4.5 Article

Effect of Metal Ion Modified TS-1 on Cyclization Properties of 6-Hydroxyhexanoic Acid

Journal

CATALYSIS LETTERS
Volume 151, Issue 12, Pages 3501-3508

Publisher

SPRINGER
DOI: 10.1007/s10562-021-03546-3

Keywords

6-hydroxyhexanoic acid; Cyclization; epsilon-caprolactone; Metals; Titanium-silicalite-1(TS-1)

Funding

  1. China's National Key Research and Development Program [2017YFC0804801]

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In this study, TS-1 samples modified by different metal ions were prepared using the equal volume impregnation method and applied to the cyclization reaction of 6-hydroxyhexanoic acid. It was found that Mg2+ and Co2+ modification increased the yield of epsilon-caprolactone, while Zn2+ modification decreased the yield.
In this study, Titanium-silicalite-1 (TS-1) samples modified by different metal ions to form M-TS-1 (M = Mg2+, Zn2+, Co2+, with a load of 5%) were prepared by equal volume impregnation method. The physical properties of the samples were characterized by FT-IR, N-2 adsorption-desorption, XRD, UV-vis. The catalysts were applied to the cyclization reaction of 6-hydroxyhexanoic acid, and the effects of catalyst type, reaction temperature, catalyst dosage and reaction pressure on the yield of epsilon-caprolactone were investigated. The experimental results showed that the catalytic capacity of catalysts modified by different metal ions are different. The addition of Mg2+ and Co2+ increased the pore size of TS-1, provided more catalytic active sites and accelerated the mass transfer of 6-hydroxycaproic acid. The yield of epsilon-caprolactone modified by Mg2+ and Co2+ increased by 6.88% and 13.93%, respectively. The addition of Zn2+ reduced the specific surface area and pore size of TS-1, and the yield of epsilon-caprolactone decreased by 3.12%. This study showed that under the relatively optimized process conditions (the temperature of 300 degrees C, the reaction pressure of 1.3 kPa and the catalyst dosage was 5%) the yield of epsilon-caprolactone of TS-1 modified by Co2+ was up to 74.5%.The process developed in this study has promising application potential in the industrial production of epsilon-caprolactone. Graphic TS-1 modified by metal ions prepared by equal volume impregnation method should be used in the cyclization reaction of 6-hydroxycaproic acid, and epsilon-caprolactone can be obtained with high yield. The reaction mechanism is that the hydroxyl and hydrogen in 6-hydroxycaproic acid are unstable in the catalyst, and it is easy to break and combine with water to remove and form epsilon-caprolactone. Due to the high reaction temperature, some oligomers are formed, and its reaction equation is as follows.

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