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The viscosities of the pre-polymer blends are shown to be adequately low for self-healing, and exhibit a high ROMP reactivity to form cross-linked networks with enhanced thermal mechanical properties.
Transients upon exposure to four various gas blends are shown.
The infrared spectra of chitosan films with and without addition of 2% or 4% green tea extracts and their blends are shown in Figure 2.
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Without cross-linking, the toughness of the cast blends was shown to systematically decrease as the PTFE content was increased.
The tensile properties of PBT/ABS/MGE blends were shown to be relatively insensitive to PBT melt viscosity or reactive compatibilization.
The gelation mechanisms with and without phase separation were proposed and the effect of the two transitions on the structures of the ternary blends were shown by SEM pictures.
At last, the viscoelastic properties of PE/PA blends were shown to be significantly influenced by clay addition and content, through various mechanisms which involve changes in dispersed phase interfacial area, in blend morphology, in clay localization and in interphase structure.
The in vitro drug release profile of ceftriaxone sodium in enzyme-free simulated gastric fluid (SGF) followed by enzyme-free simulated intestinal fluid (SIF) from the CAP-coated calcium alginate beads prepared with various sodium alginate-polymer blends is shown in Fig. 6.
Whereas the use of biodiesel blends was shown to cause a reduction in PM mass emissions in the fine and ultrafine range on the order of 41 45%, there was a shift in the size distribution with greater formation of nanoparticulates as the blending percentage increased (Chien et al., 2009).
Cross sections of PPSU, PPSU/MWCNT and PPSU/FMWCNT blend are shown in Fig. 6d f.
The SEM micrographs of top surface of PPSU, PPSU/MWCNT and PPSU/FMWCNT blend are shown in Fig. 6a c.
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