Steacie Institute for Molecular Sciences, National Research Council, Ottawa, ON, CanadaK1A 0R6.
Phys Chem Chem Phys. 2010 Jul 14;12(26):6961-9. doi: 10.1039/c000353k. Epub 2010 May 12.
This work is a systematic attempt to determine the possibilities and the limitations of the (43)Ca high field solid state NMR in the study of cement-based materials. The low natural abundance (0.135%) and small gyromagnetic ratio of (43)Ca present a serious challenge even in a high magnetic field. The NMR spectra of a number of cement compounds of known structure and composition are examined. The spectra of several phases important in cement science, e.g., anhydrous beta di-calcium silicate (beta-C(2)S) and tri-calcium (C(3)S) silicate were obtained for the first time and the relation of spectroscopic and structural parameters is discussed. The method was also applied to the hydrated C(3)S and synthetic calcium silicate hydrates (C-S-H) of different composition in order to understand the state of calcium and transformations in the structure during hydrolysis. The spectra of hydrated C(3)S reveals a calcium environment similar to that of the C-S-H samples and 11 A Tobermorite. These observations support the validity of using layered crystalline C-S-H systems as structural models for the C-S-H that forms in the hydration of Portland cement.
这项工作是系统地尝试确定(43)Ca 高场固态 NMR 在水泥基材料研究中的可能性和局限性。即使在高磁场中,(43)Ca 的天然丰度低(0.135%)和磁旋比小也带来了严重的挑战。研究了许多具有已知结构和组成的水泥化合物的 NMR 谱。首次获得了水泥科学中一些重要相的光谱,例如无水β二钙硅酸钙(β-C(2)S)和三钙(C(3)S)硅酸盐,并讨论了光谱和结构参数之间的关系。该方法还应用于不同组成的水化 C(3)S 和合成硅酸钙水合物(C-S-H),以了解水解过程中钙的状态和结构的转化。水化 C(3)S 的光谱揭示了类似于 C-S-H 样品和 11 A 托贝莫来石的钙环境。这些观察结果支持使用层状结晶 C-S-H 系统作为波特兰水泥水化过程中形成的 C-S-H 的结构模型的有效性。