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With suitable and reversible operating conditions, the RGPP led to deposit tuneable titanium oxynitride coatings, usually difficult to reach by conventional reactive sputtering.
Asymmetric supercapacitor cells are assembled by pairing up an optimized nanocomposite electrode with an activated carbon negative electrode, which exhibits a wide reversible operating voltage of 2.0 V and a high energy density of 39.6 Wh kg−1.
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The two electrodes to be used in the device are reversible, i.e. capable of reversibly operating as the cathode and as the anode.
In this subsection, works dealing with fragile reversible watermarking operating on transformed domain are presented.
In conclusion, highly complex dynamic systems were generated from networks of different reversible reactions operating simultaneously: primarily imine formation/hydrolysis, transimination, hemithioacetal/hemithioaminal formation, and nitroaldol reactions.
In principle, this would result in eight main types of reversible reactions operating concertedly: hemiaminal, hemithioaminal, hemithioacetal, aminal, and hydrate formation; and nitroaldol- and aza-nitroaldol reactions (Scheme 1).
This mechanism has escaped prior detection because it is reversible and operates within a subset of host tissues and cells.
A reaction A → B inhibited by I becomes: Ī + A → Ī + B. Only in the absence of I, represented by pseudo species Ī, educt A can react to form product B. Sometimes it can make sense to define regulatory rules that depend on the direction at which one or more reversible reactions operate.
In this study, the design of complementary ECDs with two reversible redox electrodes operating in series is presented.
This subsection is dedicated to present some of the main works implementing fragile reversible watermarking by operating in the spatial domain.
Maximum rate of heat transfer from the source in a reversible power cycle, operating between a defined source and sink is defined in Equation 4: Q ˙ CA = T 1 − T CA / α 1 (4).
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