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The resolution of ion mobility spectrometry (IMS) is of paramount importance for both post-ionization separations and structural characterization of ions that have similar ion-neutral collision cross sections; however, the instrumental features that lead to increased resolution also decrease ion transmission through the drift cell.
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X-ray absorption near edge structure at the Si K- and L3,2-edges exhibited composition-dependent phase separation and structural re-ordering of the Si-ncs and silicon nitride host matrix under different post-deposition annealing conditions and generally supported the trends observed in the PL spectra.
Details of their separation and structural elucidation will be reported elsewhere.
In addition, the XANES spectra provided evidence of composition-dependent phase separation and structural re-ordering of both the Si-ncs and the nitride host matrix upon annealing.
The model can be used as a design tool to study the effects of electrode separation and structural thickness on squeezed-film damping for different modes.
All the molecules were designed on the basis of hydrogen bond acceptors, carbonyl, fluoro groups with precise spatial separation and structural features of lipophilicity, positive charge at neutral pH and presence of aromatic rings.
All the molecules have been designed on the basis of the presence of specific recognition patterns consisting of hydrogen bond acceptors (or electron donors), carbonyl, chloro groups with precise spatial separation and structural features (lipophilicity, positive charge at neutral pH and presence of aromatic rings).
The conditions for enzymatic release, fluorescent labeling, separation and structural identification of N-glycans were the same as those reported previously [20], [21], [22].
Interfacing ion mobility spectrometry to mass spectrometry (IMS MS) has enabled mass spectrometric analyses to extend into an extra dimension, providing unrivalled separation and structural characterization of lowly populated species in heterogeneous mixtures.
This review discusses recent developments in analytical methods available for the sensitive separation, detection and structural characterization of heparin contaminants.
The following 3D morphometric parameters were calculated to describe the bone mass and microstructure: BMD, the percent bone volume (BV/TV), trabecular thickness (Tb.Th), trabecular number (Tb.N), trabecular separation (Tb.Sp), and structural model index (SMI).
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