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Design of Nonionic Surfactants for Supercritical Carbon Dioxide
Authors:JB McClain  DE Betts  DA Canelas  ET Samulski  JM DeSimone  JD Londono  HD Cochran  GD Wignall  D Chillura-Martino  R Triolo
Affiliation:J. B. McClain, D. E. Betts, D. A. Canelas, E. T. Samulski, J. M. DeSimone, Department of Chemistry, University of North Carolina, CB 3290, Venable and Kenan Laboratories, Chapel Hill, NC 27599, USA. J. D. Londono, H. D. Cochran, G. D. Wignall, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA. D. Chillura-Martino and R. Triolo, Departimento di Chimica Fisica, University of Palermo, 90123 Palermo, Italy.
Abstract:Interfacially active block copolymer amphiphiles have been synthesized and their self-assembly into micelles in supercritical carbon dioxide (CO2) has been demonstrated with small-angle neutron scattering (SANS). These materials establish the design criteria for molecularly engineered surfactants that can stabilize and disperse otherwise insoluble matter into a CO2 continuous phase. Polystyrene-b-poly(1,1-dihydroperfluorooctyl acrylate) copolymers self-assembled into polydisperse core-shell-type micelles as a result of the disparate solubility characteristics of the different block segments in CO2. These nonionic surfactants for CO2 were shown by SANS to be capable of emulsifying up to 20 percent by weight of a CO2-insoluble hydrocarbon into CO2. This result demonstrates the efficacy of surfactant-modified CO2 in reducing the large volumes of organic and halogenated solvent waste streams released into our environment by solvent-intensive manufacturing and process industries.
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