Denitrification and desulphurization of industrial biowastes via hydrothermal modification

•Hydro-char was solid fuels with less nitrogen and sulfur contents.•At most 60% of N and 70% of S were removed from solid phase after modified.•Liquid phase could enrich most of N and S in form of ionic-N and -S respectively.•Conversion pathways of N and S during hydrothermal process was provided. I...

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Published inBioresource technology Vol. 254; pp. 121 - 129
Main Authors Zhuang, Xiuzheng, Zhan, Hao, Huang, Yanqin, Song, Yanpei, Yin, Xiuli, Wu, Chuangzhi
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.04.2018
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Summary:•Hydro-char was solid fuels with less nitrogen and sulfur contents.•At most 60% of N and 70% of S were removed from solid phase after modified.•Liquid phase could enrich most of N and S in form of ionic-N and -S respectively.•Conversion pathways of N and S during hydrothermal process was provided. In attempt to decrease NOX and SO2 emission from thermochemical utilization, three industrial biowastes (penicillin mycelia waste, sewage sludge and peat waste) contained high nitrogen (N) and sulfur (S) were chosen to investigate the denitrification and desulphurization of hydrothermal modification. The results demonstrated that hydrothermal modification destroyed the structure of N- and S-containing components, thereby altering their existed conformations. Inorganic-N (N-IN) and most of amino-N/polyamide-N (N-A) were enriched by liquid phase in the forms of NH4+-N and soluble organic-N (Org-N), respectively; subsequently, Org-N could further decompose to NH4+-N at higher temperature. Residual N in hydrochars was converted from N-A to heterocyclic-N (pyrrolic-N, pyridinic-N and quaternary-N) via hydrolysis and cyclization. Similarly, over 60% of S was remove form biowastes at 240 °C. In solid phase, part of organic-S was altered to thiophenes-S after modified, while the remainder was transformed to inorganic-S; but the variation of inorganic-S in hydrochars strongly affected by its specific species.
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ISSN:0960-8524
1873-2976
DOI:10.1016/j.biortech.2018.01.061