Direct Synthesis of Formic acid from Carbon Dioxide by Hydrogenation over Ruthenium Metal Doped Titanium Dioxide Nanoparticles in Functionalized Ionic Liquid

IF 0.9 Q4 CHEMISTRY, PHYSICAL
V. Srivastava
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引用次数: 0

Abstract

Presently worldwide manufacturing of formic acid follows the permutation of methanol and carbon monoxide in the presence of a strong base. But due to the use of toxic CO molecules and easy availability of CO2 molecules in the atmosphere, most of the research has been shifted from the conventional method of formic acid synthesis to direct hydrogenation of CO2 gas using different homogenous and heterogeneous catalysts. The study aims to develop a reaction protocol to achieve easy CO2 hydrogenation to formic acid using an Ionic liquid reaction medium. We used the sol-gel method followed by calcination (over 250oC for 5 hours) to synthesize two types of ruthenium metal-doped TiO2 nanoparticles (with and without ionic liquids) Ru@TiO2@IL and Ru@TiO2. We report the application NR2 (R= CH3) containing imidazolium-based ionic liquids to achieve a good reaction rate and get agglomeration free ruthenium metal-doped TiO2 nanoparticles along with easy product isolation due to the presence of NR2 (R= CH3) functionality in ionic liquid structure. We synthesized various NR2 (R= CH3) functionalized ionic liquids such as 1-Butyl-3-methylimidazolium Chloride, 1,3-di(N,N-dimethylaminoethyl)-2-methylimidazolium trifluoromethane sulfonate ([DAMI][TfO]), 1,3-di(N,N-dimethylaminoethyl)-2-methylimidazolium bis (trifluoromethylsulfonyl) imide ([DAMI][NTf2]) and 1-butyl-3-methylimidazolium chloride ionic liquids were synthesized as per the reported procedure. We quickly developed two typed of Ru metal-doped TiO2 nanoparticles using the sol-gel method. After calcination, both Ru@TiO2@IL (3.2 wt% Ru), and Ru@TiO2 (1.7 wt% Ru) materials were characterized by XRD, FTIR, TEM, ICP-AES, EDS, and XANES analysis. After understanding the correct structural arrangement of Ru metal over TiO2 support, we utilized both Ru@TiO2@IL (3.2 wt% Ru) and Ru@TiO2 (1.7 wt% Ru) the materials as a catalyst for direct hydrogenation of CO2 in the presence of water. We functionalized [DAMI] [TfO] ionic liquid. After understanding the correct morphology and physiochemical analysis of Ru@TiO2@IL (3.2 wt% Ru), and Ru@TiO2 (1.7 wt% Ru) catalysts, we examined their application in CO2 reduction and formic acid synthesis. Here we demonstrated the preparation and characterization of TiO2 supported Ru nanoparticles with and without ionic liquid. We also noticed the significant effect of functionalized [DAMI] [TfO] ionic liquid and water to improve the formic acid yield during the optimization. Last, we also checked the stability of the catalyst by recycling the same till the 7th run.
在功能化离子液体中,金属钌掺杂二氧化钛纳米颗粒加氢直接合成甲酸
目前世界范围内甲酸的生产遵循甲醇和一氧化碳在强碱存在下的排列。但由于使用有毒的CO分子和大气中CO2分子的易得性,大多数研究已经从传统的甲酸合成方法转向使用不同的均相和多相催化剂直接加氢CO2气体。该研究旨在开发一种反应方案,以实现简单的二氧化碳加氢到甲酸的离子液体反应介质。我们采用溶胶-凝胶法制备了两种金属钌掺杂TiO2纳米粒子(含和不含离子液体)Ru@TiO2@IL和Ru@TiO2。由于离子液体结构中存在NR2 (R= CH3)的官能团,我们将含有NR2 (R= CH3)的咪唑基离子液体应用于纳米TiO2纳米颗粒的制备,获得了良好的反应速率,得到了无团聚的金属钌掺杂TiO2纳米颗粒,并且易于产物分离。我们合成了各种NR2 (R= CH3)功能化的离子液体,如1-丁基-3-甲基咪唑氯、1,3-二(N,N-二甲氨基乙基)-2-甲基咪唑三氟甲烷磺酸盐([DAMI][TfO])、1,3-二(N,N-二甲氨基乙基)-2-甲基咪唑双(三氟甲基磺酰基)亚胺([DAMI][NTf2])和1-丁基-3-甲基咪唑氯离子液体。我们利用溶胶-凝胶法快速制备了两种钌金属掺杂的TiO2纳米颗粒。煅烧后的Ru@TiO2@IL (3.2 wt% Ru)和Ru@TiO2 (1.7 wt% Ru)材料通过XRD, FTIR, TEM, ICP-AES, EDS和XANES分析进行了表征。在了解了Ru金属在TiO2载体上的正确结构安排后,我们利用Ru@TiO2@IL (3.2 wt% Ru)和Ru@TiO2 (1.7 wt% Ru)两种材料作为催化剂,在水存在下直接加氢CO2。我们将[DAMI] [TfO]离子液体功能化。在了解Ru@TiO2@IL (3.2 wt% Ru)和Ru@TiO2 (1.7 wt% Ru)催化剂的正确形态和理化分析后,我们研究了它们在CO2还原和甲酸合成中的应用。在这里,我们展示了有和没有离子液体的TiO2负载的Ru纳米颗粒的制备和表征。在优化过程中,我们还注意到功能化的[DAMI] [TfO]离子液体和水对提高甲酸收率的显著作用。最后,我们还通过回收催化剂来检查催化剂的稳定性,直到第7次运行。
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来源期刊
Current Organocatalysis
Current Organocatalysis CHEMISTRY, PHYSICAL-
CiteScore
2.00
自引率
0.00%
发文量
28
期刊介绍: Current Organocatalysis is an international peer-reviewed journal that publishes significant research in all areas of organocatalysis. The journal covers organo homogeneous/heterogeneous catalysis, innovative mechanistic studies and kinetics of organocatalytic processes focusing on practical, theoretical and computational aspects. It also includes potential applications of organocatalysts in the fields of drug discovery, synthesis of novel molecules, synthetic method development, green chemistry and chemoenzymatic reactions. This journal also accepts papers on methods, reagents, and mechanism of a synthetic process and technology pertaining to chemistry. Moreover, this journal features full-length/mini review articles within organocatalysis and synthetic chemistry. It is the premier source of organocatalysis and synthetic methods related information for chemists, biologists and engineers pursuing research in industry and academia.
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