Petroleum coke‐derived activated cokes were prepared and used for the adsorptive removal of a single‐ring naphthenic acid (NA) from synthetic oil sands process affected water (OSPW). CO2 activation produced carbon with a larger mesopore volume fraction (0.67) than steam activation (0.25). Interestingly, prolonging the activation time of CO2 from 6 to 9 h led to a simultaneous increase in specific surface area (276–405 m2/g) and mesopore volume (0.51–0.67). Furthermore, a positive relationship was found between the pseudo‐second‐order kinetic rate constant and the mesoporous volume of the activated coke. This suggests both the importance of pore size on kinetics and the fact that physical activation with a reagent such as CO2 may be better suited than chemical activation due to its ability to create mesopores. Although enlarging the pores and accelerating the adsorption rate, post‐oxidation had detrimental effects on adsorption capacity, resulting in a decrease in equilibrium adsorbed amount from 115 to 34 mg/g, a 70% decrease, when post‐oxidized with O2, due to the negative charge of oxygen‐containing functional groups. On the other hand, the measured adsorption capacity increased by over 60% when activated coke was treated with ammonia, a result of the positively charged nitrogen‐containing surface groups. Finally, in real OSPW, the activated coke had a much lower capacity for total acid‐extractable organics than for the model NA. Therefore, activated petroleum coke may not be the best choice for treating raw tailings pond water and may be better suited for polishing.
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