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:
JAPAN ATOM ENERGY RES INST,TAKASAKI RADIAT CHEM RES ESTAB,DEPT DEV,TAKASAKI,GUNMA 37012,JAPANJAPAN ATOM ENERGY RES INST,TAKASAKI RADIAT CHEM RES ESTAB,DEPT DEV,TAKASAKI,GUNMA 37012,JAPAN
GAO, DY
YOSHIDA, M
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JAPAN ATOM ENERGY RES INST,TAKASAKI RADIAT CHEM RES ESTAB,DEPT DEV,TAKASAKI,GUNMA 37012,JAPANJAPAN ATOM ENERGY RES INST,TAKASAKI RADIAT CHEM RES ESTAB,DEPT DEV,TAKASAKI,GUNMA 37012,JAPAN
YOSHIDA, M
ASANO, M
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JAPAN ATOM ENERGY RES INST,TAKASAKI RADIAT CHEM RES ESTAB,DEPT DEV,TAKASAKI,GUNMA 37012,JAPANJAPAN ATOM ENERGY RES INST,TAKASAKI RADIAT CHEM RES ESTAB,DEPT DEV,TAKASAKI,GUNMA 37012,JAPAN
ASANO, M
FUKUZAKI, H
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JAPAN ATOM ENERGY RES INST,TAKASAKI RADIAT CHEM RES ESTAB,DEPT DEV,TAKASAKI,GUNMA 37012,JAPANJAPAN ATOM ENERGY RES INST,TAKASAKI RADIAT CHEM RES ESTAB,DEPT DEV,TAKASAKI,GUNMA 37012,JAPAN
FUKUZAKI, H
KAETSU, I
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JAPAN ATOM ENERGY RES INST,TAKASAKI RADIAT CHEM RES ESTAB,DEPT DEV,TAKASAKI,GUNMA 37012,JAPANJAPAN ATOM ENERGY RES INST,TAKASAKI RADIAT CHEM RES ESTAB,DEPT DEV,TAKASAKI,GUNMA 37012,JAPAN
机构:
Korea Atom Energy Res Inst, Adv Radiat Technol Inst, Jeongeup 580185, Jeollabuk Do, South KoreaKorea Atom Energy Res Inst, Adv Radiat Technol Inst, Jeongeup 580185, Jeollabuk Do, South Korea
Jung, Chan-Hee
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机构:
Lee, Byoung-Min
Hwang, In-Tae
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机构:
Korea Atom Energy Res Inst, Adv Radiat Technol Inst, Jeongeup 580185, Jeollabuk Do, South KoreaKorea Atom Energy Res Inst, Adv Radiat Technol Inst, Jeongeup 580185, Jeollabuk Do, South Korea
Hwang, In-Tae
Choi, Jae-Hak
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Korea Atom Energy Res Inst, Adv Radiat Technol Inst, Jeongeup 580185, Jeollabuk Do, South KoreaKorea Atom Energy Res Inst, Adv Radiat Technol Inst, Jeongeup 580185, Jeollabuk Do, South Korea
Choi, Jae-Hak
Nho, Young-Chang
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Korea Atom Energy Res Inst, Adv Radiat Technol Inst, Jeongeup 580185, Jeollabuk Do, South KoreaKorea Atom Energy Res Inst, Adv Radiat Technol Inst, Jeongeup 580185, Jeollabuk Do, South Korea