Influence of mid-chain radicals on acrylate free radical polymerization: Effect of ester alkyl group

被引:51
作者
Sato, E [1 ]
Emoto, T [1 ]
Zetterlund, PB [1 ]
Yamada, B [1 ]
机构
[1] Osaka City Univ, Grad Sch Engn, Dept Appl & Bioappl Chem, Osaka 5588585, Japan
关键词
backbiting; branched polymer; ESR/EPR; persistent radical; radical polymerization; unsaturated end group;
D O I
10.1002/macp.200400140
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 benzene solution polymerizations of tertbutyl acrylate (tBA) and 2-ethylhexyl acrylate (EHA) have been investigated with respect to the effects of mid-chain radicals (MCRs) on the rate of polymerization, the total radical concentration, the apparent rate coefficients for propagation, termination, and beta-fragmentation, the contents of unsaturated end groups and branching, and the molecular weight distribution. The EHA polymerization involves a considerably higher concentration of MCR and is more significantly affected by MCR than the tBA polymerization. The MCR content as estimated by electron paramagnetic resonance (EPR) spectroscopy during photosensitized EHA polymerization was as high as 70% of the total radical concentration at 25 degreesC. However, no H-1 and C-13 NMR resonances due to unsaturated ends and branching, respectively, were detected for the poly(EHA) obtained at 25 degreesC. These findings indicate that a high MCR content does not directly correspond to significant MCR effects on the polymer structure. The rate constants for mutual reaction (k(t)(')) and beta-fragmentation (k(f)) of MCR were estimated for the two assumed cases where MCR was consumed solely by (i) mutual reaction, and (ii) beta-fragmentation, based on the aftereffect of the photosensitized EHA polymerization monitored by EPR spectroscopy at 25 degreesC; k(t)(')= 3.5 x 10(3) L . mol . s(-1) and k(f) = 4.2 x 10(-2) s(-1). These rate coefficients were compared with those for reactions of structurally similar radicals.
引用
收藏
页码:1829 / 1839
页数:11
相关论文
共 41 条
[1]   Chain transfer to polymer in free-radical solution polymerization of n-butyl acrylate studied by NMR spectroscopy [J].
Ahmad, NM ;
Heatley, F ;
Lovell, PA .
MACROMOLECULES, 1998, 31 (09) :2822-2827
[2]   Effect of the intramolecular chain transfer to polymer on PLP/SEC experiments of alkyl acrylates [J].
Arzamendi, G ;
Plessis, C ;
Leiza, JR ;
Asua, JM .
MACROMOLECULAR THEORY AND SIMULATIONS, 2003, 12 (05) :315-324
[3]  
Azukizawa M, 2000, MACROMOL CHEM PHYSIC, V201, P774, DOI 10.1002/(SICI)1521-3935(20000401)201:7<774::AID-MACP774>3.3.CO
[4]  
2-B
[5]   ELECTRON-SPIN RESONANCE STUDY OF RADICALS IN PHOTOPOLYMERIZED DI(METH)ACRYLATE NETWORK [J].
BEST, ME ;
KASAI, PH .
MACROMOLECULES, 1989, 22 (06) :2622-2627
[6]   Determination of free-radical propagation rate coefficients of butyl, 2-ethylhexyl, and dodecyl acrylates by pulsed-laser polymerization [J].
Beuermann, S ;
Paquet, DA ;
McMinn, JH ;
Hutchinson, RA .
MACROMOLECULES, 1996, 29 (12) :4206-4215
[7]   Chain-length dependence of termination rate coefficients in acrylate and methacrylate homopolymerizations investigated via the SP-PLP technique [J].
Buback, M ;
Egorov, M ;
Feldermann, A .
MACROMOLECULES, 2004, 37 (05) :1768-1776
[8]   Applications of esr techniques to the study of free: Radical processes and kinetics in acrylic polymerizations [J].
Chang, HR ;
Lau, W ;
Parker, HY ;
Westmoreland, DG .
MACROMOLECULAR SYMPOSIA, 1996, 111 :253-263
[9]   Chain transfer to polymer: A convenient route to macromonomers [J].
Chiefari, J ;
Jeffery, J ;
Mayadunne, RTA ;
Moad, G ;
Rizzardo, E ;
Thang, SH .
MACROMOLECULES, 1999, 32 (22) :7700-7702
[10]  
Couvreur L, 2001, MACROMOL SYMP, V174, P197, DOI 10.1002/1521-3900(200109)174:1<197::AID-MASY197>3.0.CO