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Benzyl dimethylamine

The resin is more than 90% DGEBA with the remaining material predominately at n=1. The curing agent, nadic methyl anhydride (NMA), is manufactured by Allied Chemical. The catalyst was benzyl dimethylamine (BDMA). All materials were stored in a desiccator to minimize moisture pickup. [Pg.276]

Dicyandiamide is a true latent catalyst for epoxy resin curing. It is also considered to be the workhorse of one-component adhesives due to its ease of use, excellent performance properties, long shelf stability, and low toxicity. In certain admixtures with DGEBA, it has demonstrated a room temperature storage life in excess of 4 years. Dicyandiamide is usually added to the solid epoxy resin in concentrations of about 3 to 6 pph. It melts at about 150°C. Cures can be conducted in the range of 120 to 175°C but are very slow at the lower temperatures. As a result, it is common practice to add accelerators such as benzyl-dimethylamine (BDMA) and mono- or dichlorophenyl substituted ureas to these systems. [Pg.246]

The matrix material for the laminates for this investigation was a typical flame retardant epoxy resin system used in PWB technology. The epoxy resin was a brominated diglycidyl ether of bisphenol-A cured with dicyandiamide and catalyzed by benzyl dimethylamine. [Pg.380]

Ring-Metallation of Benzyl Dimethylamine, iV9iV-Dunethylamline and Benzyl Alcohol... [Pg.200]

Catalyst benzyl dimethylamine. Catalyst Arquad quarternary ammonium salt. ... [Pg.116]

Empol 1040 (a high-molecular-weight tricarboxy acid) 20pbw, and benzyl-dimethylamine (a cure catalyst) 1 pbw. This composite has room-temperature ultimate tensile strength of 690 MPa in the fiber direction and 210 MPa in the cross-fiber direction. It lends itself to wet layup techniques and can be finished to prevent stress corrosion. The material also has excellent properties in a cryogenic environment [ ]. [Pg.284]

Synthesis from sucrose ester/half-ester derivatives, monoepoxide and diisocyanate. Sucrose "penta"-soyate (the methanol insoluble fraction of the soap-free product) was reacted at 100°C for 4 hours with a mixture in xylene of 1 mole equivalent cyclic anhydride e.g., phthalic or tetrahydrophthalic anhydride and monoepoxide e.g., styrene oxide or Cardura E (the glycidyl ester of versatic acid), branched C9-Cfatty acids, in the presence of N-benzyl dimethylamine as catalyst. A faster rate was achieved with the phthalic system. The course of reaction between half ester carboxyl groups and epoxide groups was followed by acid value. About 90% reaction was achieved in all cases and to the product was added 1.0 mole toluene diisocyanate (the meucimum amount without gelation) and dibutyl tin dilaurate as catalyst. [Pg.194]

Benzyl cyanide) see Benzeneacetonitrile n-Benzyl dimethylamine (/V,/V-Dimethylbenzylamine) 103-83-3 C... [Pg.42]

V,/V-Dimethylaniline (DMA) (Dimethyl benzene) see Xylene (A,A-Dimethylbenzylamine) see n-Benzyl dimethylamine 121-69-7 T... [Pg.61]

Benzyl dimethylamine 2- (Diethylamino)ethanol N,N-Diethylhydroxylamine 2- (Dimethylamino)ethanol N,N-Dimethylcyclohexylamine N,N-Dimethylethylamine Promethazine hydrochloride Triallylamine Triethanolamine Triethanolamine >70%... [Pg.143]


See other pages where Benzyl dimethylamine is mentioned: [Pg.128]    [Pg.214]    [Pg.74]    [Pg.202]    [Pg.740]    [Pg.40]    [Pg.74]    [Pg.740]    [Pg.47]    [Pg.107]    [Pg.107]    [Pg.120]    [Pg.69]    [Pg.40]    [Pg.128]    [Pg.214]    [Pg.434]    [Pg.244]    [Pg.157]    [Pg.173]    [Pg.211]    [Pg.198]    [Pg.415]    [Pg.120]    [Pg.120]    [Pg.816]    [Pg.850]    [Pg.280]    [Pg.280]    [Pg.215]    [Pg.154]    [Pg.166]    [Pg.58]    [Pg.115]    [Pg.441]   
See also in sourсe #XX -- [ Pg.198 , Pg.415 ]

See also in sourсe #XX -- [ Pg.166 , Pg.363 ]

See also in sourсe #XX -- [ Pg.353 , Pg.354 ]




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