TY - JOUR
T1 - Tuning the nanofiltration performance of thin film strong polyelectrolyte hydrogel composite membranes by photo-grafting conditions
AU - Bernstein, Roy
AU - Antón, Enrique
AU - Ulbricht, Mathias
N1 - Funding Information:
R.B. gratefully acknowledges the ‘Young Scientists Exchange Program’ of the BMBF-MOST Water Technology Cooperation for the financial support. Further thanks are due to Mr. Smail Boukercha, Center for Scanning Electron Microscopy at the University of Duisburg-Essen, for conducting the SEM analyses and Sartorius Stedim A.S. for providing the base membranes.
PY - 2013/1/5
Y1 - 2013/1/5
N2 - Polyethersulfone ultrafiltration membranes were converted into charged nanofiltration membranes having a strong polyelectrolyte hydrogel as selective barrier layer through the UV-photo initiated graft polymerization technique. This was accomplished by using vinyl sulfonic acid as the functional monomer and N,N'-methylenbisacrylamide as a cross linker monomer (Bernstein et al., ACS Applied Materials & Interfaces, 4 (2012) 3438-3446). In this research the resulting composite membranes were further characterized using different methods (ATR-FTIR spectroscopy, zeta potential, contact angle, scanning electron microscopy). ATR-FTIR data were used to quantify the degree of grafting. The composite membranes' zeta potential was negative throughout the pH range and as high as -70. mV. The hydrogel composite membranes were also very hydrophilic with a contact angle of 11°. The membrane performance-salt rejection and water permeability-obtained at varied functionalization conditions-molecular weight cut-off of the base membrane, monomer concentration, cross linker fraction, UV irradiation intensity and time-was systematically investigated and the results were correlated to the membrane characterization data. Separation performance was also tested using mixed salt solutions. Larger composite membrane samples were prepared and long-term stability of nanofiltration (NF) performance was evaluated in cross-flow experiments. The performance of the best of the newly fabricated composite membranes was comparable to other polyelectrolyte-based NF membranes as well as to some commercial NF membranes presented in the literature.
AB - Polyethersulfone ultrafiltration membranes were converted into charged nanofiltration membranes having a strong polyelectrolyte hydrogel as selective barrier layer through the UV-photo initiated graft polymerization technique. This was accomplished by using vinyl sulfonic acid as the functional monomer and N,N'-methylenbisacrylamide as a cross linker monomer (Bernstein et al., ACS Applied Materials & Interfaces, 4 (2012) 3438-3446). In this research the resulting composite membranes were further characterized using different methods (ATR-FTIR spectroscopy, zeta potential, contact angle, scanning electron microscopy). ATR-FTIR data were used to quantify the degree of grafting. The composite membranes' zeta potential was negative throughout the pH range and as high as -70. mV. The hydrogel composite membranes were also very hydrophilic with a contact angle of 11°. The membrane performance-salt rejection and water permeability-obtained at varied functionalization conditions-molecular weight cut-off of the base membrane, monomer concentration, cross linker fraction, UV irradiation intensity and time-was systematically investigated and the results were correlated to the membrane characterization data. Separation performance was also tested using mixed salt solutions. Larger composite membrane samples were prepared and long-term stability of nanofiltration (NF) performance was evaluated in cross-flow experiments. The performance of the best of the newly fabricated composite membranes was comparable to other polyelectrolyte-based NF membranes as well as to some commercial NF membranes presented in the literature.
KW - Membrane modification
KW - Nanofiltration membrane
KW - Polyelectrolyte hydrogel
KW - UV-photo polymerization
UR - http://www.scopus.com/inward/record.url?scp=84871791188&partnerID=8YFLogxK
U2 - 10.1016/j.memsci.2012.09.034
DO - 10.1016/j.memsci.2012.09.034
M3 - Article
AN - SCOPUS:84871791188
SN - 0376-7388
VL - 427
SP - 129
EP - 138
JO - Journal of Membrane Science
JF - Journal of Membrane Science
ER -