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Sulphur transformation during pyrolysis of an Australian lignite.

Authors :
Zhang, Dongke
Yani, Setyawati
Source :
Proceedings of the Combustion Institute; Jul2011, Vol. 33 Issue 2, p1747-1753, 7p
Publication Year :
2011

Abstract

Abstract: Transformation of various sulphur forms, including inherent and added pyrite, sulphates (CaSO<subscript>4</subscript> and FeSO<subscript>4</subscript>) and organic sulphur, during pyrolysis of an Australian lignite was studied using TGA, TGA-MS and a fixed bed reactor, supplemented by sulphur form analysis. It was shown that hydrogen sulphide (H<subscript>2</subscript>S) and a small quantity of sulphur dioxide (SO<subscript>2</subscript>) were released during the pyrolysis of the pyrite-lignite blend. However, only SO<subscript>2</subscript> was detected during the pyrolysis of the lignite with high pyrite content. Inorganic matter was found to help retaining some of the inorganic sulphur, including pyrite, in the char. Inherent sulphates decomposed at much lower temperatures than the added sulphates, releasing SO<subscript>2</subscript> rather than H<subscript>2</subscript>S. The inherent sulphates in the lignite were dominated by iron sulphates which started to decompose and release SO<subscript>2</subscript> at around 500K and all sulphate had been decomposed at 1073K. The retention of organic sulphur in the high organic sulphur lignite was higher than in its acid washed lignite sample, due to the interaction between inherent inorganic matter with the organic sulphur retaining the organic sulphur in the solid phase. SO<subscript>2</subscript> was the only sulphur gas produced during pyrolysis of acid washed lignite. A comprehensive mechanism of sulphur transformation during pyrolysis of lignite was proposed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15407489
Volume :
33
Issue :
2
Database :
Supplemental Index
Journal :
Proceedings of the Combustion Institute
Publication Type :
Academic Journal
Accession number :
57142071
Full Text :
https://doi.org/10.1016/j.proci.2010.07.074