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4-(2-呋喃基)-3-丁烯-2-酮在不同铼相上的水相加氢反应

Aqueous Phase Hydrogenation of 4-(2-Furyl)-3-buten-2-one over Different Re Phases.

作者信息

Díaz Claudio Ignacio C, Araya-López Claudio, Dongil A B, Escalona Nestor

机构信息

Departamento de Ingeniería Química y Bioprocesos, Escuela de Ingeniería, Pontificia Universidad Católica de Chile, Avenida Vicuña Mackenna 4860, Macul, Santiago 7820436, Chile.

Millenium Nuclei on Catalytic Processes towards Sustainable Chemistry (CSC), Santiago 7820436, Chile.

出版信息

Molecules. 2024 Aug 14;29(16):3853. doi: 10.3390/molecules29163853.

Abstract

4-(2-furyl)-3-buten-2-one (FAc) is obtained by aldol condensation of furfural and acetone and has been used in hydrodeoxygenation reactions to obtain fuel products using noble metal catalysts. The hydrogenation of FAc in the aqueous phase using metallic- and Re oxide-supported catalysts on graphite was studied, within a temperature range of 200-240 °C, in a batch reactor over a 6 h reaction period. The catalysts were characterized using N adsorption-desorption, TPR-H, TPD-NH, XRD, and XPS analyses. Catalytic reactions revealed that metallic rhenium and rhenium oxide-supported catalysts are active for the hydrogenation and Piancatelli rearrangement of FAc. Notably, metallic rhenium exhibited a fourfold higher initial rate than rhenium oxide, which was attributed to the higher dispersion of Re in the Re/G catalyst over graphite. Re/G and ReOx/G catalysts tended to rearrange and hydrogenate FAc to 2-(2-oxopropyl)cyclopenta-1-one in water.

摘要

4-(2-呋喃基)-3-丁烯-2-酮(FAc)通过糠醛和丙酮的羟醛缩合反应制得,并已用于使用贵金属催化剂的加氢脱氧反应以获得燃料产品。研究了在间歇反应器中,在200-240℃的温度范围内,在6小时的反应时间内,使用负载在石墨上的金属和氧化铼催化剂对水相中FAc的氢化反应。使用N吸附-脱附、TPR-H、TPD-NH、XRD和XPS分析对催化剂进行了表征。催化反应表明,金属铼和负载氧化铼的催化剂对FAc的氢化和Piancatelli重排具有活性。值得注意的是,金属铼的初始速率比氧化铼高四倍,这归因于Re在石墨上的Re/G催化剂中具有更高的分散度。Re/G和ReOx/G催化剂倾向于在水中将FAc重排并氢化为2-(2-氧代丙基)环戊-1-酮。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5025/11357411/6a9a2489d263/molecules-29-03853-g001.jpg

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