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Publications (8/8 displayed)
- 2024Effect of environmental temperature and semi‐crystalline order on the toughening of polyamide 1010 by <scp>2D</scp> nanomaterials
- 2024Balancing thermal conductivity, dielectric, and tribological properties in polyamide 1010 with 2D nanomaterialscitations
- 2019Deployment of 4P, the high-speed phenotyping data processing platform on the France Grilles infrastructure.
- 2019Deployment of 4P, the high-speed phenotyping data processing platform on the France Grilles infrastructure.
- 2019Dielectric properties of epoxy/POSS and PE/POSS systems
- 2018Electrical Breakdown Properties of Clay-Based LDPE Blends and Nanocompositescitations
- 2016Dielectric properties of epoxy/montmorillonite nanocomposites and nanostructured epoxy/SiO2/Montmorillonite Microcompositescitations
- 2016Functional Nanomaterials For Electric Power Industry
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article
Effect of environmental temperature and semi‐crystalline order on the toughening of polyamide 1010 by <scp>2D</scp> nanomaterials
Abstract
<jats:title>Abstract</jats:title><jats:sec><jats:label/><jats:p>By incorporating nanomaterials into polymer matrices, nanocomposites can be produced with enhanced properties, combining the ease of processing thermoplastics with the superior physical characteristics of nanoparticles. In this study, fully bio‐based polyamide 1010 was used as the polymer matrix, with graphene oxide (GO), hexagonal‐boron nitride (h‐BN), and molybdenum disulfide (MoS<jats:sub>2</jats:sub>), both individually and in hybrids, serving as fillers. The tensile behavior of these nanocomposites was evaluated at room temperature and −40 °C, along with their morphology and microstructure. Results showed that the nanomaterials slightly shifted the polymer's crystallization temperature upward, indicating a small nucleating effect, but also hindered the development of crystalline domains, reducing the crystallization kinetics. Despite no change in the final crystalline form, nanocomposites with h‐BN and MoS<jats:sub>2</jats:sub> showed lower microstructural order as evidenced by XRD. Regarding tensile behavior, GO provided the greatest toughening at room temperature due to its larger lateral dimensions and good chemical affinity with the matrix. However, at low temperatures, h‐BN‐based nanocomposites maintained the toughening effect better than GO‐based ones. This can be attributed to the lower order of the polymer's semi‐crystalline structure promoted by h‐BN, allowing greater energy dissipation. Surprisingly, hybrid fillers did not exhibit synergistic effects, with one nanomaterial hampering the effect of the other. However, SEM analysis indicated that the fracture mechanisms of the nanocomposites remained unchanged from the neat polymer, which makes them interesting options for applications that require desirable mechanical properties at a wide temperature range.</jats:p></jats:sec><jats:sec><jats:title>Highlights</jats:title><jats:p><jats:list list-type="bullet"> <jats:list-item><jats:p>GO showed the best toughening of polyamide 1010 at room temperature.</jats:p></jats:list-item> <jats:list-item><jats:p>Toughening at room temperature is mainly due to nanomaterials physical traits.</jats:p></jats:list-item> <jats:list-item><jats:p>Most nanofillers lowered polyamide's overall microstructural order.</jats:p></jats:list-item> <jats:list-item><jats:p>Toughening at −40 °C is mainly due to lower microstructural order.</jats:p></jats:list-item> </jats:list></jats:p></jats:sec>