Free-Radical Homo- and Copolymerization of Vinyl Acetate and n-Butyl Acrylate: Kinetic Studies by Online 1H NMR Kinetic Experiments
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作者:
Abdollahi, Mahdi
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Res Inst Petr Ind RIPI, Polymer Synth Res Ctr, Polymer Sci & Technol Div, Tehran, IranRes Inst Petr Ind RIPI, Polymer Synth Res Ctr, Polymer Sci & Technol Div, Tehran, Iran
Abdollahi, Mahdi
[1
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Massoumi, Bakhshali
[2
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Yousefi, Mohammad Reza
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Payame Noor Univ, Tabriz Branch, Dept Chem, Tabriz, IranRes Inst Petr Ind RIPI, Polymer Synth Res Ctr, Polymer Sci & Technol Div, Tehran, Iran
Yousefi, Mohammad Reza
[2
]
Ziaee, Farshid
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Iran Polymer & Petrochem Inst, Tehran, IranRes Inst Petr Ind RIPI, Polymer Synth Res Ctr, Polymer Sci & Technol Div, Tehran, Iran
Ziaee, Farshid
[3
]
机构:
[1] Res Inst Petr Ind RIPI, Polymer Synth Res Ctr, Polymer Sci & Technol Div, Tehran, Iran
[2] Payame Noor Univ, Tabriz Branch, Dept Chem, Tabriz, Iran
Free-radical homo- and copolymerization of vinyl acetate (VAc) and n-butyl acrylate (BA) in benzene-d(6) were performed by using benzoyl peroxide as an initiator at 70 degrees C. Polymerization kinetic was followed by online H-1 NMR kinetic experiments. Significant drift in the comonomer mixture composition with reaction progress was observed. Reactivity ratios of VAc and BA were calculated by terminal unit model (TUM) as well as by simplified penultimate unit model (PUM) with r(VAc) = 0. It was found that copolymer composition can be described well by the TUM. "Lumped" kinetic parameter (k(p).k(t)(-0.5)) was estimated from experimental data. A good fitting between the theoretical and experimental drifts in the comonomer mixture and copolymer compositions with reaction progress was observed. (C) 2011 Wiley Periodicals, Inc. J Appl Polym Sci 123: 543-553, 2012