Zaneta Senselova

Mrs. Zaneta Senselova


Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 December 2025 in Polymers
Verified
Journal Article
Open access
PDF file
AIAbdullah Iftikhar
Abdullah Iftikhar
AMAllan Manalo
Allan Manalo
ZSZaneta Senselova
Zaneta Senselova
Wahid FerdousWahid Ferdous
Wahid Ferdous
MPMazhar Peerzada
Mazhar Peerzada
BBBrahim M. Benmokrane
Brahim M. Benmokrane
This study investigates hygrothermal durability of bio-epoxy composites reinforced with carbon, E-glass, basalt, and flax fibres. Fibre yarns and bio-composites were exposed for 3000 h at 60 °C and 98% relative humidity. The tensile strength reduction in the fibres and the interfacial shear strength (IFSS) reduction in the composites were assessed after ageing. Chemical deterioration was evaluated using energy-dispersive X-ray spectroscopy (EDS); morphological changes in fibres and composites fracture surfaces were examined using a scanning electron microscope (SEM). Results indicated that the durability was significantly influenced by fibre types. Tensile strength reduction was higher in carbon, glass and basalt compared to flax yarns because of chemical degradation of the sizing layer in synthetic fibres, while only physical damage was observed in flax. The IFSS reduction was highest in flax composites (10%), and lowest in carbon (4%). EDS indicated the hydrolysis and erosion of fibre sizing, with reduced silica content in glass and basalt fibres. SEM revealed matrix-dominated failure in carbon/bio-epoxy, interfacial debonding in glass and basalt composites, fibre slip and pull-out in flax/bio-epoxy. Overall, the results highlighted damage propagation pathways and demonstrated that bio-epoxy composites exhibited reasonable performance under hygrothermal ageing, supporting their potential as a sustainable alternative in durability-critical applications.

12 March 2026 in Polymers
Verified
Journal Article
Open access
PDF file
ZSZaneta Senselova
Zaneta Senselova
AMAllan Manalo
Allan Manalo
AIAbdullah Iftikhar
Abdullah Iftikhar
OMAR ALAJARMEHOMAR ALAJARMEH
OMAR ALAJARMEH
Sayanthan RamakrishnanSayanthan Ramakrishnan
Sayanthan Ramakrishnan
BBBrahim M. Benmokrane
Brahim M. Benmokrane
This study investigates the degradation mechanisms of glass-fibre- and carbon-fibre-reinforced polymer (GFRP and CFRP, respectively) composites fabricated either with epoxy, vinyl-ester, or bio-epoxy resins under a hygrothermal environment. Composite laminates were manufactured using the vacuum-assisted resin infusion technique and exposed to high moisture and elevated in-service temperatures of 23 °C (room temperature), 40 °C and 60 °C for up to 125 days. Changes in the physical, microstructural, chemical and mechanical properties were then assessed. CFRP and GFRP composites showed distinct differences in their hygrothermal ageing depending on the resin system used in the manufacturing. CFRP composites consistently demonstrated higher stability than GFRP composites. Epoxy resin exhibited high resistance to water absorption and hydrolysis under hygrothermal exposure. After 125 days at 60 °C, glass/epoxy (GE) and carbon/epoxy (CE) composites retained 79.0% and 72.1% of their tensile strength and 46.9% and 72.6% of their interlaminar shear strength (ILSS), respectively. Vinyl-ester composites showed high mechanical retention, with glass/vinyl-ester (GV) and carbon/vinyl-ester (CV) retaining 70.8% and 83.1% of tensile strength and 67.5% and 80.3% of ILSS, respectively. Despite this mechanical stability, evidence of hydrolysis indicated ongoing chemical degradation of the vinyl-ester resin under prolonged hygrothermal exposure. In contrast, bio-epoxy composites exhibited relatively low overall durability. Glass/bio-epoxy (GB) retained 126.5% tensile strength and 68.8% ILSS, whereas carbon/bio-epoxy retained 61.0% tensile strength and 44.3% ILSS after 125 days at 60 °C. Overall, fibre and resin types were found to have a significant effect on the hygrothermal ageing of polymer composites.