Flow Semi-continuous Mechanochemistry as a Versatile and Efficient Tool for the Synthesis of Hydrocalumite and the Isomerization of Glucose to Fructose

IF 2.8 3区 化学 Q2 CHEMISTRY, APPLIED
Antonio M. Pérez-Merchán, Ramón Moreno-Tost, Irene Malpartida, Cristina García-Sancho, Juan Antonio Cecilia, Josefa M. Mérida-Robles, Pedro Maireles-Torres
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引用次数: 0

Abstract

In this work, hydrocalumite, a layered double hydroxide with formula Ca2Al(OH)6Cl·2H2O, has been prepared for the first time using flow semi-continuous mechanochemistry with a DYNO®-MILL RESEARCH LAB (Willy A. Bachofen AG, Switzerland), with stoichiometric amount of reactants in water, after only 5 min at 25 °C. Hydrocalumite, before and after thermal treatment, was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TG–DTA) and N2 sorption at − 196 °C. Moreover, calcined hydrocalumite has been evaluated as catalyst for the isomerization of glucose to fructose, a catalytic process which has also been performed in the same flow semi-continuous mechanochemical reactor. This mechanochemical system, unlike conventional ball milling, allows working in semi-continuous and/or continuous mode, using solvents and allowing heating control up to temperatures of 80 °C. The isomerization of glucose to fructose was successfully carried out in this reactor, demonstrating that hydrocalumite prepared by mechanochemistry is more active than that prepared by co-precipitation. The optimization of several experimental variables (reaction temperature and time, glucose/catalyst weight ratio and concentration of glucose in water) has resulted in a 23.5% fructose yield, with a glucose conversion of 38.1%, after 1 h of reaction, at 50 °C, with a 17 wt% glucose and a glucose/catalyst weight ratio of 6. However, the highest fructose productivity was reached under similar experimental conditions, but after only 5 min, with a value of 0.50 kgfructose LH2O−1 h−1 (equivalent to 15 kgfructose Kgcat−1 h−1), which is susceptible to be improved by implementing a continuous mode, assisted with a liquid pump, in the mechanochemical reactor. Therefore, this work has evidenced the versatility and potential of this new flow semi-continuous mechanochemical reactor for the synthesis of crystalline layered double hydroxides, under sustainable experimental conditions, and to perform catalytic processes with high performance, using water as solvent and atmospheric conditions.

Abstract Image

流式半连续机械化学是合成氢铝石和将葡萄糖异构化为果糖的多功能高效工具
在这项工作中,首次使用 DYNO®-MILL RESEARCH LAB(Willy A. Bachofen AG,瑞士)的流动半连续机械化学法制备了氢钙石(一种层状双氢氧化物,其化学式为 Ca2Al(OH)6Cl-2H2O),在 25 °C 下只需 5 分钟即可在水中制备出等量的反应物。通过 X 射线衍射 (XRD)、X 射线光电子能谱 (XPS)、热重分析 (TG-DTA) 和 - 196 °C 下的 N2 吸附,对热处理前后的氢铝土进行了表征。此外,还对煅烧氢铝土作为葡萄糖异构化为果糖的催化剂进行了评估,这一催化过程也是在同一流动半连续机械化学反应器中进行的。这种机械化学系统与传统的球磨法不同,可以在半连续和/或连续模式下工作,使用溶剂,加热温度最高可控制在 80 °C。葡萄糖到果糖的异构化反应就是在该反应器中成功进行的,这表明通过机械化学法制备的氢铝土比通过共沉淀法制备的氢铝土更具活性。通过优化几个实验变量(反应温度和时间、葡萄糖/催化剂重量比以及葡萄糖在水中的浓度),在 50 °C、葡萄糖重量比为 17 wt%、葡萄糖/催化剂重量比为 6 的条件下,反应 1 小时后,果糖产量为 23.5%,葡萄糖转化率为 38.1%。然而,在类似的实验条件下,仅 5 分钟就达到了最高的果糖生产率,果糖生产率为 0.50 kgfructose LH2O-1 h-1(相当于 15 kgfructose Kgcat-1 h-1)。因此,这项工作证明了这种新型流动半连续机械化学反应器的多功能性和潜力,可在可持续的实验条件下合成结晶层状双氢氧化物,并在以水为溶剂和大气条件下进行高性能催化过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Topics in Catalysis
Topics in Catalysis 化学-物理化学
CiteScore
5.70
自引率
5.60%
发文量
197
审稿时长
2 months
期刊介绍: Topics in Catalysis publishes topical collections in all fields of catalysis which are composed only of invited articles from leading authors. The journal documents today’s emerging and critical trends in all branches of catalysis. Each themed issue is organized by renowned Guest Editors in collaboration with the Editors-in-Chief. Proposals for new topics are welcome and should be submitted directly to the Editors-in-Chief. The publication of individual uninvited original research articles can be sent to our sister journal Catalysis Letters. This journal aims for rapid publication of high-impact original research articles in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis.
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