Synthesis of High Molecular Weight Poly(glycerol monomethacrylate) via RAFT Emulsion Polymerization of Isopropylideneglycerol Methacrylatefree
High molecular weight water-soluble polymers are widely used as flocculants or thickeners. However, synthesis of such polymers via solution polymerization invariably results in highly viscous fluids, which makes subsequent processing somewhat problematic. Alternatively, such polymers can be prepared...
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Zusammenfassung: | High molecular weight water-soluble polymers are widely used as flocculants or thickeners. However, synthesis of
such polymers via solution polymerization invariably results in highly viscous fluids, which makes subsequent processing
somewhat problematic. Alternatively, such polymers can be prepared as colloidal dispersions; in principle, this is advantageous
because the particulate nature of the polymer chains ensures a much lower fluid viscosity. Herein we exemplify the latter
approach by reporting the convenient one-pot synthesis of high molecular weight poly(glycerol monomethacrylate) (PGMA) via
the reversible addition−fragmentation chain transfer (RAFT) aqueous emulsion polymerization of a water-immiscible protected
monomer precursor, isopropylideneglycerol methacrylate (IPGMA) at 70 °C, using a water-soluble poly(glycerol
monomethacrylate) (PGMA) chain transfer agent as a steric stabilizer. This formulation produces a low-viscosity aqueous
dispersion of PGMA−PIPGMA diblock copolymer nanoparticles at 20% solids. Subsequent acid deprotection of the
hydrophobic core-forming PIPGMA block leads to particle dissolution and affords a viscous aqueous solution comprising high
molecular weight PGMA homopolymer chains with a relatively narrow molecular weight distribution. Moreover, it is shown that
this latex precursor route offers an important advantage compared to the RAFT aqueous solution polymerization of glycerol
monomethacrylate since it provides a significantly faster rate of polymerization (and hence higher monomer conversion) under
comparable conditions. |
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DOI: | 10.1021/acs.macromol.8b00294 |