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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 |
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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.
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doi_str_mv | 10.1016/j.jes.2015.06.012 |
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[Display omitted]</description><identifier>ISSN: 1001-0742</identifier><identifier>EISSN: 1878-7320</identifier><identifier>DOI: 10.1016/j.jes.2015.06.012</identifier><identifier>PMID: 26969055</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>BOF-slag ; Carbon Dioxide - chemistry ; Carbon Sequestration ; Carbonation ; Hot Temperature ; Industrial Waste - analysis ; Mineral CO2 sequestration ; Oxygen - chemistry</subject><ispartof>Journal of environmental sciences (China), 2016-03, Vol.41, p.99-111</ispartof><rights>2015</rights><rights>Copyright © 2015. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-2b2c790b6b432bb94fb433793cdb36546a96ec3672e2f338e6e14898127ded4c3</citedby><cites>FETCH-LOGICAL-c489t-2b2c790b6b432bb94fb433793cdb36546a96ec3672e2f338e6e14898127ded4c3</cites><orcidid>0000-0002-8956-5643</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26969055$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Su, Tung-Hsin</creatorcontrib><creatorcontrib>Yang, Huai-Jen</creatorcontrib><creatorcontrib>Shau, Yen-Hong</creatorcontrib><creatorcontrib>Takazawa, Eiichi</creatorcontrib><creatorcontrib>Lee, Yu-Chen</creatorcontrib><title>CO2 sequestration utilizing basic-oxygen furnace slag: Controlling factors, reaction mechanisms and V–Cr concerns</title><title>Journal of environmental sciences (China)</title><addtitle>J Environ Sci (China)</addtitle><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]</description><subject>BOF-slag</subject><subject>Carbon Dioxide - chemistry</subject><subject>Carbon Sequestration</subject><subject>Carbonation</subject><subject>Hot Temperature</subject><subject>Industrial Waste - analysis</subject><subject>Mineral CO2 sequestration</subject><subject>Oxygen - chemistry</subject><issn>1001-0742</issn><issn>1878-7320</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kM1u1TAQhSMEoqXwAGyQlyyadGwndgIrFPEnVeoG2FqOM7n4KrGLJ0EtK96BN-RJ8OWWLlnNWXznSPMVxXMOFQeuLvbVHqkSwJsKVAVcPChOeavbUksBD3MG4CXoWpwUT4j2AFA30DwuToTqVAdNc1pQfyUY4bcNaU129TGwbfWz_-HDjg2WvCvjze0OA5u2FKxDRrPdvWJ9DGuK83zAJuvWmOicJczpMLGg-2qDp4WYDSP78vvnrz4xF4PDFOhp8WiyM-Gzu3tWfH739lP_oby8ev-xf3NZurrt1lIMwukOBjXUUgxDV085SN1JNw5SNbWynUInlRYoJilbVMhzseVCjzjWTp4VL4-71yn-fdAsnhzOsw0YNzJca9FKXYPKKD-iLkWihJO5Tn6x6dZwMAfXZm-ya3NwbUCZ7Dp3XtzNb8OC433jn9wMvD4CmJ_87jEZch6zg9EndKsZo__P_B_HHJFK</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Su, Tung-Hsin</creator><creator>Yang, Huai-Jen</creator><creator>Shau, Yen-Hong</creator><creator>Takazawa, Eiichi</creator><creator>Lee, Yu-Chen</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8956-5643</orcidid></search><sort><creationdate>20160301</creationdate><title>CO2 sequestration utilizing basic-oxygen furnace slag: Controlling factors, reaction mechanisms and V–Cr concerns</title><author>Su, Tung-Hsin ; Yang, Huai-Jen ; Shau, Yen-Hong ; Takazawa, Eiichi ; Lee, Yu-Chen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-2b2c790b6b432bb94fb433793cdb36546a96ec3672e2f338e6e14898127ded4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>BOF-slag</topic><topic>Carbon Dioxide - chemistry</topic><topic>Carbon Sequestration</topic><topic>Carbonation</topic><topic>Hot Temperature</topic><topic>Industrial Waste - analysis</topic><topic>Mineral CO2 sequestration</topic><topic>Oxygen - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Su, Tung-Hsin</creatorcontrib><creatorcontrib>Yang, Huai-Jen</creatorcontrib><creatorcontrib>Shau, Yen-Hong</creatorcontrib><creatorcontrib>Takazawa, Eiichi</creatorcontrib><creatorcontrib>Lee, Yu-Chen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of environmental sciences (China)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Su, Tung-Hsin</au><au>Yang, Huai-Jen</au><au>Shau, Yen-Hong</au><au>Takazawa, Eiichi</au><au>Lee, Yu-Chen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CO2 sequestration utilizing basic-oxygen furnace slag: Controlling factors, reaction mechanisms and V–Cr concerns</atitle><jtitle>Journal of environmental sciences (China)</jtitle><addtitle>J Environ Sci (China)</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>41</volume><spage>99</spage><epage>111</epage><pages>99-111</pages><issn>1001-0742</issn><eissn>1878-7320</eissn><abstract>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.
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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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