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Curing polyamides

The outdoor durability of epoxy bonded joints is very dependent on the type of epoxy adhesive, specific formulation, nature of the surface preparation, and specific environmental conditions encountered in service. The data shown in Fig. 15.19, for a two-part room temperature cured polyamide epoxy adhesive with a variety of fillers, illustrates the differences in performance that can occur due to formulation changes. Excellent outdoor durability is provided on aluminum adherends when chromic-sulfuric acid etch or other chemical pretreatments are used. [Pg.331]

Winterpoxy. [Pester Int L] Low tenq>. curing polyamide qx>xy primer and topcoat... [Pg.408]

Winterzinc. [Porter Int l.] Low tenq>. curing polyamide qx y organic zinc-rich ]ximer. [Pg.408]

In many adhesives formulations, the resin portion is the same or similar and what determines its properties is the hardener or catalyst that is used to cure the resin. Thus, depending on the hardener, epoxy adhesives may be referred to as amine-cured, anhydride-cured, polyamide-cured, or novolac-cured. Polyurethanes may be polyol-cured or hydroxypolyester-cured. [Pg.5]

Natural rubber, unvulcanized Natural rubber, cured Polyamide, Nylon 6 Polyamide, Nylon 6,6... [Pg.96]

Data from Reference 23. The aluminum adherend was 6061-T6 alloy the adhesive was two-part, room-temperature-curing polyamide epoxy. The conversion coating was Alodine 1200. [Pg.258]

The two-part epoxy adhesive, readily available in hardware stores or other consumer outlets, comes in two tubes. One tube contains the epoxy resin, the other contains an amine hardener. Common diamine room temperature epoxy curing agents are materials such as the polyamides, available under the trade name Versamid. These polyamides are the reaction products of dimer acids and aUphatic diamines such as diethylenetriamine [111-40-0] ... [Pg.232]

Nonvinyl polymers cured by TAG include polyamides (120), polyamide—polyurethane blends (121), caprolactone polymers (122), terephthalate polymers (123), epoxy resins (124), and acryflc epoxies (125). [Pg.88]

Pubhcations on curing polymers with TAIC include TEE—propylene copolymer (135), TEE—propylene—perfluoroaHyl ether (136), ethylene—chlorotrifluoroethylene copolymers (137), polyethylene (138), ethylene—vinyl acetate copolymers (139), polybutadienes (140), PVC (141), polyamide (142), polyester (143), poly(ethylene terephthalate) (144), sdoxane elastomers (145), maleimide polymers (146), and polyimide esters (147). [Pg.88]

Only a few commercial uses for TDA per se have been found. In epoxy curing appHcations, 2,4- I DA has been used as a component of a eutectic mixture with short chain aUphatic glycidal ether resins (46) as well as by itself (46,47) TDA (46) and single isomers (47) are also used as amine curatives. TDA can be used as a chain extender in polyurethanes (48,49). TDA is cited as a monomer in making aromatic polymers with unique properties, eg, amorphous polyamides (50), powdered polyamides (51), and low melting, whoUy aromatic polyamides (52). [Pg.239]

The bisphenol A-derived epoxy resins are most frequendy cured with anhydrides, aUphatic amines, or polyamides, depending on desired end properties. Some of the outstanding properties are superior electrical properties, chemical resistance, heat resistance, and adhesion. Conventional epoxy resins range from low viscosity Hquids to soHd resins. [Pg.363]

Polyamides provide RT cure of epoxy-terrninated resins as weU as flexibiHzation they are derived by reaction of dimerized vegetable oil fatty acids (dimer acids) with polyamines. [Pg.367]

For solvent-based ambient cure systems polyamides are often the hardeners of choice. For heat-cured systems, anhydrides are used to provide higher heat-resistance systems but at the expense of flexibiHty. [Pg.367]

Ambient-cure systems are often based on lower molecular-weight soHd epoxy resins cured with aUphatic polyamines or polyamides. Curing normally occurs at ambient temperatures with a working life (pot life) of 8—24 h, depending on the formulation. Epoxy—poly amine systems are typically used for maintenance coatings in oil refineries, petrochemical plants, and in many marine appHcations. Such coverings are appHed by spray or bmsh. These are used widely where water immersion is encountered, particularly in marine appHcations (see COATINGS, MARINE). [Pg.370]

Elevated temperatures are necessary for cure and the chemical resistance of the laminates is inferior to those from unmodified resins. Because of problems in handling, the polyamides have found only limited use with epoxy resins, mainly for coating and adhesive applications. [Pg.769]


See other pages where Curing polyamides is mentioned: [Pg.260]    [Pg.352]    [Pg.572]    [Pg.262]    [Pg.260]    [Pg.352]    [Pg.572]    [Pg.262]    [Pg.226]    [Pg.247]    [Pg.514]    [Pg.517]    [Pg.17]    [Pg.20]    [Pg.20]    [Pg.361]    [Pg.10]    [Pg.251]    [Pg.306]    [Pg.65]    [Pg.162]    [Pg.365]    [Pg.366]    [Pg.46]    [Pg.47]    [Pg.263]    [Pg.275]    [Pg.364]    [Pg.367]    [Pg.522]    [Pg.761]    [Pg.151]    [Pg.138]    [Pg.404]    [Pg.443]    [Pg.1077]   
See also in sourсe #XX -- [ Pg.84 ]




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