Interception of internal phosphorus release from sediments by lanthanum-modified shrimp shell biochar in two application modes

被引:4
|
作者
Cheng, Fulong [1 ,2 ,3 ]
Zhang, Zuo [2 ]
Zhao, Changxin [2 ]
Peng, Yuting [2 ]
Liao, Maoyu [1 ,3 ]
Fan, Jianxin [1 ,3 ]
机构
[1] Chongqing Jiaotong Univ, Chongqing Engn Lab Environm Hydraul Engn, Chongqing 400074, Peoples R China
[2] Chongqing Three Gorges Univ, Chongqing 404100, Peoples R China
[3] Chongqing Jiaotong Univ, Sch River & Ocean Engn, Chongqing 400074, Peoples R China
基金
中国国家自然科学基金;
关键词
Biochar; Lanthanum; Sediment; Phosphorus; DGT; Eutrophication; PHOSPHATE; PRECIPITATION; REMOVAL; WATER;
D O I
10.1016/j.jclepro.2024.143450
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Lanthanum (La)-modified biochar has been widely investigated as a phosphate adsorbent material. However, its effectiveness and mechanism as an amendment material to manage sediment internal phosphorus (P) release under anoxic conditions is still unclear. Thus, a lanthanum carbonate-modified shrimp shell biochar (LBC-1) was synthesized for controlling sediment P release, and the efficacy, mechanism, and sediment microbial community impact of LBC-1 under two application modes (addition and capping) were investigated. The maximum adsorption capacity of LBC-1 for phosphate was 79.5 mg/g, superior to most La-modified biochar materials. The generation of LaPO4 4 and Ca5(PO4)3(OH) 5 (PO 4 ) 3 (OH) precipitates and the formation of inner-sphere complexes were the main adsorption mechanisms of LBC-1 for phosphate. Both the LBC-1 addition and capping treatments successfully blocked sediment P release under anoxic conditions, with the removal efficiencies of DGT-labile P in the overlying water being 97.7-99.7% and 97.5-99.5%, respectively. The conversion of the mobile P forms to the stable HCl-P form in sediments played an important role in the interception of internal P release by the LBC-1 addition treatment. Furthermore, the LBC-1 addition treatment also prevented internal P release by effectively adsorbing DGT-labile P in the interstitial water due to the excellent P adsorption capacity of LBC-1. However, the prevention of P release from sediments by the LBC-1 capping treatment was mainly attributed to the efficient adsorption of DGT-labile P by LBC-1 at the sediment/overlying water interface. The release of P driven by sulfate- reducing bacteria (SRB) was a key mechanism for the migration of P from sediment to interstitial water. The LBC1 addition treatment reduced the relative abundance of SRB in the surface sediment and might inhibit the release of sediment P into the interstitial water, whereas the LBC-1 capping treatment had little effect on the relative abundance of SRB. In practice, the LBC-1 capping was easier to manipulate than the LBC-1 addition. These findings confirmed that sediment remediation using the LBC-1 capping treatment has great potential to manage internal P loading in eutrophic water bodies.
引用
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页数:15
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