Removal of ammonium-nitrogen from groundwater using a fully passive permeable reactive barrier with oxygen-releasing compound and clinoptilolite.

A novel fully passive permeable reactive barrier (PRB) with oxygen-releasing compound (ORC) and clinoptilolite was proposed for the removal of ammonium-nitrogen from groundwater. The PRB involves a combination of oxygen release, biological nitrification, ion exchange, and bioregeneration. A pilot-scale performance comparison experiment was carried out employing three parallel columns to assess the proposed PRB. The results showed that the PRB achieved nearly complete [Formula: see text] depletion (>99%). [Formula: see text] of 5.23-10.88 mg/L was removed, and [Formula: see text] of <1.93 mg/L and [Formula: see text] of 2.03-19.67 mg/L were generated. Ion exchange and biological nitrification both contributed to [Formula: see text] removal, and the latter played a dominant role under the condition of sufficient oxygen. Biological nitrification favored a delay in sorption saturation and a release of exchange sites. The ORC could sufficiently, efficiently supply oxygen for approximately 120 pore volumes. The clinoptilolite ensured a robust [Formula: see text] removal in case of temporary insufficient biological activities. No external alkalinity sources had to be supplied and no inhibition of aerobic metabolism occurred. The ceramicite had a negligible effect on the biomass growth. Based on the research findings, a full-scale continuous wall PRB was installed in Shenyang, China in 2012.

Ammonium-nitrogen-contaminated groundwater remediation by a sequential three-zone permeable reactive barrier (multibarrier) with oxygen-releasing compound (ORC)/clinoptilolite/spongy iron: column studies.

A novel sequential permeable reactive barrier (multibarrier), composed of oxygen-releasing compound (ORC)/clinoptilolite/spongy iron zones in series, was proposed for ammonium-nitrogen-contaminated groundwater remediation. Column experiments were performed to: (1) evaluate the overall NH4(+)-N removal performance of the proposed multibarrier, (2) investigate nitrogen transformation in the three zones, (3) determine the reaction front progress, and (4) explore cleanup mechanisms for inorganic nitrogens. The results showed that NH4 (+)-N percent removal by the multibarrier increased up to 90.43 % after 21 pore volumes (PVs) at the influent dissolved oxygen of 0.68∼2.45 mg/L and pH of 6.76∼7.42. NH4(+)-N of 4.06∼10.49 mg/L was depleted and NOx(-)-N (i.e., NO3 (-)-N + NO2(-)-N) of 4.26∼9.63 mg/L was formed before 98 PVs in the ORC zone. NH4(+)-N of ≤4.76 mg/L was eliminated in the clinoptilolite zone. NOx(-)-N of 10.44∼12.80 mg/L was lost before 21 PVs in the spongy iron zone. The clinoptilolite zone length should be reduced to 30 cm. Microbial nitrification played a dominant role in NH4(+)-N removal in the ORC zone. Ion exchange was majorly responsible for NH4(+)-N elimination in the clinoptilolite zone. Chemical reduction and hydrogenotrophic denitrification both contributed to NOx(-)-N transformation, but the chemical reduction capacity decreased after 21 PVs in the spongy iron.

Ammonium removal from groundwater using a zeolite permeable reactive barrier: a pilot-scale demonstration.

In situ remediation of ammonium-contaminated groundwater is possible through a zeolite permeable reactive barrier (PRB); however, zeolite's finite sorption capacity limits the long-term field application of PRBs. In this paper, a pilot-scale PRB was designed to achieve sustainable use of zeolite in removing ammonium (NH(4)(+)-N) through sequential nitrification, adsorption, and denitrification. An oxygen-releasing compound was added to ensure aerobic conditions in the upper layers of the PRB where NH(4)(+)-N was microbially oxidized to nitrate. Any remaining NH(4)(+)-N was removed abiotically in the zeolite layer. Under lower redox conditions, nitrate formed during nitrification was removed by denitrifying bacteria colonizing the zeolite. During the long-term operation (328 days), more than 90% of NH(4)(+)-N was consistently removed, and approximately 40% of the influent NH(4)(+)-N was oxidized to nitrate. As much as 60% of the nitrate formed in the PRB was reduced in the zeolite layer after 300 days of operation. Removal of NH(4)(+)-N from groundwater using a zeolite PRB through bacterial nitrification and abiotic adsorption is a promising approach. The zeolite PRB has the advantage of achieving sustainable use of zeolite and immediate NH(4)(+)-N removal.