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When the PCL content in the blend was increased to 50%, the mechanical property for elongation was significantly improved without sacrificing the pores on the membrane surface that help tissue segments adhere the membrane.
It was found that, in comparison with the unfilled PMMA/SAN blends, the phase separation temperature of the filled polymer blend was increased, and the thermodynamic interaction parameter was correspondingly decreased, suggesting that the phase stability of PMMA/SAN mixtures is enhanced by the incorporation of silica.
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As the H2 concentration in the fuel blend is increased, the displacement flame velocity and local triple flame speed increase progressively due to the enhanced chemical reactivity, diffusivity, and preferential diffusion caused by H2 addition.
Assuming a fully adiabatic combustion chamber, LES always predicts an M flame shape and does not capture the V to M shape transition observed in the experiments when the hydrogen concentration in the fuel blend is increased.
The surface potential and second harmonic signal relaxation time, τe, decrease more than 5×104 times when the amount of PEO in the blend is increased from 2 to 25%, while the rotational diffusion time always remains less than τe.
In addition, relative to neat PE, the tensile modulus of a 70/30 wt% PE/starch blend is increased by 20% in the damaged starch case (vs. 10% in the blend made by melt mixing) while the reduction in tensile strength is significantly smaller than that found in melt-mixed blends.
The duration of injection for butanol blends was increased to obtain a stoichiometric mixture.
As the amount of polyether in the blends was increased, the melting endotherm of DMU became much broader and shifted to lower temperatures, indicating extensive mixing with PEO.
Tensile modulus and strength of the blends were increased while elongation at break decreased by increasing PLA content.
The mechanical properties of the ternary blends are increased when a proper amount of MA-PP is added.
Thermal analysis revealed that the crystallinity and crystallisation/melting temperatures of LPET BPET blends were increased compared with LPET.
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CEO of Professional Science Editing for Scientists @ prosciediting.com