Construction of biochar-based organohalide-respiring bacterial agent for remediation of 2,4,6-trichlorophenol contaminated soil.

Construction of an efficient bio-reductive dechlorination system remains challenging due to the narrow ecological niche and low-growth rate of organohalide-respiring bacteria during field remediation. In this study, a biochar-based organohalide-respiring bacterial agent was obtained, and its performance and effects on indigenous microbial composition, diversity, and inter-relationship in soil were investigated. A well-performing material, Triton X-100 modified biochar (BC600-TX100), was found to have the superior average pore size, specific surface area and hydrophicity, compared to other materials. Interestingly, Pseudomonas aeruginosa CP-1, which is capable of 2,4,6-TCP dechlorination, showed a 348 times higher colonization cell number on BC600-TX100 than that of BC600 after 7 d. Meanwhile, the dechlorination rate in soil showed the highest (0.732 d-1) in the BC600-TX100 bacterial agent than in the other agents. The long-term performance of the BC600-TX100 OHRB agent was also verified, with a stable dechlorination activity over six cycles. Soil microbial community analysis found the addition of the BC600-TX100 OHRB agent significantly increased the relative abundance of genus Pseudomonas from 1.53 % to 11.2 %, and Pseudomonas formed a close interaction relationship with indigenous microorganisms, creating a micro-ecological environment conducive to reductive dechlorination. This study provides a feasible bacterial agent for the in-situ bioremediation of soil contaminated organohalides. ENVIRONMENTAL IMPLICATION: Halogenated organic compounds are a type of toxic, refractory, and bio-accumulative persistent compounds widely existed in environment, widely detected in the air, water, and soil. In this study, we provide a feasible bacterial agent for the in-situ bioremediation of soil contaminated halogenated organic compounds. The application of biochar provides new insights for "Turning waste into treasure", which meets with the concept of green chemistry.

Polar electric field-modulated peroxymonosulfate selective activation for removal of organic contaminants via non-radical electron transfer process.

Nonradical electron transfer process (ETP) in peroxomonosulfate (PMS) based advanced oxidation processes (AOPs) is regarded promising for selective degradation of organic contaminants in water, however, the subjective modulation strategy and the definitive mechanistic elucidation of ETP are still lacking. Herein, we proposed a heretofore unreported yet efficient ETP indution approach by construction of polar electrical field on biochar via nonmetallic elements co-doping. Physicochemical characterizations and density functional theory (DFT) calculations verified the electronegativity difference among boron, nitrogen, and sulfur elements bestowed robust local electric fields on biochar surface (BC-BNS), which effectively enhanced the adsorption complexation and charge transfer between biochar and PMS. Compared to the other single-doped or co-doped biochar, BC-BNS exhibited superior catalytic performance of PMS activation for degradation of atrazine (ATZ) (kobs=0.036 min-1), as well as various kinds of electron-rich organics. The remarkable catalytic degradation capacity was further verified in various aqueous matrices and background factors, representing the excellent selectivity. Analysis of contribution from reactive oxygen species and electrochemical testing together substantiated the role of polar electric fields in facilitating the modulation from singlet oxygen (1O2) to ETP as a prevailing mechanism. DFT calculations and apparent interactions revealed the dissociation of S-O bond was thermodynamically favored within this potent localized electric field, which further induced the cleavage of OO bond and ultimately promoted the dual electron transfer between ATZ and PMS. The superiority of BC-BNS/PMS system was further validated with the low ecotoxicity caused by enhanced dechlorination, the low energy consumption, and the long-term effectiveness. The novel modulation principle and atomic-level mechanism exploration gave suggestions for advancing ETP-dominated AOP to remove recalcitrant contaminants during water treatment and restoration.

Microplastics contamination in groundwater of a drinking-water source area, northern China.

Although the contamination of microplastics (MPs) in groundwater has been anticipated, their occurrence, distribution, and composition require further understanding. In this study, the occurrence and distributions of MPs were investigated in shallow groundwater from an important water source district in Tianjin city of northern China. The abundance, the physical morphology, the chemical composition, and the potential correlations of the determined MPs with human activities were thoroughly characterized. MPs were determined from all ten sampling sites with the abundance ranged between 17.0 ± 2.16 to 44.0 ± 1.63 n/L, revealing the ubiquitous existed MPs contamination. Based on the physical categorization, fiber (44.74%) was the most abundant shape, while blue (31.02%) and transparent (26.09%) were the most prevalent colors. The dominant size of MPs was smaller than 200 µm which accounted for 73.10%. A total of seven types of MPs were determined with polyethylene, polyethylene terephthalate, and polystyrene as the main types, of which, polypropylene showed strong positive correlations with polystyrene, indicating the possible similar sources of them. Besides, the determined MPs in groundwater were greater in areas with the high population density and strong population activity, indicating their high correlation with human activity. The study highlighted the presence of MPs in groundwater of drinking water source in northern China and provided useful information for evaluating the potential ecological effects on water quality safety and human health brought by MPs.