Sentence examples for most favourable phase from inspiring English sources

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When the extrusion time is not long enough, the MWCNTs do not have the chance to further migrate to the thermodynamically most favourable phase.

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A new thin layer chromatographic system consisting of polyaniline modified silica gel (S2) as stationary phase with 2%% aqueous (1-methylimidazolium chloride) as eco-friendly mobile phase is most favourable for the identification and separation of three-component mixtures of organic dyes.

It may be concluded that the use of thin-layer chromatographic system consisting of polyaniline-modified silica gel (S2) as stationary phase with 2% aqueous 1-methylimidazolium chloride as eco-friendly mobile phase is most favourable for the identification and separation of three-component mixtures of tartrazine, alizarin red S and brilliant blue, bromo-cresol purple and xylenol orange.

These results are surprising given previous observations, that in general the smallest subunits on the periphery of the complex are the most favourable to unfold and dissociate in the gas phase [24], [26].

The differential migration of dyes (TZ, BB, AR, XO and BP R F = 0.55, 0.03, 0.26, 0.05 and 0.02, respectively) achieved with M3 mobile phase on Pani@SG-ES stationary phase, and hence, this TLC system was considered most favourable for ternary separations such as TZ-BB-AR, TZ-AR-XO and TZ-AR-BP (Table 4).

Low ionic strength of the aqueous phase and a pH value of 3 4 are the most favourable conditions to achieve the highest generation rate of free radicals in the organic phase under the conditions of PTC polymerization.

The compatibilization effect observed was found to be dependent upon the liquid crystalline phase temperature range of the compatibilizer, with the most favourable being in a liquid crystalline state during fibre melt extrusion and hot drawing, thus contributing a lubricating effect to the blend and giving enhanced physical properties as a result.

Sarilumab 150 mg and sarilumab 200 mg q2w had the most favourable efficacy, safety and dosing convenience and are being further evaluated in Phase III.

Overall, oral vorinostat at a dose of 400 mg daily provided the most favourable risk benefit profile and, thus, this dose has been selected for a second Phase IIB trial currently ongoing at multiple centres.

dose had the most favourable toxicity profile of the higher dose levels evaluated, and data from the entire Phase I programme identify 400 mg b.i.d.

Both analytical tools, in combination with economical variables, provide a powerful methodological procedure finding the most favourable heat integration and, by this, they help in the technological decision making and in the design phase.

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