Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
42699 | Applied Catalysis A: General | 2009 | 8 Pages |
The conversion of 1,4-butanediol to 2,3-dihydrofuran and tetrahydrofuran over Co–SiO2 and Co,Pd–SiO2 catalysts with 0.09, 0.46, 0.90 and 1.90 wt.% Pd have been investigated in a liquid phase. The Co loading was 40 wt.%. The catalysts were prepared by mechanochemical techniques and characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and temperature-programmed reduction (TPR) methods. The catalysts with 0.46 and 0.90% Pd were the best for the 1,4-butanediol cyclization. Palladium decreases the reduction temperature of cobalt phase by 165–185 °C down to 240–260 °C optimum concerning the yield of 2,3-dihydrofuran. It was found by XPS method that an optimum in the degree of cobalt reduction for the reaction of 1,4-butanediol cyclization exists in the region 7–12%. The comparison of nominal catalysts composition and XPS data suggests surface enrichment with palladium after reduction.
Graphical abstractConversion of 1,4-butanediol into 2,3-dihydrofuran and tetrahydrofuran over Co–SiO2 and Co,Pd–SiO2 catalysts has been studied in a liquid phase. Co–SiO2 catalyst's selectivity to 2,3-dihydrofuran and tetrahydrofuran changes drastically after Pd-promotion. Figure optionsDownload full-size imageDownload as PowerPoint slideCatalysts were prepared by mechanochemical treatment of Co3O4, PdCl2 and SiO2.