Control of methyl methacrylate radical polymerization via Enhanced Spin Capturing Polymerization (ESCP)

被引:21
作者
Zang, Lin [1 ]
Wong, Edgar H. H. [1 ,3 ]
Barner-Kowollik, Christopher [1 ]
Junkers, Tanja [1 ,2 ]
机构
[1] Karlsruhe Inst Technol, Inst Tech Chem & Polymerchem, Engesserstr 18, D-76128 Karlsruhe, Germany
[2] Univ Hasselt, Inst Mat Res IMO, B-3590 Diepenbeek, Belgium
[3] Univ New S Wales, Ctr Adv Macromol Design, Sydney, NSW 2052, Australia
关键词
Methyl methacrylate (MMA); Nitrone/nitroxide; Enhanced (termination) spin capturing polymerization (ESCP); COPOLYMERIZATION PROPAGATION KINETICS; THIOKETONE-MEDIATED POLYMERIZATION; RAFT PROCESS; STYRENE; NITRONES;
D O I
10.1016/j.polymer.2010.06.040
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The nitrone mediated polymerization of methyl methacrylate (MMA) via the enhanced (termination) spin capturing polymerization (ESCP) process is made possible via the addition of small amounts of styrene (between 5 and 10 vol.%) to the reaction mixture. Efficient control over the molecular weight between 7000 and 57,000 g mol(-1) (at 60 degrees C) yields macromolecules that feature a mid-chain alkoxyamine functionality and are rich in methyl methacrylate. The collated kinetic and molecular weight data allow for a deduction of the spin capturing constant, C-SC, in the range between 0.15 and 0.30. During the ESCP process, the number average molecular weight, M-n of the formed mid-chain functional polymer is constant up to high monomer to polymer conversions (i.e. 80%). The high degree of alkoxyamine mid-chain functionality present in the generated polymeric material is evidenced via a subsequent nitroxide-mediated polymerization process employing the formed ESCP polymer, indicating a chain extension from 37,700 to 118,000 g mol(-1) with a concomitant reduction in polydispersity (from 2.3 to 1.5). (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3821 / 3825
页数:5
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