材料
Online ISSN : 1880-7488
Print ISSN : 0514-5163
ISSN-L : 0514-5163
非ニュートン流停止後の応力緩和
Na-Polyacrylate の最長緩和機構
黒岩 城雄中村 亦夫
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1966 年 15 巻 152 号 p. 297-301

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It is assumed that the substances described in the present paper have elements of viscoelastic mechanism which are non-linear at large stresses, but become linear at small stresses in behaviors of flow and internal deformation. In this case the generalized Maxwell formula (1) may be reduced to Eq. (2) at the terminal region of stress relaxation following non-Newtonian flow.
dσ(t)/dt=σmj=1j(t)/dt=σmj=1{-σj(t)/τj} (1)
dσ(t)*/dt=σmj=1j(t)*/dt=σmj=1{-σj(t)*j°} (2)
The asterisk in the equation refers to small stresses. τj°is the relaxation time of the jth mechanism in its ordinary sense at small stresses. By integrating Eq. (2),
σ(t)*mj=1σj(0)*e-tj° (3)
where σj(0)*, as an integration constant, is the extrapolated value of the stress to t=0, under which the viscoelastic mechanisms obey Newtonian and Hookean laws. Dividing Eq. (3) by γ:
σ(t)*/γ=σmj=1ηj(0)*e-tj° (4)
where ηj(0)*j(0)*/γ. On the analogy of the linear viscoelastic theory ηj(0)* seems to be equal to ηj°=τj°Gj°which may prevail in the viscoelastic behaviors under small stresses. If t>>τm°(the slowest relaxation time), Eq. (4) will become:
σ(t)*/γ=ηm(0)*e-t/τm° (5)
where the mechanisms of smaller relaxation time than τm°are neglected. According to the theory presented here, the relaxation curves plotted by log{σ(t)/γ}vs. t must become a single straight line at the final process of relaxations, independent of γ values under the steady flow.
However, the experimental curves for the materials investigated here become almost straight lines in parallel after the initial rapid relaxations. This phenomenon may be interpreted by the following formula.
ηm(0)*≡τm°Gm(0)*≠τm°Gm°≡ηm° (6)
Therefore, the effects of non-Newtonian flow seem to have influence on the whole processes of the relaxation and to be characterized as follows; the maximum relaxation time is not altered, but the distribution function Gm°is depressed with increase of the shearing rate under the flow. These phenomena must be derived from the shear break-down of secondary structures under the shear, where the secondary structures seem to contribute mainly to the slowest relaxation mechanism. The evidence of structural break-down of the samples under the flow is certified by the method of Jobling et al..
By comparison of dependencies of ηm(0)* and ηa on γ, the following relations are expected:
limγ→0ηm(0)*m°≅η=limγ→0ηa (7)
log ηa vs. logγ and log ηm(0)* vs. logγ curves at various concentrations seems to be subject to reduction to the master curve, respectively, by the identically reduced variables for both cases.
τm°increases exponentially with concentration in Na-PAA solutions.

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