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In this work a detailed analysis of the nature of the L10 ordering transition in confined nanoparticle geometries is presented based upon results obtained for surface concentrations, order parameter profiles and calculated canonical distribution functions.
We used simulated concentrations in the first model layer for surface concentrations, and used annual average concentrations for PM2.5 and the maximum 6-month average of the 1-hr daily maximum for ozone, consistent with the epidemiology studies.
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Applications of satellite observations are discussed for case studies of specific events, for estimates of surface concentrations, and to improve emission inventories of trace gases and aerosols.
At steady state, the incorporation of incident atoms does not change the ratio of surface concentrations for matrix atoms.
The wafers were subsequently analyzed for Cr surface concentrations using Rutherford backscattering.
The neutron reflectometry data for two surface concentrations of the block copolymer (0.6 and 1.2 mg m−2) were analysed using the kinematic approximation.
No polyethylene oxide was desorbed from the interface, the surface concentration was identical for both surface concentrations of polymethyl methacrylate and of the same value as that obtained in the absence of a spread polymethyl methacrylate film.
Neutron reflectivity was measured for both surface concentrations using three different sets of neutron scattering length density contrast conditions, and models for the distribution of PEG and lysozyme content in the layers were obtained by simultaneous regression of all contrast condition data sets.
The purpose of this manuscript is to present a visible light polymerization-based amplification system that uses the biofunctional photoinitiator streptavidin-eosin isothiocyanate (SA-EITC) as a new method for quantifying surface concentrations of biotinylated nucleic acid targets.
Here, we develop a nonenzymatic method for quantifying surface concentrations of labeled DNA targets by coupling regulated amounts of polymer growth to complementary biomolecular binding on array-based biochips.
The model of mass transport taking into account mobile chemical interactions in the Nernst-type diffusion layer is used for the estimation of surface concentration of Sn II) and Co II) citrate complexes.
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