After biological treatment, coke wastewater contains small amounts of phenolic compounds resistant to such treatment. The removal of phenols and COD from coke wastewater subjected to biological treatment was studied. The adsorbents used were granular activated carbon and the resins XAD-2, AP-246 and OC-1074. Equilibrium, kinetics and column assays were carried out, fitting the equilibrium data to Langmuir and Freundlich models and the kinetic data to the Lagergren equation. The best results were obtained with GAC, which presented higher adsorption capacities. In the equilibrium assays, the adsorption capacities (Q) found were 1.48 mg g −1 for GAC versus 0.07 and 0.04 mg g −1 for resins AP-246 and OC-1074, respectively. In the kinetic assays, the values of the Lagergren adsorption parameter, q e , were 1.69, 0.15 and 0.14 mg g −1 for GAC, AP-246 and OC-1074, respectively. In the column assays, the dynamic capacity of GAC for up to 480 bed volumes was 1.82 mg mL −1 . No saturation was obtained for this volume due to the asymptotic shape of the breakthrough curve, whereas for the same percolated volume, the resins AP-246 and OC-1074 were saturated. These two resins presented similar saturation capacities of around 1.1 mg mL −1 .

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The upgrading of diluted methane emissions into valuable products can be accomplished at low temperatures (200 °C) by the direct partial oxidation of methanol over copper-exchanged zeolite catalysts. The reaction has been studied in a continuous fixed-bed reactor loaded with a Cu–mordenite catalyst, according to a three-step cyclic process: adsorption of methane, desorption of methanol, and reactivation of the catalyst. The purpose of the work is the use of methane emissions as feedstocks, which is challenging due to their low methane concentration and the presence of oxygen. Methane concentration had a marked influence on methane adsorption and methanol production (decreased from 164 μmol/g Cu for pure methane to 19 μmol/g Cu for 5% methane). The presence of oxygen, even in low concentrations (2.5%), reduced methane adsorption drastically. However, methanol production was only affected slightly (average decrease of 9%), concluding that methane adsorbed on the active centers yielding methanol is not influenced by oxygen.