Branched polyacrylamides (PAMs) have
shown tremendous potential
in wastewater treatment, papermaking, and oil drilling due to their
unique molecular structure, remarkable shear stability, and effective
flocculability. Efficient approaches for their industrial-scale production
have attracted increasing attention. Herein, we report a facile, scalable,
highly efficient, and cost-effective strategy for the production of
branched PAMs through UV polymerization of acrylamide (AM) initiated
with a novel water-soluble macro-photoinitiator. Through precipitation
copolymerization of AM and 2-hydroxy-1-[4-(2-acryloyloxyethoxy)phenyl]-2-methyl-1-propanone
(M2959), poly(AM-co-M2959)s bearing photoinitiator
moieties on the backbone were successfully synthesized, which showed
excellent water solubility and high photoinitiation efficiency. Most
importantly, both the branching degree and main-chain length of the
branched PAMs were controllable, given that the molar mass and photoinitiating
group content of poly(AM-co-M2959)s could be effectively
controlled by adjusting the monomer feed ratio of AM/M2959. The rheological
properties of the resultant branched PAMs were characterized in detail,
and excellent water solubility and shear resistance were observed,
confirming the well-defined branched structure of the as-prepared
PAMs. Due to their facile synthesis, simplicity of operation, and
high photoinitiation efficiency, these novel macro-photoinitiators
have great potential as a versatile platform for the preparation of
various branched polymers containing different functional groups (not
limited to branched PAMs).