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A small volume of dispersion was diluted down to approximately 1 mg/ml with isopropyl alcohol.
Yang et al. [18] recommended an alternate form of (Equation 1), when the specific energy input is stable and the volume of dispersion is constant: L = B t n (2).
As the organic phase fraction is increased, the interfacial area expressed on the basis of a unit volume of dispersion or aqueous phase, first increases, passes through a maximum and then decreases.
Factors affecting IL-DLLME (sample pH, IL amount, volume of dispersion solvent and sodium chloride percentage) were optimized by means of an experimental design, obtaining the most favorable results when using 117.5 mg of IL and 418 μL of MeOH to extract the compounds from the aqueous soil extracts at pH 5.20 containing 30% (w/v) NaCl.
With the increase of W/C ratio or liquid phase in cement pastes the elastic deformation drops from 0.83% to 0.27%, while the volume of dispersion when the paste starts flowing increases from 0.63% to 1.31% due to cement particle redistribution under shear stress.
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Yang et al. [32] recommended a modified version of Equation 1 in the case that the sonication specific energy and the volume of nanofluid dispersion are fixed.
The above gravimetric data allowed us to determine the absorption coefficient α: from a known volume of initial dispersion, several dilutions were done and the absorbance at a wavelength of 660 nm was measured[11, 17, 24].
Four mL volume of the dispersion was drawn into a syringe.
The volume of each dispersion was ultimately adjusted to 100 mL with purified water.
Lison et al. (2008) considered mass concentration, particle number, surface area and also the applied volume of NP dispersion as crucial factors for reliable conclusions on nanoparticle cytotoxicity.
Theoretically, extension of the CLIP test to more than two traits could be performed by studying the maximal volume of the dispersion of the points around the straight line under the pleiotropism assumption.
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