Anaerobic digestion of poultry manure is limited by the excessive levels of nitrogen and the high concentration of dry matter. These limitations are usually overcome either by applying procedures to remove nitrogen or by employing pretreatments that allows to solubilise organic matter. In this work, the treatment of poultry manure was enhanced by co-digestion with pig manure through the methodological determination of optimal mixtures combined together with a thermochemical pretreatment coupled to ammonia stripping. The optimum poultry-pig mixture, resulting in a 24%:76% (volume basis) poultry-pig manure, was determined by applying a methodology based on linear programming which calculates the proportions of the blend which returns the maximum methane production while keeping a stable process. Pretreatment batch experiments, consisting of increasing both temperature and pH simultaneously with ammonia stripping process was optimised for a temperature of 90 °C and a pH of 10 resulting in a nitrogen removal efficiency of 72% and a 1.2-fold higher methane production in comparison to the unpretreated mixture. Continuous anaerobic co-digestion of pretreated optimum mixture enhanced the COD removal efficiency by 37% when compared with the treatment of unpretreated feedstock (37% vs 27%, respectively). This study indicates that combining blending optimisation of substrates, thermochemical pretreatments and ammonia stripping procedures prior to anaerobic co-digestion becomes a good strategy to overtake the limitations offered by solid- and nitrogen-rich substrates, such as poultry manure.
Low oxygen levels (μgO2L(-1)) in anaerobic reactors are quite common and no relevant consequences are expected. On the contrary, higher concentrations could affect the process. This work aimed to study the influence of oxygen (4.3 and 8.8mgO2L(-1), respectively) on the different microbial activities (hydrolytic, acidogenic and methanogenic) of thermophilic anaerobic biomass and on the methanogenic community structure. Batch tests in presence of oxygen were conducted using specific substrates for each biological activity and a blank (with minimum oxygen) was included. No effect of oxygen was observed on the hydrolytic and acidogenic activities. In contrast, the methane production rate decreased by 40% in all oxygenated batches and the development of active archaeal community was slower in presence of 8.8mgO2L(-1). However, despite this sensitivity of methanogens to oxygen at saturation levels, the inhibition was reversible.
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