Abstract

The purpose of this study was to evaluate the feasibility of utilizing sewage sludge as a source of aluminosilicate to synthesise geopolymer cement. Sewage sludge was calcined at various temperatures to enhance its geopolymer reactivity. Sodium hydroxide and sodium silicate solution mixture was used as an alkaline activator. The geopolymer mortars' setting time, flow workability, unconfined compressive strength (UCS), pore volume, and water absorption characteristics, wet-dry cycles and TCLP characteristics were measured. X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) were used for microstructural analysis. The results showed that the highest 7-day UCS of up to 18.9 MPa was obtained, corresponding to a 270.6% strength increase over the control. The microstructural analysis showed that the optimal mechanical and physical properties were obtained when the sewage sludge was calcined at 750 °C showing that calcining the sewage sludge increases the geopolymer reactivity. The UCS decreases with the increase in wet dry cycles but the geopolymer composites were still within the minimum strength requirement of 3.5 MPa. TCLP showed that the leachability of the produced geopolymers is below the permissible limit. Geopolymer mortar made from sewage sludge ash can be utilized for various concrete and building applications without the risk of short- or long-term environmental contamination.

Full Text
Paper version not known

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.