Synthesis of ZrB 2 Powders from ZrO 2 , BN , and C
Submicrometer (200–800 nm) ZrB 2 powders have been successfully prepared via a new ZrO 2 –C– BN precursor powder system at a relatively low temperature (1550°C) for 1.5 h. As a moderate cost boron source, BN has a well‐defined stoichiometry and low impurity. Both thermodynamic and experimental resul...
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Veröffentlicht in: | Journal of the American Ceramic Society 2016-01, Vol.99 (1), p.16-19 |
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container_title | Journal of the American Ceramic Society |
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creator | Yan, Chunlei Liu, Rongjun Zhang, Changrui Cao, Yingbin Long, Xianhai |
description | Submicrometer (200–800 nm) ZrB
2
powders have been successfully prepared via a new ZrO
2
–C–
BN
precursor powder system at a relatively low temperature (1550°C) for 1.5 h. As a moderate cost boron source,
BN
has a well‐defined stoichiometry and low impurity. Both thermodynamic and experimental results indicated that ZrC was formed below 1300°C, a temperature required for ZrB
2
formation. Moreover, the reaction of ZrC–
BN
mixture at 1300°C indicated that the ZrC acted as an effective direct reducing reagent for
BN
to form ZrB
2
, indicating that the pathway involving the formation of intermediate phase ZrC determined the formation mechanism. |
doi_str_mv | 10.1111/jace.14027 |
format | Article |
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2
powders have been successfully prepared via a new ZrO
2
–C–
BN
precursor powder system at a relatively low temperature (1550°C) for 1.5 h. As a moderate cost boron source,
BN
has a well‐defined stoichiometry and low impurity. Both thermodynamic and experimental results indicated that ZrC was formed below 1300°C, a temperature required for ZrB
2
formation. Moreover, the reaction of ZrC–
BN
mixture at 1300°C indicated that the ZrC acted as an effective direct reducing reagent for
BN
to form ZrB
2
, indicating that the pathway involving the formation of intermediate phase ZrC determined the formation mechanism.</description><identifier>ISSN: 0002-7820</identifier><identifier>EISSN: 1551-2916</identifier><identifier>DOI: 10.1111/jace.14027</identifier><language>eng</language><ispartof>Journal of the American Ceramic Society, 2016-01, Vol.99 (1), p.16-19</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c767-16135f85814f1c9fa0041099cbcbd4845f719b46c3cff9a8b3dbfb7abe6f508a3</citedby><cites>FETCH-LOGICAL-c767-16135f85814f1c9fa0041099cbcbd4845f719b46c3cff9a8b3dbfb7abe6f508a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids></links><search><contributor>Fahrenholtz, W.</contributor><creatorcontrib>Yan, Chunlei</creatorcontrib><creatorcontrib>Liu, Rongjun</creatorcontrib><creatorcontrib>Zhang, Changrui</creatorcontrib><creatorcontrib>Cao, Yingbin</creatorcontrib><creatorcontrib>Long, Xianhai</creatorcontrib><title>Synthesis of ZrB 2 Powders from ZrO 2 , BN , and C</title><title>Journal of the American Ceramic Society</title><description>Submicrometer (200–800 nm) ZrB
2
powders have been successfully prepared via a new ZrO
2
–C–
BN
precursor powder system at a relatively low temperature (1550°C) for 1.5 h. As a moderate cost boron source,
BN
has a well‐defined stoichiometry and low impurity. Both thermodynamic and experimental results indicated that ZrC was formed below 1300°C, a temperature required for ZrB
2
formation. Moreover, the reaction of ZrC–
BN
mixture at 1300°C indicated that the ZrC acted as an effective direct reducing reagent for
BN
to form ZrB
2
, indicating that the pathway involving the formation of intermediate phase ZrC determined the formation mechanism.</description><issn>0002-7820</issn><issn>1551-2916</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNotj01LAzEYhIMouFYv_oKcxa3vm49NcrSLX1Dagj15WZJsXmyxXUkE6b93q85hhpnDwMPYNcIUR91tfUxTVCDMCatQa6yFw-aUVQAgamMFnLOLUrZjRWdVxcTrYf_1nsqm8IH4W55xwVfDd59y4ZSH3Tgtx-mWzxaj-X3P20t2Rv6jpKv_nLD148O6fa7ny6eX9n5eR9OYGhuUmqy2qAijIw-gEJyLIYZeWaXJoAuqiTISOW-D7AMF40NqSIP1csJu_m5jHkrJibrPvNn5fOgQuiNsd4TtfmHlDxe0RG8</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Yan, Chunlei</creator><creator>Liu, Rongjun</creator><creator>Zhang, Changrui</creator><creator>Cao, Yingbin</creator><creator>Long, Xianhai</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201601</creationdate><title>Synthesis of ZrB 2 Powders from ZrO 2 , BN , and C</title><author>Yan, Chunlei ; Liu, Rongjun ; Zhang, Changrui ; Cao, Yingbin ; Long, Xianhai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c767-16135f85814f1c9fa0041099cbcbd4845f719b46c3cff9a8b3dbfb7abe6f508a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yan, Chunlei</creatorcontrib><creatorcontrib>Liu, Rongjun</creatorcontrib><creatorcontrib>Zhang, Changrui</creatorcontrib><creatorcontrib>Cao, Yingbin</creatorcontrib><creatorcontrib>Long, Xianhai</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of the American Ceramic Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yan, Chunlei</au><au>Liu, Rongjun</au><au>Zhang, Changrui</au><au>Cao, Yingbin</au><au>Long, Xianhai</au><au>Fahrenholtz, W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of ZrB 2 Powders from ZrO 2 , BN , and C</atitle><jtitle>Journal of the American Ceramic Society</jtitle><date>2016-01</date><risdate>2016</risdate><volume>99</volume><issue>1</issue><spage>16</spage><epage>19</epage><pages>16-19</pages><issn>0002-7820</issn><eissn>1551-2916</eissn><abstract>Submicrometer (200–800 nm) ZrB
2
powders have been successfully prepared via a new ZrO
2
–C–
BN
precursor powder system at a relatively low temperature (1550°C) for 1.5 h. As a moderate cost boron source,
BN
has a well‐defined stoichiometry and low impurity. Both thermodynamic and experimental results indicated that ZrC was formed below 1300°C, a temperature required for ZrB
2
formation. Moreover, the reaction of ZrC–
BN
mixture at 1300°C indicated that the ZrC acted as an effective direct reducing reagent for
BN
to form ZrB
2
, indicating that the pathway involving the formation of intermediate phase ZrC determined the formation mechanism.</abstract><doi>10.1111/jace.14027</doi><tpages>4</tpages></addata></record> |
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title | Synthesis of ZrB 2 Powders from ZrO 2 , BN , and C |
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