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A set of 46 model compounds was used to demonstrate that the method is accurate, reproducible and predictive.
Batch experiments under anoxic conditions with nitrate as electron acceptor revealed that the biodegradation of the model compounds was lower than under aerobic conditions.
Thermodynamic examination of the systems using 2,3-di-O and 6-O-methylcelluloses (23MC and 6MC) as cellulose model compounds was carried out by differential scanning calorimetry.
The LC enantioseparation of chiral acidic and zwitterionic drugs selected as model compounds was optimized using chlorine containing cellulose based chiral stationary phases and polar organic mobile phases.
The X-ray analysis of one of these model compounds was performed and its crystal structure is described/compared to that of sildenafil.
Additionally, the thermal stability of the resulted polymers with various model compounds was studied to confirm the proposed polymerization mechanism and the final polymerization structures.
Similar(46)
Kinetic models for hydrocracking of model compounds were not analyzed.
Model compounds were synthesised and their chemical shifts assigned.
Mixtures of the two model compounds were used as the model systems of poly urethane urea).
To ascertain the hydrodeoxygenation activity of this catalyst under liquefaction conditions, model compounds were investigated.
Model compounds were synthesized for the correct assignment of 13C n.m.r.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com