Naimah Ibrahim
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Preferred name
Naimah Ibrahim
Official Name
Ibrahim, Naimah
Alternative Name
Ibrahim, Naimah
Ibrahim, N.
Naimah, I.
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Scopus Author ID
23767004300
Researcher ID
AAA-9532-2021

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  • Publication
    Advancement in recycling waste tire activated carbon to potential adsorbents
    ( 2022-12-01)
    Umi Fazara Md Ali
    ;
    Hussin F.
    ;
    Subash Chandra Bose Gopinath
    ;
    Aroua M.K.
    ;
    Khamidun M.H.
    ;
    Jusoh N.
    ;
    Naimah Ibrahim
    ;
    Ahmad S.F.K.
    Waste tires have been identified as one of the contributors to environmental problems and the issue of inadequate landfill spaces. The lack of consistent and systematic approaches such as specific regulations/laws or mechanisms of waste management to waste tires, limited application of technology for recycling waste tires and lack of awareness on the impacts of waste tires problem, make waste tires a source of environmental pollution. Various researches have been conducted on recycling waste tires into polymer bends, and materials to harden concretes, fuels and adsorbent. Researchers suggested that pyrolysis is the current trend of recycling waste tire to harvest the saleable pyrolysis oil and the recycled carbon black. Therefore, this review attempts to compile relevant knowledge about the potential of adsorbent derived from waste tires to be applied in the removal of various types of pollutants like heavy metals, organic pollutants, dye and air/gaseous pollutant. Studies were carried out on revealing the properties and the characteristics of activated carbon derived from waste tire as effective adsorbent which influence the application performance at liquid or gas phase. In addition, the challenges in the production of activated carbon derived from waste tire were discussed.
  • Publication
    Sulfur dioxide removal by calcium-modified fibrous KCC-1 mesoporous silica: kinetics, thermodynamics, isotherm and mass transfer mechanism
    ( 2022-04-01)
    Hanif M.A.
    ;
    Naimah Ibrahim
    ;
    Khairuddin Md Isa
    ;
    Umi Fazara Md Ali
    ;
    Tuan Abdullah T.A.
    ;
    Jalil A.A.
    The removal of sulfur dioxide from industrial flue gas through dry flue gas desulfurization method commonly involves the use of adsorption process with porous sorbent. The efficiency of this process is highly dependent on the adsorption capacity and the adsorption rate of SO2 onto the sorbent materials. The use of KCC-1 mesoporous silica modified with calcium metal additives (Ca/KCC-1) in SO2 adsorption is examined in a fixed bed reactor system. The adsorption capacity of Ca/KCC-1 is found to be critically governed by the reaction temperature and inlet SO2 concentration where low values of both parameters are favorable to achieve the highest adsorption capacity of 3241.94 mg SO2/g sorbent. SO2 molecules are adsorbed on the surface of Ca/KCC-1 by both physisorption and chemisorption processes as assumed by the Avrami kinetic model. Thermodynamic study shows that the process is exothermic and spontaneous in nature, and changes from an ordered stage on the surface of KCC-1 towards an increasingly random stage. The process is well explained by Freundlich isotherm model indicating a slightly heterogeneous process and moderate adsorption capacity. The adsorption stage is limited by film diffusion at the initial stage and by intraparticle diffusion during the transfer of SO2 into the network of pores before adsorption takes place on the active sites.
  • Publication
    Exsolution enhancement of metal-support CO oxidation perovskite catalyst with parameter modification
    ( 2021-05-24)
    Lew G.L.
    ;
    Naimah Ibrahim
    ;
    Abdullah S.
    ;
    Wan Daud W.R.
    ;
    Wan Khairunnisa Wan Ramli
    This study aimed to further tune the capability of active metal exsolution onto the surface of the CO oxidative perovskite catalyst La0.7Ce0.1Co0.3Ni0.1Ti0.6O3 by tuning the reducing parameter. Under same calcination temperature of 800℃, XRD analysis shown that the precursors with calcination duration of 6 hours (S2T8H6) was able to achieve similar crystalline structure to those with calcination duration of 12 hours (S2T8H12). In order for the active metal (CoNi) to be exsolved onto the perovskite surface, reducing parameter such as temperature and duration are deemed crucial to the reduction process. The exsolution of the active metals was observed when the samples were treated under reducing condition with varying temperatures of 550℃ and 700℃ and duration from 200 to 300 minutes. Through comparison with their EDX readings, S2T8H6 treated under 700℃ and 300 minutes (S2T8H6-R7H5) achieved the highest weight percentage of surface Cobalt and Nickel of 3.83 and 2.81. It was clear that by tuning the temperature and duration of reduction, the exsolution of the active metals onto the surface of the perovskite could be improved resulting in better exposure and dispersion of active metals onto the surface of catalyst.
  • Publication
    The role of sodium surface species on oxygen charge transfer in the Pt/YSZ system
    ( 2012-08-01)
    Naimah Ibrahim
    ;
    Danai Poulidi
    ;
    Maria Elena Rivas
    ;
    Iain D. Baikie
    ;
    Ian S. Metcalfe
    The role of sodium surface species in the modification of a platinum (Pt) catalyst film supported on 8 mol% yttria-stabilised-zirconia (YSZ) was investigated under a flow of 20 kPa oxygen at 400°C. Cyclic and linear sweep voltammetry were used to investigate the kinetics of the oxygen charge transfer reaction. The Pt/YSZ systems of both 'clean' and variable-coverage sodium-modified catalyst surfaces were also characterised using SEM, XPS and work function measurements using the Kelvin probe technique. Samples with sodium coverage from 0.5 to 100% were used. It was found that sodium addition modifies the binding energy of oxygen onto the catalyst surface. Cyclic voltammetry experiments showed that higher overpotentials were required for oxygen reduction with increasing sodium coverage. In addition, sodium was found to modify oxygen storage and/or adsorption and diffusion increasing current densities at higher cathodic overpotential. Ex situ XPS measurements showed the presence of sodium hydroxide, carbonate and/or oxide species on the catalyst surface, while the Kelvin probe technique showed a decrease of approximately 250 meV in the work function of samples with more than 50% sodium coverage (compared to a nominally 'clean' sample).
  • Publication
    The role of sodium surface species on electrochemical promotion of catalysis in a Pt/YSZ system: The case of ethylene oxidation
    ( 2013-04-23)
    Naimah Ibrahim
    ;
    Danai Poulidi
    ;
    Ian S. Metcalfe
    The role of sodium addition as foreign (impurity) species on the electrochemical promotion of ethylene oxidation in a Pt/YSZ system was investigated. It was found that the presence of sodium surface species on the catalyst surface can significantly affect its catalytic and electrocatalytic properties, but there is no clear evidence at this stage that such species are necessary for the observation of EPOC. Under negative polarisation, low coverage sodium was found to have a pronounced effect on the electrochemical promotion of ethylene oxidation as an electronic promoter. The reaction changed behaviour from electrophilic at low sodium coverage (0.11%) and low to intermediate oxygen partial pressure (pO2 ⩽ 3.0 kPa) to electrophobic at high sodium coverage (65%) and under high oxygen partial pressures (pO2 = 8.0 kPa). In between the two sets of conditions, the reaction showed volcano-type behaviour depending on the coverage of sodium and gas-phase oxygen partial pressure.
  • Publication
    Microplastics and nanoplastics: Recent literature studies and patents on their removal from aqueous environment
    ( 2022-03-01)
    Hanif M.A.
    ;
    Naimah Ibrahim
    ;
    Farrah Aini Dahalan
    ;
    Umi Fazara Md Ali
    ;
    Masitah Hasan
    ;
    Jalil A.A.
    The presence of microplastics (MP) and nanoplastics (NP) in the environment poses significant hazards towards microorganisms, humans, animals and plants. This paper is focused on recent literature studies and patents discussing the removal process of these plastic pollutants. Microplastics and nanoplastics can be quantified by counting, weighing, absorbance and turbidity and can be further analyzed using scanning electron microscopy (SEM), dynamic light scattering (DLS), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, surface-enhanced Raman spectroscopy and Raman tweezers. Mitigation methods reported are categorized depending on the removal characteristics: (i) Filtration and separation method: Filtration and separation, electrospun nanofiber membrane, constructed wetlands; (ii) Capture and surface attachment method: coagulation, flocculation and sedimentation (CFS), electrocoagulation, adsorption, magnetization, micromachines, superhydrophobic materials and microorganism aggregation; and (iii) Degradation method: photocatalytic degradation, microorganism degradation and thermal degradation; where removal efficiency between 58 and 100% were reported. As these methods are significantly distinctive, the parameters which affect the MP/NP removal performance e.g., pH, type of plastics, presence of interfering chemicals or ions, surface charges etc. are also discussed. 42 granted international patents related to microplastics and nanoplastics removal are also reviewed where the majority of these patents are focused on separation or filtration devices. These devices are efficient for microplastics up to 20 μm but may be ineffective for nanoplastics or fibrous plastics. Several patents were found to focus on methods similar to literature studies e.g., magnetization, CFS, biofilm and microorganism aggregation; with the addition of another method: thermal degradation.
  • Publication
    Oil palm waste-derived reduced graphene oxide (rGO) for dynamic adsorption of dye in a fixed-bed system
    ( 2024-01-01)
    Mohd Ali Jinnah S.N.H.
    ;
    Umi Fazara Md Ali
    ;
    Subash Chandra Bose Gopinath
    ;
    Naimah Ibrahim
    ;
    Razi Ahmad
    ;
    Mohamed Zuki F.
    This study focuses on investigating the dynamic adsorption of Rhodamine B (RhB) from reduced graphene oxide (rGO) derived from oil palm waste. The synthesis of rGO from palm kernel shell (PKS) was achieved through double oxidation and carbonization method, resulting in a yield of 73.5 wt%. The reduction of oxygen-containing functionalities process using PKS was confirmed by FTIR spectroscopy, microscopic evaluation, and X-ray diffraction analyses. Laboratory-scale fixed-bed experiments were conducted with various process parameters. Both PKS and rGO were used as adsorbents, and a comparison was made based on breakthrough curve analysis, adsorption capacity and percentage removal of dye. The adsorption kinetics of RhB on PKS and rGO were best described by the non-linear Yoon-Nelson model, with a high adsorption capacity of 88.32 mg/g and 195.24 mg/g respectively. Using both PKS and rGO, the maximum adsorption capacity was observed when using 10 cm bed depth column, inlet dye concentration of 5 mg/L, flow rate of 12 mL/min and pH of 7. PKS exhibited good dye removal with an efficiency of 66.54%. Meanwhile, the exothermic behavior highlighted the potential of utilizing rGO for maximum dye removal, achieving an efficiency of 90.35%. This study justifies rGO as a cost-effective superior dye removal adsorbent, providing new prospect for large-scale dye removal.
  • Publication
    Influence of carbonisation temperature on the surface pore characteristics of acid-treated oil palm empty fruit bunch activated carbon
    ( 2020-07-01)
    Ahmad N.
    ;
    Naimah Ibrahim
    ;
    Fu P.Y.
    ;
    Razi Ahmad
    Carbonisation process affects the surface physical and chemical properties of an activated carbon. Therefore, this work aims to investigate the influence of carbonisation temperature from 400 to 550° C during activation with 85% phosphoric acid (H3PO4) on the surface pore characteristics of activated carbon produced from oil palm empty fruit bunch (EFB) for nitric oxide (NO) removal from gas streams. Pore and morphological characterisation showed that EFB carbonised at 400° C (EFBC-400) is microporous and has a uniform pore structure with 98% micropore volume. Increasing carbonisation temperature resulted in pore enlargement from 2.8 to 4.7 nm and increment in pore heterogeneity and BET surface area from 215 to 759 m2/g. However, the NO breakthrough experiment indicated that EFBC-400 is more favourable for low-temperature NO removal, due to the importance of microporosity in adsorption of NO. Further study will look at the kinetics of NO removal and the adsorbent regeneration.
      1
  • Publication
    Nitric oxide removal by zinc chloride activated oil palm empty fruit bunch fibre
    ( 2021-01-01)
    Lin Cha Soon
    ;
    Naimah Ibrahim
    ;
    Norhidayah Ahmad
    ;
    Muhammad Adli Hanif
    ;
    Abdullah S.
    Nitric oxide (NO) emission is known to pose detrimental effects towards the environment and human beings. Low-temperature NO removal by activated carbon from agricultural waste materials is affordable due to the use of low-cost materials as precursor and elimination of the need for flue gas reheating. The use of chemical agents in activated carbon production improves the performance of waste materials in NO removal. The performance of NO removal was investigated via breakthrough experiment using oil palm empty fruit bunch (EFB) activated with zinc chloride (ZnCl2) at different concentrations (0.1, 0.5, and 1.5 M). Activation of EFB with 0.5 M ZnCl2 resulted in the formation of well-defined micropores, but the use of higher concentration of ZnCl2 resulted in widening of developed pores and intense pore blockage which reduce the accessibility of NO molecules to the adsorption sites. An adsorption isotherm study conducted using 0.5 M ZnCl2/EFB sample with varying NO concentration between 300-1000 ppm indicated that the adsorption process was best defined by Langmuir isotherm model. In addition, adsorption kinetic was investigated at different temperatures; i.e. 100, 150, 200, 250 and 300 °C. NO removal was found to follow Avrami kinetic model at T=100 °C, while upon further increase in temperature, the process was better fitted to the pseudo-second order kinetic model. NO adsorption capacity increases significantly beyond 250 °C up to 1000 mg/g. The activation energy of NO adsorption fell into two distinct regions: -4.73 kJ/mol at 100-200 °C and 84.04 kJ/mol at 200-300 °C. At lower temperature, the adsorption process was exothermic and followed physisorption path, while the increase in reaction temperature led to slower rate of reaction. It was concluded that the removal of NO using EFB modified with ZnCl2 at optimized condition could be a promising alternatives for treating NO-containing flue gas.
      1
  • Publication
    Influence of leachate matrix on oxidation performance of ozonation and aops
    ( 2022-12-15)
    Kow S.H.
    ;
    Fahmi Muhammad Ridwan
    ;
    Che Zulzikrami Azner Abidin
    ;
    Najihah Abdul Rashid
    ;
    Naimah Ibrahim
    ;
    Abdul Haqi Ibrahim
    ;
    Ong Soon An
    ;
    Wikurendra E.A.
    ;
    Handayani D.
    Landfill leachate is a critical environmental issue that should be adequately treated to prevent it from spreading to the environment. This study explored the influence of raw leachate matrix and treated leachate matrix on O3, O3/H2O2, and O3/PS performance. O3 and AOPs were conducted in a laboratory-scale batch reactor. The findings showed the degradation of p-cresol, COD, and humic substances was much slower in treated leachate matrix than in raw leachate matrix. However, color was found easier to remove in treated leachate. The results revealed a synergic effect between molecular O3 and dissolved organic matter in the raw leachate as the O3 performance was enhanced in the presence of raw leachate matrix, except for color removal. The highest degradation of more than 90% was achieved in O3 /H2 O2 to remove COD, p-cresol, and humic substances, although it is the most affected by the leachate matrix. This study provides vital insight into the notable performance of O3 /PS in color removal regardless of the influence of leachate matrix, suggesting that the sulfate radical-induced oxidation outperformed O3 and O3 /H2 O2 in reducing nitrogen-containing compounds.
      1