4.7 Article

Ammonium removal and recovery from effluent of AnMBR treating real domestic wastewater using polymeric hydrogel

Journal

SEPARATION AND PURIFICATION TECHNOLOGY
Volume 296, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.seppur.2022.121376

Keywords

Anaerobic membrane bioreactor; Adsorption; Ammonium-nitrogen; Desorption; Poly (acrylic acid) hydrogel; Resource recovery

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This study proposes the use of poly (acrylic acid) hydrogel as a post-treatment method for AnMBRs to remove and recover NH4+-N, thus promoting the circular economy and the adoption of AnMBR technology. The results show that PAA hydrogels have excellent adsorption capacities for NH4+-N and can be regenerated multiple times with minimal decline in adsorption capacity. The use of a strategic recirculation of HCl solution as an eluent also shows promise in concentrating NH4+-N as resources. Economically, the PAA hydrogel-based adsorption/desorption process coupled with eluent recirculation is cost-effective for removing and recovering NH4+-N from AnMBR effluent. Overall, this study has the potential to expand the application of AnMBRs and contribute to innovations in sustainable wastewater treatment.
Anaerobic membrane bioreactor (AnMBR) technology has been considered promising to transform domestic wastewater (DWW) treatment as a net energy producer via bioenergy recovery. However, ammonium-nitrogen (NH4+-N) in DWW cannot be removed by anaerobic process, which raises the risk of eutrophication and prevents the wide-scale adoption of AnMBRs. This study proposed adsorption/desorption by poly (acrylic acid) (PAA) hydrogel as the post-treatment of AnMBRs to remove and recover NH4+-N, thus simultaneously promoting AnMBR technology and the circular economy. Batch experiment results showed that NH4+-N could be rapidly adsorbed by PAA hydrogels within 30 min with excellent maximum adsorption capacities of 110.6-120.8 mg N/L (10-50 degrees C). Furthermore, PAA hydrogels retained 81.1 % of NH4+-N adsorption capacity when treating AnMBR effluent, preliminarily suggesting their practical feasibility in complex water matrix. Thereafter, PAA hydrogels were packed into a bench-scale fixed-bed column. Up to 98.5% of NH4+-N in AnMBR effluent could be captured in the hydrogel column at the breakthrough point at flow rate of 0.5 mL/min, achieving a polished effluent concentration of <1.5 mg N/L and thus meeting the strictest discharge regulations. The hydrogel column could be regenerated for 10 adsorption/desorption cycles with an insignificant decline in adsorption capacity of -4.7%, highlighting its excellent reusability. More importantly, we for the first time proposed the strategic recirculation of 1 mol/l HCl solution as eluent and obtained an NH4+-N enrichment factor of -10 over four rounds of adsorption/desorption, demonstrating the promise of this strategy to concentrate NH4+-N as resources. The economic analysis based on our experimental results showed that PAA hydrogel-based adsorption/desorption process coupled with eluent recirculation has the potential to remove and recover NH4+-N from AnMBR effluent cost-effectively. Overall, this study could potentially expand the application of AnMBRs and foster innovations in sustainable wastewater treatment.

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