Direct interfacial polymerization onto thin ceramic hollow fibers

Evelien Maaskant, Patrick de Wit, Nieck E. Benes* (Corresponding Author)

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

7 Citations (Scopus)
55 Downloads (Pure)

Abstract

Membrane separation under harsh conditions, such as high-p,T or in the presence of aggressive chemicals, requires a robust membrane support. In academia commonly ceramic disks are used for this purpose, but these disks posses a too low surface-area-to-volume ratio for practical applications. Ceramic hollow fibers potentially provide a much larger specific surface area, but applying a defect free thin selective layer on such structures is more intricate. Here we show the successful preparation of a thin polyamide layer on a thin porous hollow α-alumina fiber by interfacial polymerization of piperazine with trimesoyl chloride. Two aspects of the fabrication method are identified as particularly crucial for obtaining a high quality selective layer: i) the layer the ceramic surface should have a sufficient amount of hydroxyl groups for covalent attachment in order to avoid delamination, and ii) controlled drying steps are necessary to avoid local surplus or lack of liquid on the outer surface of the ceramic. To increase the hydroxyl group concentration, and to facilitate the presence of sufficient reactants in a large volume of small pores, the fibers have been coated with a layer of γ-alumina. Sufficiently long drying steps (20 mm) have been employed to avoid uneven drying over the length of the fiber. The obtained fibers show clean water fluxes in the range of 2–5 L m−2 h−1 bar−1 combined with a retention of Rose Bengal above 99%.

Original languageEnglish
Pages (from-to)296-301
Number of pages6
JournalJournal of membrane science
Volume550
Early online date6 Jan 2018
DOIs
Publication statusPublished - 15 Mar 2018

Fingerprint

Ceramic fibers
Ceramics
Polymerization
hollow
polymerization
ceramics
Drying
fibers
Fibers
Aluminum Oxide
drying
Hydroxyl Radical
Alumina
Membranes
Rose Bengal
aluminum oxides
Nylons
membranes
Polyamides
Delamination

Keywords

  • Interfacial polymerization
  • Polyamide
  • Inorganic porous hollow fiber

Cite this

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title = "Direct interfacial polymerization onto thin ceramic hollow fibers",
abstract = "Membrane separation under harsh conditions, such as high-p,T or in the presence of aggressive chemicals, requires a robust membrane support. In academia commonly ceramic disks are used for this purpose, but these disks posses a too low surface-area-to-volume ratio for practical applications. Ceramic hollow fibers potentially provide a much larger specific surface area, but applying a defect free thin selective layer on such structures is more intricate. Here we show the successful preparation of a thin polyamide layer on a thin porous hollow α-alumina fiber by interfacial polymerization of piperazine with trimesoyl chloride. Two aspects of the fabrication method are identified as particularly crucial for obtaining a high quality selective layer: i) the layer the ceramic surface should have a sufficient amount of hydroxyl groups for covalent attachment in order to avoid delamination, and ii) controlled drying steps are necessary to avoid local surplus or lack of liquid on the outer surface of the ceramic. To increase the hydroxyl group concentration, and to facilitate the presence of sufficient reactants in a large volume of small pores, the fibers have been coated with a layer of γ-alumina. Sufficiently long drying steps (20 mm) have been employed to avoid uneven drying over the length of the fiber. The obtained fibers show clean water fluxes in the range of 2–5 L m−2 h−1 bar−1 combined with a retention of Rose Bengal above 99{\%}.",
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Direct interfacial polymerization onto thin ceramic hollow fibers. / Maaskant, Evelien; de Wit, Patrick; Benes, Nieck E. (Corresponding Author).

In: Journal of membrane science, Vol. 550, 15.03.2018, p. 296-301.

Research output: Contribution to journalArticleAcademicpeer-review

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