TY - JOUR
T1 - A facile method to functionalize engineering solid membrane supports for rapid and efficient oil-water separation
AU - Jing, Benxin
AU - Wang, Haitao
AU - Lin, Kun Yi
AU - McGinn, Paul J.
AU - Na, Chongzheng
AU - Zhu, Yingxi
N1 - Funding Information:
This work is supported by the US Department of Energy, Division of Materials Science, under Award DEFG02-07ER46390 . B.J., H.W., and K.-Y.L. are grateful to the postdoctoral research support from the Notre Dame Sustainable Energy Initiative . We also thank the Notre Dame Integrated Imaging Facility (NDIIF) for technical assistance in SEM and Prof. Haifeng Gao at Notre Dame to allow us to use his polymer characterization facility.
PY - 2013/10/4
Y1 - 2013/10/4
N2 - A facile and low-cost method is developed to functionalize engineering metal membrane supports, such as stainless steel (SS), with epoxy-containing polymer poly(glycidyl methacrylate) (PGMA) to produce a versatile and universal platform for subsequent surface modification. With a PGMA anchoring layer, we have demonstrated that hydrogel particles, such as polyacrylamide-co- poly(acrylic acid) (PAM-co-PAA), can be subsequently grafted to form functional polymer membranes for rapid and efficient oil-water separation. By contact angle and AFM measurement, we have confirmed that PAM-co-PAA hydrogel particle layer grafted on a PGMA-modified SS surface exhibits excellent selectivity as required for liquid-liquid separation, showing high affinity to water but not to oils as an ideal membrane for oil-water separation. To evaluate the separation efficiency, a simple flow-through device is employed to separate free-floating oil from water in the mixture of varied initial oil volume fraction and oil composition. Under substantially high pump flow rate up to 1.3 L/min, PAM-co-PAA hydrogel treated SS mesh can achieve excellent separation efficiency with less than 5% oil or water in the respective filtrate at the flux of as high as 540 m3/(m2·h) and retentate at the flux of 1.95 m 3/(m2·h). This separation efficiency is better than, or comparable to, the maximal performance achieved using conventional gravity methods at much lower flow rate. Similar approach could be also adapted to graft superhydrophobic and superoleophilic polymer membranes with PGMA-treated engineering support to separate water from oil.
AB - A facile and low-cost method is developed to functionalize engineering metal membrane supports, such as stainless steel (SS), with epoxy-containing polymer poly(glycidyl methacrylate) (PGMA) to produce a versatile and universal platform for subsequent surface modification. With a PGMA anchoring layer, we have demonstrated that hydrogel particles, such as polyacrylamide-co- poly(acrylic acid) (PAM-co-PAA), can be subsequently grafted to form functional polymer membranes for rapid and efficient oil-water separation. By contact angle and AFM measurement, we have confirmed that PAM-co-PAA hydrogel particle layer grafted on a PGMA-modified SS surface exhibits excellent selectivity as required for liquid-liquid separation, showing high affinity to water but not to oils as an ideal membrane for oil-water separation. To evaluate the separation efficiency, a simple flow-through device is employed to separate free-floating oil from water in the mixture of varied initial oil volume fraction and oil composition. Under substantially high pump flow rate up to 1.3 L/min, PAM-co-PAA hydrogel treated SS mesh can achieve excellent separation efficiency with less than 5% oil or water in the respective filtrate at the flux of as high as 540 m3/(m2·h) and retentate at the flux of 1.95 m 3/(m2·h). This separation efficiency is better than, or comparable to, the maximal performance achieved using conventional gravity methods at much lower flow rate. Similar approach could be also adapted to graft superhydrophobic and superoleophilic polymer membranes with PGMA-treated engineering support to separate water from oil.
KW - Hydrogel membrane
KW - Oil-water separation
KW - PGMA surface modification
UR - http://www.scopus.com/inward/record.url?scp=84885022230&partnerID=8YFLogxK
U2 - 10.1016/j.polymer.2013.08.030
DO - 10.1016/j.polymer.2013.08.030
M3 - Article
AN - SCOPUS:84885022230
SN - 0032-3861
VL - 54
SP - 5771
EP - 5778
JO - Polymer
JF - Polymer
IS - 21
ER -