Abstract
The photopolymerization of styrene in presence of an efficient, eco-friendly, and a cost-effective photoinitiator, curcumin, which is found in turmeric root, has been reported for the first time. The catalytic concentration (10−6 M) of curcumin is effective to photoinitiate the polymerization of styrene. The kinetic data, inhibiting effect of benzoquinone and electron spin resonance studies, indicate that the polymerization proceeds via a free radical mechanism. The system follows non-ideal kinetics (Rp ∝ [Cur]0.36 [Sty]1.04) due to both primary radical termination and degradative chain transfer reactions. The broad peaks due to methine and methylene protons in 1H-NMR (nuclear magnetic resonance [NMR]) spectrum and a band of resonances at 145–146 ppm in 13C-NMR indicate atactic nature of the polystyrene formed. The maximum conversion at 30 ± 0.2 °C in 17 h has been limited to 23% without gelation. The formation of radicals and mechanism of polymerization are also discussed.
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