Magnetic adsorbents displaying switchable ion-exchange behaviour

by Willett, Thomas Clifford

Type Thesis
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Magnetic bioseparations based on non-porous adsorbents offer a low-fouling alternative to the porous materials required by conventional adsorbent separation techniques. Interest in magnetic bioseparations has been limited by the high cost of suitable magnetic absorbents. In this study a variety of techniques - including Ce(IV) initiation, surface ATRP and sulfonyl activation – were used to graft ion-exchanging polyelectrolyte surfaces on low cost non-porous polyvinyl alcohol-magnetite supports.…

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Summary

Magnetic bioseparations based on non-porous adsorbents offer a low-fouling alternative to the porous materials required by conventional adsorbent separation techniques. Interest in magnetic bioseparations has been limited by the high cost of suitable magnetic absorbents. In this study a variety of techniques - including Ce(IV) initiation, surface ATRP and sulfonyl activation – were used to graft ion-exchanging polyelectrolyte surfaces on low cost non-porous polyvinyl alcohol-magnetite supports. Grafting of poly(2-vinyl pyridine) and poly(methacrylic acid) was fully characterised using solid and liquid state FTIR. Dense polyelectrolyte layers were seen, with Ce(IV) grafted layers accounting for up to 49% of grafted support mass. Values for ATRP and tresyl activations were 41% and 25% of support mass respectively. These included layers which correspond to the brush regime (2R\(_f\)/D > 8), as determined by Flory Radius calculations. The above matrices were subsequently analysed with bind and elute studies using a model mixture of acidic and basic proteins. Switchable ion-exchange behaviour was demonstrated, with anion binding capacity >25 mg/g support at pH 5 and cation binding >25 mg/g seen for Ce(IV) grafted supports. Improved elution by pH was also seen, with up to 73% of bound lysozyme removed during a single elution at pH 5.

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Edition Statements

  • Publication Date:2009

Thesis Information

  • Degree:Ph.D.
  • University:University of Birmingham

Publication Statements

  • Language:eng
  • Publication Date:2009

Edition Identifiers

  • ethos:512492

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