Investigation of aerobic and anaerobic ammonium-oxidising bacteria presence in a small full-scale wastewater treatment system comprised by UASB reactor and three polishing ponds.

This work applied PCR amplification method and Fluorescence in situ hybridisation (FISH) with primers and probes specific for the anammox organisms and aerobic ammonia-oxidising beta-Proteobacteria in order to detect these groups in different samples from a wastewater treatment system comprised by UASB reactor and three polishing (maturation) ponds in series. Seven primer pairs were used in order to detect Anammox bacteria. Positive results were obtained with three of them, suggesting that Anammox could be present in polishing pond sediments. However, Anammox bacteria were not detected by FISH, indicating that they were not present in sediment samples, or they could be present but below FISH detection limit. Aerobic ammonia- and nitrite-oxidising bacteria were verified in water column samples through Most Probable Number (MPN) analysis, but they were not detected in sediment samples by FISH. Ammonia removal efficiencies occurred systematically along the ponds (24, 32, and 34% for polishing pond 1, 2, and 3, respectively) but the major reaction responsible for this removal is still unclear. Some nitrification might have occurred in water samples because some nitrifying bacteria were present. Also Anammox reaction might have occurred because Anammox genes were detected in the sediments, but probably this reaction was too low to be noticed. It is important also to consider that some of the ammonia removal observed might be related to NH(3) stripping, associated with the pH increase resulting from the intensive photosynthetic activity in the ponds (mechanism under investigation). Therefore, it can be concluded that more than one mechanism (or reaction) might be involved in the ammonia removal in the polishing ponds investigated in this study.

Characterisation of pathogenic bacteria in a UASB-polishing pond system using molecular techniques.

Molecular techniques have been commonly used to detect and quantify pathogenic bacteria in food, clinical and environmental samples, but in wastewater treatment plants few studies have been carried out. This work applied PCR with a specific set of primers to investigate pathogenic bacteria in a wastewater plant comprised of a UASB reactor followed by polishing ponds. In addition, in-situ hybridisation technique (FISH) was used to estimate the abundance of Escherichia coli in the system. According to the PCR results it was observed that Escherichia coli and Salmonella enterica subsp. enterica were not completely removed in the system, since they were detected either in the raw sewage or UASB and pond effluents. Shigella dysenteriae and Enterococcus spp. were detected in raw sewage and UASB, but not in the pond effluent. In contrast Staphylococcus aureus and Helicobacter pylori were not detected in any samples. The quantification of E. coli using FISH revealed values in the range of 10(7) cells/100 mL for raw sewage and 10(6) cells/100 mL for pond effluent, slightly higher than values obtained by traditional techniques. Finally the results show the applicability of PCR method for monitoring pathogenic bacteria in wastewater systems; however, more samples need to be analysed in order to certify the applicability of FISH to estimate pathogenic bacteria in WWT effluents.

Thermal hygienization of excess anaerobic sludge: a possible self-sustained application of biogas produced in UASB reactors.

The main current trends in final disposal of sludge from Wastewater Treatment Plants (WTP) include: safe use of nutrients and organic matter in agriculture, sludge disinfection and restricted use in landfill. As to sludge hygienization, helminth eggs have been used as a major parameter to determine the effectiveness of such process, and its inactivation can be reached by means of thermal treatment, under varying temperature and other conditions. In such context, the objective of this research was to determine how effectively biogas produced in UASB reactors could be used as a source of calorific energy for the thermal hygienization of excess anaerobic sludge, with Ascaris lumbricoides eggs being used as indicator microorganisms, and whether the system can operate on a self-sustained basis. The experiments were conducted in a pilot-scale plant comprising one UASB reactor, two biogas holders and one thermal reactor. The investigation proved to be of extreme importance to developing countries, since it leads to a simplified and fully self-sustainable solution for sludge hygienization, while making it possible to reuse such material for agricultural purposes. It should be also noted that using biogas from UASB reactors is more than sufficient to accomplish the thermal hygienization of all excess sludge produced by this system, when used for treating domestic sewage.

Inactivation of E. coli and helminth eggs in aerobic and anaerobic effluents using UV radiation.

This paper evaluates the performance of a simplified bench-scale UV-photoreactor used to inactivate Escherchia coli and eggs of Ascaris lumbricoides. The photoreactor consisted of a tubular unit constructed with PVC tube, 100 mm diameter and 45 cm total height, with a low-pressure mercury lamp adapted in the centre of the tube. The reactor was tested to disinfect the effluent from a trickling filter and from an UASB reactor, both fed with domestic sewage. The results showed an excellent performance of the photoreactor, with very high E. coli inactivation efficiencies being observed for the aerobic effluent (in the range of 4 to 5 log-units, for doses varying from 50.7 to 13.6 mW x s x cm(-2)) and also for the effluent from the UASB reactor (usually above 4 log-units, for doses of 20.3 and 13.6 mW x s x cm(-2)). In relation to the inactivation of helminth eggs, it was observed that UV radiation significantly affected the development of eggs of Ascaris lumbricoides, with the better results being obtained for radiation times of 40 and 60 seconds (doses of 13.6 and 20.3 mW x s x cm(-2), respectively), when approximately 65% of the eggs remained in the stage of single cell and only 9 to 10% were able to fully develop to the stage of motile larva.