journal article·2014-11

Hydrophilic modification of PVDF microfiltration membranes by adsorption of facial amphiphile cholic acid

Meng-Xin Hu, Ji-Nian Li, Shi-Lin Zhang, Liang Li, Zhi-Kang Xu

Publisher page

Abstract

Amphiphilic molecules have been widely used in surface modification of polymeric materials. Bile acids are natural biological compounds and possess special facial amphiphilic structure with a unusual distribution of hydrophobic and hydrophilic regions. Based on the facial amphiphilicity, cholic acid (CA), one of the bile acids, was utilized for the hydrophilic modification of poly(vinylidene fluoride) (PVDF) microfiltration membranes via the hydrophobic interactions between the hydrophobic face of CA and the membrane surfaces. Ethanol, methanol, and water were respectively used as solvent during CA adsorption procedure. Their polarity affects the CA adsorption amount, as similar to CA concentration and adsorption time. There are no changes on the membrane surface morphology after CA adsorption. The hydrophilicity of PVDF membranes is greatly enhanced and the water drops permeates into the CA modified membranes quickly after modification. All these factors benefit to the permeation flux of membrane for water. When CA concentration is higher than 0.088 M, the water permeation flux is doubled as compared with the nascent PVDF membrane and shows a good stability during filtration procedure. These results reveal the promising potential of facial amphiphilic bile acids for the surface modification of polymeric materials.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Membrane Separation Technologies · Advanced Sensor and Energy Harvesting Materials · Electrospun Nanofibers in Biomedical Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (24)

Show source-provided references
1. Liu · J. Membr. Sci. · 2011 · 375 · 110.1016/j.memsci.2011.03.014 ↗
2. Venault · J. Membr. Sci. · 2014 · 454 · 25310.1016/j.memsci.2013.11.050 ↗
3. Lang · Polym. Adv. Technol. · 2011 · 22 · 172010.1002/pat.1662 ↗
4. Zhao · J. Polym. Res. · 2013 · 20 · 5810.1007/s10965-012-0058-4 ↗
5. Wei · Colloid Surf. B · 2013 · 110 · 2210.1016/j.colsurfb.2013.04.008 ↗
6. Boributh · J. Membr. Sci. · 2009 · 342 · 9710.1016/j.memsci.2009.06.022 ↗
7. Du · Water Res. · 2009 · 43 · 455910.1016/j.watres.2009.08.008 ↗
8. Peng · J. Appl. Polym. Sci. · 2013 · 130 · 311210.1002/app.39516 ↗
9. Lin · Langmuir · 2013 · 29 · 1018310.1021/la401336y ↗
10. Guo · Macromol. Res. · 2013 · 21 · 112710.1007/s13233-013-1142-2 ↗
11. Theodoly · Langmuir · 2009 · 25 · 78110.1021/la8030254 ↗
12. Lockwood · Surf. Sci. Rep. · 2008 · 63 · 25510.1016/j.surfrep.2008.02.002 ↗
13. Erdinc · Colloid Surf. B · 2010 · 75 · 19410.1016/j.colsurfb.2009.08.031 ↗
14. Zhu · Acc. Chem. Res. · 2002 · 35 · 53910.1021/ar0101180 ↗
15. Madenci · Curr. Opin. Colloid Interface Sci. · 2010 · 15 · 10910.1016/j.cocis.2009.11.010 ↗
16. Schefer · Langmuir · 2012 · 28 · 599910.1021/la300384u ↗
17. Mukhopadhyay · Curr. Sci. · 2004 · 87 · 1666
18. Trillo · RSC Adv. · 2014 · 4 · 559810.1039/c3ra47160h ↗
19. Nakamura · J. Am. Chem. Soc. · 2004 · 126 · 876910.1021/ja049463l ↗
20. Pal · Polym. Chem. · 2014 · 5 · 127510.1039/C3PY01317K ↗
21. Shao · Macromolecules · 2012 · 45 · 192410.1021/ma202506b ↗
22. Posa · Colloid Surf. B · 2012 · 94 · 31710.1016/j.colsurfb.2012.02.014 ↗
23. Travaglini · J. Phys. Chem. B · 2013 · 117 · 924810.1021/jp405342v ↗
24. Travaglini · Chem. Commun. · 2012 · 48 · 1201110.1039/c2cc36030f ↗