Poly(acrylic acid);
Reversible Addition Fragmentation Chain Transfer (RAFT);
Reversible addition-fragmentation/macromolecular design by inter-change of xanthates (RAFT/MADIX);
Gamma irradiation;
Trithiocarbonate;
Xanthate;
FRAGMENTATION CHAIN TRANSFER;
LIVING RADICAL POLYMERIZATION;
BLOCK-COPOLYMERS;
POLY(ACRYLIC ACID);
GAMMA-IRRADIATION;
DRUG-DELIVERY;
AQUEOUS-MEDIA;
POLYMERS;
WATER;
POLY(N-ISOPROPYLACRYLAMIDE);
D O I:
10.1016/j.radphyschem.2017.01.046
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The kinetic investigation of one-pot synthesis of poly(acrylic acid) (PAA) prepared via gamma radiation induced controlled polymerization was reported. PAA homopolymers were prepared by Reversible Addition Fragmentation Chain Transfer (RAFT) polymerization in the presence of trithiocarbonate-based chain transfer agent (CTA) 2-(Dodecylthiocarbonothioylthio)-2-methylpropionic acid (DDMAT) and also by Reversible Addition-Fragmentation/Macromolecular Design by Inter-change of Xanthates (RAFT/MADlX) polymerization in the presence of a xanthate based CTA O-ethyl-S-(1-methoxycarbonyl) ethyl dithiocarbonate (RA1). The polymerizations were performed at room temperature by the virtue of ionizing radiation. Protic solvents were used for the RAFT polymerization of AA considering environmental profits. The linear first-order kinetic plot, close control of molecular weight by the monomer/CTA molar ratio supported that the polymerization proceeds in a living fashion. The linear increase in molecular weight with conversion monitored by Size Exclusion Chromatography (SEC) is another proof of controlling of polymerization. [Monomer]/[RAFT] ratio and conversion was controlled to obtain PAA in the molecular weight range of 6900-35,800 with narrow molecular weight distributions. Reaction kinetics and effect of the amount of RAFT agent were investigated in detail. Between two different types of CTA, trithiocarbonate based DDMAT was found to be more efficient in terms of low dispersity (D) and linear first-order kinetic behavior for the radiation induced controlled synthesis of PAA homopolymers.
机构:
Russian Technol Univ, M V Lomonosov Inst Fine Chem Technol, MIREA, Moscow 119571, RussiaRussian Technol Univ, M V Lomonosov Inst Fine Chem Technol, MIREA, Moscow 119571, Russia
Serkhacheva, Natalia S.
Galynskaya, Kseniya S.
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Russian Technol Univ, M V Lomonosov Inst Fine Chem Technol, MIREA, Moscow 119571, RussiaRussian Technol Univ, M V Lomonosov Inst Fine Chem Technol, MIREA, Moscow 119571, Russia
Galynskaya, Kseniya S.
Prokopov, Nikolay I.
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Russian Technol Univ, M V Lomonosov Inst Fine Chem Technol, MIREA, Moscow 119571, RussiaRussian Technol Univ, M V Lomonosov Inst Fine Chem Technol, MIREA, Moscow 119571, Russia
Prokopov, Nikolay I.
Mineeva, Kseniya O.
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M V Lomonosov Moscow State Univ, Dept Chem, Moscow 119991, RussiaRussian Technol Univ, M V Lomonosov Inst Fine Chem Technol, MIREA, Moscow 119571, Russia
Mineeva, Kseniya O.
V. Plutalova, Anna
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M V Lomonosov Moscow State Univ, Dept Chem, Moscow 119991, RussiaRussian Technol Univ, M V Lomonosov Inst Fine Chem Technol, MIREA, Moscow 119571, Russia
V. Plutalova, Anna
V. Chernikova, Elena
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M V Lomonosov Moscow State Univ, Dept Chem, Moscow 119991, RussiaRussian Technol Univ, M V Lomonosov Inst Fine Chem Technol, MIREA, Moscow 119571, Russia