High performance aromatic polyimide fibers, 3. A polyimide synthesized from 3,3′,4,4′‐biphenyltetracarboxylic dianhydride and 2,2′‐dimethyl‐4,4′‐diaminobiphenyl

Abstract A new high molecular weight aromatic polyimide has been synthesized from 3,3′,4,4′‐biphenyltetracarboxylic dianhydride (BPDA) and 2,2′‐dimethyl‐4,4′‐diaminobiphenyl (DMB) in p ‐chlorophenol at elevated temperature. BPDA‐DMB fibers have been spun by a dry‐jet wet spinning method. The fibers were elongated and annealed at elevated temperatures above 400°C to achieve excellent mechanical properties. In seven times drawn fibers, the BPDA‐DMB molecule packs into a triclinic unit cell with dimensions of a = 2,10(2) nm, b = 1,523(8) nm, c = 4,12(7) nm, α = 61,2(6)°, β = 50,7(7)°, and γ = 78,9(6)° with the number of chain repeating units per unit cell ( Z ) is sixteen. After annealing at elevated temperatures, the fibers produce a small modification of the unit cell [ a = 2,048(6) nm, b = 1,529(5) nm, c = 4,00(2) nm, α = 62,1(3)°, β = 52,2(3)° and γ = 79,6(3)°]. By increasing the draw ratio, both the crystallinity and crystal orientation increase. The BPDA‐DMB fibers possess a decomposition temperature of 530°C in nitrogen and 500°C in air at a 5% weight loss when the heating rate is 10°C/min. After extensive drawing, BPDA‐DMB fibers exhibit a tensile strength of 3,3 GPa and a tensile modulus of over 130 GPa. Dynamic mechanical behavior of the fibers show both α (glass transition) and β (sub‐glass transition) relaxations above room temperature. The nature of the sub‐glass transition behavior is described as a noncooperative motion attributed to the diamine portion of the molecule. The activation energy for this relaxation in as‐spun fibers is 109 kJ/mol and increases to 144 kJ/mol by increasing the draw ratio. This β relaxation is found to be crystallinity dependent. The α transition is also suppressed by crystallinity which increases with draw ratio.