材料科学
复合材料
环氧树脂
表面改性
纳米复合材料
极限抗拉强度
润湿
抗弯强度
氮化硼
接触角
纤维
模数
硼
复合数
六方氮化硼
纳米压痕
相间
聚合物纳米复合材料
体积分数
抗剪强度(土壤)
聚合物
X射线光电子能谱
弯曲模量
硅烷化
碳化
氢氧化钠
弹性模量
石墨烯
作者
Jerrin Joy Varughese,Lince Mathew Thomas,Arun Sam Varghese,Dinah Ann Varughese,T. P. Sumangala,M. S. Sreekanth
摘要
ABSTRACT A dual interfacial engineering strategy is proposed to enhance the mechanical and interlaminar performance of carbon fiber (CF)‐reinforced epoxy (EP) nanocomposites by simultaneously silanizing CF and exfoliated hexagonal boron nitride nanosheets (hBNNs). Sodium hydroxide assisted hydroxylation, followed by 3‐aminopropyltriethoxysilane (APTES) functionalization, enabled covalent integration at the fiber–matrix and filler–matrix interfaces. XPS analysis confirmed the formation of SiOSi and SiOB linkages on APTES functionalized hBNNs, establishing a chemically interconnected interface. Wettability improved significantly, with the contact angle reducing from 85.48° for untreated CF to 74.46° after salinization of CF. The dual‐functionalized epoxy composite exhibited a tensile strength of 409 ± 9 MPa and modulus of 32.05 ± 2 GPa, corresponding to enhancements of 22% and 67.45%, respectively, over pristine CF/EP. Flexural strength increased from 492 ± 6 MPa to 537 ± 11 MPa, while interlaminar shear strength improved from 37.08 ± 0.06 to 43.50 ± 0.04 MPa, demonstrating superior resistance to shear‐driven failure. Fiber volume fraction was consistently maintained within 41% with void content less than 5%, confirming that the performance gains arise from interfacial engineering. The chemically integrated hybrid network induces constrained interphase regions and cooperative stress‐transfer pathways in the polymer matrix, generating a positive synergistic effect beyond additive reinforcement behavior.
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