Affiliation:
1. Polytechnic Institute of Zhejiang University Quzhou Zhejiang 324000 P. R. China
2. Institute of Zhejiang University‐Quzhou Quzhou Zhejiang 324000 P. R. China
3. Quzhou University Quzhou 324000 P. R. China
4. State Key Laboratory of Chemical Engineering Zhejiang University Hangzhou Zhejiang 310027 P. R. China
5. BASF Advanced Chemicals Co. Ltd. Shanghai 200137 P. R. China
6. Henan Polytechnic University Jiaozuo 454003 P. R. China
Abstract
AbstractMechanistic understanding of free radical polymerization (FRP) in aqueous solution is hindered by the lack of kinetic coefficient data. Here, we investigated the propagation rate coefficient (kp) for FRP of HEMA in aqueous solution. The kp at 80 °C increased by 6 times as the monomer weight fraction in aqueous system decreases from 100 wt.% to 6 wt.%, that is., from 6.0 × 103 to 3.3 × 104 L·moL−1·s−1. This increase in kp is associated with the increase in pre‐exponential factor (A), which suggests an increase in entropy with increasing water molecules in the polymerization system. To investigate the effect of solvent on kp, pulse‐laser polymerization in solvents of different hydrogen bonding affinity, that is, 50 wt.% butyl propionate (BP) and dimethyl formamide (DMF), are conducted. The kp obtained are in order of kp,bulk∼kp,BP > kp,DMF, suggesting that the intermolecular hydrogen bonding at carbonyl moieties critically affects the geometry of transition state quasi‐equilibrium in propagation. We underpinned this observation by analyzing the carbonyl and alkene moieties of HEMA in different solvents using infrared (IR) spectroscopy. The mechanistic analyses and insights relating to hydrogen bonding and functional moieties can be relevant for future studies involving non‐aqueous solvents promoting hydrogen bonds.