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A full factorial design at three levels was used, varying temperature (T) and concentration of soluble solids in the osmotic solution (SSC).
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Preliminarily, a factorial design was carried out in which the independent variables were transmembrane pressure (40, 50 and 60 bar) and temperature (20, 30 and 40 °C) of the process, and the dependent variables were pH, content of soluble solids, acidity, concentration of phenolic compounds and those of monomeric and total anthocyanins, colour index, colour density, and permeate flux.
ABA was shown to stimulate invertase activity in the apoplast of grape berries and there was a rise of ABA concentration in the berry (with high time resolution) that clearly preceded the accumulation of soluble solids (hexoses) in the berries.
Regarding the effect of soluble solids in the reactor network feed stream; for cSHF, higher glucose concentration and yield are achieved for enzymatic hydrolysis with washed solids compared with non-separated pretreated material.
Regarding the effect of soluble solids in the feed stream to the reactor network, for SHF higher glucose concentration and yield are achieved for enzymatic hydrolysis with washed solids.
(1) Y X = m f (1 − f IS ) / ρ L C X m i x X M W xylan M W xylose The numerator of the first term is the mass of soluble xylose in the system, the product of the final slurry mass (biomass plus water plus acid), the mass fraction of soluble solids in the final slurry (converted to volume with the density) and the concentration of xylose in the soluble fraction.
The ratio of soluble solids to titratable acidity was also calculated.
Solid loss of carrot particulates during digestion is a result of diffusion of soluble solids and surface erosion.
The aim of this work was to investigate the genetic determination of soluble solid concentrations, titratable acidity, and individual sugars and acids in grape berries.
The physiological stage of fruit was assessed through measurement of soluble solid content (SSC).
Conversely, when FCS or 5% BSA was first incubated with DMSO-dissolved curcuminoids followed by solid curcuminoids, the final concentration of soluble curcuminoids remained essentially constant.
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