Soluble polyelectrolyte complexes composed of poly(ethylene oxide)-block-poly(sodium methacrylate) and poly(methacryloyloxyethyl trimethylammonium chloride)

被引:45
作者
Holappa, S [1 ]
Andersson, T [1 ]
Kantonen, L [1 ]
Plattner, P [1 ]
Tenhu, H [1 ]
机构
[1] Univ Helsinki, Dept Chem, Polymer Chem Lab, FIN-00014 Helsinki, Finland
关键词
polyelectrolyte complex; poly(ethylene oxide)-block-poly(methacrylic acid); light scattering;
D O I
10.1016/j.polymer.2003.10.055
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Complexation between poly(methacryloyloxyethyl trimethylammonium chloride), PMOTAC, and poly(ethylene oxide)-blockpoly(sodium methacrylate), PEO-block-PMANa with MANa blocks with two different molecular weights has been investigated by light scattering, LS, viscosimetry and conductivity measurements. Owing to the PEO blocks the polyelectrolyte complexes are water-soluble particles. Effects of the ratio of the oppositely charged monomer units, the ionic strength of the solution, and solution pH have been studied. With the 1:1 mixing ratio stable polyelectrolyte, complexes, PECs, with spherical shape were formed. When either the cationic or anionic component was in excess, charged non-stoichiometric complexes were formed. The complexes were stable also in solutions with comparatively high ionic strength, though stronger secondary aggregation was observed. By changing the solution pH the degree of dissociation of PEO-block-PMANa could be adjusted. In the vicinity of the pK(a,average) of PMAA, a minimum in the particle size and a maximum in the solution conductivity were observed. In solutions with lower pH, a typical self-complexation of PEO-block-PMAA was detected. Also, unexpected interactions between PMOTAC and the self-complexes of PEO-block-PMAA were observed. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7907 / 7916
页数:10
相关论文
共 37 条
[1]   Complexation of linear and poly(ethylene oxide)-grafted poly(methacryl oxyethyl trimethylammonium chloride) with poly(ethylene oxide-block-sodium methacrylate) [J].
Andersson, T ;
Holappa, S ;
Aseyev, V ;
Tenhu, H .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2003, 41 (13) :1904-1914
[2]  
ANDERSSON T, IN PRESS
[3]   KINETICS AND MECHANISM OF INTERPOLYELECTROLYTE EXCHANGE AND ADDITION-REACTIONS [J].
BAKEEV, KN ;
IZUMRUDOV, VA ;
KUCHANOV, SI ;
ZEZIN, AB ;
KABANOV, VA .
MACROMOLECULES, 1992, 25 (17) :4249-4254
[4]   QUANTITATIVE STUDIES OF INTERACTION BETWEEN COMPLEMENTARY POLYMERS AND OLIGOMERS IN SOLUTIONS [J].
BARANOVSKY, VY ;
LITMANOVICH, AA ;
PAPISOV, IM ;
KABANOV, VA .
EUROPEAN POLYMER JOURNAL, 1981, 17 (09) :969-979
[5]   Structural analysis in interpolyelectrolyte complex formation of sodium poly(styrenesulfonate) and diallyldimethylammonium chloride-acrylamide copolymers by viscometry [J].
Brand, F ;
Dautzenberg, H .
LANGMUIR, 1997, 13 (11) :2905-2910
[6]   Soluble complexes from poly(ethylene oxide)-block-polymethacrylate anions and N-alkylpyridinium cations [J].
Bronich, TK ;
Kabanov, AV ;
Kabanov, VA ;
Yu, K ;
Eisenberg, A .
MACROMOLECULES, 1997, 30 (12) :3519-3525
[7]   Thermo-responsive polymer nanoparticles with a core-shell micelle structure as site-specific drug carriers [J].
Cammas, S ;
Suzuki, K ;
Sone, C ;
Sakurai, Y ;
Kataoka, K ;
Okano, T .
JOURNAL OF CONTROLLED RELEASE, 1997, 48 (2-3) :157-164
[8]  
DAUTSENBERG H, 2001, PHYS CHEM POLYELECTR, V99, pCH20
[9]   Polyelectrolyte complex formation in highly aggregating systems. 1. Effect of salt: Polyelectrolyte complex formation in the presence of NaCl [J].
Dautzenberg, H .
MACROMOLECULES, 1997, 30 (25) :7810-7815
[10]   Stoichiometry and structure of polyelectrolyte complex particles in diluted solutions [J].
Dautzenberg, H ;
Hartmann, J ;
Grunewald, S ;
Brand, F .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1996, 100 (06) :1024-1032