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Triallyl isocyanurate, TAIC

Triallyl cyanurate (TAC), 2 265-267 Triallyl isocyanurate (TAIC), 2 265-267 Triallyl isocyanurate (TAIC), 5 204 Triaminotriethylamine molecular formula, 5 712t... [Pg.966]

Triallyl cyanurate (TAC) and triallyl isocyanurate (TAIC) are used as crosslinking agents for methacrylates and UP resins to improve heat and solvent resistance as well as thermooxidative stability. [Pg.74]

Curing of multicomponent systems consisting of BPA/DC, BMI and diallyl or triallyl esters (triallyl isocyanurate TAIC in particular) results in high Tgvalues. Such compositions consist of BPA/DC, BMI, TAIC, diallyl phthalate and dicumyl peroxide [127], BPA/DC prepolymer, BMI, TAIC, /erf.butyl peroxide, Zn acetate and DABCO [128] or BMI/trimethylene bis(4-aminobenzoate) prepolymer, BPA/DC, Zn octoate and TAIC [129]. [Pg.56]

Crosslinking agent, Triallyl isocyanurate (TAIC) 87, 398-401, 564, 773, 843, 849, 850 Crosslinking agent, Triallyl phosphate (TAP) 773, 823, 780... [Pg.1396]

The second kind is that of polyfunctional agents that could promote cross-linking (against chain scissioning). Trimethylol propane trimethacrylate (TMPTMA), trimethylol propane triacrylate (TMPTA) or triallyl isocyanurate (TAIC) belong to this category (Figure 9.3). [Pg.267]

Triallyl Isocyanurate (TAIC) Trimethylolpropane triacrylate (TMPTA) Trimethylolpropane trimethacrylate (TMPTMA)... [Pg.268]

Figure 7.24 Chemical structure of triallyl isocyanurate (TAIC). Figure 7.24 Chemical structure of triallyl isocyanurate (TAIC).
MBM), triallyl isocyanurate (TAIC), and triallyl cyanurate (TAC). These coagents provide a more stable free radical source by reacting with the free radicals formed from peroxide decomposition. These more stable free radicals formed by the combination of the decomposed organic peroxide and the coagent are then more likely to react with the HNBR polymer to form effective cross-links. An excellent study of the interaction of peroxides and coagents was conducted by Zeon Chemicals and shows the utility of statistical experimental design and response surface methods to provide a comprehensive picture of this interaction [8]. The compounds used in this... [Pg.107]

The mechanism of the reaction is first an abstraction of a hydrogen atom from the polymer chain, leading to the formation of a reactive radical site [6]. Then two polymer radicals can combine, which results in a polymer network. The network formed by those reactions is very irregular, fn order to improve the network the addition of compounds with multiple double bonds, for example, triaUyl cyanurate (TAG), triallyl isocyanurate (TAIC), trimethylol propane trimethacrylate (TMPTA), or ethylene dimethaciylate (EDMA) is necessary [6]. They are often referred to as activators. The effect is described as an addition to the radical site at the polymer chain and transfer of the radical to the activator. The network is formed by reaction of the transferred radical with another chain. [Pg.355]

In addition to identifying the type of peroxide used, these GC-MS techniques will also identify the type of co-agent (e.g., triallyl cyanurate (TAC) or triallyl isocyanurate (TAIC)) used. [Pg.27]

See other pages where Triallyl isocyanurate, TAIC is mentioned: [Pg.673]    [Pg.440]    [Pg.115]    [Pg.109]    [Pg.74]    [Pg.97]    [Pg.144]    [Pg.109]    [Pg.400]    [Pg.112]    [Pg.213]    [Pg.265]    [Pg.63]    [Pg.500]    [Pg.500]    [Pg.180]    [Pg.29]   
See also in sourсe #XX -- [ Pg.256 , Pg.265 ]



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Isocyanurate

Isocyanurates

Triallyl

Triallyl isocyanurate

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