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Melting was possible due to the crystallization of stearate chains when LS was purified by precipitation.
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Meanwhile, the Al2O3/HfO2/Al2O3 trilayer structure on TiN-coated Si shows relatively rough interface and surface due to the crystallization of HfO2 and TiN interlayers or possible interfacial diffusion between various layers at 600°C. Figure 2 shows the XPS depth profile of Al2O3/HfO2/Al2O3 on TiN-coated Si by Ar ion etching.
This may be due to the crystallization conditions (pH, precipitants) or that a monomeric form has been crystallized.
The combined effects will enrich the remaining core liquid in Fe, due to crystallization at the center, and to snow Fe downward from above due to the crystallization at the surface.
The improvement in the quality of the film is due to the crystallization of the amorphous film during annealing.
Well-defined features appear for a calcination temperature of 450 °C, due to the crystallization of the zinc oxide.
Crystallization at 70°C followed by cooling to room temperature (two-step crystallization) also yielded two separate LS domains, due to the crystallization of PEO within the interfibrillar regions.
Due to the crystallization of the solvents, the remaining solution becomes more concentrated.
The imperfections that are generated in the lipid core due to the crystallization increase the drug load and reduce, although not completely, the drug expulsion [ 84, 85].
This is due to the crystallization conditions requiring high concentrations of ammonium sulfate (200 mM) that compete with fosfomycin for binding in the active site of the enzyme.
This is due to the low crystallization temperature (<200°C) of the GeSb8Te film.
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