Network structure and glass transition of epoxy resins cured with active ester

1993 ◽  
Vol 40 (2) ◽  
pp. 613-619 ◽  
Author(s):  
S. Nakamura ◽  
M. Arima
Soft Matter ◽  
2020 ◽  
Vol 16 (32) ◽  
pp. 7470-7478 ◽  
Author(s):  
Mika Aoki ◽  
Atsuomi Shundo ◽  
Satoru Yamamoto ◽  
Keiji Tanaka

Network structure in an epoxy resin, which became more heterogeneous with increasing pre-curing temperature, affected the glass transition dynamics and solvent crack behavior.


Author(s):  
Istebreq A. Saeedi ◽  
Sunny Chaudhary ◽  
Thomas Andritsch ◽  
Alun S. Vaughan

AbstractReactive molecular additives have often been employed to tailor the mechanical properties of epoxy resins. In addition, several studies have reported improved electrical properties in such systems, where the network architecture and included function groups have been modified through the use of so-called functional network modifier (FNM) molecules. The study reported here set out to investigate the effect of a glycidyl polyhedral oligomeric silsesquioxane (GPOSS) FNM on the cross-linking reactions, glass transition, breakdown strength and dielectric properties of an amine-cured epoxy resin system. Since many previous studies have considered POSS to act as an inorganic filler, a key aim was to consider the impact of GPOSS addition on the stoichiometry of curing. Fourier transform infrared spectroscopy revealed significant changes in the cross-linking reactions that occur if appropriate stoichiometric compensation is not made for the additional epoxide groups present on the GPOSS. These changes, in concert with the direct effect of the GPOSS itself, influence the glass transition temperature, dielectric breakdown behaviour and dielectric response of the system. Specifically, the work shows that the inclusion of GPOSS can result in beneficial changes in electrical properties, but that these gains are easily lost if consequential changes in the matrix polymer are not appropriately counteracted. Nevertheless, if the system is appropriately optimized, materials with pronounced improvements in technologically important characteristics can be designed.


Polymers ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 1302
Author(s):  
Younggi Hong ◽  
Munju Goh

Epoxy resin (EP) is one of the most famous thermoset materials. In general, because EP has a three-dimensional random network, it possesses thermal properties similar to those of a typical heat insulator. Recently, there has been substantial interest in controlling the network structure of EP to create new functionalities. Indeed, the modified EP, represented as liquid crystalline epoxy (LCE), is considered promising for producing novel functionalities, which cannot be obtained from conventional EPs, by replacing the random network structure with an oriented one. In this paper, we review the current progress in the field of LCEs and their application to highly thermally conductive composite materials.


2020 ◽  
Vol 1 (9) ◽  
pp. 3182-3188
Author(s):  
Hsing-Ying Tsai ◽  
Yasuyuki Nakamura ◽  
Takehiro Fujita ◽  
Masanobu Naito

Epoxy resins incorporating aromatic disulfide bonds demonstrated improved adhesive properties with increasing temperature below their glass transition points.


2000 ◽  
Vol 44 (4) ◽  
pp. 961-972 ◽  
Author(s):  
Jeffry J. Fedderly ◽  
Gilbert F. Lee ◽  
John D. Lee ◽  
Bruce Hartmann ◽  
Karel Dušek ◽  
...  

2013 ◽  
Vol 787 ◽  
pp. 408-412
Author(s):  
Jiao Yan Ai ◽  
Quan Chen ◽  
Xiao Bo Wang

Two kinds of polyester bis (p-hydroxybenzoic acid) butanediolatepolyester (BDPET) and bis (p-hydroxybenzoic acid) diethylene glycol (DGPET) were synthesized through melting transesterification reaction.Then the epoxy resins were modified with BDPET or DGPET,and nanoTiO2. The composites were characterized by DSC and SEM. The experimental results showed that the polyester can act as an effective toughening modifier for the epoxy resin. The mechanical properties of the composites were greatly improved and reached to the maxium at 4wt.%PET. The PET/EP system modified by adding suitable amount of nanoTiO2have better performance.The glass transition temperature (Tg) of PET/EP and nanoTiO2/PET/EP system improved about 20°Cand 27.8°C,respectively.


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