Introducing Chemical Transport Selectivity into Gold Nanotubule Membranes

Abstract

We recently described polymeric membranes that contain a collection of monodisperse Au nanotubules with inside diameters of molecular dimensions (<1 nm). W showed that these membranes can be used to cleanly separate small molecules on the basis of molecular size. These membranes can also show charge-based transport selectivity which can be reversible switched between cation and anion-selective states. In addition to molecular size- and charge-based selectivity, chemical interactions (e.g., hydrogen bonding or hydrophobic interactions) between the membrane material and the molecule to be transport can be used to control transport selectivity. The introduction of such chemically-based transport selectivity into the Au nanotubule membranes is described here. This was accomplished by chemisorbing thiols (R-SH) to the Au tubule surfaces. Membranes derivatized with two different R groups - the hydrophobic R = -C16H33 and the more hydrophilic R = -C2H4-OH - were prepared. We show here that the rate and selectivity of transport in these membranes is dramatically altered by the chemical identity of the R group.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 1998
Accession Number
ADA349563

Entities

People

  • Charles R. Martin
  • John C. Hulteen

Organizations

  • Colorado State University

Tags

Communities of Interest

  • Advanced Electronics

DTIC Thesaurus Topics

  • Chemistry
  • Coefficients
  • Diameters
  • Diffusion Coefficient
  • Fullerenes
  • Hydrophilic Properties
  • Hydrophobic Properties
  • Membranes
  • Military Research
  • Molecules
  • Plating
  • Pyridines
  • Small Molecules
  • Transport Properties
  • Transport Ships
  • United States
  • United States Government

Fields of Study

  • Chemistry

Readers

  • Electrochemical Surface Science
  • Nanocomposite Materials Science
  • Underwater engineering and Marine Technology.