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  1. Lim JV, Bee ST, Sin LT, Ratnam CT, Bee SL
    Polymers (Basel), 2022 Dec 15;14(24).
    PMID: 36559863 DOI: 10.3390/polym14245494
    This study investigates the thermal effect of supercritical water treatment at different temperatures (150, 175, 200 °C) and semi-vacuum state (-0.08 MPa) on graphite flakes which are then incorporated into nylon 610. The treatment is deemed to increase the surface activity of nanofillers through the formation of oxygen-containing functional groups. X-ray diffraction (XRD) analysis indicated that the crystal structure of the flakes remained similar before and after supercritical water treatment. Fourier transform infrared spectroscopy (FTIR) also showed the presence of hydrogen bonding between the flakes and the polymer matrix through the appearance of amide bands. The intensity of the amide peaks is higher for nanocomposites with treated flakes than untreated ones. Furthermore, scanning electron microscopy (SEM) showed that at higher wt%, aggregation will occur, which leads to a weakening in physical properties. The tensile strength of nanocomposites with treated flakes decreased with increasing wt%, while those with untreated flakes increased with increasing wt%. Young's modulus of all the nanocomposites generally increased with increasing wt%. The highest tensile strength obtained is 967.02 kPa, while that of neat nylon 610 is 492.09 kPa. This enhancement in mechanical properties can be attributed to the intact structure of the graphite flakes and the interaction between the flakes and the nylon 610 matrix. A higher temperature of water treatment was discovered to cause higher oxidation levels on surface of the nanofillers but would result in some structural damage. The optimum nylon 610 nanocomposite synthesized was the one that was incorporated with 1.5 wt% graphite flakes treated at 150 °C and -0.08 MPa, as it has the highest tensile strength.
  2. Lim JV, Bee ST, Sin LT, Ratnam CT, Abdul Hamid ZA
    Polymers (Basel), 2022 Nov 01;14(21).
    PMID: 36365653 DOI: 10.3390/polym14214660
    In this study, water at high temperatures (150, 175, 200 °C) and in a vacuum state (-0.1 MPa) was applied to graphite nanosheets to enhance surface activity to promote the formation of oxygen-containing functional groups through supercritical water treatment. Nylon 610 nanocomposites (with treated or untreated nanosheets as nanofillers) were then synthesized using interfacial polymerization. X-ray diffraction (XRD) analysis showed that the water treatment did not alter the crystal structure of the carbon nanosheets. Additionally, Fourier transform infrared spectroscopy (FTIR) analysis showed the presence of amide peaks within the nanocomposites, indicating the presence of hydrogen bonding between the nanosheets and the polymer matrix. The intensity of the amide peaks was higher for nanocomposites combined with treated nanosheets than untreated ones. This hydrogen bonding is beneficial to the conductivity of the nanocomposites. The conductivity of treated nanosheets/nylon nanocomposites generally decreased with increasing wt%, while the conductivity of untreated nanosheets/nylon nanocomposites increased with increasing wt%. The decrementing of conductivity in the treated nanosheets/nylon nanocomposites is due to the agglomeration of the nanosheets within the composite. This is in in line with scanning electron microscopy (SEM) results which showed that at higher wt%, the aggregation condition tended to occur. The highest conductivity obtained is 0.004135 S/m, as compared to the conductivity of neat nylon 610, which is 10-14 S/m. This improvement in electrical properties can be attributed to the intact structure of the nanosheets and the interaction between the nanofillers and the nylon 610 matrix. The optimum nylon 610 nanocomposite synthesized was the one incorporated with 0.5 wt% graphite nanosheets treated at 200 °C and -0.1 MPa, which possess the highest conductivity.
  3. Bee ST, Ooi Ker Qi N, Sin LT, Ng HM, Lim JV, Ratnam CT, et al.
    Polymers (Basel), 2021 Dec 10;13(24).
    PMID: 34960885 DOI: 10.3390/polym13244334
    This work was conducted to investigate the effect of carbon nanotube (CNT) on the mechanical-physico properties of the electron beam irradiated polyvinyl alcohol (PVOH) blends. The increasing of CNT amount up to 1.5 part per hundred resin (phr) has gradually improved tensile strength and Young's modulus of PVOH/CNT nanocomposites due to effective interlocking effect of CNT particles in PVOH matrix, as evident in SEM observation. However, further increments of CNT, amounting up to 2 phr, has significantly decreased the tensile strength and Young's modulus of PVOH/CNT nanocomposits due to the CNT agglomeration at higher loading level. Irradiation was found to effectively improve the tensile strength of PVOH/CNT nanocomposites by inducing the interfacial adhesion effect between CNT particles and PVOH matrix. This was further verified by the decrement values of d-spacing of the deflection peak. The increasing of CNT amounts from 0.5 phr to 1 phr has marginally induced the wavenumber of O-H stretching, which indicates the weakening of hydrogen bonding in PVOH matrix. However, further increase in CNT amounts up to 2 phr was observed to reduce the wavenumber of O-H stretching due to poor interaction effect between CNT and PVOH matrix. Electron beam irradiation was found to induce the melting temperature of all PVOH/CNT nanocomposite by inducing the crosslinked networks.
  4. Lim JV, Bee ST, Tin Sin L, Ratnam CT, Abdul Hamid ZA
    Polymers (Basel), 2021 Oct 14;13(20).
    PMID: 34685309 DOI: 10.3390/polym13203547
    Carbon can form different allotropes due to its tetravalency. Different forms of carbon such as carbon nanotubes (CNTs), carbon nanofibers, graphene, fullerenes, and carbon black can be used as nanofillers in order to enhance the properties of polymer nanocomposites. These carbon nanomaterials are of interest in nanocomposites research and other applications due to their excellent properties, such as high Young's Modulus, tensile strength, electrical conductivity, and specific surface area. However, there are some flaws that can be found in the carbon nanoparticles such as tendency to agglomerate, insoluble in aqueous or organic solvents or being unreactive with the polymer surface. In this study, the aim is to study functionalization in order to rectify some of these shortcomings by attaching different functional groups or particles to the surface of these carbon nanoparticles; this also enables the synthesis of high-performance polymer nanocomposites. The main findings include the effects of functionalization on carbon nanoparticles and the applications of polymer nanocomposites with carbon nanoparticles as nanofillers in the industry. Additionally, the different methods used to produce polymer composites such as in situ polymerization, solution mixing and melt blending are studied, as these methods involve the dispersion of carbon nanofillers within the polymer matrix.
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