Mohd Fairul Sharin Abdul Razak
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Mohd Fairul Sharin Abdul Razak
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Mohd Fairul Sharin, Abdul Razak
Alternative Name
Razak, Mohd Fairul Sharin Abdul
Razak, Mohd Fairul Shahrin Abd
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Scopus Author ID
57219181022

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  • 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
    Preparation of water-base immobilized N doped TiO2 using DSAT technique for photocatalytic degradation of methylene blue dye
    ( 2022-01-01)
    Natar N.S.
    ;
    Ikhwan S.
    ;
    Nazeri N.S.
    ;
    Hamzah S.R.
    ;
    Rosli M.A.
    ;
    Ghani N.I.
    ;
    Ishak M.A.M.
    ;
    Mohd Fairul Sharin Abdul Razak
    ;
    Azami M.S.
    ;
    Nawawi W.I.
    Photocatalytic degradation of TiO2 photocatalyst under suspension mode has widely been studied among researchers. However, the application is limited due to the complexity in separation and non-recyclability of photocatalyst. Immobilization is one of the promising methods to overcome this problem. Most of the prepared immobilization modes showed lower photocatalytic activity compared with the suspension due to the chemical reaction of solvent with modified TiO2. Therefore, a free solvent or water-base preparation of immobilized TiO2 is critical in retaining its photocatalytic activity. Immobilization via double-sided adhesive tape (DSAT) was introduced previously by our research team, it works the best of others in replacing polymer binder in immobilization system making it a free solvent preparation process. The aim of this research is to prepare immobilized unmodified TiO2 and N doped TiO2 by using water-base DSAT technique. The presence of N element was detected for all modified N doped TiO2 samples confirmed by FTIR and EDX analysis. The N incorporated in modified TiO2 has reduced the band gap energy from 3.0 to 2.8 eV as observed by UV–Vis/DRS analysis. This explained the photoactivity under MB dye degradation is 2.1 times faster under N doped TiO2 where the photodegradation rate for unmodified and optimum N doped TiO2 (TN1-45) were 0.065 and 0.138 min−1 respectively. Immobilized TiO2/DSAT and TN1-450/DSAT have shown a significant photocatalytic performance where it was only reduced to 15% from suspension to immobilized mode. It can be considered higher performance as compared to the normal immobilization under solvent. It also better than suspension mode by considering of its reusability that able to sustain the photoactivity of immobilized TN1-450/DSAT for at least for 12 cycles.
      1