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The free‐radical copolymerization propagation kinetics of the bio‐renewable monomer γ‐methyl‐α‐methylene‐γ‐butyrolactone (MeMBL) with styrene (ST) and with methyl methacrylate (MMA) have been investigated by the pulsed laser polymerization (PLP)—size exclusion chromatography (SEC) technique, in addition to DSC and proton NMR measurements. Monomer reactivity ratios for bulk MeMBL/ST and MeMBL/MMA copolymerizations are rMeMBL = 0.80 ± 0.04 and rST = 0.34 ± 0.04 and rMeMBL = 3.0 ± 0.3 and rMMA = 0.33 ± 0.01, respectively, with no significant variation with temperature found between 22 and 90 °C. The implicit penultimate unit effect (IPUE) model best represents the composition‐averaged copolymerization propagation rate coefficient, kp,cop for the MeMBL/ST system. Arrhenius parameters were estimated for MeMBL homopolymerization and found to be quite similar to those of MMA. DSC results show that copolymers of well controlled composition can be produced to suit specific Tg requirements over a much higher temperature range than possible with current acrylic glasses.magnified image

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The propagation kinetics and copolymerization behavior of the biorenewable monomer γ-methyl-α-methylene-γ-butyrolactone (MeMBL) are studied using the pulsed laser polymerization (PLP)/size exclusion chromatography (SEC) technique. The propagation rate coefficient for MeMBL is 15% higher than that of its structural analogue, methyl methacrylate (MMA), with a similar activation energy of 21.8 kJ·mol(-1). When compared to MMA, MeMBL is preferentially incorporated into copolymers when reacted with styrene (ST), MMA, and n-butyl acrylate (BA); the monomer reactivity ratios fit from bulk MeMBL/ST, MeMBL/MMA, and MeMBL/BA copolymerizations are r(MeMBL) = 0.80 ± 0.04 and r(ST) = 0.34 ± 0.04, r(MeMBL) = 3.0 ± 0.3 and r(MMA) = 0.33 ± 0.01, and r(MeMBL) = 7.0 ± 2.0 and r(BA) = 0.16 ± 0.03, respectively. In all cases, no significant variation with temperature was found between 50 and 90 °C. The implicit penultimate unit effect (IPUE) model was found to adequately fit the composition-averaged copolymerization propagation rate coefficient, k(p,cop), for the three systems.

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