Industrial applications of the aggregation of block copolymers in supercritical CO2: a SANS study

被引:0
|
作者
F. Lo Celso
A. Triolo
F. Triolo
J. McClain
J.M. Desimone
R.K. Heenan
H. Amenitsch
R. Triolo
机构
[1] University of Palermo,
[2] Department of Physical Chemistry,undefined
[3] viale delle Scienze,undefined
[4] 90128 Palermo,undefined
[5] Italy,undefined
[6] HMI-BENSC,undefined
[7] 14109 Berlin,undefined
[8] Germany,undefined
[9] Mount Sinai School of Medicine,undefined
[10] New York,undefined
[11] NY 10029,undefined
[12] USA,undefined
[13] Department of Chemistry,undefined
[14] University of North Carolina,undefined
[15] Chapel Hill,undefined
[16] NC 27599-3290,undefined
[17] USA,undefined
[18] Rutherford Appleton Laboratory,undefined
[19] Chilton OX11 0QX,undefined
[20] UK,undefined
[21] Sincrotrone Elettra,undefined
[22] 34012 Trieste,undefined
[23] Italy,undefined
来源
Applied Physics A | 2002年 / 74卷
关键词
PACS: 61.12.Ex; 61.25.Hq; 64.75.+g;
D O I
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学科分类号
摘要
Industrial applications of supercritical carbon dioxide (scCO2) rely upon the rather selective and easily adjustable solvent ability of CO2. CO2 near the critical point is a poor solvent for high molecular weight (HMW) hydrocarbon polymers, while it is a very good solvent for amorphous fluorinated polymers. By increasing the pressure, CO2 becomes a good solvent even for HMW hydrogenated chains. Specially engineered amphiphilic di-block copolymers, with CO2-philic and CO2-phobic portions, are expected to undergo trough a monomer–aggregate transition when the solvent density of the scCO2 changes. Here small-angle neutron scattering (SANS) results are reported for a block copolymer dissolved in liquid and supercritical CO2. Time-resolved small-angle X-ray scattering (TR-SAXS) results are also reported.
引用
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页码:s1427 / s1429
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