Effect of environmental temperature and semi‐crystalline order on the toughening of polyamide 1010 by 2D nanomaterials

IF 4.8 2区 材料科学 Q2 MATERIALS SCIENCE, COMPOSITES Polymer Composites Pub Date : 2024-09-10 DOI:10.1002/pc.29019
Gabriel M. Pinto, Emna Helal, Hélio Ribeiro, Eric David, Nicole R. Demarquette, Guilhermino J. M. Fechine
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Abstract

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 (MoS2), 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 MoS2 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.Highlights GO showed the best toughening of polyamide 1010 at room temperature. Toughening at room temperature is mainly due to nanomaterials physical traits. Most nanofillers lowered polyamide's overall microstructural order. Toughening at −40 °C is mainly due to lower microstructural order.

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环境温度和半结晶阶次对二维纳米材料增韧聚酰胺 1010 的影响
通过在聚合物基体中加入纳米材料,可以生产出性能更强的纳米复合材料,将热塑性塑料的易加工性与纳米粒子的优异物理特性结合起来。本研究以完全生物基的聚酰胺 1010 为聚合物基体,以氧化石墨烯(GO)、六方氮化硼(h-BN)和二硫化钼(MoS2)单独或混合作为填料。对这些纳米复合材料在室温和 -40 °C 下的拉伸行为及其形态和微观结构进行了评估。结果表明,纳米材料使聚合物的结晶温度略微上移,表明其具有微小的成核效应,但同时也阻碍了结晶畴的形成,降低了结晶动力学。尽管最终的结晶形式没有改变,但从 XRD 中可以看出,含有 h-BN 和 MoS2 的纳米复合材料显示出较低的微观结构有序性。在拉伸行为方面,由于 GO 的横向尺寸较大,且与基体的化学亲和性较好,因此其在室温下的韧性最大。然而,在低温条件下,h-BN 基纳米复合材料比 GO 基纳米复合材料能更好地保持增韧效果。这可能是由于 h-BN 促进了聚合物半结晶结构的低阶化,从而允许更大的能量耗散。令人惊讶的是,混合填料并没有表现出协同效应,一种纳米材料阻碍了另一种纳米材料的效果。不过,扫描电镜分析表明,纳米复合材料的断裂机制与纯聚合物相比没有变化,这使它们成为需要在宽温度范围内具有理想机械性能的应用领域的有趣选择。室温下增韧的主要原因是纳米材料的物理特性。大多数纳米填料都降低了聚酰胺的整体微结构有序性。-40°C下的增韧主要是由于微观结构阶次降低。
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来源期刊
Polymer Composites
Polymer Composites 工程技术-材料科学:复合
CiteScore
7.50
自引率
32.70%
发文量
673
审稿时长
3.1 months
期刊介绍: Polymer Composites is the engineering and scientific journal serving the fields of reinforced plastics and polymer composites including research, production, processing, and applications. PC brings you the details of developments in this rapidly expanding area of technology long before they are commercial realities.
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