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基于聚合物纳米孔膜的疏水性 conformally initiated chemical vapor deposition 分离。

Polymeric nanopore membranes for hydrophobicity-based separations by conformal initiated chemical vapor deposition.

机构信息

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.

出版信息

Nano Lett. 2011 Feb 9;11(2):677-86. doi: 10.1021/nl103799d. Epub 2010 Dec 17.

Abstract

High-aspect ratio hydrophobic, cylindrical nanopores having diameters as low as 5 nm are rapidly fabricated using conformal vapor deposition of fluorinated polymeric layers into porous track-etched polycarbonate membranes. The resultant selectivity of these membranes for pairs of small molecules of similar size, but of different hydrophobicity, arises from solute-pore wall interactions emphasized by confinement. Increasing selectivity was observed as pore diameter decreased and as the surface of the pore became more hydrophobic. Cylindrical pores provided higher selectivity than bottleneck-shaped pores having the same minimum diameter. A maximum selectivity of 234 was achieved between mesitylene and phloroglucinol by the best performing membrane. Membranes with small fluorinated pores exhibited an effective cutoff based on the polar surface area of the molecules, with limited correlation with solute size. This technology could lead to a new generation of membrane separations based on specific interactions.

摘要

高纵横比的疏水、圆柱形纳米孔,其直径低至 5nm,是通过将氟化聚合物层共形气相沉积到多孔径迹蚀刻聚碳酸酯膜中来快速制造的。这些膜对具有相似尺寸但疏水性不同的小分子对的选择性来自于溶质-孔壁相互作用,这种作用受到限制。随着孔径的减小和孔表面变得更加疏水,选择性增加。与具有相同最小直径的瓶颈形孔相比,圆柱形孔提供了更高的选择性。通过性能最佳的膜,间二甲苯和间苯三酚之间的最大选择性达到 234。具有小氟化孔的膜根据分子的极性表面积表现出有效的截止,与溶质尺寸的相关性有限。这项技术可能会导致基于特定相互作用的新一代膜分离。

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