Influence of iron-modified biochar on phosphate transport and deposition in saturated porous media under varying pH, ionic strength, and biochar dosage

IF 8.1 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Chemosphere Pub Date : 2025-02-01 Epub Date: 2024-12-22 DOI:10.1016/j.chemosphere.2024.143932
Rakesh Kumar , Jasmeet Lamba , Sushil Adhikari , Nitesh Kasera , Henry Allen Torbert
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Abstract

Phosphorus (P) is one of the essential nutrients required for plants; however, loss of phosphorus from agricultural areas results in water quality impairment. This research aims to investigate the transport and deposition of phosphate at different solution chemistries and phosphate-biochar dosages under (a) individual phosphate flow, (b) phosphate transport followed by biochar, and (c) co-transport of biochar-phosphate in saturated porous media. Breakthrough curves (BTCs) for phosphate were generated to understand the effect of pine raw biochar (BC) and iron-modified biochar (Fe-BC) on phosphate transport and deposition under varying solutions, pH (5.5 ± 0.1–10.5 ± 0.1), ionic strength (0–10 mM), phosphate (10–20 mg/L), and biochar dosages (100–200 mg/L) in saturated porous media. Results revealed increased deposition of BC and Fe-BC at high ionic strength (IS), i.e., 10 mM compared to 0 mM. The BTCs of phosphate (10–20 mg/L) transport at increasing IS showed delayed elute and long tailing curves compared to BTCs of tracer. Further, phosphate transport using BTCs in biochar-mediated saturated porous media was investigated at 10–20 mg/L phosphate, where maximum retardation (37%) was observed at pH 6.7 ± 0.1 and 0 mM IS due to the availability of active sites for 10 mg/L phosphate using Fe-BC than BC. The BTCs of phosphate transport at pH 6.7 ± 0.1 and 0–10 mM IS showed 37% and 40% phosphate deposition in Fe-BC-mediated columns for 0 mM and 10 mM, respectively, than BC-mediated columns. For BC, maximum phosphate adsorption was observed at pH 5.5 ± 0.1, whereas for Fe-BC, it was observed at pH 6.7 ± 0.1 at 10 mM IS. The least adsorption was observed at pH of 10.5 ± 0.1 for both BC and Fe-BC. Similar phosphate retardation BTCs for BC and Fe-BC at 10 mM were observed with adsorption of 40% phosphate for 100–200 mg/L biochar dosages. Besides, co-transport and deposition of biochar and phosphate, considering with and without ripening effect, reported high phosphate retardation using Fe-BC than BC at pH of 6.7 ± 0.1 and 10 mM IS due to chemical non-equilibrium and mass transfer. Taken together, iron-modified biochar (Fe-BC) showed significant adsorptive potential for phosphate management in saturated porous media. Overall, modeling of transport and deposition of phosphate and biochar are significant to understanding fate, nutrient mobility & management, biochar-phosphate interactions, and remediation designs in saturated porous media.

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铁改性生物炭在不同 pH 值、离子强度和生物炭用量条件下对饱和多孔介质中磷酸盐迁移和沉积的影响。
磷是植物必需的营养物质之一;然而,农业地区磷的流失导致水质受损。本研究旨在研究磷酸盐在不同溶液化学和磷酸盐-生物炭剂量下的运输和沉积(a)单独的磷酸盐流动,(b)磷酸盐运输后的生物炭,以及(c)饱和多孔介质中生物炭-磷酸盐的共运输。在饱和多孔介质中,pH(5.5-10.5)、离子强度(0-10 mM)、磷酸盐(10-20 mg/L)和生物炭用量(100-200 mg/L)不同的溶液条件下,通过生成磷酸盐的突破曲线(btc)来了解松木生生物炭(BC)和铁改性生物炭(Fe-BC)对磷酸盐运输和沉积的影响。结果表明,在高离子强度(IS)下,BC和Fe-BC的沉积量增加,即10 mM比0 mM。磷酸盐(10-20 mg/L)在高离子强度(IS)下的运输比示踪剂的btc表现出延迟的洗脱和长尾曲线。此外,在10-20 mg/L的磷酸盐条件下,研究了btc在生物炭介导的饱和多孔介质中的磷酸盐运输,其中在pH 6.7±0.1和0 mM IS下观察到最大的延迟(37%),这是由于Fe-BC比BC具有10 mg/L磷酸盐的活性位点。在pH 6.7±0.1和0-10 mM IS下,fe - bc介导柱的磷酸盐转运btc分别为0 mM和10 mM,比bc介导柱的磷酸盐沉积37%和40%。BC在pH为5.5±0.1时对磷酸盐的吸附最大,而Fe-BC在pH为6.7±0.1时对磷酸盐的吸附最大。在pH为10.5±0.1时,BC和Fe-BC的吸附量最小。在100-200 mg/L的生物炭剂量下,40%的磷酸盐对10 mM的BC和Fe-BC的吸附效果相似。此外,在pH 6.7±0.1和10 mM IS条件下,由于化学不平衡和传质,Fe-BC对生物炭和磷酸盐的共转运和沉积效果优于BC。综上所述,铁改性生物炭在饱和多孔介质中表现出显著的磷酸盐管理吸附潜力。总的来说,模拟磷酸盐和生物炭的迁移和沉积对于理解饱和多孔介质中的命运、生物炭-磷酸盐相互作用和修复设计具有重要意义。
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来源期刊
Chemosphere
Chemosphere 环境科学-环境科学
CiteScore
15.80
自引率
8.00%
发文量
4975
审稿时长
3.4 months
期刊介绍: Chemosphere, being an international multidisciplinary journal, is dedicated to publishing original communications and review articles on chemicals in the environment. The scope covers a wide range of topics, including the identification, quantification, behavior, fate, toxicology, treatment, and remediation of chemicals in the bio-, hydro-, litho-, and atmosphere, ensuring the broad dissemination of research in this field.
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