Roslinda Shamsudin

High Sensitivity pH Sensor Based on Porous Silicon (PSi) Extended Gate Field-Effect Transistor

In this study, porous silicon (PSi) was prepared and tested as an extended gate field-effect transistor (EGFET) for pH sensing. The prepared PSi has pore sizes in the range of 500 to 750 nm with a depth of approximately 42 µm. The results of testing PSi for hydrogen ion sensing in different pH buffer solutions reveal that the PSi has a sensitivity value of 66 mV/pH that is considered a super Nernstian value. The sensor considers stability to be in the pH range of 2 to 12. The hysteresis values of the prepared PSi sensor were approximately 8.2 and 10.5 mV in the low and high pH loop, respectively. The result of this study reveals a promising application of PSi in the field for detecting hydrogen ions in different solutions.

Temperature-Driven Structural and Morphological Evolution of Zinc Oxide Nano-Coalesced Microstructures and Its Defect-Related Photoluminescence Properties

In this paper, we address the synthesis of nano-coalesced microstructured zinc oxide thin films via a simple thermal evaporation process. The role of synthesis temperature on the structural, morphological, and optical properties of the prepared zinc oxide samples was deeply investigated. The obtained photoluminescence and X-ray photoelectron spectroscopy outcomes will be used to discuss the surface structure defects of the prepared samples. The results indicated that the prepared samples are polycrystalline in nature, and the sample prepared at 700 °C revealed a tremendously c-axis oriented zinc oxide. The temperature-driven morphological evolution of the zinc oxide nano-coalesced microstructures was perceived, resulting in transformation of quasi-mountain chain-like to pyramidal textured zinc oxide with increasing the synthesis temperature. The results also impart that the sample prepared at 500 °C shows a higher percentage of the zinc interstitial and oxygen vacancies. Furthermore, the intensity of the photoluminescence emission in the ultraviolet region was enhanced as the heating temperature increased from 500 °C to 700 °C. Lastly, the growth mechanism of the zinc oxide nano-coalesced microstructures is discussed according to the reaction conditions.

Low temperature production of wollastonite from limestone and silica sand through solid-state reaction

Abstract Wollastonite was produced using solid-state reaction from limestone and silica sand. Limestone containing a high percentage of CaO (55.10%) and silica sand with 99% SiO2 were used as starting materials. The ratios of limestone/sand used were 1:1, 2:1 and 3:1 with various firing temperatures, namely 1100, 1200, 1300, 1400 and 1450 °C. The raw materials and fired products were characterised for mineral phases, chemical composition of content such as CaO, SiO2 and loss on ignition (LOI), density and microstructure. CaSiO3 with an α-phase was detected at firing temperatures as low as 1300 °C, together with olivine and quartz phases, obtained from a 1:1 ratio. No α-CaSiO3 was detected for 2:1 and 3:1 ratios; only olivine and larnite phases were present. The density of the product was 2.93 g cm−3, which is close to the theoretical value, with a specific surface area of 3.23 m2 g−1. This study shows that the Malaysian limestone and silica sand can produce good properties of wollastonite materials.

Amperometric Non-Enzymatic Hydrogen Peroxide Sensor Based on Aligned Zinc Oxide Nanorods

Zinc oxide (ZnO) nanorods (NRs) have been synthesized via the hydrothermal process. The NRs were grown over a conductive glass substrate. A non-enzymatic electrochemical sensor for hydrogen peroxide (H2O2), based on the prepared ZnO NRs, was examined through the use of current-voltage measurements. The measured currents, as a function of H2O2 concentrations ranging from 10 μM to 700 μM, revealed two distinct behaviours and good performance, with a lower detection limit (LOD) of 42 μM for the low range of H2O2 concentrations (first region), and a LOD of 143.5 μM for the higher range of H2O2 concentrations (second region). The prepared ZnO NRs show excellent electrocatalytic activity. This enables a measurable and stable output current. The results were correlated with the oxidation process of the H2O2 and revealed a good performance for the ZnO NR non-enzymatic H2O2 sensor.

Effect of autoclaving and sintering on the formation of β-wollastonite.

β-wollastonite (β-CaSiO3) was synthesized from rice husk ash and calcium carbonate, and a study of the effects of the autoclaving and sintering steps is presented here. Autoclaving and sintering at 8h and 2h yielded the β-wollastonite phase in full, with improved crystallinity. Nucleation between rice husk ash and calcium oxide occurred around 135 °C, pressure 0.24 MPa, and growth proved to be more crystalline after the ripening period. For shorter processing times, and for both unsintered and unautoclaved samples, cristobalite and unstable tricalcium silicate phases were present. Crystallite size was increased by longer sintering times but reduced by longer autoclaving times. The β-wollastonite obtained had a random branch-like structure. In conclusion, the introduction of the autoclaving step successfully obtained β-wollastonite from a reaction between rice husk ash and calcium oxide.

Synthesis and Characterization of Nano-Wollastonite from Rice Husk Ash and Limestone

Wollastonite, CaSiO3 material was prepared from rice husk ash, as the source for SiO2 and limestone, source for CaO using sol-gel method. Rice husk ash and CaO powder was mixed together in 100ml distilled water with the rice husk ash/CaO ratios of 45:55 and 40:60. The mixed solution was place in the autoclave and heated at 135°C for 4 hours and calcined at 950°C for 1 and 2 hours. From the XRD results,ratio of 45:55 exhibited that b-wollastonite is the major phase and the minor phase is only contributed by cristoballite and by calcining the mixture for 2hrs would yield better crystallinity. Both of the rice husk ash:CaO ratios produced wollastonite materials in cylinder structures. Wollastonite with nano size grain was obtained for an hour calcination and 2 hrs of calcination would increase the grain size over 100 nm for ratio, 45:55 and 40:60.Therefore in order to get the nano size of wollastonite material, period of calcination process has to be controlled.

A Study on the UV Photoresponse of Hydrothermally Grown Zinc Oxide Nanorods With Different Aspect Ratios

We report on the effect of the aspect ratio of zinc oxide (ZnO) nanorods (NRs) prepared by the hydrothermal process. It was found that increasing the precursor molar amount resulted in the decrease of the aspect ratio of ZnO NRs. Furthermore, the aspect ratios showed a significant effect on the structural and optical properties of the prepared ZnO NRs. The ZnO NRs were fabricated into a metal-semiconductor-metal (MSM) UV photodetector. The performances of the prepared MSM ZnO NRs were also studied, and the high aspect ratio showed that the highest responsivity had a value of 33 A/W at a bias voltage of 5 V and a wavelength of 380 nm. The responsivity, rise time, and full time of the prepared ZnO NRs showed a trend of behavior as the molar amount of the precursor was varied.

Investigation of thermal properties of Al–Si matrix reinforced fine SiCp composites

Abstract The characterisation of thermal expansion coefficient and thermal conductivity of Al–Si matrix alloy and Al–Si alloy reinforced with fine SiCp (5 and 20 wt-%) composites fabricated by stir casting process are investigated. The results show that with increasing temperature up to 350°C, thermal expansion of composites increases and slowly reduces when the temperature reaches to 500°C. The values of both thermal expansion and conductivity of composites are less than those for Al–Si matrix. Microstructure and particles/matrix interface properties play an important role in the thermal properties of composites. Thermal properties of composites are strongly dependent on the weight percentage of SiCp.

Bioactivity and cell compatibility of β-wollastonite derived from rice husk ash and limestone

The aim of this study was to prepare β-wollastonite using a green synthesis method (autoclaving technique) without organic solvents and to study its bioactivity. To prepare β-wollastonite, the precursor ratio of CaO:SiO2 was set at 55:45. This mixture was autoclaved for 8 h and later sintered at 950 °C for 2 h. The chemical composition of the precursors was studied using X-ray fluorescence (XRF), in which rice husk ash consists of 89.5 wt % of SiO2 in a cristobalite phase and calcined limestone contains 97.2 wt % of CaO. The X-ray diffraction (XRD) patterns after sintering showed that only β-wollastonite was detected as the single phase. To study its bioactivity and degradation properties, β-wollastonite samples were immersed in simulated body fluid (SBF) for various periods of time. Throughout the soaking period, the molar ratio of Ca/P obtained was in the range of 1.19 to 2.24, and the phase detected was amorphous calcium phosphate, which was confirmed by scanning electron microscope with energy dispersive X-ray analysis (SEM/EDX) and XRD. Fourier-transform infrared spectroscopy (FTIR) analysis indicated that the peaks of the calcium and phosphate ions increased when an amorphous calcium phosphate layer was formed on the surface of the β-wollastonite sample. A cell viability and proliferation assay test was performed on the rice husk ash, calcined limestone, and β-wollastonite samples by scanning electron microscope. For heavy metal element evaluation, a metal panel that included As, Cd, Pb, and Hg was selected, and both precursor and β-wollastonite fulfilled the requirement of an American Society for Testing and Materials (ASTM F1538-03) standard specification. Apart from that, a degradation test showed that the loss of mass increased incrementally as a function of soaking period. These results showed that the β-wollastonite materials produced from rice husk ash and limestone possessed good bioactivity, offering potential for biomedical applications.

The Suitability of Rice Straw Ash as a Precursor for Synthesizing β-Wollastonite

In this study, β-wollastonite is produced from a reaction between silica (SiO2) and calcium oxide (CaO) with the SiO2/Cao ratio of 55:45. Rice straw ash is chosen as the source for SiO2 instead of rice husk ash because the straw can yield up to 85% of silica even though this percentage is lower than those silica yielded from rice husk ash. It is found that period of autoclaving and sintering play an important role in producing the wollastonite. As shown in the XRD results, a single phase β-wollastonite is obtained after 8 h of autoclaving and 3 h of sintering at 950 °C. The produced β-wollastonite phase also shows a good crystallinity but needs longer sintering time compared with wollastonite produced using rice husk ash. DTA graph shows a chemical reaction between silica and calcium oxide started to occur at 788.3°C. IR spectroscopic analysis data confirm that the IR peaks at 681, 894 and 931 cm-1 are due to the β-Wollastonite phase. Form the results obtained, it can be concluded that rice straw ash is comparable to rice husk ash as a precursor in producing β-Wollastonite material.