Department of Chemistry "Ugo Schiff" & Consorzio per lo Sviluppo dei Sistemi a Grande Interfase (CSGI), University of Florence, Via della Lastruccia, 3, 50019 Sesto Fiorentino, Italy.
Department of Nuclear Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Phys Chem Chem Phys. 2021 Feb 4;23(4):2630-2636. doi: 10.1039/d0cp06251k.
Calcium silicate hydrate (C-S-H) is the main binding product of ordinary Portland concrete (OPC). Unfortunately, OPC production generates ∼5% of all anthropomorphic CO2. Among the most promising green alternatives, magnesium silicate hydrate (M-S-H) is a colloidal gel equivalent to C-S-H which exhibits weaker mechanical properties. Here we investigated the effect of the inclusion of aluminosilicate nanoclays (HNTs) on the microstructure of the silicate hydrate gels as a strategy to ultimately improve their mechanical properties. The microstructure of C-S-H and M-S-H gels synthesized with and without carboxylic or polycarboxylic functionalised HNTs (HNT-COOH, HNT-PAA) was investigated by a multi-technique approach including small- and wide-angle X-ray scattering (SWAXS) and scanning electron microscopy (SEM). The results indicate that, during C-S-H formation in solution, HNTs decrease the size of the disk-like globules with little influence on the spacing of calcium silicate layers. In the case of M-S-H, the presence of functionalised HNTs has a reduced effect on the hydrate structure as a result of the weaker interaction of the carboxylic moieties with Mg2+ ions. SEM investigation on the synthesized composites shows that HNT-PAA are better included in the hydration products. Moreover, in the proximity of the PAA functionalised surfaces, less extended aggregates are formed. The morphology at the micron scale for M-S-H and C-S-H with HNT-COOH is conserved.
硅酸钙水合物(C-S-H)是普通波特兰水泥(OPC)的主要结合产物。不幸的是,OPC 的生产会产生约 5%的人为 CO2。在最有前途的绿色替代品中,硅酸镁水合物(M-S-H)是一种与 C-S-H 相当的胶态凝胶,其机械性能较弱。在这里,我们研究了包含铝硅酸盐纳米粘土(HNTs)对硅酸盐水凝胶微观结构的影响,作为最终改善其机械性能的策略。通过包括小角和广角 X 射线散射(SWAXS)和扫描电子显微镜(SEM)在内的多种技术方法研究了在有无羧酸或多羧酸官能化 HNTs(HNT-COOH、HNT-PAA)的情况下合成的 C-S-H 和 M-S-H 凝胶的微观结构。结果表明,在溶液中形成 C-S-H 时,HNTs 会减小盘状小球的尺寸,而对硅酸钙层的间距影响不大。在 M-S-H 的情况下,由于羧酸部分与 Mg2+离子的相互作用较弱,官能化 HNTs 对水合结构的影响较小。对合成复合材料的 SEM 研究表明,HNT-PAA 更好地包含在水合产物中。此外,在 PAA 官能化表面附近,形成的延伸聚集体较少。具有 HNT-COOH 的 M-S-H 和 C-S-H 的微米尺度形貌得以保留。