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Additively manufactured graphene enhanced nylon with inhibited coiling, entropically favorable linear conformations for hydrogen barrier applications 增材制造的石墨烯增强尼龙具有抑制卷绕,熵有利的线性构象,用于氢障应用
IF 12 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-10-01 DOI: 10.1016/j.aiepr.2025.07.002
Mohammed Alkrunz , Chanaka Sandaruwan , Shanavas Shajahan , Basel Al Tawil , Mohd Yusuf Khan , Naga Venkateswara Rao Nulakani , Dalaver Anjum , Andreas Schiffer , Yahya Zweiri , Yarjan Abdul Samad
Hydrogen is vital to sustainable energy systems, yet developing efficient and cost-effective gas barrier materials for hydrogen storage remains a challenge. This study investigates the hydrogen barrier performance of 3D-printed nanocomposites based on Polyamide-12 (PA12) filled with 0–2 wt% of few layer formulated graphene inks (PAG). A unique printing pattern facilitated uniform graphene dispersion within the polymer matrix. Mechanical tests revealed a 11 % increase in tensile strength and a 50 % rise in Young’s modulus at 2 wt% graphene, confirming effective reinforcement. Thermogravimetric analysis showed a 40 °C increase in degradation temperature, indicating enhanced thermal stability. Additionally, thermal conductivity improved by 170 %, and electrical percolation was achieved at just 0.5 wt% loading, enhancing electrostatic discharge safety. Molecular dynamics simulations demonstrated that graphene reduced polymer chain coiling, improved crystalline order, and strengthened hydrogen bonding within the matrix. Most notably, gas permeability tests revealed an 11-fold reduction in hydrogen permeability at 1.5 wt% filler, at least 40 % lower than state-of-the-art materials. These findings position 3D-printed graphene/PA12 nanocomposites as a superior solution for advanced, safe, and efficient hydrogen storage applications.
氢对可持续能源系统至关重要,但开发高效、经济的储氢气体屏障材料仍然是一个挑战。本研究研究了基于聚酰胺-12 (PA12)填充0-2 wt%的少层配方石墨烯油墨(PAG)的3d打印纳米复合材料的隔氢性能。一种独特的印刷模式促进了石墨烯在聚合物基体中的均匀分散。机械测试显示,在2 wt%石墨烯的情况下,抗拉强度增加11%,杨氏模量增加50%,证实了有效的增强。热重分析表明,降解温度提高了40°C,表明热稳定性增强。此外,导热性提高了170%,在0.5 wt%的负载下实现了电渗透,提高了静电放电的安全性。分子动力学模拟表明,石墨烯减少了聚合物链卷曲,改善了晶体秩序,并加强了基体内的氢键。最值得注意的是,气体渗透性测试显示,在1.5 wt%的填料中,氢气渗透率降低了11倍,比最先进的材料低至少40%。这些发现将3d打印石墨烯/PA12纳米复合材料定位为先进、安全和高效的储氢应用的卓越解决方案。
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引用次数: 0
Ultra-expanded microcellular shape memory polymer foams via supercritical foaming for recyclable oil absorption and improved thermal insulation 超膨胀微孔形状记忆聚合物泡沫通过超临界发泡可回收吸油和提高绝热
IF 12 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-10-01 DOI: 10.1016/j.aiepr.2025.08.002
Jialong Chai , Guilong Wang , Chao Wei , Xinyang Li , Runze Shao , Guoqun Zhao
Shape memory foams (SMFs) have garnered significant attention as smart, sustainable solutions for diverse applications, including environmental remediation and thermal insulation. However, their practical utility has often been constrained by limited expansion ratios resulted poor porosity, which hinder performance in key areas such as oil absorption and heat retention. In this study, we report the fabrication of ultralight SMFs based on the environmentally friendly supercritical foaming method. The exceptional miscibility of the polymer blends, validated by molecular dynamics analysis and thermo behaviors, enables the formation of foams with an extraordinarily high expansion ratio. This process yields microcellular structures with an ultralow density of 0.0265 g cm−3, significantly enhancing both the porosity and surface area of the material. The high expansion ratio directly translates to superior oil absorption capacity, as the increased pore volume and interconnected microstructure facilitate rapid uptake and retention of oils. Simultaneously, the expanded cellular architecture imparts outstanding thermal insulation properties, effectively minimizing heat transfer and energy loss. The excellent shape memory behavior and recyclability, further underscoring their potential for sustainable applications. This research introduces a robust and eco-friendly strategy for producing high-performance SMFs with unprecedented expansion ratios, offering a versatile approach for environmental protection and energy conservation.
形状记忆泡沫(smf)作为一种智能、可持续的解决方案,在环境修复和隔热等各种应用中得到了广泛关注。然而,它们的实际应用往往受到有限的膨胀比的限制,导致孔隙率低,从而影响了吸油和保温等关键领域的性能。在这项研究中,我们报道了基于环境友好的超临界发泡方法制备超轻SMFs。通过分子动力学分析和热行为验证,聚合物共混物具有优异的混相性,能够形成具有极高膨胀率的泡沫。该工艺产生的微细胞结构具有0.0265 g cm−3的超低密度,显著提高了材料的孔隙率和表面积。高膨胀率直接转化为优越的吸油能力,因为增加的孔隙体积和相互连接的微观结构有助于快速吸收和保留油。同时,扩展的蜂窝结构赋予出色的隔热性能,有效地减少热量传递和能量损失。优异的形状记忆性能和可回收性,进一步强调了其可持续应用的潜力。该研究介绍了一种强大而环保的策略,用于生产具有前所未有膨胀比的高性能smf,为环境保护和节能提供了一种通用方法。
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引用次数: 0
Engineered interface design in polymer composites: Simultaneous enhancement of thermal conductivity and tribological properties for industrial applications 聚合物复合材料的工程界面设计:工业应用中热导率和摩擦学性能的同时增强
IF 12 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-10-01 DOI: 10.1016/j.aiepr.2025.06.001
Liang He , Hongbo Shen , Jinghui Zhang , Shuning Liu , Xiaobo Liu , Lifen Tong
The escalating demand for high-performance electronics necessitates innovative dielectric materials capable of efficient heat dissipation and robust interfacial stability. Herein, we present an interfacial engineering approach to fabricate multifunctional polyarylene ether nitrile (PEN)-based composite films, addressing critical challenges in thermal management and wear resistance. Through designing co-deposition process, heterostructure fillers (Ag-SiCws, Ag-BNNS, and SiCws-BNNS) were synthesized and functionalized by polydopamine (PDA) and polyethyleneimine (PEI), ensuring optimal dispersion and interfacial adhesion within the PEN matrix. Results show that different heterostructure fillers are inconsistent for constructing heat transfer pathways, but all of them can achieve effective attenuation of interfacial phonon scattering. At the same time, the formation mechanism of heat conduction channels in the multi-component PEN-based films is deeply deduced with the help of finite element analysis and tribological behavior analysis. The excellent frictional performance is not only attributed to the rigid skeleton of filler, but also the synergistic effect of interfacial optimization, which effectively suppresses the accumulation of frictional heat during the sliding process. In addition, the effectiveness of interfacial optimization was further confirmed by a combination of mechanical and electrical property tests. Therefore, this study provides a way to solve the heat dissipation problem of electronic devices and to improve the stability and lifetime.
对高性能电子产品不断升级的需求需要能够高效散热和强大界面稳定性的创新介电材料。在此,我们提出了一种界面工程方法来制造多功能聚芳醚腈(PEN)基复合薄膜,解决了热管理和耐磨性方面的关键挑战。通过设计共沉积工艺,合成异质结构填料Ag-SiCws、Ag-BNNS和SiCws-BNNS,并以聚多巴胺(PDA)和聚乙烯亚胺(PEI)进行功能化,保证了PEN基质内的最佳分散和界面粘附。结果表明,不同异质结构填料在构建换热通道时存在差异,但均能有效地衰减界面声子散射。同时,借助有限元分析和摩擦学行为分析,深入推导了多组分pen基薄膜中热传导通道的形成机理。优异的摩擦性能不仅归功于填料的刚性骨架,还归功于界面优化的协同作用,有效抑制了滑动过程中摩擦热的积累。此外,力学性能和电学性能的结合试验进一步证实了界面优化的有效性。因此,本研究为解决电子器件的散热问题,提高其稳定性和寿命提供了一条途径。
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引用次数: 0
Facile and scalable preparation of poly(vinyl alcohol) hydrogels: Insights into thermal kinetics, combustion behavior, and flame retardancy 聚乙烯醇水凝胶的简易和可伸缩制备:热动力学,燃烧行为和阻燃性的见解
IF 12 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-10-01 DOI: 10.1016/j.aiepr.2025.06.003
Sang Yun Jeong , Hyewon Song , Keunhye Koo , Jong Seok Lim , Hui Hun Cho , Jun Hyuk Heo , Jung Heon Lee
A flame-retardant (FR) hydrogel with controllable size and shape was synthesized using only poly(vinyl alcohol) (PVA) and ammonium polyphosphate (APP). The self-assembled PVA-APP (PA) hydrogel was formed via hydrogen bonding, enabling customizable shapes and sizes by simply shaking and stacking. Its dimensions were up to 250 × 400 × 2 mm3. In PA-n (n = APP/PVA mass ratio; n = 4, 6, and 8), PA-6 exhibited a compressive strength of 16.17 kPa and fracture elongation of 238 %. The hydrogel can be rolled for portability and retains its structure and performance after unfolding, ensuring its suitability for long-term storage. Moreover, PA-6 achieved a limited oxygen index of 39.22 % and peak heat-release rate of 157.97 kW/m2, demonstrating excellent FR properties. Organic and structural analyses before and after combustion revealed that the FR mechanism involved air pathways, phosphate radical chelation, char formation, and gas dilution. In addition, the PA hydrogel exhibited excellent thermal protection performance when applied to various substrates, including pig skin, paper, and polyurethane foam, and was effectively used as a fire blanket to suppress flames in a model car. These findings highlight the potential of PA hydrogels for broad applications in various industrial fields.
以聚乙烯醇(PVA)和聚磷酸铵(APP)为原料合成了粒径和形状可控的阻燃水凝胶。这种自组装的PVA-APP (PA)水凝胶是通过氢键形成的,可以通过简单的摇动和堆叠来定制形状和大小。其尺寸可达250 × 400 × 2毫米。在PA-n (n = APP/PVA质量比,n = 4,6和8)中,PA-6的抗压强度为16.17 kPa,断裂伸长率为238%。水凝胶可以卷起来携带,并且在展开后保持其结构和性能,确保其适合长期储存。此外,PA-6的限氧指数为39.22%,峰值放热率为157.97 kW/m2,表现出优异的FR性能。燃烧前后的有机和结构分析表明,FR机制涉及空气途径、磷酸根螯合、炭形成和气体稀释。此外,PA水凝胶应用于各种基材(包括猪皮、纸张和聚氨酯泡沫)时表现出优异的热防护性能,并有效地用作模型车中的防火毯来抑制火焰。这些发现突出了PA水凝胶在各种工业领域的广泛应用潜力。
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引用次数: 0
Gel alloy: One-step prepared stratified complementary hydrogel with multifunctions for deflagration substances packaging 凝胶合金:一步制备的层状多功能互补水凝胶,用于爆燃物质的包装
IF 12 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-10-01 DOI: 10.1016/j.aiepr.2025.09.001
He Ming Song , Yong Mei Chen , Xin Yi Zhao , Yang Yang , Feng Xu , Miklós Zrínyi
Multifunctional hydrogels often face performance trade-offs inherent in homogeneous systems, while conventional methods for constructing stratified hydrogels struggle to reconcile simplicity, stability, and functionality. Herein, we introduce Gel Alloy, a three-layer hydrogel prepared via one-step self-assembly at room temperature, characterized by its alloy-like stratified complementary structure. This innovative design enables synergistic functionality, achieving combined properties that exceed the sum of individual layers. The resulting Gel Alloy exhibits exceptional integrated performance, including flame retardancy up to 1300 °C, high compressive strength (6.8 MPa), puncture resistance (111.3 MPa), and durability in saline-wet environments. These attributes effectively overcome classical functional trade-offs in protective materials, making it suitable for packaging deflagration-prone substances. This study offers fundamental insights into synergy-driven material enhancement and opens a new avenue for designing high-performance materials for critical applications.
多功能水凝胶通常面临均相系统固有的性能权衡,而构建分层水凝胶的传统方法则难以调和简单性、稳定性和功能性。本文介绍了一种在室温下一步自组装制备的三层水凝胶Gel Alloy,其特点是具有类似合金的分层互补结构。这种创新的设计实现了协同功能,实现了超过单个层总和的综合性能。由此产生的凝胶合金具有优异的综合性能,包括高达1300°C的阻燃性,高抗压强度(6.8 MPa),抗穿刺性(111.3 MPa),以及在盐湿环境中的耐久性。这些属性有效地克服了保护材料的经典功能权衡,使其适合包装易爆物质。这项研究为协同驱动的材料增强提供了基本的见解,并为设计关键应用的高性能材料开辟了新的途径。
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引用次数: 0
Asymmetric multilayer-porous structure of MXene nanocomposites with absorption-dominated high electromagnetic interference shielding performance 非对称多层多孔结构的MXene纳米复合材料具有吸收为主的高电磁干扰屏蔽性能
IF 12 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-10-01 DOI: 10.1016/j.aiepr.2025.07.003
Guirong Hu , Lingfeng Cui , Yuzhu Xiong , Jiao-Jing Shao
There are limited reports on multilayer MXene-based electromagnetic interference shielding (EMI) nanocomposites featuring low-reflectivity characteristics with MXene nanocomposite films serving as electromagnetic wave reflection layers. In this study, the first combination of asymmetric porous structures with sequence-dependent gradient loss mechanisms, a MXene/cellulose nanofiber (MC) nanocomposite film was used as the electromagnetic wave reflecting layer, while Nickel-plated multi-walled carbon nanotube/iron tetroxide-loaded reduced graphene oxide/cellulose nanofiber/waterborne polyurethane (Ni@MCNT/Fe3O4@rGO/CNF/WPU(NFCW)) porous nanocomposites served as the absorbing layer. Four types of NFCW&MC asymmetric multilayer-porous nanocomposites were prepared with varying assembly orders through a layer-by-layer self-assembly method. Benefiting from the asymmetric multilayer-porous structure design, all four NFCW&MC asymmetric multilayer-porous nanocomposites exhibited absorption-dominated (A over R) EMI shielding mechanisms. The loss processes of electromagnetic waves in the nanocomposites were simulated using finite element analysis. Notably, different assembly orders resulted in distinct loss mechanisms, affecting the values of A and R for the nanocomposites. In particular, the asymmetric multilayer-porous nanocomposite with the optimal assembly order demonstrated an EMI shielding effectiveness of 57.4 dB and an A value of 0.807. Therefore, the findings of this study provide valuable insights for the development of absorption-dominated MXene nanocomposites.
利用多层MXene纳米复合材料薄膜作为电磁波反射层,具有低反射率特性的电磁干扰屏蔽(EMI)纳米复合材料的报道有限。本研究首次结合了具有序列依赖梯度损耗机制的不对称多孔结构,采用MXene/纤维素纳米纤维(MC)纳米复合膜作为电磁波反射层,镀镍多壁碳纳米管/四氧化二铁负载还原氧化石墨烯/纤维素纳米纤维/水性聚氨酯(Ni@MCNT/Fe3O4@rGO/CNF/WPU(NFCW))多孔纳米复合材料作为吸波层。采用逐层自组装方法制备了4种不同组装顺序的NFCW&;MC非对称多层多孔纳米复合材料。得益于非对称多层多孔结构设计,四种非对称多层多孔纳米复合材料均表现出以吸收为主(A / R)的电磁干扰屏蔽机制。采用有限元方法模拟了电磁波在纳米复合材料中的损耗过程。值得注意的是,不同的组装顺序会导致不同的损失机制,从而影响纳米复合材料的A和R值。特别是,具有最佳组装顺序的非对称多层多孔纳米复合材料的EMI屏蔽效能为57.4 dB, A值为0.807。因此,本研究结果为吸附型MXene纳米复合材料的发展提供了有价值的见解。
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引用次数: 0
Industrial-grade carbon fiber reinforced epoxy vitrimer composites: Reprocessing, repairing and recycling 工业级碳纤维增强环氧树脂复合材料:再加工、修复和回收
IF 12 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-10-01 DOI: 10.1016/j.aiepr.2025.07.005
Mei Fang , Xiang Liu , Jinchuan Chen , Yuezhan Feng , Ming Huang , Chuntai Liu , Changyu Shen
Carbon fiber reinforced thermoset composites (CFRP) have demonstrated significant potential for industrial applications. However, their permanent cross-linked networks pose challenges for reprocessing, repairing, and recycling. The advent of vitrimers, featuring dynamic cross-linked networks, offers a promising solution to these limitations. Herein, industrial-scale production of carbon fiber (CF) reinforced vitrimer composite was achieved using a prepreg process with a matrix of polyether sulfone (PES)-modified epoxy vitrimer (V-PES). The CF/V-PES composite exhibits suitable thermal and mechanical properties, including a glass transition temperature (Tg) of 86.2 °C and a storage modulus of 16 GPa. The dynamic transesterification reaction of vitrimer matrix imparts dynamic properties to CF/V-PES composite, enabling significant stress relaxation and creep behavior at temperatures above 200 °C, with a relaxation activation energy (Eτ) of 65.43 kJ/mol. These dynamic properties facilitate macroscopic shape memory behavior, reprocessing, and repair of interlayer cracks. The process conditions pressure, temperature, and time were optimized through orthogonal experiments. Furthermore, leveraging the dynamic transesterification reaction with ethylene glycol (EG), the V-PES matrix can be rapidly degraded in EG solution at 180 °C, enabling closed-loop recycling of CF/V-PES composites. These exceptional capabilities in reprocessing, repairing, and recycling underscore the tremendous potential of CF/V-PES composite for advanced engineering applications.
碳纤维增强热固性复合材料(CFRP)已显示出巨大的工业应用潜力。然而,它们的永久交联网络对后处理、修复和回收提出了挑战。具有动态交联网络特征的玻璃体的出现,为这些限制提供了一个有希望的解决方案。本文采用聚醚砜(PES)改性环氧玻璃体(V-PES)为基体的预浸工艺,实现了碳纤维(CF)增强玻璃体复合材料的工业规模生产。CF/V-PES复合材料具有良好的热性能和力学性能,包括玻璃化转变温度(Tg)为86.2℃,存储模量为16 GPa。在200℃以上的温度下,CF/V-PES复合材料具有明显的应力松弛和蠕变行为,弛豫活化能(Eτ)为65.43 kJ/mol。这些动态特性有利于宏观形状记忆行为、再加工和层间裂纹的修复。通过正交试验对工艺条件、压力、温度、时间进行优化。此外,利用与乙二醇(EG)的动态酯交换反应,V-PES基质可以在180°C的EG溶液中快速降解,从而实现CF/V-PES复合材料的闭环回收。CF/V-PES复合材料在后处理、修复和回收方面的卓越能力凸显了其在先进工程应用方面的巨大潜力。
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引用次数: 0
Re-evaluating bioplastic blend wastes through mechanical recycling and chemical modification 通过机械回收和化学改性对生物塑料混合废料进行再评价
IF 9.9 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-07-01 DOI: 10.1016/j.aiepr.2025.03.001
Sanaz Soleymani Eil Bakhtiari , Islam Shyha , Dongyang Sun , Mohammadreza Nofar , Reza Salehiyan
The escalating environmental challenges posed by conventional plastics have amplified the importance of biodegradable polymers as sustainable alternatives. However, addressing their recyclability and reprocessing is critical to enhancing their environmental and economic viability. This review delves into the multiple reprocessing of biodegradable polymer blends, focusing on mechanical recycling's effects on their structure, properties, and performance. Unlike single polymers, blends offer tailored properties by combining the strengths of individual components, making them more suitable for diverse applications. However, their complex morphologies and phase interactions demand unique strategies for effective recycling.
Key findings highlight that polymer blends, such as PLA/PHB and PLA/PBAT, exhibit greater resilience to repeated processing compared to their pure counterparts, owing to enhanced intermolecular interactions and progressive crystallinity. Compatibilizers, including chain extenders like Joncryl®, play a pivotal role in mitigating degradation by improving phase adhesion and maintaining mechanical and thermal properties. Rheological analyses reveal the critical interplay between phase morphology and processing conditions, emphasizing the importance of tailoring blend compositions and additives for optimal recyclability.
This review sets itself apart by providing the first comprehensive examination of the effects of multiple mechanical reprocessing cycles specifically on biodegradable polymer blends, filling a significant gap in the literature. By addressing current challenges, it offers a roadmap for advancing biodegradable materials toward a circular economy.
传统塑料带来的不断升级的环境挑战放大了可生物降解聚合物作为可持续替代品的重要性。然而,解决它们的可回收性和再加工问题对于提高它们的环境和经济可行性至关重要。本文综述了生物可降解聚合物共混物的多重再处理,重点介绍了机械回收对其结构、性能和性能的影响。与单一聚合物不同,共混物通过结合单个组分的优势提供定制的性能,使其更适合各种应用。然而,它们复杂的形态和相相互作用需要独特的策略来有效地回收。主要研究结果强调,聚合物共混物,如PLA/PHB和PLA/PBAT,由于增强的分子间相互作用和渐进结晶度,与纯聚合物相比,对重复加工表现出更大的弹性。增容剂,包括像Joncryl®这样的扩链剂,通过改善相粘合和保持机械和热性能,在减轻降解方面发挥着关键作用。流变分析揭示了相形态和加工条件之间的关键相互作用,强调了定制混合成分和添加剂的重要性,以获得最佳的可回收性。这篇综述通过首次全面研究多种机械后处理循环对生物可降解聚合物混合物的影响而使自己与众不同,填补了文献中的重大空白。通过解决当前的挑战,它为推动生物可降解材料向循环经济发展提供了路线图。
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引用次数: 0
Advances in lead-free flexible piezoelectric materials for energy and evolving applications 能源用无铅柔性压电材料及其应用进展
IF 9.9 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-07-01 DOI: 10.1016/j.aiepr.2025.04.001
Jacem Zidani , Latifa Tajounte , Abdellah Benzaouak , Noureddine Touach , Adam Duong , Moneim Zannen , Abdelilah Lahmar
The review highlights the advancements in flexible lead-free piezoelectric materials, emphasizing their potential for energy harvesting and sustainable energy. Although normal piezoelectric materials such as lead zirconate titanate (PZT) have great efficiency, their lead content causes environmental issues. This research focuses on replacement materials like biodegradable polymers and bismuth sodium titanate (BNT), which not only show interesting piezoelectric capabilities but also have advantages in terms of flexibility and biocompatibility. In order to increase piezoelectric performance while maintaining flexibility, it is advised to include inorganic fillers into polymer matrices, therefore qualifying these materials for usage in biomedical and wearable electronics applications. The evaluation also covers the issues resulting from the great usage of these resources, including e-waste and the need of sustainable solutions. The general message of the research underlines the need of developing new piezoelectric materials able to effectively gather mechanical energy from different sources, therefore promoting self-sustaining systems and reducing reliance on traditional power sources. The review also underlines how lead-free piezoelectric materials can boost power density and chemical oxygen demand (COD) removal rates in microbial fuel cells (MFCs), therefore promoting sustainable energy solutions that turn organic waste into bioelectricity.
这篇综述强调了柔性无铅压电材料的进展,强调了它们在能量收集和可持续能源方面的潜力。虽然普通压电材料如锆钛酸铅(PZT)具有很高的效率,但其含铅量造成了环境问题。本研究的重点是生物可降解聚合物和钛酸铋钠(BNT)等替代材料,它们不仅具有有趣的压电性能,而且在柔韧性和生物相容性方面具有优势。为了在保持柔性的同时提高压电性能,建议在聚合物基体中加入无机填料,从而使这些材料适用于生物医学和可穿戴电子应用。评估还涵盖了大量使用这些资源所产生的问题,包括电子废物和可持续解决方案的需要。这项研究的总体信息强调了开发新型压电材料的必要性,这种材料能够有效地从不同的来源收集机械能,从而促进自我维持系统,减少对传统能源的依赖。该综述还强调了无铅压电材料如何提高微生物燃料电池(mfc)的功率密度和化学氧需求(COD)去除率,从而促进将有机废物转化为生物电的可持续能源解决方案。
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引用次数: 0
Recent advancement in MXene-based nanomaterials for flame retardant polymers and composites 用于阻燃聚合物和复合材料的mxene基纳米材料的最新进展
IF 9.9 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-07-01 DOI: 10.1016/j.aiepr.2025.03.002
Yakubu Adekunle Alli , Abayomi Bamisaye , Onome Ejeromedoghene , Olusegun Oluwaseun Jimoh , Samuel Oluwadadepo Oni , Gerald Chekwube Ezeamii , Chukwurimazu Ozoemezim , Adeniyi Sunday Ogunlaja , Suraya Abdul Rashid , Baljinder K. Kandola
This review explores the advancements in MXene-based nanomaterials as flame-retardant additives for polymers and composites, driven by increasing fire safety demands across industries. It highlights the critical role of flame-retardant materials in mitigating fire hazards in structures, electronics, transportation, and textiles, emphasizing the need for innovative solutions due to stricter safety regulations. MXenes, a class of two-dimensional nanomaterials with unique structural properties such as high surface area, tunable composition, and superior thermal stability, are presented as promising candidates. The review discusses various synthesis and incorporation techniques for MXenes in polymer matrices, showcasing improvements in flame retardancy, mechanical properties, and thermal stability. Additionally, it emphasizes the multifunctionality of MXenes, which offer conductivity, electromagnetic shielding, and mechanical reinforcement alongside flame suppression. In conclusion, the review underscores MXenes' potential to address challenges in flame-retardant materials, advocating for further research to optimize their applications and explore synergies with other agents to enhance safety and sustainability in engineering materials.
这篇综述探讨了基于mxene的纳米材料作为聚合物和复合材料阻燃添加剂的进展,这是由各行各业日益增长的消防安全需求所驱动的。它强调了阻燃材料在减轻结构、电子、运输和纺织品中的火灾危险方面的关键作用,强调了由于更严格的安全法规,需要创新的解决方案。MXenes是一类二维纳米材料,具有独特的结构特性,如高表面积、可调成分和优越的热稳定性,被认为是有前途的候选者。综述了MXenes在聚合物基体中的各种合成和掺入技术,展示了其在阻燃性、机械性能和热稳定性方面的改进。此外,它强调了MXenes的多功能性,它提供导电性,电磁屏蔽和机械加固以及火焰抑制。总之,该综述强调了MXenes在解决阻燃材料挑战方面的潜力,提倡进一步研究以优化其应用,并探索与其他剂的协同作用,以提高工程材料的安全性和可持续性。
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引用次数: 0
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Advanced Industrial and Engineering Polymer Research
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