Phosphorus immobilisation in sediment by using iron rich by-product as affected by water pH and sulphate concentrations

化学 环境化学 修正案 富营养化 沉积物 孵化 缺氧水域 溶解 吸附 硫黄 吸附 营养物 地质学 古生物学 生物化学 有机化学 物理化学 政治学 法学
作者
Lei Xia,Toon van Dael,Benoit Bergen,Erik Smolders
出处
期刊:Science of The Total Environment [Elsevier]
卷期号:864: 160820-160820 被引量:3
标识
DOI:10.1016/j.scitotenv.2022.160820
摘要

Iron (Fe) rich by-product from drinking water treatment plants can be added to rivers and lakes to immobilise phosphorus (P) in sediment and lower eutrophication risks. This study was set up to investigate the P immobilisation efficiency of an Fe rich by-product as affected by the pH and sulphate (SO4) concentration in the overlying water. Both factors are known to inhibit long-term P immobilisation under anoxic conditions. A static sediment-water incubation was conducted at varying buffered water pH values (6, 7 and 8) and different initial SO4 concentrations (0-170 mg SO4 L-1) with or without Fe rich by-product amendment to the sediment. In the unamended sediment, the P release to the overlying water was highest, and up to 6 mg P L-1, at lowest water pH due to higher reductive dissolution of Fe(III) oxyhydroxides. The Fe rich by-product amendment to the sediment largely reduced P release from sediment by factors 50-160 depending on pH, with slightly lowest immobilisation at highest pH 8, likely because of pH dependent P sorption. The total sulphur (S) concentrations in the overlying water reduced during incubation. The P release in unamended sediments increased from 2.7 mg L-1 to 4.2 mg L-1 with higher initial SO4 concentrations, suggesting sulphide formation during incubation and FeS precipitation that facilitates release of P. However, no such SO4 effects were found where Fe rich by-product was applied that lowered P release to <0.1 mg L-1 illustrating high stability of immobilised P in amended sediments. This study suggests that Fe rich by-product is efficient for P immobilisation but that loss of Fe in low pH water may lower its long-term effect.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
RC_Wang应助科研通管家采纳,获得10
刚刚
充电宝应助科研通管家采纳,获得10
刚刚
刚刚
领导范儿应助科研通管家采纳,获得10
刚刚
科研通AI5应助科研通管家采纳,获得10
刚刚
田様应助科研通管家采纳,获得10
刚刚
1秒前
丘比特应助科研通管家采纳,获得10
1秒前
CodeCraft应助科研通管家采纳,获得30
1秒前
sutharsons应助科研通管家采纳,获得30
1秒前
归海含烟完成签到,获得积分10
1秒前
科研通AI2S应助科研通管家采纳,获得10
1秒前
shire应助科研通管家采纳,获得10
1秒前
Orange应助科研通管家采纳,获得10
1秒前
思源应助科研通管家采纳,获得10
1秒前
RC_Wang应助科研通管家采纳,获得10
1秒前
研友_VZG7GZ应助科研通管家采纳,获得10
1秒前
充电宝应助科研通管家采纳,获得10
2秒前
顾矜应助科研通管家采纳,获得10
2秒前
大个应助科研通管家采纳,获得10
2秒前
2秒前
2秒前
匹诺曹发布了新的文献求助10
2秒前
唐画完成签到 ,获得积分10
2秒前
2秒前
2秒前
淡淡采白关注了科研通微信公众号
3秒前
tY完成签到,获得积分20
3秒前
傲娇的凡旋应助卢健辉采纳,获得10
4秒前
CodeCraft应助calbee采纳,获得10
4秒前
6秒前
6秒前
sw98318完成签到,获得积分10
7秒前
impala完成签到,获得积分10
7秒前
7秒前
欣喜访旋发布了新的文献求助10
7秒前
朱江涛完成签到 ,获得积分10
8秒前
角鸮完成签到,获得积分10
8秒前
zly完成签到 ,获得积分10
9秒前
雨霧雲完成签到,获得积分10
9秒前
高分求助中
Continuum Thermodynamics and Material Modelling 3000
Production Logging: Theoretical and Interpretive Elements 2700
Social media impact on athlete mental health: #RealityCheck 1020
Ensartinib (Ensacove) for Non-Small Cell Lung Cancer 1000
Unseen Mendieta: The Unpublished Works of Ana Mendieta 1000
Bacterial collagenases and their clinical applications 800
El viaje de una vida: Memorias de María Lecea 800
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 量子力学 光电子学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3527961
求助须知:如何正确求助?哪些是违规求助? 3108159
关于积分的说明 9287825
捐赠科研通 2805882
什么是DOI,文献DOI怎么找? 1540070
邀请新用户注册赠送积分活动 716926
科研通“疑难数据库(出版商)”最低求助积分说明 709808