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This paper summarizes the results of experimental and numerical research focused on determination of the behavior and bond strength limits of what are currently the most widespread industrial glues used for anchor bonding.
Compared with single La2Zr2O7 coating, the bonding strength of the composite coatings was improved by 40%, owing to the anchor-bond of Al2O3 coating and La2Zr2O7 coating.
In the present research work, the strengthening the beams in shear have been carried out by using mechanically anchored bonded GFRP sheets.
The mixture of sulphuric acid and hydrogen peroxide can slightly etch the outer walls of CNTs, which benefits the anchoring bonding between the CNTs inner walls and Al matrix, and improves the interface stability, hence exploits the load bearing capacity of the CNTs inner walls and eventually leads to the effective load transfer between Al and CNTs.
At this point, the force in the sheet was developed by the first row of anchors and a combination of anchor and bond in the region surrounding the second row of anchors.
Research on systems to mechanically anchor externally bonded FRP strengthening systems has included anchor spikes, transverse wrapping, U-Anchors, longitudinal chases, FRP strips, plate anchors, bolted angles, cylindrical hollow sections, ductile anchorage systems, and other miscellaneous systems.
This may point to the role of specific binding in rigidifying the ligand pose in related binding pockets (in this case, the prevailing feature was the cation-π contact with anchoring hydrogen bond by the hydroxyl/thiol functional group).
The N-terminal Kac always formed the anchoring hydrogen bond with the conserved asparagine (N140).
Detailing varies between studies, but in general, the FRP sheets being anchored are bonded to the plates, which are either bolted or bonded to the concrete substrate.
Other shared but non-residue specific interactions include the anchoring hydrogen bonds at the hinge, and a key interaction with a main chain carbonyl group.
This mode is stabilized by suggesting alternative hydrogen bond anchor points in the ligand binding domain as potential leads for future drug design.
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