Abstract
Membranes with tailorable surface chemistry have applications in a wide range of industries. Synthesizing membranes from poly(chloromethyl styrene) directly incorporates an alkyl halide surface-bound initiator which can be used to install functional groups via SN2 chemistry or graft polymerization techniques. In this work, poly(chloromethyl styrene) membranes were synthesized through electrospinning. After fabrication, membranes were crosslinked with a diamine, and the chemical resistance of the membranes was evaluated by exposure to 10 M nitric acid, ethanol, or tetrahydrofuran for 24 h. The resulting membranes had diameters on the order of 2–5 microns, porosities of >80%, and permeance on the order of 10,000 L/m2/h/bar. Crosslinking the membranes generally increased the chemical stability. The degree of crosslinking was approximated using elemental analysis for nitrogen and ranged from 0.5 to 0.9 N%. The poly(chloromethyl styrene) membrane with the highest degree of crosslinking did not dissolve in THF after 24 h and retained its high permeance after solvent exposure. The presented chemically resistant membranes can serve as a platform technology due to their versatile surface chemistry and can be used in membrane manufacturing techniques that require the membrane to be contacted with organic solvents or monomers. They can also serve as a platform for separations that are performed in strong acids.
Original language | English |
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Article number | 870 |
Journal | Membranes |
Volume | 13 |
Issue number | 11 |
DOIs | |
State | Published - Nov 2023 |
Funding
This work is funded by the US Department of Energy Early Career Research Award (DE-SC0021260) within the Isotope Program, formerly in the Office of Nuclear Physics. J.S. and A.J. were also supported by undergraduate research awards from the Case Western Reserve University SOURCE program, now the Office of Undergraduate Research.
Keywords
- adsorptive chromatography
- chloromethyl styrene
- electrospinning
- microfiltration
- non-woven membranes
- polyvinyl benzyl chloride