Dynamic cure kinetics of epoxy resins using an amine-containing borate as a latent hardener

2012 ◽  
Vol 61 (6) ◽  
pp. 959-965 ◽  
Author(s):  
Qiao Yan Liu ◽  
Jin Bin Chen ◽  
Shu Mei Liu ◽  
Jian Qing Zhao
2009 ◽  
Vol 112 (5) ◽  
pp. 3119-3126 ◽  
Author(s):  
Garima Tripathi ◽  
Deepak Srivastava

2002 ◽  
Vol 383 (1-2) ◽  
pp. 119-127 ◽  
Author(s):  
D Roşu ◽  
C.N Caşcaval ◽  
F Mustątǎ ◽  
C Ciobanu

1986 ◽  
Vol 32 (2) ◽  
pp. 3761-3773 ◽  
Author(s):  
Antonio Moroni ◽  
Jovan Mijovic ◽  
Eli M. Pearce ◽  
Cheu Ching Foun

2011 ◽  
Vol 236-238 ◽  
pp. 2058-2062
Author(s):  
Hong Jun Zhou ◽  
Guo Qiang Yin ◽  
Miao Hong Zhuang ◽  
Jian Fang Ge ◽  
Xuan Lin

The cure kinetics of epoxy/epoxy-grafted nano-aluminum oxide using 4, 4'-diaminodiphenylsulphone (DDS) as the curing agent was studied by nonisothermal differential scanning calorimetry (DSC) at different heating rates. The activation energy (Ea) was determined by Flynn-Wall-Ozawa method, and kinetic model was predicted by Málek method. TheEa values of epoxy/nano-aluminum oxide/DDS systems are generally higher than those of epoxy /DDS. These imply that the addition of nano-aluminum oxide would inhibit the chain mobility of the epoxy resins. Furthermore, autocatalytic model was found to be appropriate to describe the kinetics of above mentioned reactions. The predicted curves fit well with the experimentally obtained curves.


1992 ◽  
Vol 4 (1) ◽  
pp. 41-48 ◽  
Author(s):  
R. M. V. G. K. Rao ◽  
A. Padma ◽  
H. S. Patel

Differential scanning calorimeny was used to study the cure kinetics of three epoxy resin systems cured with two hardeners: diaminodiphenylmethane (DDM) and a poly (keto-amine) (PA). The results showved that the curing of the epoxy resins by PA occurs at higher temperatures and the activation energy for PA curing was higher compared with the DDM curing process, showing the er reactivity of PA.


2010 ◽  
Vol 123-125 ◽  
pp. 955-958
Author(s):  
De Wen Zhou ◽  
Li Yan Liang ◽  
Man Geng Lu

A series of dimeric liquid crystalline (LC) epoxy monomers containing azo groups with different length of central spacers were synthesized. The mesogenic behavior of these monomers was characterized by differential scanning calorimetry(DSC), polarized optical microscopy (POM) and wide-angle X-Ray diffraction(WAXS). Like other dimeric LC epoxy monomers, the melting points, clear points and mesophase of these compounds were influenced by the carbon numbers of the central spacers. Cure kinetics of these monomers with anhydride was studied by non-isothermal DSC at different heating rates. With the increasing of conversion, the values of activation energy show a tendency to decrease. The formation and development of LC phase during curing were also studied by POM. Finally LC thermosets with nematic phase were obtained.


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