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The room temperature adsorption FTIR results show that O H dissociation is the primary reaction pathway.
Metabolic switching to C-21 emerged as the primary reaction pathway when the substrate was engineered to prevent 16α- and 17-hydroxylation, and all enzymes also epoxidized the double bond at C-16.
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These comparisons show that the selectivities for epoxidation, via primary reaction pathways, increase with increasing reaction temperatures.
The analysis of primary reaction pathways for hydrocarbon species was used to demonstrate the inhibition mechanisms of ignition in hydrogen:oxygen mixtures excited by non-equilibrium discharge plasma.
Results of these analyses suggest that the primary reaction pathways for cleavage of the C C bond take place through activated complexes based on ethyl (C2H5) and ethylidene (CHCH3) species.
Furthermore, these analyses suggest that while the more abundant surface species (e.g., adsorbed atomic hydrogen, ethylidyne, and vinylidene species) are not directly involved in the primary reaction pathways, they affect the observed kinetic rates through blocking of sites.
Nitrotyrosine adducts are formed in vivo by two primary reaction pathways.
Towards the goal of establishing kinetic database for low-temperature combustion (T < 1000 K) of mid-sized biodiesel surrogates, the study uses quantum chemistry and statistical kinetic methods to investigate three <span class="lh">primary unimolecular reaction pathways of methyl octanoate peroxy radicals, including dissociation, isomerization and concerted elimination.
Moreover, gold species are responsible for the second reaction pathway via primary partial oxidation of propene to oxygenates and further reaction with NO and R-CN and R-NCO active intermediates as observed on Au/H-Beta and Au/H-ZSM-5.
Testing at low conversion showed that propene was the main primary product from propane ammoxidation and that the reaction pathway on these catalysts was similar to that on other efficient catalytic systems.
Sensitivity and species flux analyses were used to identify the primary reactions and kinetics pathways for the conditions studied.
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