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First normal stress

Polyolefin melts have a high degree of viscoelastic memory or elasticity. First normal stress differences of polyolefins, a rheological measure of melt elasticity, are shown in Figure 9 (30). At a fixed molecular weight and shear rate, the first normal stress difference increases as MJM increases. The high shear rate obtained in fine capillaries, typically on the order of 10 , coupled with the viscoelastic memory, causes the filament to swell (die swell or... [Pg.317]

Fig. 9. First normal stress differences of polypropylene of different molecular weight and distribution (30) see Table 4 for key. To convert N /m to... Fig. 9. First normal stress differences of polypropylene of different molecular weight and distribution (30) see Table 4 for key. To convert N /m to...
Fig. 22. Shear viscosity Tj and first normal stress difference (7) vs shear rate 7 for a low density polyethylene at 150°C (149), where (Q) — parallel plate ... Fig. 22. Shear viscosity Tj and first normal stress difference (7) vs shear rate 7 for a low density polyethylene at 150°C (149), where (Q) — parallel plate ...
A sliding plate rheometer (simple shear) can be used to study the response of polymeric Hquids to extension-like deformations involving larger strains and strain rates than can be employed in most uniaxial extensional measurements (56,200—204). The technique requires knowledge of both shear stress and the first normal stress difference, N- (7), but has considerable potential for characteri2ing extensional behavior under conditions closely related to those in industrial processes. [Pg.192]

Non-linear viscoelastic flow phenomena are one of the most characteristic features of polymeric liquids. A matter of very emphasised interest is the first normal stress difference. It is a well-accepted fact that the first normal stress difference Nj is similar to G, a measure of the amount of energy which can be stored reversibly in a viscoelastic fluid, whereas t12 is considered as the portion that is dissipated as viscous flow [49-51]. For concentrated solutions Lodge s theory [52] of an elastic network also predicts normal stresses, which should be associated with the entanglement density. [Pg.10]

Fig. 19. Shear stress and first normal stress difference plotted as a function of shear rate for different molar masses, and b at different concentrations of polystyrene in toluene... [Pg.37]

As a result, we find for sols that the divergence of the above zero shear viscosity rj0 and of two other linear viscoelastic material functions, first normal stress coefficient and equilibrium compliance 7°, depends on the divergence... [Pg.177]

We can also calculate other viscoelastic properties in the limit of low shear rate (linear viscoelastic limit) near the LST. The above simple spectrum can be integrated to obtain the zero shear viscosity 0, the first normal stress coefficient if/1 at vanishing shear rate, and the equilibrium compliance J... [Pg.194]

The corresponding first normal stress difference N t) = tu(t) — t22( ) as predicted from Eq. 4-2... [Pg.196]

Fig. 13. Shear stress t12 and first normal stress difference N1 during start-up of shear flow at constant rate, y0 = 0.5 s 1, for PDMS near the gel point [71]. The broken line with a slope of one is predicted by the gel equation for finite strain. The critical strain for network rupture is reached at the point at which the shear stress attains its maximum value... Fig. 13. Shear stress t12 and first normal stress difference N1 during start-up of shear flow at constant rate, y0 = 0.5 s 1, for PDMS near the gel point [71]. The broken line with a slope of one is predicted by the gel equation for finite strain. The critical strain for network rupture is reached at the point at which the shear stress attains its maximum value...
Quotient of the first normal stress difference N ) and the square of the shear rate (y) in the limit of zero shear rate... [Pg.162]

Various investigations have considered the effects of titanate treatments on melt rheology of filled thermoplastics [17,41]. Figure 10, for example, shows that with polypropylene filled with 50% by weight of calcium carbonate, the inclusion of isopropyl triisostearoyl titanate dispersion aid decreases melt viscosity but increases first normal stress difference. This suggests that the shear flow of the polymer is promoted by the presence of titanate treatment, and is consistent with the view that these additives provide ineffective coupling between filler particles and polymer matrix [42]. [Pg.169]

Fig. 10. Viscosity and first normal stress difference vs. shear stress for polypropylene (at 200 °C) filled with calcium carbonate (50 wt%) with and without a titanate coupling agent (TTS ) (O, ) pure polypropylene (PP) (A,A) PP/CaC03=50 50 (by wt.) ( , ) PP/CaC03=50 50 with TTS (1 wt%). The open symbols were obtained from a cone and plate instrument and the closed symbols from a slit/capillary rheometer. Fig. 10. Viscosity and first normal stress difference vs. shear stress for polypropylene (at 200 °C) filled with calcium carbonate (50 wt%) with and without a titanate coupling agent (TTS ) (O, ) pure polypropylene (PP) (A,A) PP/CaC03=50 50 (by wt.) ( , ) PP/CaC03=50 50 with TTS (1 wt%). The open symbols were obtained from a cone and plate instrument and the closed symbols from a slit/capillary rheometer.
First normal stress function, pt t — p22 at steady state in steady simple shear flow. [Pg.161]

This behaviour of the extinction angles is in accordance with eq. (1.3), if % = In fact, for a second order fluid the first normal stress difference increases with the square of the shear rate, whereas the shear stress increases with the first power of this rate (constant viscosity). As a consequence, it follows from eq. (1.3) that cot 2% increases linearly. From this fact the above mentioned linear behaviour of the extinction angle curve is deduced, since... [Pg.180]

In Sections 1.2 and 1.3 only the measurements of shear stress p and of first normal stress difference (/>u — p22) have been discussed. To... [Pg.182]

In Chapter 1 the validity of a stress-optical law has been presumed. Furthermore, it has been shown for several polymer systems that this law is, at least approximately, valid and that the second normal stress difference (p22 — p33) must be very small compared with the first normal stress difference (pn — 22). In the present chapter some theoretical considerations of a more general character will be reviewed in order to indicate reasons for this special behaviour of flowing polymer systems. Some additional experimental results will be given. [Pg.188]


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Examples of first normal-stress differences

First Normal Stress Function

First normal stress coefficient defined

First normal stress coefficient from viscosity data

First normal stress difference

First normal stress difference negative values

First normal stress growth coefficient

First normal-stress coefficient

Negative first normal stress differences

Non-Newtonian shear viscosity and first normal stress coefficient of polymer melts

Normal stress

Normal-stress coefficients difference, first

Parameters Influencing the First Normal Stress Difference

Zero-shear first normal stress coefficient

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