Banjuraizah Johar
Thumbnail Image
Preferred name
Banjuraizah Johar
Official Name
Banjuraizah, Johar
Main Affiliation
Scopus Author ID
36782257500
Researcher ID
ELA-9787-2022

Research Output

Filters

1
3
Reset filters

Settings
Now showing 1 - 3 of 3
  • Publication
    Formation of bio-based derived dicalcium silicate ceramics via mechanochemical treatment: physical, XRD, SEM and FTIR analyses
    ( 2023-07)
    Siti Nur Hazwani Yunus
    ;
    Khor Shing Fhan
    ;
    Banjuraizah Johar
    ;
    Nur Maizatul Shima Adzali
    ;
    Nur Hazlinda Jakfar
    ;
    Cheng Ee Meng
    ;
    Emma Ziezie Mohd Tarmizi
    ;
    Zainal Abidin Talib
    Beta-dicalcium silicate plays an important role in modern technology, but its tendency for polymorphic transformation results in the dusting phenomenon, is a major challenge. Therefore, mechanochemical treatment is used to reduce the particle size to retain the stability of the polymorph. In this study, pure dicalcium silicate ceramics of β-monoclinic structure with P 121/c1 space group were synthesized using calcium oxide and silicate powders derived from calcined eggshells and rice husks, respectively. The powders were mixed in a 2:1 molar ratio by mechanochemical treatment and heat-treated in the air at temperatures ranging from 900°C to 1100°C for 2 h. The results reveal that pure betadicalcium silicate formed at 1100°C without adding stabilizers. The properties of the pristine and sintered bodies were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, and scanning electron microscopy (SEM). SEM revealed that the grain and pore sizes increase with rising sintering temperatures. FTIR spectra indicate the existence of Si-O bonds in -4 4 SiO tetrahedrons on all the samples. The sample sintered at 1000°C attains the lowest bulk density (1.2463 g/cm3), whereas the apparent porosity is the highest (62.5%). The reason for this trend is due to the decomposition of carbonate into CO2 gas. The densification onset for the sample sintered at 1100°C as the bulk density rises and grain size achieves 6.06 μm. This study further explains the effect of sintering temperatures on the physical, structural, and morphological properties of Ca2SiO4 which would also be useful for further optimization of its use.
  • Publication
    The Microstructural and Bioactivity Behavior of Magnesium Alloy Filled with Bioglass for Biomedical Application
    ( 2022-01-24)
    Nur Maizatul Shima Adzali
    ;
    Dahlan N.F.
    ;
    Banjuraizah Johar
    ;
    Baharom N.A.
    Magnesium alloy have known as degradable implant material due to biodegradable properties. However, by developed Mg alloy matrix composites containing a bioceramic will produced more biodegradable and does not need second surgical to remove the implants in body. Powder metallurgy route was used to fabricate the AZ91/BG composite by mixing, compacting and sintering. Mg alloy (AZ91) was reinforced with 0, 3, 6, and 9 wt% of bioglass (BG) before compact and sintered at 400°C for 2 hours. The Vickers hardness, scanning electron microscope, and x-ray diffraction are used to investigate the effect of BG particles addition on the mechanical properties and microstructure of the composite AZ91/BG. Bioactivity behaviour was studied by immersion test of AZ91/BG composite into phosphate buffered saline (PBS) solution for 72 hours. The results showed that as the addition of BG increases from 3 to 9 wt%, the hardness of AZ91/BG decrease from 43.3HV to 27.9HV. The result also showed the formation of protective layers or apatite layer on the surface of AZ91/BG composite after immersed in PBS solution for 72 hours. Phase analysis by XRD shows the presence of peak Ca10(OH)2(PO4)6 as the BG increased from 3 to 9 wt%. As a conclusion, AZ91/3BG shows the optimum composite for biomedical application based on its properties and bioactivity behaviour.
  • Publication
    Phase Analysis of Bio-Based Derived Tricalcium Disilicate From 2CaO:1SiO2 By X-ray Diffraction
    ( 2021-12-14)
    Siti Nur Hazwani Yunus
    ;
    Fhan K.S.
    ;
    Banjuraizah Johar
    ;
    Nur Maizatul Shima Adzali
    ;
    Jakfar N.H.
    ;
    Cheng Ee Meng
    In this paper, tricalcium disilicate was formed from dicalcium silicate compound powder, synthesised via a mechanochemical technique using a stoichiometric 2CaO:1SiO2. Compound CaO and SiO2 were derived from the bio-waste of eggshell and rice husk at the calcination temperature of 900oC and 800oC, respectively. The dicalcium disilicate powder was sintered for 2 hours at different temperatures ranging from 1150oC to 1350oC. Using X-ray diffraction with Rietveld analysis, it was found that the amount of tricalcium disilicate with monoclinic (beta) crystal structure increases on sintering temperature at the expense of dicalcium silicate. The complete formation of single-phase tricalcium disilicate began at a sintering temperature of 1300oC. The effect of sintering temperatures on the crystallisation and phase transition of dicalcium silicate is reported. The size of crystallites depends on the sintering temperature. The finding of this study rebound to the benefit of society by reducing the risk-off pollution cause by accessive redundant bio-waste eggshell and rice husk and also reduced the amount of CaO and SiO2 used in the fabrication of Ca3Si2O7