Process for preparing monomer complexes
View Patent ↗Disclosed are processes for preparing monomer complexes that include contacting 2,3,5,6-tetraminopyridine free base in water with 2,5-dihydroxy terephthalic acid dipotassium salt to form an aqueous mixture, and adjusting the pH of the aqueous mixture to within the range of from about (3) to about (5) to precipitate the monomer complex. Processes of polymerizing the monomer complexes, polyareneazoles, filaments and yarns are also disclosed.
1. A process for making a polyareneazole comprising:
contacting a molar excess in a ratio of at least 1.05 to 1 of a 2,3,5,6-tetraaminopyridine free base in water with a 2,5-dihydroxy terephthalic acid salt to form an aqueous mixture,
adjusting the pH of the aqueous mixture to within the range of from about 3 to about 5 to precipitate a monomer complex, and
polymerizing the monomer complex to form a polyareneazole having an inherent viscosity of at least about 25 dl/g at 30° C. at a polymer concentration of 0.05 g/dl in methane sulfonic acid.
2. The process of claim 1 wherein the molar ratio is in excess of about 1.075 to 1.
3. The process of claim 2 wherein the molar ratio is in excess of about 1.15 to 1.
4. The process of claim 1 wherein the pH is adjusted by adding orthophosphoric acid to the aqueous mixture.
5. The process of claim 1 , wherein the 2,5-dihydroxy terephthalic acid salt is an alkaline salt or an ammonium salt of 2,5-dihydroxy terephthalic acid.
6. The process of claim 5 , wherein the alkaline salt is 2,5-dihydroxy terephthalic acid dipotassium salt.
7. The process of claim 1 , wherein the pH of the aqueous mixture is adjusted to within the range of from about 4.3 to about 4.6 to precipitate the monomer complex.
8. The process of claim 1 , wherein the polyareneazole is poly(1,4-(2,5-dihydroxy)phenylene-2,6-pyrido[2,3-d:5,6-d′]bisimidazole).
9. A process for making a monomer complex comprising:
contacting 2,3,5,6-tetraminopyridine free base in water with 2,5-dihydroxy terephthalic acid dipotassium salt to form an aqueous mixture, and
adjusting the pH of the aqueous mixture to within the range of from about 3 to about 5 to precipitate the monomer complex,
wherein the molar ratio of the 2,3,5,6-tetraminopyridine free base to the 2,5-dihydroxy terephthalic acid dipotassium salt is in excess of about 1.05 to 1.
10. The process of claim 9 wherein the molar ratio is in excess of about 1.075 to 1.
11. The process of claim 10 wherein the molar ratio is in excess of about 1.15 to 1.
12. The process of claim 9 wherein the pH is adjusted by adding dilute orthophosphoric acid to the aqueous mixture.
13. The process of claim 9 , wherein the pH of the aqueous mixture is adjusted to within a range of from about 4.3 to about 4.6 to precipitate the monomer complex.