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Shearing the polymer leads to a temperature increase due to viscous dissipation. However, the temperature increase is small since the shear rate is highest near the wall, which is maintained isothermal by the temperature control system and since the shear is imposed only for a brief duration. No variation in temperature during shear is recorded by a thermocouple positioned near the sample
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Shearing the polymer leads to a temperature increase due to viscous dissipation. However, the temperature increase is small since the shear rate is highest near the wall, which is maintained isothermal by the temperature control system and since the shear is imposed only for a brief duration. No variation in temperature during shear is recorded by a thermocouple positioned near the sample.
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35
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0343944986
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The temperature chosen, 220 °C, was higher than the Hoffman-Weeks equilibrium melting temperature for PP-300/6, which was determined to be 190 °C. Holding at this temperature for 5 min was deemed to be adequate to erase melt memory effects since higher temperatures (up to 240 °C) or longer holding times did not have any measurable difference on the crystallization kinetics
-
The temperature chosen, 220 °C, was higher than the Hoffman-Weeks equilibrium melting temperature for PP-300/6, which was determined to be 190 °C. Holding at this temperature for 5 min was deemed to be adequate to erase melt memory effects since higher temperatures (up to 240 °C) or longer holding times did not have any measurable difference on the crystallization kinetics.
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36
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0343944985
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-6 s) for the present experiments
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-6 s) for the present experiments.
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0043002852
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0342638972
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Nonlinear viscoelastic data obtained using a capillary rheometer indicate that PP-300/6 is shear thinning. Fitting this data to a power law model yields a value of about 0.38 for the power law exponent
-
Nonlinear viscoelastic data obtained using a capillary rheometer indicate that PP-300/6 is shear thinning. Fitting this data to a power law model yields a value of about 0.38 for the power law exponent.
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39
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0343944984
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shear = 12 s) show that the spherulitic core has a lower melting temperature than the oriented skin. This suggests that the core might have crystallized at a lower temperature than the skin
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shear = 12 s) show that the spherulitic core has a lower melting temperature than the oriented skin. This suggests that the core might have crystallized at a lower temperature than the skin.
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43
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0342638966
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17 (Figure 5). This is misleading. The steep increase in force and the subsequent decay between 10 and 20 s in Figure 6 of ref 14 is the viscoelastic response of the polymer melt to step strain. Neither the time scale nor the magnitude of the overshoot observed in the rheometer torque in Figure 5 of ref 17 change with the imposed strain rate, suggesting that the overshoot might be an artifact of the experimental setup (repositioning of the polymer, as suggested by the authors). In both these references, the increase in stress at later times results from an increase in modulus of the polymer due to crystallization with no evidence that these are oriented
-
17 (Figure 5). This is misleading. The steep increase in force and the subsequent decay between 10 and 20 s in Figure 6 of ref 14 is the viscoelastic response of the polymer melt to step strain. Neither the time scale nor the magnitude of the overshoot observed in the rheometer torque in Figure 5 of ref 17 change with the imposed strain rate, suggesting that the overshoot might be an artifact of the experimental setup (repositioning of the polymer, as suggested by the authors). In both these references, the increase in stress at later times results from an increase in modulus of the polymer due to crystallization with no evidence that these are oriented.
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44
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0343509251
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cryst = 141 °C for ∼6 s of shear are qualitatively similar to that in Figure 1a in the work of Andersen and Carr
-
cryst = 141 °C for ∼6 s of shear are qualitatively similar to that in Figure 1a in the work of Andersen and Carr (Andersen, P. G. and Carr, S.H. J. Mat. Sci. 1975, 10, 870-886.) which was obtained from an iPP fiber with well-developed α-iPP crystal structure having strong uniaxial orientation of parent crystallites (c axis along the fiber), bearing the associated crosshatched "daughter" crystallites.
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Wang, P.3
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Hsiao, B.S.6
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0016510939
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which was obtained from an iPP fiber with well-developed α-iPP crystal structure having strong uniaxial orientation of parent crystallites (c axis along the fiber), bearing the associated crosshatched "daughter" crystallites
-
cryst = 141 °C for ∼6 s of shear are qualitatively similar to that in Figure 1a in the work of Andersen and Carr (Andersen, P. G. and Carr, S.H. J. Mat. Sci. 1975, 10, 870-886.) which was obtained from an iPP fiber with well-developed α-iPP crystal structure having strong uniaxial orientation of parent crystallites (c axis along the fiber), bearing the associated crosshatched "daughter" crystallites.
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Andersen, P.G.1
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0001211193
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Jones, A. T.; Aizlewood, J. M.; Beckett, D. R. Makromol. Chem. 1964, 75, 134-158.
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0032003918
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Eckstein, A.; Suhm, J.; Friedrich, C.; Maier, R.-D.; Sassmannshausen, J.; Bochmann, M.; Mulhaupt, R. Macromolecules 1998, 31, 1335-1340.
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0342638963
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Figure 4 in ref 24
-
Figure 4 in ref 24.
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54
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0343944980
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z = 407 000 g/mol) was sheared at a temperature of 150 °C for shearing times of ∼20 s at wall shear stresses around 0.1 MPa. No upturn was seen in the birefringence observed during shear
-
z = 407 000 g/mol) was sheared at a temperature of 150 °C for shearing times of ∼20 s at wall shear stresses around 0.1 MPa. No upturn was seen in the birefringence observed during shear.
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55
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0001302524
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Flow induced orientation and structure formation
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Meijer, H. E. H., Ed.; VCH: NY
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