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- W2067207456 abstract "The occurrence of a molecular complex between poly(ethylene oxide) (PEO) and p-dihydroxybenzene (hydroquinone) has been determined using different experimental techniques such as differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WAXD), and Fourier transform infrared spectroscopy (FTIR). From DSC investigations, an ethylene oxide/hydroquinone molar ratio of 2/1 was deduced. During the heating, the molecular complex undergoes a peritectic reaction and spontaneously transforms into a liquid phase and crystalline hydroquinone (incongruent melting). A triclinic unit cell (a = 1.17 nm, b = 1.20 nm, c = 1.06 nm, α = 78°, β = 64°, γ = 115°), containing eight ethylene oxide (EO) monomers and four hydroquinone molecules, has been determined from the analysis of the X-ray diffraction fiber patterns of stretched and spherulitic films. The PEO chains adopt a helical conformation with four monomers per turn, which is very similar to the 72 helix of the pure polymer. A crystal structure is proposed on the basis of molecular packing considerations and X-ray diffraction intensities. It consists of a layered structure with an alternation of PEO and small molecules layers, both layers being stabilized by an array of hydrogen bonds. The morphology of PEO–HYD crystals was studied by small angle X-ray scattering and DSC. As previously shown for the PEO–resorcinol complex, PEO–HYD samples crystallize with a lamellar thickness corresponding to fully extended or integral folded chains. The relative proportion of lamellae with different thicknesses depends on the crystallization temperature and time. Finally, the observed morphologies are discussed in terms of intermolecular interactions and chain mobility. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 1197–1208, 1999" @default.
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- W2067207456 date "1999-06-15" @default.
- W2067207456 modified "2023-10-16" @default.
- W2067207456 title "Morphology and crystal structure of the poly(ethylene oxide)-hydroquinone molecular complex" @default.
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- W2067207456 doi "https://doi.org/10.1002/(sici)1099-0488(19990615)37:12<1197::aid-polb1>3.0.co;2-c" @default.
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