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Unidirectional fibre reinforced geopolymer matrix composites

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posted on 2021-11-13, 22:55 authored by Welter, Michael

Geopolymers have been suggested in the literature as matrix materials for fibre reinforced composites due to a unique combination of low-temperature synthesis and high temperature stability. This study investigated several key aspects of fibre reinforced geopolymer matrix composites in order to improve the basic knowledge of these materials. It was demonstrated that geopolymer matrix composites show great potential as fire-resistant materials for near room temperature applications. In particular, basalt fibre composites were of great interest due to their comparatively low cost and good mechanical performance. Microstructural investigations indicated that basalt fibres can potentially be used in geopolymer matrices up to 600°C. However, the success of the application of geopolymer matrix composites at higher temperatures is seen as critical and depends on further development of suitable matrices.  Several compositions within a sodium-metahalloysite model matrix system were evaluated in order to identify a suitable formulation for composite fabrication. An average compressive strength of ~ 79 MPa and flexural strength and modulus of ~ 10 MPa and 8.5 GPa, respectively, were achieved for the best batch of the main matrix composition. By optimising the matrix composition, the mechanical properties could be significantly improved, achieving an extremely high maximum compressive strength value of 145 MPa. Issues with reproducibility and the influence of various aspects of the fabrication process are discussed.  The room temperature flexural properties of unidirectional fibre reinforced composite bars with basalt, carbon and alumina fibres were investigated. Besides the fibre type, the effects of several other parameters including fibre sizing, matrix strength, span-to-depth ratio and specimen dimensions on the flexural properties and the failure behaviour of the composites were studied. Significant improvements to the mechanical properties were achieved with all fibre types. However, the mechanical behaviour was highly influenced by the elastic modulus of the fibre. Furthermore, it was shown that the composite properties were affected by the overall sample dimensions, the testing span and the mixing time of the geopolymer binder. The alumina fibre composites achieved the highest flexural stress with a maximum value of 470 MPa and a fibre content of ~ 30 vol.-%. Basalt and carbon fibre composites showed maximum flexural strength values around 200 MPa. Although all composite types displayed considerable post-fracture strength, only the basalt composites failed in tensile mode. The applicability of the weak matrix composites (WMC) concept to describe the mechanical behaviour of geopolymer matrix composites was discussed.  The fibre-matrix interactions were analysed between room temperature and 1000°C by means of electron microscopy, EDS and x-ray diffraction. All fibres were found to be chemically stable under the highly alkaline conditions of the geopolymer synthesis and showed no significant reaction with the geopolymer matrix at room temperature. The results indicate that basalt fibre composites may be used up to 600°C without significant degradation of the fibre. The heating of the carbon fibre composites to 600°C had drastic effect on the strength and integrity of the composite, in particular, when using sized carbon fibres. The alumina fibres showed good wetting and bonding behaviour but otherwise little reaction with the matrix even after heating to 1000°C.


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Date of Award



Te Herenga Waka—Victoria University of Wellington

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Author Retains Copyright

Degree Discipline


Degree Grantor

Te Herenga Waka—Victoria University of Wellington

Degree Level


Degree Name

Doctor of Philosophy

ANZSRC Type Of Activity code

970103 Expanding Knowledge in the Chemical Sciences

Victoria University of Wellington Item Type

Awarded Doctoral Thesis



Victoria University of Wellington School

School of Chemical and Physical Sciences


MacKenzie, Kenneth