First solvent-free synthesis of poly(N-methylolacrylamide) via frontal free-radical polymerization

被引:60
作者
Chen, Li
Hu, Ting
Yu, Huan
Chen, Su
Pojman, John A.
机构
[1] Nanjing Univ Technol, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China
[2] Univ So Mississippi, Dept Chem & Biochem, Hattiesburg, MS 39406 USA
关键词
ammonium persulfate; frontal polymerization (FP); kinetics (polym.); nanosilica; polyamides; poly(N-methylolacrylamide) (PNMA); radical polymerization; self-sustaining; solid monomers; solid-state polymerization;
D O I
10.1002/pola.22176
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report the first synthesis of poly (N-methylolacrylamide) (PNMA) via free-radical frontal polymerization (FP) with solid monomers at ambient pressure. The appropriate amounts of reactants (N-methylolacrylamide) (NMA) and initiator (ammonium persulfate) were mixed together at ambient temperature without solvent. FP was initiated by heating the wall of the tube with a soldering iron, and the resultant hot fronts were allowed to self-propagate throughout the reaction vessel. Once initiated, no further energy was required for polymerization to occur. To suppress the fingers of molten monomer, a small amount of nanosilica was added. We also produced PNMA with dimethyl sulfoxide (DMSO) or N-methyl-2-pyrrolidone, as solvent by FP, to study the macrokinetics in FP of PNMA without fillers. The front velocity and front temperature dependence on the ammonium persulfate and N-methyl-2-pyrrolidone concentration were investigated. The polymer was analyzed by thermogravimetric analysis. Results show that without postpolymerization solvent removal, waste production can be reduced. Solvent-free FP could be exploited as a means for preparation of PNMA with the potential advantage of higher throughput than solvent-based methods. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:4322 / 4330
页数:9
相关论文
共 63 条
[1]  
Ainsworth W. J., 2001, ACS SYM SER, V793, P112, DOI DOI 10.1021/BK-2001-0793.CH008
[2]   Synthesis of porous macrospheres from amino-polymers [J].
Baltieri, RC ;
Innocentini-Mei, LH ;
Tamashiro, WMSC ;
Peres, L ;
Bittencourt, E .
EUROPEAN POLYMER JOURNAL, 2002, 38 (01) :57-62
[3]   Effect of orientation on thermoset frontal polymerization [J].
Bazile, M ;
Nichols, HA ;
Pojman, JA ;
Volpert, V .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2002, 40 (20) :3504-3508
[4]  
BEGISHEV VP, 1973, DOKL AKAD NAUK SSSR, V208, P892
[5]  
Bidali S, 2003, E-POLYMERS
[6]   Spherically propagating thermal polymerization fronts [J].
Binici, B ;
Fortenberry, DI ;
Leard, KC ;
Molden, M ;
Olten, N ;
Popwell, S ;
Pojman, JA .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2006, 44 (04) :1387-1395
[7]   Effect of convection on a propagating front with a solid product: Comparison of theory and experiments [J].
Bowden, G ;
Garbey, M ;
Ilyashenko, VM ;
Pojman, JA ;
Solovyov, SE ;
Taik, A ;
Volpert, VA .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (04) :678-686
[8]   Reactivity of oxetane monomers in photoinitiated cationic polymerization [J].
Bulut, U ;
Crivello, JV .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2005, 43 (15) :3205-3220
[9]  
Chechilo N. M., 1975, Dokl. Phys. Chem, V221, P392
[10]  
Chechilo N. M., 1976, Dokl. Phys. Chem, V230, P840