BACKGROUND: In this work, a comprehensive study of the respirometric and physical-chemical methods has been performed to evaluate the information provided by these two methodologies in order to assess the biodegradable organic matter fractions of wastewater.
The anaerobic treatment of sulphate-rich wastewater causes sulphate reducing bacteria (SRB) and methanogenic archaea (MA) to compete for the available substrate. The outcome is lower methane yield coefficient and, therefore, a reduction in the energy recovery potential of the anaerobic treatment. Moreover, in order to assess the overall chemical oxygen demand (COD) balance, it is necessary to determine how much dissolved CH(4) is lost in the effluent. The aim of this study is to develop a detailed and reliable method for assessing the COD mass balance and, thereby, to establish a more precise methane yield coefficient for anaerobic systems treating sulphate-rich wastewaters. A submerged anaerobic membrane bioreactor (SAMBR) treating sulphate-rich municipal wastewater was operated at 33 °C for an experimental period of 90 d, resulting in a high COD removal (approximately 84%) with a methane-enriched biogas of 54 ± 15% v/v. The novelty of the proposed methodology is to take into account the sulphide oxidation during COD determination, the COD removed only by MA and the dissolved CH(4) lost with the effluent. The obtained biomethanation yield (333 L CH(4) kg(-1) COD(REM MA)) is close to the theoretical value, which confirms the reliability of the proposed method.
A generalized low-order model of the biofilm in a microbial fuel cell (MFC), suitable for use in real-time engineering applications, is presented. It is based on the description of the charge transfer, diffusion process, and charge accumulation in the biofilm. Since the dynamic processes in an MFC are ruled mainly by the biofilm, it can be used for many different diffusion-based MFC types by just changing the boundary conditions. Different mode operations like batch, fed-batch, continuous, etc., are also possible. The time-responses of voltage, substrate concentration on the surface of the electrode, and Faradaic and capacitive currents have been tested under several experimental conditions.
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