2021
DOI: 10.1016/j.seppur.2021.118331
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Effect of thermal processing on brominated 6FDA-DAM for effective propylene/propane separation

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Cited by 10 publications
(5 citation statements)
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“…The molecular structure of hyper‐coPIs was investigated using FT‐IR. As shown in Figure 3A, the in‐plane and out‐of‐plane bending of CNC at 1363/cm and 723/cm and the stretching vibration of CO at 1783 and 1722/cm could be clearly observed 37–39 . It confirms that imidization has been successfully promoted in all the membranes.…”
Section: Resultssupporting
confidence: 53%
See 1 more Smart Citation
“…The molecular structure of hyper‐coPIs was investigated using FT‐IR. As shown in Figure 3A, the in‐plane and out‐of‐plane bending of CNC at 1363/cm and 723/cm and the stretching vibration of CO at 1783 and 1722/cm could be clearly observed 37–39 . It confirms that imidization has been successfully promoted in all the membranes.…”
Section: Resultssupporting
confidence: 53%
“…As shown in Figure 3A, the in-plane and out-of-plane bending of C N C at 1363/cm and 723/cm and the stretching vibration of C O at 1783 and 1722/cm could be clearly observed. [37][38][39] It confirms that imidization has been successfully promoted in all the membranes. The aromatic C C stretching at both 1668/cm is from the benzene rings.…”
Section: Characterization Of Membranessupporting
confidence: 62%
“…This indicated that the resultant product included a mixture of different substitutions of BrPI- x depending on the number and location of the brominated group. As the degree of bromination increased, the integrated peak area of benzylic protons ( H a ) at 2.00 and 2.23 ppm decreased, whereas the integrated peak area of –CH 2 –Br– ( H e ) at 4.18 and 4.37 ppm increased. , The degree of bromination of BrPI-1 was approximately 7.78% from NMR analysis. The 1 H NMR spectra and TGA curves of BrPI- x (1–4) with controlled degrees of bromination are shown in Figures S7 and S8 with a detailed explanation.…”
Section: Resultsmentioning
confidence: 91%
“…Brominated 6FDA-DAM (called 6FDA-DAM-Br hereinafter) was synthesized using a slightly version of a method reported in the literature. , 6FDA-DAM (1.0 g) and NBS (0.16 g) were dissolved in chloroform (60 mL) in a round-bottom flask. After the reactants dissolved fully, AIBN (0.002 g) was added as an initiator with vigorous stirring.…”
Section: Experimental Sectionmentioning
confidence: 99%
“…[1][2][3][4][5][6] Membrane-based separation is an attractive alternative for many molecular separations due to its energy-saving and highly efficient advantages. 4,[7][8][9][10] At present, polymer membranes are widely used in industry, [11][12][13][14][15] but they also encounter the problem of plasticization and the bottleneck of a tradeoff between selectivity and permeability. [16][17][18] Therefore, promising membrane materials with excellent performance are always desired in membrane separation technology.…”
Section: Introductionmentioning
confidence: 99%