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The well-defined structure prompts us to understand the nature of the catalytic active sites, and to demonstrate that the catalyst activity is linearly proportional to the concentration of FeN2 sites.
Similar to viscosity reduction, the experimental results demonstrate that the catalyst Cu(C11H7O2 2 shows high activity in the aspect of upgrading heavy components.
These results demonstrate that the catalyst particle architecture directly affects polymer composition, offering the perspective of making high-performance polyethylene from a single reactor system using this modified Phillips catalyst.
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It was demonstrated that the catalyst has an enhanced activity and sulfur tolerance during naphthalene hydrogenation.
Catalytic studies demonstrated that the catalyst containing 1.0% Ru and based on MN-270 is the most active.
It was demonstrated that the catalyst worked well for a variety of aziridines producing the corresponding oxazolidinones in good yields and excellent regio-selectivities.
Electrochemical experiments demonstrated that the catalyst exhibited excellent hydrogen evolution reaction (HER) activity with large cathode currents (small overpotential of 184 mV for 10 mA cm−2 current density) and a Tafel slope as small as 62 mV per decade.
Under these conditions the conversion of benzyl alcohol reached 100% after 2 h and it was demonstrated that the catalyst can be recycled three times without significant loss of activity.
Obtaining the polarization curves for the fabricated MEAs (Pt loading ∼0.4 mg cm−2) and a commercial MEA (ElectroChem, Pt loading ∼1 mg cm−2) demonstrated that the catalyst prepared by two-step sensitization activation coating procedure possesses a good performance despite of its lower Pt content.
Several research results demonstrated that the catalyst is one of an important part to control the morphology of the nanowires.
The above results demonstrated that, the catalyst performed in excellence both in DMO conversion and in EG Selectivity.
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CEO of Professional Science Editing for Scientists @ prosciediting.com