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The blends were analysed with differential scanning calorimetry.
Melting and crystallisation behaviours of the blends were analysed by differential scanning calorimetry (DSC).
The phase morphologies of the obtained blends were analysed using SEM, etching experiments and image analysis.
The curing kinetics of the neat resin and of PC/epoxy blends were analysed in detail by dynamic differential scanning calorimetry.
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The errors stemming from the sc lattice assumption for these blends are analysed.
A large range of blends is analysed with different glycerol (plasticizer):starch contents ratios (0.14 0.54) and various PCL concentrations (up to 40 wt.%).
The influence of various parameters on the detection of methanol, tert-butyl alcohol (TBA) and tert-butyl methylether (TBME) in hydrocarbon blends is analysed by u.v.-visible spectroscopy.
The interfacial thickness in reactively compatibilized polymer blends is analysed with ellipsometry for the blend system polyamide 12/(polystyrene/poly styrene-co-maleic anhydride)) polystyrene/poly styrene-co-maleicem polystyrene/poly styrene-co-maleic
The behaviour of these blends was analysed with the aid of a theoretical model developed by Piorkowska et al. and furnished additional support for the correctness of the particle-size effect based on the principle of 'stress-induced displacement misfit' proposed by Argon et al. previously.
The transport properties of water and sodium dodecyl sulfate (SDS) in membranes of the PANi CA blends and of CA were analysed.
The hydrolytic degradation behaviour and some other properties were analysed for blends of microbial poly 3-hydroxybutyrate) [poly 3-hydroxybutyrate poly(3-hydroxybutyrate-co-3-hydroxyvalerate) [P 3HB-co-3HV); 3HV content, 22.3 mol%].
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