The present study was aimed at the development of a strategy for removing and degrading perfluorohexanoic acid (PFHxA) from industrial process waters at concentrations in the range 60-200 mg L-1. The treatment train consisted of nanofiltration (NF) separation followed by electrochemical degradation of the NF concentrate. Using a laboratory-scale system and working in the total recirculation mode, the DowFilm NF270 membrane provided PFHxA rejections that varied in the range 96.6-99.4% as the operating pressure was increased from 2.5 to 20 bar. The NF operation in concentration mode enabled a volume reduction factor of 5 and increased the PFHxA concentration in the retentate to 870 mg L-1. Results showed that the increase in PFHxA concentration and the presence of calcium sulfate salts did not induce irreversible membrane fouling. The NF retentate was treated in a commercial undivided electrochemical cell provided with two parallel flow-by compartments separated by bipolar boron doped diamond (BDD) electrode, BDD counter anode, and counter cathode. Current densities ranging from 20 to 100 A m-2 were examined. The electrochemical degradation rate of PFHxA reached 98% and was accompanied by its efficient mineralization, as the reduction of total organic carbon was higher than 95%. Energy consumption, which was 15.2 kWh m-3 of treated NF concentrate, was minimized by selecting operation at 50 A m-2. While most of the previous research on the treatment of perfluoroalkyl substances (PFASs) focused on the removal of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS), these compounds have been phased out by chemical manufacturers. Our findings are relevant for the treatment of PFHxA, which appears to be one of the present alternatives to long-chain PFASs thanks to its lower bioaccumulative potential than PFOA and PFOS. However, PFHxA also behaves as a persistent pollutant. Moreover, our results highlight the potential of combining membrane separation and electrochemical oxidation for the efficient treatment of PFAS-impacted waters.

The recovery of energy and valuable compounds from exhaust gases in the iron and steel industry deserves special attention due to the large power consumption and CO₂ emissions of the sector. In this sense, the hydrogen content of coke oven gas (COG) has positioned it as a promising source toward a hydrogen-based economy which could lead to economic and environmental benefits in the iron and steel industry. COG is presently used for heating purposes in coke batteries or furnaces, while in high production rate periods, surplus COG is burnt in flares and discharged into the atmosphere. Thus, the recovery of the valuable compounds of surplus COG, with a special focus on hydrogen, will increase the efficiency in the iron and steel industry compared to the conventional thermal use of COG. Different routes have been explored for the recovery of hydrogen from COG so far: i) separation/purification processes with pressure swing adsorption or membrane technology, ii) conversion routes that provide additional hydrogen from the chemical transformation of the methane contained in COG, and iii) direct use of COG as fuel for internal combustion engines or gas turbines with the aim of power generation. In this study, the strengths and bottlenecks of the main hydrogen recovery routes from COG are reviewed and discussed.