Self-healing kinetics and the stereoisomers of dicyclopentadiene

被引:87
作者
Mauldin, Timothy C.
Rule, Joseph D.
Sottos, Nancy R.
White, Scott R.
Moore, Jeffrey S.
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Aerosp Engn, Urbana, IL 61801 USA
[4] Univ Illinois, Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
关键词
ring-opening metathesis polymerization; endo-dicyclopentadiene; exo-dicyclopentadiene; autonomic healing; self-healing;
D O I
10.1098/rsif.2006.0200
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
While original epoxy resin-based self-healing systems used the commercially available endo-isomer of dicyclopentadiene (DCPD), the exo-stereoisomer is known to have much faster olefin metathesis reaction rates with first-generation Grubbs' catalyst. Here, we measure the energy to failure of healed specimens as a function of healing time and compare the kinetics of damage repair for endo- and exo-DCPD, and mixtures of the two isomers. Using catalyst loading levels previously reported to be effective for endo-DCPD, exo-DCPD was found to heal approximately 20 times faster than the endo-isomer, but with a lower healing efficiency. The fracture toughness of the repaired specimens decreased when the exo content of the blends was greater than 40% and, for the pure exo-DCPD, when the catalyst loadings were below 1%. Possible causes of the reduced healing efficiencies of the exo-DCPD healing agent are discussed.
引用
收藏
页码:389 / 393
页数:5
相关论文
共 18 条
[1]   In situ poly(urea-formaldehyde) microencapsulation of dicyclopentadiene [J].
Brown, EN ;
Kessler, MR ;
Sottos, NR ;
White, SR .
JOURNAL OF MICROENCAPSULATION, 2003, 20 (06) :719-730
[2]   Retardation and repair of fatigue cracks in a microcapsule toughened epoxy composite - Part II: In situ self-healing [J].
Brown, EN ;
White, SR ;
Sottos, NR .
COMPOSITES SCIENCE AND TECHNOLOGY, 2005, 65 (15-16) :2474-2480
[3]   Fracture testing of a self-healing polymer composite [J].
E. N. Brown ;
N. R. Sottos ;
S. R. White .
Experimental Mechanics, 2002, 42 (4) :372-379
[4]  
FU Q, 2001, POLYM PREPR, V42, P341
[5]  
Ivin K. J., 1997, OLEFIN METATHESIS ME
[6]   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
[7]   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
[8]   RING-OPENING POLYMERIZATION OF NORBORNENE SUBSTITUTED WITH AMINE AND AMMONIUM GROUPS [J].
LARROCHE, C ;
LAVAL, JP ;
LATTES, A ;
BASSET, JM .
JOURNAL OF ORGANIC CHEMISTRY, 1984, 49 (11) :1886-1890
[9]   Characterization of diene monomers as healing agents for autonomic damage repair [J].
Liu, Xing ;
Lee, Jong Keun ;
Yoon, Sung Ho ;
Kessler, Michael R. .
JOURNAL OF APPLIED POLYMER SCIENCE, 2006, 101 (03) :1266-1272
[10]   (eta(3)-Allyl)palladium(II) and palladium(II) nitrile catalysts for the addition polymerization of norbornene derivatives with functional groups [J].
Mathew, JP ;
Reinmuth, A ;
Melia, J ;
Swords, N ;
Risse, W .
MACROMOLECULES, 1996, 29 (08) :2755-2763