Synthesis and solution rheology of poly[(stearyl methacrylate)-stat-([2-(methacryloyloxy)ethyl] trimethyl ammonium iodide)]

被引:13
作者
Vesterinen, Arja-Helena [1 ]
Rich, Jaana [1 ]
Seppala, Jukka [1 ]
机构
[1] Aalto Univ, Sch Sci & Technol, Polymer Technol Res Grp, FIN-00076 Aalto, Finland
关键词
Amphiphilic; Polyelectrolyte; Solution rheology; BLOCK-COPOLYMERS; STEARYL METHACRYLATE; POLYMER-SOLUTIONS; RADICAL COPOLYMERIZATION; AQUEOUS-MEDIA; VISCOSITY; STYRENE; POLYELECTROLYTES; ARCHITECTURE; ASSOCIATION;
D O I
10.1016/j.jcis.2010.07.073
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Poly([stearyl methacrylate]-stat-[2-(dimethylamino) ethyl methacrylate]) was synthesised through radical polymerisation using 1,1-diphenyl ethylene (DPE) as a molecular weight controlling agent. The amino groups were further quaternised into a cationic form in order to increase water solubility. Solubility of the polymers in water and a mixed solvent was studied with rotational rheometry. The resulting poly[(stearyl methacrylate)-stat-([2-(methacryloyloxy)ethyl] trimethyl ammonium iodide)] was soluble in water when the amount of stearyl methacrylate (SMA) in the polymer was less than 17 mol%. At higher SMA content, solubility strongly decreased but could be improved by using an organic co-solvent. Viscosity of the SMA-based statistical co-polymers is strongly dependent on polymer composition but solvent quality also has an influence, and the fluidic character can be either Newtonian or shear-thinning, or a weak gel can be formed. Concentration dependence behaviour deviates from that of typical polyelectrolytes. SMA polymers retain low viscosity up to rather high concentrations, but above a certain limiting concentration, the viscosity rapidly increases. This phenomenon is stronger with a higher amount of hydrophobic side-chain. At high co-polymer concentrations no entanglement formation was observed, and theological behaviour indicates that SMA segments form aggregates in water solution. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:478 / 484
页数:7
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