Ring-opening polymerization of trimethylene carbonate to poly(trimethylene carbonate) diol over a heterogeneous high-temperature calcined CeO2 catalyst
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作者:
Tamura, Masazumi
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Tohoku Univ, Grad Sch Engn, Aoba Ku, Aoba 6-6-07, Sendai, Miyagi 9808579, JapanTohoku Univ, Grad Sch Engn, Aoba Ku, Aoba 6-6-07, Sendai, Miyagi 9808579, Japan
Tamura, Masazumi
[1
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Matsuda, Keitaro
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Tohoku Univ, Grad Sch Engn, Aoba Ku, Aoba 6-6-07, Sendai, Miyagi 9808579, JapanTohoku Univ, Grad Sch Engn, Aoba Ku, Aoba 6-6-07, Sendai, Miyagi 9808579, Japan
Matsuda, Keitaro
[1
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Nakagawa, Yoshinao
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Tohoku Univ, Grad Sch Engn, Aoba Ku, Aoba 6-6-07, Sendai, Miyagi 9808579, JapanTohoku Univ, Grad Sch Engn, Aoba Ku, Aoba 6-6-07, Sendai, Miyagi 9808579, Japan
Nakagawa, Yoshinao
[1
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Tomishige, Keiichi
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Tohoku Univ, Grad Sch Engn, Aoba Ku, Aoba 6-6-07, Sendai, Miyagi 9808579, JapanTohoku Univ, Grad Sch Engn, Aoba Ku, Aoba 6-6-07, Sendai, Miyagi 9808579, Japan
Tomishige, Keiichi
[1
]
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[1] Tohoku Univ, Grad Sch Engn, Aoba Ku, Aoba 6-6-07, Sendai, Miyagi 9808579, Japan
CeO2 calcined at 1273 K showed higher activity per surface area than other metal oxides in the ring-opening polymerization of trimethylene carbonate under neat conditions without any additives, providing metal-free and additive-free poly(trimethylene carbonate) diols with no ether bonds with high selectivity. It was demonstrated that CeO2 was a robust and reusable heterogeneous catalyst.