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In Situ Capturing and Absorption of Sulfur Gases Formed during Thermal Treatment of South African Coals

[Image: see text] The objective of this study, the first of its kind on these specific South African low-sulfur coals, was to capture H(2)S and SO(2) produced under inert and oxidizing conditions from sulfur compounds present in the coals. The capturing agents were calcium and magnesium oxides forme...

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Autores principales: Matjie, Ratale H., Lesufi, Jeanett M., Bunt, John R., Strydom, Christien A., Schobert, Harold H., Uwaoma, Romanus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645234/
https://www.ncbi.nlm.nih.gov/pubmed/31458111
http://dx.doi.org/10.1021/acsomega.8b01359
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author Matjie, Ratale H.
Lesufi, Jeanett M.
Bunt, John R.
Strydom, Christien A.
Schobert, Harold H.
Uwaoma, Romanus
author_facet Matjie, Ratale H.
Lesufi, Jeanett M.
Bunt, John R.
Strydom, Christien A.
Schobert, Harold H.
Uwaoma, Romanus
author_sort Matjie, Ratale H.
collection PubMed
description [Image: see text] The objective of this study, the first of its kind on these specific South African low-sulfur coals, was to capture H(2)S and SO(2) produced under inert and oxidizing conditions from sulfur compounds present in the coals. The capturing agents were calcium and magnesium oxides formed during the transformation of calcite and dolomite. The effectiveness of two different scrubbing solutions (0.15 M cadmium acetate and 1.1 M potassium hydroxide) for absorption of volatilized H(2)S and SO(2) was also investigated. The bituminous coal (coal A) contained dolomite, calcite, pyrite, and organic sulfur. Lignite (coal B) had a high organic sulfur content and contained gypsum, no or low dolomite and pyrite contents, and no calcite. A third sample (coal C) was prepared by adding 5 wt % potassium carbonate to coal A. Under oxidizing conditions and at elevated temperatures, FeS(2) produced Fe(2)O(3), FeO, and SO(2). It transformed to FeS and released H(2)S under inert conditions. Organic sulfur interacted with organically bound calcium and magnesium at 400 °C in an inert atmosphere to form calcium sulfate and oldhamite ((Ca,Mg)S). CaO, produced from calcite or dolomite, reacted with SO(2) and O(2) at 950 °C to form calcium sulfate. Treatment of lignite at 400–950 °C resulted in 96–98% evolution of sulfur as gases. Hydrogen sulfide formation increased with the increasing thermal treatment temperature under inert conditions for the three coals. Under oxidizing conditions, sulfur dioxide formation decreased with the increasing temperature when heating coals B and C. The lowest ratio (0.01) of H(2)S to SO(2) was achieved during thermal treatment of the blend of coal and potassium carbonate (coal C), implying that almost all of sulfur was retained in the coal C ash/char samples. In situ capturing of sulfur gases by CaO and MgO and by the added K(2)CO(3) in coal C to form calcium/magnesium/potassium sulfates and potassium/calcium/magnesium aluminosilicate glasses during utilization of these and similar coals could reduce the percentage of sulfur volatilized from the coals by 54–100%, thereby potentially decreasing their impact on the environment.
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spelling pubmed-66452342019-08-27 In Situ Capturing and Absorption of Sulfur Gases Formed during Thermal Treatment of South African Coals Matjie, Ratale H. Lesufi, Jeanett M. Bunt, John R. Strydom, Christien A. Schobert, Harold H. Uwaoma, Romanus ACS Omega [Image: see text] The objective of this study, the first of its kind on these specific South African low-sulfur coals, was to capture H(2)S and SO(2) produced under inert and oxidizing conditions from sulfur compounds present in the coals. The capturing agents were calcium and magnesium oxides formed during the transformation of calcite and dolomite. The effectiveness of two different scrubbing solutions (0.15 M cadmium acetate and 1.1 M potassium hydroxide) for absorption of volatilized H(2)S and SO(2) was also investigated. The bituminous coal (coal A) contained dolomite, calcite, pyrite, and organic sulfur. Lignite (coal B) had a high organic sulfur content and contained gypsum, no or low dolomite and pyrite contents, and no calcite. A third sample (coal C) was prepared by adding 5 wt % potassium carbonate to coal A. Under oxidizing conditions and at elevated temperatures, FeS(2) produced Fe(2)O(3), FeO, and SO(2). It transformed to FeS and released H(2)S under inert conditions. Organic sulfur interacted with organically bound calcium and magnesium at 400 °C in an inert atmosphere to form calcium sulfate and oldhamite ((Ca,Mg)S). CaO, produced from calcite or dolomite, reacted with SO(2) and O(2) at 950 °C to form calcium sulfate. Treatment of lignite at 400–950 °C resulted in 96–98% evolution of sulfur as gases. Hydrogen sulfide formation increased with the increasing thermal treatment temperature under inert conditions for the three coals. Under oxidizing conditions, sulfur dioxide formation decreased with the increasing temperature when heating coals B and C. The lowest ratio (0.01) of H(2)S to SO(2) was achieved during thermal treatment of the blend of coal and potassium carbonate (coal C), implying that almost all of sulfur was retained in the coal C ash/char samples. In situ capturing of sulfur gases by CaO and MgO and by the added K(2)CO(3) in coal C to form calcium/magnesium/potassium sulfates and potassium/calcium/magnesium aluminosilicate glasses during utilization of these and similar coals could reduce the percentage of sulfur volatilized from the coals by 54–100%, thereby potentially decreasing their impact on the environment. American Chemical Society 2018-10-26 /pmc/articles/PMC6645234/ /pubmed/31458111 http://dx.doi.org/10.1021/acsomega.8b01359 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Matjie, Ratale H.
Lesufi, Jeanett M.
Bunt, John R.
Strydom, Christien A.
Schobert, Harold H.
Uwaoma, Romanus
In Situ Capturing and Absorption of Sulfur Gases Formed during Thermal Treatment of South African Coals
title In Situ Capturing and Absorption of Sulfur Gases Formed during Thermal Treatment of South African Coals
title_full In Situ Capturing and Absorption of Sulfur Gases Formed during Thermal Treatment of South African Coals
title_fullStr In Situ Capturing and Absorption of Sulfur Gases Formed during Thermal Treatment of South African Coals
title_full_unstemmed In Situ Capturing and Absorption of Sulfur Gases Formed during Thermal Treatment of South African Coals
title_short In Situ Capturing and Absorption of Sulfur Gases Formed during Thermal Treatment of South African Coals
title_sort in situ capturing and absorption of sulfur gases formed during thermal treatment of south african coals
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645234/
https://www.ncbi.nlm.nih.gov/pubmed/31458111
http://dx.doi.org/10.1021/acsomega.8b01359
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