کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1883197 | 1533544 | 2009 | 5 صفحه PDF | دانلود رایگان |

Cross-linking polymerization initiated by high-energy radiation is a very attractive technique for the fabrication of high-performance composite materials. The method offers many advantages compared to conventional energy- and time-consuming thermal curing processes. Free radical and cationic poly-addition chemistries have been investigated in some details by various research groups along the previous years. A high degree of control over curing kinetics and material properties can be exerted by adjusting the composition of matrix precursors as well as by acting on process parameters.However, the comparison with state-of-the-art thermally cured composites revealed the lower transverse mechanical properties of radiation-cured composites and the higher brittleness of the radiation-cured matrix. Improving fiber–matrix adhesion and upgrading polymer network toughness are thus two major challenges in this area. We have investigated several points related to these issues, and particularly the reduction of the matrix shrinkage on curing, the wettability of carbon fibers, the design of fiber–matrix interface and the use of thermoplastic toughening agents. Significant improvements were achieved on transverse strain at break by applying original surface treatments on the fibers so as to induce covalent coupling with the matrix. A drastic enhancement of the KIC value exceeding 2 MPa m1/2 was also obtained for acrylate-based matrices toughened with high Tg thermoplastics.
Journal: Radiation Physics and Chemistry - Volume 78, Issues 7–8, July–August 2009, Pages 557–561