{"title":"脱钙对水泥浆中C-S-H凝胶微观结构的影响","authors":"Zhen He, Lei Wang, Y. Shao, Xinhua Cai","doi":"10.3969/J.ISSN.1007-9629.2011.03.002","DOIUrl":null,"url":null,"abstract":"Effect of decalcification on microstructure of C-S-H gel in ASTMⅠcement paste were studied by X-ray fluorescence spectrometer(XRF),X-ray diffraction(XRD),infrared spectroscopy with Fourier transform(FTIR) and ~(29)Si MAS NMR with deconvolution technique.It is shown from test results that the decalcification process can be divided into two stages.When the molar ratio of CaO to SiO_2 in the pastes at 3,28 d is lowered from~2.78 to~2.00,almost all of CH is removed and C-S-H gel is partially decalcified, the average chain length(ACL) of C-S-H is increased from 2.4 to 4.4 for 3 d paste and from 2.9 to 5.8 for 28 d paste respectively,and I(Q~2)/I(Q~1) is also increased.While the molar ratio of CaO to SiO_2 in the pastes comes to~1.83,decalcification of C-S-H gel occurs.C-S-H polymerizes and I(Q~2)/I(Q~1) increases largely in this stage,which results in further increase of ACL to 6.2 for 3 d paste and 9.9 for 28 d paste.The mechanism of increase of C-S-H polymerization could be transformation of dimeric C-S-H toward highly polymerized C-S-H.However,Al doping could affect the stability of C-S-H microstructure. In molecular level,the existence of the pure bridging silicon-oxy tetrahedrons in C-S-H is beneficial to the optimization of the microstructure.","PeriodicalId":39562,"journal":{"name":"Jianzhu Cailiao Xuebao/Journal of Building Materials","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"12","resultStr":"{\"title\":\"Effect of decalcification on C-S-H gel microstructure in cement paste\",\"authors\":\"Zhen He, Lei Wang, Y. Shao, Xinhua Cai\",\"doi\":\"10.3969/J.ISSN.1007-9629.2011.03.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Effect of decalcification on microstructure of C-S-H gel in ASTMⅠcement paste were studied by X-ray fluorescence spectrometer(XRF),X-ray diffraction(XRD),infrared spectroscopy with Fourier transform(FTIR) and ~(29)Si MAS NMR with deconvolution technique.It is shown from test results that the decalcification process can be divided into two stages.When the molar ratio of CaO to SiO_2 in the pastes at 3,28 d is lowered from~2.78 to~2.00,almost all of CH is removed and C-S-H gel is partially decalcified, the average chain length(ACL) of C-S-H is increased from 2.4 to 4.4 for 3 d paste and from 2.9 to 5.8 for 28 d paste respectively,and I(Q~2)/I(Q~1) is also increased.While the molar ratio of CaO to SiO_2 in the pastes comes to~1.83,decalcification of C-S-H gel occurs.C-S-H polymerizes and I(Q~2)/I(Q~1) increases largely in this stage,which results in further increase of ACL to 6.2 for 3 d paste and 9.9 for 28 d paste.The mechanism of increase of C-S-H polymerization could be transformation of dimeric C-S-H toward highly polymerized C-S-H.However,Al doping could affect the stability of C-S-H microstructure. In molecular level,the existence of the pure bridging silicon-oxy tetrahedrons in C-S-H is beneficial to the optimization of the microstructure.\",\"PeriodicalId\":39562,\"journal\":{\"name\":\"Jianzhu Cailiao Xuebao/Journal of Building Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"12\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Jianzhu Cailiao Xuebao/Journal of Building Materials\",\"FirstCategoryId\":\"1087\",\"ListUrlMain\":\"https://doi.org/10.3969/J.ISSN.1007-9629.2011.03.002\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Engineering\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jianzhu Cailiao Xuebao/Journal of Building Materials","FirstCategoryId":"1087","ListUrlMain":"https://doi.org/10.3969/J.ISSN.1007-9629.2011.03.002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Engineering","Score":null,"Total":0}
引用次数: 12
摘要
采用x射线荧光光谱仪(XRF)、x射线衍射仪(XRD)、红外傅立叶变换光谱仪(FTIR)和~(29)Si MAS NMR反褶积技术研究了脱钙对ASTMⅠ水泥浆中C-S-H凝胶微观结构的影响。试验结果表明,脱钙过程可分为两个阶段。当膏体中CaO / SiO_2的摩尔比在3,28 d时从~2.78降低到~2.00时,CH几乎全部被去除,C-S-H凝胶部分脱钙,C-S-H的平均链长(ACL)从3 d的2.4增加到4.4,28 d的2.9增加到5.8,I(Q~2)/I(Q~1)也有所增加。当膏体中CaO与SiO_2的摩尔比达到~1.83时,C-S-H凝胶发生脱钙,C-S-H发生聚合,I(Q~2)/I(Q~1)大幅增加,使3 d膏体的ACL进一步提高到6.2,28 d膏体的ACL进一步提高到9.9。C-S-H聚合增加的机理可能是二聚体C-S-H向高聚合的C-S-H转化。Al掺杂会影响C-S-H微观结构的稳定性。在分子水平上,C-S-H中纯桥接硅氧四面体的存在有利于结构的优化。
Effect of decalcification on C-S-H gel microstructure in cement paste
Effect of decalcification on microstructure of C-S-H gel in ASTMⅠcement paste were studied by X-ray fluorescence spectrometer(XRF),X-ray diffraction(XRD),infrared spectroscopy with Fourier transform(FTIR) and ~(29)Si MAS NMR with deconvolution technique.It is shown from test results that the decalcification process can be divided into two stages.When the molar ratio of CaO to SiO_2 in the pastes at 3,28 d is lowered from~2.78 to~2.00,almost all of CH is removed and C-S-H gel is partially decalcified, the average chain length(ACL) of C-S-H is increased from 2.4 to 4.4 for 3 d paste and from 2.9 to 5.8 for 28 d paste respectively,and I(Q~2)/I(Q~1) is also increased.While the molar ratio of CaO to SiO_2 in the pastes comes to~1.83,decalcification of C-S-H gel occurs.C-S-H polymerizes and I(Q~2)/I(Q~1) increases largely in this stage,which results in further increase of ACL to 6.2 for 3 d paste and 9.9 for 28 d paste.The mechanism of increase of C-S-H polymerization could be transformation of dimeric C-S-H toward highly polymerized C-S-H.However,Al doping could affect the stability of C-S-H microstructure. In molecular level,the existence of the pure bridging silicon-oxy tetrahedrons in C-S-H is beneficial to the optimization of the microstructure.