Synthesis of polyarylate by one-pot reaction using reactive distillation condensation polymerization starting from terephthalic/isophthalic acids, bisphenol A, and acetic anhydride mixture systems

Citation
T. Iwamoto et al., Synthesis of polyarylate by one-pot reaction using reactive distillation condensation polymerization starting from terephthalic/isophthalic acids, bisphenol A, and acetic anhydride mixture systems, KOBUNSH RON, 56(1), 1999, pp. 31-40
Citations number
15
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
KOBUNSHI RONBUNSHU
ISSN journal
03862186 → ACNP
Volume
56
Issue
1
Year of publication
1999
Pages
31 - 40
Database
ISI
SICI code
0386-2186(1999)56:1<31:SOPBOR>2.0.ZU;2-M
Abstract
We invented a new and effective process for the preparation of polyarylate using reactive distillation condensation polymerization. The concept of the reactive condensation polymerization came from the application of reactive distillation, which is usually used for the synthesis of eater compounds o f low molecular weight, to the condensation polymerization. Applying this n ew method to the one-pot reaction for the synthesis of polyarylate starting from terephthalic/isophthalic acids, bisphenol A, and acetic anhydride in the presence of a high boiling solvent such as biphenyl/diphenyl ether, we developed a simple process for manufacturing polyarylate. This one-pot reac tion for the synthesis of polyarylate consists of 4 unit processes that inc lude acetylation of bisphenol A with acetic anhydride, condensation polymer ization of bisphenol A diacetate with terephthalic/isophthalic acids by rem oving acetic acid in the presence of biphenyl/diphenyl ether, further conde nsation polymerization of the prepolymer by removal of acetic acid with bip henyl/diphenyl ether vapor, while feeding the biphenyl/diphenyl ether mixed solvent, and finally, evaporation of the biphenyl/diphenyl. ether from the molten polyarylate using a self-cleaning type twin screw extruder. The pol yarylate obtained from this one-pot synthesis showed goad mechanical proper ties which are comparable to those of the commercially available polyarylat e.