2019
DOI: 10.1016/j.seppur.2019.02.036
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MOF-801 incorporated PEBA mixed-matrix composite membranes for CO2 capture

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Cited by 144 publications
(65 citation statements)
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“…In addition, it seems that permeability of the specified gases was not affected significantly by PL addition, as a result of the molecular structure of PEBA chain, which is composed of compact homochiral sheets. This form makes it difficult for molecules to pack and rearrange and fill space [17], even at the lowest concentration of GA (PEBA2). When GA loading was increased from 0.05 to 0.4 wt.%, permeability of CO 2 and CH 4 gases increased from 88.12 to 197.86 Barrer (increasing by~56%) and from 3.74 to 6.10 (increasing by~39%) Barrer, respectively ( Figure 10A), where the presence of GA restricts the conformational freedom of PEBA chains in its vicinity, which may frustrate PEBA chain ability to group together and cause a curvature of the surface at the nanoscale [58], thus increments of the PEBA amorphous structure, fractional free volume and chain mobility as a result of decreasing in the crystallinity of the synthesized membranes (confirmed by the XRD and FTIR results), which causes a significant increase in CO 2 permeability and a little in CH 4 permeability of the synthesized membranes [59].…”
Section: Gas Permeation Performancementioning
confidence: 99%
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“…In addition, it seems that permeability of the specified gases was not affected significantly by PL addition, as a result of the molecular structure of PEBA chain, which is composed of compact homochiral sheets. This form makes it difficult for molecules to pack and rearrange and fill space [17], even at the lowest concentration of GA (PEBA2). When GA loading was increased from 0.05 to 0.4 wt.%, permeability of CO 2 and CH 4 gases increased from 88.12 to 197.86 Barrer (increasing by~56%) and from 3.74 to 6.10 (increasing by~39%) Barrer, respectively ( Figure 10A), where the presence of GA restricts the conformational freedom of PEBA chains in its vicinity, which may frustrate PEBA chain ability to group together and cause a curvature of the surface at the nanoscale [58], thus increments of the PEBA amorphous structure, fractional free volume and chain mobility as a result of decreasing in the crystallinity of the synthesized membranes (confirmed by the XRD and FTIR results), which causes a significant increase in CO 2 permeability and a little in CH 4 permeability of the synthesized membranes [59].…”
Section: Gas Permeation Performancementioning
confidence: 99%
“…Among these polymer membranes, PEBA is classified as one of the most promising polymer membranes with high efficiency in CO 2 separation due to its high CO 2 permeability and CO 2 /CH 4 selectivity [15,16]. In order to improve their permeability and selectivity and make them fulfil the industrial requirements and increase stability for the long term, PEBA mixed-matrix composite membranes (MCM) were developed to address these aspects through mixing or modifying PEBA by other additives or chemical treatments [17,18].…”
Section: Introductionmentioning
confidence: 99%
“…They are used for separation [110]. Different researchers have reported membrane used for the capture of harmful gases in literature [17, 111,112] as they are environmentally benign and efficient in energy consumption [113] and exhibit technical and cost-related merits [114].…”
Section: Membranesmentioning
confidence: 99%
“…Various studies on the use of membrane for the capture of CO 2 and H 2 S, have also been reported [110,112,[122][123][124][125][126].…”
Section: Fig 5 Separation Of Different Molecules Using Membrane [118]mentioning
confidence: 99%
“…PEBA 1657, a polyether block amide composed of 40% polyamide (PA) and 60% polyethylene oxide (PEO), was selected as the polymer material. The impacts of different fillers including MOFs, [25][26][27][28][29][30] carbon nanotubes, 31,32 zeolites, [33][34][35] and other 2D and 3D inorganic materials [36][37][38] were investigated to enhance the CO 2 \CH 4 separation properties of PEBA. It is expected that the flexible structure of polymer chains displays sufficient compatibility with the particles to prohibit sieve-in-a-cage and rigidification defects at the polymer-particle interface.…”
Section: Introductionmentioning
confidence: 99%