Polymers, amorphous, curing

Polymer mechanical properties are one from the most important ones, since even for polymers of different special-purpose function a definite level of these properties always requires [20]. Besides, in Ref [48] it has been shown, that in epoxy polymers curing process formation of chemical network with its nodes different density results to final polymer molecular characteristics change, namely, characteristic ratio C, which is a polymer chain statistical flexibility indicator [23]. If such effect actually exists, then it should be reflected in the value of cross-linked epoxy polymers deformation-strength characteristics. Therefore, the authors of Ref [49] offered limiting properties (properties at fracture) prediction techniques, based on a methods of fractal analysis and cluster model of polymers amorphous state structure in reference to series of sulfur-containing epoxy polymers [50]. 

Only a few commercial uses for TDA per se have been found. In epoxy curing appHcations, 2,4- I DA has been used as a component of a eutectic mixture with short chain aUphatic glycidal ether resins (46) as well as by itself (46,47) TDA (46) and single isomers (47) are also used as amine curatives. TDA can be used as a chain extender in polyurethanes (48,49). TDA is cited as a monomer in making aromatic polymers with unique properties, eg, amorphous polyamides (50), powdered polyamides (51), and low melting, whoUy aromatic polyamides (52). 

Experimental results are presented that show that high doses of electron radiation combined with thermal cycling can significantly change the mechanical and physical properties of graphite fiber-reinforced polymer-matrix composites. Polymeric materials examined have included 121 °C and 177°C cure epoxies, polyimide, amorphous thermoplastic, and semicrystalline thermoplastics. Composite panels fabricated and tested included four-ply unidirectional, four-ply [0,90, 90,0] and eight-ply quasi-isotropic [0/ 45/90]s. Test specimens with fiber orientations of [10] and [45] were cut from the unidirectional panels to determine shear properties. Mechanical and physical property tests were conducted at cold (-157°C), room (24°C) and elevated (121°C) temperatures. 

Thermoplastic polymers can be heated and cooled reversibly with no change to their chemical structure. Thermosets are processed or cured by a chemical reaction which is irreversible they can be softened by heating but do not return to their uncured state. The polymer type will dictate whether the compound is completely amorphous or partly crystalline at the operating temperature, and its intrinsic resistance to chemicals, mechanical stress and electrical stress. Degradation of the basic polymer, and, in particular, rupture of the main polymer chain or backbone, is the principal cause of reduction of tensile strength. 

Cured polymers of butadiene with low cross-link density do not tend to cold flow and are useful elastomers. These vulcanized elastomers crystallize when stretched, but when the stress is removed, the restoring force is largely entropy and most of the crystals melt and the chains return to the random conformation.The tensile strength is increased dramatically when large amounts of carbon black or amorphous silica are added. 

TPEs are blends of various amorphous rubbers such as ethylene-propylene and of polyolefin semicrystalline plastics such as PP. They are part of the family of TP olefins (TPOs). TPOs are mechanical blends consisting of a hard plastic and softer rubber. They are considered different from blends that are dynamically thermoplastic vulcanized (TPV) a process in which the elastomer phase is cured during mixing of the polymers.84 94... 

In an earlier analysis, it was shown that the main argument for the existence of inhomogeneous crosslinking — the appearance of nodular structure particularly when etched fracture surfaces are examined — is not at all characteristic of cured epoxies. Similar nodular structures could also be seen in other amorphous polymers. 

A differential scanning calorimeter (DSC 1-B, Perkin-Elmer Corporation) was used to determine the extent of cure 10-mg to 20-mg specimens were tested at a scanning rate of 10°C/min. An exothermic peak on the thermograph indicates the heat of reaction whereas an endothermic peak in the amorphous polymer indicates the presence of residual stresses or the occurrence of a transition such as the glass transition. The presence of an exothermic peak in the DSC-scan of a pre-cured sample is an indication of incomplete curing. 

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