Abstract

Alkali-activated ZnO–geopolymer composites were synthesised using metakaolin to investigate their photocatalytic degradation efficiency toward methylene blue and α-pinene under 253.7 nm irradiation. Composites prepared with bulk Si/Al molar ratios (1 and 2), ZnO/Al loadings (0.10, 0.15, and 0.20), were characterised using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), N2-sorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV-vis spectroscopy. A custom-built flow cell was used for gas-phase α-pinene degradation, while aqueous methylene blue degradation was evaluated under batch conditions. A key finding of the study was that increasing ZnO content led to matrix densification, reduced surface area, and blue shifting of the adsorption band. Structural studies revealed that ZnO was integrated into the geopolymer framework through bonding with aluminium within the composite. The highest 160 mg/L methylene blue removal (91.05%) was achieved by a geopolymer with Si/Al ratio of 2 and attributed to naturally occurring TiO2 phases in the metakaolin coupled with a high surface area. These samples exhibited superior continuous α-pinene degradation, with a maximum removal of 26.93%, which was attributed to reduced Al–OH surface groups and lower hydrophilicity, favouring VOC adsorption. Significantly, this research identifies the critical parameters of incorporating ZnO into a geopolymer framework, suggesting that both the concentration of ZnO added, and the microstructural modification induced by ZnO play important roles in determining photocatalytic activity. This study revealed how ZnO influences the physicochemical characteristics of geopolymers, and the remediation mechanism of pollutants from aqueous and gaseous environments.
Original languageEnglish
Article number106125
JournalCement and Concrete Composites
Volume162
Early online date21 May 2025
DOIs
Publication statusE-pub ahead of print - 21 May 2025

Data Availability Statement

Data will be made available on request

Acknowledgements

The authors would like to thank the technical staff at The University of Bath for their support with material characterisation. We are particularly gratefully to Dr G. Kociok-Köhn for assistance XRD, Dr T. Woodman for support with solid-state NMR, Dr O. Camus for assistance with N2-sorption, Dr P. Fletcher for support with SEM and TEM imaging, W. Bazeley for help with constructing the novel flow cell and Dr K. Proctor for their expertise on TD-GCMS.

Funding

This study is sponsored by the University of Bath Research Scholarship Award (J Wilson).

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