Published January 15, 2014 | Version Supplemental Material
Journal Article Open

A facile route to the preparation of mixed matrix polyvinylidene fluoride membranes with in-situ generated polyethyleneimine particles

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

Abstract

The development of mixed matrix polymeric membranes with embedded functional particles/nanomaterials has been an active area of research during the last two decades. Such membranes are being designed to carry out multiple functions (e.g. retention, sorption and catalysis) with improved properties and performance over those of commercial membranes. Polymeric particles could provide greater flexibility for the preparation of mixed matrix membranes with improved particle–matrix compatibility, particle loading, flux and permselectivity. In this article, we describe a facile and simple route to the preparation of mixed matrix polyvinylidene fluoride (PVDF) membranes embedded with branched polyethylenimine (PEI) particles. The critical step of our novel methodology is the in-situ generation of crosslinked PEI micro/nanoparticles (with diameters ranging from 400 nm to 3 μm) in the membrane casting solution using epichlorohydrin as crosslinker. This eliminates the need to utilize inverse emulsion polymerization techniques to synthesize PEI particles prior to the membrane casting. Using non-solvent induced phase separation (NIPS), we successfully prepared mixed matrix PVDF membranes with uniform particle distribution and PEI particle loadings ranging from 27 to 48 wt%. Our novel membrane preparation route exhibits many advantages including simplicity, scalability and versatility. Preliminary experiments show that our new mixed matrix PVDF membranes with embedded PEI particles can serve as weak-base membrane absorbers for proteins such as bovine serum albumin.

Additional Information

© 2013 Elsevier B.V. Received 24 June 2013. Received in revised form 17 August 2013. Accepted 19 August 2013. Available online 3 September 2013. This research was carried out at the Korea Advanced Institute of Science and Technology (KAIST) and at the California Institute of Technology (Caltech). Funding for KAIST was provided by the EEWS Initiative (NT080607C0209721) and the National Research Foundation of Korea (NRF) [MEST Grant no. 2012M1A2A2026588]. Funding for Caltech was provided by the National Science Foundation (NSF) of United States [CBET EAGER Award 0948485]. We thank Dr. BeomSik Kim of the Korea Research Institute of Chemical Technology (KRICT) for providing us access to their SurPASS electrokinetic analyzer. MSD thanks Dr. Walter Kosar of Arkema (King of Prussia, PA) for providing the Kynar 761 PVDF samples.

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Identifiers

Eprint ID
42770
Resolver ID
CaltechAUTHORS:20131202-103609251

Funding

EEWS Initiative
NT080607C0209721
National Research Foundation of Korea (NRF) Ministry of Education, Science and Technology (MEST)
2012M1A2A2026588
NSF CBET EAGER Award
09484805

Dates

Created
2013-12-02
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Updated
2021-11-10
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