Abstract
The ammonia nitrogen (NH4+-N) in the biogas liquid is exposing serious ecological risks to the environment. Electrochemical membrane processes have the advantages of high efficiency and environmental sustainability in treating NH4+-N. However, precisely designing the efficient catalytic interface is difficult, and the mechanism and the path of NH4+-N removal are unclear. To address this issue, this study designed a highly cross-linked structure oxidized carbon nanotube/polypyrrole (OCNT–PPy) electrical membrane by precisely controlling the polymerization time (optimization for 60 min), minimizing interfacial electron transfer resistance, and achieving excellent electrochemical performance. The prepared OCNT-PPy electrical membrane with applied 3 V achieved 99% NH4+-N removal within 20 min, 3 times higher than the 0 V OCNT-PPy group. Mechanism analysis revealed that hydroxyl radicals (•OH) and active chlorine synergistically contributed to the removal of NH4+-N, and most of NH4+-N (about 71.35%) was oxidized into nitrogen gas (N2). Furthermore, the OCNT-PPy electrical membrane with 3 V was used to directly treat the diluted actual fermentation biogas liquid. The permeation flux increased by 67%, and the total organic carbon (TOC) enhanced removal of 11.2%, and the fluorescent organic substances were completely removed compared with the 0 V group. This work developed a scalable and high-efficiency electrochemical membrane platform for high-efficiency NH4+-N removal of biogas liquid and provided a new inspiration for the precise design of the catalytic reaction interface.
| Original language | English |
|---|---|
| Article number | 125677 |
| Journal | Journal of Membrane Science |
| Volume | 754 |
| DOIs | |
| State | Published - Jul 2026 |
Keywords
- Ammonia nitrogen (NH-N) removal
- Biogas liquid treatment
- Electrochemical membrane
- Membrane fouling control
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