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Differences in the wear behavior are rationalized in terms of the coating hardness and structure.
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Stress levels and energy-to rupture increase in the order: L-SIBS <3-SIBS <4-SIBS and this behavior is rationalized in terms of the covalent junction points, entanglements, and hard block domain reinforcement.
This behavior is rationalized with a change in the primary strain mechanism from domain switching at low temperatures to a reversible electric field-induced transition from an ergodic relaxor state to a long-range order at high temperatures.
The different buckling behaviors, dependent on the constituent phases, are rationalized in the light of the disparity in mechanical properties.
Such differences are rationalized in terms of polymer analyte interactions.
In this work we present evidence that this behavior can be rationalized in terms of the donor acceptor intermolecular chemical hardness (ηDA).
We introduce the notion of strong activity rules, which allow simple, consistent bidding strategies while precluding all behaviors that cannot be rationalized in this way.
The complex behavior of the photoresponses is rationalized in terms of recombination losses, band edge energy tails and hindered transport across the oxide thin film.
The non-selectivity in the adsorption behavior of the type-II suppressor is rationalized in terms of anion/cation pairing effects of the poly-cationic suppressor and the anion-modified copper substrate.
So the unjust was rationalized in service of safe streets.
Such a condition can be rationalized in two possible ways.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com