Synthesis of SrO–Al2O3 Solid Base Catalysts from Strontium Hydroxide and Aluminum Alkoxide by a Solid-liquid Interface Reaction

IF 0.6 4区 工程技术 Q4 ENERGY & FUELS Journal of The Japan Petroleum Institute Pub Date : 2021-03-01 DOI:10.1627/JPI.64.103
H. Matsuhashi, Asako Iwamoto, Misaho Sasaki, Kana Yoshida, H. Aritani
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引用次数: 5

Abstract

Alkaline earth metal oxides such as MgO are well known to show activities as solid base catalysts. The preparation, active site structure, and application of MgO to numerous base-catalyzed organic reactions have been extensively investigated1)~4). Strontium oxide (SrO) has a higher base strength among the alkaline earth metal oxides, because strontium (Sr) has lower electronegativity within the group of alkaline earth metals. The base strength increases in the order MgO < CaO < SrO < BaO5),6). Therefore, SrO is expected to achieve higher catalytic activity in various organic reactions. SrO catalysts are applicable to many base-catalyzed reactions, such as aldol condensation5), nitroaldol reaction7), Michel addition8),9), Cannizzaro reaction10), transesterification11)~18), Tishchenko reaction19),20), diacetone alcohol decomposition6), and amination of alkene21). However, fewer studies have been carried out with SrO than MgO as the base catalyst, particularly the preparation and application of SrO as a base catalyst, partially because of the difficulties associated with the preparation of SrO. Alkaline earth metal oxides are usually obtained by thermal decomposition of the corresponding hydroxide or carbonate at elevated temperatures2),3). For example, Mg(OH)2 is converted to MgO by thermal decomposition around 650 K22),23). However, the melting point of Sr(OH)2 is slightly lower than the decomposition temperature of the hydroxide24). Consequently, Sr(OH)2 first melts and then decomposes as the temperature increases. The decomposition of Sr(OH)2 in the liquid phase results in solid SrO with low surface area. In contrast, thermal decomposition of SrCO3 to SrO requires very high temperatures (>1073 K) because of the high thermal stability of SrCO37),10),25)~29). Therefore, the conventional thermal decomposition method is not appropriate for SrO catalyst preparation from the hydroxide or carbonate. To overcome these problems, we investigated solid-liquid interface reaction for the preparation of SrO base catalyst. In general, a metal alkoxide with high reactivity to[Regular Paper]
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氢氧化锶和醇铝固液界面反应合成SrO-Al2O3固体碱催化剂
众所周知,氧化镁等碱土金属氧化物具有固体碱催化剂的活性。MgO的制备、活性位点结构以及在多种碱催化有机反应中的应用已经得到了广泛的研究(1)~4)。在碱土金属氧化物中,氧化锶(SrO)具有较高的碱强度,因为在碱土金属基团中,锶(Sr)具有较低的电负性。基体强度的增大顺序为MgO < CaO < SrO < BaO5),6)。因此,SrO有望在各种有机反应中获得更高的催化活性。SrO催化剂适用于许多碱催化反应,如醛醇缩合反应(5)、硝基醇反应(7)、Michel加成反应(8)、9)、Cannizzaro反应(10)、酯交换反应(11)~18)、Tishchenko反应(19)、20)、二丙酮醇分解(6)、烯烃胺化反应(21)。然而,与氧化镁相比,以SrO作为碱催化剂进行的研究较少,特别是SrO作为碱催化剂的制备和应用,部分原因是SrO的制备存在困难。碱土金属氧化物通常是由相应的氢氧化物或碳酸盐在高温下热分解得到的2),3)。例如,Mg(OH)2在650 k2左右通过热分解转化为MgO(22),23)。而Sr(OH)2的熔点略低于氢氧化物的分解温度(24)。因此,随着温度的升高,Sr(OH)2首先熔化,然后分解。Sr(OH)2在液相中的分解产生了低表面积的固体SrO。相比之下,SrCO3的热分解需要非常高的温度(>1073 K),因为SrCO37),10),25)~29)具有很高的热稳定性。因此,传统的热分解方法不适用于氢氧化物或碳酸盐制备SrO催化剂。为了克服这些问题,我们研究了固液界面反应制备SrO碱催化剂。一种对[普通纸张]具有高反应性的金属醇氧化合物
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来源期刊
Journal of The Japan Petroleum Institute
Journal of The Japan Petroleum Institute 工程技术-工程:石油
CiteScore
1.70
自引率
10.00%
发文量
29
审稿时长
>12 weeks
期刊介绍: “Journal of the Japan Petroleum Institute”publishes articles on petroleum exploration, petroleum refining, petrochemicals and relevant subjects (such as natural gas, coal and so on). Papers published in this journal are also put out as the electronic journal editions on the web. Topics may range from fundamentals to applications. The latter may deal with a variety of subjects, such as: case studies in the development of oil fields, design and operational data of industrial processes, performances of commercial products and others
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