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In general, blending the lignins in Voranol 270 increased the viscosity of the polyol.
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The large difference between the viscosity of the polyols and the ethylene glycols that inversely correlate with nucleation times indicates that the kinetic effects observed cannot be attributed solely to solution viscosity.
The molecular weight polyol produced by DMC catalyst increases from Mn = 3700 to more than 6000, and the viscosity of polyol decreases by combining with ILs.
Viscosity of the mixture of the polyether polyol (Voranol 270) and lignin (HEL and HKL) was determined using a Brookfield dial reading rotary viscometer (Model LVT).
Viscosity of polyol is critical to the preparation of polyurethane foam and cellular structure of resultant foam.
In addition, the siloxane functionalized polyols also effectively reduced the viscosity of the coatings formulations.
Interactions between the sugar substitutes were found to affect the viscosity of the matrices, whereas flavor release was not affected by interactions between the polyols and bulking agents investigated.
Under the polyol-rich condition, a part of the polyol can be pyrolyzed to carbonized structures although most undergo combustion to supply the energy for nanoparticle formation.
Due to the bio-based content of the polyol backbone, the synthesized polyol had both excellent biodegradability and low cytotoxicity.
The thermodynamic role of the polyol (polyhydric alcohol fuel) must be understood in terms of reaction catalyst for a given thermochemical reaction process.
In a typical polyol process, the solid precursor is suspended in the liquid polyol, and then the solution or the suspension is stirred and heated to a given temperature which can reach the boiling point of the polyol.
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