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Substrate strength

Post-crosslinkable and substrate reactive polymers are widely used to Improve water and solvent resistance, strength, substrate adhesion and block resistance In binders, adhesives and coatings. The surprisingly rich chemistry of a new class of functional monomers (eg. 1 and 2) related to standard amide/aldehyde (amlnoplast) condensates, but which eliminate aldehyde emissions, was elucidated by monomeric model and mechanistic studies and discussed In the preceeding paper (1). Results with these monomers In copolymer systems are reported here. [Pg.467]

Since the adsorption of a protein to a surface is basically a reversible process, changes of pH, ionic strength, substrate concentration, temperature, etc. may detach the biomolecule from the carrier (Carr and Bowers, 1980). In addition to the simplicity of the procedure, the advantage of adsorptive immobilization is that it does not need nonphysiologi-cal coupling conditions or chemicals potentially impairing enzyme or cell functions. An activity loss is therefore seldom observed. [Pg.51]

Method Membrane thickness Operation Economy Composition control Adhesion strength Substrate requirement... [Pg.116]

Besides the material based characteristics, the difference of density of the used particle/substrate combination is a very important criterion. The difference of density influences the contrast of the radiographic tests. Tungsten carbides were used as mechanically resistant particles and titanium based alloys as substrate. The substrate material is marked by an advantageous relation of strength to density. This material is often used in aeronautics, astronautics, and for modification of boundary layers. The density of tungsten carbide (15.7 g/cm ) is about 3.5 times higher than the density of titanium (4.45-4.6 g/cm ). [Pg.543]

Molecular adsorbates usually cover a substrate with a single layer, after which the surface becomes passive with respect to fiirther adsorption. The actual saturation coverage varies from system to system, and is often detenumed by the strength of the repulsive interactions between neighbouring adsorbates. Some molecules will remain intact upon adsorption, while others will adsorb dissociatively. This is often a frinction of the surface temperature and composition. There are also often multiple adsorption states, in which the stronger, more tightly bound states fill first, and the more weakly bound states fill last. The factors that control adsorbate behaviour depend on the complex interactions between adsorbates and the substrate, and between the adsorbates themselves. [Pg.294]

The balance between these different types of bonds has a strong bearing on the resulting ordering or disordering of the surface. For adsorbates, the relative strength of adsorbate-substrate and adsorbate-adsorbate interactions is particularly important. Wlien adsorbate-substrate interactions dominate, well ordered overlayer structures are induced that are arranged in a superlattice, i.e. a periodicity which is closely related to that of the substrate lattice one then speaks of commensurate overlayers. This results from the tendency for each adsorbate to seek out the same type of adsorption site on the surface, which means that all adsorbates attempt to bond in the same maimer to substrate atoms. [Pg.1758]

As we have seen the nucleophile attacks the substrate m the rate determining step of the Sn2 mechanism it therefore follows that the rate of substitution may vary from nucleophile to nucleophile Just as some alkyl halides are more reactive than others some nucleophiles are more reactive than others Nucleophilic strength or nucleophilicity, is a measure of how fast a Lewis base displaces a leaving group from a suitable substrate By measuring the rate at which various Lewis bases react with methyl iodide m methanol a list of then nucleophihcities relative to methanol as the standard nucleophile has been compiled It is presented m Table 8 4... [Pg.337]

Acryhc modifiers for cement impact strength and adhesion to substrates are discussed in reference 211. Both water-soluble acryhc and acryhc emulsion polymers are used in the ceramic industry as temporary binders, deflocculants, and additive components in ceramic bodies and glazes (212) (see Ceramcs). [Pg.172]

The cured polymers are hard, clear, and glassy thermoplastic resins with high tensile strengths. The polymers, because of their highly polar stmcture, exhibit excellent adhesion to a wide variety of substrate combinations. They tend to be somewhat britde and have only low to moderate impact and peel strengths. The addition of fillers such as poly (methyl methacrylate) (PMMA) reduces the brittleness somewhat. Newer formulations are now available that contain dissolved elastomeric materials of various types. These mbber-modifted products have been found to offer adhesive bonds of considerably improved toughness (3,4). [Pg.178]

Lasdy, the importance of electroceramic substrates and insulators should not be overlooked. Here one strives to raise the breakdown strength by eliminating the interesting conduction mechanisms just described. Spark plugs, high voltage insulators, and electronic substrates and packages are made from ceramics like alumina, mullite [55964-99-3] and porcelain [1332-58-7]. [Pg.309]

Fig. 26. Qualitative compatison of substrate materials for optical disks (187) An = birefringence IS = impact strength BM = bending modulus HDT = heat distortion temperature Met = metallizability WA = water absorption Proc = processibility. The materials are bisphenol A—polycarbonate (BPA-PC), copolymer (20 80) of BPA-PC and trimethylcyclohexane—polycarbonate (TMC-PC), poly(methyl methacrylate) (PMMA), uv-curable cross-linked polymer (uv-DM), cycHc polyolefins (CPO), and, for comparison, glass. Fig. 26. Qualitative compatison of substrate materials for optical disks (187) An = birefringence IS = impact strength BM = bending modulus HDT = heat distortion temperature Met = metallizability WA = water absorption Proc = processibility. The materials are bisphenol A—polycarbonate (BPA-PC), copolymer (20 80) of BPA-PC and trimethylcyclohexane—polycarbonate (TMC-PC), poly(methyl methacrylate) (PMMA), uv-curable cross-linked polymer (uv-DM), cycHc polyolefins (CPO), and, for comparison, glass.
The most commonly used reinforcement for high pressure decorative and industrial laminates is paper (qv). The strong substrate layers, or filler, are kraft paper. Kraft is a brown paper made from a sulfate pulp process (8). It consists of both short cellulose fibers from hardwoods and long fibers from conifers. The long fibers impart most of the wet strength required for resin saturation processes. [Pg.532]

Other reinforcements that may be used in the substrate layers of decorative laminates and throughout the stmcture of industrial laminates are woven fabrics of glass or canvas and nonwoven fabrics of various polymeric monofilaments such as polyester, nylon, or carbon fibers. Woven and nonwoven fabrics tend to be much stronger than paper and have much more uniform strength throughout the x—y plane. They greatly enhance properties of laminates such as impact and tear strength. [Pg.532]

Finishing and Fabrication. Since laminates are normally pressure cured in flat-bed presses and pHes overextend the plates, laminates have rough or uneven edges when removed from the press. These edges are sawed off and the back of the laminate is often sanded to improve the strength of subsequent bonding to various substrates. [Pg.534]


See other pages where Substrate strength is mentioned: [Pg.309]    [Pg.249]    [Pg.309]    [Pg.113]    [Pg.29]    [Pg.137]    [Pg.137]    [Pg.302]    [Pg.306]    [Pg.309]    [Pg.249]    [Pg.309]    [Pg.113]    [Pg.29]    [Pg.137]    [Pg.137]    [Pg.302]    [Pg.306]    [Pg.456]    [Pg.1708]    [Pg.2413]    [Pg.605]    [Pg.64]    [Pg.242]    [Pg.393]    [Pg.441]    [Pg.490]    [Pg.354]    [Pg.323]    [Pg.70]    [Pg.358]    [Pg.250]    [Pg.28]    [Pg.92]    [Pg.94]    [Pg.234]    [Pg.251]    [Pg.134]    [Pg.135]    [Pg.136]    [Pg.137]    [Pg.204]    [Pg.153]   
See also in sourсe #XX -- [ Pg.165 ]




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