Among the greatest challenges to the full implementation of biological sulfate reduction are the cost and availability of the electron source. With the development of the biofuel industry, new organic substrates have become available. Therefore, this work sought to compare the performance of a sulfidogenic process utilizing either lactate or glycerol as the substrate for sulfate-reducing bacteria (SRB) growth. Although sulfate reduction is energetically more favorable with lactate, glycerol is a less expensive alternative because excess production is forecasted with the worldwide development of the biodiesel industry. Continuous experiments were performed in a fluidized bed (FB) reactor containing activated carbon as a carrier for a mixed bacterial population composed of sulfate-reducing and fermentative bacteria. During the lactate-fed phases, incomplete oxidation of lactate to acetate by SRB was the dominant metabolic pathway resulting in as much as 90 % sulfate reduction and high acetate concentrations (2.7 g L(-1)). Conversely, in the glycerol-fed phases, glycerol degradation resulted from syntrophic cooperation between sulfate-reducing and fermentative bacteria that produce butyrate along with acetate (1.0 g L(-1)) as oxidation products. To our knowledge, this is the first report of butyrate formation during sulfate reduction in a glycerol-fed continuous-flow reactor. Sulfate concentrations were reduced by about 90 % (from 2,000 to 100-300 mg L(-1)) when glycerol was being fed to the reactor. Since the FB reactor was able to stand a change from lactate to glycerol, this reactor is recommended as the preferred option should glycerol be selected as a cost-effective alternative to lactate for continuous sulfate reduction.

No abstract

The data presented in this paper are related to the research article “Ammonia recovery from food waste digestate using solar heat-assisted stripping-absorption” [1] . The raw and filtered data are associated to daily monitoring of NH 4 concentration of food waste digestate, pH of digestate and absorption solution and temperature of food waste digestate throughout experiments at different conditions. In addition, data of temperature monitoring in different points of solar-heat assisted stripping-absorption device are presented. The data could help further studies aiming to improve this system. The detailed data of these experiments could help to improve the performance and to reduce costs of nitrogen recovery from digestate using stripping-absorption technology.

It has recently come to our attention that the below point in the Acknowledgements section has been missed to include in the article 'Phosphorus recovery from liquid digestate by chemical precipitation using low-cost ion sources'

RESUMO O fosfogesso (FG) é um dos principais subprodutos da produção de ácido fosfórico para fertilizantes. Esse sólido é constituído principalmente de sulfato de cálcio di-hidratado, podendo conter também metais tóxicos e acidez residual (pH 2-3). A disposição em pilhas próximas às usinas é o principal método de disposição, entretanto isso não soluciona os problemas ambientais, uma vez que pode haver lixiviação das pilhas de resíduo pela água da chuva, contaminando o solo e os corpos d’água. Portanto, a disposição do FG é um desafio para a indústria de fertilizantes. O FG pode ser utilizado como fonte de sulfato para a produção de sulfeto em reatores anaeróbios, utilizando bactérias redutoras de sulfato (BRS). O sulfeto gerado pode ser utilizado posteriormente para a produção de enxofre elementar ou usado na precipitação de metais de transição. No presente trabalho, avaliou-se a viabilidade do uso do FG como fonte de sulfato para as BRS em um reator contínuo de leito fluidizado alimentado com glicerol p.a. como substrato, e estudou-se a influência da variável tempo de detenção hidráulica (TDH) real no processo de biorredução do sulfato. Este último foi determinado em 15 ± 2,6 e 9,7 ± 1,2 h, respectivamente, para os valores teóricos de 10 e 8 horas, a partir do uso de cloreto de lítio como traçador. Para a razão DQO/SO4 2- igual a 1,9, obteve-se remoção de sulfato de 73 ± 11 e 75 ± 12%, respectivamente, para os TDHs 15 ± 2,6 e 9,7 ± 1,2 h. As taxas de remoção específicas de sulfato foram de 0,106 ± 0,04 e 0,179 ± 0,07 gSO4 2-/gSSV.d, respectivamente, para os TDHs 15 ± 2,6 e 9,7 ± 1,2 h.