Low-temperature cure high-performance cyanate ester resins/microencapsulated catalyst systems

被引:19
作者
Chen, Feng [1 ,2 ]
Yuan, Li [1 ,2 ]
Gu, Aijuan [1 ,2 ]
Lin, Chao [1 ,2 ]
Liang, Guozheng [1 ,2 ]
机构
[1] Soochow Univ, Dept Mat Sci & Engn, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Jiangsu, Peoples R China
[2] Soochow Univ, Jiangsu Key Lab Adv Funct Polymer Design & Applic, Dept Polymer Sci & Engn, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
SUPPORTED PALLADIUM CATALYST; RESIN SYSTEMS; MECHANICAL-PROPERTIES; COUPLING REACTIONS; KINETICS; RELEASE;
D O I
10.1002/pen.23455
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The encapsulated catalyst can be released under stimulation conditions to control the polymerization reaction. In this study, poly(urea-formaldehyde) (PUF) microcapsules (MCs) filled with dibutyltin dilaurate (DBTDL) catalyst (PUF/DBTDL MCs) were applied to bisphenol A dicyanate ester (BADCy) resins to develop a novel low temperature cure high performance BADCy/MCs systems. The effect of PUF/DBTDL MCs on the reactivity of BADCy was investigated. The mechanical property, the thermal property, the water uptake, and the dielectric property of cured BADCy/MCs resin systems were discussed in detail. Results indicate that roughly varying the content of the encapsulated DBTDL can easily and safely adjust the polymerization temperature. The BADCy systems with proper content of MCs cured at low temperature show excellent mechanical property, good thermal property, low water uptake, and low dielectric property. When the content of MCs is 0.125 wt%, the cured BADCy/MCs system has the optimal integrated properties owing to the formation of more uniform crosslinked structure and high conversion of cyanate ester (OCN) groups resulting from the slow release of DBTDL catalyst through the wall shell under heating condition. POLYM. ENG. SCI., 2013. (c) 2013 Society of Plastics Engineers
引用
收藏
页码:1871 / 1877
页数:7
相关论文
共 29 条
[1]   KINETICS AND MODELING OF THERMAL POLYCYCLOTRIMERIZATION OF AROMATIC DICYANATES [J].
BAUER, M ;
BAUER, J ;
KUHN, G .
ACTA POLYMERICA, 1986, 37 (11-12) :715-719
[2]   Microwave-assisted Suzuki coupling reactions with an encapsulated palladium catalyst for batch and continuous-flow transformations [J].
Baxendale, Ian R. ;
Griffiths-Jones, Charlotte M. ;
Ley, Steven V. ;
Tranmer, Geoffrey K. .
CHEMISTRY-A EUROPEAN JOURNAL, 2006, 12 (16) :4407-4416
[3]   Microcapsule induced toughening in a self-healing polymer composite [J].
Brown, EN ;
White, SR ;
Sottos, NR .
JOURNAL OF MATERIALS SCIENCE, 2004, 39 (05) :1703-1710
[4]   Polydimethylsiloxane-based self-healing materials [J].
Cho, SH ;
Andersson, HM ;
White, SR ;
Sottos, NR ;
Braun, PV .
ADVANCED MATERIALS, 2006, 18 (08) :997-+
[5]   A Novel Hybrid Catalyst System and Its Effects on the Curing, Thermal, and Dielectric Properties of Cyanate Ester [J].
Dai, Shankai ;
Zhuo, Dongxian ;
Gu, Aijuan ;
Liang, Guozheng ;
Yuan, Li .
POLYMER ENGINEERING AND SCIENCE, 2011, 51 (11) :2236-2244
[6]   Polymer crosslinking controlled by release of catalyst encapsulated in polycarbonate micro-spheres [J].
Deyrail, Y ;
Zydowicz, N ;
Cassagnau, P .
POLYMER, 2004, 45 (18) :6123-6131
[7]  
Fink JohannesKarl., 2005, REACTIVE POLYM FUNDA
[8]  
Goetter R. W., 2008, U. S. Patent, Patent No. [01,82,943A1, 0182943]
[9]   Kinetic parameters of a cyanate ester resin catalyzed with different proportions of nonylphenol and cobalt acetylacetonate catalyst [J].
Gómez, CM ;
Recalde, IB ;
Mondragon, M .
EUROPEAN POLYMER JOURNAL, 2005, 41 (11) :2734-2741
[10]  
Hamerton I., 1994, Chemistry and Technology of Cyanate Ester Resins, Blackie Academic