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Adhesives apphcations

In the automated lay-up system, each layer of veneer (with exception of the top surface veneer) passes under an automatic adhesive appHcation system. This may be a spray appHcation, a curtain coater, or an extmder, each of which is designed to apply a uniform adhesive spread on the upper face of each veneer. After all except the top veneer have been spread with adhesive and laid together, the top veneer is added. The me of the veneer—adhesive assembly at this point should be about 8%. [Pg.384]

The diverse nature of the cyanoacrylate adhesives appHcations illustrates vividly that there is no truly typical appHcation. The number of appHcations ia which these adhesives are used is being expanded daily as technological improvements continue to broaden their capabiUties. [Pg.179]

Peel tests are accompHshed using many different geometries. In the simplest peel test, the T-peel test, the adherends are identical in size, shape, and thickness. Adherends are attached at thek ends to a tensile testing machine and then separated in a "T" fashion. The temperature of the test, as well as the rate of adherend separation, is specified. The force requked to open the adhesive bond is measured and the results are reported in terms of newtons per meter (pounds per inch, ppi). There are many other peel test configurations, each dependent upon the adhesive appHcation. Such tests are well described in the ASTM hterature. [Pg.232]

G-5—G-9 Aromatic Modified Aliphatic Petroleum Resins. Compatibihty with base polymers is an essential aspect of hydrocarbon resins in whatever appHcation they are used. As an example, piperylene—2-methyl-2-butene based resins are substantially inadequate in enhancing the tack of 1,3-butadiene—styrene based random and block copolymers in pressure sensitive adhesive appHcations. The copolymerization of a-methylstyrene with piperylenes effectively enhances the tack properties of styrene—butadiene copolymers and styrene—isoprene copolymers in adhesive appHcations (40,41). Introduction of aromaticity into hydrocarbon resins serves to increase the solubiHty parameter of resins, resulting in improved compatibiHty with base polymers. However, the nature of the aromatic monomer also serves as a handle for molecular weight and softening point control. [Pg.354]

Although most aromatic modified C-5 resins are typically higher softening point resins, certain appHcations, such as adhesives, require lower softening points. Copolymerization of a C-8—C-10 vinyl aromatic fraction with piperylenes in the presence of a C-4—C-8 mono-olefin chain-transfer stream yields resins with softening points ranging from 0—40°C (44). A particular advantage of these Hquid resins is the fact that they eliminate the need for plasticizers or oils in some pressure sensitive adhesive appHcations. [Pg.354]

In order to increase the solubiUty parameter of CPD-based resins, vinyl aromatic compounds, as well as other polar monomers, have been copolymerized with CPD. Indene and styrene are two common aromatic streams used to modify cyclodiene-based resins. They may be used as pure monomers or contained in aromatic steam cracked petroleum fractions. Addition of indene at the expense of DCPD in a thermal polymerization has been found to lower the yield and softening point of the resin (55). CompatibiUty of a resin with ethylene—vinyl acetate (EVA) copolymers, which are used in hot melt adhesive appHcations, may be improved by the copolymerization of aromatic monomers with CPD. As with other thermally polymerized CPD-based resins, aromatic modified thermal resins may be hydrogenated. [Pg.355]

Terpolymers from dimethy]-a.-methy]styrene (3,4-isomer preferred)—a-methylstyrene—styrene blends in a 1 1 1 weight ratio have been shown to be useful in adhesive appHcations. The use of ring-alkylated styrenes aids in the solubiHty of the polymer in less polar solvents and polymeric systems (75). Monomer concentrations of no greater than 20% and temperatures of less than —20° C are necessary to achieve the desired properties. [Pg.356]

Heteroatom functionalized terpene resins are also utilized in hot melt adhesive and ink appHcations. Diels-Alder reaction of terpenic dienes or trienes with acrylates, methacrylates, or other a, P-unsaturated esters of polyhydric alcohols has been shown to yield resins with superior pressure sensitive adhesive properties relative to petroleum and unmodified polyterpene resins (107). Limonene—phenol resins, produced by the BF etherate-catalyzed condensation of 1.4—2.0 moles of limonene with 1.0 mole of phenol have been shown to impart improved tack, elongation, and tensile strength to ethylene—vinyl acetate and ethylene—methyl acrylate-based hot melt adhesive systems (108). Terpene polyol ethers have been shown to be particularly effective tackifiers in pressure sensitive adhesive appHcations (109). [Pg.357]

Substituted heat-reactive resins are most widely used in contact-adhesive appHcations and, to a lesser extent, in coatings (77,78) -butylphenol, cresol, and nonylphenol are most frequendy used. The alkyl group increases compatibiHty with oleoresinous varnishes and alkyds. In combination with these resins, phenoHcs reduce water sensitivity. Common appHcations include baked-on and electrical insulation varnishes, and as modifiers for baking alkyds, rosin, and ester gum systems. Substituted heat-reactive resins are not used for air-dry coatings because of theh soft, tacky nature in the uncured state substituted nonheat-reactive phenoHcs are the modifying resin of choice in this case. [Pg.303]

Aqueous dispersions are used in fiber bonding, paper coating, friction and abrasive appHcations, and laminates and wood bonding. PhenoHc dispersions improve the strength of latex-contact adhesive appHcations. Epoxy-modified phenoHc dispersions are prepared by dispersion of the phenoHc epoxy resin. The systems are used for baked primer appHcations and bonding requirements. Minimum baking conditions are 20 min at 150°C (25). [Pg.303]

Adhesives. High concentration (>10%) solutions of poly(ethylene oxide) exhibit wet tack properties that are used in several adhesive appHcations. The tackiness disappears when the polymer dries and this property can be successfully utilized in appHcations that require adhesion only in moist conditions. PEO is also known to form solution complexes with several phenoHc and phenoxy resins. Solution blends of PEO and phenoxy resins are known to exhibit synergistic effects, leading to high adhesion strength on aluminum surfaces. Adhesive formulations are available from the manufacturers. [Pg.344]

High purity 4-dodecylphenol is used to produce specialty surfactants by its reaction with ethylene oxide. The low color of high purity 4-dodecylphenol is important in this appHcation from a standpoint of aesthetics. 4-Dodecylphenol is also used to produce phenoHc resins which are used in adhesive appHcations and printing inks. 4-Dodecylphenol is also used as an epoxy curing catalyst where the addition of 4-dodecylphenol accelerates curing of the epoxy resin to a hard, nontacky soHd. [Pg.67]

Adhesives and Sealants. Most industrial adhesives contain surface active components and additives, and air entrainment during their mechanical appHcation can significantly reduce joint strength. Defoamers are usually formulated into adhesives to protect users against such difficulties. Additional benefits, such as improved uniformity of products, increased throughput and reduced labor costs can also result from the use of defoamers during adhesive appHcation. The footwear and nonwoven fabric industries are extensive users of defoamers in this way. [Pg.466]

The type of chloroprene polymers used is perhaps best illustrated by the variety of special products, designed for adhesive appHcations, that Du Pont has developed. These are described ia Table 8. Standard polymer grades are also often used, especially to modify adhesive properties and to reduce cost. [Pg.546]

Some grades of polyurethane and polyester copolymers are used as hot-melt adhesives. AppHcations include shoe manufacture and as an adhesive interlayer in coextmsion. [Pg.20]

Keywords Adhesive apphcations. Adhesive components. Joining technology. Primers, Risk minimization... [Pg.215]

Leong WH. Developing an underfill process for dense flip-chip apphcations. In Proc. 1996 lEEE/CPMT Int. Electronics Mfg. Technol Symp. Oct. 1996 10-17. lost EM, McNeiUy K, Sexton P. Silver flakes for state of the art conductive adhesive apphcations. Proc. Seventh Int. Microelectronics Conf. 1992 442-8. [Pg.73]

Instantly install and fix the glass after the glass adhesive apphcation. [Pg.416]


See other pages where Adhesives apphcations is mentioned: [Pg.379]    [Pg.231]    [Pg.255]    [Pg.356]    [Pg.357]    [Pg.357]    [Pg.358]    [Pg.518]    [Pg.260]    [Pg.8]    [Pg.5]    [Pg.86]    [Pg.449]    [Pg.468]    [Pg.470]    [Pg.522]    [Pg.318]    [Pg.117]    [Pg.544]    [Pg.546]    [Pg.19]    [Pg.362]    [Pg.8]    [Pg.379]    [Pg.19]    [Pg.362]    [Pg.190]    [Pg.700]    [Pg.992]    [Pg.992]    [Pg.272]   
See also in sourсe #XX -- [ Pg.539 ]




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Apphcations

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