کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
60038 1419454 2013 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Vapor-phase selective dehydration of 1,4-butanediol to 3-buten-1-ol over ZrO2 catalysts modified with alkaline earth metal oxides
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Vapor-phase selective dehydration of 1,4-butanediol to 3-buten-1-ol over ZrO2 catalysts modified with alkaline earth metal oxides
چکیده انگلیسی

Modified ZrO2 catalysts were prepared by doping with alkaline earth metal oxides (CaO, SrO, or BaO) in a wet impregnation method. The catalysts were characterized by N2 physisorption, X-ray diffraction, and temperature-programmed desorption (TPD) with NH3 and CO2. Their catalytic performance in the vapor-phase selective dehydration of 1,4-butanediol (BDO) to 3-buten-1-ol (BTO) was investigated. The results showed that the alkaline earth metal can change the acid–base properties on the catalyst surface and thus affect BDO conversion and BTO product selectivity. For ZrO2 catalyst modified by CaO, Ca2+ entered the ZrO2 crystal lattice and formed Ca-O-Zr hetero-linkages. These allowed the CaO/ZrO2 catalyst to maintain a high acid density and generate a large number of basic sites when compared with unmodified ZrO2. In contrast, SrO and BaO reacted with ZrO2 to generate the corresponding zirconates, which resulted in decreased acid density on the catalyst surface. Of the catalysts tested, CaO/ZrO2 showed the best catalytic performance. The highest yield of BTO was 60.5% and was achieved at 350 °C over CaO/ZrO2 catalyst. The key point for highly selective dehydration of BDO to BTO resided in the synergistic effect between acid and base sites on the catalyst surface.

摘要通过将Ag催化的羧化偶联反应与Ru催化的交叉复分解反应串联, 用端炔/二氧化碳/端烯基取代的溴代物和甲基丙烯酸甲酯高效高产率地合成了一系列官能团化的炔酸酯.

Modified ZrO2 catalysts doped with alkaline earth metal oxides exhibit excellent catalytic performance in the vapor-phase selective dehydration of 1,4-butanediol to 3-buten-1-ol. The high catalytic activity is attributed to the rich content of acid-base bifunctional reaction centers.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chinese Journal of Catalysis - Volume 34, Issue 6, June 2013, Pages 1159–1166
نویسندگان
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