首页 > 最新文献

Composites Science and Technology最新文献

英文 中文
Low-dielectric and hydrophobic thermotropic liquid crystalline polyester composites reinforced with hollow glass microspheres for next-generation electronic board materials 中空玻璃微球增强低介电疏水性热致液晶聚酯复合材料,用于下一代电子电路板材料
IF 9.8 1区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-09-25 DOI: 10.1016/j.compscitech.2025.111395
Jun-Hyeop Lee, Ya-Rin Shin, Gyeong-Ig Hwang, Shinwoo Lee, Jongho Moon, Young Gyu Jeong
In this study, composites based on thermotropic liquid crystalline polymers (TLCP) and incorporated with hollow glass microspheres (HGM) were prepared via a melt compounding technique facilitated by masterbatch dilution, followed by subsequent shaping through injection molding. The influence of HGM loading (2–10 wt%) on the microstructure, thermal behavior, rheological and mechanical properties, dielectric performance, and hydrophobicity of the composites was comprehensively investigated. Electron microscopy and infrared spectroscopy confirmed uniform dispersion of HGM and strong interfacial hydrogen bonding with the TLCP matrix. X-ray diffraction revealed that HGM disrupts TLCP crystallinity, while differential scanning calorimetry demonstrated a decrease in crystallization and melting temperatures with increasing filler content. Thermogravimetric analysis showed excellent thermal stability, with char yields increasing from 38.2 % for neat TLCP to 48.8 % for TLCP/HGM10. Rheological testing revealed enhanced melt viscosity and viscoelastic moduli, and dynamic mechanical analysis indicated restricted chain mobility and increased glass transition temperatures. Importantly, the dielectric constant (Dk ∼2.43) and loss (Df ∼0.0284) at 2 MHz decreased by approximately 20 % and 59 %, respectively, for TLCP/HGM10 compared to neat TLCP, and these experimental values correlated well with theoretical predictions based on the Maxwell-Garnett model. Water contact angle tests further showed improved surface hydrophobicity, increasing from 77.4° to 88.8° with HGM addition. These results collectively demonstrate that the incorporation of HGM simultaneously enhances the thermal, dielectric, and moisture-resistance characteristics of TLCP composites, making them promising candidates for high-frequency and moisture-resilient electronic applications.
在本研究中,通过母粒稀释的熔融复合技术制备了基于热致液晶聚合物(TLCP)并加入中空玻璃微球(HGM)的复合材料,随后通过注塑成型。研究了HGM (2-10 wt%)对复合材料的微观结构、热行为、流变力学性能、介电性能和疏水性的影响。电镜和红外光谱证实了HGM的均匀分散和与TLCP基体的强界面氢键。x射线衍射显示HGM破坏了TLCP的结晶度,而差示扫描量热法显示随着填料含量的增加,结晶和熔化温度降低。热重分析表明,TLCP/HGM10的炭产率由纯TLCP的38.2%提高到48.8%。流变学测试表明熔体粘度和粘弹性模量增强,动态力学分析表明链迁移率受限,玻璃化转变温度升高。重要的是,与纯TLCP相比,TLCP/HGM10在2 MHz时的介电常数(Dk ~ 2.43)和损耗(Df ~ 0.0284)分别降低了约20%和59%,这些实验值与基于Maxwell-Garnett模型的理论预测具有良好的相关性。水接触角试验进一步表明,添加HGM后,表面疏水性从77.4°提高到88.8°。这些结果共同表明,HGM的加入同时增强了TLCP复合材料的热、介电和防潮特性,使其成为高频和湿弹性电子应用的有希望的候选者。
{"title":"Low-dielectric and hydrophobic thermotropic liquid crystalline polyester composites reinforced with hollow glass microspheres for next-generation electronic board materials","authors":"Jun-Hyeop Lee,&nbsp;Ya-Rin Shin,&nbsp;Gyeong-Ig Hwang,&nbsp;Shinwoo Lee,&nbsp;Jongho Moon,&nbsp;Young Gyu Jeong","doi":"10.1016/j.compscitech.2025.111395","DOIUrl":"10.1016/j.compscitech.2025.111395","url":null,"abstract":"<div><div>In this study, composites based on thermotropic liquid crystalline polymers (TLCP) and incorporated with hollow glass microspheres (HGM) were prepared via a melt compounding technique facilitated by masterbatch dilution, followed by subsequent shaping through injection molding. The influence of HGM loading (2–10 wt%) on the microstructure, thermal behavior, rheological and mechanical properties, dielectric performance, and hydrophobicity of the composites was comprehensively investigated. Electron microscopy and infrared spectroscopy confirmed uniform dispersion of HGM and strong interfacial hydrogen bonding with the TLCP matrix. X-ray diffraction revealed that HGM disrupts TLCP crystallinity, while differential scanning calorimetry demonstrated a decrease in crystallization and melting temperatures with increasing filler content. Thermogravimetric analysis showed excellent thermal stability, with char yields increasing from 38.2 % for neat TLCP to 48.8 % for TLCP/HGM10. Rheological testing revealed enhanced melt viscosity and viscoelastic moduli, and dynamic mechanical analysis indicated restricted chain mobility and increased glass transition temperatures. Importantly, the dielectric constant (<em>D</em><sub>k</sub> ∼2.43) and loss (<em>D</em><sub>f</sub> ∼0.0284) at 2 MHz decreased by approximately 20 % and 59 %, respectively, for TLCP/HGM10 compared to neat TLCP, and these experimental values correlated well with theoretical predictions based on the Maxwell-Garnett model. Water contact angle tests further showed improved surface hydrophobicity, increasing from 77.4° to 88.8° with HGM addition. These results collectively demonstrate that the incorporation of HGM simultaneously enhances the thermal, dielectric, and moisture-resistance characteristics of TLCP composites, making them promising candidates for high-frequency and moisture-resilient electronic applications.</div></div>","PeriodicalId":283,"journal":{"name":"Composites Science and Technology","volume":"272 ","pages":"Article 111395"},"PeriodicalIF":9.8,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145155618","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Thermally conductive and electromagnetic interference shielding polydimethylsiloxane composites with vertically oriented carbon fibers obtained by gravity-magnetic actuation 采用重力磁致动法制备了具有导热和屏蔽电磁干扰性能的垂直取向碳纤维聚二甲基硅氧烷复合材料
IF 9.8 1区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-09-24 DOI: 10.1016/j.compscitech.2025.111393
Jinlong Wang, Yonggang Shangguan, Qiang Zheng
With the rapid advancement of the highly integrated microelectronics industry, the growing demand for composite materials that offer both high thermal conductivity and effective electromagnetic interference (EMI) shielding to ensure the long-term stability of electronic devices is becoming increasingly significant. However, achieving high through-plane thermal conductivity remains challenging due to the difficulty in establishing continuous thermal conduction pathways through the composite thickness. In this work, polydimethylsiloxane (PDMS) composites with vertically oriented Carbon fiber (CF) structures were successfully fabricated through cast molding and gravity-magnetic field co-induced CF alignment. At 23.5 vol% CF content, the composite exhibits a through-plane thermal conductivity of 12.26 W/(m⋅K), a thermal conductivity enhancement (TCE) of 7500 %, and an electromagnetic interference shielding efficiency (EMI SE) of 27.9 dB. In addition, the influences of CF content on the anisotropic thermal conductivity and EMI shielding properties of the composites were examined. This CF/PDMS composites with vertically aligned CF structures have a broad range of potential applications in thermal management and EMI shielding, such as thermal interface materials in high-power chips, LEDs, 5G RF modules.
随着高度集成的微电子工业的快速发展,对既能提供高导热性又能有效屏蔽电磁干扰(EMI)以确保电子器件长期稳定性的复合材料的需求日益增长。然而,由于难以通过复合材料厚度建立连续的热传导路径,因此实现高的通平面导热性仍然具有挑战性。在本研究中,通过铸造成型和重力-磁场共诱导碳纤维取向,成功制备了具有垂直取向碳纤维结构的聚二甲基硅氧烷(PDMS)复合材料。当CF含量为23.5 vol%时,复合材料的通平面导热系数为12.26 W/(m·K),导热系数增强(TCE)为7500 %,电磁干扰屏蔽效率(EMI SE)为27.9 dB。此外,还考察了CF含量对复合材料各向异性导热性能和电磁干扰屏蔽性能的影响。这种具有垂直排列CF结构的CF/PDMS复合材料在热管理和EMI屏蔽方面具有广泛的潜在应用,例如大功率芯片,led, 5G射频模块中的热界面材料。
{"title":"Thermally conductive and electromagnetic interference shielding polydimethylsiloxane composites with vertically oriented carbon fibers obtained by gravity-magnetic actuation","authors":"Jinlong Wang,&nbsp;Yonggang Shangguan,&nbsp;Qiang Zheng","doi":"10.1016/j.compscitech.2025.111393","DOIUrl":"10.1016/j.compscitech.2025.111393","url":null,"abstract":"<div><div>With the rapid advancement of the highly integrated microelectronics industry, the growing demand for composite materials that offer both high thermal conductivity and effective electromagnetic interference (EMI) shielding to ensure the long-term stability of electronic devices is becoming increasingly significant. However, achieving high through-plane thermal conductivity remains challenging due to the difficulty in establishing continuous thermal conduction pathways through the composite thickness. In this work, polydimethylsiloxane (PDMS) composites with vertically oriented Carbon fiber (CF) structures were successfully fabricated through cast molding and gravity-magnetic field co-induced CF alignment. At 23.5 vol% CF content, the composite exhibits a through-plane thermal conductivity of 12.26 W/(m⋅K), a thermal conductivity enhancement (TCE) of 7500 %, and an electromagnetic interference shielding efficiency (EMI SE) of 27.9 dB. In addition, the influences of CF content on the anisotropic thermal conductivity and EMI shielding properties of the composites were examined. This CF/PDMS composites with vertically aligned CF structures have a broad range of potential applications in thermal management and EMI shielding, such as thermal interface materials in high-power chips, LEDs, 5G RF modules.</div></div>","PeriodicalId":283,"journal":{"name":"Composites Science and Technology","volume":"272 ","pages":"Article 111393"},"PeriodicalIF":9.8,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145155620","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhanced dielectric and energy storage performance of polyetherimide doping with molecular semiconductor all-organic composites 聚醚酰亚胺掺杂分子半导体全有机复合材料提高介电和储能性能
IF 9.8 1区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-09-24 DOI: 10.1016/j.compscitech.2025.111391
Mingyang Zhang , Likun Zang , Hui Tong , Fuyuan Liu
Polyetherimide (PEI), as a kind of high-temperature dielectrics, still face the issue of current leakage under thermo-electrical coupling fields, leading to a sharp degradation of energy storage performance. In this study, an intrinsic PEI with superior comprehensive properties was synthesized using 4,4'-(4,4′-isopropylidenediphenoxy)bis(phthalic anhydride) (BPADA) and 2,2-bis[4-(4-aminophenoxy)phenyl] propane (BAPP). Through molecular design, an "electron gate" mechanism was introduced via σ-π hyperconjugation effects, effectively suppressing long-range charge delocalization. The resulting intrinsic PEI achieves an energy storage density (Ud) of 1.93 J/cm3 at 150 °C, which is 20.6 % higher than that of commercial Ultem™ PEI film (1.6 J/cm3). Further modification was conducted by doping with three molecular semiconductors: 3,4,9,10-perylenetetracarboxylic diimide (PTCDI), 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTCDA), and 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA). Density Functional Theory (DFT) simulations and Low-Energy Inverse Photoemission Spectroscopy (LEIPS) experiments reveal that all three semiconductors exhibit higher electron affinity than the intrinsic PEI. Additionally, Thermally Stimulated Depolarization Current (TSDC) reveals that the incorporation of molecular semiconductors increases trapped charges and trap energy level compared to intrinsic PEI. Both experimental and simulation results consistently demonstrate that molecular semiconductor doping can enhance energy storage performance by constructing deep trap sites within the PEI matrix. Experimental results demonstrate that at 150 °C, the 0.125 % PTCDI-doped PEI achieves a breakdown strength of 545 MV/m, an Ud of 3.71 J/cm3, and a charge-discharge efficiency (η) of 90.13 % (vs. 436 MV/m, 1.93 J/cm3, and 94.67 % for intrinsic PEI). This research provides an effective strategy for improving the capacitive performance of polymer dielectrics under thermo-electrical coupling conditions.
聚醚酰亚胺(PEI)作为一种高温电介质,在热电耦合场下仍然面临着电流泄漏的问题,导致储能性能急剧下降。本研究以4,4′-(4,4′-异丙基二苯氧基)双邻苯酐(BPADA)和2,2-双[4-(4-氨基苯氧基)苯基]丙烷(BAPP)为原料合成了具有优异综合性能的本征PEI。通过分子设计,通过σ-π超共轭效应引入了“电子门”机制,有效抑制了远距离电荷离域。在150°C下,本构PEI的储能密度(Ud)达到1.93 J/cm3,比商用Ultem™PEI膜(1.6 J/cm3)高20.6%。通过掺杂3种分子半导体:3,4,9,10-苝四羧基二亚胺(PTCDI)、1,4,5,8-萘四羧基二酐(NTCDA)和3,4,9,10-苝四羧基二酐(PTCDA)进行进一步修饰。密度泛函理论(DFT)模拟和低能逆光电发射光谱(LEIPS)实验表明,这三种半导体都表现出比本征PEI更高的电子亲和力。此外,热激发去极化电流(TSDC)表明,与本质PEI相比,分子半导体的掺入增加了捕获电荷和捕获能级。实验和模拟结果一致表明,分子半导体掺杂可以通过在PEI矩阵内构建深阱位来提高储能性能。实验结果表明,在150°C下,掺0.125% ptcdi的PEI击穿强度为545 MV/m, Ud为3.71 J/cm3,充放电效率(η)为90.13%(本质PEI为436 MV/m, 1.93 J/cm3, 94.67%)。该研究为提高热电耦合条件下聚合物电介质的电容性能提供了一种有效的策略。
{"title":"Enhanced dielectric and energy storage performance of polyetherimide doping with molecular semiconductor all-organic composites","authors":"Mingyang Zhang ,&nbsp;Likun Zang ,&nbsp;Hui Tong ,&nbsp;Fuyuan Liu","doi":"10.1016/j.compscitech.2025.111391","DOIUrl":"10.1016/j.compscitech.2025.111391","url":null,"abstract":"<div><div>Polyetherimide (PEI), as a kind of high-temperature dielectrics, still face the issue of current leakage under thermo-electrical coupling fields, leading to a sharp degradation of energy storage performance. In this study, an intrinsic PEI with superior comprehensive properties was synthesized using <strong>4,4'-(4,4′-isopropylidenediphenoxy)bis(phthalic anhydride) (BPADA)</strong> and <strong>2,2-bis[4-(4-aminophenoxy)phenyl] propane (BAPP)</strong>. Through molecular design, an \"electron gate\" mechanism was introduced via <strong>σ-π hyperconjugation effects</strong>, effectively suppressing long-range charge delocalization. The resulting intrinsic PEI achieves an energy storage density (<strong><em>U</em><sub>d</sub></strong>) of <strong>1.93 J/cm<sup>3</sup> at 150 °C</strong>, which is <strong>20.6 % higher</strong> than that of commercial Ultem™ PEI film (1.6 <strong>J/cm<sup>3</sup></strong>). Further modification was conducted by doping with three molecular semiconductors: 3,4,9,10-perylenetetracarboxylic diimide <strong>(PTCDI), 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTCDA), and 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA). Density Functional Theory (DFT)</strong> simulations and <strong>Low-Energy Inverse Photoemission Spectroscopy (LEIPS)</strong> experiments reveal that all three semiconductors exhibit <strong>higher electron affinity</strong> than the intrinsic PEI. Additionally, Thermally Stimulated Depolarization Current (TSDC) reveals that the incorporation of molecular semiconductors increases trapped charges and trap energy level compared to intrinsic PEI. Both experimental and simulation results consistently demonstrate that molecular semiconductor doping can enhance energy storage performance by constructing deep trap sites within the PEI matrix. Experimental results demonstrate that at 150 <strong>°C,</strong> the 0.125 % PTCDI-doped PEI achieves a breakdown strength of 545 MV/m, an <strong><em>U</em><sub>d</sub></strong> of 3.71 J/cm<sup>3</sup>, and a charge-discharge efficiency <strong>(</strong><em>η</em><strong>)</strong> of 90.13 % (vs. 436 MV/m, 1.93 J/cm<sup>3</sup>, and 94.67 % for intrinsic PEI). This research provides an effective strategy for improving the capacitive performance of polymer dielectrics under thermo-electrical coupling conditions.</div></div>","PeriodicalId":283,"journal":{"name":"Composites Science and Technology","volume":"272 ","pages":"Article 111391"},"PeriodicalIF":9.8,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145155619","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Continuous construction of gradient modulus interphase in CF/PA6 composites with enhanced interfacial properties and reduced porosity CF/PA6复合材料中梯度模量界面相的连续构建增强了界面性能并降低了孔隙率
IF 9.8 1区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-09-23 DOI: 10.1016/j.compscitech.2025.111392
Guang Yang , Jinze Cui , Kewen Zeng , Yutai Luo , Feng Bao , Jiali Yu , Caizhen Zhu , Jian Xu , Huichao Liu
Chopped ultra-thin carbon fiber tape reinforced polyamide 6 (PA6) composites are considered promising materials for balancing the mechanical properties and ease of processing, particularly due to their in-plane quasi-isotropy, which facilitate structural design and manufacturing in the industry. However, further advancement is hindered by the weak interfacial bonding and modulus mismatch between carbon fiber (CF) and PA6 matrix, as well as high porosity of the CF/PA6 composites. In this work, plasma treatment and mixed COOH-carbon nanotubes (CNTs)/PA6 sizing methods are proposed to enhance the surface roughness (Ra) and surface energy of the CF. Compared to untreated CF, the Ra value and surface energy of the modified CF increased by 45.1 % and 69.7 %, respectively. After 0.6 wt% COOH-CNTs modification, the tensile strength, Young's modulus, and interlaminar shear strength (ILSS) of the composites reach 900.0 MPa, 48.4 GPa, and 62.3 MPa, which are respectively 24.9 %, 19.8 %, and 36.9 % higher than those of the unmodified composites. In particular, the porosity is reduced to 1.22 %, which is 73.3 % lower than that of unmodified composites. Moreover, the [email protected] wt% CNT/PA6 composites exhibit mitigatory modulus gradient across the interphase. This work synergistically enhances the interface adhesion and reduces the porosity of the CF/PA6 composites via a large-scale continuous modification technology.
短切超薄碳纤维带增强聚酰胺6 (PA6)复合材料被认为是一种很有前途的材料,因为它具有平衡机械性能和易于加工的特点,特别是由于其面内准各向同性,这有助于工业上的结构设计和制造。然而,碳纤维(CF)与PA6基体之间的界面结合较弱,模量不匹配,以及CF/PA6复合材料的高孔隙率阻碍了进一步的发展。本文提出了等离子体处理和混合cooh -碳纳米管(CNTs)/PA6上浆方法来提高CF的表面粗糙度(Ra)和表面能。与未经处理的CF相比,改性CF的Ra值和表面能分别提高了45.1%和69.7%。经0.6 wt% COOH-CNTs改性后,复合材料的抗拉强度、杨氏模量和层间剪切强度(ILSS)分别达到900.0 MPa、48.4 GPa和62.3 MPa,比未改性的复合材料分别提高24.9%、19.8%和36.9%。特别是孔隙率降低到1.22%,比未改性的复合材料降低了73.3%。此外,wt% CNT/PA6复合材料在界面上表现出减缓的模量梯度。本工作通过大规模连续改性技术,协同增强了CF/PA6复合材料的界面附着力,降低了其孔隙率。
{"title":"Continuous construction of gradient modulus interphase in CF/PA6 composites with enhanced interfacial properties and reduced porosity","authors":"Guang Yang ,&nbsp;Jinze Cui ,&nbsp;Kewen Zeng ,&nbsp;Yutai Luo ,&nbsp;Feng Bao ,&nbsp;Jiali Yu ,&nbsp;Caizhen Zhu ,&nbsp;Jian Xu ,&nbsp;Huichao Liu","doi":"10.1016/j.compscitech.2025.111392","DOIUrl":"10.1016/j.compscitech.2025.111392","url":null,"abstract":"<div><div>Chopped ultra-thin carbon fiber tape reinforced polyamide 6 (PA6) composites are considered promising materials for balancing the mechanical properties and ease of processing, particularly due to their in-plane quasi-isotropy, which facilitate structural design and manufacturing in the industry. However, further advancement is hindered by the weak interfacial bonding and modulus mismatch between carbon fiber (CF) and PA6 matrix, as well as high porosity of the CF/PA6 composites. In this work, plasma treatment and mixed COOH-carbon nanotubes (CNTs)/PA6 sizing methods are proposed to enhance the surface roughness (Ra) and surface energy of the CF. Compared to untreated CF, the Ra value and surface energy of the modified CF increased by 45.1 % and 69.7 %, respectively. After 0.6 wt% COOH-CNTs modification, the tensile strength, Young's modulus, and interlaminar shear strength (ILSS) of the composites reach 900.0 MPa, 48.4 GPa, and 62.3 MPa, which are respectively 24.9 %, 19.8 %, and 36.9 % higher than those of the unmodified composites. In particular, the porosity is reduced to 1.22 %, which is 73.3 % lower than that of unmodified composites. Moreover, the <span><span><span>[email protected]</span></span><svg><path></path></svg></span> wt% CNT/PA6 composites exhibit mitigatory modulus gradient across the interphase. This work synergistically enhances the interface adhesion and reduces the porosity of the CF/PA6 composites via a large-scale continuous modification technology.</div></div>","PeriodicalId":283,"journal":{"name":"Composites Science and Technology","volume":"272 ","pages":"Article 111392"},"PeriodicalIF":9.8,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145155710","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cellulose nanofibers-enabled interfacial engineering for thermally conductive composites with superior mechanical durability 具有优异机械耐久性的导热复合材料的纤维素纳米纤维界面工程
IF 9.8 1区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-09-23 DOI: 10.1016/j.compscitech.2025.111390
Wen-yan Wang , Yan-ji Yin , Yuan-chao Jiang , Rui Han , Min Nie
Cellulose nanofibers (CNFs), derived from renewable biomass, offer exceptional mechanical properties, a high aspect ratio, and abundant surface hydroxyl groups, making them highly attractive for polymer composite functionalization. In this study, CNFs are employed as both dispersing and reinforcing agents to address the dual challenges of filler aggregation and poor interfacial adhesion in nylon-based thermally conductive composites. By leveraging their strong hydrogen bonding capability, CNFs not only enable the uniform dispersion of boron nitride (BN) fillers in aqueous systems but also facilitate the construction of robust interfacial networks within the polymer matrix. Using a simple vacuum-assisted filtration and compression molding strategy, we fabricated laminated composites featuring highly aligned BN structures. This unique architecture promotes the formation of efficient thermal pathways, resulting in an in-plane thermal conductivity of 4.5 Wm−1K−1 at 24.5 wt% BN—an 1857 % enhancement over pure nylon. Simultaneously, the CNF-induced interfacial reinforcement leads to excellent mechanical strength and fatigue resistance, with the composite retaining 92 % of its thermal conductivity and 85 % of its tensile strength after 100,000 bending cycles. These findings demonstrate the significant potential of CNF-assisted interfacial engineering for developing high-performance, thermoplastic-based thermal management materials suitable for flexible electronics and other advanced applications.
纤维素纳米纤维(CNFs)来源于可再生生物质,具有优异的机械性能、高长径比和丰富的表面羟基,使其在聚合物复合功能化方面具有很高的吸引力。在这项研究中,CNFs被用作分散剂和增强剂,以解决尼龙基导热复合材料中填料聚集和界面粘附不良的双重挑战。CNFs利用其强大的氢键能力,不仅使氮化硼(BN)填料在水体系中均匀分散,而且有助于在聚合物基体中构建坚固的界面网络。使用简单的真空辅助过滤和压缩成型策略,我们制造了具有高度排列BN结构的层压复合材料。这种独特的结构促进了高效热通道的形成,导致在24.5% wt% bn时的面内导热系数为4.5 Wm−1K−1,比纯尼龙提高了1857%。同时,cnf诱导的界面增强带来了优异的机械强度和抗疲劳性能,在10万次弯曲循环后,复合材料保持了92%的导热系数和85%的抗拉强度。这些发现证明了cnf辅助界面工程在开发适用于柔性电子和其他先进应用的高性能热塑性热管理材料方面的巨大潜力。
{"title":"Cellulose nanofibers-enabled interfacial engineering for thermally conductive composites with superior mechanical durability","authors":"Wen-yan Wang ,&nbsp;Yan-ji Yin ,&nbsp;Yuan-chao Jiang ,&nbsp;Rui Han ,&nbsp;Min Nie","doi":"10.1016/j.compscitech.2025.111390","DOIUrl":"10.1016/j.compscitech.2025.111390","url":null,"abstract":"<div><div>Cellulose nanofibers (CNFs), derived from renewable biomass, offer exceptional mechanical properties, a high aspect ratio, and abundant surface hydroxyl groups, making them highly attractive for polymer composite functionalization. In this study, CNFs are employed as both dispersing and reinforcing agents to address the dual challenges of filler aggregation and poor interfacial adhesion in nylon-based thermally conductive composites. By leveraging their strong hydrogen bonding capability, CNFs not only enable the uniform dispersion of boron nitride (BN) fillers in aqueous systems but also facilitate the construction of robust interfacial networks within the polymer matrix. Using a simple vacuum-assisted filtration and compression molding strategy, we fabricated laminated composites featuring highly aligned BN structures. This unique architecture promotes the formation of efficient thermal pathways, resulting in an in-plane thermal conductivity of 4.5 Wm<sup>−1</sup>K<sup>−1</sup> at 24.5 wt% BN—an 1857 % enhancement over pure nylon. Simultaneously, the CNF-induced interfacial reinforcement leads to excellent mechanical strength and fatigue resistance, with the composite retaining 92 % of its thermal conductivity and 85 % of its tensile strength after 100,000 bending cycles. These findings demonstrate the significant potential of CNF-assisted interfacial engineering for developing high-performance, thermoplastic-based thermal management materials suitable for flexible electronics and other advanced applications.</div></div>","PeriodicalId":283,"journal":{"name":"Composites Science and Technology","volume":"272 ","pages":"Article 111390"},"PeriodicalIF":9.8,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145155622","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Necklace-structured FeCoNi@N-doped porous carbon nanofibers with strong magnetic coupling for high-performance microwave absorption 项链结构FeCoNi@N-doped多孔碳纳米纤维强磁耦合高性能微波吸收
IF 9.8 1区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-09-19 DOI: 10.1016/j.compscitech.2025.111389
Shuai Liu , Qunfu Fan , Sijia Li , Yicang Huang , Yujie Chen , Hezhou Liu
One-dimensional (1D) carbon-based magnetic fibers, characterized by rational multicomponent regulation and refined microstructure design, have emerged as promising candidates for high-performance electromagnetic wave (EMW) absorption. However, conventional 1D absorbers often suffer from densely aggregated and randomly oriented magnetic nanoparticles embedded in carbon matrices, which severely restricts magnetic coupling and consequently compromises magnetic loss capabilities. In this study, 1D necklace-structured nitrogen-doped porous carbon nanofibers embedded with FeCoNi nanoparticles (FeCoNi@NPCNFs) were successfully fabricated through a synergistic combination of hydrothermal synthesis, coaxial electrospinning, and controlled carbonization. By precisely regulating the spatial arrangement of magnetic nanoparticles, we achieved uniform dispersion and enhanced interparticle magnetic interactions within the NPCNFs, resulting in stronger magnetic anisotropy and elevated saturation magnetization. Impressively, the well-designed necklace-like FeCoNi@NPCNFs demonstrated a minimum reflection loss (RLmin) of −52.36 dB at an ultrathin thickness of 1.46 mm, accompanied by a broad effective absorption bandwidth (EAB) of 5.52 GHz (11.70–17.22 GHz) measured at 1.66 mm, which significantly outperformed single-component FeCoNi@CNFs (RLmin = −17.08 dB, EAB = 4.75 GHz). Such excellent EMW absorption performance can be attributed to the multiple magnetic coupling networks, as well as the multiple interface polarization among the biphasic FeCoNi alloys, N-doped carbon species, and the core-shell porous structure. This work proposes a groundbreaking design strategy for high-efficiency, ultra-thin magnetic fibrous EMW absorbers.
一维(1D)碳基磁性纤维具有合理的多组分调节和精细的微观结构设计,是高性能电磁波(EMW)吸收的有希望的候选者。然而,传统的一维吸收体经常受到密集聚集和随机取向的磁性纳米颗粒嵌入碳基体的影响,这严重限制了磁耦合,从而影响了磁损耗能力。在本研究中,通过水热合成、同轴静电纺丝和可控碳化的协同作用,成功制备了嵌入FeCoNi纳米颗粒(FeCoNi@NPCNFs)的一维项链状氮掺杂多孔碳纳米纤维。通过精确调节磁性纳米颗粒的空间排列,我们实现了NPCNFs内均匀分散和增强粒子间磁相互作用,从而增强了磁性各向异性和提高了饱和磁化强度。令人惊讶的是,设计良好的项链状FeCoNi@NPCNFs在超薄厚度为1.46 mm时的最小反射损耗(RLmin)为- 52.36 dB,同时在1.66 mm处测量的有效吸收带宽(EAB)为5.52 GHz (11.70-17.22 GHz),显著优于单分量FeCoNi@CNFs (RLmin = - 17.08 dB, EAB = 4.75 GHz)。这种优异的EMW吸收性能可归因于双相FeCoNi合金的多重磁耦合网络、双相FeCoNi合金之间的多重界面极化、n掺杂碳种以及核壳多孔结构。这项工作提出了一种突破性的设计策略,用于高效率,超薄磁性纤维EMW吸收器。
{"title":"Necklace-structured FeCoNi@N-doped porous carbon nanofibers with strong magnetic coupling for high-performance microwave absorption","authors":"Shuai Liu ,&nbsp;Qunfu Fan ,&nbsp;Sijia Li ,&nbsp;Yicang Huang ,&nbsp;Yujie Chen ,&nbsp;Hezhou Liu","doi":"10.1016/j.compscitech.2025.111389","DOIUrl":"10.1016/j.compscitech.2025.111389","url":null,"abstract":"<div><div>One-dimensional (1D) carbon-based magnetic fibers, characterized by rational multicomponent regulation and refined microstructure design, have emerged as promising candidates for high-performance electromagnetic wave (EMW) absorption. However, conventional 1D absorbers often suffer from densely aggregated and randomly oriented magnetic nanoparticles embedded in carbon matrices, which severely restricts magnetic coupling and consequently compromises magnetic loss capabilities. In this study, 1D necklace-structured nitrogen-doped porous carbon nanofibers embedded with FeCoNi nanoparticles (FeCoNi@NPCNFs) were successfully fabricated through a synergistic combination of hydrothermal synthesis, coaxial electrospinning, and controlled carbonization. By precisely regulating the spatial arrangement of magnetic nanoparticles, we achieved uniform dispersion and enhanced interparticle magnetic interactions within the NPCNFs, resulting in stronger magnetic anisotropy and elevated saturation magnetization. Impressively, the well-designed necklace-like FeCoNi@NPCNFs demonstrated a minimum reflection loss (RL<sub>min</sub>) of −52.36 dB at an ultrathin thickness of 1.46 mm, accompanied by a broad effective absorption bandwidth (EAB) of 5.52 GHz (11.70–17.22 GHz) measured at 1.66 mm, which significantly outperformed single-component FeCoNi@CNFs (RL<sub>min</sub> = −17.08 dB, EAB = 4.75 GHz). Such excellent EMW absorption performance can be attributed to the multiple magnetic coupling networks, as well as the multiple interface polarization among the biphasic FeCoNi alloys, N-doped carbon species, and the core-shell porous structure. This work proposes a groundbreaking design strategy for high-efficiency, ultra-thin magnetic fibrous EMW absorbers.</div></div>","PeriodicalId":283,"journal":{"name":"Composites Science and Technology","volume":"272 ","pages":"Article 111389"},"PeriodicalIF":9.8,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145155624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Composite structures spring back, modeling and sensitivity analysis 复合材料结构回弹、建模及灵敏度分析
IF 9.8 1区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-09-19 DOI: 10.1016/j.compscitech.2025.111371
Quentin Maréchal , Mohamed Ichchou , Bruno Berthel , Michelle Salvia , Pascal Fossat , Olivier Bareille , Mohamed Chabchoub
This paper deals with the modeling and sensitivity analysis of spring back for composite made structures. Spring back is a well-known phenomenon connected to the manufacturing of composite parts. It is a multi-physical process involving chemical, thermal, and mechanical issues. The prediction of the spring back is necessary in order to improve the quality of the production while respecting the manufacturing rules and tolerances. This paper specifically addresses a very important question. Indeed when the spring back is connected to a great number of parameters that need to be characterized accordingly, not all of them are of relevance for the prediction. The paper implements a sensitivity analysis process leading to a hierarchy of the needed parameters. Specifically for the composite tested in this paper, it is shown that the cure shrinkage coefficients are the most important parameters that need to be characterized precisely. This conclusion could help make relevant experimental characterization for the final target which is the relevant prediction of the spring back.
本文研究了复合材料结构回弹的建模和灵敏度分析。回弹是复合材料零件制造过程中常见的现象。它是一个涉及化学、热和机械问题的多物理过程。为了在遵守制造规则和公差的前提下提高产品质量,回弹预测是必要的。这篇论文专门讨论了一个非常重要的问题。事实上,当回弹与大量需要相应表征的参数相连接时,并非所有参数都与预测相关。本文实现了一个敏感性分析过程,从而得到所需参数的层次结构。具体到本文所测试的复合材料,表明固化收缩系数是最重要的参数,需要精确表征。这一结论有助于对最终目标即回弹的相关预测进行相关的实验表征。
{"title":"Composite structures spring back, modeling and sensitivity analysis","authors":"Quentin Maréchal ,&nbsp;Mohamed Ichchou ,&nbsp;Bruno Berthel ,&nbsp;Michelle Salvia ,&nbsp;Pascal Fossat ,&nbsp;Olivier Bareille ,&nbsp;Mohamed Chabchoub","doi":"10.1016/j.compscitech.2025.111371","DOIUrl":"10.1016/j.compscitech.2025.111371","url":null,"abstract":"<div><div>This paper deals with the modeling and sensitivity analysis of spring back for composite made structures. Spring back is a well-known phenomenon connected to the manufacturing of composite parts. It is a multi-physical process involving chemical, thermal, and mechanical issues. The prediction of the spring back is necessary in order to improve the quality of the production while respecting the manufacturing rules and tolerances. This paper specifically addresses a very important question. Indeed when the spring back is connected to a great number of parameters that need to be characterized accordingly, not all of them are of relevance for the prediction. The paper implements a sensitivity analysis process leading to a hierarchy of the needed parameters. Specifically for the composite tested in this paper, it is shown that the cure shrinkage coefficients are the most important parameters that need to be characterized precisely. This conclusion could help make relevant experimental characterization for the final target which is the relevant prediction of the spring back.</div></div>","PeriodicalId":283,"journal":{"name":"Composites Science and Technology","volume":"272 ","pages":"Article 111371"},"PeriodicalIF":9.8,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145155621","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dielectric breakdown behaviors and high-voltage damages of 3D braided carbon fiber/epoxy resin composites 三维编织碳纤维/环氧树脂复合材料的介电击穿行为及高压损伤
IF 9.8 1区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-09-18 DOI: 10.1016/j.compscitech.2025.111388
Sheng Liu, Bohong Gu, Baozhong Sun
Dielectric breakdown of carbon fiber reinforced polymers is a key factor affecting the lightning protection design of engineering applications. This paper presented a coupled phase field-electrical-thermal model to reveal dielectric breakdown evolution and damage morphology of three-dimensional (3D) braided carbon fiber/epoxy composites. Finite element analysis (FEA) results show that dielectric breakdown occurs in the shortest conductive path along the electrical field direction. The braided yarns outside the shortest path also exhibit a breakdown tendency, which weakens the dielectric breakdown voltage. Testing results verify that dielectric breakdown voltage decreases from 3250 V to 337.5 V as the increasing carbon fiber yarns. Increasing the equivalent length of braided yarn along the loading direction decreases the dielectric breakdown voltage. Furthermore, a similar elliptical damage is observed at the surface braided knot from both the FEA model and the testing results. The verified model finds that both electric potential and current density distributions within the composite undergo abrupt transitions upon complete dielectric breakdown, which further reveals the dielectric breakdown progress.
碳纤维增强聚合物的介电击穿是影响工程应用防雷设计的关键因素。本文提出了一种相场-电-热耦合模型来揭示三维编织碳纤维/环氧复合材料的介电击穿演化和损伤形态。有限元分析结果表明,介质击穿发生在沿电场方向的最短导电路径上。在最短路径以外的编织纱线也表现出击穿的倾向,这削弱了介质击穿电压。测试结果表明,随着碳纤维纱的增加,介质击穿电压从3250 V降低到337.5 V。沿加载方向增加编织纱的等效长度可降低介质击穿电压。此外,从有限元模型和试验结果来看,编织结表面出现了相似的椭圆损伤。经过验证的模型发现,复合材料内部的电势和电流密度分布在介质完全击穿后都发生了突变,进一步揭示了介质击穿的过程。
{"title":"Dielectric breakdown behaviors and high-voltage damages of 3D braided carbon fiber/epoxy resin composites","authors":"Sheng Liu,&nbsp;Bohong Gu,&nbsp;Baozhong Sun","doi":"10.1016/j.compscitech.2025.111388","DOIUrl":"10.1016/j.compscitech.2025.111388","url":null,"abstract":"<div><div>Dielectric breakdown of carbon fiber reinforced polymers is a key factor affecting the lightning protection design of engineering applications. This paper presented a coupled phase field-electrical-thermal model to reveal dielectric breakdown evolution and damage morphology of three-dimensional (3D) braided carbon fiber/epoxy composites. Finite element analysis (FEA) results show that dielectric breakdown occurs in the shortest conductive path along the electrical field direction. The braided yarns outside the shortest path also exhibit a breakdown tendency, which weakens the dielectric breakdown voltage. Testing results verify that dielectric breakdown voltage decreases from 3250 V to 337.5 V as the increasing carbon fiber yarns. Increasing the equivalent length of braided yarn along the loading direction decreases the dielectric breakdown voltage. Furthermore, a similar elliptical damage is observed at the surface braided knot from both the FEA model and the testing results. The verified model finds that both electric potential and current density distributions within the composite undergo abrupt transitions upon complete dielectric breakdown, which further reveals the dielectric breakdown progress.</div></div>","PeriodicalId":283,"journal":{"name":"Composites Science and Technology","volume":"272 ","pages":"Article 111388"},"PeriodicalIF":9.8,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145106933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bio-inspired overlapping curl structures for toughening bio-based epoxy: A study on the fracture phenomena 生物基环氧树脂增韧的仿生重叠卷曲结构:断裂现象研究
IF 9.8 1区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-09-16 DOI: 10.1016/j.compscitech.2025.111374
Zhiyuan Xu , Ran Tao , Kunal Masania , Sofia Teixeira de Freitas
In this study, a 3D-printed biomimetic overlapping curl structure inspired by spider silk molecular structure, containing sacrificial bonds and hidden lengths, is studied as a toughening mechanism for a bio-based epoxy. Experimental results of the fracture phenomena of the overlapping curl-reinforced bio-based epoxy identify three toughening mechanisms triggered by the overlapping curl: (1) crack re-initiation, (2) overlapping curl bridging, and (3) epoxy ligament. First, the integrated overlapping curl creates a void within the epoxy matrix. As the crack tip reaches the end of this void, the crack re-initiates. Then, as the hidden length of overlapping curl unfolds, it leads to a bridging effect in resisting crack growth. In addition, for the smallest hidden length, an epoxy ligament is formed due to crack branching, significantly improving the energy release rate. The epoxy fracture energy release rate increased by 13 %. The overall modest improvement is attributed to the large plastic dissipation energy of the epoxy and the relatively low overlapping curl load-capacity. However, when expanding the design space numerically, it was shown that as the failure load of the overlapping curl increases, the bridging effect increases progressively. The introduction of the bio-inspired overlapping curl structure into bio-based epoxy proves the concept of a toughening strategy for developing high-performance sustainable composite materials.
在这项研究中,受蜘蛛丝分子结构的启发,3d打印仿生重叠卷曲结构,包含牺牲键和隐藏长度,研究了生物基环氧树脂的增韧机制。通过对重叠旋度增强生物基环氧树脂断裂现象的实验研究,确定了重叠旋度触发的三种增韧机制:(1)裂纹再萌生,(2)重叠旋度桥接,(3)环氧韧带。首先,集成的重叠卷曲在环氧树脂基体中产生空隙。当裂纹尖端到达空洞的末端时,裂纹重新开始。然后,随着重叠卷曲的隐藏长度展开,它在抵抗裂纹扩展中起到桥接作用。此外,在最小的隐藏长度下,由于裂纹分支形成环氧韧带,显著提高了能量释放率。环氧树脂断裂能释放率提高13%。整体的适度改善是由于环氧树脂的塑性耗散能大,而重叠旋度荷载能力相对较低。然而,当数值扩展设计空间时,表明随着重叠旋度破坏载荷的增大,桥接效应逐渐增大。将仿生重叠卷曲结构引入生物基环氧树脂中,证明了开发高性能可持续复合材料的增韧策略的概念。
{"title":"Bio-inspired overlapping curl structures for toughening bio-based epoxy: A study on the fracture phenomena","authors":"Zhiyuan Xu ,&nbsp;Ran Tao ,&nbsp;Kunal Masania ,&nbsp;Sofia Teixeira de Freitas","doi":"10.1016/j.compscitech.2025.111374","DOIUrl":"10.1016/j.compscitech.2025.111374","url":null,"abstract":"<div><div>In this study, a 3D-printed biomimetic overlapping curl structure inspired by spider silk molecular structure, containing sacrificial bonds and hidden lengths, is studied as a toughening mechanism for a bio-based epoxy. Experimental results of the fracture phenomena of the overlapping curl-reinforced bio-based epoxy identify three toughening mechanisms triggered by the overlapping curl: (1) crack re-initiation, (2) overlapping curl bridging, and (3) epoxy ligament. First, the integrated overlapping curl creates a void within the epoxy matrix. As the crack tip reaches the end of this void, the crack re-initiates. Then, as the hidden length of overlapping curl unfolds, it leads to a bridging effect in resisting crack growth. In addition, for the smallest hidden length, an epoxy ligament is formed due to crack branching, significantly improving the energy release rate. The epoxy fracture energy release rate increased by 13<!--> <!-->%. The overall modest improvement is attributed to the large plastic dissipation energy of the epoxy and the relatively low overlapping curl load-capacity. However, when expanding the design space numerically, it was shown that as the failure load of the overlapping curl increases, the bridging effect increases progressively. The introduction of the bio-inspired overlapping curl structure into bio-based epoxy proves the concept of a toughening strategy for developing high-performance sustainable composite materials.</div></div>","PeriodicalId":283,"journal":{"name":"Composites Science and Technology","volume":"272 ","pages":"Article 111374"},"PeriodicalIF":9.8,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145155623","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Compressive behaviour and micromechanical modelling of steel-reinforced resin under monotonic and cyclic loading 单调和循环加载下钢增强树脂的压缩行为和微观力学模型
IF 9.8 1区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Pub Date : 2025-09-15 DOI: 10.1016/j.compscitech.2025.111387
Angeliki Christoforidou , Abishek Baskar , Entela Kane , Marko Pavlovic
Steel-Reinforced Resin (SRR) is a particulate material originally developed as an injectant for anchoring applications. More recently, it has been proposed as a filler material for cavities embedding mechanical connectors in FRP–steel hybrid bridges. In this context, the compressive behaviour of SRR becomes critical due to the multiaxial stress states and fatigue demands at a joint scale. This paper presents a comprehensive experimental and numerical investigation of SRR under monotonic, incremental cyclic, and fatigue compressive loading in unconfined conditions. A custom triaxial setup is also used to evaluate pressure sensitivity and strength enhancement due to confinement under monotonic loading. In parallel, micromechanical finite element models are developed to simulate the interactions between the resin matrix and the steel balls at the microscale, incorporating interface damage, friction, and cohesive failure. The models reproduce the observed nonlinear behaviour and reveal distinct Poisson's ratio responses in tension and compression, offering deeper insight into the mechanisms governing stiffness degradation, strain softening, and plateau behaviour.
钢增强树脂(SRR)是一种颗粒材料,最初是作为锚固应用的注入剂开发的。最近,它被提出作为一种填充材料,用于在frp -钢混合桥中嵌入机械连接器的空腔。在这种情况下,由于多轴应力状态和关节尺度的疲劳需求,SRR的压缩行为变得至关重要。本文对无侧限条件下单调、增量循环和疲劳压缩载荷下的SRR进行了全面的实验和数值研究。定制的三轴装置也用于评估压力敏感性和强度增强,因为约束在单调载荷下。同时,开发了微力学有限元模型来模拟树脂基体与钢球在微观尺度上的相互作用,包括界面损伤、摩擦和内聚破坏。这些模型再现了观察到的非线性行为,并揭示了拉伸和压缩中不同的泊松比响应,为控制刚度退化、应变软化和平台行为的机制提供了更深入的见解。
{"title":"Compressive behaviour and micromechanical modelling of steel-reinforced resin under monotonic and cyclic loading","authors":"Angeliki Christoforidou ,&nbsp;Abishek Baskar ,&nbsp;Entela Kane ,&nbsp;Marko Pavlovic","doi":"10.1016/j.compscitech.2025.111387","DOIUrl":"10.1016/j.compscitech.2025.111387","url":null,"abstract":"<div><div>Steel-Reinforced Resin (SRR) is a particulate material originally developed as an injectant for anchoring applications. More recently, it has been proposed as a filler material for cavities embedding mechanical connectors in FRP–steel hybrid bridges. In this context, the compressive behaviour of SRR becomes critical due to the multiaxial stress states and fatigue demands at a joint scale. This paper presents a comprehensive experimental and numerical investigation of SRR under monotonic, incremental cyclic, and fatigue compressive loading in unconfined conditions. A custom triaxial setup is also used to evaluate pressure sensitivity and strength enhancement due to confinement under monotonic loading. In parallel, micromechanical finite element models are developed to simulate the interactions between the resin matrix and the steel balls at the microscale, incorporating interface damage, friction, and cohesive failure. The models reproduce the observed nonlinear behaviour and reveal distinct Poisson's ratio responses in tension and compression, offering deeper insight into the mechanisms governing stiffness degradation, strain softening, and plateau behaviour.</div></div>","PeriodicalId":283,"journal":{"name":"Composites Science and Technology","volume":"272 ","pages":"Article 111387"},"PeriodicalIF":9.8,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145119192","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Composites Science and Technology
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1