Mohd Fairul Sharin Abdul Razak
Thumbnail Image
Preferred name
Mohd Fairul Sharin Abdul Razak
Official Name
Mohd Fairul Sharin, Abdul Razak
Alternative Name
Razak, Mohd Fairul Sharin Abdul
Razak, Mohd Fairul Shahrin Abd
Main Affiliation
Scopus Author ID
57219181022

Research Output

Filters

2
2
Reset filters

Settings
Now showing 1 - 2 of 2
  • Publication
    The role of Nitrogen-Doped TiO2 supported by platinum catalyst synthesized via various mode preparations for photocatalytic nnhancement
    ( 2022-11-01)
    Natar N.S.
    ;
    Ghani N.I.A.
    ;
    Hamzah S.R.
    ;
    Rosli M.A.
    ;
    Muhamad N.A.
    ;
    Azami M.S.
    ;
    Ishak M.A.M.
    ;
    Mohd Fairul Sharin Abdul Razak
    ;
    Nawawi W.I.
    The limitations of TiO2 as a photocatalyst such as the larger bandgap energy, which only activates under the UV region, give a lower photocatalytic activity. This study reports the role of the N and Pt co-dopant on the modification of the TiO2 photocatalyst for photocatalytic degradation of methylene blue dye under different mode preparations, i.e., sequential and vice-versa modes. The sequential mode preparation of the N and Pt co-dopant TiO2 photocatalyst consisted of the initial preparation of the N-doped TiO2 (N-TiO2) under the calcination method, which was then further doped with platinum (Pt) through the photodeposition process labeled as NPseq-TiO2, while the vice-versa mode was labeled as PNrev-TiO2. About 1.58 wt.% of N element was found in the NPseq-TiO2 photocatalyst, while there was no presence of N element detected in PNrev-TiO2, confirmed through an elemental analyzer (CHNS-O) and (EDX) analysis. The optimum weight percentage of Pt for both modes was detected at about ±2.0 wt.%, which was confirmed by inductively coupled plasma-emission spectroscopy (ICP-OES). The photoactivity under methylene blue (MB) dye degradation of the NPseq-TiO2 photocatalyst was 2 and 1.5 times faster compared to the unmodified TiO2 and PNrev-TiO2, where the photodegradation rates were, ca., 0.065 min−1 and 0.078 min−1, respectively. This was due to the N elements being incorporated with the TiO2 lattice, which was proven by UV-Vis/DRS where the bandgap energy of NPseq-TiO2 was reduced from 3.2 eV to 2.9 eV. In addition, the N generated a stronger PL signal due to the formation of oxygen vacancies defects on the surface of the NPseq-TiO2 photocatalyst. The higher specific surface area as well as higher pore volume for the NPseq-TiO2 photocatalyst enhanced its photocatalytic activity. Moreover, the NPseq-TiO2 showed the lowest COD value, and it was completely mineralized after 7 h of light irradiation. The preparation order did not affect the Pt dopant but did for the N element. Therefore, it is significant to investigate different mode preparations of the N and Pt co-dopant for the modification of TiO2 to produce a good-quality photocatalyst for photocatalytic study under the photodegradation of MB dye.
      1  9
  • Publication
    Effect of Photoetching Process onto Immobilized PANI/TiO2Films towards Photocatalytic Degradation of RR2 dye
    ( 2020-11-24)
    Mohd Fairul Sharin Abdul Razak
    ;
    Mohd Nazry Salleh
    ;
    Nawawi W.I.
    ;
    Natar N.
    Polyaniline (PANI) and P-25 Titanium dioxide (TiO2) was fabricated as immobilized P-25TiO2/PANI/ENR/PVC film and reported on the photocatalytic study. PANI and TiO2 was immersed into the organic solvent and being coated onto glass plates under influenced of ENR/PVC polymeric binder by using a dip-coating method. It was found that, the removal of RR2 dye nearly good as suspension system after the pre-irradiation process. Based on COD and BET results, it showed that the optimum time of etching process was 7 hours irradiation time. This pre-irradiation process enhanced the removal of dye due to leached out of excessive binder and also exhibit visible light active after insertion of PANI into the immobilized system.
      17  2