Estudo da atividade metanogênica específica de diferentes lodos anaeróbios / Study of specific methanogenic activity of different anaerobic sludges

RESUMO O estudo da atividade metanogênica específica (AME) constitui uma importante ferramenta para o controle operacional de reatores anaeróbios, pois apresenta parâmetros de monitoramento da eficiência e estabilidade de um reator biológico. Nesse sentido, o presente trabalho visou determinar a AME de lodos provenientes de reatores anaeróbios de fluxo ascendente (UASB - upflow anaerobic slugde blanket) de duas indústrias cervejeiras (lodos A e B), uma de processamento de grãos (lodo C), uma leiteira (lodo D) e uma de processamento de couro (lodo E). Os ensaios foram conduzidos em batelada, em ambiente aclimatado a 35°C, utilizando um equipamento para monitorar a geração de biogás em função do tempo de digestão. Também foi realizada a qualificação do gás metano presente no biogás gerado pelos diferentes lodos. O maior valor de AME obtido e a maior porcentagem do gás metano produzido, para uma concentração de biomassa de 5,0 gSTV.L-1 e 4,0 gDQO.L-1 de glicose, foram para o lodo B: 0,36 gDQO-CH4.gSTV-1.d-1 e 58,9%, respectivamente.

ABSTRACT The study of Specific Methanogenic Activity (SMA) is an important tool for operational control of anaerobic reactors, as it presents parameters to monitor the efficiency and stability of a biological reactor. For this reason, the present article aimed to determine the SMA of sludges from UASB reactors, of two different brewing industries (sludges A and B), a grain processing industry (sludge C), a dairy industry (sludge D), and a leather processing industry (sludge E). Assays were performed in batch, at an acclimatized environment (35°C), using a device equipment to monitor the generation of biogas due to digestion time. Also, the quantity of methane gas was measured in the biogas generated by the different sludges. The best SMA value obtained and the greater percentage of methane gas generated, with a biomass concentration of 5.0 gSTV.L-1, and a glucose concentration of 4.0 gCOD.L-1, were for sludge B, with 0.36 gCOD-CH4.gSTV-1.d-1 and 58.9%, respectively.

Production of rhamnolipids in solid-state cultivation: Characterization, downstream processing and application in the cleaning of contaminated soils.

Pseudomonas aeruginosa UFPEDA 614 produced a rhamnolipid biosurfactant when grown on sugarcane bagasse impregnated with a solution containing glycerol. Biosurfactant levels reached 40 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of liquid used, the biosurfactant levels were similar to those obtained in submerged liquid culture of a medium identical to the impregnating solution. The properties of the biosurfactant were very similar to those obtained with rhamnolipids produced in submerged culture, with a critical micelle concentration of 46.8 mg/L and an emulsification index at 24 h of over 90% against gasoline. The surface properties were maintained after autoclaving of the fermented solids, meaning that it is possible to minimize safety risks by killing the producing organism with a heat treatment of the solids prior to product extraction. The biosurfactant was used in the washing of soils contaminated with gasoline. An aqueous biosurfactant solution was 3.2-fold more efficient than water in leaching organic material from the soil, demonstrating the viability of application of rhamnolipids in the bioremediation of soils contaminated with gasoline.

Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture.

In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this problem. In the current work, we optimized the production of a rhamnolipid biosurfactant by Pseudomonas aeruginosa UFPEDA 614, grown on a solid medium impregnated with a solution containing glycerol. During the study, we increased the production of the biosurfactant over tenfold, with levels reaching 172 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of impregnating solution added to the solid support, this yield is of the order of 46 g/L, which is comparable with the best results that have been obtained to date in submerged liquid cultivation. Our results suggest that there is a great potential for using solid-state cultivation for the production of rhamnolipids.