Residence time effects on sorption and desorption mechanisms of phosphate and myo-inositol hexakisphosphate on allophane

• Sorption and desorption of phosphate on allophane were investigated using NMR. • PO 4 sorption kinetics were four times faster than IHP at both pH 4 and 6. • NMR revealed initial inner-sphere complexes transforming into AlPO 4 and Al-IHP. • Formation of AlPO 4 and Al-IHP surface precipitates on allophane begins within munites of contact. • Surface precipitation of amorphous AlPO 4 and Al-IHP reduced phosphate desorption over time. Understanding the molecular-scale mechanisms of phosphate (PO 4 ) and inositol hexakisphosphate (IHP) interactions with allophane is critical for predicting phosphorus (P) retention in volcanic ash soils. This study investigated the sorption and desorption behavior of PO 4 and IHP on allophane over residence times of 60 days at pH 4 and 6, integrating macroscopic kinetics and isotherms with solid-state 31 P and 27 Al NMR spectroscopy. Allophane showed strong sorption affinity for both PO 4 and IHP, with PO 4 sorption increasing markedly at lower pH (from 0.89 mmol g −1 at pH 6 to 1.36 mmol g −1 at pH 4), while IHP sorption was less pH-dependent. Sorption followed a biphasic kinetic pattern: an initial rapid phase driven by ligand exchange, followed by a slower phase involving minor structural reorganization. PO 4 exhibited faster sorption kinetics than IHP, with rate constants nearly four times higher at both pH levels. NMR spectroscopy revealed that both PO 4 and IHP initially formed inner-sphere surface complexes on allophane, rapidly initiating surface precipitation of AlPO 4 and Al-IHP, particularly under acidic conditions, indicating that the surface precipitation processes are initiated durting the early stages of sorption. These surface precipitates became increasingly dominant with longer residence times and coincided with reduced phosphate desorption. These findings highlight the critical roles of residence time and pH in regulating PO 4 and IHP binding mechanisms on allophane, providing molecular-level insights into legacy P dynamics and substantiating allophane’s function as a long-term sink for both inorganic and organic phosphorus in Andisols.

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Publication Details

Journal
Geoderma
Published
2025-09-01
DOI
https://doi.org/10.1016/j.geoderma.2025.117488
Citations
1
Primary Topic
Phosphorus and nutrient management
Type
article
Field-Weighted Citation Impact
1.00
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article

Residence time effects on sorption and desorption mechanisms of phosphate and myo-inositol hexakisphosphate on allophane

Keiichi Noguchi, Yohey Hashimoto, T. Nakajima
1 citations
Geoderma
Phosphorus and nutrient management
1.00
article

Residence time effects on sorption and desorption mechanisms of phosphate and myo-inositol hexakisphosphate on allophane

Keiichi Noguchi, Yohey Hashimoto, T. Nakajima
article en
1 citations

Abstract

• Sorption and desorption of phosphate on allophane were investigated using NMR. • PO 4 sorption kinetics were four times faster than IHP at both pH 4 and 6. • NMR revealed initial inner-sphere complexes transforming into AlPO 4 and Al-IHP. • Formation of AlPO 4 and Al-IHP surface precipitates on allophane begins within munites of contact. • Surface precipitation of amorphous AlPO 4 and Al-IHP reduced phosphate desorption over time. Understanding the molecular-scale mechanisms of phosphate (PO 4 ) and inositol hexakisphosphate (IHP) interactions with allophane is critical for predicting phosphorus (P) retention in volcanic ash soils. This study investigated the sorption and desorption behavior of PO 4 and IHP on allophane over residence times of 60 days at pH 4 and 6, integrating macroscopic kinetics and isotherms with solid-state 31 P and 27 Al NMR spectroscopy. Allophane showed strong sorption affinity for both PO 4 and IHP, with PO 4 sorption increasing markedly at lower pH (from 0.89 mmol g −1 at pH 6 to 1.36 mmol g −1 at pH 4), while IHP sorption was less pH-dependent. Sorption followed a biphasic kinetic pattern: an initial rapid phase driven by ligand exchange, followed by a slower phase involving minor structural reorganization. PO 4 exhibited faster sorption kinetics than IHP, with rate constants nearly four times higher at both pH levels. NMR spectroscopy revealed that both PO 4 and IHP initially formed inner-sphere surface complexes on allophane, rapidly initiating surface precipitation of AlPO 4 and Al-IHP, particularly under acidic conditions, indicating that the surface precipitation processes are initiated durting the early stages of sorption. These surface precipitates became increasingly dominant with longer residence times and coincided with reduced phosphate desorption. These findings highlight the critical roles of residence time and pH in regulating PO 4 and IHP binding mechanisms on allophane, providing molecular-level insights into legacy P dynamics and substantiating allophane’s function as a long-term sink for both inorganic and organic phosphorus in Andisols.

GeodermaVol. 461
Tokyo University of Agriculture and Technology (JP)
Openalex Percentile: Top 19%
Phosphorus and nutrient management
1.00
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