Physical Properties and Hydration Behavior of 3CaO⋅Al2O3 Composition by Quenching after Fusion

N. Tsuyuki, H. Otake, Tsugio Miyakawa, J. Kasai
{"title":"Physical Properties and Hydration Behavior of 3CaO⋅Al2O3 Composition by Quenching after Fusion","authors":"N. Tsuyuki, H. Otake, Tsugio Miyakawa, J. Kasai","doi":"10.2109/JCERSJ1950.94.1091_636","DOIUrl":null,"url":null,"abstract":"The melt of 3CaO⋅Al2O3 (G-C3A) composition in the presence of a small amount of SiO2 was synthesized by rapid quenching after fusion. Furthermore, the physical properties and the hydration behavior of G-C3A were investigated. G-C3A results in a lowering of lattice constant, a decrease of specific gravity and an increase of free CaO compared with C3A. The hydration was not completed even on 10 days curing, and 3CaO⋅Al2O3⋅6H2O hydrate grew very slowly. It is thought that Al(OH)4- eluted from G-C3A is remarkably depressed against Ca2+. The molar ratio (CaO/Al2O3) in case of G-C3A was given 2.7 after 10 days curing but closely approached to 1.0 after 6 hours curing in case of C3A. Namely, as glass phase is formed on G-C3A surface, the strain occurs in inner layer. Therefore, it is difficult to elute Al(OH)4- by breaking -Al-O-Al- bonds. Although the elution of Al(OH)4- by NaOH is considerable, the growth of the hydrate cannot be expected because of depression of the elution of Ca2+. The results of surface analysis by ESCA showed that the binding energy of inner shell electron of Ca, Al, and Si combined with O (oxygen) in G-C3A is 0.7-0.8eV higher than C3A. Consequently, as the elution of Ca2+ and Al(OH)4- is depressed, the hydration reaction becomes inactive.","PeriodicalId":17274,"journal":{"name":"Journal of the Ceramic Association, Japan","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1986-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Ceramic Association, Japan","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2109/JCERSJ1950.94.1091_636","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The melt of 3CaO⋅Al2O3 (G-C3A) composition in the presence of a small amount of SiO2 was synthesized by rapid quenching after fusion. Furthermore, the physical properties and the hydration behavior of G-C3A were investigated. G-C3A results in a lowering of lattice constant, a decrease of specific gravity and an increase of free CaO compared with C3A. The hydration was not completed even on 10 days curing, and 3CaO⋅Al2O3⋅6H2O hydrate grew very slowly. It is thought that Al(OH)4- eluted from G-C3A is remarkably depressed against Ca2+. The molar ratio (CaO/Al2O3) in case of G-C3A was given 2.7 after 10 days curing but closely approached to 1.0 after 6 hours curing in case of C3A. Namely, as glass phase is formed on G-C3A surface, the strain occurs in inner layer. Therefore, it is difficult to elute Al(OH)4- by breaking -Al-O-Al- bonds. Although the elution of Al(OH)4- by NaOH is considerable, the growth of the hydrate cannot be expected because of depression of the elution of Ca2+. The results of surface analysis by ESCA showed that the binding energy of inner shell electron of Ca, Al, and Si combined with O (oxygen) in G-C3A is 0.7-0.8eV higher than C3A. Consequently, as the elution of Ca2+ and Al(OH)4- is depressed, the hydration reaction becomes inactive.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
3CaO·Al2O3熔后淬火的物理性质及水化行为
在少量SiO2的存在下,采用快速淬火的方法合成3CaO⋅Al2O3 (G-C3A)成分的熔体。进一步研究了G-C3A的物理性质和水化行为。与C3A相比,G-C3A降低了晶格常数,降低了比重,增加了游离CaO。固化10 d水化未完成,3CaO⋅Al2O3⋅6H2O水合物生长缓慢。从G-C3A中洗脱的Al(OH)4-被认为对Ca2+有明显的抑制作用。G-C3A的摩尔比(CaO/Al2O3)在固化10天后为2.7,而C3A在固化6小时后接近1.0。即当G-C3A表面形成玻璃相时,应变发生在内层。因此,通过破坏-Al- o -Al-键来洗脱Al(OH)4-是困难的。虽然NaOH对Al(OH)4-的洗脱作用是相当大的,但由于Ca2+的洗脱作用受到抑制,水合物的生长不能预期。ESCA表面分析结果表明,G-C3A中Ca、Al和Si与O(氧)结合的内壳电子结合能比C3A高0.7-0.8eV。因此,由于Ca2+和Al(OH)4-的洗脱被抑制,水合反应变得不活跃。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Effect of Carbon Monoxide on the Sintering of SiC Whisker-Zirconia Composite Preparation and Properties of LiTaO3 Thin Films by Dipping Method Distribution of Impregnated Component and Nonuniformity of Colloidal Silica in Porous Glass Synthesis of High-Purity ZrF4 by Chemical Vapour Deposition Si//3N//4 FORMATION IN THE CARBOTHERMAL REDUCTION PROCESS OF A MAGADIITE-POLYACRYLONITRILE INTERCALATION COMPOUND.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1