Hospital wastewater contains high concentrations of pharmaceuticals, which pose risks to receiving waters. In this study, a pilot plant consisting of six moving bed biofilm reactors (MBBRs) in series (with the intention to integrate Biological Oxygen Demand (BOD) removal, nitrification and denitrification as well as prepolishing Chemical Oxygen Demand (COD) for ozonation) was built to integrate pharmaceutical removal and intermittent feeding of the latter reactors aimed for micropollutant removal. Based on the experimental resultss, nitrifying MBBRs achieved higher removal as compared to denitrifying MBBRs except for azithromycin, clarithromycin, diatrizoic acid, propranolol and trimethoprim. In the batch experiments, nitrifying MBBRs showed the ability to remove most of the analysed pharmaceuticals, with degradation rate constants ranging from 5.0 × 10 h to 2.6 h. In general, the highest degradation rate constants were observed in the nitrifying MBBRs while the latter MBBRs showed lower degradation rate constant. However, when the degradation rate constants were normalised to the respective biomass, the intermittently fed reactors presented the highest specific activity. Out of the 22 compounds studied, 17 compounds were removed with more than 20%.

Previous studies have demonstrated that aerobic moving bed biofilm reactors (MBBRs) remove pharmaceuticals better than activated sludge. Thus we used a MBBR system to polish the effluent of an activated sludge wastewater treatment plant. To overcome that effluent contains insufficient organic matter to sustain enough biomass, the biofilm was intermittently fed with raw wastewater. The capacity of pharmaceutical degradation was investigated by spiking pharmaceuticals. Actual removal during treatment was assessed by sampling the inlets and outlets of reactors. The removal of the majority of pharmaceuticals was enhanced through the intermittent feeding of the MBBR. First-order rate constants for pharmaceutical removal, normalised to biomass, were significantly higher compared to other studies on activated sludge and suspended biofilms, especially for diclofenac, metoprolol and atenolol. Due to the intermittently feeding, degradation of diclofenac occurred with a half-life of only 2.1h and was thus much faster than any hitherto described wastewater bioreactor treatment.

Wastewater from wet lime(stone)-gypsum flue gas desulphurisation (FGD) processes in coal-fired power plants contains nitrate. Where case selective catalytic reduction (SCR) of NOx is applied the wastewater can also contain ammonia. For the removal of both nitrate and ammonia, biological processes are an attractive option. A bottle-neck for application of biological processes might be the high chloride concentration and relatively high temperature of the wastewater. Therefore research work was performed in fluid-bed reactors at pilot-plant scale for both biological nitrification and denitrification. Biological nitrification was studied up to 34 gCl−/l and nitrite was the main product formed. Biological denitrification was effective up to at least 45 gCl−/l. Both nitrate and nitrite were removed effectively.

Further biological polishing of micropollutants in WWTP effluents is limited by the lack of available carbon for cometabolic degradation. Metabolism of polyhydroxyalkanoates (PHAs) stored intracellularly during enhanced biological phosphorus removal (EBPR) could serve as carbon source for post-denitrification and micropollutant cometabolism. The removal of nine micropollutants (i.e., pharmaceuticals and corrosion inhibitors) was investigated by using Moving Bed Biofilm Reactors (MBBRs), selecting phosphorus (PAO) or glycogen (GAO) accumulating organisms under different redox conditions. Three laboratory-scale MBBRs were operated in sequencing-batch mode under cyclical anaerobic and aerobic/anoxic conditions for phosphorus removal. Batch experiments were performed to evaluate the biodegradation potential of micropollutants along with the utilization of internally stored PHA. Experiments showed that aerobic PAO were able to efficiently remove most of the targeted micropollutants. The removal of benzotriazole, 5-methyl-1H-benzotriazole, carbamazepine, ketoprofen and diclofenac occurred simultaneously to phosphorus uptake and terminated when phosphorus was no longer available. Denitrifying PAO and aerobic GAO exhibited lower removal of micropollutants than aerobic PAO. Degradation profiles of stored PHA suggested a diverse utilization of the different fractions of PHA for phosphorus and micropollutant removal, with PHV (poly 3-hydroxyvalerate) most likely used for the cometabolism of targeted micropollutants.

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