Surface-initiated atom transfer radical polymerization: A new method for preparation of polymeric membrane adsorbers

被引:132
作者
Singh, Nripen [1 ]
Wang, Jun [2 ]
Ulbricht, Mathias [2 ]
Wickramasinghe, S. Ranil [3 ]
Husson, Scott M. [1 ]
机构
[1] Clemson Univ, Dept Chem & Biomol Engn, Clemson, SC 29634 USA
[2] Univ Duisburg Essen, Lehrstuhl Tech Chem 2, D-45141 Essen, Germany
[3] Colorado State Univ, Dept Chem & Biol Engn, Ft Collins, CO 80525 USA
基金
美国国家科学基金会;
关键词
ATRP; graft polymerization; ion exchange; protein separation; surface modification;
D O I
10.1016/j.memsci.2007.10.007
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This contribution demonstrates a method for preparing high-capacity membrane adsorbers by growing surface-tethered, charged polymer nanolayers from the surfaces of regenerated cellulose (RC) membranes (average pore diameter 1 p,m). Surface-initiated atom transfer radical polymerization was used to grow the cation-exchanger poly(acrylic acid) (PAA). By varying the polymerization time, the thickness of the nanolayer was controlled. Characterization was done by ATR-FTIR spectroscopy to follow the modification steps. Water flux measurements illustrated that polymerization time could be used to decrease average effective pore sizes controllably. Pore-size distributions measured by liquid dewetting permporometry also confirmed that polymer chains were grown from the surface of the membrane pores. Static and dynamic binding capacities were measured for lysozyme on the PAA-modified RC membranes. Capacities initially increase with increasing modification times and reach maximum values of 98.5 mg/ml (static) and 71.2 mg/ml (dynamic). Confocal laser scanning microscopy (CLSM) was used to visualize binding of fluorescently labeled lysozyme on the unmodified and PAA-modified membranes. CLSM of labeled membranes also showed that the modification procedure had no detrimental effects on the membrane pore structure. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 72
页数:9
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