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Growth of Nanosized Calcite through Gas−Solid Carbonation of Nanosized Portlandite under Anisobaric Conditions
The gas−solid carbonation of nanosized portlandite was experimentally investigated using a static bed reactor under anisobaric conditions. The effects of initial CO2 pressure (10−40 bar), reaction temperature (30 and 60 °C), and relative humidity were investigated. Three steps of the carbonation pro...
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Published in: | Crystal growth & design 2010-11, Vol.10 (11), p.4823-4830 |
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description | The gas−solid carbonation of nanosized portlandite was experimentally investigated using a static bed reactor under anisobaric conditions. The effects of initial CO2 pressure (10−40 bar), reaction temperature (30 and 60 °C), and relative humidity were investigated. Three steps of the carbonation process were determined: (1) instantaneous CO2 mineralization during CO2 injection period. From 25 to 40 wt % of initial portlandite grains were transformed into calcite during the CO2 injection period (from 0.9 to 2 min). (2) Fast CO2 mineralization after gas injection period ( |
doi_str_mv | 10.1021/cg100714m |
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The effects of initial CO2 pressure (10−40 bar), reaction temperature (30 and 60 °C), and relative humidity were investigated. Three steps of the carbonation process were determined: (1) instantaneous CO2 mineralization during CO2 injection period. From 25 to 40 wt % of initial portlandite grains were transformed into calcite during the CO2 injection period (from 0.9 to 2 min). (2) Fast CO2 mineralization after gas injection period (<5 h) followed by (3) a slow CO2 mineralization until an equilibrium state (<24 h). The results revealed high efficiency from portlandite-to-calcite transformation (>95%). For this case, the mineralization of CO2 does not form a protective carbonate layer around the reacting particles of portlandite as typically observed by other gas−solid carbonation methods. This method could be efficiently performed to produce nanosized calcite. Moreover, the separation of calcite particles from the fluid phase is most simple compared with precipitation methods. A kinetic pseudo-second-order model was satisfactorily used to describe the three CO2 mineralization steps except for the carbonation reaction initiated at 40 bar. In this latter case, a kinetic pseudo-first-order model was satisfactorily used; indicating that the slow CO2 mineralization step appears less significant during the carbonation process.</description><identifier>ISSN: 1528-7483</identifier><identifier>EISSN: 1528-7505</identifier><identifier>DOI: 10.1021/cg100714m</identifier><language>eng</language><publisher>Washington,DC: American Chemical Society</publisher><subject>Cross-disciplinary physics: materials science; rheology ; Earth Sciences ; Environmental Sciences ; Exact sciences and technology ; Geochemistry ; Global Changes ; Materials science ; Methods of crystal growth; physics of crystal growth ; Phase diagrams and microstructures developed by solidification and solid-solid phase transformations ; Physics ; Precipitation ; Sciences of the Universe ; Theory and models of crystal growth; physics of crystal growth, crystal morphology and orientation</subject><ispartof>Crystal growth & design, 2010-11, Vol.10 (11), p.4823-4830</ispartof><rights>Copyright © 2010 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a390t-d6f89b9dedcb94c64645f42078a8c74eb437f1e7eb6601b1fc0b6e228edc42c33</citedby><cites>FETCH-LOGICAL-a390t-d6f89b9dedcb94c64645f42078a8c74eb437f1e7eb6601b1fc0b6e228edc42c33</cites><orcidid>0000-0003-3149-531X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23382595$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://insu.hal.science/insu-00549812$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Montes-Hernandez, G</creatorcontrib><creatorcontrib>Daval, D</creatorcontrib><creatorcontrib>Chiriac, R</creatorcontrib><creatorcontrib>Renard, F</creatorcontrib><title>Growth of Nanosized Calcite through Gas−Solid Carbonation of Nanosized Portlandite under Anisobaric Conditions</title><title>Crystal growth & design</title><addtitle>Cryst. Growth Des</addtitle><description>The gas−solid carbonation of nanosized portlandite was experimentally investigated using a static bed reactor under anisobaric conditions. The effects of initial CO2 pressure (10−40 bar), reaction temperature (30 and 60 °C), and relative humidity were investigated. Three steps of the carbonation process were determined: (1) instantaneous CO2 mineralization during CO2 injection period. From 25 to 40 wt % of initial portlandite grains were transformed into calcite during the CO2 injection period (from 0.9 to 2 min). (2) Fast CO2 mineralization after gas injection period (<5 h) followed by (3) a slow CO2 mineralization until an equilibrium state (<24 h). The results revealed high efficiency from portlandite-to-calcite transformation (>95%). For this case, the mineralization of CO2 does not form a protective carbonate layer around the reacting particles of portlandite as typically observed by other gas−solid carbonation methods. This method could be efficiently performed to produce nanosized calcite. Moreover, the separation of calcite particles from the fluid phase is most simple compared with precipitation methods. A kinetic pseudo-second-order model was satisfactorily used to describe the three CO2 mineralization steps except for the carbonation reaction initiated at 40 bar. In this latter case, a kinetic pseudo-first-order model was satisfactorily used; indicating that the slow CO2 mineralization step appears less significant during the carbonation process.</description><subject>Cross-disciplinary physics: materials science; rheology</subject><subject>Earth Sciences</subject><subject>Environmental Sciences</subject><subject>Exact sciences and technology</subject><subject>Geochemistry</subject><subject>Global Changes</subject><subject>Materials science</subject><subject>Methods of crystal growth; physics of crystal growth</subject><subject>Phase diagrams and microstructures developed by solidification and solid-solid phase transformations</subject><subject>Physics</subject><subject>Precipitation</subject><subject>Sciences of the Universe</subject><subject>Theory and models of crystal growth; physics of crystal growth, crystal morphology and orientation</subject><issn>1528-7483</issn><issn>1528-7505</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNptkM1KxDAURoMoqKML36AbFwrV_LVNl0PRGWFQQV2HJE2mGTrJkHQUfQLXPqJPYsvoiODqXrjnfHA_AE4QvEAQo0s1RxAWiC53wAHKMEuLDGa7PztlZB8cxriAPZQTcgBWk-BfuibxJrkVzkf7puukEq2ynU66Jvj1vEkmIn6-fzz41g63IL0TnfXur3TvQ9cKVw_i2tU6JGNno5ciWJVUfjj0TjwCe0a0UR9_zxF4ur56rKbp7G5yU41nqSAl7NI6N6yUZa1rJUuqcprTzFAMCyaYKqiWlBQG6ULLPIdIIqOgzDXGrBcoVoSMwPkmtxEtXwW7FOGVe2H5dDzj1sU1hzCjJUP4GfXw2QZWwccYtNkaCPKhV77ttWdPN-xKRCVaE4RTNm4FTAjDWZn9ckJFvvDr4Pp3_8n7ArbZhhc</recordid><startdate>20101103</startdate><enddate>20101103</enddate><creator>Montes-Hernandez, G</creator><creator>Daval, D</creator><creator>Chiriac, R</creator><creator>Renard, F</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-3149-531X</orcidid></search><sort><creationdate>20101103</creationdate><title>Growth of Nanosized Calcite through Gas−Solid Carbonation of Nanosized Portlandite under Anisobaric Conditions</title><author>Montes-Hernandez, G ; Daval, D ; Chiriac, R ; Renard, F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a390t-d6f89b9dedcb94c64645f42078a8c74eb437f1e7eb6601b1fc0b6e228edc42c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Cross-disciplinary physics: materials science; rheology</topic><topic>Earth Sciences</topic><topic>Environmental Sciences</topic><topic>Exact sciences and technology</topic><topic>Geochemistry</topic><topic>Global Changes</topic><topic>Materials science</topic><topic>Methods of crystal growth; physics of crystal growth</topic><topic>Phase diagrams and microstructures developed by solidification and solid-solid phase transformations</topic><topic>Physics</topic><topic>Precipitation</topic><topic>Sciences of the Universe</topic><topic>Theory and models of crystal growth; physics of crystal growth, crystal morphology and orientation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Montes-Hernandez, G</creatorcontrib><creatorcontrib>Daval, D</creatorcontrib><creatorcontrib>Chiriac, R</creatorcontrib><creatorcontrib>Renard, F</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Crystal growth & design</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Montes-Hernandez, G</au><au>Daval, D</au><au>Chiriac, R</au><au>Renard, F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Growth of Nanosized Calcite through Gas−Solid Carbonation of Nanosized Portlandite under Anisobaric Conditions</atitle><jtitle>Crystal growth & design</jtitle><addtitle>Cryst. Growth Des</addtitle><date>2010-11-03</date><risdate>2010</risdate><volume>10</volume><issue>11</issue><spage>4823</spage><epage>4830</epage><pages>4823-4830</pages><issn>1528-7483</issn><eissn>1528-7505</eissn><abstract>The gas−solid carbonation of nanosized portlandite was experimentally investigated using a static bed reactor under anisobaric conditions. The effects of initial CO2 pressure (10−40 bar), reaction temperature (30 and 60 °C), and relative humidity were investigated. Three steps of the carbonation process were determined: (1) instantaneous CO2 mineralization during CO2 injection period. From 25 to 40 wt % of initial portlandite grains were transformed into calcite during the CO2 injection period (from 0.9 to 2 min). (2) Fast CO2 mineralization after gas injection period (<5 h) followed by (3) a slow CO2 mineralization until an equilibrium state (<24 h). The results revealed high efficiency from portlandite-to-calcite transformation (>95%). For this case, the mineralization of CO2 does not form a protective carbonate layer around the reacting particles of portlandite as typically observed by other gas−solid carbonation methods. This method could be efficiently performed to produce nanosized calcite. Moreover, the separation of calcite particles from the fluid phase is most simple compared with precipitation methods. A kinetic pseudo-second-order model was satisfactorily used to describe the three CO2 mineralization steps except for the carbonation reaction initiated at 40 bar. In this latter case, a kinetic pseudo-first-order model was satisfactorily used; indicating that the slow CO2 mineralization step appears less significant during the carbonation process.</abstract><cop>Washington,DC</cop><pub>American Chemical Society</pub><doi>10.1021/cg100714m</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-3149-531X</orcidid></addata></record> |
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subjects | Cross-disciplinary physics: materials science rheology Earth Sciences Environmental Sciences Exact sciences and technology Geochemistry Global Changes Materials science Methods of crystal growth physics of crystal growth Phase diagrams and microstructures developed by solidification and solid-solid phase transformations Physics Precipitation Sciences of the Universe Theory and models of crystal growth physics of crystal growth, crystal morphology and orientation |
title | Growth of Nanosized Calcite through Gas−Solid Carbonation of Nanosized Portlandite under Anisobaric Conditions |
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