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Thickness of dielectric shell around metal core with diameter D. The core volume fraction.
In many long-term clinical studies, cast metal posts have shown good adaptability to the configuration and angulation of root canal walls as well as an ideal connection to the metal core, with no possibility of separation [1].
Biofilm adhesiveness - a measure for biostabilization capacity - was determined with a modified magnetic particle induction (MagPI) system (Figure 6), e.g. using an improved electromagnetic inductor containing a highly magnetisable μ metal core with low remanence.
The results of this study indicate that the loss of reactivity in the metal core with burnup is less than half that of a MOX core and its breeding ratio remains nearly constant.
The results of extended X-ray absorption fine structure at Pd K and Pt LIII edges showed that Pt was surface-enriched or anchored on the Pd metal core with an increase of the Pt content.
Muskens and co-workers [10] derived a simple equation for measuring thickness of dielectric shell (h) around metal core with weakly dispersed imaginary part of dielectric function in core-shell systems embedded in dielectric medium in a quasi-static regime, which for usual dielectric shells like water and glass is expressed as: 1 − a ≃ Δ λ SPR h Δ λ SPR max (8).
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In this metamaterial, which we call metaconcrete, the stone, sand, and gravel aggregates of standard concrete are replaced with spherical inclusions consisting of a heavy metal core coated with a soft outer layer.
Lately, core-shell nanostructures of metal core covered with protective oxide layer have been proposed as good SERS substrates for high-temperature Raman sensing [2, 3, 5, 8 10].
We report a core shell approach that combines silver nanoparticles as the metal core component with Eu Lu2O3 as the phosphor shell component.
The obtained results indicate that the investigated additives are either actively incorporated into the formed CEI layer (in case of Al, Ti as metal core) or interacting with decomposition products (in case of B as metal core) resulting in lower charge-transfer impedance and hence improved long-term cycling behavior.
In order to further study the O2-binding properties of ALKBH4, we followed the optical changes of the Fe(II) metal core upon interaction with the dioxygen analogue NO, as performed in the EPR experiments reported earlier.
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