Spontaneously self-assembled dual-layer mixed matrix membranes containing mass-produced mesoporous TiO2 for CO2 capture

Sang Jin Kim, Won Seok Chi, Harim Jeon, Jong Hak Kim, Rajkumar Patel

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Herein, a high performance mixed matrix membrane (MMM) is reported, through control of the solvent evaporation rate based on the spontaneous self-assembly of mesoporous TiO2 (m-TiO2) fillers in a poly(vinyl chloride)-g-poly(oxyethylene methacrylate) (PVC-g-POEM) graft copolymer matrix. In particular, a facile, non-hydrothermal and mass-producible preparation method for m-TiO2 is described. Slow solvent evaporation resulted in the formation of dual-layer MMMs consisting of a top PVC-g-POEM rich layer over a bottom m-TiO2 rich layer, whereas fast evaporation led to the case of single-layer MMMs. Both CO2 permeability and CO2/N2 selectivity increased as the m-TiO2 content increased up to 20 wt% for single-layer as well as dual-layer MMMs, due to loose packing structures and increased chain flexibility. However, above 20 wt% loading, dual-layer MMMs exhibited much higher CO2 permeabilities and CO2/N2 selectivities than single-layer MMMs, resulting from self-assembled dual-layer architecture as well as better interfacial adhesion properties. Scanning electron microscopy (SEM), X-ray diffraction (XRD), and density measurements revealed that the PVC-g-POEM graft copolymer chains penetrated into the m-TiO2 rich layer to generate web-like interconnected structures, forming proper pore sizes for selective CO2 transport. The dual-layer MMMs exhibited excellent improvements in CO2 permeability of over 3000% from 46.2 to 1430.9 Barrer (1 Barrer = 1×10-10 cm3 (STP) cm /cm2 s cmHg) with a CO2/N2 selectivity of 22.4, which was only slightly below the upper bound (2008).

Original languageEnglish
Pages (from-to)62-72
Number of pages11
JournalJournal of Membrane Science
Volume508
DOIs
Publication statusPublished - 2016 Jun 15

Fingerprint

Permeability
Evaporation
Graft copolymers
membranes
Membranes
matrices
Transplants
X-Ray Diffraction
Electron Scanning Microscopy
Self assembly
Pore size
Fillers
Adhesion
permeability
X ray diffraction
selectivity
Scanning electron microscopy
chlorides
copolymers
poly(vinyl chloride)-g-poly(oxyethylene methacrylate)

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Materials Science(all)
  • Physical and Theoretical Chemistry
  • Filtration and Separation

Cite this

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title = "Spontaneously self-assembled dual-layer mixed matrix membranes containing mass-produced mesoporous TiO2 for CO2 capture",
abstract = "Herein, a high performance mixed matrix membrane (MMM) is reported, through control of the solvent evaporation rate based on the spontaneous self-assembly of mesoporous TiO2 (m-TiO2) fillers in a poly(vinyl chloride)-g-poly(oxyethylene methacrylate) (PVC-g-POEM) graft copolymer matrix. In particular, a facile, non-hydrothermal and mass-producible preparation method for m-TiO2 is described. Slow solvent evaporation resulted in the formation of dual-layer MMMs consisting of a top PVC-g-POEM rich layer over a bottom m-TiO2 rich layer, whereas fast evaporation led to the case of single-layer MMMs. Both CO2 permeability and CO2/N2 selectivity increased as the m-TiO2 content increased up to 20 wt{\%} for single-layer as well as dual-layer MMMs, due to loose packing structures and increased chain flexibility. However, above 20 wt{\%} loading, dual-layer MMMs exhibited much higher CO2 permeabilities and CO2/N2 selectivities than single-layer MMMs, resulting from self-assembled dual-layer architecture as well as better interfacial adhesion properties. Scanning electron microscopy (SEM), X-ray diffraction (XRD), and density measurements revealed that the PVC-g-POEM graft copolymer chains penetrated into the m-TiO2 rich layer to generate web-like interconnected structures, forming proper pore sizes for selective CO2 transport. The dual-layer MMMs exhibited excellent improvements in CO2 permeability of over 3000{\%} from 46.2 to 1430.9 Barrer (1 Barrer = 1×10-10 cm3 (STP) cm /cm2 s cmHg) with a CO2/N2 selectivity of 22.4, which was only slightly below the upper bound (2008).",
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Spontaneously self-assembled dual-layer mixed matrix membranes containing mass-produced mesoporous TiO2 for CO2 capture. / Kim, Sang Jin; Chi, Won Seok; Jeon, Harim; Kim, Jong Hak; Patel, Rajkumar.

In: Journal of Membrane Science, Vol. 508, 15.06.2016, p. 62-72.

Research output: Contribution to journalArticle

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AU - Kim, Sang Jin

AU - Chi, Won Seok

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AU - Patel, Rajkumar

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AB - Herein, a high performance mixed matrix membrane (MMM) is reported, through control of the solvent evaporation rate based on the spontaneous self-assembly of mesoporous TiO2 (m-TiO2) fillers in a poly(vinyl chloride)-g-poly(oxyethylene methacrylate) (PVC-g-POEM) graft copolymer matrix. In particular, a facile, non-hydrothermal and mass-producible preparation method for m-TiO2 is described. Slow solvent evaporation resulted in the formation of dual-layer MMMs consisting of a top PVC-g-POEM rich layer over a bottom m-TiO2 rich layer, whereas fast evaporation led to the case of single-layer MMMs. Both CO2 permeability and CO2/N2 selectivity increased as the m-TiO2 content increased up to 20 wt% for single-layer as well as dual-layer MMMs, due to loose packing structures and increased chain flexibility. However, above 20 wt% loading, dual-layer MMMs exhibited much higher CO2 permeabilities and CO2/N2 selectivities than single-layer MMMs, resulting from self-assembled dual-layer architecture as well as better interfacial adhesion properties. Scanning electron microscopy (SEM), X-ray diffraction (XRD), and density measurements revealed that the PVC-g-POEM graft copolymer chains penetrated into the m-TiO2 rich layer to generate web-like interconnected structures, forming proper pore sizes for selective CO2 transport. The dual-layer MMMs exhibited excellent improvements in CO2 permeability of over 3000% from 46.2 to 1430.9 Barrer (1 Barrer = 1×10-10 cm3 (STP) cm /cm2 s cmHg) with a CO2/N2 selectivity of 22.4, which was only slightly below the upper bound (2008).

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