C-(N)-S-H and N-A-S-H gels: Compositions and solubility data at 25°C and 50°C

被引:56
作者
Gomez-Zamorano, Lauren [1 ,2 ]
Balonis, Magdalena [3 ,4 ]
Erdemli, Bartu [2 ]
Neithalath, Narayanan [5 ]
Sant, Gaurav [2 ,6 ]
机构
[1] Univ Autonoma Nuevo Leon, Programa Doctoral Ingn Mat, Fac Ingn Mecan & Elect, San Nicolas De Los Garza, Mexico
[2] Univ Calif Los Angeles, Dept Civil & Environm Engn, Lab Chem Construct Mat LC2, Los Angeles, CA USA
[3] Univ Calif Los Angeles, Dept Mat Sci & Engn, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Inst Technol Adv, Los Angeles, CA USA
[5] Arizona State Univ, Sch Sustainable Engn & Built Environm, Tempe, AZ USA
[6] Univ Calif Los Angeles, Calif Nanosyst Inst CNSI, Los Angeles, CA USA
基金
美国国家科学基金会;
关键词
calcium silicate hydrate; cements; geopolymers; solubility; thermodynamics; CALCIUM SILICATE HYDRATE; ALKALI-ACTIVATED MATERIALS; MOLAL THERMODYNAMIC PROPERTIES; PORTLAND-CEMENT; SOLID-SOLUTIONS; PART I; MODEL; PHASE; GEOPOLYMERS; PASTES;
D O I
10.1111/jace.14715
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Calcium silicate hydrates containing sodium [C-(N)-S-H], and sodium aluminosilicate hydrates [N-A-S-H] are the dominant reaction products that are formed following reaction between a solid aluminosilicate precursor (eg, slags, fly ash, metakaolin) and an alkaline activation agent (eg NaOH) in the presence of water. To gain insights into the thermochemical properties of such compounds, C-(N)-S-H and N-A-S-H gels were synthesized with compositions: 0.8Ca/Si1.2 for the former, and 0.25Al/Si0.50 (atomic units) for the latter. The gels were characterized using thermogravimetric analysis (TGA), scanning electron microscopy with energy-dispersive X-ray microanalysis (SEM-EDS), and X-ray diffraction (XRD). The solubility products (K-S0) of the gels were established at 25 degrees C and 50 degrees C. Self-consistent solubility data of this nature are key inputs required for calculation of mass and volume balances in alkali-activated binders (AABs), and to determine the impacts of the precursor chemistry on the hydrated phase distributions; in which, C-(N)-S-H and N-A-S-H compounds dominate the hydrated phase assemblages.
引用
收藏
页码:2700 / 2711
页数:12
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