Studies on Curing Kinetics of Epoxy Resin / Modified Amine System

2013 ◽  
Vol 652-654 ◽  
pp. 121-126 ◽  
Author(s):  
Dong Bo Guan ◽  
Zhong Yi Cai ◽  
Xiao Jie Zhai ◽  
Wei Guo Yao ◽  
Shou Jun Wang ◽  
...  
Keyword(s):  
Activation Energy ◽  
Kinetic Model ◽  
Epoxy Resin ◽  
Reaction Kinetic ◽  
Reaction Order ◽  
Curing Kinetics ◽  
Curing Conditions ◽  
Reaction Kinetic Model ◽  
Amine System ◽  
Kinetics Of

In this paper, E51 epoxy resin with 1050B modified polyamine and 1055B Modified polyamide was studied by non-isothermal DSC, and then we use Kissinger and Ozawa methods to calculate the activation energy and reaction order n, obtained its curing reaction kinetic model, and the reaction is a complicated reaction, at last we determine the E51 epoxy resin and 1050B modified polyamine / 1055B Modified polyamide curing conditions.

Curing Kinetics of Phenol Formaldehyde Resin Modified with Sodium Silicate

2012 ◽  
Vol 184-185 ◽  
pp. 1471-1479
Author(s):  
Jin Sun ◽  
Xiao Feng Zhu ◽  
Xiao Bo Wang ◽  
Rui Hang Lin ◽  
Zhen Zhong Gao
Keyword(s):  
Activation Energy ◽  
Sodium Silicate ◽  
Reaction Order ◽  
Phenol Formaldehyde ◽  
Curing Kinetics ◽  
Curing Temperature ◽  
Formaldehyde Resin ◽  
Exponential Factor ◽  
Curing Reaction ◽  
Kinetics Of

The curing kinetics of PF resin modified with sodium silicate had been investigated by differential scanning calorimetry (DSC). The kinetic analysis was performed at heating rates of 5, 10, 15, and 20°C/min，respectively. The kinetic parameters such as reaction order and activation energy were solved by Kissinger and Crane equation. The relationship between curing temperature and heating rate was also investigated. The activation energy and the curing reaction order，which were obtained by kinetic calculation, are 83.00kJ/mol and 0.917, respectively. The curing reaction kinetics equations were built by the obtained best curing temperature, reaction order, pre-exponential factor and reaction rate constant.

Curing Kinetics of Silicone Epoxy Resin Containing Fluorene

2014 ◽  
Vol 936 ◽  
pp. 28-33 ◽  
Author(s):  
Wei Xing Deng ◽  
Yuan Wei Zhong ◽  
Jie Qin ◽  
Xue Bing Huang ◽  
Jin Wen Peng
Keyword(s):  
Activation Energy ◽  
Differential Scanning Calorimetry ◽  
Ftir Spectroscopy ◽  
Epoxy Resin ◽  
1H Nmr ◽  
Chemical Structure ◽  
Curing Kinetics ◽  
Curing Agent ◽  
Scanning Calorimetry ◽  
Kinetics Of

A new epoxy resin based on dichlorosilane and 9,9-bis (4-hydroxyphenyl) fluorene was synthesized to produce a highly heat-resistant network. The chemical structure was characterized with FTIR spectroscopy and 1H-NMR. 4-4′-Diaminodiphenylsulfone (DDS) was used as the curing agent. The curing kinetics of different epoxy/DDS systems were investigated using non-isothermal differential scanning calorimetry (DSC). The results showed that the values of activation energy (E) were affected by the chemical structure of epoxy resin, and BPEBF exhibited lower curing reactivity towards DDS compared to E-51.

Effect of pre-curing process on epoxy resin foaming using carbon dioxide as blowing agent

2016 ◽  
Vol 53 (2) ◽  
pp. 181-197 ◽  
Author(s):  
Jiaxun Lyu ◽  
Tao Liu ◽  
Zhenhao Xi ◽  
Ling Zhao
Keyword(s):  
Carbon Dioxide ◽  
Epoxy Resin ◽  
Curing Kinetics ◽  
Batch Process ◽  
Average Cell Size ◽  
Average Cell ◽  
Curing Conditions ◽  
Foaming Process ◽  
Epoxy Resin System ◽  
Kinetics Of

A thermosetting epoxy resin system consisting of diglycidylether of bisphenol A (DGEBA) and m-xylylenediamine (MXDA) was successfully foamed by carbon dioxide (CO2) using two-step batch process. Isothermal curing kinetics of epoxy system was developed to help control the pre-curing degree of resin under different pre-curing conditions. Samples with different pre-curing degrees were prepared and then foamed via temperature-rising foaming process. It was found that the pre-curing degree was a crucial index for the foamability of epoxy resin. The effects of pre-curing conditions on curing reaction as well as further foaming results were investigated, and the results showed that the pre-curing degree from 37.7% to 46.3% was the proper foaming range for the chosen epoxy resin. With increasing pre-curing degrees from 37.7% to 51.6%, viscosity and elasticity of pre-cured resins increased, and correspondingly, average cell size of epoxy foams decreased from 329.8 µm to 60.8 µm while cell density increased from 1.4 × 105 cells/cm3 to 8.6 × 105 cells/cm3. Furthermore, the foamed samples with the same pre-curing degree had similar cell morphology regardless of pre-curing conditions.

scholarly journals Effect of Surface Treatment of Halloysite Nanotubes (HNTs) on the Kinetics of Epoxy Resin Cure with Amines

Polymers ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 930 ◽  
Author(s):  
Vahideh Akbari ◽  
Maryam Jouyandeh ◽  
Seyed Mohammad Reza Paran ◽  
Mohammad Reza Ganjali ◽  
Hossein Abdollahi ◽  
...  
Keyword(s):  
Activation Energy ◽  
Epoxy Resin ◽  
Low Cost ◽  
Halloysite Nanotubes ◽  
Diffusion Control ◽  
Heating Rates ◽  
Scanning Calorimetry ◽  
Epoxy Amine ◽  
Amine System ◽  
Kinetics Of

The epoxy/clay nanocomposites have been extensively considered over years because of their low cost and excellent performance. Halloysite nanotubes (HNTs) are unique 1D natural nanofillers with a hollow tubular shape and high aspect ratio. To tackle poor dispersion of the pristine halloysite (P-HNT) in the epoxy matrix, alkali surface-treated HNT (A-HNT) and epoxy silane functionalized HNT (F-HNT) were developed and cured with epoxy resin. Nonisothermal differential scanning calorimetry (DSC) analyses were performed on epoxy nanocomposites containing 0.1 wt.% of P-HNT, A-HNT, and F-HNT. Quantitative analysis of the cure kinetics of epoxy/amine system made by isoconversional Kissinger–Akahira–Sunose (KAS) and Friedman methods made possible calculation of the activation energy (Eα) as a function of conversion (α). The activation energy gradually increased by increasing α due to the diffusion-control mechanism. However, the average value of Eα for nanocomposites was lower comparably, suggesting autocatalytic curing mechanism. Detailed assessment revealed that autocatalytic reaction degree, m increased at low heating rate from 0.107 for neat epoxy/amine system to 0.908 and 0.24 for epoxy/P-HNT and epoxy/A-HNT nanocomposites, respectively, whereas epoxy/F-HNT system had m value of 0.072 as a signature of dominance of non-catalytic reactions. At high heating rates, a similar behavior but not that significant was observed due to the accelerated gelation in the system. In fact, by the introduction of nanotubes the mobility of curing moieties decreased resulting in some deviation of experimental cure rate values from the predicted values obtained using KAS and Friedman methods.

Curing kinetics of epoxy resin using epoxidized cardanol as diluent with/without fortifier

1988 ◽  
Vol 129 (2) ◽  
pp. 277-284 ◽  
Author(s):  
M.B. Patel ◽  
R.G. Patel ◽  
V.S. Patel
Keyword(s):  
Epoxy Resin ◽  
Curing Kinetics ◽  
Kinetics Of

Investigating the relationship between tack and degree of conversion in DGEBA-based epoxy resin cured with dicyandiamide and diuron

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Ali Kuliaei ◽  
Iraj Amiri Amraei ◽  
Seyed Rasoul Mousavi
Keyword(s):  
Epoxy Resin ◽  
Reaction Order ◽  
Theoretical Data ◽  
Cure Kinetics ◽  
Diglycidyl Ether ◽  
Degree Of Conversion ◽  
Ozawa Method ◽  
Heating Rates ◽  
Scanning Calorimetry ◽  
Kinetics Of

Abstract The purpose behind this research was to determine the optimum formulation and investigate the cure kinetics of a diglycidyl ether of bisphenol-A (DGEBA)-based epoxy resin cured by dicyandiamide and diuron for use in prepregs. First, all formulations were examined by the tensile test, and then, the specimens with higher mechanical properties were further investigated by viscometry and tack tests. The cure kinetics of the best formulation (based on tack test) in nonisothermal mode was investigated using differential scanning calorimetry at different heating rates. Kissinger and Ozawa method was used for determining the kinetic parameters of the curing process. The activation energy obtained by this method was 71.43 kJ/mol. The heating rate had no significant effect on the reaction order and the total reaction order was approximately constant ( m + n ≅ 2.1 $m+n\cong 2.1$ ). By comparing the experimental data and the theoretical data obtained by Kissinger and Ozawa method, a good agreement was seen between them. By increasing the degree of conversion, the viscosity decreased; as the degree of conversion increased, so did the slope of viscosity. The results of the tack test also indicated that the highest tack could be obtained with 25% progress of curing.

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