TY - JOUR
T1 - Thermodynamically enhancing propionic acid degradation by using sulfate as an external electron acceptor in a thermophilic anaerobic membrane reactor
AU - Qiao, Wei
AU - Takayanagi, Kazuyuki
AU - Li, Qian
AU - Shofie, Mohammad
AU - Gao, Fang
AU - Dong, Renjie
AU - Li, Yu You
N1 - Funding Information:
This work was partially supported by The Beijing Municipal Science and Technology Plan Projects ( D151100005115001 & Z151100001115010 ), the National Natural Science Foundation of China ( 51408599 ), and the Chinese Universities Scientific Fund (2016QC050).
Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2016/12/1
Y1 - 2016/12/1
N2 - In this study, sulfate was employed as an external electron acceptor for enhancing the degradation of propionate in a thermophilic anaerobic membrane reactor (AnMBR). The organic loading rate (OLR) was increased gradually from the initial 3.9 kg-COD/m3d to the inhibiting OLR of 14.6 kg-COD/m3d. Feeding was stopped for 98 days but the process did not recover until 500 mg/L of sulfate was added into the AnMBR. After that, the enhanced propionate degradation was achieved up to an OLR of 15 kg-COD/m3d with a reduced sulfate addition of 300 mg/L. However, the thermodynamic calculation indicated that the syntrophic propionic acid degradation, coupled with methanogenesis, was unfavorable with a △G of +3 kJ/mol under the enhanced conditions. Conversely, the utilization of propionic acid by sulfate reduction bacterial (SRB) would be more favourable by having a much lower △G of −180 kJ/mol. The hydrogen conversion was presumed to go through the methanogenesis pathway according to the thermodynamic results. The mechanism of the propionic and hydrogen metabolism was supported as well by comparing the microbial communities with and without sulfate addition. As a result, the role of the sulfate enhancing propionic degradation can be concluded by combining the process performance, thermodynamic, and microbiology results.
AB - In this study, sulfate was employed as an external electron acceptor for enhancing the degradation of propionate in a thermophilic anaerobic membrane reactor (AnMBR). The organic loading rate (OLR) was increased gradually from the initial 3.9 kg-COD/m3d to the inhibiting OLR of 14.6 kg-COD/m3d. Feeding was stopped for 98 days but the process did not recover until 500 mg/L of sulfate was added into the AnMBR. After that, the enhanced propionate degradation was achieved up to an OLR of 15 kg-COD/m3d with a reduced sulfate addition of 300 mg/L. However, the thermodynamic calculation indicated that the syntrophic propionic acid degradation, coupled with methanogenesis, was unfavorable with a △G of +3 kJ/mol under the enhanced conditions. Conversely, the utilization of propionic acid by sulfate reduction bacterial (SRB) would be more favourable by having a much lower △G of −180 kJ/mol. The hydrogen conversion was presumed to go through the methanogenesis pathway according to the thermodynamic results. The mechanism of the propionic and hydrogen metabolism was supported as well by comparing the microbial communities with and without sulfate addition. As a result, the role of the sulfate enhancing propionic degradation can be concluded by combining the process performance, thermodynamic, and microbiology results.
KW - 16S rRNA
KW - Anaerobic membrane reactor
KW - Hydrogen
KW - Propionic acid
KW - Thermodynamic
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U2 - 10.1016/j.watres.2016.10.013
DO - 10.1016/j.watres.2016.10.013
M3 - Article
C2 - 27736707
AN - SCOPUS:84990840516
SN - 0043-1354
VL - 106
SP - 320
EP - 329
JO - Water Research
JF - Water Research
ER -