The stability of nanosized materials differs significantly from the stability of bulk materials. In this study a thermodynamic analysis on the simultaneous oxidation and re-reduction of small metallic cobalt crystallites in the presence of water and hydrogen as a function of the crystallite diameter was performed as a model for catalyst deactivation in the Fischer-Tropsch synthesis. It is shown that spherical cobalt crystallites with a diameter less than 4.4 nm are likely to be oxidized under realistic Fischer-Tropsch synthesis conditions (p(H)(2)(O)/p(H)(2) < 1.5, T = 493 K).

Supported metal particles play an important role in heterogeneous catalysis. It has been shown lately that the size of the metal crystallites in the supported metal catalysts has a profound effect on the catalytic activity, thus necessitating the need for synthesis methods aimed at a strict control of the metal crystallite size in these catalysts. The classical methods used to synthesize supported metal catalysts typically yield a wide metal crystallite size distribution, and average crystallite sizes which are difficult to control. Suitable techniques have been developed to obtain supported metal catalysts with defined crystallite size distributions, inter alia impregnation of reverse micelle microemulsions, colloid impregnation following reverse micelle precipitation or crystallization, and deposition-precipitation. Using these techniques, a series of supported Ru/γ-Al 2 O 3 , Co/SiO 2 , Fe/γ-Al 2 O 3 , Fe/C, and Au/ZnO catalysts have been prepared and characterized.

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Renewable biowaste-derived carbon dots have garnered immense interest owing to their exceptional optical, fluorescence, chemical, and environmentally friendly attributes, which have been exploited for the detection of metals, non-metals, and organics in the environment. In the present study, water-soluble fluorescent carbon dots (CDs) were synthesized via facile green microwave pyrolysis of pine-cone biomass as precursors, without any chemical additives. The synthesized fluorescent pine-cone carbon dots (PC-CDs) were spherical in shape with a bimodal particle-size distribution (average diameters of 15.2 nm and 42.1 nm) and a broad absorption band of between 280 and 350 nm, attributed to a π-π* and n-π* transition. The synthesized PC-CDs exhibited the highest fluorescent (FL) intensity at an excitation wavelength of 360 nm, with maximum emission of 430 nm. The synthesized PC-CDs were an excellent fluorescent probe for the selective detection of Cu2+ in aqueous solution, amidst the presence of other metal ions. The FL intensity of PC-CDs was exceptionally quenched in the presence of Cu2+ ions, with a low detection limit of 0.005 μg/mL; this was largely ascribed to Cu2+ ion binding interactions with the enriched surface functional groups on the PC-CDs. As-synthesized PC-CDs are an excellent, cost effective, and sensitive probe for detecting and monitoring Cu2+ metal ions in wastewater.

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A physical mixture of Macadamia-derived activated carbon and cationic attapulgite clay was investigated for total chromium removal in aqueous solution. The parameters influencing the adsorption of chromium on the sorbents were investigated, and it was shown that pH 3, contact time 2 hours, concentration 50 mg L À1 and calculated adsorption capacity of 96.28 mg g À1 were the optimal parameters. The process of adsorption was better described by Freundlich adsorption isotherm, and the kinetic modelling data suggested a chemisorption mechanism described by pseudo-second-order (PSO) rate model. Ionic strength studies demonstrated that the removal of anionic Cr(VI) species was mostly affected by the presence of anions like Cl À and NO À 3 , while the removal of the cationic Cr(III) species was affected largely by cations NH þ 4 >Na þ >K þ. Overall, the removal mechanism involved adsorption, reduction and ion exchange processes.

Three-dimensional hierarchical porous carbon prepared from microwave pyrolysis of pinecone. The carbon material aid Ag–AgBr photocatalytic attributes and enhanced the activity on removal of tetracycline.