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The fracture surface of adhesive failure at the Sup10HT specimen is very similar to the one at AF163-2 (smooth and flat).
At room temperature (RT) as well as at +80°C (HT), the fracture surface of adhesive failure is quite smooth and flat.
The modification treatment of the surface of adhesive paste consist of a porous causes densification on the surface of recycled coarse aggregates, resulting in higher density and lower absorption ratio compared to low-quality recycled aggregates as shown in Sect.
In summary, the presented analysis shows that owing to the reversible adsorption of the polymer chains onto the solid surface of adhesive particles (and therefore deceleration of chain relaxation), applied energy by external deformations during a fast flow can be stored in the stretched polymer chains, instead of being dissipated by their chain-scale Rouse-like relaxation.
Mature pollen grains collected from wild-type and amiR-atpv42b-1 flowers after anther dehiscence were spread onto the surface of adhesive tapes, and directly observed under a JSM-6360LV scanning electron microscope (JEOL) at an accelerating voltage of 20 kV.
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The out-of-plane stresses (σzz and τyz and τxz) and von-Mises stress (σe) components on mid-surface of adhesive layer are determined for different FRP composite plates made of Graphite/Epoxy (Gr/E), Glass/Epoxy (Gl/E) and Boron/Epoxy (B/E) materials with varied laminate stacking sequence viz.
Images of real engineering surfaces, surfaces of adhesive wear particles and trabecular bone were used for the tests.
Fibroblasts were next cultured within 3-D microwells and on 2-D patterned surfaces with similar surface areas of adhesive contact in order to clarify whether this actin filament assembly was a function of contact dimensionality.
Previous studies analyzing cell functions in response to both cell shape and surface area of adhesive contact were, to the best of our knowledge, exclusively limited to engineered 2-D surfaces.
A predictive understanding of the cellular response to physical cues necessitates the development of tools that allow for independent control of surface area of adhesive contact, substrate stiffness, and dimensionality.
The focus here was to determine how the surface area of adhesive contact and substrate rigidity differentially regulate actin cytoskeleton assembly in 2-D versus 3-D environments, and how this impacts cell phenotypes.
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