کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1390342 1500883 2013 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Catalytic dehydration of fructose to 5-hydroxymethylfurfural over Nb2O5 catalyst in organic solvent
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آلی
پیش نمایش صفحه اول مقاله
Catalytic dehydration of fructose to 5-hydroxymethylfurfural over Nb2O5 catalyst in organic solvent
چکیده انگلیسی

The catalytic dehydration of fructose to 5-hydroxymethylfurfural (HMF) in DMSO was performed over Nb2O5 derived from calcination of niobic acid at various temperatures (300–700 °C). The catalysts were characterized by powder X-ray diffraction, N2 physical adsorption, temperature-programed desorption of NH3, n-butylamine titration using Hammett indicators, infrared spectroscopy of adsorbed pyridine, and X-ray photoelectron spectroscopy. It was found that both catalytic activity and surface acid sites decrease with increasing calcination temperatures. The Nb2O5 derived from calcination of niobic acid at 400 °C reveals the maximum yield of HMF among all the catalysts, although the amount of acid sites on the catalyst is lower than that on the sample calcined at 300 °C. The results suggest that the presence of larger amounts of strong acid sites on the surface of the Nb2O5 calcined at 300 °C may promote side reactions. The Nb2O5 prepared at 400 °C shows 100% fructose conversion with 86.2% HMF yield in DMSO at 120 °C after 2 h. The activity of the catalyst decreases gradually during recycle because of coke deposition; however, it can be fully recovered by calcination at 400 °C for 2 h, suggesting that this catalyst is of significance for practical applications.

Figure optionsDownload as PowerPoint slideHighlights
► 5-Hydroxymethylfurfural was synthesized by the catalytic dehydration of fructose.
► Nb2O5 calcined at 400 °C is a highly efficient catalyst.
► 100% fructose conversion with 86.2% HMF yield was obtained at 120 °C for 2 h.
► This Nb2O5 catalyst was deactivated gradually during recycle due to carbon deposition.
► The activity of the catalyst can be fully recovered by calcination.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Carbohydrate Research - Volume 368, 7 March 2013, Pages 78–83
نویسندگان
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