TY - JOUR
T1 - Simultaneous removal of tetrachloroethylene and nitrate with a novel sulfur-packed biocathode system
T2 - The synergy between bioelectrocatalytic dechlorination and sulfur autotrophic denitrification
AU - Chen, Fan
AU - Ye, Yin
AU - Fan, Beilei
AU - Lv, Miao
AU - Liang, Bin
AU - Liu, Wenzong
AU - Cheng, Hao Yi
AU - Chen, Yanlong
AU - Liu, Yang
AU - Wang, Yuheng
AU - Wang, Aijie
AU - Li, Zhiling
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/7/1
Y1 - 2022/7/1
N2 - The co-contamination of tetrachloroethylene (PCE) and nitrate is ubiquitous in groundwater, posing a serious threat to human health. The lack of a sustainable electron donor source and the inhibitory effect of nitrate on dechlorination make it difficult to achieve simultaneous removal of PCE and nitrate. Here, a novel process coupling bioelectrocatalytic dechlorination and elemental sulfur (S0)-based autotrophic denitrification (eBD-SAD) was established for efficient simultaneous removal of PCE and nitrate. The accelerated nitrate removal in the S0-packed biocathode system mitigated the competition for electrons between reductive dechlorination and denitrification. The 95.9% removal of nitrate within 12 h, 87.2% removal of PCE within 48 h, and stable pH of 7.05–7.49 were achieved at an optimized voltage of 0.5 V. The potential dechlorinators (e.g., Pseudomonas, Chryseobacterium, Desulfovibrio, Mesorhizobium, Geobacter) was significantly enriched in the biocathode biofilm. The S0 particle biofilm was mainly dominated by denitrifiers (e.g., Arcobacter, Pseudomonas, Azospira, Ralstonia). The positive interactions between electroactive and dechlorination bacteria in the cathode biofilm, as well as the S0 autotrophic denitrifiers and non-S0-respiring bacteria in the S0 particle biofilm, might play important roles in the simultaneous removal of PCE and nitrate. This study proposes a novel method for accelerated electro-biodechlorination by alleviating nitrate competition with the SAD process and opens an appealing avenue for the efficient remediation of groundwater co-contaminated with chlorinated aliphatic hydrocarbons and nitrate.
AB - The co-contamination of tetrachloroethylene (PCE) and nitrate is ubiquitous in groundwater, posing a serious threat to human health. The lack of a sustainable electron donor source and the inhibitory effect of nitrate on dechlorination make it difficult to achieve simultaneous removal of PCE and nitrate. Here, a novel process coupling bioelectrocatalytic dechlorination and elemental sulfur (S0)-based autotrophic denitrification (eBD-SAD) was established for efficient simultaneous removal of PCE and nitrate. The accelerated nitrate removal in the S0-packed biocathode system mitigated the competition for electrons between reductive dechlorination and denitrification. The 95.9% removal of nitrate within 12 h, 87.2% removal of PCE within 48 h, and stable pH of 7.05–7.49 were achieved at an optimized voltage of 0.5 V. The potential dechlorinators (e.g., Pseudomonas, Chryseobacterium, Desulfovibrio, Mesorhizobium, Geobacter) was significantly enriched in the biocathode biofilm. The S0 particle biofilm was mainly dominated by denitrifiers (e.g., Arcobacter, Pseudomonas, Azospira, Ralstonia). The positive interactions between electroactive and dechlorination bacteria in the cathode biofilm, as well as the S0 autotrophic denitrifiers and non-S0-respiring bacteria in the S0 particle biofilm, might play important roles in the simultaneous removal of PCE and nitrate. This study proposes a novel method for accelerated electro-biodechlorination by alleviating nitrate competition with the SAD process and opens an appealing avenue for the efficient remediation of groundwater co-contaminated with chlorinated aliphatic hydrocarbons and nitrate.
KW - Biocathode systems
KW - Competition mitigation
KW - Denitrification
KW - Functional bacteria interaction
KW - Groundwater bioremediation
KW - Reductive dechlorination
UR - http://www.scopus.com/inward/record.url?scp=85126359558&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2022.135793
DO - 10.1016/j.cej.2022.135793
M3 - 文章
AN - SCOPUS:85126359558
SN - 1385-8947
VL - 439
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 135793
ER -