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Polyamine adduct

Dezincing, lead refining by, 14 754-755 DGEBA-aromatic polyamine adduct system, 10 416, 417. See also Diglycidyl ether of bisphenol A (DGEBA)... [Pg.257]

Properties Short-chain aliphatic poly amine Oxyalkylated short-chain poly amine Long-chain polyamine adduct Aromatic poly amine adduct Polyamide... [Pg.367]

Polyamine-adduct-cured coal tar 71 125-500 4 h 6h Two components, high build, cures down to —5°C when substrate ice-free... [Pg.96]

Polyamines. Aliphatic polyamines cure epoxy resins via their epoxy groups at ambient temperature. Excess amine is generally prereacted with the epoxy resin to form a polyamine adduct. Amines react with monomeric or dimeric fatty acids to form polyamidoamines. Polyamine-adduct-cured epoxy resins have a high chemical resistance. Polyamidoamine-cured epoxy resins exhibit good adhesion and flexibility. [Pg.71]

Chem. Descrip. Aliphatic polyamine adduct (80%) in water Uses Hardener for solid epoxy resin disps. or emulsified liq. resins for use in water-reducible coatings on metallic substrates, corrosion-protection primers (in combination with Beckopox EH 386w)... [Pg.107]

Chem. Descrip. Polyamine adduct Uses Epoxy curing agent for coatings... [Pg.324]

Chem. Descrip. Aq. microgel disp. of polyamine adduct in water and ethylene glycol monopropyl ether... [Pg.334]

Nikolic, G. Zlatkovic, S. Cakic, M Cakic, S. Lacnjevac, C Rajic, Z. (2010). Fast Fourier Transform IR Characterization of Epoxy GY Systems Crosslinked with Aliphatic and Cydoahphatic EH Polyamine Adducts. Sensors, Vol.lO, No.l, 0anuary 2010), pp. 684-696, ISSN 1424-8220. [Pg.282]

Fig. 6. Chemical resistance of a DGEBA—aromatic polyamine adduct. Post-cured substrate sandblasted mild steel film thickness 300-350 /zm cure 7 d at 20°C. D Degraded resistant. Fig. 6. Chemical resistance of a DGEBA—aromatic polyamine adduct. Post-cured substrate sandblasted mild steel film thickness 300-350 /zm cure 7 d at 20°C. D Degraded resistant.
The hardeners for cold-setting systems include aliphatic and cycloaliphatic amines and polyamines, adducts of polyamines and epoxy resins, phenol-amine combinations, and condensates of polyamines and dimerized fatty acids (polyaminoamides). Whereas amine hardeners must be used in a stoichiometric ratio to the reactive epoxy groups, polyaminoamides may be overdosed to a certain extent and thus used to elasticize the adhesive resin. [Pg.36]

In order to address the issues of volatility and toxicity associated with low MW aliphatic amines, different chemical modifications are adopted to derive amine cross-linkers with higher MW and hence lower volatility. Some commercially important derivatives are polyamine adducts, amine terminated polyamides, amidoamines, Mannich bases, and phenalkamines. [Pg.104]


See other pages where Polyamine adduct is mentioned: [Pg.367]    [Pg.367]    [Pg.257]    [Pg.269]    [Pg.285]    [Pg.286]    [Pg.285]    [Pg.286]    [Pg.367]    [Pg.367]    [Pg.74]    [Pg.75]    [Pg.934]    [Pg.934]    [Pg.2703]    [Pg.2726]    [Pg.2753]    [Pg.13]    [Pg.104]    [Pg.104]    [Pg.104]   
See also in sourсe #XX -- [ Pg.104 ]




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