Enhancing the phosphorus content of layered double hydroxide fertilizers by intercalating polymeric phosphate instead
Maarten Everaert1, Fien Degryse2, Mike J McLaughlin2
1Division of Soil and Water Management, Department of Earth and Environmental Science, KU Leuven, Kasteelpark Arenberg 20, B-3001 Heverlee, Belgium.
Hypothesis:
Layered double hydroxide (LDH) loaded with orthophosphate (PO4) are suggested as slow-release P fertilizers. However, PO4-LDHs have a low maximal P content, related to high charge HPO42-/PO43- anions occupying the anion exchange capacity (AEC) of LDHs. We postulate that the P content of LDHs can be enhanced by exchanging them with polymeric-P (i.e. trimetaphosphate, P3O9), which has a lower molar charge/P ratio than its monomer.
Experiments:
Adsorption capacities were compared between PO4 and P3O9 for as-synthesized and calcined MgAl LDHs with Mg/Al ratio of 2, 3, or 4; the P-LDHs were characterized (XRD, FTIR). Dialysis and soil incubation experiments were performed with PO4-LDHs, P3O9-LDHs, and corresponding soluble fertilizers to compare their P release and P solubility (CaCl2 extract).
Findings:
The P adsorption capacities were 1.25-1.60 fold larger for P3O9 compared to PO4, yet the high theoretical P contents with P3O9 were not achieved (incomplete loading, P3O9 depolymerization). P3O9-Mg3Al released polymeric-P whereas P3O9-Mg2Al released depolymerized PO4, and P release from P3O9-LDHs was slower than that of PO4-LDHs. With soil incubation, soluble P from P3O9-LDH was initially lower but later converged to that of PO4-LDH as result of continued hydrolysis, yet did not exceed that of the soluble P3O9 and PO4 fertilizers.
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