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Polymer of intrinsic microporosity (PIM-1) is characterized by a developed microporous structure. Needle-free Nanospider™ electrospinning of the PIM-1 solution with subsequent pyrolysis either under vacuum or in argon-hydrogen medium (7 vol% H 2) at 900–1200 °C results in PIM-1 based carbon nanofibers (CNF) self-supporting mats. The samples were thoroughly characterized by N 2 and CO 2 adsorption using the BET, BJH, Dubinin-Radushkevich (DR), NLDFT and GCMC methods, CO 2 uptake, and by Raman spectroscopy, elemental analysis, electrical conductivity, SEM. Since the N 2 adsorption is found to be inapplicable, the presence of microporosity in the CNF is confirmed by CO 2 adsorption (273 K) by the DR, NLDFT and GCMC methods. The CNF reach micropore specific surface area of 919 m2 g−1, micropore volume of 0.257 cm3 g−1 and CO 2 uptake of 4.01 mmol g−1, which is higher than for initial PIM-1. Pt/PIM-1 CNF self-supporting mat, was successfully tested as anode for HT-PEM fuel cell. Carbon dioxide adsorption method unveils PIM-1 carbon nanofiber microporosity exceeding PIM-1 microporosity. [Display omitted] • Electrospun PIM-1 carbon nanofibers are mostly ultramicroporous. • Microporosity characteristics of PIM-1 CNF exceed the ones for PIM-1. • PIM-1 CNF specific surface area reaches 919 m2 g−1 • CO 2 uptake for PIM-1 CNF is higher than for PIM-1. • Pt/PIM-1 CNF mats can be used as anodes in HT-PEM fuel cell. [ABSTRACT FROM AUTHOR]

High strength flame-resistant semi-ladder fibers of the "Lola" family (PNBI) have been obtained by an acid-free and more environmentally friendly method with controlled heating of precursor fibers in an inert atmosphere. The suggested two-step method consists in preparation of a prepolymer (PANI-O) in N-methylpyrrolidone. The prepared PANI-O dopes were additionally modified by introducing a certain part of a non-solvent (ethanol) to smooth the interdiffusion mass-transfer and prepare defectless precursor fibers. A detailed study of the thermal behavior of the PANI-O fibers by DSC and TGA shows that the maximum exothermic effect is observed at 320–370 °C, associated with formation of a ladder structure, i.e., transformation of the PANI-O into the PNBI-O. As a result, after the heat treatment, the flame-resistant PNBI "Lola" family fibers were obtained with an oxygen index of up to 83, tensile strength of ∼500 MPa, relative elongation of ∼5% and elastic modulus of ∼12 GPa. Flame-resistant semi-ladder PNBI fibers were obtained by acid-free environmentally friendly way through PANI-O prepolymer stage. [Display omitted] • PNBI fibers were obtained by an environmentally friendly way. • PNBI fibers were obtained through a PANI-O prepolymer stage. • Ethanol addition leads to defectless pre-polymer fibers by dry-wet spinning. • LOI of 83 for the H 3 PO 4 impregnated PNBI fibers was obtained. • Outstanding mechanical properties were recorded for the obtained PNBI fibers. [ABSTRACT FROM AUTHOR]

Semi-ladder high-molecular polynaphthoylenebenzimidazoles (PNBI) were synthesized through polyaminonaphtoyleneimide (PANI) formation and thermal cyclization at 350 °C. The structures of PANIs and PNBIs were confirmed by NMR, GPC and FTIR. Polymer films were obtained from PANI pre-polymer by solution-cast technique. After thermal cyclization, the PNBI films exhibit excellent mechanical properties: tensile strength of 95–174 MPa, Young's modulus of 1.5–2.4 GPa and elongation at break of 10–50%. The PNBIs are located near the upper bound of the 1991 Robeson diagram for O 2 /N 2 , H 2 /N 2 and H 2 /CH 4 gas pairs, while the PNBI with a hexafluoroisopropylidene bridge (PNBI-4) overcomes it for CO 2 /CH 4 , approaching the upper bound of the 2008 Robeson diagram. A peculiarity of the synthesized polymers is lower gas diffusion coefficients and higher gas solubility coefficients, which are close to polypyrrolones and PIM family polymers. The higher PNBI diffusion selectivity identifies them as organic molecular sieves, as confirmed by the specific surface area of PNBI-4, which is close to PIM-1. The data obtained allows to classify the studied PNBIs as unexpected PIM relatives. The synthesized PNBIs are polymer molecular sieves and, unexpectedly, belong to the polymer of intrinsic microporosity family. [Display omitted] • The PNBI gas transport properties have been obtained. • The studied PNBIs lie on the upper bounds of the 1991 Robeson diagrams. • PNBI-4 is higher than the upper bound on the 1991 Robeson diagram for CO 2 /CH 4. • PNBI-4 is approaching the upper bound of the 2008 Robeson diagram for CO 2 /CH 4. • PNBI-4 possesses a microporous structure similar to the one of PIM-1. [ABSTRACT FROM AUTHOR]