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Thermomechanics of polymers

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Pharmacy/Thermomechanics/Elastomers/Telechelics

Part of the book series: Advances in Polymer Science ((POLYMER,volume 76))

Abstract

This article reviews recent developments in polymer thermomechanics both in theory and experiment. The first section is concerned with theories of thermomechanics of polymers both in rubbery and solid (glassy and crystalline) states with special emphasis on relationships following from the thermomechanical equations of state. In the second section, some of the methods of thermomechanical measurements are briefly described. The third section deals with the thermomechanics of molecular networks and rubberlike materials including such technically important materials as filled rubbers and block and graft copolymers. Some recent data on thermomechanical behaviour of bioelastomers are also described. In the fourth section, thermomechanics of solid polymers both in undrawn and drawn states are discussed with a special focus on the molecular and structural interpretation of thermomechanical experiments. The concluding remarks stress the progress in the understanding of the thermomechanical properties of polymers.

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Abbreviations

a0 :

radius of unstrained sample

a, a1, a2 :

parameters of van der Waals equation of state of a network

e:

uniform (volume) strain

f:

retractive force

fs :

entropy component of retractive force

fu :

energy component of retractive force

p:

number of statistical segments

r:

end-to-end distance of network chains

rmax :

maximum extension of network chains

〈r2〉:

mean square end-to-end distance of network chains in undeformed sample

〈r2〉0 :

mean square end-to-end distance of unperturbed chains

〈r2〉i :

mean square end-to-end distance of network chains in the reference state

w:

degree of crystallinity

xi :

generalized coordinate

A0 :

cross-sectional area of sample

C:

heat capacity

C:

constant in the Gaussian equation of state for-rubber elasticity

C1, C2 :

constants in the Mooney-Rivlin equation

\(D',D_m ,\bar D_m\) :

strain functions in van der Waals equation of state

E:

modulus of elasticity (Young modulus)

Ec :

conformational energy of chains

E′:

modulus of elasticity of filled rubbers

Ef :

internal energy changes in filled rubbers

E‖ :

modulus of elasticity along the draw axis

E⊥ :

modulus of elasticity perpendicular to the draw axis

Ecr :

modulus of elasticity of crystalline lattice

EAB :

modulus of elasticity of amorphous intrafibrillar regions

EAI :

modulus of elasticity of amorphous interfibrillar regions

F:

free energy

F*:

Free energy of deformation of solids

G:

free enthalpy

G*:

free enthalpy of deformation of solids

G0 :

shear modulus

H:

enthalpy

H*:

enthalpy of deformation of solids

K:

modulus of elasticity (volume)

L0 :

length of undeformed samples

L:

length of deformed samples

Li :

length of samples in the reference state

M:

twisting couple

P:

pressure

Q:

heat

S:

entropy

T:

absolute temperature

V:

volume

U:

internal energy

U*:

internal energy of deformation of solids

W:

mechanical work

X:

portion of interfibrillar amorphous regions

α:

volume thermal expansivity

α* :

degree of deformation

β:

linear thermal expansivity

β‖ :

linear thermal expansivity along the orientation axis

β⊥ :

linear thermal expansivity perpendicular to orientation axis

βcr :

linear thermal expansivity of crystalline lattice

βAB :

linear thermal expansivity of intrafibrillar amorphous regions

βAI :

linear thermal expansivity of interfibrillar amorphous regions

β:

linear thermal expansivity under the angle Ï•

γ:

= (∂ ln 〈r2〉0/∂ ln V)T, L

γS :

shear deformation

γ′:

= γ/2

δ:

solubility parameter

ε:

strain (uniaxial)

η:

heat to work ratio

κ:

volume compressibility

κL :

linear compressibility

λ:

elongation (or compression) ratio

λQ :

elongation corresponding to inversion of heat

λu :

elongation corresponding to inversion of internal energy

λm :

limiting elongation

λf :

elongation corresponding to inversion of force

μ:

Poisson's ratio

ν:

number of elastically active network chains

ξ, ξi :

generalized force

σ:

stress

Ï„:

shear stress

Ï•:

angle with the draw direction

ω:

internal energy to work ratio

θ:

twisting angle

PE:

polyethylene

LDPE:

low density polyethylene

HDPE:

high density polyethylene

PP:

polypropylene

PA:

polyamide

PS:

polystyrene

PET:

poly(ethylene terephthalate)

NR:

natural rubber

PDMS:

polydimethylsiloxane

EPR:

ethylene-propylene rubber

SBR:

styrene-butadiene rubber

PCR:

polychloroprene rubber

NBR:

nitrile-butadiene rubber

PBR:

polybutadiene rubber

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Godovsky, Y.K. (1986). Thermomechanics of polymers. In: Dušek, K. (eds) Pharmacy/Thermomechanics/Elastomers/Telechelics. Advances in Polymer Science, vol 76. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-15830-8_2

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