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The thermal stability of the respective blends is higher than that of the POT HNO3 and PMT HNO3 salts.
At higher crystallization temperatures, the crystallization rate of the blends is higher than both the pure homopolymers, resulting in phase separation morphology.
The storage modulus, E′, of the iPP/sPP blends is higher than that of sPP homopolymer in the temperature range from −90 to 100 °C.
The average strength of the hydrogen bond in the cured ER/PEO blends is higher than in the pure MCDEA-cured ER.
The results indicate that the content of collagen on the surface of the blends is higher than expected, and that such enrichment is more evident for the blends containing a lower percentage of collagen.
However, T1ρHs of star PMMA/phenolic blends are relatively smaller than those of linear PMMA/phenolic blends, implying that the degree of homogeneity of star PMMA/phenolic blends is higher than those of linear PMMA/phenolic blends.
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This is why model predictions for PS/PMMA (20/80, 30/70) blends are higher than experimental results.
The activation energies of the blends are higher than that of the neat resin.
The Tgs of PSI100/P4VPy and PSI100/P2VPy blends are higher than those calculated from the additivity rule.
Again, Tg values of the blends are higher than the component ones, but now a dependence on the composition of the mixture is observed.
The relative amount and the average strength of the hydrogen bonds in the blends were higher than those in the pure novolac resin.
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