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The equilibrium melting points (Tm0) of the blends were determined using the Hoffman-Weeks procedure.
Cloud points of poly(ϵ-caprolactone) (PCL /polystyrene (PS) blends were determined using the thermooptical analysis (t.o.a).
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The distribution of processing oil in two olefinic thermoplastic elastomer (OTPE) blends was determined using dielectric spectroscopy.
To determine the effect of chitosan and genipin on hydrogel electrostatic character, the free amine content within hydrogel blends was determined using a ninhydrin assay.
The boundary between the mesophase (M1) of block copolymer and the homogeneous phase (H) of block copolymer/homopolymer blend was determined using oscillatory shear rheometry, and the boundary between the homogeneous phase (H) and two-phase liquid mixture (L1+L2) with L1 being disordered block copolymer and L2 being macrophase-separated homopolymer was determined using cloud point measurement.
Moisture sorption isotherms of pure pullulan, alginate and blend films were determined using the gravimetric method at 25, 35 and 45 °C.
The effects of antioxidants and storage on oxidation stability of croton biodiesel and its blends with petro-diesel were determined using PetroOxy equipment.
The expected 'phase diagram' for the blend system was determined using indirect techniques, i.e. differential scanning calorimetry and transmission electron microscopy.
In this work, the mixing quality of a multi-component blend of particles is determined using Multivariate Image Analysis of RGB images combined with the Grey Level Co-occurrence Matrix (GLC M texture analysis.
The pure error of the experimental data was determined using replicate blends in the design and was found to be 0.3 °C for freeze point and 2.6 × 10−3 cSt for viscosity.
These scores are determined using a blend of more than two dozen indicators, including financial credit scores — and for many people, these have dropped.
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