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Anhydride cure

Anhydride curing agents - corrosive, severe sensitizers dusts may be sensitizers high toxicity... [Pg.145]

Epoxy (Anhydride-Cured) Epoxy resins may be crosslinked with various anhydrides by using a tertiary amine accelerator and heat. These cured polymers generally have good chemical resistance especially to acids. [Pg.44]

A Kinetic Study of an Anhydride-Cured Epoxy Polymerization... [Pg.275]

The resin system selected to initiate these studies is a step-growth anhydride cured epoxy. The approach to the kinetic analysis is that which is prevalent in the chemical engineering literature on reactor design and analysis. Numerical simulations of oligomeric population density distributions approximate experimental data during the early stages of the cure. Future research will... [Pg.275]

Tanaka and Kakiuchi (6) proposed catalyst activation via a hydrogen donor such as an alcohol as a refinement to the mechanism discussed by Fischer (7) for anhydride cured epoxies in the presence of a tertiary amine. The basic catalyst eliminates esterification reactions (8). Shechter and Wynstra ( ) further observed that at reaction conditions BDMA does not produce a homopolymerization of oxiranes. [Pg.276]

Polystyrene insulation on magnet wire 0.49 Encapsulated with phthalic anhydride cured bisphenol A-epichlorohydrin epoxide (epoxy hot melt cast). Impregnated. [Pg.158]

Fig. 20. Plot of the exponent ras a function of the chain lengths between two branching points. Open symbols results by Colby et al. [118,119] for branched polyesters. The variation of this length was achieved by co-condensation of trifunctional monomers with increasing fraction of bifunctional units. Filled symbols refer to polydicyanurates (N Nj ), anhydride cured phenyl monoglycidyl ether with a small fraction of bisphenol A diglyci-dylether as crosslinker (N=8Nj ) and end-functionalized 3-arm polystyrene stars crosslinked by diisocyanate (N 40 N ). N denotes the number of repeating units between two branching points... Fig. 20. Plot of the exponent ras a function of the chain lengths between two branching points. Open symbols results by Colby et al. [118,119] for branched polyesters. The variation of this length was achieved by co-condensation of trifunctional monomers with increasing fraction of bifunctional units. Filled symbols refer to polydicyanurates (N Nj ), anhydride cured phenyl monoglycidyl ether with a small fraction of bisphenol A diglyci-dylether as crosslinker (N=8Nj ) and end-functionalized 3-arm polystyrene stars crosslinked by diisocyanate (N 40 N ). N denotes the number of repeating units between two branching points...
Figure 35 shows the result for the scaled forward scattering from randomly cross linked polyester chains which were prepared by anhydride curing of phe-nylglycidylether in the presence of bisphenol A diglycidylether [173-175]. The data could be fitted with Eq. (91) with values for g and which are collected in Table 5. [Pg.185]

Fig. 35. Plot of the reduced osmotic modulus from anhydride cured linear and cross-linked phenylglycidylethers [165,173-175]... Fig. 35. Plot of the reduced osmotic modulus from anhydride cured linear and cross-linked phenylglycidylethers [165,173-175]...
This paper rerports an investigation of the yield behavior of several amine and anhydride cured DGEBA resin systems. The Argon theory is used to assess the controlling molecular parameters from the experimental results. Such parameters are then compared with the known chemical structures of the resins. The mechanisms of plastic flow in thermoset polymers such as epoxies is demonstrated. [Pg.137]

The plastic deformation in several amine and anhydride cured epoxy resins has been studied. The experimental results have been reasonably interpreted by the Argon theory. The molecular parameters determined from the data based on the theory reflect the different molecular structures of the resins studied. However, these parameters are in similar enough range to also show the structural similarity in these DGEBA based systems. In general, the mechanisms of plastic deformation in epoxy resins below T are essentially identical to those in amorphouE thermoplastics. The yield stress level being related to the modulus that controls the intermolecular energy due to molecular deformation will, however, be affected by the crosslinks in the thermosets. [Pg.143]

The anhydride cured epoxies displayed a prominent carbonyl group of HHPA. The peak at 70 ppm was assigned to the products of the reacted epoxide groups. This peak was predominant in all four groups, piperidine-CTBN, MPDA, HHPA and NMA-DMBA. [Pg.101]

Tertiary amines are used to accelerate both amine and anhydride cures of epoxy resins (B-67MI11501). Certain heterocyclic amines have been used for this purpose, including pyridine and piperidine. In the case of anhydride cures, the use of an amine catalyst not only accelerates the cure, but also improves the thermal stability of the cured resin. [Pg.407]

The catalytic effect has been explained in terms of the activation of the anhydride by interaction with the amine to give a zwitterionic intermediate (47 Scheme 10) (B-68MI11501). Imidazoles have also been suggested as accelerators for anhydride cures (68USP3394105). A review of the patent literature (B-77MI11502) shows that several heterocyclic compounds are of interest as curatives for epoxy resins. [Pg.407]

The results of DSC studies on the anhydride cure of epoxy resins are summarised in Table 2. These studies have confirmed that the cure mechanism is complex. The early stages show autocatalytic features while the later stages are complicated by the effects of diffusion control. Intermediate stages of cure can show an approximation to overall kinetic orders of 1 or 2. In general the isothermal DSC data are easier to... [Pg.129]

Table 2. Summary of DSC kinetic results on anhydride cure... [Pg.130]

Reference to Table 14 will show the effect of increasing levels of APES on the compressive properties of an anhydride cured epoxide/silica microballoon foam, the APES being added on the resin content. The notation w/r (wt% resin) has been used in the tables. Both the yield stress and strain to failure increased steadily with increased silane content, with a corresponding increase in compressive modulus. At the 5 wt% level there was no real increase in yield stress but a marked increase in strain to failure, resulting in a lower modulus. However, at the 4% level the compressive strength was more than double that of the nonsilane control. [Pg.41]


See other pages where Anhydride cure is mentioned: [Pg.55]    [Pg.20]    [Pg.277]    [Pg.279]    [Pg.281]    [Pg.283]    [Pg.285]    [Pg.287]    [Pg.314]    [Pg.407]    [Pg.56]    [Pg.323]    [Pg.431]    [Pg.176]    [Pg.146]    [Pg.183]    [Pg.187]    [Pg.105]    [Pg.106]    [Pg.329]    [Pg.136]    [Pg.142]    [Pg.241]    [Pg.242]    [Pg.111]    [Pg.111]    [Pg.120]    [Pg.126]    [Pg.55]   
See also in sourсe #XX -- [ Pg.126 , Pg.128 , Pg.129 ]




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Curing anhydride

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