[Bmim]FeCl4 mediated inhibition and toxicity during anaerobic digestion: Dose-response kinetics, biochar-dependent detoxification and microbial resistance

化学 离子液体 生物炭 戒毒(替代医学) 产酸作用 厌氧消化 酰胺 丙酸盐 生物转化 药物化学 有机化学 甲烷 催化作用 替代医学 病理 医学 热解
作者
Jingyi Li,Yilin Yao,Yongsen Shi,Jingchun Tang,Samir I. Gadow,Rutao Liu,Qigui Niu
出处
期刊:Water Research [Elsevier]
卷期号:210: 117969-117969 被引量:29
标识
DOI:10.1016/j.watres.2021.117969
摘要

[Bmim]FeCl4, or 1‑butyl‑3-methylimidazolium tetrachloroferrate, is a typical ionic liquid (IL). Its recyclable, magnetic, multicomponent, and solvent-free nature makes it a particularly attractive ionic liquid for use in industrial processes. Despite its widespread use, the potential hazards that [Bmim]FeCl4 might pose to the environment, including productive microorganisms, have not been explored. In this study, the dose-response of [Bmim]FeCl4 in anaerobic digestion (AD) was investigated to assess the potential toxification and biochar-dependent detoxification in microbial communities, including enzymatic activity and molecule docking dynamics. Our results showed that methane production (31.52 mLmax/gVS) was sharply inhibited following [Bmim]FeCl4 treatment. Moreover, increasing the dosage of [Bmim]FeCl4 caused more dissolved organic matter (DOM) to be generated. Interestingly, 0.4 g/L of [Bmim]FeCl4 could stimulate the high activity of microbial hydrolase and ATPase. However, a higher concentration of 2.65 g/L prevented these enzymatic processes from continuing. At the cellular level, higher concentration of [Bmim]FeCl4 (>0.4 g/L) increased malondialdehyde (MDA) levels, leading to a higher cell lethal rate and weakening of the secondary structures of protein (especially, the amide I region). At the molecular level, the competitive H-bonding in the active sites caused low activity and consummated more energy. At the community level, structural equation modeling (SEM) revealed that [Bmim]FeCl4 and biochar were the main drivers for microbial community succession. For instance, high [Bmim]FeCl4 (8 g/L) benefited the growth of Clostridium sensu_stricto (from ≤1% to 27%). It is worth mentioning that biochar reversed the inhibition with high α-diversity, which caused a resurgence in the activity of previously inhibited ATPase and hydrolase. H2-trophic methanogens (Methanolinea and Methaofastidisoum) were sensitive to [Bmim]FeCl4 and decreased linearly while acetoclastic methanogens (Methanosaeta) were unchanged. These findings were consistent with the short-term activity tests and further verified by functional analysis.
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