锁磷剂和增氧剂对沉积物内源污染物钴的吸附
作者:
作者单位:

(1.河海大学水文水资源与水利工程科学国家重点实验室,江苏 南京210098;2.河海大学全球变化与水循环国际合作联合实验室,江苏 南京210098 )

作者简介:

李敏娟(1995—),女,助理工程师,硕士,主要从事环境水文及水环境保护研究。E-mail:867724810@qq.com

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中图分类号:

X524

基金项目:

国家自然科学基金(41971047);湖南省水利基金(XSKJ2019081-42);水文水资源与水利工程科学国家重点实验室“一带一路”水与可持续发展科技基金(2020491811)


Adsorption of endogenous pollutant Co in sediments, by phosphorus-locking agent and oxygen-enhancing agent
Author:
Affiliation:

(1.State Key Laboratory of Hydrology-Water Resources and Hydraulic Engineering, Hohai University, Nanjing 210098, China;2.Joint International Research Laboratory of Global Change and Water Cycle, Nanjing 210098, China )

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    摘要:

    为探究不同吸附材料(锁磷剂和增氧剂)对沉积物内源污染物Co的影响机制,以太湖梅梁湾为研究区域,设计3组室内模拟试验(对照组、增氧剂组及锁磷剂组),基于高分辨率平衡式间隙水采样(HR-Peeper)装置采集4个阶段(加入吸附材料后的第4天、30天、90天、150天)水样,解析原位覆盖条件下沉积物剖面溶解态Co、Fe(Ⅱ)、Mn的垂向分布特征及相互作用机制。结果表明:锁磷剂和增氧剂未造成水体中的pH值和Eh值的剧烈变化;沉积物剖面中溶解态Co质量浓度降低了1.29%~45.87%,且30.d时的吸附效果最好;增氧剂组及锁磷剂组沉积物水界面Co释放通量较对照组分别降低了1.00.μg/(m2·d)和1.19.μg/(m2·d);沉积物剖面Co的释放受铁、锰的氧化还原控制,且主要受锰的氧化还原控制;增氧剂对钴的吸附效果优于锁磷剂,且有效吸附时间更久。

    Abstract:

    In order to explore the influence mechanism of different adsorbents (phosphorus-locking agent and oxygen-enhancing agent) on the endogenous pollutant Co in sediments, the Meiliang Bay of Taihu Lake was selected as the study area. Three groups of indoor simulation experiments, including the control group, oxygen-enhancing group and phosphorus-locking group, were designed in this study. Water samples were collected in four stages (the 4th, 30th, 90th and 150th day after the addition of adsorbents) based on the high-resolution pore water sampling device (HR peeper). The vertical distribution characteristics and interaction mechanism of dissolved Co, Fe(Ⅱ) and Mn in sediment profile under the in-situ coverage were explored. The results show that phosphorus-locking agent and oxygen-enhancing agent did not cause drastic changes in Eh and pH in the water body. The dissolved Co concentration in the sediment profile decreased by 1.29%-45.87% while the adsorption effect was the best at 30th day. Comparing with the control group, the release flux of Co at the sediment-water interface of oxygen-enhancing group and phosphorus-locking group decreased by 1.00.μg/(m2·d) and 1.19 μg/(m2·d), respectively. The release of Co in the sediment profile was controlled by the redox of Fe and Mn, and mainly by the redox of Mn. In addition, the adsorption effect of oxygen-enhancing agent on Co was better than that of phosphorus-locking agent, and the reaction time was also longer.

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李敏娟,燕文明,陈翔,等.锁磷剂和增氧剂对沉积物内源污染物钴的吸附[J].河海大学学报(自然科学版),2022,50(4):90-97.(LI Minjuan, YAN Wenming, CHEN Xiang, et al. Adsorption of endogenous pollutant Co in sediments, by phosphorus-locking agent and oxygen-enhancing agent[J]. Journal of Hohai University (Natural Sciences),2022,50(4):90-97.(in Chinese))

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  • 收稿日期:2021-09-15
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  • 在线发布日期: 2022-07-25
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