The solution property of amphiphilic graft copolymer has been examined by means of NMR,TEM and viscometry. It is found that water and toluene are selective solvent for PSt- g- PEO. When it is dissolved in water, micel...The solution property of amphiphilic graft copolymer has been examined by means of NMR,TEM and viscometry. It is found that water and toluene are selective solvent for PSt- g- PEO. When it is dissolved in water, micelle can be formed with hydrophobic PSt backbone as the core and hydrophilic PEO side chains as the shell. On the other hand, in selective solvent toluene, the reversed- micelle can be formed with PEO as core and PSt as the shell. In toluene, with an increase in concentration, the conformation of PSt- g- PEO can be transformed from stretched single molecule to spherical reversed- micelle. The critical micelle concentration(CMC) is determined at different temperature and with the increase of temperature and the content of PEO the reversed- micelle can be formed in lower concentrations.展开更多
Amphiphilic graft copolymers having poly（phthalazinone ether sulfone ketone）（PPESK） backbones and poly（ethylene glycol） side chains were synthesized through a modified Williamson ether method.Initially,chloromet...Amphiphilic graft copolymers having poly（phthalazinone ether sulfone ketone）（PPESK） backbones and poly（ethylene glycol） side chains were synthesized through a modified Williamson ether method.Initially,chloromethylated PPESK（CMPPESK） was prepared using chloromethylether as chloromethylation agent.Then,PPESK-g-PEGs were synthesized via the coupling of CMPPESK with alkoxides formed from PEG mono methyl ether（PEG-OH） and sodium hydride.Two PEG-OHs with the average molecular weight of 350 g/mol and 750 g/mol,respectively were used as the grafting reactants.The grafting of PEG-OHs onto PPESK backbones was confirmed by FT-IR,1H-NMR and solid13C CP-MAS NMR.The grafting degrees of PEG-OH were calculated from1H-NMR analysis,and the obtained results were approximately consistent with those from TGA analysis.The resultant PPESK-g-PEG copolymers were hydrophilic,but water insoluble,rendering them potential candidates as surface modifying additive for PPESK porous membranes.展开更多
Preparation of an amphiphilic graft copolymer having poly(phthalazinone ether sulfone ketone)(PPESK) as main chains was carried out by atom transfer radical polymerization(ATRP).The precursor,chloromethylated PPESK (C...Preparation of an amphiphilic graft copolymer having poly(phthalazinone ether sulfone ketone)(PPESK) as main chains was carried out by atom transfer radical polymerization(ATRP).The precursor,chloromethylated PPESK (CMPPESK),was prepared by using chioromethylether as chloromethylation agent.Then,poly(ethylene glycol) methyl ether methacrylate(PEGMA) was used as monomer to synthesize PPESK-g-P(PEGMA) by ATRP method under the catalysis of a cuprous chloride/2,2'-bipyridyl system.PPESK/PPESK-g-P(PEGMA) blend m...展开更多
文摘The solution property of amphiphilic graft copolymer has been examined by means of NMR,TEM and viscometry. It is found that water and toluene are selective solvent for PSt- g- PEO. When it is dissolved in water, micelle can be formed with hydrophobic PSt backbone as the core and hydrophilic PEO side chains as the shell. On the other hand, in selective solvent toluene, the reversed- micelle can be formed with PEO as core and PSt as the shell. In toluene, with an increase in concentration, the conformation of PSt- g- PEO can be transformed from stretched single molecule to spherical reversed- micelle. The critical micelle concentration(CMC) is determined at different temperature and with the increase of temperature and the content of PEO the reversed- micelle can be formed in lower concentrations.
文摘Amphiphilic graft copolymers having poly（phthalazinone ether sulfone ketone）（PPESK） backbones and poly（ethylene glycol） side chains were synthesized through a modified Williamson ether method.Initially,chloromethylated PPESK（CMPPESK） was prepared using chloromethylether as chloromethylation agent.Then,PPESK-g-PEGs were synthesized via the coupling of CMPPESK with alkoxides formed from PEG mono methyl ether（PEG-OH） and sodium hydride.Two PEG-OHs with the average molecular weight of 350 g/mol and 750 g/mol,respectively were used as the grafting reactants.The grafting of PEG-OHs onto PPESK backbones was confirmed by FT-IR,1H-NMR and solid13C CP-MAS NMR.The grafting degrees of PEG-OH were calculated from1H-NMR analysis,and the obtained results were approximately consistent with those from TGA analysis.The resultant PPESK-g-PEG copolymers were hydrophilic,but water insoluble,rendering them potential candidates as surface modifying additive for PPESK porous membranes.
基金supported by the"973"program of China(No.2009CB623402)Engineering Research Center of Ministry of Education of China(No.JD09011)
文摘Preparation of an amphiphilic graft copolymer having poly(phthalazinone ether sulfone ketone)(PPESK) as main chains was carried out by atom transfer radical polymerization(ATRP).The precursor,chloromethylated PPESK (CMPPESK),was prepared by using chioromethylether as chloromethylation agent.Then,poly(ethylene glycol) methyl ether methacrylate(PEGMA) was used as monomer to synthesize PPESK-g-P(PEGMA) by ATRP method under the catalysis of a cuprous chloride/2,2'-bipyridyl system.PPESK/PPESK-g-P(PEGMA) blend m...
