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Branched polymeric media: Boron-chelating resins from hyperbranched polyethylenimine

  • Himanshu Mishra
  • , Changjun Yu
  • , Dennis P. Chen
  • , William A. Goddard
  • , Nathan F. Dalleska
  • , Michael R. Hoffmann
  • , Mamadou S. Diallo
  • Division of Chemistry and Chemical Engineering
  • AquaNano, LLC
  • California Institute of Technology Division of Engineering and Applied Science
  • Korea Advanced Institute of Science and Technology

Research output: Contribution to journalArticlepeer-review

Abstract

Extraction of boron from aqueous solutions using selective resins is important in a variety of applications including desalination, ultrapure water production, and nuclear power generation. Today's commercial boron-selective resins are exclusively prepared by functionalization of styrene-divinylbenzene (STY-DVB) beads with N-methylglucamine to produce resins with boron-chelating groups. However, such boron-selective resins have a limited binding capacity with a maximum free base content of 0.7 eq/L, which corresponds to a sorption capacity of 1.16 ± 0.03 mMol/g in aqueous solutions with equilibrium boron concentration of ∼70 mM. In this article, we describe the synthesis and characterization of a new resin that can selectively extract boron from aqueous solutions. We show that branched polyethylenimine (PEI) beads obtained from an inverse suspension process can be reacted with glucono-1,5-d-lactone to afford a resin consisting of spherical beads with high density of boron-chelating groups. This resin has a sorption capacity of 1.93 ± 0.04 mMol/g in aqueous solution with equilibrium boron concentration of ∼70 mM, which is 66% percent larger than that of standard commercial STY-DVB resins. Our new boron-selective resin also shows excellent regeneration efficiency using a standard acid wash with a 1.0 M HCl solution followed by neutralization with a 0.1 M NaOH solution.

Original languageEnglish
Pages (from-to)8998-9004
Number of pages7
JournalEnvironmental Science and Technology
Volume46
Issue number16
DOIs
Publication statusPublished - 21 Aug 2012
Externally publishedYes

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