Investigating the effect of pyrolysis temperature on bio-oil composition in bio-epoxy composites, indicating a path for partially bio-based resins.
In this study, we develop bio-epoxy composites incorporating bio-oils obtained from the pyrolysis of almond and walnut shells at 400 °C and 600 °C, with the aim of evaluating their potential as renewable precursors for epoxy resin modification. The influence of pyrolysis temperature on bio-oil yield and chemical composition is examined to identify phenolic-rich fractions relevant to epoxy curing. Bio-oil production increased with temperature, reaching 40.46% for walnut shells and 36.84% for almond shells at 600 °C. Chemical analysis revealed that aromatic compounds, particularly phenolics, were the major constituents associated with epoxy curing reactivity. For walnut hulls, the total aromatic fraction increased from 30.4% at 400 °C to 35.2% at 600 °C, while almond hulls showed an increase from 23.8% to 26.1% over the same temperature range. Incorporation of bio-oil into the epoxy matrix promoted three-dimensional network formation through reactions between epoxy groups and the functional moieties present in the bio-oil, resulting in a higher cross-linking degree, Young’s modulus, and tensile strength. However, compared to neat epoxy, the bio-oil-modified systems exhibited reduced storage modulus (E′) and glass transition temperature (Tg), attributed to the plasticizing effect of lighter oxygenated species. Overall, although bio-oil incorporation decreases Tg and cross-linking degree, it still provides a viable pathway toward partially bio-based epoxy resins with enhanced stiffness and competitive mechanical performance.
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Hidalgo et al. (2026) studied this question.
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