Radical polymerization behavior of 3-(N-2-methacryloyloxyethyl-N,N-dimethyl)ammonato-propanesulfonate in water

The homogeneous polymerization of 3-(N-2-methacryloyloxyethyl-N,N-dimethyl)ammonatopropanesulfonate (MDAPS) with potassium peroxydisulfate (KPS) was kinetically in situ investigated in water by means of FT-near IR spectroscopy. The overall activation energy of the polymerization was calculated to be 16.0 kcal/mol. The initial polymerization rate (R-p) at 40 degreesC was expressed by R-p = k[KPS](0.65)[MDAPS](1.0). The presence of alkaline metal salts was observed to accelerate the polymerization. The order of acceleration at 40 degreesC was CsCl > KCl > NaCl > LiCl when the chloride salts were used. NaCl showed higher acceleration effect than NaF. NaBr and NaI exhibited retardation and inhibition effect, respectively, because of reduction of KPS and its primary radical with bromide and iodide ions. The polymerization of MDAPS with KPS in water in the presence of NaCl at 2.0 mol/l gave R-p = k[KPS](0.70)[MDAPS](1.4) at 40 degreesC. The overall activation energy of the polymerization in the presence of NaCl was estimated to be 11.6 kcal/mol being considerably lower value compared with that in its absence. The syndiotacticity of poly(MDAPS) tended to increase with rising temperature and decrease in the presence of NaCl. (C) 2003 Elsevier Ltd. All rights reserved.