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The ionic conductance behavior of the polymeric electrolyte was investigated as solid Mg2+-ion conductors.
The viscoelastic behavior of the polymeric matrix is considered as stress-dependent and thermo-rheologically complex.
The electrochemical behavior of the polymeric films was systematically investigated using differential pulse voltammetry (DPV) to demonstrate the high affinity of the biohybrid interfaces for Cu II) ions.
The reason could simply be the inherent behavior of the polymeric solution, i.e., the correlational structure seen in the sample used in the training step did not continue outside the sample space.
Below Tg these relaxation processes are practically unaffected by changes in the length of the diol units and the softening behavior of the polymeric model networks.
Numerically, 3D finite elements simulations were conducted to replicate the normal impact conditions while incorporating the time-dependent constitutive behavior of the polymeric elements contributing during the impact: the racket constituents (the foam and the compact) and the ball.
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The magnetic behavior of these polymeric complexes was measured as a function of magnetic field strength (0 60 kOe) at 4 K and as a function of temperature (4 300 K) at magnetic field strength of 30 kOe.
The magnetic behavior of these polymeric complexes was measured as a function of magnetic field strength (0 60 kOe) at 4 K and as a function of temperature (4 300 K) at a magnetic field strength of 30 kOe, indicating that they all exhibited features of soft ferromagnet.
Surprisingly, these effects cancel each other in the global packing behavior of this polymeric system.
A combination of pH and temperature to trigger release behavior of these polymeric micelles was discussed by comparing the encapsulated molecule release ability under various pH and temperature conditions and analyzing chemical structural changes of the polymer before and after the triggering.
Ultimately, additional FE calculations confirm that the friction plays a key role in the energy dissipation process, alongside with the rate-dependent behavior and architecture of the polymeric constituents.
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behavior of the whole
behavior of the young
behavior of the dissimilar
behavior of the closed
behavior of the giant
behavior of the combined
behavior of the Spanish
behavior of the wealthy
behavior of the intestinal
behavior of the critical
behavior of the corresponding
behavior of the recycled
behavior of the theoretical
behavior of the polymers
behavior of the stamped
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