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where DsFfAwAsρr, and ρs are deswollen weight of the sample, fraction insoluble, sample weight, weight of the absorbed solvent corrected for swelling increment, density of rubber, and density of solvent, respectively.
The porosity was calculated from (3). (3) Porosity = (w − w 0 ) ρ V T, where w0 and w are the weights of SPHC particles before and after immersion, ρ is the density of solvent, and V T is the total volume of SPHC particles.
M is the mass of the protein molecule in Dalton; No is Avogadro's number, 6.023 × 10; v2 is the partial specific volume of the protein; typical value is 0.73 cm/g; ρ is the density of solvent (1.0 g/cm for H2O); η is the viscosity of the solvent (0.01 g/cm-s for H2O).
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Spatial and temporal variability of BTEX compounds was associated with, in order of importance based on partial R, traffic signal density within 450 m of the monitors, kernel-weighted density of solvent-use industries within 500 m, and reference site mean.
where Wsf is the weight fraction of the solvent, ρ0 is the density of the solvent, Wrf is the weight fraction of the polymer in the swollen specimen, and ρ1 is the density of the polymer.
The volume fraction of a rubber network in the swollen phase is calculated from equilibrium swelling data as: V 2 = W 2 / d 2 / W 1 / d 1 + W 2 / d 2, where W1 is the weight fraction of the solvent, d1 is the density of the solvent, W2 is the weight fraction of the polymer in the swollen specimen and d2 is the density of the polymer.
The volume fraction of a rubber network in the swollen phase Vr is calculated from equilibrium swelling data using Flory Rehner equation [27], V r = W 2 / d 2 / W 1 / d 1 + W 2 / d 2, where W1 is the weight fraction of the solvent, d1 is the density of the solvent, W2 is the weight fraction of the polymer in the swollen specimen and d2 is the density of the polymer.
The value of V r is determined from equilibrium swelling data with the help of Flory Rehner equation [33], V_r = ({W_2 /d_2 })/{{({W_1 /d_1 }) + ({W_2 /d_2 })}} where W 1 represents a weight fraction of the solvent, d 1 is the density of the solvent, W 2 represents a weight fraction of the polymer in the swollen specimen and d 2 is the density of the polymer.
Increasing the density of the solvent or/and increasing the pressure of the solvent will also increase the cavitation threshold [24, 25].
Where, do: density of pure solvent ds: density of solution m : molarity of solution M : molecular weight of solute β o : adiabatic compressibility of pure solvent β s : adiabatic compressibility of solution.
Density of the solvent.
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