scholarly journals Bending and Compressive Analysis of Epoxy Resins Modified with Low-polar Solvent Solution of Polysulphone

2018 ◽  
Vol 55 (3) ◽  
pp. 295-298
Author(s):  
Vasile Bria ◽  
Cristian Muntenita ◽  
Iulia Graur
Keyword(s):  
Energy Storage ◽  
Epoxy Resin ◽  
Epoxy Resins ◽  
Polar Solvent ◽  
High Porosity ◽  
Three Point Bending ◽  
Mobility Of Charge Carriers ◽  
Bio Compatibility ◽  
Epoxy Systems ◽  
Excellent Stability

The memory shape materials seem to be extremely promising materials for medical applications especially as inserts to support the muscular system. In the case of memory shape polymers a supplementary issue is related to their bio-compatibility such as they can be rejected by the organism even their properties are fitting the requirements. Present study started from the hypothesis that mixing the epoxy resin with other polymers some valuable materials could be obtained especially for energy storage. The epoxy resins possess extraordinary properties (relatively to other thermoset polymers) but they also show an excellent stability that generates problems when this type of materials should be neutralized. Epoxy resins also show low water or other liquids absorption due to their low porosity and they cannot be used for energy storage applications when mobility of charge carriers is ensured by liquid phase. A polymer with high porosity used for membrane formation is the polysulfone and, in this regard, tests were performed to analyse the ways to mix an epoxy resin with polysulfone. The idea had generated a study regarding the properties of such a mixture together with the condition that had to be reached to successfully get the mixture. Low-polar solvent solution of polysulfone had been obtained with 1-methyl-2-pyrrolidinone. After compatibility tests, 15 and 20% of this solution was added to the components of the epoxy systems -with the epoxy resin -and formed materials were analysed by mechanical means-compressive and three-point bending - the surprise was that some materials had showed memory shape properties.

The Mechanical Properties of Organic Modified Epoxy Resin

2020 ◽  
Vol 43 (3) ◽  
pp. 10-14
Author(s):  
Georgel MIHU ◽  
Claudia Veronica UNGUREANU ◽  
Vasile BRIA ◽  
Marina BUNEA ◽  
Rodica CHIHAI PEȚU ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Composite Materials ◽  
Epoxy Resin ◽  
Epoxy Matrix ◽  
Epoxy Resins ◽  
Mechanical Tests ◽  
Organic Modification ◽  
Three Point Bending ◽  
Modified Epoxy

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.

scholarly journals Tailored for simplicity: creating high porosity, high performance bio-based macroporous polymers from foam templates

2014 ◽  
Vol 16 (4) ◽  
pp. 1931-1940 ◽  
Author(s):  
Thomas H. M. Lau ◽  
Ling L. C. Wong ◽  
Koon-Yang Lee ◽  
Alexander Bismarck
Keyword(s):  
Epoxy Resin ◽  
Epoxy Resins ◽  
High Performance ◽  
High Porosity ◽  
Macroporous Polymers

High porosity, high performance macroporous biobased epoxy resins are produced by curing foam templates produced by mechanical frothing of a highly viscous epoxy resin.

scholarly journals Determination of the cross-linking degree of unmodified epoxy resin by cycloaliphatic polyamine and polyamidamin hardeners by ftir spectroscopy

2003 ◽  
Vol 57 (11) ◽  
pp. 563-567 ◽  
Author(s):  
Sasa Zlatkovic ◽  
Goran Nikolic ◽  
Jakov Stamenkovic
Keyword(s):  
Epoxy Resin ◽  
Epoxy Resins ◽  
Optimal Time ◽  
Cross Linking ◽  
Stoichiometric Ratio ◽  
Film Hardness ◽  
Epoxy Groups ◽  
Epoxy Systems ◽  
Unmodified Epoxy

Unmodified epoxy resin GY250 was crosslinked by the cycloaliphatic polyamino hardener HY847 and polyamidamine hardener HY848 in the different mass ratios. The degree of crosslinking of the epoxy resin and the quantity of unreacted epoxy groups were determined by a spectroscopic FTIR method. The optimal time of complete crosslinking, as a criterion of the degree, was determined by measuring the film hardness indirectly (JUS H.C8.055). The optimal stoichiometric ratio of 100:18:32 (GY250:HY847:HY848) was defined by correlating parameters which directly depend on the degree of crosslinking and the period of application of the epoxy resins, as a prerequisite for forming 2-component epoxy systems which are comparatively more elastic adhesive and waterproof.

Epoxy Resin Embedment

1968 ◽  
Vol 26 ◽  
pp. 100-101
Author(s):  
J. G. Adams ◽  
M. M. Campbell ◽  
H. Thomas ◽  
J. J. Ghldonl
Keyword(s):  
Electron Microscopy ◽  
Electron Beam ◽  
Epoxy Resin ◽  
Light Microscope ◽  
Epoxy Resins ◽  
Image Contrast ◽  
Tissue Preservation ◽  
Resin System ◽  
Excellent Quality

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).

scholarly journals Studies on the Modification of Commercial Bisphenol-A-Based Epoxy Resin Using Different Multifunctional Epoxy Systems

2021 ◽  
Vol 2 (2) ◽  
pp. 419-430
Author(s):  
Ankur Bajpai ◽  
James R. Davidson ◽  
Colin Robert
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Bisphenol A ◽  
Epoxy Resin ◽  
Tensile Fracture ◽  
Chemical Structures ◽  
Amino Phenol ◽  
Epoxy Systems

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.

scholarly journals Thermophysical Properties of Multifunctional Syntactic Foams Containing Phase Change Microcapsules for Thermal Energy Storage

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1790
Author(s):  
Francesco Galvagnini ◽  
Andrea Dorigato ◽  
Luca Fambri ◽  
Giulia Fredi ◽  
Alessandro Pegoretti
Keyword(s):  
Thermal Conductivity ◽  
Energy Storage ◽  
Phase Change ◽  
Epoxy Resin ◽  
Storage Modulus ◽  
Thermal Energy ◽  
Thermal Energy Storage ◽  
Neat Epoxy ◽  
Low Density ◽  
Syntactic Foams

Syntactic foams (SFs) combining an epoxy resin and hollow glass microspheres (HGM) feature a unique combination of low density, high mechanical properties, and low thermal conductivity which can be tuned according to specific applications. In this work, the versatility of epoxy/HGM SFs was further expanded by adding a microencapsulated phase change material (PCM) providing thermal energy storage (TES) ability at a phase change temperature of 43 °C. At this aim, fifteen epoxy (HGM/PCM) compositions with a total filler content (HGM + PCM) of up to 40 vol% were prepared and characterized. The experimental results were fitted with statistical models, which resulted in ternary diagrams that visually represented the properties of the ternary systems and simplified trend identification. Dynamic rheological tests showed that the PCM increased the viscosity of the epoxy resin more than HGM due to the smaller average size (20 µm vs. 60 µm) and that the systems containing both HGM and PCM showed lower viscosity than those containing only one filler type, due to the higher packing efficiency of bimodal filler distributions. HGM strongly reduced the gravimetric density and the thermal insulation properties. In fact, the sample with 40 vol% of HGM showed a density of 0.735 g/cm3 (−35% than neat epoxy) and a thermal conductivity of 0.12 W/(m∙K) (−40% than neat epoxy). Moreover, the increase in the PCM content increased the specific phase change enthalpy, which was up to 68 J/g for the sample with 40 vol% of PCM, with a consequent improvement in the thermal management ability that was also evidenced by temperature profiling tests in transient heating and cooling regimes. Finally, dynamical mechanical thermal analysis (DMTA) showed that both fillers decreased the storage modulus but generally increased the storage modulus normalized by density (E′/ρ) up to 2440 MPa/(g/cm3) at 25 °C with 40 vol% of HGM (+48% than neat epoxy). These results confirmed that the main asset of these ternary multifunctional syntactic foams is their versatility, as the composition can be tuned to reach the property set that best matches the application requirements in terms of TES ability, thermal insulation, and low density.

scholarly journals An Effective Method for Preparation of Liquid Phosphoric Anhydride and Its Application in Flame Retardant Epoxy Resin

Materials ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2205
Author(s):  
Qian Li ◽  
Yujie Li ◽  
Yifan Chen ◽  
Qiang Wu ◽  
Siqun Wang
Keyword(s):  
Flame Retardant ◽  
Epoxy Resin ◽  
Epoxy Resins ◽  
Oxygen Index ◽  
Decomposition Temperature ◽  
Ease Of Use ◽  
Limiting Oxygen Index ◽  
Good Thermal Stability ◽  
Low Viscosity ◽  
The Impact

A novel liquid phosphorous-containing flame retardant anhydride (LPFA) with low viscosity was synthesized from 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) and methyl tetrahydrophthalic anhydride (MeTHPA) and further cured with bisphenol-A epoxy resin E-51 for the preparation of the flame retardant epoxy resins. Both Fourier transform infrared spectroscopy (FT-IR), mass spectrometry (MS) and nuclear magnetic resonance (NMR) measurements revealed the successful incorporation of DOPO on the molecular chains of MeTHPA through chemical reaction. The oxygen index analysis showed that the LPFA-cured epoxy resin exhibited excellent flame retardant performance, and the corresponding limiting oxygen index (LOI) value could reach 31.2%. The UL-94V-0 rating was achieved for the flame retardant epoxy resin with the phosphorus content of 2.7%. With the addition of LPFA, the impact strength of the cured epoxy resins remained almost unchanged, but the flexural strength gradually increased. Meanwhile, all the epoxy resins showed good thermal stability. The glass transition temperature (Tg) and thermal decomposition temperature (Td) of epoxy resin cured by LPFA decreased slightly compared with that of MeTHPA-cured epoxy resin. Based on such excellent flame retardancy, low viscosity at room temperature and ease of use, LPFA showed potential as an appropriate curing agent in the field of electrical insulation materials.

Thermal Stabilities and the Thermal Degradation Kinetics Study of the Flame Retardant Epoxy Resins

2014 ◽  
Vol 1053 ◽  
pp. 263-267 ◽  
Author(s):  
Xiu Juan Tian
Keyword(s):  
Thermal Stability ◽  
Thermal Degradation ◽  
Flame Retardant ◽  
Epoxy Resin ◽  
Epoxy Resins ◽  
Degradation Kinetics ◽  
Thermal Degradation Kinetics ◽  
Thermal Stabilities ◽  
Degradation Kinetic ◽  
Modified Epoxy

Thermal stability and thermal degradation kinetics of epoxy resins with 2-(Diphenylphosphinyl)-1, 4-benzenediol were investegated by thermogravimetric analysis (TGA) at different heating rates of 5 K/min, 10 K/min, 20 K/min and 40 K/min. The thermal degradation kinetic mechanism and models of the modified epoxy resins were determined by Coast Redfern method.The results showed that epoxy resins modified with the flame retardant had more thermal stability than pure epoxy resin. The solid-state decomposition mechanism of epoxy resin and the modified epoxy resin corresponded to the controlled decelerating ځ˽̈́˰̵̳͂͆ͅ˼˰̴̱̾˰̸̵̈́˰̵̸̳̱̹̽̾̓̽˰̶̳̹̾̈́̿̾̓ͅ˰̶˸ځ˹˰̵̵͇͂˰̃˸́˽ځ˹2/3. The introduction of phosphorus-containing flame retardant reduced thermal degradation rate of epoxy resins in the primary stage, and promote the formation of carbon layer.

Effect of Cure State on Stress Relaxation in 3501-6 Epoxy Resin

1997 ◽  
Vol 119 (3) ◽  
pp. 262-265 ◽  
Author(s):  
S. R. White ◽  
A. B. Hartman
Keyword(s):  
Stress Relaxation ◽  
Epoxy Resin ◽  
Creep Compliance ◽  
Numerical Technique ◽  
Matrix Material ◽  
Relaxation Modulus ◽  
Master Curves ◽  
Creep Tests ◽  
Three Point Bending ◽  
Direct Inversion

Little experimental work has been done to characterize how the viscoelastic properties of composite material matrix resins develop during cure. In this paper, the results of a series of creep tests carried out on 3501–6 epoxy resin, a common epoxy matrix material for graphite/epoxy composites, at several different cure states is reported. Beam specimens were isothermally cured at increasing cure temperatures to obtain a range of degrees of cure from 0.66 to 0.99. These specimens were then tested in three-point bending to obtain creep compliance over a wide temperature range. The master curves and shift functions for each degree of cure case were obtained by time-temperature superposition. A numerical technique and direct inversion were used to calculate the stress relaxation modulus master curves from the creep compliance master curves. Direct inversion was shown to be adequate for fully cured specimens, however it underpredicts the relaxation modulus and the transition for partially cured specimens. Correlations with experimental stress relaxation data from Kim and White (1996) showed that reasonably accurate results can be obtained by creep testing followed by numerical conversion using the Hopkins-Hamming method.

Ozone Resistance of Vulcanizates Based on XNB Rubber

2021 ◽  
Vol 410 ◽  
pp. 686-691
Author(s):  
Evgeniy S. Bochkarev ◽  
Dmitriy S. Vostrikov ◽  
Oleg O. Tuzhikov
Keyword(s):  
Epoxy Resin ◽  
Magnesium Oxide ◽  
Polyvinyl Chloride ◽  
Flow Rate ◽  
Epoxy Resins ◽  
Butadiene Rubber ◽  
Express Method ◽  
Elastomeric Materials ◽  
Main Period ◽  
Ozone Resistance

The paper represents ozone resistance of rubbers based on carboxylated nitrile butadiene rubber cured with epoxy resins and magnesium oxide. Ozone resistance was investigated using the express-method at a flow rate of the ozone-air mixture of 9 l/h and ozone content of 9 mg/l. In the method used, the “time to cracking start” indicator was taken as the basic indicator of ozone resistance. The second indicator characterizing the ozone resistance of elastomeric materials was the "rate of destruction" in the main period of destruction. There has been evaluated the effect of dissolved polyvinyl chloride in epoxy resin ED-20 on the properties of vulcanizates. There has been investigated the Increase in destruction time under the action of ozone.

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