Issue 56, 2018, Issue in Progress

Synthesis and characterization of new polyimides from diphenylpyrene dianhydride and ortho methyl substituted diamines

Abstract

Three new polyimides were synthesized via one-step polycondensation from 3,8-diphenylpyrene-1,2,6,7-tetracarboxylic dianhydride (DPPD) with two diamines with ortho methyl substitution (MBDAM and HFI) and one diamine without ortho substituents (BAPHF). The effect of diamine structure in DPPD based polyimides' physical, thermal, mechanical and gas transport properties has been studied. The polyimide structure was confirmed by FTIR and 1H NMR. All polymers show high thermal stability with decomposition temperatures above 493 °C, and glass transition temperatures above 336 °C. Changes in packing density of polyimide membranes were assessed by wide angle X-ray diffraction and correlated to fractional free volume FFV. Polyimides based on rigid DPPD dianhydride exhibited an improved gas permeability and selectivity when ortho methyl substituents are present in the diamine used for polyimide synthesis. DPPD-MBDAM polyimide showed the best gas productivity values with 565 barrer CO2 permeability and a selectivity of 16 for CO2/CH4.

Graphical abstract: Synthesis and characterization of new polyimides from diphenylpyrene dianhydride and ortho methyl substituted diamines

Article information

Article type
Paper
Submitted
13 Jul 2018
Accepted
29 Aug 2018
First published
12 Sep 2018
This article is Open Access
Creative Commons BY license

RSC Adv., 2018,8, 31881-31888

Synthesis and characterization of new polyimides from diphenylpyrene dianhydride and ortho methyl substituted diamines

R. Sulub-Sulub, M. I. Loría-Bastarrachea, J. L. Santiago-García and M. Aguilar-Vega, RSC Adv., 2018, 8, 31881 DOI: 10.1039/C8RA05991H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements