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1.
Membranes (Basel) ; 11(4)2021 Apr 08.
Artigo em Inglês | MEDLINE | ID: mdl-33918006

RESUMO

A series of new poly(ethylene oxide) (PEO)-based copolyimides varying in hard segment structure are reported in this work as CO2 selective separation membranes. Their structural diversity was achieved by using different aromatic dianhydrides (4,4'-oxydiphthalic anhydride (ODPA), 4,4'-(hexafluoroisopropylidene)diphthalic anhydride (6FDA)) and diamines (4,4'-oxydianiline (ODA), 4,4'-(4,4'-isopropylidene-diphenyl-1,1'- diyldioxy)dianiline (IPrDA), 2,3,5,6-tetramethyl-1,4-phenylenediamine (4MPD)), while keeping the content of PEO (2000 g/mol) constant (around 50%). To get a better insight into the effects of hard segment structure on gas transport properties, a series of aromatic polyimides with the same chemistry was also studied. Both series of polymers were characterized by 1HNMR, FTIR, WAXD, DSC, TGA, and AFM. Permeabilities for pure He, O2, N2, and CO2 were determined at 6 bar and at 30 °C, and for CO2 for pressures ranging from 1 to 10 bar. The results show that OPDA-ODA-PEO is the most permeable copolyimide, with CO2 permeability of 52 Barrer and CO2/N2 selectivity of 63, in contrast to its fully aromatic analogue, which was the least permeable among polyimides. 6FDA-4MPD-PEO ranks second, with a two times lower CO2 permeability and slightly lower selectivity, although 6FDA-4MPD was over 900 times more permeable than OPDA-ODA. As an explanation, partial filling of hard domain free voids by PEO segments and imperfect phase separation were proposed.

2.
J Phys Chem A ; 113(8): 1481-8, 2009 Feb 26.
Artigo em Inglês | MEDLINE | ID: mdl-19170575

RESUMO

Two series of new aromatic polyimides were synthesized from 2,5-bis(4-aminophenyl)-1,3,4-oxadiazole and 2,5-diamino-pyridine and various diamidedianhydrides and dietherdianhydride via high-temperature polycondensation in N-methyl-2-pyrrolidinone. The structures of polymers were characterized by means of FTIR, (1)H NMR spectroscopy, and elemental analysis; the results showed an agreement with the proposed structure. The polymers exhibited high glass-transition temperatures (T(g) = 199-290 degrees C) and high thermal stability with decomposition temperatures (T(d)) in the range of 437-510 degrees C. The optical properties, that is, absorption and photoluminescence (PL) of synthesized polymers, were investigated in solution and in solid state as a blend with inert poly(methyl methacrylate) (PMMA). The polymers in solution emitted violet-blue light in the range of 417-453 nm depending on the polymer structure. The polymers containing pyridine rings in the backbone emitted light at a longer wavelength than polymers with oxadiazole units. The effect of solvent polarity on polymer emission was found. Additionally, the photoluminescence properties of the polymers before and after protonation with HCl were tested.

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