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The parameters κexp and κtheor were useful in the further part of the study to analyse the effect of the PU structure itself on SFE parameters of the polymer film obtained from that PU.
The parameters κexp and κtheor were useful in the further part of the study to analyse the effect of the PU structure itself on SEP parameters of the polymer coating obtained from that PU.
The additive models were then developed and they confirmed that the SFE values for polyurethanes may be modified over a wide span: 20 50 mJ/m while the specific value may be controlled by the PU structure which is defined by the type of initial diisocyanate, polyol, and isocyanate prepolymer chain extender.
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The melting points of the synthesized PU structures were between 245-265°C 245-265°C5, 6).
The PU structures were embedded in a cream for topical applications on murine skin.
The PU structures showed a good stability, melting points between 245-265°C 245-265°Cs between 150-400 nm.
Mice were divided into five equal groups (2 mice for blank cream and each PU structures type, respectively).
In this research PU structures were synthesized using a well-known procedure, the interfacial polyaddition combined with spontaneous emulsification.
In vitro characterization of similar PU structures was already done by our team by testing of mesenchymal stem cells (MSCs) viability.
Polyurethane (PU) structures with high stability and sizes ranging from nano- to micro-scale were obtained by interfacial polyaddition combined with spontaneous emulsification.
The purpose of the present investigation was to develop aliphatic PU structures with a diameter in the range of 100-300 nm in the absence of a catalyst.
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