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M-PHENYLENE BISMALEIMIDE

PHENYLDIPHENYL see TBC750 PHENYL-DRANE see SPC500 N,N -(m-PHENYLENE)BISMALEIMIDE see BKL750 m-PHENYLENEBIS(METHYLAMINE) see XHS800 2,2 -(l,3-... [Pg.1836]

Reaction between a,a -(p-phenylene)-bis(N-phenylnitrone) and m-phenylene-bismaleimide gives an isoxazolidine polymer (86) that does not melt above 300°. 92 93 The polymer 87 obtained from the same nitrone and ethylene dimethacrylate has a lower melting point... [Pg.250]

Beilstein Handbook Reference) 1,3-Bismaleimidobenzene BRN 0249503 1,3-Dimale-imidobenzene m-Dimaleimidobenzene EINECS 221-112-8 HVA 2 HVA-2 curing agent Maleimide, N,N -(m-phenylene)di- m-PHDM m-Phenylenebismaleimide N,N -(m-Phenylene)bismaleimide 1,1 -(1,3-... [Pg.488]

One of the curing characteristics that we would like to control is reversion, which can occur in compounds containing natural rubber. There is more than one approach to reducing the amount of reversion. We can use sulfur donors or increase the ratio of accelerator concentration to sulfur concentration, or we could carry out the vulcanization at a reduced temperature for a longer period. However, these approaches give rise to effects that will have to be compensated. Another approach is use of additives such as certain bisimides, e.g., N,N -m-phenylene-biscitraconimide and N,N -/m-phenylene-bismaleimides (Datta et al., 1997, 1998 Datta and Ivan, 1995) or trialkoxysilylalkylpoly-sulfides such as bis-(3-triethoxisilylpropyl)-tetrasulflde (Tan and Wolff, 1985). [Pg.357]

PA-6 (100-0) or PA-6,66,610 terpolymer or PA-69/ chlorinated PE (0-100)/L101 RI Internal mixer at 225 °C/seiective solvent extraction/FTIR/mechanicai properties/ also blends containing m-phenylene bismaleimide or trimethyioipropane triacrylate + RI Coran and Patel 1983a... [Pg.558]

This chapter discusses the effect of addition of a reactive monomer, namely, m-phenylene bismaleimide (BMI) in the composite processing stage on the processing and end-use properties. Various particulate fillers were used for making composites and their properties were compared with respect to processing and end-use properties. [Pg.190]

See other pages where M-PHENYLENE BISMALEIMIDE is mentioned: [Pg.642]    [Pg.115]    [Pg.109]    [Pg.100]    [Pg.109]    [Pg.823]    [Pg.16]    [Pg.16]    [Pg.740]    [Pg.617]    [Pg.627]    [Pg.635]    [Pg.361]    [Pg.699]    [Pg.916]    [Pg.264]    [Pg.187]    [Pg.190]    [Pg.193]   


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M-phenylene

M-phenylene bismaleimid

M-phenylene bismaleimid

PHENYLENE BISMALEIMIDE

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