The range of surface coating methods

2006 ◽  
Author(s):  
P Shipway
Keyword(s):  
Surface Coating ◽  
Coating Methods

Structural Repair/Retrofit of Brick Masonry Walls

2021 ◽  
Vol 3 (1) ◽  
pp. 5-9
Author(s):  
R.H. Atkinson
Keyword(s):  
Nondestructive Evaluation ◽  
Surface Coating ◽  
Base Isolation ◽  
Masonry Wall ◽  
Masonry Structure ◽  
Brick Masonry ◽  
Seismic Resistance ◽  
Masonry Walls ◽  
Structural Repair ◽  
Coating Methods

The various methods presently available for the repair of brick masonry walls are reviewed. Particular attention is given to structural repair made necessary as the result of earthquake induced damage or retrofit measures to be applied to an existing masonry structure to increase seismic resistance. Among the techniques discussed are: crack injection with epoxy or resin, crack or void injection with a cement based grout, surface coating methods, base isolation, repointing or limited replacement of damaged elements and installation of steel reinforcing elements. Use of nondestructive evaluation methods to determine the initial damaged state and the condition of the repaired masonry wall will also be presented.

Antithrombin III Binding to Surface Immobilized Heparin and Its Relation to F Xa Inhibition

1987 ◽  
Vol 58 (04) ◽  
pp. 1064-1067 ◽  
Author(s):  
K Kodama ◽  
B Pasche ◽  
P Olsson ◽  
J Swedenborg ◽  
L Adolfsson ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Ionic Strength ◽  
Surface Coating ◽  
Antithrombin Iii ◽  
Lower Class ◽  
Biologically Active ◽  
High Affinity ◽  
Heparin Coating ◽  
Continuous Surface ◽  
Approximate Molecular Weight

SummaryThe mode of F Xa inhibition was investigated on a thromboresistant surface with end-point attached partially depoly-merized heparin of an approximate molecular weight of 8000. Affinity chromatography revealed that one fourth of the heparin used in surface coating had high affinity for antithrombin III (AT). The heparin surface adsorbed AT from both human plasma and solutions of purified AT. By increasing the ionic strength in the AT solution the existence of high and low affinity sites could be shown. The uptake of AT was measured and the density of available high and low affinity sites was found to be in the range of 5 HTid 11 pic.omoles/cmf, respectively Thus the estimated density of biologically active high and low ailmity heparm respectively would be 40 and 90 ng/cm2 The heparin coating did not take up or exert F Xa inhibition by itself. With AT adsorbed on both high and low affinity heparin the surface had the capacity to inhibit several consecutive aliquots of F Xa exposed to the surface. When mainly high affinity sites were saturated with AT the inhibition capacity was considerably lower. Tt was demonstrated that the density of AT on both high and low affinity heparin determines the F Xa inhibition capacity whereas the amount of AT on high affinity sites limits the rate of the reaction. This implies that during the inhibition of F Xa there is a continuous surface-diffusion of AT from sites of a lower class to the high affinity sites where the F Xa/AT complex is formed and leaves the surface. The ability of the immobilized heparin to catalyze inhibition of F Xa is likely to be an important component for the thromboresistant properties of a heparin coating with non-compromized AT binding sequences.

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