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The polymer matrix structure and the interface are strongly influenced by filler in semi-crystalline polymer composites because the fillers have the potential to nucleate the polymer crystallization.
Therefore, adding greater than 2 at.% Sn addition may dramatically affect the mechanical properties of Nb/Nb5Si3 composites because the solid solution (Nb,Ti SS has been shown to dominate the toughness of such materials.
Although the CP-SiCf/SiC composites also fractured in a non-brittle manner, their bending strength and fracture energy were much lower than the UD-SiCf/SiC composites because the SiC fibers aligned in 90° direction did not work for toughening and strengthening the SiCf/SiC composites.
Results showed that the CdS QDs had been successfully deposited onto the surface of npg-C3N4 with a good dispersion, and the two components formed stable composites because the CdS QDs can be anchored by the rolled and curled edges of npg-C3N4.
By careful examination of results (Fig. 9), we can observe that the conductivity of PANI/G composites is higher than counterpart PANI/MWCNTs composites because the surface area of graphene sheets is higher than CNTs.
In the early stage, CDM was built to study damage development for single-ply or laminate composites because the damage mechanisms of UD composites were relatively easy to quantify.
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The formation of zirconia and silicon dioxide from the oxidation of ZrB2/SiC improved the ablation resistance of the composites, because of the evaporation at elevated temperature, which absorbed heat from the flame and reduced the erosive attack to carbon fibers and SiC matrix.
The intermetallic compounds (Al13Fe4, AlFe3) were exhibited in the composites because of the reaction between SUS316L and Al during the SPS process.
Furthermore, the introduction of POM species can not only improve the light adsorption and redox activity of the TiO2, but also promote the photochemical stability of the plasmonic composites because of the relatively narrow band gap and low reversible redox potential of polyoxoanion.
The methanol permeability is suppressed in these Q-PVA/Q-chitosan composites because of the confined swelling in the presence of the fillers, shrinking the free volume size.
Such composites depart from usual elastic composites because (i) the properties of the constituents are highly contrasted, and (ii) the axial geometry of each fiber is continuous over a distance much larger than the Representative Elementary Volume size.
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