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In this study, a green zero-valent iron-loaded carbon composite (ZVI-SCG) was synthesized using coffee grounds and FeCl3 solution through two-steps method, and the synthesized ZVI-SCG was used in the activation of peroxydisulfate (PDS) to degrade Levofloxacin (LEX). Results revealed that ZVI-SCG exhibited a great potential for LEX removal by adsorption and catalytic degradation in the ZVI-SCG/PDS system, and 99% of LEX was removed in the ZVI-SCG/PDS system within 60 min. ZVI-SCG/PDS system showed a high reactivity toward LEX degradation under realistic environmental conditions. Also, the ZVI-SCG/PDS system could effectively degrade several quinolone antibiotics including gatifloxacin, ciprofloxacin and LEX in single and simultaneous removal modes. A potential reaction mechanism of LEX degradation by ZVI-SCG/PDS system was proposed, SO 4 •- , HO•, O 2 • - and 1 O 2 involved in radical and non-radical pathways took part in catalytic degradation of LEX by ZVI-SCG/PDS system, but HO• might be the main reactive species for LEX degradation. The possible degradation pathway of LEX was also proposed based on the identified ten intermediate products, LEX degradation was successfully achieved through decarboxylation, opening ring and hydroxylation processes. The potential toxicity of LEX and its oxidation products decreased significantly after treatment. This study provides a promising strategy of water treatment for the antibiotics-containing wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

The applicability of sludge biochar catalyst (SBC) coupling with ultrasound (US) irradiation for the simultaneous removal of Pb(II) and phenol was firstly investigated in this study. Results indicate that Pb(II) removal of SBC/US process was superior to that of SBC without US. The inhibitory order of the coexisting anions on Pb(II) removal was PO 4 3- > HCO 3 -  > NO 3 -  > F - > SO 4 2- > Cl - . Also, several coexisting metals ions inculding Cr(VI), Ni(II) and Cu(II) could be removed in a simultaneous manner with Pb(II). A high removal performance of Pb(II) by SBC/US process and its synergism with phenol oxidation had been successfully achieved. The simultaneous removal efficiencies of Pb(II) and phenol were high up to 95% within 60 min at optimum reaction conditions. Four kinds of Pb species inculding Pb 0 , PbCO 3 , PbO and Pb(OH) 2 were formed during the reaction, whereas five kinds of transformation compounds of phenol such as 1,4-benzoquinone, acetic acid, formic acid, maleic acid and propionic acid were detected. Both HO and O 2 - contributed to the oxidation of phenol by SBC/US process, but HO was dominant radical. A reaction mechanism for the synergistic removal of Pb(II) and phenol by SBC/US process involving in four stages-namely adsorption, precipitation, reduction and Fenton-like oxidation processes was proposed. This study demonstrates that SBC/US process could be considered as a potential candidate for the remediation of real wastewaters containing Pb(II) and phenol., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

In this study, the feasibility of a novel Ca-Ag 3 PO 4 composite with visible light irradiation for the phenanthrene (PHE) degradation and algae inactivation in artificial seawater was firstly investigated. The experimental findings revealed that Ag 3 PO 4 phase was sucessfully formed on the Ca-based material, and the presence of Ca-based material could effectively keep Ag 3 PO 4 particles stable. An excellent performance on PHE degradation or algae inactivation was observed from Ca-Ag 3 PO 4 composite under visible light irradiation. The degradation of PHE or inactivation of algae not only could be efficiently achieved in the single mode, but also could be successfully achieved in the coexisting mode. Above 96% of PHE and algae were simultaneously removed within 12 h in the Ca-Ag 3 PO 4 /visible light system. It was further observed that the degradation of PHE and/or inactivation of algae increased with the increase of Ca-Ag 3 PO 4 dosage. HO was the primary radical responsible for PHE degradation, whereas HO and Ag + released from Ca-Ag 3 PO 4 mainly contributed to the algae inactivation. A possible mechanism involving the catalytic removal of PHE and algae by Ca-Ag 3 PO 4 under visible light irradiation was proposed. This study provides helpful guide for the simultaneous removal of various pollutants in real seawater., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Biodegradable plastics, as alternatives to conventional plastics, are increasingly used, but their interactions with organic pollutants are still unknown. In this study, the sorption and desorption behaviors on a type of biodegradable plastic-poly(butylene adipate co-terephtalate) (PBAT) were investigated, and at the same time two types of conventional plastics-polyethylene (PE c and PE v ) and polystyrene (PS) were used for comparison. Phenanthrene (PHEN) was chosen as one of representative organic pollutants. Results indicated that the sorption and desorption capacities of PBAT were not only higher than those of the other types of microplastics, but also higher than those of carbonaceous geosorbents. The surface area normalized results illustrated that sorption and desorption of the microplastics were positively correlated with their abundance of rubbery subfraction. The sorption kinetic results showed that the sorption rates of PBAT and PE c were higher than PE v and PS. The effects of water chemistry factors including salinity, dissolved organic matter and Cu 2+ ion on the sorption process displayed the same trend, but the degrees of influence on the four microplastics differed. The degrees of influence were mainly dependent on the abundance of rubbery subfraction for microplastics. These findings indicate that the biodegradable poly(butylene adipate co-terephtalate) microplastics are actually stronger vectors than the conventional microplastics, and crystallization characteristics of the microplastics have great influences on the vector effect., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Sediments were collected from three mangrove wetlands in the Pearl River Estuary (PRE) of South China to investigate spatial and temporal distributions of polybrominated diphenyl ethers (PBDEs), decabromodiphenyl ethane (DBDPE) and 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE). Concentrations of ΣPBDEs, DBDPE and BTBPE in mangrove sediments of the PRE ranged from 1.25-206, 0.364-34.9, and not detected-0.794 ng g(-1) dry weight, respectively. The highest concentrations of ΣPBDEs, DBDPE and BTBPE were found at the mangrove wetland from Shenzhen, followed by Zhuhai and Guangzhou, showing the dependence on the proximity to urban areas. PBDEs were the predominant brominated flame retardants (BFRs) in mangrove sediments. The concentrations of ΣPBDEs, DBDPE and BTBPE in sediment cores showed an increasing trend from the bottom to top layers, reflecting the increasing usage of these BFRs. The inventories of ΣPBDEs, DBDPE and BTBPE in mangrove sediments were 1962, 245, and 4.10 ng cm(-2), respectively. This is the first study to report the occurrence of DBDPE and BTBPE in mangrove ecosystems., (Copyright © 2014 Elsevier Ltd. All rights reserved.)