Characteristics of algae-derived biochars and their sorption and remediation performance for sulfamethoxazole in marine environment

吸附 生物炭 环境修复 环境化学 化学 藻类 生物利用度 吸附 沉积物 污染 植物 有机化学 生态学 生物 生物信息学 古生物学 热解
作者
Man Zhao,Xiaohan Ma,Xinrui Liao,Siyu Cheng,Qiang Liu,He‐Fang Wang,Hao Zheng,Xiaoyun Li,Xianxiang Luo,Jian Zhao,Fengmin Li,Baoshan Xing
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:430: 133092-133092 被引量:80
标识
DOI:10.1016/j.cej.2021.133092
摘要

The performance of algae-derived biochars (ABCs) on sorption and remediation of antibiotic pollution in marine environment is poorly understood. A batch of biochars were produced from two marine algae waste (Enteromorpha prolifera and seaweed residuals) at 300–700 °C (EM300–700 and SW300–700) to investigate their sorption of sulfamethoxazole (SMX) in seawater, as well as their performance in remediation of SMX polluted marine sediment. Regardless the heating temperature (HTT), ABCs with relatively low C contents (29.6–37.4%), but high contents of O (16.6–28.9%) and N (0.75–3.48%), possessed lower surface area, but more abundant minerals (ash content 33.5–63.5%), richer heteroatom-containing functional groups than the terrestrial plant silvergrass-derived biochars (SGBCs). The maximum sorption capacities of ABCs increased from 2896 to 4212 mg kg−1 to 4874–4879 mg kg−1 as the HTT increased from 300 to 700 °C, higher than those of the SGBCs (1017–3515 mg kg−1). SMX sorption on the ABCs was dominantly through cation bridging, followed by negative charge-assisted H-bond, π-π electron donor–acceptor interaction, and pore filling. Moreover, the mixing and capping of SW700 effectively decreased SMX bioavailability in the sediment, equivalent to a commercial activated carbon. These results provide the strategies for in-situ remediation of antibiotic-contaminated marine sediments using designer biochars from marine algae waste.
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