Effect of a heterogeneous network on glass transition dynamics and solvent crack behavior of epoxy resins

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.

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.


2021 ◽  
Author(s):  
OMAR RODRIGUEZ-UICAB ◽  
JANDRO L. ABOT ◽  
FRANCIS AVILÉS

The cyclic thermoresistive response of individual carbon nanotube yarns (CNTYs) embedded into epoxy resins is investigated. The influence of the temperature at which the epoxy resin cures on the thermoresistive response is investigated by using two epoxy resins, one that cures at room temperature and the other one that cures at 130 °C. Heating-cooling cycles ranging from room temperature (RT, 25 °C) to 80 °C, incremental cycles (RT to 40 °C, RT to 60 °C and RT to 80 °C) and incremental heating-dwell cycles are applied to monofilament composites, while their electrical resistance is simultaneously recorded. The monofilament composites showed a negative temperature coefficient of resistance during the heating-cooling cycles of -7.07x10-4 °C-1 for specimens cured at high temperature, and -5.93x10-4 °C-1 for specimens cured at room temperature. The hysteresis after the different heating-cooling cycles was slightly smaller for specimens cured at 130 °C, in comparison to specimens cured at room temperature. Several factors including the intrinsic thermoresistivity of CNTY, level of infiltration and the effect of curing temperature may explain the thermoresistive sensitivity of the monofilament composites.


Polymers ◽  
2019 ◽  
Vol 11 (7) ◽  
pp. 1191 ◽  
Author(s):  
Evgeniy M. Chistyakov ◽  
Ivan V. Terekhov ◽  
Aleksey V. Shapagin ◽  
Sergey N. Filatov ◽  
Vladimir P. Chuev

The method of optical wedge revealed that the optimum temperature for compatibility of hexakis(4-acetamidophenoxy)cyclotriphosphazene (ACP) and DER-331 epoxy resin is in the range of 220–260 °C. The interdiffusion time of components at these temperatures is about 30 min. The TGA and differential scanning calorimetry (DSC) methods revealed the curing temperature of 280 °С for this composition. IR spectroscopy confirmed that the reaction between the resin and ACP is completed within 10 min. According to the DSC data, a glass transition temperature of 130 °С was estimated for the cured resin. Combustion test UL-94 demonstrated that the obtained material can be assigned to the fireproof category of V-0. Burning droplets were not formed during the burning. The coke formed during the combustion of samples possessed a dense and porous structure. The shape of pores is closed, while their size is in the range of 0.2–200 µm.


2008 ◽  
Vol 56 ◽  
pp. 297-302
Author(s):  
Peter B.S. Bailey ◽  
S.A. Hayes ◽  
R.J. Hand ◽  
B. Zhang

The results of an initial investigation into the monitoring of water absorption and chemical degradation in epoxy matrix composites using evanescent wave spectroscopy are presented. While conventional silica glasses have too low a refractive index and too short an IR transmission window to be useful as unclad sensing elements in most resin systems, chalcogenide glasses offer suitable refractive indices and infrared transmission windows. Arsenic selenide compositions with gallium or tellurium additions were initially investigated as they have been successfully demonstrated in other fibre sensing applications. However their glass transition point lies near or below the curing temperature for many commercial epoxy resins and thus germanium-antimony-lead sulphide glasses were also investigated as they display higher glass transition temperatures. The fibres were embedded in a representative matrix resin by casting samples of epoxy resin around sections of fibre. The end faces were prepared to allow an infrared beam to be passed along the fibre and the samples were subjected to hygrothermal aging. Changes in the transmitted spectra were observed, and photoelasticity was used to monitor the occurrence of fibre fragmentation. Both the arsenic selenide based compositions and the germanium-antimony-lead sulphide compositions displayed minimal bonding with the epoxy resin, so a simple silane treatment was used to improve adhesion.


2017 ◽  
Vol 898 ◽  
pp. 2294-2301 ◽  
Author(s):  
Chen Yu Zhang ◽  
Yong Liu ◽  
Ke Qing Han ◽  
Xue Feng Chang ◽  
Mu Huo Yu

In this paper, Polyborosilazane (PBSZ) was successfully synthesized and used as curing agents for epoxy resin. FTIR, TGA, XRD, SEM were used to analyze the curing mechanism, curing temperature and thermal stability of the curing system. The results indicated that PBSZ could be used as curing agents for bisphenol A epoxy resin when its usage amount was 30-60 wt.% at the temperature between 100 ∼ 150 °C. Additionally, the thermal stability of PBSZ cured epoxy resin samples were better than that of epoxy resin cured with 4, 4-diaminodiphenylsulfone (DDS), showing a higher residual weight at 900°C. As PBSZ content increased, the residual weight of PBSZ cured epoxy resin at 900°C increased. When PBSZ content was 30%, the surface of cured epoxy resins was smooth without obvious defects. However, the surface became coarse when PBSZ content was further increased.


Author(s):  
J. G. Adams ◽  
M. M. Campbell ◽  
H. Thomas ◽  
J. J. Ghldonl

Since the introduction of epoxy resins as embedding material for electron microscopy, the list of new formulations and variations of widely accepted mixtures has grown rapidly. Described here is a resin system utilizing Maraglas 655, Dow D.E.R. 732, DDSA, and BDMA, which is a variation of the mixtures of Lockwood and Erlandson. In the development of the mixture, the Maraglas and the Dow resins were tested in 3 different volumetric proportions, 6:4, 7:3, and 8:2. Cutting qualities and characteristics of stability in the electron beam and image contrast were evaluated for these epoxy mixtures with anhydride (DDSA) to epoxy ratios of 0.4, 0.55, and 0.7. Each mixture was polymerized overnight at 60°C with 2% and 3% BDMA.Although the differences among the test resins were slight in terms of cutting ease, general tissue preservation, and stability in the beam, the 7:3 Maraglas to D.E.R. 732 ratio at an anhydride to epoxy ratio of 0.55 polymerized with 3% BDMA proved to be most consistent. The resulting plastic is relatively hard and somewhat brittle which necessitates trimming and facing the block slowly and cautiously to avoid chipping. Sections up to about 2 microns in thickness can be cut and stained with any of several light microscope stains and excellent quality light photomicrographs can be taken of such sections (Fig. 1).


Author(s):  
Georgel MIHU ◽  
Claudia Veronica UNGUREANU ◽  
Vasile BRIA ◽  
Marina BUNEA ◽  
Rodica CHIHAI PEȚU ◽  
...  

Epoxy resins have been presenting a lot of scientific and technical interests and organic modified epoxy resins have recently receiving a great deal of attention. For obtaining the composite materials with good mechanical proprieties, a large variety of organic modification agents were used. For this study gluten and gelatin had been used as modifying agents thinking that their dispersion inside the polymer could increase the polymer biocompatibility. Equal amounts of the proteins were milled together and the obtained compound was used to form 1 to 5% weight ratios organic agents modified epoxy materials. To highlight the effect of these proteins in epoxy matrix mechanical tests as three-point bending and compression were performed.


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.


2021 ◽  
Vol 2 (2) ◽  
pp. 419-430
Author(s):  
Ankur Bajpai ◽  
James R. Davidson ◽  
Colin Robert

The tensile fracture mechanics and thermo-mechanical properties of mixtures composed of two kinds of epoxy resins of different chemical structures and functional groups were studied. The base resin was a bi-functional epoxy resin based on diglycidyl ether of bisphenol-A (DGEBA) and the other resins were (a) distilled triglycidylether of meta-amino phenol (b) 1, 6–naphthalene di epoxy and (c) fluorene di epoxy. This research shows that a small number of multifunctional epoxy systems, both di- and tri-functional, can significantly increase tensile strength (14%) over neat DGEBA while having no negative impact on other mechanical properties including glass transition temperature and elastic modulus. In fact, when compared to unmodified DGEBA, the tri-functional epoxy shows a slight increase (5%) in glass transition temperature at 10 wt.% concentration. The enhanced crosslinking of DGEBA (90 wt.%)/distilled triglycidylether of meta-amino phenol (10 wt.%) blends may be the possible reason for the improved glass transition. Finally, the influence of strain rate, temperature and moisture were investigated for both the neat DGEBA and the best performing modified system. The neat DGEBA was steadily outperformed by its modified counterpart in every condition.


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