The synthesis of N-A-S-H gel with high Si/Al ratios (>2) has been rarely reported in the literature, leaving the establishment of a reliable synthesis route as an open challenge. This paper aims to synthesize N-A-S-H gels with Si/Al ratios ranging from 1 to 3 and establish their thermodynamic database. The effects of reaction temperature, reaction time, initial Si/Al, concentration of reactants and pH of the matrix on the Si/Al ratios of the synthesized N-A-S-H gel were investigated. Results showed that N-A-S-H gels with target Si/Al ratios can be synthesized by controlling the concentration of reactants, pH and initial Si/Al ratios. The solubility products of the obtained N-A-S-H gels were determined via dissolution tests at different temperatures, to determine thermodynamic data. The development of this experimentally derived thermodynamic database of N-A-S-H gels constitutes a crucial step in the advancement of thermodynamic modeling of geopolymer, providing valuable insight into geopolymer reactions and phase assemblages.

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This study is undertaken to explore the relationship between the reaction products and the drying shrinkage of alkali-activated slag (AAS) with the varying hydroxide dosage. AAS pastes were firstly produced with either Al(OH)3 or Mg(OH)2 to investigate the effects of hydroxide on the composition of reaction products and the drying shrinkage of AAS. Secondly, the main reaction products formed in AAS pastes, viz. C4AH13, M4AH10, C-S-H, C-A-S-H and C-M-S-H, were synthesized individually. Synthetic products were then taken to cast the respective paste sample to examine the performance against the drying exposure. The results show that adding Mg(OH)2 indeed improved the shrinkage resistance of AAS. This is primarily connected to the increased crystalline phases, namely the hydrotalcite-like phases and the unreacted Mg(OH)2. Whereas adding Al(OH)3 did not relieve the drying shrinkage of AAS as the interlayer spacing of C-A-S-H was enlarged, which in turn allowed for more shrinkage. Further, the investigation of individual synthetic products illustrates that their drying shrinkage scales satisfied the following order: C4AH13 < M4AH10 < C-M-S-H < C-S-H < C-A-S-H. Moreover, the shrinkage scale of C-S-H was found to evolve as the Ca/Si ratio decreased.@en

In this paper, the atomic structures of sodium aluminosilicate hydrate (N–A–S–H) gels with different Si/Al ratios are studied by molecular dynamics simulation. An N–A–S–H gel model was obtained from the polymerization of Si(OH)₄ and Al(OH)₃ monomers with the use of a reactive force field (ReaxFF). The simulated atomic structural features, such as the bond length, bond angle, and simulated X-ray diffraction pattern of the gel structure are in good accordance with the experimental results in the literature. Si–O–Al is found to be preferred over Si–O–Si in the N–A–S–H gel structure according to the amount of T–O–T bond angles and distribution of Si⁴(mAl). Pentacoordinate Al is identified in all simulated N–A–S–H models. It provides strong support to current knowledge that pentacoordinate Al in geopolymer does not only come from raw material. Furthermore, the structural analysis results also show that N–A–S–H gel with lower Si/Al ratios has a more cross-linked and compacted structure.

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This study presents a comprehensive experimental investigation on the fracture properties of hardened alkali-activated slag/fly ash (AASF) pastes in relation to the microstructure formation and reaction product composition. The main reaction product in AASF is C-(N-)A-S-H gel along with minor hydrotalcite phase, with the polymerization of C-(N-)A-S-H gel substantially governed by its Ca/Si ratio. Strong positive correlations are identified between the Ca/Si ratios of C-(N-)A-S-H gel and the fracture properties K_Ic (J_tip), whereas, the compressive strength of AASF pastes is primarily determined by its capillary porosity (>0.01 μm). The disagreements between the Ca/Si ratios and corresponding intrinsic mechanical properties of C-(N-)A-S-H gel as proof by contradiction indicate that the fracture properties K_Ic (J_tip) of AASF pastes could be dominated by a cohesion/adhesion-based mechanism. These findings provide promising guidance for fine-tuning the fracture properties of AASF and also advise on the tailoring strategies for high-performance composite such as strain-hardening geopolymer composite.

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The understanding of sodium aluminosilicate hydrate (N-A-S-H) gel is still limited due to its complex and amorphous structure. Recently, molecular dynamics simulation has provided a unique opportunity to better understand the structure of N-A-S-H gel from nanoscale. In this work, the N-A-S-H gel structure was obtained by simulating the polymerization of Si and Al monomers by molecular dynamics. The simulated polymerization process is in good agreement with the experimental results especially in terms of the reaction rate of Si and Al species. The atomic structural features of the N-A-S-H gel were analyzed in terms of bond length and bond angle information, simulated X-ray diffraction (XRD) and Qn distribution. A significant finding is the existence of pentacoordinate Al in all simulated N-A-S-H structures, indicating that pentacoordinate Al in geopolymer does not only come from raw material. Besides, the results show that a smaller Si/Al ratio led to a more crosslinked and compacted structure of N-A-S-H gel.@en