Mesoporous Gallium Oxide as Catalyst for the Synthesis of Propyl N-Octylcarbamate from CO2, n-Propanol and n-Octylamine

Javishk Shah, J. Ort, M. Carreon
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Abstract

Background: There is an increasing interest to consider carbon dioxide as a resource and a business opportunity rather than a waste with a disposal cost. Among the several specific motivations to produce platform chemicals such as carbamates from CO2 are the low or zero cost of this feedstock and the potential to be a more economic efficient route. However, this pathway requires the development of materials with tunable morphologies and textural properties that display enhanced catalytic performance, distinctive structural and adsorption properties than those of conventional materials. Gallium oxide can be rationally engineered into crystalline porous materials which combine highly desirable properties, such as controlled morphology, uniform micropores, and high surface areas with exceptional chemical and thermal stability. Method: The synthesis was performed in a batch reactor with mesoporous gallium oxide as catalyst while n-octylamine and nproponal were the reactants. The reactor was pressured with CO2. The temperature of the reaction was at 200°C and the reaction time is 24 h. Results: High surface area γ-mesostructured gallium oxide was tested as a catalyst for the synthesis of carbamates from CO2. The mesostructured catalysts displayed a high conversion of ≈ 69%, much higher than their non-mesostructured counterparts. After recycling the catalysts the γ-gallium oxide phase was preserved and displayed only a slight decrease in catalytic activity. The selectivity of carbamates was higher at small pore diameters which can be attributed to the enhanced diffusion of the linear chain carbamate compared to the branched urea derivatives. Conclusion: The results from this work demonstrate the successful use of mesostructured gallium oxide for the synthesis of carbamates from CO2. The high conversion of the mesostructured γ-gallium oxide compared to the non-mesostructured catalysts can be attributed to the high surface area.
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介孔氧化镓催化CO2、正丙醇和正辛胺合成正辛氨基甲酸丙酯
背景:人们越来越有兴趣将二氧化碳视为一种资源和商业机会,而不是一种需要处理成本的废物。从二氧化碳中生产氨基甲酸酯等平台化学品的几个具体动机之一是这种原料的成本低或为零,并且有可能成为一种更经济有效的途径。然而,这一途径需要开发具有可调形态和结构特性的材料,这些材料要比传统材料表现出增强的催化性能、独特的结构和吸附特性。氧化镓可以合理地设计成晶体多孔材料,这些材料结合了非常理想的特性,例如控制形态,均匀的微孔,具有优异的化学和热稳定性的高表面积。方法:以介孔氧化镓为催化剂,正辛胺和非丙烯为反应物,在间歇式反应器中进行合成。反应堆用二氧化碳加压。反应温度为200℃,反应时间为24 h。结果:测试了高表面积γ-介结构氧化镓作为CO2合成氨基甲酸酯的催化剂。介观结构催化剂的转化率约为69%,远高于非介观结构催化剂。催化剂回收后γ-氧化镓相保留,催化活性略有下降。氨基甲酸酯在小孔径下的选择性更高,这可归因于与支链脲衍生物相比,线性链氨基甲酸酯的扩散增强。结论:本工作的结果证明了介结构氧化镓在CO2合成氨基甲酸酯中的成功应用。与非介观结构催化剂相比,介观结构的γ-氧化镓的高转化率可归因于高表面积。
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