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Attempts at introducing faster assays resulted in several spectrophotometric methods for reaction product (ammonia, hydroxamate, methacrylamide, benzamide, etc).
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In this paper numerical results are reviewed [D.L. Ropp, J.N. Shadid, C.C. Ober, Studies of the accuracy of time integration methods for reaction-diffusion equations, J. Comput. Phys.
A novel method for reaction synthesis is proposed.
This chapter discusses the sequential response surface modeling method for reaction kinetics.
The pulse corona plasma has been used as an activation method for reaction of methane and carbon dioxide, the product was C2 hydrocarbons and by-products were CO and H2.
The tagmentation reactions were cleaned up using Zymo Clean & Concentrate™ columns in which the elution volume was related to the initial reaction volume (see Methods), except for reaction D for which the recommended minimum column elution volume (6 μl) was used.
There is a need for an intermediate range data-evaluation method for reactions with rates too fast for the classical, graphical method but not fast enough to justify extensive computations.
This phenomenon is also similarly observed under other methods for the reaction part.
Methods for coupling reaction and transport, such as sequential iteration approach (SIA) and predictor corrector approach are incorporated into the code to make the model versatile.
Due to the inherent heterogeneities of porous media, such use of lab-measured rate laws may introduce errors, leading to a need to develop methods for upscaling reaction rates.
Another 11 cycles were performed with the reaction time progressively reduced from 4 h to 6 s for the purpose of enriching the most efficient DNA sequences (see Materials and Methods for the reaction time allowed for each cycle).
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