4.7 Article

Sewage sludge valorisation by hydrothermal carbonization: A new method to enhance nitrogen removal in hydrochar catalyzed with Ni-Mg-Al layered double oxides

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JOURNAL OF CLEANER PRODUCTION
卷 386, 期 -, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.jclepro.2023.135880

关键词

Sludge; Layered double hydroxides; Layered double oxides; Hydrothermal carbonization; Nitrogen removal

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Hydrothermal carbonization is an effective method to treat sludge, but the high nitrogen content in the sludge hydrochar causes environmental pollution. This study used layered double oxides (LDO) catalysts to catalytically remove nitrogen during hydrothermal carbonization. The LDO catalysts significantly improved nitrogen removal, achieving more than 57.00% at 240 degrees C. Additionally, by adjusting the metal ratio of the catalysts, the acid-base sites could be modified to produce low nitrogen hydrochar.
Hydrothermal carbonization is a technology that can quickly treat sludge. However, the high nitrogen content of the sludge hydrochar will produce NOx and pollute the environment, which influences the utilization of hydrochar as a fuel. Therefore, the calcined Ni-Al and Ni-Mg-Al layered double hydroxides (LDH) catalyst, named layered double oxides (LDO), were used for catalytic nitrogen removal during hydrothermal carbonization. Compared with the sample without catalyst, the layered double oxides catalyst showed excellent nitrogen removal capability, which can reach more than 57.00% at 240 degrees C. LDH catalyst enhanced the destruction of sludge structure to effectively realize the transfer of nitrogen-containing substances from solid phase to aqueous phase, which decreased the content of organic-N in hydrochar and increased the content of ammonia nitrogen and total nitrogen in aqueous phase to 4184 and 6463 mg/L, respectively with Ni-Mg-Al LDO at 240 degrees C. Moreover, this study also adjusted the acid-base sites by changing the metal ratio of catalysts, which was the key to produce the low nitrogen hydrochar. The acid sites were beneficial to inhibit the Maillard reaction and the basic sites can promote the decomposition of extracellular polymer (EPS). The possible removal pathways were proposed in this study.

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