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In Honor of Nobel Laureate Dr. Aaron Ciechanover

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SIPS 2025 takes place from November 17-20, 2025 at the Dusit Thani Mactan Resort in Cebu, Philippines

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More than 400 abstracts submitted from over 50 countries
Abstracts Still Accepted for a Limited Time



Featuring many Nobel Laureates and other Distinguished Guests

ADVANCED PROGRAM

Orals | Summit Plenaries | Round Tables | Posters | Authors Index


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Oral Presentations


SESSION:
CompositeTuePM2-R1
Meyers International Symposium (11th Intl. Symp. on Composite, Ceramic & Nano Materials Processing, Characterization & Applications)
Tue. 18 Nov. 2025 / Room: Dusit 1
Session Chairs: Sergio Monteiro; Student Monitors: TBA

15:25: [CompositeTuePM208] OS
COLD SINTERING OF HYDROXYAPATITE USING PHOSPHORIC ACID AS TRANSIENT LIQUID PHASE
Pedro Henrique Poubel Mendonça Da Silveira1; Derick Horrana Souza Trindade1; Ary Machado De Azevedo1; Sergio Monteiro1; Marcelo Henrique Prado Da Silva1
1Military Institute of Engineering, Rio de Janeiro, Brazil
Paper ID: 37 [Abstract]

Cold Sintering Process (CSP) was employed to densify hydroxyapatite (HAp) using phosphoric acid (H₃PO₄) as a transient liquid phase at low temperature. HAp powders synthesized by aqueous precipitation were CSP-processed at 200 °C under 600 MPa for 30 min with H₃PO₄ contents of 5 or 10 wt% at 1 or 2 M. Apparent density (Archimedes), biaxial flexural strength (three-ball method, ABNT NBR ISO 6872), X-ray diffraction (XRD), and scanning electron microscopy (SEM) were used to correlate processing, microstructure, and properties. Despite the low thermal budget, CSP achieved apparent densities of 2.44–2.55 g cm⁻³, corresponding to 77.64–84.21% of the theoretical density. The 5%–2 M condition reached the highest densification (84.21%), whereas 10%–1 M delivered the best mechanical performance (σ_f = 36.08 ± 8.88 MPa), indicating that strength is not governed by densification alone. XRD confirmed predominance of the HAp phase (ICDD 00-009-0432) for all groups; average crystallite sizes ranged from 34.35 to 56.92 nm, with specific surface area increasing as crystallite size decreased (up to 87.53 m² g⁻¹). SEM revealed a microstructural evolution consistent with dissolution–reprecipitation: from porous, weakly coalesced networks (5%–1 M) to denser, better-bridged grains (10%–1 M), while excessive acidity (10%–2 M) promoted local fragility. Overall, tailoring the chemistry of the transient liquid phase enables efficient, phase-preserving, and energy-saving densification of HAp via CSP, offering a viable route for bioceramics where low processing temperatures and controlled microstructures are required.

For composite production, commercial corn starch plasticized with 30% glycerol was used. Ubim fibers were sourced from the local market in Belém (PA) and subjected to peeling and milling processes to optimize adhesion to the polymer matrix. The composites were processed using a single-screw extruder in five TPS/fiber ratios (0, 5, 10 and 15 wt.%). Films and test specimens were molded by hot pressing under standardized parameters. The composites were characterized through density, hardness (ASTM D2240), tensile strength (ASTM D638), and impact tests, as well as microstructural analyses by scanning electron microscopy (SEM) and phase evaluation by X-ray diffraction (XRD).

The results showed that the addition of ubim fibers to the thermoplastic starch composites significantly increased tensile strength, demonstrating the effectiveness of natural reinforcement in enhancing the mechanical properties of the polymer matrix. SEM analyses revealed morphological changes, highlighting good interfacial adhesion between the ubim fibers and TPS, which is essential for efficient stress transfer. XRD indicated the presence of semi-crystalline structures influenced by fiber incorporation. These findings confirm that the use of natural fibers, such as ubim, is a promising strategy for developing biodegradable composites with improved performance. Such materials exhibit high potential for sustainable plastic packaging applications, combining mechanical performance with reduced environmental impact.

References:
[1] J. Guo, R. Floyd, S. Lowum, J.-P. Maria, T. Herisson de Beauvoir, J.-H. Seo, C.A. Randall, Annu. Rev. Mater. Res. 49 (2019) 275–295.
[2] A. Ndayishimiye, M.Y. Sengul, T. Sada, S. Dursun, S.H. Bang, Z.A. Grady, K. Tsuji, S. Funahashi, A.C.T. van Duin, C.A. Randall, Open Ceram. 2 (2020) 100019.
[3] M. Kumar, M.A. Ben Achour, M. Lasgorceix, P. Quadros, R. Mincheva, J.-M. Raquez, A. Leriche, Open Ceram. 17 (2024) 100566.


15:45 COFFEE BREAK/POSTERS - Ballroom Foyer



08:00 SUMMIT PLENARY - Dusit Ballroom
12:00 LUNCH - Tradewinds Café

SESSION:
CompositeThuPM1-R1
Meyers International Symposium (11th Intl. Symp. on Composite, Ceramic & Nano Materials Processing, Characterization & Applications)
Thu. 20 Nov. 2025 / Room: Dusit 1
Session Chairs: Lisley Madeira Coelho; Student Monitors: TBA

13:20: [CompositeThuPM102] OS
FEASIBILITY OF COLD SINTERING PROCESSING OF PURE NIOBIUM FOR ADVANCED APPLICATIONS
Pedro Henrique Poubel Mendonça Da Silveira1; Ary Machado De Azevedo1; Derick Horrana Souza Trindade1; Plínio Honorato Muella Peixoto1; Marllon Fraga Silva1; Lisley Madeira Coelho1; Sergio Monteiro1; Marcelo Henrique Prado Da Silva1
1Military Institute of Engineering, Rio de Janeiro, Brazil
Paper ID: 53 [Abstract]

Niobium is a strategic material for Brazil, a country that holds the largest global reserves of this element. However, its sintering presents significant challenges, mainly due to the high reactivity of the metal, which promotes oxide formation and hinders consolidation. This study aimed to investigate the feasibility of cold sintering of niobium at different temperatures, seeking to minimize oxidative effects and enable new technological applications. The material used was supplied by CBMM (Companhia Brasileira de Metalurgia e Mineração), and experiments were conducted at temperatures of 125 °C, 150 °C, and 175 °C. To promote the formation of a transient liquid phase, niobium powders were mixed with 10 wt.% of absolute ethanol. Sintering was performed under a simultaneous pressure of 300 MPa, with a holding time of 30 minutes at each specified temperature. After processing, the samples were characterized through density measurements, scanning electron microscopy (SEM), and X-ray diffraction (XRD) analyses. The results indicated that cold sintering of niobium was effective even at the relatively low temperatures employed. XRD analysis revealed only minor peaks corresponding to the NbO phase, indicating a low incidence of oxidation during the process. These findings demonstrate the feasibility of cold sintering pure niobium, paving the way for the development of new components and applications, with advantages in reducing processing temperatures and preserving metallic properties. The use of cold sintering techniques thus represents a promising alternative for processing highly reactive metals such as niobium.



14:20 POSTERS - Ballroom Foyer