Autonomic healing of epoxy vinyl esters via ring opening metathesis polymerization

被引:150
作者
Wilson, Gerald O. [1 ,3 ]
Moore, Jeffrey S. [3 ,4 ]
White, Scott R. [2 ,3 ]
Sottos, Nancy R. [1 ,3 ]
Andersson, H. Magnus [3 ]
机构
[1] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Aerosp Engn, Urbana, IL 61801 USA
[3] Univ Illinois, Beckman Inst, Urbana, IL 61801 USA
[4] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
关键词
D O I
10.1002/adfm.200700419
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A materials system for autonomic healing of epoxy vinyl esters is demonstrated. The system is comprised of wax microspheres containing Grubbs' catalyst and microcapsules containing exo-dicyclopentadiene (DCPD) embedded together in an epoxy vinyl ester matrix. Healing is triggered when damage in the form of a crack ruptures the microcapsules, causing DCPD to be released into the crack plane where it comes in contact and mixes with the catalyst microspheres initiating ring opening metathesis polymerization (ROMP). The chemical compatibility of the catalyst with the matrix is investigated and wax protection of the catalyst via microspheres of a sufficient size (34-98 mu m) is shown to provide a suitable barrier for protecting the catalyst from free radicals generated in situ during the curing of the epoxy vinyl ester resin. Wax protection of the catalyst also allows uninhibited curing of the matrix to proceed at room temperature. Concentration of self-healing components is varied with a view towards optimization of the recovery of virgin mechanical properties. Efficient self-healing is observed with microspheres that are smaller than those used in previous polymer matrices. Significant recovery of virgin mechanical properties is observed within 2.5 min of healing time at room temperature and the mechanical properties of healed samples after 24 h of healing time match those of existing ROMP-based self-healing systems.
引用
收藏
页码:44 / 52
页数:9
相关论文
共 23 条
[11]  
Hansen SM, 1999, CHEM-EUR J, V5, P557, DOI 10.1002/(SICI)1521-3765(19990201)5:2<557::AID-CHEM557>3.0.CO
[12]  
2-A
[13]   Catalyst morphology and dissolution kinetics of self-healing polymers [J].
Jones, AS ;
Rule, JD ;
Moore, JS ;
White, SR ;
Sottos, NR .
CHEMISTRY OF MATERIALS, 2006, 18 (05) :1312-1317
[14]   Self-healing structural composite materials [J].
Kessler, MR ;
Sottos, NR ;
White, SR .
COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING, 2003, 34 (08) :743-753
[15]   Cure kinetics of the ring-opening metathesis polymerization of dicyclopentadiene [J].
Kessler, MR ;
White, SR .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2002, 40 (14) :2373-2383
[16]   Self-activated healing of delamination damage in woven composites [J].
Kessler, MR ;
White, SR .
COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING, 2001, 32 (05) :683-699
[17]   Using nanoparticles to create self-healing composites [J].
Lee, JY ;
Buxton, GA ;
Balazs, AC .
JOURNAL OF CHEMICAL PHYSICS, 2004, 121 (11) :5531-5540
[18]  
NELSON GL, 1975, SYNTHESIS-STUTTGART, P105
[19]   A hollow fibre reinforced polymer composite encompassing self-healing and enhanced damage visibility [J].
Pang, JWC ;
Bond, IP .
COMPOSITES SCIENCE AND TECHNOLOGY, 2005, 65 (11-12) :1791-1799
[20]   Wax-protected catalyst microspheres for efficient self-healing materials [J].
Rule, JD ;
Brown, EN ;
Sottos, NR ;
White, SR ;
Moore, JS .
ADVANCED MATERIALS, 2005, 17 (02) :205-+