Non-Ideal Polymerization Kinetics of a Cationic Double Charged Acryl Monomer and Solution Behavior of the Resulting Polyelectrolytes
✍ Scribed by Ricardo Losada; Christine Wandrey
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 153 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Abstract
The radical polymerization of bis‐1,3(N,N,N‐trimethylammonium)‐2‐propylmethacrylate dichloride revealed non‐ideality with 0.59 and 4.4 for the reaction orders of the initiator and monomer concentration, respectively. Further, autoacceleration was observed from less than 10% conversion onwards. Degradative chain transfer to the monomer was concluded to explain the initiator exponent. Monomer association and electrostatic effects are hypothesized to govern the monomer exponent and autoacceleration. The exponential concentration dependent increase of the viscosity of the monomer solution and the relatively low overall activation energy E~a~ = 31.5 kJ · mol^−1^ support the hypothesis. Counterion activity measurements confirmed strong counterion condensation as expected for a charge distance of 0.12 nm.
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