Control of porous morphology in suspension polymerized poly(divinylbenzene) resins using oligomeric porogens

F.S. Macintyre, D.C. Sherrington

Research output: Contribution to journalArticle

75 Citations (Scopus)

Abstract

Porous poly(divinylbenzene) (DVB) resins have been prepared using suspension polymerization with toluene and an oligomer as coporogens. The oligomers investigated were poly(propylene glycol) 1000 (PPG 1000), poly(propylene glycol) 4000 (PPG 4000), and poly(dimethylsiloxane) (PDMS). The porogen was used in a 1/1 vol/vol ratio with DVB, and with each oligomeric coporogen the full compositional range 100 vol % toluene to 100 vol % oligomer was examined. As predicted from previous knowledge of the effect of different solvent porogens, toluene yielded a highly microporous resin with a large dry state surface area (similar to650 m(2) g(-1)), whereas each oligomeric porogen yielded a highly macroporous resin with rather low surface area similar to15-50 m(2) g(-1). Using mixtures of toluene and oligomer as coporogens, we speculated that it might be possible to produce a resin with a strongly bimodal pore size distribution with one population of pores in the micropore region, and one in the macropore region. This proved to be the case with a mixture 80 vol % toluene and 20 vol % PDMS. Unexpectedly, however, the surface area of the poly(DVB) resins was found to rise significantly (similar to100 m(2) g(-1)) in shifting from toluene as sole porogen to a mixture with a low level of oligomeric coporogen (similar to4-6 vol %). Further increase in the level of oligomer led to the predicted fall in surface area. Overall, therefore, it is clear that use of oligomers, particularly as coporogens with solvent porogens, provides a valuable methodology for fine-tuning the porous morphology of poly(DVB) resins.
LanguageEnglish
Pages7628-7636
Number of pages8
JournalMacromolecules
Volume37
Issue number20
DOIs
Publication statusPublished - 5 Oct 2004

Fingerprint

divinyl benzene
Propylene Glycol
Toluene
Glycols
Oligomers
Propylene
Suspensions
Resins
Dimethylpolysiloxanes
Surface states
Polydimethylsiloxane
Pore size
Tuning
Polymerization

Keywords

  • CO-ETHYLENE DIMETHACRYLATE)
  • MONODISPERSE
  • PARTICLES
  • BEADS
  • POLY(STYRENE-CO-DIVINYLBENZENE)
  • MATRICES
  • MONOMERS

Cite this

Macintyre, F.S. ; Sherrington, D.C. / Control of porous morphology in suspension polymerized poly(divinylbenzene) resins using oligomeric porogens. In: Macromolecules. 2004 ; Vol. 37, No. 20. pp. 7628-7636.
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abstract = "Porous poly(divinylbenzene) (DVB) resins have been prepared using suspension polymerization with toluene and an oligomer as coporogens. The oligomers investigated were poly(propylene glycol) 1000 (PPG 1000), poly(propylene glycol) 4000 (PPG 4000), and poly(dimethylsiloxane) (PDMS). The porogen was used in a 1/1 vol/vol ratio with DVB, and with each oligomeric coporogen the full compositional range 100 vol {\%} toluene to 100 vol {\%} oligomer was examined. As predicted from previous knowledge of the effect of different solvent porogens, toluene yielded a highly microporous resin with a large dry state surface area (similar to650 m(2) g(-1)), whereas each oligomeric porogen yielded a highly macroporous resin with rather low surface area similar to15-50 m(2) g(-1). Using mixtures of toluene and oligomer as coporogens, we speculated that it might be possible to produce a resin with a strongly bimodal pore size distribution with one population of pores in the micropore region, and one in the macropore region. This proved to be the case with a mixture 80 vol {\%} toluene and 20 vol {\%} PDMS. Unexpectedly, however, the surface area of the poly(DVB) resins was found to rise significantly (similar to100 m(2) g(-1)) in shifting from toluene as sole porogen to a mixture with a low level of oligomeric coporogen (similar to4-6 vol {\%}). Further increase in the level of oligomer led to the predicted fall in surface area. Overall, therefore, it is clear that use of oligomers, particularly as coporogens with solvent porogens, provides a valuable methodology for fine-tuning the porous morphology of poly(DVB) resins.",
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Control of porous morphology in suspension polymerized poly(divinylbenzene) resins using oligomeric porogens. / Macintyre, F.S.; Sherrington, D.C.

In: Macromolecules, Vol. 37, No. 20, 05.10.2004, p. 7628-7636.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Control of porous morphology in suspension polymerized poly(divinylbenzene) resins using oligomeric porogens

AU - Macintyre, F.S.

AU - Sherrington, D.C.

PY - 2004/10/5

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N2 - Porous poly(divinylbenzene) (DVB) resins have been prepared using suspension polymerization with toluene and an oligomer as coporogens. The oligomers investigated were poly(propylene glycol) 1000 (PPG 1000), poly(propylene glycol) 4000 (PPG 4000), and poly(dimethylsiloxane) (PDMS). The porogen was used in a 1/1 vol/vol ratio with DVB, and with each oligomeric coporogen the full compositional range 100 vol % toluene to 100 vol % oligomer was examined. As predicted from previous knowledge of the effect of different solvent porogens, toluene yielded a highly microporous resin with a large dry state surface area (similar to650 m(2) g(-1)), whereas each oligomeric porogen yielded a highly macroporous resin with rather low surface area similar to15-50 m(2) g(-1). Using mixtures of toluene and oligomer as coporogens, we speculated that it might be possible to produce a resin with a strongly bimodal pore size distribution with one population of pores in the micropore region, and one in the macropore region. This proved to be the case with a mixture 80 vol % toluene and 20 vol % PDMS. Unexpectedly, however, the surface area of the poly(DVB) resins was found to rise significantly (similar to100 m(2) g(-1)) in shifting from toluene as sole porogen to a mixture with a low level of oligomeric coporogen (similar to4-6 vol %). Further increase in the level of oligomer led to the predicted fall in surface area. Overall, therefore, it is clear that use of oligomers, particularly as coporogens with solvent porogens, provides a valuable methodology for fine-tuning the porous morphology of poly(DVB) resins.

AB - Porous poly(divinylbenzene) (DVB) resins have been prepared using suspension polymerization with toluene and an oligomer as coporogens. The oligomers investigated were poly(propylene glycol) 1000 (PPG 1000), poly(propylene glycol) 4000 (PPG 4000), and poly(dimethylsiloxane) (PDMS). The porogen was used in a 1/1 vol/vol ratio with DVB, and with each oligomeric coporogen the full compositional range 100 vol % toluene to 100 vol % oligomer was examined. As predicted from previous knowledge of the effect of different solvent porogens, toluene yielded a highly microporous resin with a large dry state surface area (similar to650 m(2) g(-1)), whereas each oligomeric porogen yielded a highly macroporous resin with rather low surface area similar to15-50 m(2) g(-1). Using mixtures of toluene and oligomer as coporogens, we speculated that it might be possible to produce a resin with a strongly bimodal pore size distribution with one population of pores in the micropore region, and one in the macropore region. This proved to be the case with a mixture 80 vol % toluene and 20 vol % PDMS. Unexpectedly, however, the surface area of the poly(DVB) resins was found to rise significantly (similar to100 m(2) g(-1)) in shifting from toluene as sole porogen to a mixture with a low level of oligomeric coporogen (similar to4-6 vol %). Further increase in the level of oligomer led to the predicted fall in surface area. Overall, therefore, it is clear that use of oligomers, particularly as coporogens with solvent porogens, provides a valuable methodology for fine-tuning the porous morphology of poly(DVB) resins.

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KW - MONODISPERSE

KW - PARTICLES

KW - BEADS

KW - POLY(STYRENE-CO-DIVINYLBENZENE)

KW - MATRICES

KW - MONOMERS

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