Sintering of a Crystallizable K2O–CaO–SrO–BaO–B2O3–SiO2 Glass with Titania Present
Crystallization and reaction kinetics of a crystallizable K2O–CaO–SrO–BaO–B2O3–SiO2 glass powder with 17–40 vol% titania powder were investigated. The initially amorphous K2O–CaO–SrO–BaO–B2O3–SiO2 glass powder formed cristobalite (SiO2) and pseudowollastonite [(Ca, Ba, Sr)SiO3] during firing. The ab...
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Veröffentlicht in: | Journal of materials research 2002-07, Vol.17 (7), p.1772-1778 |
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creator | Jean, Jau-Ho Fang, Yu-Ching Dai, Steve X. Wilcox, David L. |
description | Crystallization and reaction kinetics of a crystallizable K2O–CaO–SrO–BaO–B2O3–SiO2 glass powder with 17–40 vol% titania powder were investigated. The initially amorphous K2O–CaO–SrO–BaO–B2O3–SiO2 glass powder formed cristobalite (SiO2) and pseudowollastonite [(Ca, Ba, Sr)SiO3] during firing. The above crystalline phases were completely replaced by a crystalline phase of titanite [(Ca, Sr, Ba)TiSiO5] when the amount of added titania was greater than a critical value, e.g., 10 vol%, at 99–1100 °C. A chemical reaction taking place at the interface between titania and the glass was attributed to the above observation. The dissolved titania changed the composition of the glass, and the dissolution kinetics was much faster than the formation of cristobalite and pseudowollastonite. Activation energy analysis showed that the crystallization of titanite [(Ca,Sr,Ba)TiSiO5] was controlled by a reaction-limiting kinetics of formation for the Ti–O bond. |
doi_str_mv | 10.1557/JMR.2002.0262 |
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The initially amorphous K2O–CaO–SrO–BaO–B2O3–SiO2 glass powder formed cristobalite (SiO2) and pseudowollastonite [(Ca, Ba, Sr)SiO3] during firing. The above crystalline phases were completely replaced by a crystalline phase of titanite [(Ca, Sr, Ba)TiSiO5] when the amount of added titania was greater than a critical value, e.g., 10 vol%, at 99–1100 °C. A chemical reaction taking place at the interface between titania and the glass was attributed to the above observation. The dissolved titania changed the composition of the glass, and the dissolution kinetics was much faster than the formation of cristobalite and pseudowollastonite. Activation energy analysis showed that the crystallization of titanite [(Ca,Sr,Ba)TiSiO5] was controlled by a reaction-limiting kinetics of formation for the Ti–O bond.</description><identifier>ISSN: 0884-2914</identifier><identifier>EISSN: 2044-5326</identifier><identifier>DOI: 10.1557/JMR.2002.0262</identifier><language>eng</language><publisher>New York, USA: Cambridge University Press</publisher><ispartof>Journal of materials research, 2002-07, Vol.17 (7), p.1772-1778</ispartof><rights>Copyright © Materials Research Society 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Jean, Jau-Ho</creatorcontrib><creatorcontrib>Fang, Yu-Ching</creatorcontrib><creatorcontrib>Dai, Steve X.</creatorcontrib><creatorcontrib>Wilcox, David L.</creatorcontrib><title>Sintering of a Crystallizable K2O–CaO–SrO–BaO–B2O3–SiO2 Glass with Titania Present</title><title>Journal of materials research</title><addtitle>J. Mater. Res</addtitle><description>Crystallization and reaction kinetics of a crystallizable K2O–CaO–SrO–BaO–B2O3–SiO2 glass powder with 17–40 vol% titania powder were investigated. The initially amorphous K2O–CaO–SrO–BaO–B2O3–SiO2 glass powder formed cristobalite (SiO2) and pseudowollastonite [(Ca, Ba, Sr)SiO3] during firing. The above crystalline phases were completely replaced by a crystalline phase of titanite [(Ca, Sr, Ba)TiSiO5] when the amount of added titania was greater than a critical value, e.g., 10 vol%, at 99–1100 °C. A chemical reaction taking place at the interface between titania and the glass was attributed to the above observation. The dissolved titania changed the composition of the glass, and the dissolution kinetics was much faster than the formation of cristobalite and pseudowollastonite. Activation energy analysis showed that the crystallization of titanite [(Ca,Sr,Ba)TiSiO5] was controlled by a reaction-limiting kinetics of formation for the Ti–O bond.</description><issn>0884-2914</issn><issn>2044-5326</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNotkLFOwzAQhi0EEqUwsmdiS2s7sR2PtIICLQ3QIiSEZDmOUwxpUmxXUCbegTfkSUgoy93p16fT3QfAMYI9RAjrX13f9TCEuAcxxTugg2EchyTCdBd0YJLEIeYo3gcHzr1AiAhkcQc8zUzltTXVIqiLQAZDu3FelqX5lFmpgzFOf76-h7KtM9vWwd88wGnURibFwaiUzgXvxj8Hc-NlZWRwY7XTlT8Ee4UsnT76711wf342H16Ek3R0OTydhKo51IcMIkRxrEmkuOJREVHFuEaESkxYriApKGeKYZoznpEkkTHiONNZHjcBpjzqgpPt3pWt39baebE0TumylJWu105gRjnklDZguAWN8_pDrKxZSrsR0r4KyiJGBB3diunDmHAyfRSw4ftbXsllZk2-0OKlXtuqeUYgKFrrorEuWuuitR79Av6PdkY</recordid><startdate>20020701</startdate><enddate>20020701</enddate><creator>Jean, Jau-Ho</creator><creator>Fang, Yu-Ching</creator><creator>Dai, Steve X.</creator><creator>Wilcox, David L.</creator><general>Cambridge University Press</general><scope>BSCLL</scope><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20020701</creationdate><title>Sintering of a Crystallizable K2O–CaO–SrO–BaO–B2O3–SiO2 Glass with Titania Present</title><author>Jean, Jau-Ho ; Fang, Yu-Ching ; Dai, Steve X. ; Wilcox, David L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c262t-7011624e53c9c93f36c79e156a257dc05f697c726d79b588a4192bebd4d792693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jean, Jau-Ho</creatorcontrib><creatorcontrib>Fang, Yu-Ching</creatorcontrib><creatorcontrib>Dai, Steve X.</creatorcontrib><creatorcontrib>Wilcox, David L.</creatorcontrib><collection>Istex</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of materials research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jean, Jau-Ho</au><au>Fang, Yu-Ching</au><au>Dai, Steve X.</au><au>Wilcox, David L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sintering of a Crystallizable K2O–CaO–SrO–BaO–B2O3–SiO2 Glass with Titania Present</atitle><jtitle>Journal of materials research</jtitle><addtitle>J. Mater. Res</addtitle><date>2002-07-01</date><risdate>2002</risdate><volume>17</volume><issue>7</issue><spage>1772</spage><epage>1778</epage><pages>1772-1778</pages><issn>0884-2914</issn><eissn>2044-5326</eissn><abstract>Crystallization and reaction kinetics of a crystallizable K2O–CaO–SrO–BaO–B2O3–SiO2 glass powder with 17–40 vol% titania powder were investigated. The initially amorphous K2O–CaO–SrO–BaO–B2O3–SiO2 glass powder formed cristobalite (SiO2) and pseudowollastonite [(Ca, Ba, Sr)SiO3] during firing. The above crystalline phases were completely replaced by a crystalline phase of titanite [(Ca, Sr, Ba)TiSiO5] when the amount of added titania was greater than a critical value, e.g., 10 vol%, at 99–1100 °C. A chemical reaction taking place at the interface between titania and the glass was attributed to the above observation. The dissolved titania changed the composition of the glass, and the dissolution kinetics was much faster than the formation of cristobalite and pseudowollastonite. Activation energy analysis showed that the crystallization of titanite [(Ca,Sr,Ba)TiSiO5] was controlled by a reaction-limiting kinetics of formation for the Ti–O bond.</abstract><cop>New York, USA</cop><pub>Cambridge University Press</pub><doi>10.1557/JMR.2002.0262</doi><tpages>7</tpages></addata></record> |
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title | Sintering of a Crystallizable K2O–CaO–SrO–BaO–B2O3–SiO2 Glass with Titania Present |
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