Skip to main content
Log in

Constitutive equations from molecular network theories for polymer solutions

  • Published:
Rheologica Acta Aims and scope Submit manuscript

Summary

In this mainly expository paper, constitutive equations based on the network models ofYamamoto,Lodge, andKaye are re-derived in a common notation involving the use of base vectors embedded in the deforming macroscopic continuum. The derivations are thereby simplified in some respects and the differences of detail between the models are clarified. InLodges theory, the sub-network superposition assumption is replaced by alternative assumptions concerning the creation and loss of network segments, and the theory is extended to non-Gaussian networks.Kayes theory is extended to allow for the presence of entanglement junctions of different complexities.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

b n :

= 3/(2n l 2)

n :

= number of freely-jointed links, each of lengthl, in a strand

r :

= time-average (or ensemble-average) end-to-end vector for a typical network segment;r = magnitude ofr

A :

=Helmholtz free energy per unit volume of solution

k :

=Boltzmanns constant

T :

= absolute temperature

F(x, n, t) d 3 x=F(x 1,x 2,x 3,n, t) dx 1 dx 2 dx 3 :

= concentration at timet ofn-segments whoser-vectors lie in the range (x i u i , (x i +dx i)u i )

u 1,u 2,u 3 :

= orthonormal base vectors, fixed in space;r =x i u i

e 1,e 2,e 3 :

= linearly independent, time-dependent base vectors, embedded in the macroscopic continuum

ξ i :

= convected components ofr: r =ξ i e i

γ jj :

=e i · e j (scalar product)

c n :

= concentration ofn-segments

γ :

= det [γ ij ]

γ ij :

= element of matrix reciprocal to matrix

N * 0 :

= concentration of segments

π ij :

= stress components referred to basise 1,e 2,e 3

II ij :

=π ij+p γ ij,p arbitrary

x :

= a parameter (of values 1, 2,...) labeling segments according to the complexity of their junctions with the network

τ −1 xn :

= constant probability per unit time that an (n, x)-segment will leave the network

Ψ(ξ, n, x, t' ¦t) d 3 ξ dt' :

= concentration at timett' of (ξ, n, x)-segments which were created in the interval (t', t' + dt')

L xn :

= rate of creation, per unit volume, of (n, x)-segments

N * (t− t') dt' :

= concentration at timet≥t' of segments which were created in the interval (t', t'+dt')

CdV :

= density of configurations available to a strand having one end fixed at a given point and the other end within a volume elementdV about a second given point

p 11p 22,p 22p 33 :

= primary and secondary differences of normal cartesian stress components for a liquid in steady shear flow in which the velocity components arev 1=Gx 2,v 2=v 3=0

G :

= shear rate

Φ (r, n, T) :

= contribution toA from a typical (r, n)-segment at timet

β (r, n) :

= probability per unit time that a given (r, n)-segment will leave the network

G(r, n, t) d 3 x dt :

= concentration of (r, n)-segments created during (t, t + dt)

Ψ (ξ, n, t′¦t) d 3 ξ dt′ :

= concentration at timet≥t′ of (ξ, n)-segments which were created during (t′, t′ + dt′)

r′ :

=r(t′) r″ =r(t″)

P ij :

= components of extra stress tensor referred to basisu 1,u 2,u 3

c (t) :

= a cartesian space tensor defined byr(t) =e(*) · r(0)

h :

=r(0) in [7.22],r(t′) in [7.24]

e + :

= transpose ofe

e −1 :

= reciprocal of e

g :

=g[Q i (t), Q 2 (t)]= stress-dependent probability per unit time at timet of the loss of any given network junction

Q 1 (t), Q 2 (t) :

= functions of invariants of stress at timet, defined by [8.11], [8.12]

g″xn ≡ g [Qi(t″), Q 2(t″), x,n] :

= probability per unit time at timet″ of the loss of any given (n, x)-segment

N * xn :

= concentration of (n, x)-segmentsN 0 = concentration of junctions

s :

=N * 0/N 0, a number whose value is about 1 or 2

References

  1. Treloar, L. R. G. “The Physics of Rubber Elasticity”, 2nd Edition). (Oxford 1958).

  2. James, H. M. J. Chem. Phys.15, 651 (1947).

    Article  Google Scholar 

  3. Green, M. S. andA. V. Tobolsky, ibid.14, 80 (1946).

    Article  Google Scholar 

  4. Lodge, A. S., Trans. Faraday Soc.52, 120 (1956).

    Article  Google Scholar 

  5. Lodge, A. S., Kolloid-Z.171, 46 (1960).

    Article  Google Scholar 

  6. Yamamoto, M., J. Phys. Soc. Japan11, 413 (1956).

    Google Scholar 

  7. Yamamoto, M., ibid.12, 1148 (1957).

    Google Scholar 

  8. Yamamoto, M., ibid.13, 1200 (1958).

    Google Scholar 

  9. Kaye, A., Brit. J. Appl. Phys.17, 803 (1966).

    Google Scholar 

  10. Lodge, A. S., In Proc. 2nd Int. Congr. Rheol.: “Rheology” London 1954, 229.

  11. Lodge, A. S., “Elastic Liquids” London-New York (1964).

  12. Oldroyd, J. G., Proc. Roy. Soc.A 200, 523 (1950).

    Google Scholar 

  13. Scanlon, J., In “Rheology of Elastomers”. Ed.Mason andWookey, 58, (London 1958).

  14. Flory, P. J., Trans. Faraday Soc.56, 722 (1960).

    Article  Google Scholar 

  15. Wall, F. T., J. Chem. Phys.10, 485, eq. (1) (1942).

    Article  Google Scholar 

  16. Wang, M. C. andE. Guth, J. Chem. Phys.20, 1144 (1952).

    Article  Google Scholar 

  17. Adams, N. andA. S. Lodge, Phil. Trans.A 256, 149 (1964).

    Google Scholar 

  18. Huppler, J., Trans. Soc. Rheol.9: 2, 273 (1965).

    Article  Google Scholar 

  19. Graessley, W. W., J. Chem. Phys.43, 2696 (1965).

    Article  Google Scholar 

  20. Macdonald, I. F. andR. B. Bird, J. Phys. Chem.70, 2068 (1966).

    Google Scholar 

  21. Broadbent, J. M., A. Kaye, A. S. Lodge, andD. G. Vale, Nature, London217, 55 (1968).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Sponsored by the Mathematics Research Center, United States Army, Madison, Wisconsin, under Contract No.: DA-31-124-ARO-D-462.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lodge, A.S. Constitutive equations from molecular network theories for polymer solutions. Rheol Acta 7, 379–392 (1968). https://doi.org/10.1007/BF01984856

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01984856

Keywords

Navigation