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Diglycidyl ether of bisphenol F

Gamma irradiation curing of epoxy resins for structural adhesives — Radiation cure polymerization of commercial diglycidyl ether of bisphenol F epoxy resin has been achieved using Co-60 irradiation source, compounding the monomer with and onium salt catalyst [9],... [Pg.35]

Materials. The diglycidyl ether of bisphenol F (DGEBF), and N,N,N ,N -tetraglycidyl-4,4 -diaminodiphenylmethane (TGDDM), were received from Ciba Geigy. 4,4-diaminodiphenylmethane (DDM), was obtained fi om Aldrich. 4,4 -diaminodiphenylsulphone (DDS), was provided from Sigma Chemical. All chemicals were used without further purification. The monomers are presented in Figure 1. [Pg.261]

In epoxy materials, some of the conventional diglycidyl ether of bisphenol F has been replaced with functionalized vegetable oils, such as epoxidized linseed oil and epoxidized soybean oil. The materials have been cured using an anhydride based curing agent. [Pg.180]

Ingram, S.E., Liggat, J.J., Pethrick, R.A. Properties of epoxy nanoclay system based on diaminodiphenyl sulfone and diglycidyl ether of bisphenol F influence of post cure and structure of amine and epoxy. Polym. Int. 56, 1029-1034 (2007)... [Pg.47]

Diglycidyl ethers of bisphenol A (DGEBA or Bis A epoxies) Diglycidyl ethers of bisphenol F (DGEBF or Bis F epoxies) -low-molecular-weight epoxy coatings Epoxy phenol or cresol novolac multifunctional resins... [Pg.13]

Diglycidyl ether of bisphenol F (DGEBFyfunctionalized vegetable oils (FVOs) Acetone Cloisite SOB Homogeneous dispersion of clay filler Miyagawa et al. (2004a)... [Pg.114]

Figure 37 The front velocity as a function of the ethyleneglycol dimethacrylate mole fraction in the binary frontal polymerization with diglycidyl ether of bisphenol F. Adapted from Pojman, J. A. Griffith, J. Nichols, H. A. e-Polymers 2m, 13,1-7. ... Figure 37 The front velocity as a function of the ethyleneglycol dimethacrylate mole fraction in the binary frontal polymerization with diglycidyl ether of bisphenol F. Adapted from Pojman, J. A. Griffith, J. Nichols, H. A. e-Polymers 2m, 13,1-7. ...
Figure 4 shows the chemical formulae of other epoxy resins commonly used to prepare conductive adhesive compositions. Representative of approximately difunctional compounds are the diglycidyl ether of bisphenol-F (DGEBF) 18 and the diglycidyl ether of 1,3-dihydroxybenzene 19. Epoxy resins with a functionality higher than two are prepared by the reaction of l-chloro-2,3-epoxypropane 7 with polyfunctional starting materials. [Pg.358]


See other pages where Diglycidyl ether of bisphenol F is mentioned: [Pg.36]    [Pg.412]    [Pg.598]    [Pg.598]    [Pg.435]    [Pg.105]    [Pg.81]    [Pg.182]    [Pg.35]    [Pg.34]    [Pg.572]    [Pg.194]    [Pg.238]    [Pg.238]    [Pg.93]    [Pg.99]    [Pg.180]    [Pg.25]    [Pg.401]    [Pg.116]    [Pg.974]    [Pg.714]    [Pg.714]    [Pg.336]   
See also in sourсe #XX -- [ Pg.33 , Pg.77 ]

See also in sourсe #XX -- [ Pg.116 , Pg.122 ]




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BISPHENOL DIGLYCIDYL

Bisphenol

Bisphenol F diglycidyl ether

Bisphenol-F

Bisphenols

DIGLYCIDYL ETHER BISPHENOL

Diglycidyl ether

Diglycidyl ether of bisphenol-F epoxy

Ether of bisphenol

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