Published August 21, 2012 | Version Published + Supplemental Material
Journal Article Open

Branched Polymeric Media: Boron-Chelating Resins from Hyperbranched Polyethylenimine

  • 1. ROR icon California Institute of Technology
  • 2. ROR icon Korea Advanced Institute of Science and Technology

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.

Additional Information

© 2012 American Chemical Society. Received: April 17, 2012. Revised: July 3, 2012. Accepted: July 24, 2012. Published: July 24, 2012. This research was carried out at the California Institute of Technology and AquaNano, LLC. Selected materials characterization studies (FT-IR and SEM) were carried out at the Korea Advanced Institute of Science and Technology (KAIST). Funding for this research was provided by the U.S National Science Foundation (NSF) (CBET Award 0506951). M.S.D. and D.P.C. were supported by the KAIST EEWS Initiative (NT080607C0209721). W.A.G. III was supported partially by the KAIST World Class University (WCU) program (NRF-31-2008-000-10055).

Attached Files

Published - es301518x.pdf

Supplemental Material - es301518x_si_001.pdf

Files

es301518x.pdf

Files (2.6 MB)

Name Size Download all
md5:808df494e8d13d55fb0bfc4326541b32
1.4 MB Preview Download
md5:a8a3322bb4767ecce59654c9fe3aff5f
1.2 MB Preview Download

Additional details

Identifiers

Eprint ID
34779
Resolver ID
CaltechAUTHORS:20121009-104621400

Funding

NSF
CBET-0506951
Korea Advanced Institute of Science and Technology (KAIST)
NT080607C0209721
National Research Foundation of Korea
NRF-31-2008-000-10055

Dates

Created
2012-10-09
Created from EPrint's datestamp field
Updated
2021-11-09
Created from EPrint's last_modified field