Tensile properties epoxy resins

Bisphenol A diglycidyl ether [1675-54-3] reacts readily with methacrylic acid [71-49-4] in the presence of benzyl dimethyl amine catalyst to produce bisphenol epoxy dimethacrylate resins known commercially as vinyl esters. The resins display beneficial tensile properties that provide enhanced stmctural performance, especially in filament-wound glass-reinforced composites. The resins can be modified extensively to alter properties by extending the diepoxide with bisphenol A, phenol novolak, or carboxyl-terrninated mbbers. 

For quality cured thermoset resins, approximately one percent of the mass is soluble when subjected to long-term leaching with tetrahydrofuran. Equilibrium is approached in two weeks resin swell is not visually noticeable. The monomeric, chemical structures are such that the hydrocarbon resins exhibit more pronounced viscoelastic properties whereas, the epoxy resins are similar to elastic bodies when subjected to tensile testing at room temperature. Therein, LRF 216 is less sensitive to flaws and is more nonlinear in tensile or compressive stress-strain analysis. 

Early in the development of solid propellant, the asphalt composites were found to have poor physical properties, such as cracking under normal temperature cycling, poor tensile characteristics, etc. They were replaced with the elastomeric polymers which have become the present-day binders. The first of these was Thiokol rubber, a polysulfide rubber, whichgives the propellant with good physical properties. The presence of the sulfur atom in the Thiokol rubber decreases the performance compared to a CHO polymer thus the most frequently used binders are polyurethane, polybutadiene acrylic acid (PBAA), epoxy resin, etc. The choice of the latter binders is made with regard to physical properties rather than performance. 

Polysulfide resins combine with epoxy resins to provide adhesives and sealants with excellent flexibility and chemical resistance. These adhesives bond well to many different substrates. Tensile shear strength and elevated-temperature properties are low. However, resistance to peel forces and low temperatures is very good. Epoxy polysulfides have good adhesive properties down to -100°C, and they stay flexible to -65°C. The maximum service temperature is about 50 to 85°C depending on the epoxy concentration in the formulation. Temperature resistance increases with the epoxy content of the system. Resistance to solvents, oil and grease, and exterior weathering and aging is superior to that of most thermoplastic elastomers. 

Figure 14.2. The mechanical properties of 0.5 wt% SWNT/Epoxy composites (a) tensile test of neat epoxy resin (b) tensile test of pristine-SWNT/epoxy ...

Figure 11.13 shows that in ajute filled epoxy resin, water intake increases with time of immersion and with the amount of fiber. This jute fibers readily absorb water. A surface treatment of the jute with epoxy silane reduces the water intake. Tensile properties of a composite containing surface treated fiber remain constant up to a moisture content of 5%. 

Analyses have been carried out assuming a cavitated particle, that is, the particle is replaced by a void (see the section Cavitation of the Rubber Particles ). The analysis is applied to an annulus of epoxy resin. The volume fraction of the void is 20%. The elastic material properties used for the epoxy matrix are shown in Table I. The elastic-plastic material properties used are shown in Figure 4. Nonlinear geometric effects were included to take account of large deformations. Final failure of the cell was defined (23) to be the applied strain required for the maximum linear tensile strain in the resin to attain the value of 20%. 

The preparation of composite materials in general is a very important appHca-tion of the mechanical properties of nanodiamond. With many polymers like caoutchouc, polysiloxanes, fluoroelastomers polymethacrylates, epoxy resins, etc., composites with markedly improved mechanical characteristics have already been obtained from the noncovalent incorporation of nanodiamond by simple admixing during polymerization. The modulus of elasticity, the tensile strength, and the maximal elongation of the material all increase upon this modification. Depending on the basic polymer, just 0.1-0.5% (w/w) of nanodiamond are required to achieve this effect (Table 5.3). Polymer films can also be reinforced by the addition of nanodiamond. For a teflon film with ca. 2% of nanodiamond added, for example, friction is reduced at least 20%, and scratches inflicted by mechanical means are only half as deep as in neat teflon. 

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