期刊
CHEMOSPHERE
卷 303, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2022.134986
关键词
Leachate membrane retentate; Advanced oxidation; Eletrochemical oxidation; Electro-coagulation; Performance
资金
- Science and Technology Department of Sichuan Province [2021YFS0290]
- China Postdoctoral Science Foundation [2021M701027]
- Open Fund of Sichuan Provincial Engineering Research Center of City Solid Waste Energy and Buliding Materials Conversion and Utilization Technology [GF2022ZD004]
This study compared the performances of electrochemical oxidation (EO) and electro-coagulation (EC) technology on the treatment of leachate membrane retentate (LMR). The results showed that EO had better removal efficiency for organic carbon, UV absorption, and chromaticity, while EC had better removal efficiency for ammonia nitrogen and total nitrogen. Additionally, EO showed better performance in decomposing dissolved organic matter with complicated structures.
With the widespread use of membrane in advanced treatment of leachate, China produces a large amount of leachate membrane retentate (LMR) (asymptotic to 23.4 million tons) annually, which is usually treated by incineration or recirculation in engineering, but these technologies have many drawbacks. LMR is suitable for electrochemical treatment due to its high electrical conductivity. This study compared the performances of electrochemical oxidation (EO) and electro-coagulation (EC) technology on LMR treatment under different experimental conditions, including anode material, current density, initial pH and reaction time. We found that EO optimal conditions achieved 70.1%, 83.1%, 78.7%, 98.7%, and 69.7% removal of total organic carbon (TOC), UV absorption (at 254 nm), chromaticity, ammonia nitrogen (NH3-N), and total nitrogen (TN), respectively. Compared with EO, EC exhibited a similar removal ability for orgainics and better removals of chroma, but much less performance for removing nitrogen pollutants in the same reaction time, that is, removals of NH3-N and TN were only 31.5% and 36.2%, respectively. Meanwhile, EC showed much higher instantaneous current efficiency of COD than EO under its optimal reaction time (120 min). In addition, the UV-Vis spectra and 3D fluorescence spectra indicated that EO exhibited relatively outstanding performance in decomposing dissolved organic matter (DOM) with rather complicated structures than EC. Also, the flow field-flow fractionation technique demonstrated that EO preferentially destroy humic-like, large molecular weight DOM, and converting them to smaller
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