Membrane comprising self-assembled block copolymer and method of making same by mixing casting (ib)
A diblock copolymer, selected technology, used in chemical instruments and methods, membranes, membrane technology, etc.
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[0121] The homopolymers formed during the preparation of the diblock copolymers of the present invention, as well as the diblock copolymers, can be characterized by any known technique for their molecular weight and molecular weight distribution. For example, MALS-GPC technology can be used. This technique uses mobile phase elution, and by means of a high pressure pump, the polymer solution is passed through a column stack packed with stationary phase. The stationary phase separates the polymer sample according to chain size and then detects the polymer by three different detectors. A series of detectors can be used, for example, an ultraviolet detector (UV-detector), followed by a multi-angle laser light scattering detector (MALS-detector), in turn, followed by a refractive index detector (RI-detection). device). The UV-detector measures the light absorption of the polymer at a wavelength of 254 nm; the MALS-detector measures the scattered light of the polymer chains relati...
Embodiment 1
[0164] This example describes some of the materials used in the preparation of monomers and polymers
[0165] Maleimide, furan, diisopropyl azodicarboxylate (DIAD), triphenylphosphine (Ph 3 P), 1-hexadecanol, tetrahydrofuran (THF), ethyl acetate, N-phenylmaleimide, acetonitrile, methanol, Grubbs secondary catalyst, 3-bromopyridine, and pentane, from Sigma- Aldrich obtained and used without further processing. Dichloropentane, also obtained from Sigma-Aldrich, was treated with basic alumina prior to use.
Embodiment 2
[0167] This example illustrates exo-7-oxanorbornene-5,6-dicarboxyimide (C1), an intermediate in the preparation of the first and second monomers according to embodiments of the present invention. preparation.
[0168] In a clean 500 mL round bottom flask (RBF) equipped with a magnetic stir bar, furan (21 g, 309 mmol) was added to a solution of maleimide (25 g, 258 mmol) in 250 mL of ethyl acetate. The mixture was heated at 90 °C for 30 h. Rinse with ether (100 mL, 3X) and filter to give C1 as a white precipitate from solution. The white solid was dried under vacuum at room temperature for 24 h. C1 was obtained as the pure exo isomer in 29 g, 68% yield. 1 H-NMR (300MHz, CDCl 3 ): δ (ppm) 8.09 (s, 1H), 6.53 (s, 2H), 5.32 (s, 2H), 2.89 (s, 2H).
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