Carbothermal reduction–nitridation of titania-bearing blast furnace slag
The synthesis of (Ca,Mg)α′-Sialon ((Ca,Mg) x Si 12−3 x Al 3 x O x N 16− x ) powders using titania-bearing blast furnace slag as a starting material by carbothermal reduction–nitridation (CRN) was reported for the first time. The reaction processes were greatly affected by initial material and reacti...
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creator | Jiang, Tao Xue, Xiangxin Duan, Peining Liu, Xin Zhang, Shuhui Liu, Ran |
description | The synthesis of (Ca,Mg)α′-Sialon ((Ca,Mg)
x
Si
12−3
x
Al
3
x
O
x
N
16−
x
) powders using titania-bearing blast furnace slag as a starting material by carbothermal reduction–nitridation (CRN) was reported for the first time. The reaction processes were greatly affected by initial material and reaction parameters. With the compositions shifting range from
x
=
0.3 up to 2.0, the amount of (Ca,Mg)α′-Sialon, TiN and AlN, the solid solubility of Ca
2+ and Mg
2+, the unit cell parameters of the (Ca,Mg)α′-Sialon and the amount of elongated α′-Sialon grains increased, but β′-Sialon and SiC decreased. With the increase of synthesis temperature and holding time, the formation of (Ca,Mg)α′-Sialon in the products increased and the CRN reactions accelerated. The optimum synthesis conditions of (Ca,Mg)α′-Sialon were 1480
°C for 8
h, under which the crystalline phases of the products also included AlN, TiN and a small amount of SiC and β-CaSiO
3. The volatilization of SiO resulted in a mass loss of samples, which was enhanced with the increase of synthesis temperature and holding time. |
doi_str_mv | 10.1016/j.ceramint.2007.07.005 |
format | Article |
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x
Si
12−3
x
Al
3
x
O
x
N
16−
x
) powders using titania-bearing blast furnace slag as a starting material by carbothermal reduction–nitridation (CRN) was reported for the first time. The reaction processes were greatly affected by initial material and reaction parameters. With the compositions shifting range from
x
=
0.3 up to 2.0, the amount of (Ca,Mg)α′-Sialon, TiN and AlN, the solid solubility of Ca
2+ and Mg
2+, the unit cell parameters of the (Ca,Mg)α′-Sialon and the amount of elongated α′-Sialon grains increased, but β′-Sialon and SiC decreased. With the increase of synthesis temperature and holding time, the formation of (Ca,Mg)α′-Sialon in the products increased and the CRN reactions accelerated. The optimum synthesis conditions of (Ca,Mg)α′-Sialon were 1480
°C for 8
h, under which the crystalline phases of the products also included AlN, TiN and a small amount of SiC and β-CaSiO
3. The volatilization of SiO resulted in a mass loss of samples, which was enhanced with the increase of synthesis temperature and holding time.</description><identifier>ISSN: 0272-8842</identifier><identifier>EISSN: 1873-3956</identifier><identifier>DOI: 10.1016/j.ceramint.2007.07.005</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>(Ca,Mg)α′-Sialon ; Carbothermal reduction–nitridation ; Chemistry ; Colloidal state and disperse state ; Exact sciences and technology ; General and physical chemistry ; General, apparatus, technics of preparation ; Powder synthesis ; Powders ; Titania-bearing blast furnace slag</subject><ispartof>Ceramics international, 2008-09, Vol.34 (7), p.1643-1651</ispartof><rights>2007 Elsevier Ltd and Techna Group S.r.l.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480t-50a47b8600d31f27ed11aaa9f84af6f3b7e53ee9213c45c6fbefbdcd92e9bf943</citedby><cites>FETCH-LOGICAL-c480t-50a47b8600d31f27ed11aaa9f84af6f3b7e53ee9213c45c6fbefbdcd92e9bf943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0272884207001617$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20604156$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiang, Tao</creatorcontrib><creatorcontrib>Xue, Xiangxin</creatorcontrib><creatorcontrib>Duan, Peining</creatorcontrib><creatorcontrib>Liu, Xin</creatorcontrib><creatorcontrib>Zhang, Shuhui</creatorcontrib><creatorcontrib>Liu, Ran</creatorcontrib><title>Carbothermal reduction–nitridation of titania-bearing blast furnace slag</title><title>Ceramics international</title><description>The synthesis of (Ca,Mg)α′-Sialon ((Ca,Mg)
x
Si
12−3
x
Al
3
x
O
x
N
16−
x
) powders using titania-bearing blast furnace slag as a starting material by carbothermal reduction–nitridation (CRN) was reported for the first time. The reaction processes were greatly affected by initial material and reaction parameters. With the compositions shifting range from
x
=
0.3 up to 2.0, the amount of (Ca,Mg)α′-Sialon, TiN and AlN, the solid solubility of Ca
2+ and Mg
2+, the unit cell parameters of the (Ca,Mg)α′-Sialon and the amount of elongated α′-Sialon grains increased, but β′-Sialon and SiC decreased. With the increase of synthesis temperature and holding time, the formation of (Ca,Mg)α′-Sialon in the products increased and the CRN reactions accelerated. The optimum synthesis conditions of (Ca,Mg)α′-Sialon were 1480
°C for 8
h, under which the crystalline phases of the products also included AlN, TiN and a small amount of SiC and β-CaSiO
3. The volatilization of SiO resulted in a mass loss of samples, which was enhanced with the increase of synthesis temperature and holding time.</description><subject>(Ca,Mg)α′-Sialon</subject><subject>Carbothermal reduction–nitridation</subject><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>General, apparatus, technics of preparation</subject><subject>Powder synthesis</subject><subject>Powders</subject><subject>Titania-bearing blast furnace slag</subject><issn>0272-8842</issn><issn>1873-3956</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkMtKBDEQRYMoOD5-QXqjux4rnfQjO2XwieBG16E6XdEMPWlNMoI7_8E_9EvsZtStcKEoOLcudRk74jDnwKvT5dxQwJXzaV4A1PNJUG6xGW9qkQtVVttsBkVd5E0ji122F-MSRqOSMGO3CwztkJ4prLDPAnVrk9zgvz4-vUvBdTht2WCz5BJ6h3lLGJx_ytoeY8rsOng0lMUenw7YjsU-0uHP3GePlxcPi-v87v7qZnF-lxvZQMpLQFm3TQXQCW6LmjrOEVHZRqKtrGhrKgWRKrgwsjSVbcm2nelUQaq1Sop9drK5-xKG1zXFpFcuGup79DSsoxal4CCVGsFqA5owxBjI6pfgVhjeNQc9VaeX-rc6PVWnJ0E5Go9_EjAa7G1Ab1z8cxdQgeRlNXJnG47Gd98cBR2NI2-oc4FM0t3g_ov6Bmmriwk</recordid><startdate>20080901</startdate><enddate>20080901</enddate><creator>Jiang, Tao</creator><creator>Xue, Xiangxin</creator><creator>Duan, Peining</creator><creator>Liu, Xin</creator><creator>Zhang, Shuhui</creator><creator>Liu, Ran</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QQ</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20080901</creationdate><title>Carbothermal reduction–nitridation of titania-bearing blast furnace slag</title><author>Jiang, Tao ; Xue, Xiangxin ; Duan, Peining ; Liu, Xin ; Zhang, Shuhui ; Liu, Ran</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c480t-50a47b8600d31f27ed11aaa9f84af6f3b7e53ee9213c45c6fbefbdcd92e9bf943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>(Ca,Mg)α′-Sialon</topic><topic>Carbothermal reduction–nitridation</topic><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>General, apparatus, technics of preparation</topic><topic>Powder synthesis</topic><topic>Powders</topic><topic>Titania-bearing blast furnace slag</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiang, Tao</creatorcontrib><creatorcontrib>Xue, Xiangxin</creatorcontrib><creatorcontrib>Duan, Peining</creatorcontrib><creatorcontrib>Liu, Xin</creatorcontrib><creatorcontrib>Zhang, Shuhui</creatorcontrib><creatorcontrib>Liu, Ran</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Ceramics international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiang, Tao</au><au>Xue, Xiangxin</au><au>Duan, Peining</au><au>Liu, Xin</au><au>Zhang, Shuhui</au><au>Liu, Ran</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbothermal reduction–nitridation of titania-bearing blast furnace slag</atitle><jtitle>Ceramics international</jtitle><date>2008-09-01</date><risdate>2008</risdate><volume>34</volume><issue>7</issue><spage>1643</spage><epage>1651</epage><pages>1643-1651</pages><issn>0272-8842</issn><eissn>1873-3956</eissn><abstract>The synthesis of (Ca,Mg)α′-Sialon ((Ca,Mg)
x
Si
12−3
x
Al
3
x
O
x
N
16−
x
) powders using titania-bearing blast furnace slag as a starting material by carbothermal reduction–nitridation (CRN) was reported for the first time. The reaction processes were greatly affected by initial material and reaction parameters. With the compositions shifting range from
x
=
0.3 up to 2.0, the amount of (Ca,Mg)α′-Sialon, TiN and AlN, the solid solubility of Ca
2+ and Mg
2+, the unit cell parameters of the (Ca,Mg)α′-Sialon and the amount of elongated α′-Sialon grains increased, but β′-Sialon and SiC decreased. With the increase of synthesis temperature and holding time, the formation of (Ca,Mg)α′-Sialon in the products increased and the CRN reactions accelerated. The optimum synthesis conditions of (Ca,Mg)α′-Sialon were 1480
°C for 8
h, under which the crystalline phases of the products also included AlN, TiN and a small amount of SiC and β-CaSiO
3. The volatilization of SiO resulted in a mass loss of samples, which was enhanced with the increase of synthesis temperature and holding time.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.ceramint.2007.07.005</doi><tpages>9</tpages></addata></record> |
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language | eng |
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source | Elsevier ScienceDirect Journals |
subjects | (Ca,Mg)α′-Sialon Carbothermal reduction–nitridation Chemistry Colloidal state and disperse state Exact sciences and technology General and physical chemistry General, apparatus, technics of preparation Powder synthesis Powders Titania-bearing blast furnace slag |
title | Carbothermal reduction–nitridation of titania-bearing blast furnace slag |
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