2020
DOI: 10.1016/j.seppur.2020.116899
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Highly permeable novel PDMS coated asymmetric polyethersulfone membranes loaded with SAPO-34 zeolite for carbon dioxide separation

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Cited by 34 publications
(15 citation statements)
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“…The presence of these defects is a symptom of a membrane with low selectivity that needs to be coated to perform defect healing. Herein, we have coated the membranes with a dense PDMS layer, which is a widely used procedure for the correction of pinhole defects in membranes for gas separation [ 38 , 39 , 40 , 41 ]. The effect of PDMS on the diffusive transport through the dense membrane is negligible when there is a difference of several orders of magnitude in their intrinsic permeability coefficients, as is the case for our PEEK–WC-based MMMs.…”
Section: Resultsmentioning
confidence: 99%
“…The presence of these defects is a symptom of a membrane with low selectivity that needs to be coated to perform defect healing. Herein, we have coated the membranes with a dense PDMS layer, which is a widely used procedure for the correction of pinhole defects in membranes for gas separation [ 38 , 39 , 40 , 41 ]. The effect of PDMS on the diffusive transport through the dense membrane is negligible when there is a difference of several orders of magnitude in their intrinsic permeability coefficients, as is the case for our PEEK–WC-based MMMs.…”
Section: Resultsmentioning
confidence: 99%
“…This is attributed to the reduction of intermolecular cohesive energy because of the obstruction of more preformed hydrogen bonds by inserting zeolites 44 . At the same time, the final char yields remarkably increase from 0% of neat Pebax to 16% of Pebax/SAPO‐20% owing to the contribution of thermal stable zeolites 45–46 . Besides, the thermal weight loss trend of the MMMs slows down in the range of 450–500°C, and the temperature at the maximum thermal weight loss rate increases from 457 to 459°C.…”
Section: Resultsmentioning
confidence: 99%
“…In all the spectra, the broad peak found near 3274 cm �1 was due to stretching vibrations of H-bonded -OH 47,48 and H-bonded N-H groups. 49 The stretching peak at 2935 cm �1 was due to C-H groups [50][51][52] of the protein and the peak at 1425 cm �1 was attributed to C-H bending vibration. 38,53 The appearance of the peak at 1732 cm �1 was related to the vibration of free carbonyl groups -C¼O due to the hydrolysis of PVA.…”
Section: Ftir Analysismentioning
confidence: 99%