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The adsorption of substrates is the first stage in many catalytic processes.
Besides, bubble particles can be utilized as absorbers to facilitate adsorption of substrates due to a high-surface area.
It has been also observed that disordered mesopores are clearly contained in the amorphous carbon substance, making channels for mass transport from the substance to the nanoparticles and/or large enough space for adsorption of substrates.
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The competition between the adsorption of substrate and surfactant molecules is studied.
The doping of silicon atoms with more electropositive into metals lattices in the M-Si intermetallic compounds (IMCs) influenced the adsorption of substrate molecule on the catalyst surface, slightly leading to the different reaction routes.
For the determination of conversion a calibration curve was established for a range of substrate/H-donor ratios in presence of MP-carbonate to compensate for the different adsorption of substrate and H-donor onto the carrier.
Quartz crystal microgravimetry (QCM) revealed observable differences in both the extent and kinetics of AgNP adsorption on substrates coated with NOM and dextran sulfate.
Changing the polarity of the solvent strongly influences the adsorption equilibrium of substrates and products at the catalyst surface and hence plays an influential role on the reaction rate.
A different adsorption of the substrates onto the catalyst surface was observed owing to the hydrophilic/hydrophobic character of the catalyst, depending on the pH.
Chitosan solubility, biodegradability, reactivity, and adsorption of many substrates depend on the amount of protonated amino groups in the polymeric chain and thereby on the proportion of acetylated and nonacetylated glucosamine units.
Thus, it is further confirmed that adsorption of the substrate on the pores and surface of the electrode and the overall reaction was adsorption-controlled.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com