Ultrathin, multilayered polyelectrolyte films as nanofiltration membranes

被引:213
作者
Stanton, BW [1 ]
Harris, JJ [1 ]
Miller, MD [1 ]
Bruening, ML [1 ]
机构
[1] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
关键词
D O I
10.1021/la034603a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study shows that alternating polyelectrolyte deposition on porous supports can yield nanofiltration membranes that allow high water flux along with selective ion transport. Membranes composed of 4.5-5 layer pairs of poly(styrene sulfonate)/poly(allylamine hydrochloride) (PSS/PAH) on porous alumina allow water fluxes of 1-2 m(3) m(-2) day(-1) at 4.8 bar while exhibiting MgSO4 rejections of 96%. Rejections of CaCl2 and Na2SO4 depend on polyelectrolyte deposition conditions and the composition of the outer layer of the membrane. In general, divalent-ion rejection increases when the charge of the outer layer of the membrane has the same sign as the divalent ion being rejected. Increasing the concentration of the supporting electrolyte present during deposition of the terminating PSS layer of PSS/PAH membranes results in a higher surface charge, and hence higher Na2SO4 rejections (up to 95%). Nanofiltration with mixed solutions of NaCl and Na2SO4 yields Cl-/SO42- selectivities of about 30 when the top layer of PSS/PAH membranes is deposited from a solution of high ionic strength. Capping PSS/PAH films with a layer of PAA increases Cl-/SO42- selectivities to values as high as 80. Interestingly, Cl-/SO42- selectivities in mixed solutions are higher than those determined from single-salt measurements, presumably because diffusion potentials are different in the two cases. The high selectivities, water fluxes, and ion rejections of PSS/PAH membranes make them potentially attractive for applications in water and salt purification.
引用
收藏
页码:7038 / 7042
页数:5
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