Effect of Ordinary Portland Cement on Mechanical Properties and Microstructures of Metakaolin-Based Geopolymers

Geopolymers have been considered a sustainable alternative to ordinary Portland cement (CEM I) for its lower embodied carbon and ability to make use of industrial by-products. Additionally, its excellent engineering properties of high strength, low permeability, good chemical resistance, and excellent fire resistance also strike a chord in the minds of researchers. The goal of this study is to clarify the effect of calcium sources on the mechanical properties and microstructures of the geopolymers. CEM I was chosen as the sole calcium source, while metakaolin was used as the source material. Five distinct geopolymers were prepared, having various ratio of CEM I: 0%, 5%, 10%, 20%, and 30%. The alkali-activator was a mixture of 12 M sodium hydroxide (NaOH) and sodium silicate (Na(2)SiO(3)), utilizing compressive strength and flexural strength to evaluate the changes of the geopolymers’ mechanical properties. SEM, XRD, and FTIR were used to examine microscopic features, evaluate internal morphology, and analyze changes in components of the geopolymers containing different amounts of CEM I. The experimental results indicated that the optimal incorporation of CEM I was 5%. Under this dosage, the compressive strength and flexural strength of the geopolymers can reach 71.1 MPa and 6.75 MPa, respectively. With the incorporation of CEM I, the heat released by cement hydration can accelerate the geopolymerization reaction between silica-alumina materials and alkaline solutions. Additionally, the coexistence of N-A-S-H gel from components of an aluminosilicate mix and C-S-H gel from the CEM I promoted a more densified microstructure of the geopolymers and improved the geopolymer’s strength. However, as the amount of CEM I in the mixture increased, the geopolymer matrix was unable to provide enough water for the CEM I to hydrate, which prevented excessive CEM I from forming hydration products, weakening the workability of the matrix and eventually hindering the development of geopolymer strength.