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Additionally, it was found that higher chitosan content in the precursor blends led to thinner nanofibers.
Cooling the crystalline/crystalline polymer blends led to POM first crystallization in the PBSU melts, followed by PBSU crystallization in the POM crystal-filled PBSU melts.
By XPS N1s peak convolution, it was found that thermal treatment of blends led to dedoping when the curing temperature reached 250°C.
The produced orientation and the negative volume of mixing of the blends led to a range of LCP materials with intermediate modulus and tensile strength and slightly higher ductility.
Also, microstructure of blends studied by SEM showed that incorporation of IF-WS2 into the blends led to reduction of dispersed domain size attributed to reduction of interfacial tension due to the filler presence.
The additional compatibilization was not able to overcome the brittle nature of the Ro at large Ro contents (40%), but in the case of the 20% Ro blends, led to blends with overall improved mechanical properties compared to those of the reference blends without additional time in the melt state.
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These bimodal blends lead to significant enhancements in the mechanical properties of samples printed in the transverse orientation.
Addition of rubber to both the epoxy and the epoxy-polycarbonate blends leads to significant improvements in the critical strain energy release rate, GIC, of the cured resin.
In particular, phase separation of PLLA/PDLLA or PLLA/PLGA blends leads to partially nanofibrous scaffolds, in which PLLA forms nanofibers and PDLLA or PLGA forms the smooth (solid) surfaces on macropore walls, respectively.
The uniaxial deformation of these blend films having a PBT-crystallinity degree ranging from 31to12%2%, in unstretched blends, leads to a appreciable high segmental orientation for the crystalline PBT due to a structural transformation from lamellae to microfibrils.
The d.s.c. and SAXS studies of the blends lead to the conclusion that the PEI segments are incorporated in the amorphous layer between the stacked N-TPI crystals, regardless of the phase separation.
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