Assessment of Metal Impurity Partitioning and Speciation in Mineral Carbonation Processes Using FGD-Gypsum from Coal-Fired Power Plants under Distinct Operating Conditions
The sequestration of carbon dioxide (CO2) stands as a profoundly pivotal environmental challenge, given its potential to directly contribute to the advancement of environmental, societal, and economic objectives across a multitude of nations. In the present study, we have conducted an evaluation of...
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Published in | ACS omega Vol. 9; no. 33; pp. 35906 - 35919 |
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Language | English |
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Abstract | The sequestration of carbon dioxide (CO2) stands as a profoundly pivotal environmental challenge, given its potential to directly contribute to the advancement of environmental, societal, and economic objectives across a multitude of nations. In the present study, we have conducted an evaluation of the metal impurity partitioning and speciation in mineral carbonation processes conducted in laboratory using flue gas desulfurization (FGD) gypsums originating from both Spanish and two Chinese coal-fired power plants, each subject to distinct fuel sources and FGD operational conditions. Of the three resultant carbonation products, two exhibited CaCO3 content in the range of 81–83%, while the third registered 76.9% CaCO3 contenta variance attributed to the occurrence of metallic impurities within the initial FGD-gypsum. The partitioning and speciation of metal impurities at all stages of CO2 conversion have enabled us to proffer four potential reaction mechanisms governing carbonation efficiency: (i) conversion of metal sulfates to metal carbonate complexes, (ii) transformation of transferable elements into metal oxides and oxyhydroxide complexes, (iii) transformation of metal sulfates into diverse metal complexes, and (iv) diverse pathways of elemental transformation. Metal impurities present in FGD-gypsum lead to the formation of complexes between As and metals, thereby affecting their activity. Higher Ca/Mn, Ca/Fe, and Ca/Al ratios in one FGD-gypsum slurry enhance Ca3(AsO4)2·8H2O activity, while in another, excess Ca facilitates Mn3(AsO4)2·8H2O formation during carbonation, with coprecipitation retaining As in carbonation products. The occurrence of metallic contaminants in FGD-gypsums may exert a substantial influence on the effectiveness of CO2 conversion, thereby impacting the feasibility of using resultant carbonation products, with potential implications for environmental leaching and diminished reusability prospects. |
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AbstractList | The sequestration of carbon dioxide (CO
2
)
stands as
a profoundly pivotal environmental challenge, given its potential
to directly contribute to the advancement of environmental, societal,
and economic objectives across a multitude of nations. In the present
study, we have conducted an evaluation of the metal impurity partitioning
and speciation in mineral carbonation processes conducted in laboratory
using flue gas desulfurization (FGD) gypsums originating from both
Spanish and two Chinese coal-fired power plants, each subject to distinct
fuel sources and FGD operational conditions. Of the three resultant
carbonation products, two exhibited CaCO
3
content in the
range of 81–83%, while the third registered 76.9% CaCO
3
content—a variance attributed to the occurrence of
metallic impurities within the initial FGD-gypsum. The partitioning
and speciation of metal impurities at all stages of CO
2
conversion have enabled us to proffer four potential reaction mechanisms
governing carbonation efficiency: (i) conversion of metal sulfates
to metal carbonate complexes, (ii) transformation of transferable
elements into metal oxides and oxyhydroxide complexes, (iii) transformation
of metal sulfates into diverse metal complexes, and (iv) diverse pathways
of elemental transformation. Metal impurities present in FGD-gypsum
lead to the formation of complexes between As and metals, thereby
affecting their activity. Higher Ca/Mn, Ca/Fe, and Ca/Al ratios in
one FGD-gypsum slurry enhance Ca
3
(AsO
4
)
2
·8H
2
O activity, while in another, excess Ca
facilitates Mn
3
(AsO
4
)
2
·8H
2
O formation during carbonation, with coprecipitation retaining
As in carbonation products. The occurrence of metallic contaminants
in FGD-gypsums may exert a substantial influence on the effectiveness
of CO
2
conversion, thereby impacting the feasibility of
using resultant carbonation products, with potential implications
for environmental leaching and diminished reusability prospects. The sequestration of carbon dioxide (CO ) stands as a profoundly pivotal environmental challenge, given its potential to directly contribute to the advancement of environmental, societal, and economic objectives across a multitude of nations. In the present study, we have conducted an evaluation of the metal impurity partitioning and speciation in mineral carbonation processes conducted in laboratory using flue gas desulfurization (FGD) gypsums originating from both Spanish and two Chinese coal-fired power plants, each subject to distinct fuel sources and FGD operational conditions. Of the three resultant carbonation products, two exhibited CaCO content in the range of 81-83%, while the third registered 76.9% CaCO content-a variance attributed to the occurrence of metallic impurities within the initial FGD-gypsum. The partitioning and speciation of metal impurities at all stages of CO conversion have enabled us to proffer four potential reaction mechanisms governing carbonation efficiency: (i) conversion of metal sulfates to metal carbonate complexes, (ii) transformation of transferable elements into metal oxides and oxyhydroxide complexes, (iii) transformation of metal sulfates into diverse metal complexes, and (iv) diverse pathways of elemental transformation. Metal impurities present in FGD-gypsum lead to the formation of complexes between As and metals, thereby affecting their activity. Higher Ca/Mn, Ca/Fe, and Ca/Al ratios in one FGD-gypsum slurry enhance Ca (AsO ) ·8H O activity, while in another, excess Ca facilitates Mn (AsO ) ·8H O formation during carbonation, with coprecipitation retaining As in carbonation products. The occurrence of metallic contaminants in FGD-gypsums may exert a substantial influence on the effectiveness of CO conversion, thereby impacting the feasibility of using resultant carbonation products, with potential implications for environmental leaching and diminished reusability prospects. The sequestration of carbon dioxide (CO2) stands as a profoundly pivotal environmental challenge, given its potential to directly contribute to the advancement of environmental, societal, and economic objectives across a multitude of nations. In the present study, we have conducted an evaluation of the metal impurity partitioning and speciation in mineral carbonation processes conducted in laboratory using flue gas desulfurization (FGD) gypsums originating from both Spanish and two Chinese coal-fired power plants, each subject to distinct fuel sources and FGD operational conditions. Of the three resultant carbonation products, two exhibited CaCO3 content in the range of 81-83%, while the third registered 76.9% CaCO3 content-a variance attributed to the occurrence of metallic impurities within the initial FGD-gypsum. The partitioning and speciation of metal impurities at all stages of CO2 conversion have enabled us to proffer four potential reaction mechanisms governing carbonation efficiency: (i) conversion of metal sulfates to metal carbonate complexes, (ii) transformation of transferable elements into metal oxides and oxyhydroxide complexes, (iii) transformation of metal sulfates into diverse metal complexes, and (iv) diverse pathways of elemental transformation. Metal impurities present in FGD-gypsum lead to the formation of complexes between As and metals, thereby affecting their activity. Higher Ca/Mn, Ca/Fe, and Ca/Al ratios in one FGD-gypsum slurry enhance Ca3(AsO4)2·8H2O activity, while in another, excess Ca facilitates Mn3(AsO4)2·8H2O formation during carbonation, with coprecipitation retaining As in carbonation products. The occurrence of metallic contaminants in FGD-gypsums may exert a substantial influence on the effectiveness of CO2 conversion, thereby impacting the feasibility of using resultant carbonation products, with potential implications for environmental leaching and diminished reusability prospects.The sequestration of carbon dioxide (CO2) stands as a profoundly pivotal environmental challenge, given its potential to directly contribute to the advancement of environmental, societal, and economic objectives across a multitude of nations. In the present study, we have conducted an evaluation of the metal impurity partitioning and speciation in mineral carbonation processes conducted in laboratory using flue gas desulfurization (FGD) gypsums originating from both Spanish and two Chinese coal-fired power plants, each subject to distinct fuel sources and FGD operational conditions. Of the three resultant carbonation products, two exhibited CaCO3 content in the range of 81-83%, while the third registered 76.9% CaCO3 content-a variance attributed to the occurrence of metallic impurities within the initial FGD-gypsum. The partitioning and speciation of metal impurities at all stages of CO2 conversion have enabled us to proffer four potential reaction mechanisms governing carbonation efficiency: (i) conversion of metal sulfates to metal carbonate complexes, (ii) transformation of transferable elements into metal oxides and oxyhydroxide complexes, (iii) transformation of metal sulfates into diverse metal complexes, and (iv) diverse pathways of elemental transformation. Metal impurities present in FGD-gypsum lead to the formation of complexes between As and metals, thereby affecting their activity. Higher Ca/Mn, Ca/Fe, and Ca/Al ratios in one FGD-gypsum slurry enhance Ca3(AsO4)2·8H2O activity, while in another, excess Ca facilitates Mn3(AsO4)2·8H2O formation during carbonation, with coprecipitation retaining As in carbonation products. The occurrence of metallic contaminants in FGD-gypsums may exert a substantial influence on the effectiveness of CO2 conversion, thereby impacting the feasibility of using resultant carbonation products, with potential implications for environmental leaching and diminished reusability prospects. The sequestration of carbon dioxide (CO2) stands as a profoundly pivotal environmental challenge, given its potential to directly contribute to the advancement of environmental, societal, and economic objectives across a multitude of nations. In the present study, we have conducted an evaluation of the metal impurity partitioning and speciation in mineral carbonation processes conducted in laboratory using flue gas desulfurization (FGD) gypsums originating from both Spanish and two Chinese coal-fired power plants, each subject to distinct fuel sources and FGD operational conditions. Of the three resultant carbonation products, two exhibited CaCO3 content in the range of 81–83%, while the third registered 76.9% CaCO3 contenta variance attributed to the occurrence of metallic impurities within the initial FGD-gypsum. The partitioning and speciation of metal impurities at all stages of CO2 conversion have enabled us to proffer four potential reaction mechanisms governing carbonation efficiency: (i) conversion of metal sulfates to metal carbonate complexes, (ii) transformation of transferable elements into metal oxides and oxyhydroxide complexes, (iii) transformation of metal sulfates into diverse metal complexes, and (iv) diverse pathways of elemental transformation. Metal impurities present in FGD-gypsum lead to the formation of complexes between As and metals, thereby affecting their activity. Higher Ca/Mn, Ca/Fe, and Ca/Al ratios in one FGD-gypsum slurry enhance Ca3(AsO4)2·8H2O activity, while in another, excess Ca facilitates Mn3(AsO4)2·8H2O formation during carbonation, with coprecipitation retaining As in carbonation products. The occurrence of metallic contaminants in FGD-gypsums may exert a substantial influence on the effectiveness of CO2 conversion, thereby impacting the feasibility of using resultant carbonation products, with potential implications for environmental leaching and diminished reusability prospects. |
Author | Córdoba, Patricia |
AuthorAffiliation | Institute of Environmental Assessment and Water Research (IDÆA-CSIC), Spanish National Research Council |
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Author_xml | – sequence: 1 givenname: Patricia orcidid: 0000-0003-0596-4354 surname: Córdoba fullname: Córdoba, Patricia email: patricia.cordoba@idaea.csic.es |
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References | ref9/cit9 ref6/cit6 ref3/cit3 ref27/cit27 ref18/cit18 Gutberlet H. (ref45/cit45) 1988; 68 Parkhurst D. L. (ref36/cit36) 1999 ref11/cit11 ref25/cit25 ref16/cit16 ref29/cit29 ref43/ref43_1 ref32/cit32 ref23/cit23 ref39/cit39 ref14/cit14 ref8/cit8 ref5/cit5 ref31/cit31 ref2/cit2 Rumble J. R. (ref47/cit47) 2021 ref34/cit34 ref37/cit37 ref28/cit28 ref40/cit40 ref20/cit20 ref17/cit17 ref26/cit26 ref35/cit35 Tumati P. R. (ref38/cit38) 1991 ref19/cit19 ref21/cit21 ref12/cit12 ref15/cit15 ref42/cit42 ref46/cit46 ref41/cit41 ref22/cit22 ref13/cit13 ref33/cit33 ref4/cit4 ref30/cit30 Kamarudin R. A. (ref10/cit10) 2007; 11 ref1/cit1 ref24/cit24 ref44/cit44 ref7/cit7 |
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Snippet | The sequestration of carbon dioxide (CO2) stands as a profoundly pivotal environmental challenge, given its potential to directly contribute to the advancement... The sequestration of carbon dioxide (CO ) stands as a profoundly pivotal environmental challenge, given its potential to directly contribute to the advancement... The sequestration of carbon dioxide (CO 2 ) stands as a profoundly pivotal environmental challenge, given its potential to directly contribute to the... |
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Title | Assessment of Metal Impurity Partitioning and Speciation in Mineral Carbonation Processes Using FGD-Gypsum from Coal-Fired Power Plants under Distinct Operating Conditions |
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