Humic acid(HA),as a represent of natural organic matter widely existing in water body,dose harm to water quality and human health;however,it was commonly treated as an environmental background substance while not targ...Humic acid(HA),as a represent of natural organic matter widely existing in water body,dose harm to water quality and human health;however,it was commonly treated as an environmental background substance while not targeted contaminant in advanced oxidation processes(AOPs).Herein,we investigated the removal of HA in the alkali-activated biochar(KBC)/peroxymonosulfate(PMS)system.The modification of the original biochar(BC)resulted in an increased adsorption capacity and catalytic activity due to the introduction of more micropores,mesopores,and oxygen-containing functional groups,particularly carbonyl groups.Mechanistic insights indicated that HA is primarily chemically adsorbed on the KBC surface,while singlet oxygen(^(1)O_(2))produced by the PMS decomposition served as the major reactive species for the degradation of HA.An underlying synergistic adsorption and oxidation mechanism involving a local high concentration reaction region around the KBC interface was then proposed.This work not only provides a cost-effective solution for the elimination of HA but also advances our understanding of the nonradical oxidation at the biochar interface.展开更多
基金supported by the National Natural Science Foundation of China(No.52200049)the China Postdoctoral Science Foundation(No.2022TQ0089)the Heilongjiang Province Postdoctoral Science Foundation(No.LBHZ22181).
文摘Humic acid(HA),as a represent of natural organic matter widely existing in water body,dose harm to water quality and human health;however,it was commonly treated as an environmental background substance while not targeted contaminant in advanced oxidation processes(AOPs).Herein,we investigated the removal of HA in the alkali-activated biochar(KBC)/peroxymonosulfate(PMS)system.The modification of the original biochar(BC)resulted in an increased adsorption capacity and catalytic activity due to the introduction of more micropores,mesopores,and oxygen-containing functional groups,particularly carbonyl groups.Mechanistic insights indicated that HA is primarily chemically adsorbed on the KBC surface,while singlet oxygen(^(1)O_(2))produced by the PMS decomposition served as the major reactive species for the degradation of HA.An underlying synergistic adsorption and oxidation mechanism involving a local high concentration reaction region around the KBC interface was then proposed.This work not only provides a cost-effective solution for the elimination of HA but also advances our understanding of the nonradical oxidation at the biochar interface.
