制备了具有宽范围Ca/(Si+Al)比和Al/Si比的铝掺杂水化硅酸钙(C-A-S-H)系列样品,采用。^27Al魔角旋转固体核磁共振技术(^27AlMASNMR)半定量研究了Al在C-A-S—H结构中的配位状态。结果表明:Al在C—A—S—H结构的配位形式和位置主要取决于其初始Ca/(Si+Al)比和Al/Si比。当初始Ca/(Si+A1)比低时(0.6和0.8),Al只能取代硅酸盐链硅氧四面体结构中四配位的Si,以Al[4]的形式存在;随着Ca/(Si+Al)比的增加,部分Al开始形成Al[5]和Al[6],且随着Al/Si比的增加,Al[4]的含量减小,Al[5]和Al[6]的总量增加,但Al[4]还是占主要比例,Al[5]的量非常少。Al[4]既可取代桥四面体中的Si也可取代配对四面体中的Si,但优先取代的是桥四面体中的Si,两者取代比并非恒定,而是随着初始Ca/(Si+Al)比和Al/Si比的变化而变化。
Aluminum-substituted calcium silicate hydrate (C-A-S-H) series with various ratios of Ca/(Si+AI) and Al/Si were prepared. The Al incorporation in C-S-H structure was semi-quantitatively investigated by 27Al magic angle spinning nuclear magnetic resonance (27Al MAS NMR). The results show that the possible site and content of Al in C-S-H structure mainly depend on initial ratios of Ca/(Si+A1) and Al/Si. At low ratios of Ca/(Si+Al) of 0.6 and 0.8, A1 only substitutes 4-coordinated Si in the silicate chains. Some A1 starts to form Al[5] and Al[6] as Ca/(Si+Al) ratio increases, and the content of Al[4] decreases, but Al[4] is still dominant and Al[5] is rather limited as Al/Si ratio increases. Al can substitute Si in both bridging and pairing sites, Al-Si substitution takes priority in bridging site, and the ratio of the Al number in bridging site to that in pairing site depends on the initial ratios of Ca/(Si+A1) and Al/Si.