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Several proportions of buffer, water-acetonitrile mixture, and methanol were evaluated to obtain suitable composition of the mobile phase.
All transport, kinetic, and adsorption parameters, excepting the equilibrium adsorption constants for water and methanol, were evaluated in separate experiments.
Organic modifiers like acetonitrile and methanol were evaluated as mobile phase B. Satisfactory chromatographic separation was achieved when acetonitrile was used as mobile phase B in terms of better resolution and tailing factor.
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The catalytic activity of the catalysts towards the oxidation of methanol was evaluated by cyclic voltammetry.
Performance of the prepared catalysts for CO/CO2 hydrogenation to methanol was evaluated by using a stainless steel fixed-bed reactor at 5 MPa and 513 K.
Parametric-effects on kinetics for biodiesel production from H2SO4 catalyzed esterification of free fatty acids (FFA) with methanol are evaluated at different intervals of reaction using Taguchi method.
Glycerol dehydrogenase activity in the presence of methanol was evaluated using purified, membrane-bound G. oxydans alcohol dehydrogenase (mADH) based on the method of Adachi et al. (1978) with modifications.
The deprotonation ability of clean (i.e., carbonate- and hydroxyl-free) MgO surfaces of various morphologies towards protic molecules, such as propyne and methanol, is evaluated by following the adsorption modes and amount of dissociated species by FTIR.
AOX affinity towards methanol was evaluated via a kinetic study of enzyme activity in crude cell-free extracts of parental [ 13] and mutant H. polymorpha strains CA2 and CA4 in the presence of different methanol concentrations (0 100 mM) in the peroxidase reaction with ABTS (2,2'-azino-bis 3-ethylbenzothiazoline-6-sulphonic 2,2'-azino-bis 3-ethylbenzothiazoline-6-sulphonic 2,2'-azino-bis 3-ethylbenzothiazoline-6-sulphonic 2,2'-azino-bis 3-ethylbenzothiazoline-6-sulphonic 2,2'-azino-bis 3-ethylbenzothiazoline-6-sulphonic 2,2'-azino-bis 3-ethylbenzothiazoline-6-sulphonic
The effects of temperature and time of reaction on methanol conversion were evaluated.
The electrocatalytic properties of the catalysts for methanol oxidation were evaluated by cyclic voltammetry (CV).
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