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. 2025 Jun 10;14(12):2042.
doi: 10.3390/foods14122042.

Thin-Layer, Intermittent, Near-Infrared Drying of Two-Phase Olive Pomace: Mathematical Modeling and Effect on Recovery of Bioactive Compounds and Antioxidant Activity

Affiliations

Thin-Layer, Intermittent, Near-Infrared Drying of Two-Phase Olive Pomace: Mathematical Modeling and Effect on Recovery of Bioactive Compounds and Antioxidant Activity

Ioanna Pyrka et al. Foods. .

Abstract

The present study examined the drying kinetics of two-phase olive pomace (OP) using near-infrared (NIR) thin layer intermittent drying at 70-140 °C. For the first time, this approach was combined with color, bioactive compound retention and antioxidant activity assessment. Among tested models, the Midilli's semi-empirical model best described the drying behavior (r2 ≥ 0.99839, RMSE ≤ 0.01349). Effective diffusivity ranged from 1.417 × 10-9 to 5.807 × 10-9 m2/s, and activation energy was calculated at 23.732 kJ/mol. Drying at 140 °C reduced time by 68% compared to 70 °C. The corresponding sample had the highest total phenolics content, antioxidant activity (DPPH, CUPRAC assays) and triterpenic acid (maslinic, oleanolic) content, and a significant amount of hydroxytyrosol, despite the increased sample browning. Compared to oven-drying (140 °C), NIR was equal or better and 3.2-fold faster. The same was evidenced compared to freeze-drying, except for tyrosol recovery (1.2-fold lower in NIR). These findings were obtained using two different OP industrial samples. Given that NIR is already used industrially for food drying, the present study offers proof-of-concept for its application as a rapid and eco-friendly pretreatment of OP for food and feed uses. However, scalability challenges and the limitations of semi-empirical modeling must be addressed in the future to support industrial-scale implementation.

Keywords: antioxidants; bioactives; drying kinetics; hydroxytyrosol; mathematical modeling; near-infrared drying; olive pomace.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Experimental drying curves of olive pomace at five studied temperatures. Plots represent average of three measurements.
Figure 2
Figure 2
Experimental drying speed curves of olive pomace at five studied temperatures. Plots represent average of three measurements.
Figure 3
Figure 3
Plot of ln(MR) against drying time at studied temperatures (solid lines). Linear trendlines (dotted lines), their equation and R2 values are displayed for each curve. Plots represent average of three measurements.
Figure 4
Figure 4
Arrhenius-type relationship between effective diffusivity (Deff) and temperature (T, K).
Figure 5
Figure 5
(A) Total phenolics content (TPC) and (B) antioxidant activity (AA), using DPPH and CUPRAC assays, of olive pomace (OP1) dried at five different temperatures (70, 90, 100, 120, 140 °C). Results are expressed as mean ± standard deviation values (n = 3). Same letters above bars indicate that no significant difference was found at (p < 0.05) applying Games–Howell post hoc test.
Figure 6
Figure 6
Main phenolic compounds (hydroxytyrosol and tyrosol) and triterpenic acids (maslinic and oleanolic acids) of olive pomace (OP1) dried at five different temperatures (70, 90, 100, 120, 140 °C). Results are expressed as mean ± standard deviation values (n = 3). Different letters above bars indicate a significant difference (p < 0.05) applying Games–Howell post hoc test.
Figure 7
Figure 7
Total phenolics content (TPC) of olive pomace samples (OP1, OP2) dried with infrared radiation at 140 °C (IR), oven heating at 140 °C (OD) and freeze-drier (FD). Results are expressed as mean ± standard deviation values (n = 3). Different lowercase and capital letters above bars indicate a significant difference (p < 0.05) for OP1 and OP2, respectively, applying Games–Howell post hoc test.
Figure 8
Figure 8
Antioxidant activity (AA) of olive pomace samples (OP1, OP2), measured by DPPH● (A) and CUPRAC (B) assays and dried with infrared radiation at 140 °C (IR), oven heating at 140 °C (OD) and freeze-drier (FD). Results are expressed as mean ± standard deviation values (n = 3). Different lowercase and capital letters above bars indicate a significant difference (p < 0.05 for OP1 and OP2, respectively, applying Games–Howell post hoc test.
Figure 9
Figure 9
Main phenolic compounds (hydroxytyrosol, A and tyrosol, B) and triterpenic acids (maslinic, C and oleanolic, D acids) of olive pomace samples (OP1, OP2) dried with infrared radiation at 140 °C (IR), oven heating at 140 °C (OD) and freeze-drier (FD). Results are expressed as mean ± standard deviation values (n = 3). Different lowercase and capital letters above bars indicate a significant difference (p < 0.05) for OP1 and OP2, respectively, applying Games–Howell post hoc test.

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