Characterization of highly branched poly(methyl methacrylate) by solution viscosity and viscoelastic spectroscopy

被引:111
作者
Simon, PFW
Müller, AHE
Pakula, T
机构
[1] Univ Bayreuth, Bayreuther Inst Makromol Forsch, D-95440 Bayreuth, Germany
[2] Univ Mainz, Inst Phys Chem, D-55099 Mainz, Germany
[3] Max Planck Inst Polymer Res, D-55021 Mainz, Germany
关键词
D O I
10.1021/ma0014766
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Highly branched poly(methyl methacrylate) with an estimated degree of branching (DB) over bar = 0.074 (i.e., 3.7 branchpoints per 100 monomer units) was prepared using self-condensing group transfer copolymerization (SCVCP) of methyl methacrylate (MMA) and 2-(2-methyl-1-triethylsiloxy-1-propenyloxy)ethyl methacrylate (MTSHEMA) and fractionated by means of preparative SEC. The fractions were characterized in solution by SEC-viscosity coupling and in the melt by viscoelastic spectroscopy. In THF solution, a Mark-Houwink exponent of alpha = 0.40 was determined for the branched polymer, which is considerably lower than that of linear PMMA (alpha = 0.688). In the region between the relaxation times of the chain, tau (c), and of the segments, tau (s), of the viscoelastic spectrum of the branched polymer, both the storage and the loss moduli (log G' and log G ") are nearly equal, and the complex viscosities show a practically linear dependence on log omega with a slope of -0.54. This is attributed to a broad distribution of relaxation times and the absence of entanglements, similar to near-critical gels. The normalized chain relaxation times scale with the molecular weight with an exponent of alpha = 2.61, which again is considerably lower than the value for the linear case (alpha = 3.39).
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页码:1677 / 1684
页数:8
相关论文
共 41 条
[21]   GROUP TRANSFER AND ANIONIC-POLYMERIZATION - A CRITICAL COMPARISON [J].
MULLER, AHE .
MAKROMOLEKULARE CHEMIE-MACROMOLECULAR SYMPOSIA, 1990, 32 :87-104
[22]   Molecular parameters of hyperbranched polymers made by self-condensing vinyl polymerization .1. Molecular weight distribution [J].
Muller, AHE ;
Yan, DY ;
Wulkow, M .
MACROMOLECULES, 1997, 30 (23) :7015-7023
[23]  
MULLER MA, 1986, MAKROMOL CHEM-RAPID, V7, P575
[24]  
MUTHUKUMAR M, 1986, MACROMOLECULES, V19, P9
[25]   Solution rheology of hyperbranched polyesters and their blends with linear polymers [J].
Nunez, CM ;
Chiou, BS ;
Andrady, AL ;
Khan, SA .
MACROMOLECULES, 2000, 33 (05) :1720-1726
[26]   HYDROSILYLATION OF ALPHA,BETA-UNSATURATED NITRILES AND ESTERS CATALYZED BY TRIS(TRIPHENYLPHOSPHINE)CHLORORHODIUM [J].
OJIMA, I ;
KUMAGAI, M ;
NAGAI, Y .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1976, 111 (01) :43-60
[27]   Preparation of hyperbranched polymethacrylates by self-condensing group transfer polymerization [J].
Sakamoto, K ;
Aimiya, T ;
Kira, M .
CHEMISTRY LETTERS, 1997, (12) :1245-1246
[28]   Effects of molecular variables and architecture on the rheological behavior of dendritic polymers [J].
Sendijarevic, I ;
McHugh, AJ .
MACROMOLECULES, 2000, 33 (02) :590-596
[29]   Hyperbranched methacrylates by self-condensing group transfer polymerization [J].
Simon, PFW ;
Radke, W ;
Muller, AHE .
MACROMOLECULAR RAPID COMMUNICATIONS, 1997, 18 (09) :865-873
[30]  
SIMON PFW, UNPUB MACROMOLECULES