Abstract

This paper proposes the induction of an acid-base reaction during the formation of silico-aluminophosphate (SAP) geopolymer. Such reaction is promoted by dead burnt magnesia (DBM) and phosphate activating solution to synthesize a DBM-doped silico-aluminophosphate (DBM-SAP) geopolymer with enhanced early-age properties. The reaction mechanisms and chemistries between DBM and mono-aluminum phosphate (MAP) in aqueous solution were firstly investigated at four Mg/Al ratios. Conductivity and pH evolutions of the solution systems, in addition to X-ray diffraction (XRD) and scanning electron microscopy (SEM) results of the final precipitations indicated that the crystalline phase (i.e., Newberyite) started to precipitate at a pH of 3 approximately. Besides, the reaction between DBM and MAP produced an amorphous aluminum magnesium phosphate (Al2O3·3MgO·2P2O5) phase. The rate of such reaction was governed by the DBM/MAP ratio in the solution system. Setting time and early strength of the DBM-SAP geopolymer pastes with an optimal Mg/Al ratio (i.e., 4) in solution system were evaluated to confirm the acceleration effect of DBM-induced acid-base reaction. Experimental results showed that 20% incorporation of DBM enabled the preparation of an SAP geopolymer with an initial setting time of 8 min and 1 day compressive strength of 8.3 MPa. Phosphorrösslerite was detected in the 1d-cured geopolymer paste but disappeared after 3 days curing. Such reaction intermediate might contribute to the fast setting and achieving early strength.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.