Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Polymers wetting

Lowering of the rubbery plateau modulus increases the compliance of the polymer making faster wet-out of a substrate possible. As a result, the PSAs show more aggressive tack properties. Provided the surface energy of the substrate allows for complete polymer wetting, a PSA with improved quick-stick and faster adhesion build will be obtained. [Pg.502]

PDMS based siloxane polymers wet and spread easily on most surfaces as their surface tensions are less than the critical surface tensions of most substrates. This thermodynamically driven property ensures that surface irregularities and pores are filled with adhesive, giving an interfacial phase that is continuous and without voids. The gas permeability of the silicone will allow any gases trapped at the interface to be displaced. Thus, maximum van der Waals and London dispersion intermolecular interactions are obtained at the silicone-substrate interface. It must be noted that suitable liquids reaching the adhesive-substrate interface would immediately interfere with these intermolecular interactions and displace the adhesive from the surface. For example, a study that involved curing a one-part alkoxy terminated silicone adhesive against a wafer of alumina, has shown that water will theoretically displace the cured silicone from the surface of the wafer if physisorption was the sole interaction between the surfaces [38]. Moreover, all these low energy bonds would be thermally sensitive and reversible. [Pg.689]

In an alternative approach, MIP membranes can be obtained by generating molec-ularly imprinted sites in a non-specific matrix of a synthetic or natural polymer material during polymer solidification. The recognition cavities are formed by the fixation of a polymer conformation adopted upon interaction with the template molecule. Phase inversion methods have used either the evaporation of polymer solvent (dry phase separation) or the precipitation of the pre-synthesised polymer (wet phase inversion process). The major difficulties of this method lay both in the appropriate process conditions allowing the formation of porous materials and recognition sites and in the stability of these sites after template removal due to the lack of chemical cross-linking. [Pg.70]

Example 7.8. Steinhart et al. [288] used the formation of a precursor film to fabricate nanotubes of polymers. For this purpose a porous alumina filter with cylindrical holes of defined size is brought into contact with a polymer melt (Fig. 7.17). This is done at a temperature, where the polymer is liquid, which is significantly above room temperature. The precursor film of the polymer wets the walls of the pores within, typically a few seconds. Before the pores are filled completely the filter is removed from the melt, the sample is cooled to room temperature, and the filter material is dissolved in potassium hydroxide. [Pg.136]

When the polymer wets the solid (0 = 0), polymer films are thermodynamically stable. For 0 > 0 the films are only metastable. When a thin, metastable film is heated above the glass transition temperature, holes start to form spontaneously, usually at small defects. The holes increase in size until only a network of polymer lines is formed which eventually breaks up into individual droplets (Fig. 7.19) [150], The film stability of films with a thickness of 1-100 nm is determined by long-range surface forces, mainly van der Waals forces [151,268, 294,295],... [Pg.138]

Acid toilet cleaners Fatty amine ethoxylates Fatty alcohol EO/PO co-polymers Wetting agents with acid stability... [Pg.10]

Figure 11-10 shows the laboratory recipe for the process. We first form solutions of the separate polymers. Then the active material is dispersed as droplets of the desired size in one of the polymer solutions. The two solutions are mixed and the pH is adjusted to let the polymers precipitate. The polymer wets the active drops and forms a weak layer around them. After cooling we cross-link the polymer with an excess of formaldehyde to obtain capsules with a good strength. These need to be filtered, and the process liquid washed out. The capsules can then be dried. [Pg.123]

Major new insights into the surface science of silicone materials were catalyzed by the work of deGennes, whose theories of polymer wetting and adhesion have inspired many to explore his provocative themes [7]. These explorations focused attention on the need for a polymeric material that is well characterized, liquid over a wide molecular weight range, with controlled molecular weight distribution and crosslinkable in a controlled fashion. Dimethylpolysiloxane is the best available candidate and has become central to a revolution in polymer surface physics. [Pg.474]

Synthionic. [W hooSA] Blodt polymer wetting agents, low foaming detergents, rinse aids, defoamers. [Pg.364]

Fire the laser by double clicking on the live video. Check polymer wetting. Observe the wetted polymer after the laser is fired. Firing the laser pulse causes the polymer to melt in the vicinity of the laser pulse. There should be a distinct clear circle surrounded by a dark ring (see Fig. 4) (see Note 14). [Pg.79]

The fluorenone polyesters have very good thermal and flame resistance and produce medium char yields in the 30-60% range. They do not drip at high temperatures and will not ignite under sustained external flame exposure. Fibers can be spun from solutions of these polymers (wet or dry). They can be blended with 10% ethylene terpoly-mer without much loss in heat resistance properties, althougih not much toughening is achieved. [Pg.338]

The literature on this topic is too vast to cover in detail. A few essential points will be mentioned, the reader being directed to books such as those by Kraus (1965h) and Stern (1967) for more comprehensive reviews. It will be assumed below that if the polymer wets the filler, extensive physical... [Pg.303]

Figure 12.44. Effect of water (2.83 wt %) on damping in glass-bead-epoxy systems Vj- = 0.3). Note the appearance of a new peak at 0 C in the presence of water a shoulder also has developed on the peak near 60 C (Manson and Chiu, 1973h). Dashed line represents unfilled polymer (wet). Figure 12.44. Effect of water (2.83 wt %) on damping in glass-bead-epoxy systems Vj- = 0.3). Note the appearance of a new peak at 0 C in the presence of water a shoulder also has developed on the peak near 60 C (Manson and Chiu, 1973h). Dashed line represents unfilled polymer (wet).
These ideas are farther developed in other articles, in particnlar. Surface characterization by contact angles - polymers. Wetting and spreading, Wetting and work of adhesion, Contact angles and interfacial tension. Pre-treatments of polymers and Pretreatment of metals prior to bonding. [Pg.516]

Mai et al. reported on the use of AA-g-PP in aluminum hydroxide-filled PP homopolymer [41] and found the graft polymer to increase filler to polymer wetting and adhesion, as shown by electron microscopy of fracture surfaces. In addition, they found not only significant increases in fiexural strength but also a loss in notched impact strength. The loss in impact strength was most marked at low to moderate filler levels and was least at the 60% level, typical for fire-retardant compounds. It was... [Pg.133]

Sometimes it is more convenient to rearrange this test procedure as follows. A strip of filter paper with the colorimetric reagent, a 1 % solution of 4-nitrobenzene diazofiuoroborate in methanol, is wetted. A glass stirring rod is heated to red hot and touched to the polymer. Wet filter paper is held directly over the polymer and glass rod to allow the fumes to contact the paper. The following characteristic colours develop TDI, reddish-brown MDI, yellow and NDI, violet. [Pg.336]

K Lelhg, G Ondracek. Glass and polymer wetting and adhesion. Glastech Ber Glass Sci Tech 89 357-367, 1996. [Pg.323]


See other pages where Polymers wetting is mentioned: [Pg.394]    [Pg.52]    [Pg.52]    [Pg.182]    [Pg.209]    [Pg.551]    [Pg.3641]    [Pg.230]    [Pg.589]    [Pg.144]    [Pg.79]    [Pg.86]    [Pg.20]    [Pg.254]    [Pg.254]    [Pg.254]    [Pg.254]    [Pg.254]    [Pg.254]    [Pg.1255]    [Pg.93]    [Pg.692]    [Pg.3159]    [Pg.4511]    [Pg.233]    [Pg.4272]    [Pg.92]    [Pg.522]    [Pg.220]    [Pg.369]   
See also in sourсe #XX -- [ Pg.2 , Pg.126 ]

See also in sourсe #XX -- [ Pg.2 , Pg.126 ]




SEARCH



© 2024 chempedia.info