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Non-glycidyl ether epoxides

Although the first and still most important epoxide resins are of the glycidyl ether type, other epoxide resins have been commercially marketed in recent years. These materials are generally prepared by epoxidising unsaturated compounds using hydrogen peroxide or peracetic acid. [Pg.764]

Cyclic aliphatic epoxide resins were first introduced in the United States. Some typical examples of commercial materials are shown in Table 26.6. [Pg.764]

Compared with standard diglycidyl ether resins, the liquid cyclic aliphatic resins are paler in colour and have a much lower viscosity. Whereas in general the cyclic aliphatic resins react more slowly with amines, there is less difference with acid anhydrides. Table 26.7 provides data illustrating this point. [Pg.765]

Appearance pale straw liquid water white liquid white powder straw liquid [Pg.765]

Because of the compact structure of the cycloaliphatic resins the intensity of cross-linking occurring after cure is greater than with the standard diglycidyl ethers. The lack of flexibility of the molecules also leads to more rigid segments between the cross-links. [Pg.765]


Non-glycidyl ether epoxides Diluents, Rexibilisers tmd other Additives Structure and Properties of Cured Resins Applications... [Pg.924]

As with the other non-glycidyl ether resins the absence of the ether oxygen near to the epoxide group results in low reactivity with amine hardemers whereas activity with acid anhydride proceeds at reasonable rates. [Pg.767]

In addition to the diglycidyl ether based resins, there are also non-glycidyl ether based epoxide resins. These materials can usually be prepared by carrying out an epoxidisation reaction on an unsaturated compound using hydrogen peroxide or peracetic acid ... [Pg.106]

Non-crosslinked polystyrene with salen ligand Non-crosslinked polystyrene with onium salt residues Non-crosslinked polystyrene copolymerised with a chiral phosphine ligand 14,765 0.5-3.8" 0.7-2.3 CH2Cl2,THF, EtOAc, DMF DMF,DMSO,DMA, toluene, anisole, MeOH,MeCN, diglyme Asymmetric epoxidation Regioselective addition reaction of phenyl glycidyl ether with S-phenyl thioacetate Pt-catalysed asymmetric hydroformylation of olefins Precipitation (methanol) (r) Precipitation (diethyl ether) (r) [68] [142] [143]... [Pg.22]


See other pages where Non-glycidyl ether epoxides is mentioned: [Pg.764]    [Pg.764]    [Pg.764]    [Pg.764]    [Pg.764]    [Pg.764]    [Pg.303]    [Pg.161]    [Pg.142]    [Pg.183]    [Pg.164]    [Pg.63]    [Pg.63]    [Pg.120]    [Pg.135]    [Pg.135]    [Pg.210]    [Pg.309]    [Pg.310]    [Pg.314]    [Pg.412]    [Pg.424]    [Pg.425]    [Pg.582]    [Pg.756]    [Pg.792]    [Pg.903]    [Pg.903]    [Pg.181]    [Pg.165]   


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Epoxide resins non-glycidyl ether

Epoxides glycidyl ethers

Glycidyl ethers

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