Carbonate accelerates while humic acid inhibits ferrihydrite transformation in soil: kinetics and mechanisms of As and Pb sequestration under fluctuating redox conditions

Understanding how common soil constituents regulate iron (oxyhydr)oxide transformation is essential for predicting the stability of co-occurring lead (Pb) and arsenate [As(V)] under dynamic conditions. Here, a decoupling and comparative strategy was used to isolate carbonate- versus humic acid (HA)-driven controls on the transformation of Pb-bearing, As-bearing, and Pb-As co-bearing ferrihydrite (Fh) across six well-defined systems. An evidence chain combining kinetic experiments, spectroscopic and mineralogical analyses, and anaerobic-aerobic soil incubation linked interfacial chemistry with contaminant fate. The results showed that the transformation pathway and products of Fh were primarily dictated by the mode of surface complexation, with carbonate and HA playing distinct roles. Carbonate ions associated with Fh via weak outer-sphere and bidentate inner-sphere complexation, accelerated dissolution-recrystallization, and directed transformation toward goethite. This process simultaneously promoted the re-immobilization of Pb and As via adsorption, lattice incorporation, and PbCO 3 precipitation. In contrast, HA formed strong inner-sphere complexes; Pb further induced surface fractionation of phenolic-/carboxylic-rich HA components and promoted stable cyclic complexation, enhancing interfacial passivation and stabilizing Pb and As predominantly via edge-/surface-associated adsorption. Soil redox incubation corroborated net stabilization under fluctuating conditions, with available Pb decreasing from 104 to 29.8 mg/kg (71% removal) and available As from 61.0 to 12.6 mg/kg (79% removal), significantly outperforming the control. We conclude that carbonate functions as a transformation promoter and re-immobilization facilitator, whereas HA acts as a transformation inhibitor and surface stabilizer. These findings provide valuable insights for predicting and managing risks of Pb and As in complex, redox-fluctuating environments. • Carbonate and humic acid modulate Fe oxide cycling, driving Pb/As immobilization. • Carbonate acts as a transformation promoter through outer-sphere complexation. • Humic acid acts as a transformation inhibitor via strong inner-sphere complexation. • The pH-buffering effect of carbonate reduced Pb mobility.

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Publication Details

Journal
Soil & Environmental Health
Published
2026-02-21
DOI
https://doi.org/10.1016/j.seh.2026.100203
Primary Topic
Iron oxide chemistry and applications
Type
article
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article

Carbonate accelerates while humic acid inhibits ferrihydrite transformation in soil: kinetics and mechanisms of As and Pb sequestration under fluctuating redox conditions

Wenyan Gao, Shengguo Xue, Xi Luo, Chao Xiang et al.
Soil & Environmental Health
Iron oxide chemistry and applications
article

Carbonate accelerates while humic acid inhibits ferrihydrite transformation in soil: kinetics and mechanisms of As and Pb sequestration under fluctuating redox conditions

Wenyan Gao, Shengguo Xue, Xi Luo, Chao Xiang, Zhenyao Xia, Chuan Wu, Hai Xiao
article en

Abstract

Understanding how common soil constituents regulate iron (oxyhydr)oxide transformation is essential for predicting the stability of co-occurring lead (Pb) and arsenate [As(V)] under dynamic conditions. Here, a decoupling and comparative strategy was used to isolate carbonate- versus humic acid (HA)-driven controls on the transformation of Pb-bearing, As-bearing, and Pb-As co-bearing ferrihydrite (Fh) across six well-defined systems. An evidence chain combining kinetic experiments, spectroscopic and mineralogical analyses, and anaerobic-aerobic soil incubation linked interfacial chemistry with contaminant fate. The results showed that the transformation pathway and products of Fh were primarily dictated by the mode of surface complexation, with carbonate and HA playing distinct roles. Carbonate ions associated with Fh via weak outer-sphere and bidentate inner-sphere complexation, accelerated dissolution-recrystallization, and directed transformation toward goethite. This process simultaneously promoted the re-immobilization of Pb and As via adsorption, lattice incorporation, and PbCO 3 precipitation. In contrast, HA formed strong inner-sphere complexes; Pb further induced surface fractionation of phenolic-/carboxylic-rich HA components and promoted stable cyclic complexation, enhancing interfacial passivation and stabilizing Pb and As predominantly via edge-/surface-associated adsorption. Soil redox incubation corroborated net stabilization under fluctuating conditions, with available Pb decreasing from 104 to 29.8 mg/kg (71% removal) and available As from 61.0 to 12.6 mg/kg (79% removal), significantly outperforming the control. We conclude that carbonate functions as a transformation promoter and re-immobilization facilitator, whereas HA acts as a transformation inhibitor and surface stabilizer. These findings provide valuable insights for predicting and managing risks of Pb and As in complex, redox-fluctuating environments. • Carbonate and humic acid modulate Fe oxide cycling, driving Pb/As immobilization. • Carbonate acts as a transformation promoter through outer-sphere complexation. • Humic acid acts as a transformation inhibitor via strong inner-sphere complexation. • The pH-buffering effect of carbonate reduced Pb mobility.

Soil & Environmental HealthVol. 4(2)
Central South University (CN), China Three Gorges University (CN)
Life in Land
Openalex Percentile: Top 50%
Iron oxide chemistry and applications
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