7 research outputs found
Simple room-temperature preparation of high-yield large-area graphene oxide
Graphene has attracted much attention from researchers due to its interesting mechanical, electrochemical, and electronic properties. It has many potential applications such as polymer filler, sensor, energy conversion, and energy storage devices. Graphene-based nanocomposites are under an intense spotlight amongst researchers. A large amount of graphene is required for preparation of such samples. Lately, graphene-based materials have been the target for fundamental life science investigations. Despite graphene being a much sought-after raw material, the drawbacks in the preparation of graphene are that it is a challenge amongst researchers to produce this material in a scalable quantity and that there is a concern about its safety. Thus, a simple and efficient method for the preparation of graphene oxide (GO) is greatly desired to address these problems. In this work, one-pot chemical oxidation of graphite was carried out at room temperature for the preparation of large-area GO with ~100% conversion. This high-conversion preparation of large-area GO was achieved using a simplified Hummer’s method from large graphite flakes (an average flake size of 500 μm). It was found that a high degree of oxidation of graphite could be realized by stirring graphite in a mixture of acids and potassium permanganate, resulting in GO with large lateral dimension and area, which could reach up to 120 μm and ~8000 μm2, respectively. The simplified Hummer’s method provides a facile approach for the preparation of large-area GO
Life Cycle Assessment Studies of Jatropha (Jatropha curcas) Biodiesel Production Processed by In-situ Transesterification Method
In situ transesterification is a biodiesel production method that utilizes the original lipid-bearing agricultural products instead of purified oil as the source of triglycerides for direct transesterification. This method will eliminate the costly extraction process and reduce the long production system associated with pre-extracted oil and maximize alkyl ester yield. In this paper the production of fatty acid methyl ester (FAME) by direct in situ alkaline-catalyzed transesterification of the triglycerides (TG) in jatropha seeds was investigated and its environmental performance was compared with the conventional alkali catalyzed transesterification process using LCA as a tool. In-situ transesterification process is technically offers the advantages of the production of non-toxic jatropha seed cakes. The seed cakes after in-situ transesterification is rich in protein and is a potential source of livestock feed. However, it still generates significantly higher environmental load since in-situ transestrification needs large amount of methanol and longer duration of process. A large amount of energy will be required in methanol recovery unit
Autothermal reforming of palm empty fruit bunch bio-oil: thermodynamic modelling
This work focuses on thermodynamic analysis of the autothermal reforming of palm empty fruit bunch (PEFB) bio-oil for the production of hydrogen and syngas. PEFB bio-oil composition was simulated using bio-oil surrogates generated from a mixture of acetic acid, phenol, levoglucosan, palmitic acid and furfural. A sensitivity analysis revealed that the hydrogen and syngas yields were not sensitive to actual bio-oil composition, but were determined by a good match of molar elemental composition between real bio-oil and surrogate mixture. The maximum hydrogen yield obtained under constant reaction enthalpy and pressure was about 12 wt% at S/C = 1 and increased to about 18 wt% at S/C = 4; both yields occurring at equivalence ratio Φ of 0.31. The possibility of generating syngas with varying H2 and CO content using autothermal reforming was analysed and application of this process to fuel cells and Fischer-Tropsch synthesis is discussed. Using a novel simple modelling methodology, reaction mechanisms were proposed which were able to account for equilibrium product distribution. It was evident that different combinations of reactions could be used to obtain the same equilibrium product concentrations. One proposed reaction mechanism, referred to as the ‘partial oxidation based mechanism’ involved the partial oxidation reaction of the bio-oil to produce hydrogen, with the extent of steam reforming and water gas shift reactions varying depending on the amount of oxygen used. Another proposed mechanism, referred to as the ‘complete oxidation based mechanism’ was represented by thermal decomposition of about 30% of bio-oil and hydrogen production obtained by decomposition, steam reforming, water gas shift and carbon gasification reactions. The importance of these mechanisms in assisting in the eventual choice of catalyst to be used in a real ATR of PEFB bio-oil process was discussed
The effect of impregnation of activated carbon with SnCl2.2H2O on its porosity, surface composition and CO gas adsorption
Activated carbon was impregnated with different concentrations of SnCl .2H O. Unimpregnated and impregnated 2 2
activated carbons were analysed by means of physical adsorption and XPS and were tested for CO gas adsorption in a PSA
system. The adsorption isotherms of N at 77 K were measured and showed a Type I isotherm indicating microporous 2
carbon for all the samples. The surface area, pore volume and pore size distribution were reduced with impregnation. XPS
analysis showed an increase in the intensity of Sn3d peak with impregnation. The impregnated activated carbon showed a
very good adsorption ability of CO gas compared to the unimpregnated sample. The adsorptive species responsible for CO
gas adsorption was confirmed to be SnO instead of SnO due to the former’s comparative thermodynamic stability. 2
2002 Elsevier Science Ltd. All rights reserved