4.7 Article

Phase dissolution and improving properties of completely decomposed granite through alkali fusion method

Journal

CEMENT & CONCRETE COMPOSITES
Volume 127, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cemconcomp.2022.104407

Keywords

Completely decomposed granite; Alkali fusion; Dissolution; Reactivity; Setting time; Alkali-activated binder

Funding

  1. National Nature Science Foundation of China [52108233, 52008265, 52078300, 51978414]
  2. Royal Society, UK [IEC\NSFC \181449]

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Low-reactive completely decomposed granite (CDG) was synthesized by thermal activation with the addition of NaOH at low alkali/CDG mass ratio. This method shows potential for producing geopolymers.
Low-reactive completely decomposed granite (CDG) was successfully synthesized by thermal activation with the addition of NaOH at low alkali/CDG mass ratio of 0.1/1. During alkali fusion, the degree of amorphicity of CDG rich in kaolinite (Al2Si2O5(OH)4) increased and a significant reduction of the peak intensities occurring between 20 and 45 (o2 theta) was observed. Reactivity analysis indicated that, initial CDG requires high molar NaOH to provide a proper dissolution, whereas fused CDG exhibits high reactivity (29Si = 555.57 ppm; 27Al = 223.73 ppm) at low NaOH concentration. Moreover, results from the setting time, varied between 15 and 45 min, indicating that alkali fusion is very effective for improving the dissolution of the fused CDG under Na2SiO3 solution. However, the setting time decreases as the reaction degree accelerates. FTIR analysis of the fused CDG presented lower wavenumber band of around 975 cm-1, confirming a decline of crystalline phases. In addition, SEM-EDS characterization and alkalinity analysis showed a compactness of the structure due to the liberation of enough sodium aluminosilicate gel. Finally, results from the mechanical test (4.75-39.55 MPa) and water solubility inferred that, by enhancing the reactivity of CDG by alkali fusion and by addition of up to 15% GGBS, CDG can be optimally recycled as an alternative source material to produce geopolymers.

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