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Novel glass-ceramic composites with optical bandgap tunability were synthesised. Zinc silicate powder (ZS) was mixed with multi-walled carbon nanotubes (MWCNTs) at various mass fractions (0, 1, 2, and 3 wt %), followed by argon sintering. X-ray diffraction (XRD) analysis revealed the structural change from an amorphous ZS phase to a crystalline willemite phase (Zn 2 SiO 4) by adding MWCNTs, and the largest crystallite size was obtained for ZS with 2.0 wt% MWCNTs. Although the agglomeration of ZS and MWCNTs was observed by field emission scanning electron microscopy (FESEM), there was no chemical interaction between ZS and MWCNTs as confirmed by Fourier transform infrared spectroscopy (FTIR). MWCNTs enhanced the crystallisation, which led to the green emission of Zn 2 SiO 4 blue-shifting from 572 nm to 557 nm. The narrowed optical bandgap of Zn 2 SiO 4 was attributed to the MWCNT-induced exciton localised between the valence band and conduction band of Zn 2 SiO 4. The bandgap tuning effect of MWCNTs potentially paved new ways to mass fabricate zinc silicate-based semiconductors with desirable optical bandgap energy E g , which significantly benefits the sensor and laser-related industry. [ABSTRACT FROM AUTHOR]

This paper presents a study on synthesis and optical properties of ZnSiO:1 wt% Eu at different heat treatments. The objective of the research is to synthesize ZnSiO:1 wt% Eu phosphor by using low cost solid state reaction method with recycled waste bottle glasses as the silicate source. The X-ray diffraction results showed that the prepared ZnSiO:1 wt% Eu phosphors have a sharp diffraction peak as the heat treatment temperatures were increased from 600 to 1000 °C. Furthermore, the morphology from the Field emission scanning electron microscope analysis were shown the formation of well crystalline samples with dense packed grains due to the increment of heat treatment temperatures. Fourier transform infrared spectra has confirmed the present elements in ZnSiO:1 wt% Eu phosphors while the narrow width of Raman line spectra were observed at temperatures ranging from 700 to 1000 °C indicates good homogeneity and crystallinity of synthesized powders. In addition, the energy band gap of europium doped zinc silicate increased dramatically up to 3.62 eV at temperature of 1000 °C. Photoluminescence measurements has also exhibited the red emission corresponding to the D → F (600 nm) when viewed under blue excitation. [ABSTRACT FROM AUTHOR]

Arecanut husk (AH) was selected as a material for silica replacement in the synthesis process of glass-ceramics zinc silicate and also the fact that it has no traditional use and often being dumped and results in environmental issues. The process of pyrolysis was carried out at temperature 700 °C and above based on thermogravimetric analysis to produce arecanut husk ash (AHA). The average purity of the silica content in AHA ranged from 29.17% to 45.43%. Furthermore, zinc oxide was introduced to AHA and zinc silicate started to form at sintering temperature 700 °C and showed increased diffraction intensity upon higher sintering temperature of 600 °C to 1000 °C based on X-ray diffraction (XRD) analysis. The grain sizes of the zinc silicate increased from 1011 nm to 3518 nm based on the morphological studies carried out by field emission scanning electron microscopy (FESEM). In addition, the optical band gap of the sample was measured to be in the range from 2.410 eV to 2.697 eV after sintering temperature. From the data, it is believed that a cleaner production of low-cost zinc silicate can be achieved by using arecanut husk and have the potential to be used as phosphors materials. [ABSTRACT FROM AUTHOR]

Glass ionomer cement (GIC) is a well-known restorative material applied in dentistry. The present work aims to study the effect of hydroxyapatite (HA) addition into GIC based on physical, mechanical and structural properties. The utilization of waste materials namely clam shell (CS) and soda lime silica (SLS) glass as replacements for the respective CaO and SiO2 sources in the fabrication of alumino-silicate-fluoride (ASF) glass ceramics powder. GIC was formulated based on ASF glass ceramics, polyacrylic acid (PAA) and deionized water, while 1 wt.% of HA powder was added to enhance the properties of the cement samples. The cement samples were subjected to four different ageing times before being analyzed. In this study, the addition of HA caused an increment in density and compressive strength results along with ageing time. Besides, X-ray Diffraction (XRD) revealed the formation of fluorohydroxyapatite (FHA) phase in HA-added GIC samples and it was confirmed by Fourier Transform Infrared (FTIR) analysis which detected OH‒F vibration mode. In addition, needle-like and agglomeration of spherical shapes owned by apatite crystals were observed from Field Emission Scanning Electron Microscopy (FESEM). Based on Energy Dispersive X-ray (EDX) analysis, the detection of chemical elements in the cement samples were originated from chemical compounds used in the preparation of glass ceramics powder and also the polyacid utilized in initiating the reaction of GIC. [ABSTRACT FROM AUTHOR]

In this paper, the structural and optical properties of ZnO-SiO2-based ceramics fabricated from oil palm empty fruit bunch (OPEFB) were investigated. The OPEFB waste was burned at 600, 700 and 800 °C to form palm ash and was then treated with sulfuric acid to extract silica from the ash. X-ray fluorescence (XRF) and X-ray diffraction (XRD) analyses confirmed the existence of SiO2 in the sample. Field emission scanning electron microscopy (FESEM) showed that the particles displayed an irregular shape and became finer after leaching. Then, the solid-state method was used to produce the ZnO-SiO2 composite and the samples were sintered at 600, 800, 1000, 1200 and 1400 °C. The XRD peaks of the Zn2SiO4 showed high intensity, which indicated high crystallinity of the composite. FESEM images proved that the grain boundaries were larger as the temperature increased. Upon obtaining the absorbance spectrum from ultraviolet–visible (UV–Vis) spectroscopy, the energy band gaps obtained were 3.192, 3.202 and 3.214 eV at room temperature, 600 and 800 °C, respectively, and decreased to 3.127, 2.854 and 2.609 eV at 1000, 1200 and 1400 °C, respectively. OPEFB shows high potential as a silica source in producing promising optical materials. [ABSTRACT FROM AUTHOR]

In this study, the authors attempted to propose the very first study on fabrication and characterization of zinc-boro-silicate (ZBS) glass-ceramics derived from the ternary zinc-boro-silicate (ZnO)0.65(B2O3)0.15(RHA)0.2 glass system through a conventional melt-quenching method by incorporating rice husk ash (RHA) as the silica (SiO2) source, followed by a sintering process. Optimization of sintering condition has densified the sintered samples while embedded beta willemite (β-Zn2SiO4) and alpha willemite (α-Zn2SiO4) were proven in X-ray diffraction (XRD) analysis. Field emission scanning electron microscopy (FESEM) has shown the distribution of willemite crystals in rhombohedral shape crystals and successfully form closely-packed grains due to intense crystallization. The photoluminescence (PL) spectra of all sintered ZBS glasses presented various emission peaks at 425, 463, 487, 531, and 643 nm corresponded to violet, blue, green, and red emission, respectively. The correlation between the densification, phase transformation, microstructure, and photoluminescence of Zn2SiO4 glass-ceramic phosphor is discussed in detail. [ABSTRACT FROM AUTHOR]

In this work, waste coconut husk ash was used to prepare a ZnO-SiO2 composite. Solid-state technique was used to fabricate the composite due to its producibility, simple procedure as well as lower production cost. At high sintering temperatures ranging from 600 °C to 1000 °C, the X-ray diffraction (XRD) peaks of the Zn2SiO4 showed high intensity, which indicated high crystallinity. Furthermore, the formation of broad bands of ZnO4, Si-O-Si, and SiO4 were detected by Fourier transform infrared (FTIR) spectroscopy and the bands became narrower with the increment of sintering temperature. Besides, the morphological image from field emission scanning electron microscopy (FESEM) showed the formation of densely packed grains and smooth surface composite with the increase of sintering temperature. Upon obtaining the absorbance spectrum from Ultraviolet–Visible (UV–Vis) spectroscopy, the optical band gap was calculated to be 4.05 eV at 1000 °C. The correlation between the structural and optical properties of ZnO-SiO2 composite was discussed in detail. [ABSTRACT FROM AUTHOR]

This paper presents the electromagnetic interference properties of multi-walled carbon nanotubes (MWCNTs) as a novel nano-reinforcement filler in poly (lactic acid) (PLA)/poly (ethylene glycol) (PEG) polymer matrix that was prepared via melt blending mode. Plasticization of PLA was first carried out by PEG, which overcomes its brittleness problem, in order to enhance its flexibility. A waveguide adapter technique was used to measure the dielectric properties ε r , and S-parameters reflection (S11) and transmission (S21) coefficients. The dielectric properties, microwave attenuation performances, and electromagnetic interference shielding effectiveness (EMISE) for all the material under test have been calculated over the full X-Band (8–12 GHz) due to its importance for military and commercial applications. The prepared samples were studied while using X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), Fourier transforms infrared spectroscopy (FTIR), mechanical properties measurements, as well as thermogravimetric analysis (TGA). The results showed that the dielectric properties increased with increased multi-walled carbon nanotubes (MWCNTs) filler, as well as the shielding effectiveness of the MWCNT/PLA/PEG nanocomposites increased with the increasing of MWCNTs. The highest SE total value was found to be 42.07 dB at 12 GHz for 4 wt.% filler content. It is also observed that the attenuation values of the nanocomposites increased with an increase in MWCNTs loading, as well as the power loss values for all of the samples increased with the increase in MWCNTs loading, except the amount of the transmitted wave through the nanocomposites. [ABSTRACT FROM AUTHOR]

In this study, a nanocomposite of reduced graphene oxide (RGO) nanofiller-reinforcement poly(lactic acid) (PLA)/poly(ethylene glycol) (PEG) matrix was prepared via the melt blending method. The flexibility of PLA was improved by blending the polymer with a PEG plasticizer as a second polymer. To enhance the electromagnetic interference shielding properties of the nanocomposite, different RGO wt % were combined with the PLA/PEG blend. Using Fourier-transform infrared (FT-IR) spectroscopy, field emission scanning electron microscopy (FE-SEM) and X-ray diffraction, the structural, microstructure, and morphological properties of the polymer and the RGO/PLA/PEG nanocomposites were examined. These studies showed that the RGO addition did not considerably affect the crystallinity of the resulting nanomaterials. Thermal analysis (TGA) reveals that the addition of RGO highly improved the thermal stability of PLA/PEG nanocomposites. The dielectric properties and electromagnetic interference shielding effectiveness of the synthesized nanocomposites were calculated and showed a higher SE total value than the target value (20 dB). On the other hand, the results showed an increased power loss by increasing the frequency and conversely decreased with an increased percentage of filler. [ABSTRACT FROM AUTHOR]