Enabling the recycling of polycarbonate through reinforcement with graphene nanoplatelets

材料科学 复合材料 聚碳酸酯 渗流阈值 脆性 脆化 极限抗拉强度 渗透(认知心理学) 纳米复合材料 石墨烯 聚合物 石墨 弹性体 模数 色散(光学) 无定形固体 碳纤维 压力(语言学) 聚合物纳米复合材料 杨氏模量 延展性(地球科学) 压阻效应 休克(循环) 艾氏冲击强度试验 造型(装饰) 拉伸试验 弹性模量 动态力学分析
作者
Ozan Can Zehni,Tayyab Khan,Yubao Deng,Mark A. Bissett,William W. Sampson,Robert J. Young,Ian A. Kinloch
出处
期刊:Composites Part B-engineering [Elsevier BV]
卷期号:320: 113668-113668
标识
DOI:10.1016/j.compositesb.2026.113668
摘要

The rapid embrittlement of polycarbonate (PC) during mechanical recycling, caused by chain scission and the resulting molecular weight loss, severely limits its potential for circular use. Here, we demonstrate that the addition of graphene nanoplatelets (GNPs) enables improved recycability by simultaneously stabilizing the polymer’s molecular weight and preserving mechanical integrity. PC/GNP nanocomposites were evaluated in the as-manufactured state (R0) and after three consecutive recycling cycles (R1–R3) in terms of molecular, thermal, mechanical, and electrical properties. While neat PC exhibited catastrophic embrittlement and became too brittle for tensile testing by R3, falling apart after moulding, intermediate GNP loadings (3–5 wt. %) proved optimal. This coincides with the electrical percolation threshold (∼4.8 wt. %) and enables efficient stress transfer and crack suppression, yielding tensile strengths of ∼40–50 MPa and sustaining appreciable failure strain despite some chain scission. At higher loadings (≥7 wt. %), the Young’s modulus increased monotonically, but platelet agglomeration reduced ductility. Gel permeation chromatography (GPC) confirmed that GNPs mitigate molecular weight reduction and distribution broadening across cycles, consistent with improved macroscopic stability. Collectively, these findings establish that reinforcing amorphous polymers with percolating carbon nanofiller networks offers a viable strategy for closed-loop recycling and opens pathways toward the sustainable, high-value reuse of engineering plastics.
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