TY - JOUR
T1 - Synthesis and characterization of poly(aryl ether sulfone) PolyHIPE materials
AU - Cameron, Neil R.
AU - Sherrington, David C.
PY - 1997/9/22
Y1 - 1997/9/22
N2 - The preparation and characterization of poly(aryl ether sulfone) (PES) PolyHIPE (polymerized high internal phase emulsion) materials is described. A maleimide-terminated aryl ether sulfone macromonomer was copolymerized with styrene, divinylbenzene (DVB), or a bis(vinyl ether) species, in the continuous phase of a HIPE. Furthermore, a novel, nonaqueous HIPE methodology was employed, since only dipolar aprotic solvents were able to cosolubilize the polymeric precursor and surfactant. HIPEs of petroleum ether, dispersed in a dipolar aprotic solution of maleimide-terminated PES, PEO-PPO-PEO block copolymer surfactants, comonomer, and AIBN, were successfully prepared and polymerized. The cellular structures and porosities of the resulting materials were characterized by SEM, solvent imbibition, mercury porosimetry, and a Brunauer-Emmett-Teller (BET) treatment of nitrogen adsorption results. All were shown to possess an open-cellular morphology and a secondary pore structure within the polymer walls. Thermogravimetric analysis (TGA) of the materials indicated that critical degradation occurred at higher temperatures than in poly(styrene/DVB) PolyHIPE but lower than the PES macromonomer precursor.
AB - The preparation and characterization of poly(aryl ether sulfone) (PES) PolyHIPE (polymerized high internal phase emulsion) materials is described. A maleimide-terminated aryl ether sulfone macromonomer was copolymerized with styrene, divinylbenzene (DVB), or a bis(vinyl ether) species, in the continuous phase of a HIPE. Furthermore, a novel, nonaqueous HIPE methodology was employed, since only dipolar aprotic solvents were able to cosolubilize the polymeric precursor and surfactant. HIPEs of petroleum ether, dispersed in a dipolar aprotic solution of maleimide-terminated PES, PEO-PPO-PEO block copolymer surfactants, comonomer, and AIBN, were successfully prepared and polymerized. The cellular structures and porosities of the resulting materials were characterized by SEM, solvent imbibition, mercury porosimetry, and a Brunauer-Emmett-Teller (BET) treatment of nitrogen adsorption results. All were shown to possess an open-cellular morphology and a secondary pore structure within the polymer walls. Thermogravimetric analysis (TGA) of the materials indicated that critical degradation occurred at higher temperatures than in poly(styrene/DVB) PolyHIPE but lower than the PES macromonomer precursor.
UR - http://www.scopus.com/inward/record.url?scp=0031235071&partnerID=8YFLogxK
U2 - 10.1021/ma961403f
DO - 10.1021/ma961403f
M3 - Article
AN - SCOPUS:0031235071
SN - 0024-9297
VL - 30
SP - 5860
EP - 5869
JO - Macromolecules
JF - Macromolecules
IS - 19
ER -