Highly efficient bioregeneration of high temperature-pyrolyzed biochar after trichloroethylene adsorption through biodegradation of Dehalococcoides.

[Display omitted] • Biodegradation of biochar-adsorbed trichloroethylene (TCE) by Dhc 195 was studied. • 87.5 % of biochar-adsorbed TCE was biodegraded to ethene within 63 days. • Adsorption capacity of biochar remained 80.4% after 5-time bioregeneration cycles. • Electron transfer from Dhc 195 to TCE was mediated by biochar for biodegradation. • Biodegradation of adsorbed TCE required more VB 12 but had a wider pH tolerance. Biochars was widely employed to immobilize chlorinated aliphatic hydrocarbons (CAHs) in groundwater. Biodegradation of adsorbed CAHs may be able to regenerate biochars, but was scarcely explored. In this study, therefore, biodegradation of trichloroethylene (TCE) adsorbed on a biochar prepared at 700 °C (WBC700) by Dehalococcoides mccartyi 195 (Dhc 195) was investigated. Aqueous TCE was completely degraded to ethene by Dhc 195 within 28 days, while 87.5 % of WBC700-adsorbed TCE was degraded to ethene within 63 days. The slower biodegradation of WBC700-adsorbed TCE could be attributed to its lower accessibility to Dhc 195 caused by the steric effects of WBC700. The adsorption capacity of WBC700 for TCE remained 80.4 % after five adsorption-bioregeneration cycles, indicating that the microbial degradation could be a highly efficient method to regenerate biochars. The microbial degradation was mainly through the electron transfer from Dhc 195 to TCE mediated by biochars as electron conductor or shuttle, but was not assisted by desorption or extracellular redox active species. Compared with biodegradation of aqueous TCE, the biodegradation of WBC700-adsorbed TCE by Dhc 195 had a wider pH tolerance and required more VB 12 , due to the buffer effect and adsorption of WBC700, respectively. The obtained results could provide a cost-effective method of biochar regeneration for CAHs removal in groundwater. [ABSTRACT FROM AUTHOR]