4.6 Article

Phosphorus retention in constructed wetlands enhanced by zeolite- and clinopyroxene-dominated lava sand

Journal

HYDROLOGICAL PROCESSES
Volume 35, Issue 2, Pages -

Publisher

WILEY
DOI: 10.1002/hyp.14040

Keywords

filter materials; NMR spectroscopy; organic P species; P recycling; P saturation; sequential P extraction; vegetated soil filters; waste water cleaning

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Constructed wetlands are engineered systems for treating wastewater by sequestering nutrients and contaminants. Research on the phosphorus binding states in operating CWs found that organic and inorganic phosphorus accumulated in all CWs regardless of filter materials, with orthophosphate being the dominant pool. Different filter materials showed varying associations with phosphorus, suggesting potential for P recycling. Oxalate extractions indicated a dominance of P fractions associated with poorly crystalline Fe- and Al-(oxy)hydroxides, which might have high desorption capacity.
Constructed wetlands (CWs) are engineered systems for treating wastewater by sequestering nutrients and contaminants. Our aim was to assess the main phosphorus (P) binding states in operating CWs to assess P saturation and indications on P recycling potential of filter materials, which might be necessary under future peak P scenarios. The investigated vertical flow CWs (operation time up to 16 years) are based on either fluviatile (Fluv) sand or zeolite- (Ze-LS) and clinopyroxene (Cl-LS)-dominated lava sand. Organic and inorganic P accumulated in all CWs independent of filter materials and showed a considerable increase with operation time. Concentrations of P decreased sharply with depth in the Fluv-CWs compared to only a slight decrease in the lava sand CWs, with P concentrations of deeper horizons approximating the relatively P enriched original lava sand substrates. Orthophosphate was the dominant pool in all CWs, while the sum of organic fractions ranged between 11% and 33%. Sequential extraction indicated that P was mainly associated with Fe and Al (hydr)oxides for Fluv-CWs and Ze-LS-CWs, while Ca and Mg bound mineral phosphates dominated in Cl-LS-CWs. Oxalate extractions pointed to a clear dominance of P fractions associated with poorly crystalline Fe- and Al-(oxy)hydroxides. Solution P-31 NMR analyses revealed that inositol hexakisphosphates were a major pool of organic P in surface layers of CWs, which increased with operation time. With a maximum of 0.5% P content, filter sands do not appear to be a suitable fertilizer for direct application to agricultural fields. The dominance of inorganic, poorly crystalline P species point to potentially high desorption capacity which might be investigated further, to assess recycling potential of P or usage of filter materials as soil amendments with relatively high plant available P. The latter might become feasible and economically attractive under future P scarcity. Simultaneously, P saturation indexes (DPS) did not indicate an imminent P saturation of filters, since P accumulation was not restricted by binding to Al and Fe minerals.

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