagonal wurtzite structure with the crystallite size of 19.2 nm. The average diameter of the ZnO nanorods was 37.7 nm and the thickness was found to be 2680.2 nm. According to FESEM images, as the hydrothermal growth temperature increases, the nanorod diameter become smaller. Moreover, the thickness of the nanorods increase with the growth time. Therefore, the sample prepared at 120 °C for 4 h displayed an impressive photoresponse by achieving high current density of 0.1944 mA/cm².
This research work demonstrates compositional engineering of an organic-inorganic hybrid nano-composites for modifying absolute threshold of humidity sensors. Vanadyl-2,9,16,23-tetraphenoxy-29H,31H-phthalocyanine (VOPcPhO), an organic semiconductor, doped with Titanium-dioxide nanoparticles (TiO2NPs) has been employed to fabricate humidity sensors. The morphology of the VOPcPhO:TiO2nano-composite films has been analyzed by atomic force microscopy (AFM) and field emission scanning electron microscopy (FESEM). The sensors have been examined over a wide range of relative humidity i.e. 20-99% RH. The sensor with TiO2(90nm) shows reduced sensitivity-threshold and improved linearity. The VOPcPhO:TiO2(90nm) nano-composite film is comprised of uniformly distributed voids which makes the surface more favorable for adsorption of moisture content from environment. The VOPcPhO:TiO2nano-composite based sensor demonstrates remarkable improvement in the sensing parameter when equated with VOPcPhO sensors.
Neat cellulose acetate (CA) and CA/polysulfone (PSf) blend ultrafiltration membranes in the presence of polyvinylpyrrolidone as a pore former were prepared via a phase inversion technique. The prepared membranes were characterized by Fourier transform infrared, scanning electron microscopy, mechanical strength, water content, porosity, permeate flux and heavy metals (Pb2+, Cd2+, Zn2+ and Ni2+) rejection to comprehend the impact of polymer blend composition and additive on the properties of the modified membranes. The water flux expanded by increasing of PSf content in the polymer composition. CA/PSf (60/40) had the highest flux among prepared membranes. Prepared blend membranes were able to remove heavy metals from water in the following order: Pb2+ > Cd2+ > Zn2+ > Ni2+. The CA/PSf (80/20) blend membrane had great performance among prepared membranes due to the high heavy metals removal and permeate flux.
The objective of the present study is to evaluate the effect of incorporation of 3- acetylcoumarin (3-AC), an antibacterial agent, on the mechanical and surface morphology of glass ionomer cement (GIC). A conventional GIC, Fuji II LC, was used as a control. 3-AC was incorporated into GIC during its manipulation at percentage of 2% and 5% (wt/wt). Flexural strength of the specimens were analysed using Shimadzu AGX-Plus while morphological evaluation of the specimens were observed using Scanning Electron Microscope (SEM). Oneway analysis (ANOVA) with post-hoc Bonferroni multiple-range test was used to determine the significant differences among the groups. Statistically, the incorporation of 2% (wt/wt) of 3-AC into GIC showed a significantly lower flexural strength (p
Glass-ceramics are a group of materials that takes advantage of the various glass-forming methods before they are subsequently heat-treated in a controlled manner to effect nucleation and crystallization to produce crystalline materials. The production of glassceramic materials is to overcome the low mechanical strength in pure glassy materials. In this work, a study on the crystallisation of a soda-lime-silica glass was undertaken to ascertain how the processing parameters affect the crystallization of such glasses, viz. either via a single or two-step heat-treatment procedure, as well as the effect of soaking duration at the heat-treatment temperature. A soda-lime-silica glass system was chosen because the raw materials for producing such glasses are readily available and can be considered to be the cheapest. The glass produced was examined by thermal analysis to determine the nucleation and crystallization temperatures before they were heat-treated using a single-step and a two-stage heat-treatment procedures. The resultant glassceramics produced were characterized using x-ray diffraction as well as by scanning electron microscopy. The results thus obtained showed that a two-stage heat-treatment procedure is more successful in producing a well-crystallized glass-ceramic product.