Aromatic polyamines

Pot life definition (source) 2-part epoxy polyamide 2-part epoxy polyamine (aliphatic) 2-part epoxy polyamine (aromatic) 3-part flexibilised 2-part toughened epoxy polyamine epoxy ... 

For solidification of epoxy oligomers, numerous substances are produced, such as aliphatic polyamines, aromatic amines, dicyanoamines and their derivatives, the anhydrides of di- and polycarboxylic acids, as well as a number of catalysts for solidification. These substances impart a large variety of technological properties to epoxy oligomers. Some properties of the main solidification agents produced worldwide are listed in Table 8 [229-231]. 

To cine an epoxy adhesive, the epoxy ring must first be opened before polymerization can occur. The epoxy ring may be opened by an acid anhydride or an amine. The four general types of curing agents are aliphatic polyamine, aromatic polyamine, aeid anhydride, and catalytic. 

Polyamine (Section 22 4) A compound that contains many ammo groups The term is usually applied to a group of nat urally occurring substances including spermine spermi dine and putrescme that are believed to be involved in cell differentiation and proliferation Polycyclic aromatic hydrocarbon (Section 118) An aromatic hydrocarbon charactenzed by the presence of two or more fused benzene rings... 

Other modifications of the polyamines include limited addition of alkylene oxide to yield the corresponding hydroxyalkyl derivatives (225) and cyanoethylation of DETA or TETA, usuaHy by reaction with acrylonitrile [107-13-1/, to give derivatives providing longer pot Hfe and better wetting of glass (226). Also included are ketimines, made by the reaction of EDA with acetone for example. These derivatives can also be hydrogenated, as in the case of the equimolar adducts of DETA and methyl isobutyl ketone [108-10-1] or methyl isoamyl ketone [110-12-3] (221 or used as is to provide moisture cure performance. Mannich bases prepared from a phenol, formaldehyde and a polyamine are also used, such as the hardener prepared from cresol, DETA, and formaldehyde (228). Other modifications of polyamines for use as epoxy hardeners include reaction with aldehydes (229), epoxidized fatty nitriles (230), aromatic monoisocyanates (231), or propylene sulfide [1072-43-1] (232). 

This reaction is reported to proceed at a rapid rate, with over 25% conversion in less than 0.001 s [3]. It can also proceed at very low temperatures, as in the middle of winter. Most primary substituted urea linkages, referred to as urea bonds, are more thermally stable than urethane bonds, by 20-30°C, but not in all cases. Polyamines based on aromatic amines are normally somewhat slower, especially if there are additional electron withdrawing moieties on the aromatic ring, such as chlorine or ester linkages [4]. Use of aliphatic isocyanates, such as methylene bis-4,4 -(cyclohexylisocyanate) (HnMDI), in place of MDI, has been shown to slow the gelation rate to about 60 s, with an amine chain extender present. Sterically hindered secondary amine-terminated polyols, in conjunction with certain aliphatic isocyanates, are reported to have slower gelation times, in some cases as long as 24 h [4]. 

Polythiosemicarbazide disulfide is the most efficient aliphatic polyamine disulfide for inhibiting the thermal oxidative breakdown of polypropylene, while polyimi-noaniline disulfide and polydiiminodiphenyloxide disulfide (Fig. 3) are the most efficient aromatic polyamine disulfides. In contrast to polyethylene, the thermal oxidative breakdown period increases as the concentration increases (Fig. 4), Depending on the concentration, the flow-melt index at 230°C increases at a lower rate than in the case of commercial stabilizer Santanox (Table 2)-... 

Hyperbranched aromatic polyesters, synthesis of, 116-118 Hyperbranched aromatic polymers, 286 Hyperbranched polyamine, synthesis of, 519-520... 

Branched polyesters contain oxalkylated primary fatty amines or oxalkyl-ated polyamines together with at least trivalent oxalkylated alkanol that is responsible for branching. The condensation is achieved with a dicarboxylic acid or a dicarboxylic acid anhydride [216]. In this way, branched polyoxyalkylene mixed polyesters are formed. Suitable solvents are water or organic solvents, such as methanol, isopropanol, butanol, or aromatic hydrocarbons (e.g., toluene, xylene). 

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

Aromatic polyamines react with sugar lactones to give heterocyclic compounds having an attached open-chain polyhydroxyalkyl substituent. Thus, treatment of aldonolactones with o-phenylenediamine afforded (117) 2-polyhydroxyalkylimidazoles (100). 

Of the primary monoamines, some, such as. aniline, o-toluidine, xylidine, are colourless liquids. Others, such as p-toluidine, pseudo-cumidine and the naphthylamines, are solids. They can be distilled without decomposition and are volatile with steam. In water they are rather sparingly soluble—a 3 per cent solution of aniline can be made. The di- and polyamines are usually solids, not volatile in steam and much more soluble in water than the monoamines. The amines are basic in character, but, as a result of the negative nature of the phenyl-group, the aromatic amines are considerably weaker bases than are the aliphatic amines. Consequently aqueous solutions of the (stoicheio-metrically) neutral aniline salts are acid to litmus because of the hydrolysis which they undergo. For the same reason a small amount of the free base can be extracted with ether from an aqueous solution of an aniline salt. (Test with a solution of hydrogen chloride in ether or, after evaporation of the ether, by the reaction with bleaching powder.)... 

Earlier in this chapter we discussed the enthalpies of formation of both aliphatic and aromatic monoamines. We now turn to polyamines where an obvious question is whether the effect of multiple amino groups on enthalpies of formation is simply the additive effects... 

Commercially available hyperbranched polymers are Polyglycerol (aliphatic polyether polyol) and Polyethylenimine (aliphatic polyamine) both from Hyperpolymers, Boltom (aliphatic polyesters) from Perstorp and Hybrane (aromatic polyester amide) from DSM. 

W. Black and J. Preston, eds., High-Modulus Wholly Aromatic Fibers, Dekker, New York (1973). R. A. Campbell, cd., Advances in Polyamine Research, Raven, New York (1978). 

Curing Agent mixture of aromatic di-and polyamines (metaphenylenediamine, 42%, methylenediaminiline, 42%,... 

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