Sample records for biphenyldiamine

  1. High Flow Addition Curing Polyimides (United States)

    Chuang, Kathy C.; Vannucci, Raymond D.; Ansari, Irfan; Cerny, Lawrence L.; Scheiman, Daniel A.


    A new series of high flow PMR-type addition curing polyimides was developed, which employed the substitution of 2,2'-bis (trifluoromethyl) -4,4'-diaminobiphenyl (BTDB) for p-phenylenediamine (p -PDA) in a PMR-IL formulation. These thermoset polyimides, designated as 12F resins, were prepared from BTDB and the dimethyl ester of 4,4'- (hexafluo- roisopropylidene) -diphthalic acid (HFDE) with either nadic ester (NE) or p-aminostyrene (PAS) as the endcaps for addition curing. The 12F prepolymers displayed lower melting temperatures in DSC analysis, and higher melt flow in rheological studies than the cor- responding PMR-11 polyimides. Long-term isothermal aging studies showed that BTDB- based 12F resins exhibited comparable thermo-oxidative stability to P-PDA based PMR-11 polyimides. The noncoplanar 2- and 2'-disubstituted biphenyldiamine (BTDB) not only lowered the melt viscosities of 12F prepolymers, but also retained reasonable thermal sta- bility of the cured resins. The 12F polyimide resin with p-aminostyrene endcaps showed the best promise for long-term, high-temperature application at 343 C (650 F).


    Institute of Scientific and Technical Information of China (English)

    Zhi-hao Shen; Alexander J. Jing; Shi Jin; Hua-bin Wang; Frank W. Harris; Stephen Z. D. Cheng


    A series of "hairy-rod" polyimides, BBPA(n), with multiple alkyl side chains was prepared from 3,3′,4,4′biphenyltetracarboxylic dianhydride (BPDA) and 4,4′-biphenyldiamine substituted in the 2,2′-positions with benzoate, which was substituted in the 3,4,5-positions with ether side chains of varying lengths. The number of the methylene units, n, in these alkyl side chains were in even numbers ranging from 8 to 18. Combining techniques of one-dimensional (1D) and 2D wide angle x-ray diffraction, 1D small angle X-ray scattering, differential scanning calorimetry experiments, it was found that this series of "hairy-rod" polyimides possess a micro-phase separation between the backbones and side chains. This led to the formation of ordered structures in two different lengthscales, of which both are hexagonal packing: one is attributed to the alkyl side chains on the sub-nanometer scale, and another is for the whole polymer chains on the nanometer scale. The development of the hexagonal structure on the sub-nanometer scale was critically dependent upon the lengths of the alkyl side chains. Three relaxation processes were captured by dynamic mechanical analysis, i.e., segmental motion of the backbones, α, the melting of the side chain crystals, β1, which exits only for the materials with longer side chains (n = 18,16); and the subglass relaxation of side chains,β2. The peak relaxation temperature of the α process decreased with increasing the length of side chains, while the one of theβ2 process increased. The activation energy of the αrelaxation was relatively independent on the length of side chain, whereas, β2 process showed the increasing of activation energy with increasing the length of side chains.