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Anthracene oil has been used as raw material for the production of carbon precursors via conventional and microwave technologies. Cokes with comparable characteristics have been obtained, suggesting that their structural order is primarily reliant on the precursor rather the heating method. However, microwave route is a more energy efficient process, achieving electricity savings of up to 60%. Furthermore, graphites produced from microwave-derived precursors show an excellent graphitization degree, which makes them appropriate starting resources for the synthesis of graphene-like materials with similar characteristics to those obtained from conventional means. Therefore, microwave-assisted heating approach appears to be a suitable and energy saving alternative for the production of carbon precursors.

Gold nanoparticles (AuNPs) were homogeneously electrodeposited on nitrogen-doped reduced graphene oxide (N-rGO) to modify a glassy carbon electrode (GCE/N-rGO-Au) in order to improve the simultaneous detection of dopamine (DA), ascorbic acid (AA), and uric acid (UA). N-rGO was prepared by the hydrothermal treatment of graphene oxide (GO) and urea at 180 °C for 12 h. AuNPs were subsequently electrodeposited onto the surface of GCE/N-rGO using 1 mM HAuCl4 solution. The morphology and chemical composition of the synthesized materials were characterized by field-emission scanning electron microscopy and X-ray photoelectron spectroscopy. The electrochemical performance of the modified electrodes was investigated through cyclic voltammetry and differential pulse voltammetry measurements. Compared to GCE/rGO-Au, GCE/N-rGO-Au exhibited better electrochemical performance towards the simultaneous detection of the three analytes due to the more homogeneous distribution of the metallic nanoparticles as a result of more efficient anchoring on the N-doped areas of the graphene structure. The GCE/N-rGO-Au-based sensor operated in a wide linear range of DA (3–100 µM), AA (550–1500 µM), and UA (20–1000 µM) concentrations with a detection limit of 2.4, 58, and 8.7 µM, respectively, and exhibited satisfactory peak potential separation values of 0.34 V (AA-DA), 0.20 V, (DA-UA) and 0.54 V (AA-UA). Remarkably, GCE/N-rGO-Au showed a very low detection limit of 385 nM towards DA, not being susceptible to interference, and maintained 90% of its initial electrochemical signal after one month, indicating an excellent long-term stability.

This work describes a novel route for the preparation of pitches by oxidative polymerization of an industrial anthracene oil (AO) in a microwave semi-pilot equipment consisting in a multi-mode applicator having a 2.45 GHz magnetron with variable microwave power. The experimental five variables of microwave heating of AO air-blowing range between 320 and 380 °C (temperature), 0.2–3.9 °C min−1 (heating rate), 1.5–5 h (soaking time), 16–20.5% (air/AO ratio) and 200–1500 g (initial weight). Their effect on the overall microwave air-blowing process is evaluated by means of a statistical analysis. A detailed characterization of the pitches has been carried out in terms of ultimate analysis, softening point, solubility parameters (toluene insolubles (TI) and quinoline insolubles (QI)) and thermogravimetric analysis. The experiments were also carried out by using conventional heating for comparative purposes. The detailed study of the electric energy consumption of the overall microwave treatment allows estimating a significant electric energy saving of about 20% when compared to conventional heating thus representing an excellent result in the production of carbon precursors.

Tyre wastes and their blends with coal and a bituminous waste material obtained from the benzol distillation column of a by-product section of a coking plant were employed as a precursor for the production of activated carbons (ACs). Pyrolysis up to 850 °C followed by physical activation with CO2 produced mesoporous carbons with different pore size distributions and surface areas. The surface chemistry of the samples was studied by measuring the point of zero charge (pHpzc) and by temperature programmed desorption (TPD). The activated carbons obtained contained higher amounts of basic functional groups. Their textural and surface chemistry characteristics make them highly suitable for adsorbing anionic dyes of large molecular size, such as Congo red. The adsorption kinetics was found to conform closely to the pseudo-second-order kinetic model. To determine the adsorption mechanism, the kinetic data were also analyzed using the Weber and Morris intraparticle diffusion model and the Boyd model to distinguish between the pore and film diffusion steps. The equilibrium isotherms were of the Langmuir isotherm type. The efficiency of the low-cost ACs prepared for the removal of Congo red dye was similar to that reported in the literature for coal-based ACs and greater than that of other low-cost ACs.