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The encapsulation is modeled as a complex interface of an infinitesimal thickness.
The encapsulation is positioned in close proximity to the engine and completely surrounds the entire engine block.
According to our theoretical study, the titanocene/cyclodextrin inclusion compounds can be obtained (high interaction energy; the encapsulation is energetically favourable).
This nanosystem is well-suited for dual encapsulation of IONPs and drug molecules, because the encapsulation is achieved in a way that is similar to common drug loading.
Although the encapsulation is incomplete, maximum impact strength and maximum strain at break in tensile test can be obtained when certain combinations of SEBS-gMA and SEBS are used.
The encapsulation is followed by evaporation of the organic swelling solvent, during which the hydrophobic microsphere shrinks back to its near-original size, while the solute remains trapped within the microsphere (Figure 1). Figure 1 Routine method of encapsulation of a hydrophobic compound into a hydrophobic polymeric microsphere by swelling followed by evaporation of the swelling solvent.
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The effect of the functional groups on the encapsulation was evaluated by transmission electron microscopy.
The encapsulation was checked by FTIR ATR spectroscopy and thermogravimetric analyses.
The encapsulation was 21 μg of drug per 100 μg of SWCNTs as revealed by thermogravimetric analysis.
Therefore the encapsulation was specially designed for these detectors to have as little influence as possible on the radiation response.
Interestingly, we found that the encapsulation was stable at higher temperatures, while the guest molecules exchange dynamically at lower temperatures.
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