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The reaction of isocyanate in pressure sensitive adhesive (PSA) films adhered on to various adherends having different surface tensions was monitored by depth profiling using attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy.
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The surface concentrations of deposited films were measured electrochemically and the film thicknesses were measured by depth-profiling using the atomic force microscope.
The deformation of coating system under nanoscratch loads was quantitatively analyzed by means of depth profiling using confocal laser scanning microscopy (CLSM).
This result is obtained by means of measuring depth profiles using X-ray photoelectron spectroscopy because these spectra yield not only the chemical composition of the interface but a detailed analysis provides information on the chemical states across the interface.
The depth profile used is shown in Fig. 7e.
Chemical composition of the samples was analyzed by acquiring their compositional depth-profiles using radio-frequency Glow Discharge Optical Emission Spectroscopy (rf-GDOES), while the microstructural properties were analyzed by X-ray absorption near edge spectroscopy (XANES) and Raman spectroscopy.
The diffusion study was carried out by depth profiling of Cu using time-of-flight secondary ion mass spectrometer (ToF-SIMS) after annealing treatment at various temperatures.
The correlation was performed by depth profiling of the indentation imprints using confocal laser scanning microscopy (CLSM) and atomic force microscopy (AFM).
The resulting depth profiles were used to indicate bioturbation rates by fitting them to a simple one-dimensional advection/diffusion model with a biodiffusivity that decreases with depth.
Porosity versus normalized depth profiles were used as guides to split zones (subzones) into 30 layers.
To clarify denominations in this work: A-Scan and depth profile are used interchangeably.
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