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CO2 sequestration utilizing basic-oxygen furnace slag: Controlling factors, reaction mechanisms and V–Cr concerns

Basic-oxygen furnace slag (BOF-slag) contains >35% CaO, a potential component for CO2 sequestration. In this study, slag–water–CO2 reaction experiments were conducted with the longest reaction duration extending to 96hr under high CO2 pressures of 100–300kg/cm2 to optimize BOF-slag carbonation co...

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Published in:Journal of environmental sciences (China) 2016-03, Vol.41, p.99-111
Main Authors: Su, Tung-Hsin, Yang, Huai-Jen, Shau, Yen-Hong, Takazawa, Eiichi, Lee, Yu-Chen
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cited_by cdi_FETCH-LOGICAL-c489t-2b2c790b6b432bb94fb433793cdb36546a96ec3672e2f338e6e14898127ded4c3
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creator Su, Tung-Hsin
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description Basic-oxygen furnace slag (BOF-slag) contains >35% CaO, a potential component for CO2 sequestration. In this study, slag–water–CO2 reaction experiments were conducted with the longest reaction duration extending to 96hr under high CO2 pressures of 100–300kg/cm2 to optimize BOF-slag carbonation conditions, to address carbonation mechanisms, and to evaluate the extents of V and Cr release from slag carbonation. The slag carbonation degree generally reached the maximum values after 24hr slag–water–CO2 reaction and was controlled by slag particle size and reaction temperature. The maximum carbonation degree of 71% was produced from the experiment using fine slag of ≤0.5mm under 100°C and a CO2 pressure of 250kg/cm2 with a water/slag ratio of 5. Vanadium release from the slag to water was significantly enhanced (generally >2 orders) by slag carbonation. In contrast, slag carbonation did not promote chromium release until the reaction duration exceeded 24hr. However, the water chromium content was generally at least an order lower than the vanadium concentration, which decreased when the reaction duration exceeded 24hr. Therefore, long reaction durations of 48–96hr are proposed to reduce environmental impacts while keeping high carbonation degrees. Mineral textures and water compositions indicated that Mg-wüstite, in addition to CaO-containing minerals, can also be carbonated. Consequently, the conventional expression that only considered carbonation of the CaO-containing minerals undervalued the CO2 sequestration capability of the BOF-slag by ~20%. Therefore, the BOF-slag is a better CO2 storage medium than that previously recognized. [Display omitted]
doi_str_mv 10.1016/j.jes.2015.06.012
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In this study, slag–water–CO2 reaction experiments were conducted with the longest reaction duration extending to 96hr under high CO2 pressures of 100–300kg/cm2 to optimize BOF-slag carbonation conditions, to address carbonation mechanisms, and to evaluate the extents of V and Cr release from slag carbonation. The slag carbonation degree generally reached the maximum values after 24hr slag–water–CO2 reaction and was controlled by slag particle size and reaction temperature. The maximum carbonation degree of 71% was produced from the experiment using fine slag of ≤0.5mm under 100°C and a CO2 pressure of 250kg/cm2 with a water/slag ratio of 5. Vanadium release from the slag to water was significantly enhanced (generally &gt;2 orders) by slag carbonation. In contrast, slag carbonation did not promote chromium release until the reaction duration exceeded 24hr. However, the water chromium content was generally at least an order lower than the vanadium concentration, which decreased when the reaction duration exceeded 24hr. Therefore, long reaction durations of 48–96hr are proposed to reduce environmental impacts while keeping high carbonation degrees. Mineral textures and water compositions indicated that Mg-wüstite, in addition to CaO-containing minerals, can also be carbonated. Consequently, the conventional expression that only considered carbonation of the CaO-containing minerals undervalued the CO2 sequestration capability of the BOF-slag by ~20%. Therefore, the BOF-slag is a better CO2 storage medium than that previously recognized. 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However, the water chromium content was generally at least an order lower than the vanadium concentration, which decreased when the reaction duration exceeded 24hr. Therefore, long reaction durations of 48–96hr are proposed to reduce environmental impacts while keeping high carbonation degrees. Mineral textures and water compositions indicated that Mg-wüstite, in addition to CaO-containing minerals, can also be carbonated. Consequently, the conventional expression that only considered carbonation of the CaO-containing minerals undervalued the CO2 sequestration capability of the BOF-slag by ~20%. Therefore, the BOF-slag is a better CO2 storage medium than that previously recognized. 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However, the water chromium content was generally at least an order lower than the vanadium concentration, which decreased when the reaction duration exceeded 24hr. Therefore, long reaction durations of 48–96hr are proposed to reduce environmental impacts while keeping high carbonation degrees. Mineral textures and water compositions indicated that Mg-wüstite, in addition to CaO-containing minerals, can also be carbonated. Consequently, the conventional expression that only considered carbonation of the CaO-containing minerals undervalued the CO2 sequestration capability of the BOF-slag by ~20%. Therefore, the BOF-slag is a better CO2 storage medium than that previously recognized. [Display omitted]</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26969055</pmid><doi>10.1016/j.jes.2015.06.012</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-8956-5643</orcidid></addata></record>
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subjects BOF-slag
Carbon Dioxide - chemistry
Carbon Sequestration
Carbonation
Hot Temperature
Industrial Waste - analysis
Mineral CO2 sequestration
Oxygen - chemistry
title CO2 sequestration utilizing basic-oxygen furnace slag: Controlling factors, reaction mechanisms and V–Cr concerns
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