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  1. Mahmoudi E, Azizkhani S, Mohammad AW, Ng LY, Benamor A, Ang WL, et al.
    J Environ Sci (China), 2020 Dec;98:151-160.
    PMID: 33097147 DOI: 10.1016/j.jes.2020.05.013
    Graphene oxide is a very high capacity adsorbent due to its functional groups and π-π interactions with other compounds. Adsorption capacity of graphene oxide, however, can be further enhanced by having synergistic effects through the use of mixed-matrix composite. In this study, silica-decorated graphene oxide (SGO) was used as a high-efficiency adsorbent to remove Congo red (CR) and Cadmium (II) from aqueous solutions. The effects of solution initial concentration (20 to 120 mg/l), solution pH (pH 2 to 7), adsorption duration (0 to 140 min) and temperature (298 to 323 K) were measured in order to optimize the adsorption conditions using the SGO adsorbent. Morphological analysis indicated that the silica nanoparticles could be dispersed uniformly on the graphene oxide surfaces. The maximum capacities of adsorbent for effective removal of Cd (II) and CR were 43.45 and 333.33 mg/g based on Freundlich and Langmuir isotherms, respectively. Langmuir and Freundlich isotherms displayed the highest values of Qmax for CR and Cd (II) adsorption in this study, which indicated monolayer adsorption of CR and multilayer adsorption of Cd (II) onto the SGO, respectively. Thermodynamic study showed that the enthalpy (ΔH) and Gibbs free energy(ΔG) values of the adsorption process for both pollutants were negative, suggesting that the process was spontaneous and exothermic in nature. This study showed active sites of SGO (π-π, hydroxyl, carboxyl, ketone, silane-based functional groups) contributed to an enormous enhancement in simultaneous removal of CR and Cd (II) from an aqueous solution, Therefore, SGO can be considered as a promising adsorbent for future water pollution control and removal of hazardous materials from aqueous solutions.
  2. Mahmoudi E, Ang WL, Ng CY, Ng LY, Mohammad AW, Benamor A
    J Colloid Interface Sci, 2019 Apr 15;542:429-440.
    PMID: 30771638 DOI: 10.1016/j.jcis.2019.02.023
    Graphene oxide (GO) has gained popularity in scientific research and industry due to its superior properties, which can be controlled by the synthesis method and graphite feedstock. Despite the availability of different graphite sources, most of the reported studies used natural graphite flake (NGF) as a source of oxidation for GO synthesis. The effect of various alternative graphite feedstocks on the GO properties has not been investigated systematically. This study investigated the influence of graphite feedstock (natural and synthetic) on the characteristics and properties of GO via modified Hummer's method. Natural graphite flake (NGF), natural graphite powder (NGP), and synthetic graphite powder (SGP) were used as graphite feedstock in the study. Energy-dispersive X-ray analysis revealed that the GO produced using NGP (NGP-GO) has higher oxygen to carbon ratio in comparison to GO made from NGF (NGF-GO) and GO made from SGP (SGP-GO) (35.4, 32.7, and 32.2%, respectively), indicating higher oxidation degree for NGP-GO. Zeta potential analysis for NGP-GO, NGF-GO and SGP-GO were -47.8, -42.6 and -39.4 mV, respectively. Morphological analysis revealed that the structures of GO varied according to graphite feedstock, in which (NGP-GO) and (NGF-GO) were highly exfoliated (single-layered structure) while (SGP-GO) showed a multi-layered structure. Further testing was conducted by decorating silver (Ag) nanoparticles on the GO. The results showed that Ag could be uniformly decorated (no agglomeration) on the surface of GO-NGP, due to the presence of more functional groups. Subsequently, the antimicrobial property of Ag-NGP was the highest with an inhibition diameter of 14.7 ± 1.2 mm (30% higher than the other samples). In conclusion, the properties of GO can be tuned by selecting the suitable graphite feedstock and this might pave the way to new developments in the GO-based applications.
  3. Khoshnam M, Farahbakhsh J, Zargar M, Mohammad AW, Benamor A, Ang WL, et al.
    Sci Rep, 2021 Oct 13;11(1):20378.
    PMID: 34645890 DOI: 10.1038/s41598-021-99849-x
    In this study, hematite graphene oxide (αFe2O3-GO) powder nanocomposites and thin-film hematite graphene oxide (αFe2O3-GO) were synthesized for application in the removal of Rhodamine B (RhB) from textile wastewater. αFe2O3-GO nanomaterials were placed onto the FTO substrate to form a thin layer of nanocomposites. Different analysis including XRD, FTIR, Raman spectra, XPS, and FESEM were done to analyze the morphology, structure, and properties of the synthesized composites as well as the chemical interactions of αFe2O3 with GO. The photocatalytic performance of two synthesized composites was compared with different concentrations of αFe2O3-GO. The results showed that powder nanocomposites are more effective than thin-film composites for the removal of RhB dye. αFe2O3-GO-5% powder nanocomposites removed over 64% of dye while thin-film nanocomposites had less removal efficiencies with just under 47% removal rate. The reusability test was done for both materials in which αFe2O3-GO-5% powder nanocomposites removed a higher rate of dye (up to 63%) in more cycles (6 cycles).
  4. Ba-Abbad MM, Takriff MS, Kadhum AA, Mohamad AB, Benamor A, Mohammad AW
    Environ Sci Pollut Res Int, 2017 Jan;24(3):2804-2819.
    PMID: 27837474 DOI: 10.1007/s11356-016-8033-y
    In this study, the photocatalytic degradation of toxic pollutant (2-chlorophenol) in the presence of ZnO nanoparticles (ZnO NPs) was investigated under solar radiation. The three main factors, namely pH of solution, solar intensity and calcination temperature, were selected in order to examine their effects on the efficiency of the degradation process. The response surface methodology (RSM) technique based on D-optimal design was applied to optimise the process. ANOVA analysis showed that solar intensity and calcination temperature were the two significant factors for degradation efficiency. The optimum conditions in the model were solar intensity at 19.8 W/m(2), calcination temperature at 404 °C and pH of 6.0. The maximum degradation efficiency was predicted to be 90.5% which was in good agreement with the actual experimental value of 93.5%. The fit of the D-optimal design correlated very well with the experimental results with higher values of R (2) and R (2)adj correlation coefficients of 0.9847 and 0.9676, respectively. The intermediate mechanism behaviour of the 2-chlorophenol degradation process was determined by gas chromatography-mass spectrometry (GC-MS). The results confirmed that 2-chlorophenol was converted to acetic acid, a non-toxic compound.
  5. Ang WL, Boon Mee CAL, Sambudi NS, Mohammad AW, Leo CP, Mahmoudi E, et al.
    Sci Rep, 2020 12 03;10(1):21199.
    PMID: 33273663 DOI: 10.1038/s41598-020-78322-1
    In the present work, palm kernel shell (PKS) biomass waste has been used as a low-cost and easily available precursor to prepare carbon dots (CDs) via microwave irradiation method. The impacts of the reacting medium: water and diethylene glycol (DEG), and irradiation period, as well as the presence of chitosan on the CDs properties, have been investigated. The synthesized CDs were characterized by several physical and optical analyses. The performance of the CDs in terms of bacteria cell imaging and copper (II) ions sensing and removal were also explored. All the CDs possessed a size of 6-7 nm in diameter and the presence of hydroxyl and alkene functional groups indicated the successful transformation of PKS into CDs with carbon core consisting of C = C elementary unit. The highest quantum yield (44.0%) obtained was from the CDs synthesised with DEG as the reacting medium at irradiation period of 1 min. It was postulated that the high boiling point of DEG resulted in a complete carbonisation of PKS into CDs. Subsequently, the absorbance intensity and photoluminescence intensity were also much higher compared to other precursor formulation. All the CDs fluoresced in the bacteria culture, and fluorescence quenching occurred in the presence of heavy metal ions. These showed the potential of CDs synthesised from PKS could be used for cellular imaging and detection as well as removal of heavy metal ions.
  6. Nouri A, Ang WL, Mahmoudi E, Chua SF, Mohammad AW, Benamor A, et al.
    Chemosphere, 2023 May;322:138219.
    PMID: 36828108 DOI: 10.1016/j.chemosphere.2023.138219
    Decorating nanomaterials on graphene oxide (GO) can enhance its adsorption capacity and removal efficiency of water pollutants. In this study, for the first time, nano-sized polylactic acid (PLA) has been successfully decorated on the surface of GO through a facile synthesis approach. The adsorptive efficiency of GO-PLA for removing methylene blue (MB) and tetracycline (TC) from an aqueous solution was examined. The characterization confirmed the successful decoration of PLA on GO nanosheets with the nano size of PLA. It was hypothesized that the PLA was decorated on the surface of GO through covalent bonding between oxygen-containing functional groups and lactide molecules. The optimum adsorption parameters determined were at the adsorbent dose of 0.5 g L-1, pH 4, contact time of 120 min, and temperature of 318 K. The pseudo-second-order kinetic model described the contaminants' adsorption behaviour, and the intraparticle diffusion model revealed that both surface adsorption and intraparticle diffusion controlled the adsorption process. Langmuir isotherm model best described the adsorption behaviour of the pollutants on GO-PLA and demonstrated the maximum monolayer uptake capacities of MB (332.5 mg g-1) and TC (223.7 mg g-1). The adsorption results indicated that the uptake capacities of GO-PLA in comparison to GO have increased by approximately 70% and 110% for MB and TC, respectively. These observations reflect the remarkable role of nano-sized PLA that enhanced the adsorption capacity due to its additional functional group and larger surface area.
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