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In the pre-processing stage, the composition space is partitioned into a user-specified number of regions, over which suitable reduced chemical representations and kinetic models are generated automatically using the Directed Relation Graph with Error Propagation (DRGEP) reduction technique.
The selection of the most suitable reduced model, with real applications in some cases, should not be taken lightly, but rather an exhaustive study should be made of the suitability of the model, examining the main characteristics required in each case and particularly the controller design techniques to be used.
The model reduction method developed in this work is based on the generation of a large set of candidate reduced-order models by elimination of terms from the original model, followed by selection of suitable reduced models from the generated set through checking against T-optimality design of experiments criteria.
The computational approach for strongly coupled fluid structure interaction is used to create suitable reduced models of generic nonlinear problems.
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In this process, the starting raw material barium sulfate is reduced by a suitable reducing agent to produce barium sulfide, which is used to reduce sulfur dioxide to elemental sulfur vapor and regenerate barium sulfate.
The release mechanism relies upon the imposition of a suitable reducing potential at the gold suture resulting in an increase in local pH and thereby induces the dissolution of the polymeric binder and releases the drug.
In addition, in their presence it is possible to reduce a compound, electrochemically or photochemically using a suitable reducing agent [9, 10].
Suitable reducing agents preferably sodium borohydride is used to yield the sodium salt of FEX which is converted to the free base by pH adjustment.
Horseradish peroxidase can reduce H2O2 to OH, and ultimately to H2O (Chen and Schopfer 1999) in the presence of a suitable reducing agent, using a mechanism similar to that used by chelated Fe3+ ions or Fe3+ ions in the Fenton-like process (Abo-Farah 2010).
An important feature of our liposome formulations is the disulfide linker moiety in SS14 that, in suitable reducing environment, might promote lipoplex disassembly by reversion of the gemini surfactant to single-chain amphiphiles.
DPPH radicals react with suitable reducing agents during which the electrons become paired off and solution loses colour stoichiometrically depending on number of electrons taken up [ 3].
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