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The presence of polymer/filler interactions was confirmed by bound polymer measurements.
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MIDA has been quantitatively validated and compared by independent methods, including a biosynthesis polymer measurement (1, 2, 7, 8).
Direct comparison of these impedances is consistent with bulk polymer film measurements.
Corroborating the findings made during previous studies of this polymer, absolute measurements conducted in this study provided new detailed information regarding some of the basic parameters characterising the doping process of this conjugated polymer.
After at least five readings which were obtained for different areas of the polymer, the measurements were averaged to arrive at a final contact angle (n = 6).
To integrate these results within a framework, they develop a mathematical model that is parameterized quantitatively on their in vitro polymer length measurements, that demonstrates that the coupling they have uncovered allows for an ultrasensitive response to changes in environment.
This could be very useful when carrying out polymer adsorption measurement; however, some useful measurement like generic feature of the in situ rheology of the polymer can be done in unconsolidated porous media.
The surface energy of drugs and polymers measured by contact angle measurement was found to be an important factor, although it could not solely determine the steady state values of particle size.
In order to compare the properties of both polymers viscosimetric measurements were carried out at different integration times and using different concentrations of polymer.
For polymer adsorption measurement, the mineral sample is soaked in the polymer solution.
The composites were incubated in phosphate buffer saline at 37°C to study the in vitro degradation of the polymer by measurement of water absorption, weight loss as well as changes in the average molecular weight of the polymer and in the pH of the incubation medium as a function of the incubation time.
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