Chin Hua Chia

Citric acid modified kenaf core fibres for removal of methylene blue from aqueous solution.

Chemically modified kenaf core fibres were prepared via esterification in the presence of citric acid (CA). The adsorption kinetics and isotherm studies were carried out under different conditions to examine the adsorption efficiency of CA-treated kenaf core fibres towards methylene blue (MB). The adsorption capacity of the kenaf core fibres increased significantly after the citric acid treatment. The values of the correlation coefficients indicated that the Langmuir isotherm fitted the experimental data better than the Freundlich isotherm. The maximum adsorption capacity of the CA-treated kenaf core fibres was found to be 131.6mg/g at 60°C. Kinetic models, pseudo-first-order, pseudo-second-order and intraparticle diffusion, were employed to describe the adsorption mechanism. The kinetic data were found to fit pseudo-second-order model equation as compared to pseudo-first-order model. The adsorption of MB onto the CA-treated kenaf core fibres was spontaneous and endothermic.

Cationic and anionic modifications of oil palm empty fruit bunch fibers for the removal of dyes from aqueous solutions

Oil palm empty fruit bunch (EFB) fibers were employed to remove dyes from aqueous solutions via adsorption approaches. The EFB fibers were modified using citric acid (CA) and polyethylenimine (PEI) to produce anionic and cationic adsorbents, respectively. The CA modified EFB fibers (CA-EFB) and PEI-modified EFB fibers (PEI-EFB) were used to study the efficiency in removing cationic methylene blue (MB) and anionic phenol red (PR) from aqueous solutions, respectively, at different pHs, temperatures and initial dye concentrations. The adsorption data for MB on the CA-EFB fitted the Langmuir isotherm, while the adsorption of PR on the PEI-EFB fitted the Freundlich isotherm, suggesting a monolayer and heterogeneous adsorption behavior of the adsorption processes, respectively. Both modified fibers can be regenerated up to seven adsorption/desorption cycles while still providing as least 70% of the initial adsorption capacity.

Antibacterial performance of Ag nanoparticles and AgGO nanocomposites prepared via rapid microwave-assisted synthesis method

Silver nanoparticles and silver-graphene oxide nanocomposites were fabricated using a rapid and green microwave irradiation synthesis method. Silver nanoparticles with narrow size distribution were formed under microwave irradiation for both samples. The silver nanoparticles were distributed randomly on the surface of graphene oxide. The Fourier transform infrared and thermogravimetry analysis results showed that the graphene oxide for the AgNP-graphene oxide (AgGO) sample was partially reduced during the in situ synthesis of silver nanoparticles. Both silver nanoparticles and AgGO nanocomposites exhibited stronger antibacterial properties against Gram-negative bacteria (Salmonella typhi and Escherichia coli) than against Gram-positive bacteria (Staphyloccocus aureus and Staphyloccocus epidermidis). The AgGO nanocomposites consisting of approximately 40 wt.% silver can achieve antibacterial performance comparable to that of neat silver nanoparticles.

Direct production of biodiesel from high-acid value Jatropha oil with solid acid catalyst derived from lignin

BackgroundSolid acid catalyst was prepared from Kraft lignin by chemical activation with phosphoric acid, pyrolysis and sulfuric acid. This catalyst had high acid density as characterized by scanning electron microscope (SEM), energy-dispersive x-ray spectrometry (EDX) and Brunauer, Emmett, and Teller (BET) method analyses. It was further used to catalyze the esterification of oleic acid and one-step conversion of non-pretreated Jatropha oil to biodiesel. The effects of catalyst loading, reaction temperature and oil-to-methanol molar ratio, on the catalytic activity of the esterification were investigated.ResultsThe highest catalytic activity was achieved with a 96.1% esterification rate, and the catalyst can be reused three times with little deactivation under optimized conditions. Biodiesel production from Jatropha oil was studied under such conditions. It was found that 96.3% biodiesel yield from non-pretreated Jatropha oil with high-acid value (12.7 mg KOH/g) could be achieved.ConclusionsThe catalyst can be easily separated for reuse. This single-step process could be a potential route for biodiesel production from high-acid value oil by simplifying the procedure and reducing costs.

Exceedingly biocompatible and thin-layered reduced graphene oxide nanosheets using an eco-friendly mushroom extract strategy

Purpose A simple, one-pot strategy was used to synthesize reduced graphene oxide (RGO) nanosheets by utilizing an easily available over-the-counter medicinal and edible mushroom, Ganoderma lucidum. Methods The mushroom was boiled in hot water to liberate the polysaccharides, the extract of which was then used directly for the reduction of graphene oxide. The abundance of polysaccharides present in the mushroom serves as a good reducing agent. The proposed strategy evades the use of harmful and expensive chemicals and avoids the typical tedious reaction methods. Results More importantly, the mushroom extract can be easily separated from the product without generating any residual byproducts and can be reused at least three times with good conversion efficiency (75%). It was readily dispersible in water without the need of ultrasonication or any surfactants; whereas 5 minutes of ultrasonication with various solvents produced RGO which was stable for the tested period of 1 year. Based on electrochemical measurements, the followed method did not jeopardize RGO’s electrical conductivity. Moreover, the obtained RGO was highly biocompatible to not only colon (HT-29) and brain (U87MG) cancer cells, but was also viable towards normal cells (MRC-5). Conclusion Besides being eco-friendly, this mushroom based approach is easily scalable and demonstrates remarkable RGO stability and biocompatibility, even without any form of functionalization.

Facile hydrothermal preparation of titanium dioxide decorated reduced graphene oxide nanocomposite

A simple single-stage approach, based on the hydrothermal technique, has been introduced to synthesize reduced graphene oxide/titanium dioxide nanocomposites. The titanium dioxide nanoparticles are formed at the same time as the graphene oxide is reduced to graphene. The triethanolamine used in the process has two roles. It acts as a reducing agent for the graphene oxide as well as a capping agent, allowing the formation of titanium dioxide nanoparticles with a narrow size distribution (~20 nm). Transmission electron micrographs show that the nanoparticles are uniformly distributed on the reduced graphene oxide nanosheet. Thermogravimetric analysis shows the nanocomposites have an enhanced thermal stability over the original components. The potential applications for this technology were demonstrated by the use of a reduced graphene oxide/titanium dioxide nanocomposite-modified glassy carbon electrode, which enhanced the electrochemical performance compared to a conventional glassy carbon electrode when interacting with mercury(II) ions in potassium chloride electrolyte.

A REVIEW OF METAL OXIDE COMPOSITE ELECTRODE MATERIALS FOR ELECTROCHEMICAL CAPACITORS

With the emerging technology in the 21st century, which requires higher electrochemical performances, metal oxide composite electrodes in particular offer complementary properties of individual materials via the incorporation of both physical and chemical charge storage mechanism together in a single electrode. Numerous works reviewed herein have identified a wide variety of attractive metal oxide-based composite electrode material for symmetric and asymmetric electrochemical capacitors. The focus of the review is the detailed literature data and discussion regarding the electrochemical performance of various metal oxide composite electrodes fabricated from different configurations including binary and ternary composites. Additionally, projection of future development in hybrid capacitor coupling lithium metal oxides and carbonaceous materials are found to obtain significantly higher energy storage than currently available commercial electrochemical capacitors. This review describes the novel concept of l...

Cellulose nanofibrils: a rapid adsorbent for the removal of methylene blue

Cellulose nanofibrils (CNF) were prepared from kenaf core (KC) using acidified-chlorite bleaching method and followed by disintegration using a high speed blender. The effects of disintegration time and acid treatment on the defibrillation of holocellulose were studied. Hemicellulose was found to facilitate defibrillation, as CNF without any acid treatment was fully defibrillated after 30 min. The adsorption kinetics of CNF toward cationic dye cannot be accurately determined due to its quick adsorption performance, in which the equilibrium is achieved immediately after 1 min of contact time. The effects of acid treatment on holocellulose, pH, adsorbent dosage, temperature and dye concentration were studied and optimized. Adsorption data were fitted to both Langmuir and Freundlich models where the Langmuir model was found to be the better model to describe the adsorption process. The maximum adsorption capacity was found to be 122.2 mg g−1 at pH 9, 20 °C for the non-acid treated CNF. The CNF can be regenerated by desorption at low pH where as much as 70% of the dye adsorbed can be desorbed after 6 cycles of adsorption–desorption.

Bifunctional graphene oxide–cellulose nanofibril aerogel loaded with Fe(III) for the removal of cationic dye via simultaneous adsorption and Fenton oxidation

A highly porous cellulose nanofibril (CNF) aerogel loaded with graphene oxide–iron(III) (GO–Fe) nanocomposites was produced and used for the treatment of methylene blue (MB) in aqueous solution. The CNF aerogel serves as an adsorbent for the dye, while the GO–Fe nanocomposites play a role in the decomposition of the dye via the Fenton oxidation reaction. The aerogel exhibits rapid adsorption performance (less than 10 min) for removing MB, with a maximum adsorption capacity of 142.3 mg g−1. On the side of enhancing the MB removal, the GO in the GO–CNF nanocomposite aerogel was loaded with 1 wt% of Fe(III) to perform as a catalyst for the Fenton oxidation reaction. The MB continues to decolorize by 30.4% more after 24 h of the reaction process. Moreover, by performing Fenton oxidation for adsorbent regeneration, the adsorption capacity for nanocomposite adsorption was reduced by 52.2% after five cycles of adsorption–oxidation.

High yield production of sugars from deproteinated palm kernel cake under microwave irradiation via dilute sulfuric acid hydrolysis

Recent years, great interest has been devoted to the conversion of biomass-derived carbohydrate into sugars, such as glucose, mannose and fructose. These are important versatile intermediate products that are easily processed into high value-added biofuels. In this work, microwave-assisted dilute sulfuric acid hydrolysis of deproteinated palm kernel cake (DPKC) was systematically studied using Response Surface Methodology. The highest mannose yield (92.11%) was achieved at the optimized condition of 148°C, 0.75N H2SO4, 10min 31s and substrate to solvent (SS) ratio (w/v) of 1:49.69. Besides that, total fermentable sugars yield (77.11%), was obtained at 170°C, 0.181N H2SO4, 6min 6s and SS ratio (w/v) of 1:40. Ridge analysis was employed to further verify the optimum conditions. Thus, this work provides fundamental data of the practical use of DPKC as low cost, high yield and environmental-friendly material for the production of mannose and other sugars.