Abstract
Properties of networks, prepared by curing of diglycidyl ethers of bisphenols with some aromatic amines, have been considered. Network polymers, obtained from mixtures with different reactant ratios and at different curing temperatures (Tcure), have been chemically characterized (curing conversion, concentration of chemical crosslinks) in detail at all stages of the cure process. Polymer properties, i. e. mechanical features such as rigidity and deformability and thermal features such as Tg, heat capacity, and coefficient of thermal expansion, have been analyzed and interpreted in terms of chemical and physical (packing density) structure. Plastic deformation and some fracture peculiarities of network glasses have been examined. In a few cases, the properties of these polymers in the rubbery state have been considered. A comparison of the structure and properties of network and linear polymeric glasses has been made. It has been shown that, in the formation of the structure and properties of these polymers, an important role is played by vitrification during cure. Polymers prepared at low Tcure usually show higher mechanical properties which, however, are not due to the high density of their glassy state. The peculiarities of the mechanical behaviour and vitrification of polymers isothermally cured at different Tcure have been considered.
λ=1+ε
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Abbreviations
- α:
-
reaction conversion
- αdif :
-
diffusion conversion limit
- αtop :
-
topological conversion limit
- AN:
-
aniline
- βg :
-
cubic thermal expansion coefficient of the glassy state
- βl :
-
cubic thermal expansion coefficient of the liquid state
- Δβ(Tg):
-
thermal expansion coefficient jump at Tg
- Cp :
-
heat capacity
- ΔCp(Tg):
-
heat capacity jump at Tg
- DGER:
-
diglycidyl ether of resorcinol
- DGEBA:
-
diglycidyl ether of Bisphenol-A
- DGEOPH:
-
diglycidyl ether of orthophthalic acid
- DGEPC:
-
diglycidyl ether of pyrocathechol
- DGEHHPH:
-
diglycidyl ether of hexahydrophthalic acid
- DADMOPHM:
-
diaminodimethoxyphenylmethane
- 4,4′-DADPhS:
-
4,4′-diaminodiphenyl sulfone
- Epol :
-
electric polarization field
- E,E′:
-
Young modulus; dynamic Young modulus
- ε:
-
relative deformation
- εb :
-
elongation at break
- ε*:
-
maximum local elongation
- εy :
-
elongation at yield
- G:
-
shear modulus
- G∞ :
-
equilibrium shear modulus
- Kc :
-
rigidity modulus of a network molecular chain
- K20 :
-
packing density coefficient at 20 °C
- L⊥, L∥ :
-
length of plastic deformation zone in the front of crack tip (⊥ and ‖ the tension direction)
- m-PhDA:
-
m-phenylenediamine
- μ:
-
dipole moment
- N:
-
number of dipoles
- N(x):
-
number of crosslinks (m-PhDA molecules) with different
- x=0÷4:
-
connectivity (x) of the crosslink with entire network
- P:
-
initial molar ratio of reactive groups; P=[NH]0/[EP]0
- PhGE:
-
phenylglycidyl ether
- PETP:
-
poly(ethylene terephthalate)
- P0 :
-
saturation polarization
- PS:
-
polystyrene
- PC:
-
polycarbonate
- Q:
-
integral heat of cure reaction
- T ∞g :
-
glass transition temperature of the network at the conversion α=αtop
- T expg :
-
experimental glass transition temperature
- Tcure :
-
cure temperature
- Δ(Tg):
-
temperature interval of the glass transition
- σy :
-
yield stress
- Ï„y :
-
shear yield stress
- Ï„i :
-
average waiting time of a breaking of chemical bond at the stress σi
- U0 :
-
activation energy
- Vsp :
-
specific volume
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Oleinik, E.F. (1986). Epoxy-aromatic amine networks in the glassy state structure and properties. In: Dušek, K. (eds) Epoxy Resins and Composites IV. Advances in Polymer Science, vol 80. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-16423-5_12
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