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The three CA-RPs (CA VIII, X and XI) owe their putative lack of CA activity to substitutions of one or more active site residues [ 6, 7].
This kind of surface arrangement can provide a superior adsorption environment and more active site for the photocatalytic reaction.
In addition, synergy effect of RhMnFe/Al2O3 catalyst prepared by co-impregnation may promote the formation of more active site for ethanol formation.
Extra-large surface area is favorable for the adsorption procedure because then more active site is available for the adsorption of adsorbent.
The catalytic results demonstrated that the Sb/PAL composites perform an excellent catalytic hydrogenation with a good reusability, which was attributed to the high dispersion of Sb nanoparticles on the palygorskite fiber, providing a more active site; the similar effect was also found in TiO2/halloysite composites [38].
Of these homologues, 637 are missing one or more active site residues because they are fragments, and a further 337 are considered not to be peptidases because one or more active site residues are not conserved.
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Earlier studies have shown that the hybrid structures offer enhanced catalytic activity with more active sites [13].
In general, larger surface area often possesses a higher photocatalytic activity because of the more active sites on the surface.
The less active sites appeared to be more easily regenerated than the more active sites as the catalytic activity at TOS≥100 min was recovered following regeneration at 315°C.
The good dispersity of NiSe nanoparticles permitted the exposure of more active sites, which enhanced the activity of HER on the NiSe-RGO-PI/CNT film.
This superiority of ZnO photocatalytic activity is because it has more active sites, higher reaction rates, and is more effective in generating hydrogen peroxide[18].
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