Simultaneous nitrate and sulfide removal using a bio-electrochemical system.

This study addresses the applicability of simultaneous nitrate and sulfide removal using two-chamber bio-electrochemical systems (BES). The anode and cathode chambers of a BES were fed with the effluent of a sulfate reducing reactor and a nitrate-rich groundwater as an electron donor and acceptor sources, respectively. BES has been found to be effective for simultaneous removal of sulfide and nitrate coming from different sources and without mixing them. As a result, 10 gS/m3/d of sulfide oxidation and 7.26 gN/m3/d of nitrate reduction rates were achieved. The number of electrons used for denitrification was more than that of delivered from the anode, especially when the anode chamber was fed with the SRR effluent and operated at pH 7-7.5. It was supposed that H2S was used for denitrification in the cathode by passing through the membrane. Another reason for this might be the electrons released from the corroding steel mesh current collector.

Performance of polydimethylsiloxane membrane contactor process for selective hydrogen sulfide removal from biogas.

H2S in biogas affects the co-generation performance adversely by corroding some critical components within the engine and it has to be removed in order to improve the biogas quality. This work presents the use of polydimethylsiloxane (PDMS) membrane contactor for selective removal of H2S from the biogas. Experiments were carried out to evaluate the effects of different pH of absorption liquid, biogas flowrate and temperature on the absorption performances. The results revealed that at the lowest loading rate (91mg H2S/m2·h) more than 98% H2S and 59% CO2 absorption efficiencies were achieved. The CH4 content in the treated gas increased from 60 to 80% with nearly 5% CH4 loss. Increasing the pH (7-10) and loading rate (91-355mg H2S/m2·h) enhanced the H2S absorption capacity, and the maximum H2S/CO2 and H2S/CH4 selectivity factors were 2.5 and 58, respectively. Temperature played a key role in the process and lower temperature was beneficial for intensifying H2S absorption performance. The highest H2S fluxes at pH 10 and 7 were 3.4g/m2·d and 1.8g/m2·d with overall mass transfer coefficients of 6.91×10-6 and 4.99×10-6m/s, respectively. The results showed that moderately high H2S fluxes with low CH4 loss may be achieved by using a robust and cost-effective membrane based absorption process for desulfurization of biogas. A tubular PDMS membrane contactor was tested for the first time to remove H2S from biogas under slightly alkaline conditions and the suggested process could be a promising for real scale applications.

Biogas desulfurization using autotrophic denitrification process.

The aim of this study was to evaluate the performance of an autotrophic denitrification process for desulfurization of biogas produced from a chicken manure digester. A laboratory scale upflow fixed bed reactor (UFBR) was operated for 105 days and fed with sodium sulfide or H2S scrubbed from the biogas and nitrate as electron donor and acceptor, respectively. The S/N ratio (2.5 mol/mol) of the feed solution was kept constant throughout the study. When the UFBR was fed with sodium sulfide solution with an influent pH of 7.7, about 95 % sulfide and 90 % nitrate removal efficiencies were achieved. However, the inlet of the UFBR was clogged several times due to the accumulation of biologically produced elemental sulfur particles and the clogging resulted in operational problems. When the UFBR was fed with the H2S absorbed from the biogas and operated with an influent pH of 8-9, around 98 % sulfide and 97 % nitrate removal efficiencies were obtained. In this way, above 95 % of the H2S in the biogas was removed as elemental sulfur and the reactor effluent was reused as scrubbing liquid without any clogging problem.