Hydrotalcite Anchored Ruthenium Catalyst for CO2 Hydrogenation Reaction

2019 ◽  
Vol 16 (5) ◽  
pp. 396-408
Author(s):  
Vivek Srivastava

We developed a series of new hydrotalcite functionalized Ru catalytic system to synthesize formic acid via CO2 hydrogenation reaction. Advance analytical procedures like FTIR, N2 physisorption, ICP-OES, XPS, and TEM analysis were applied to understand the physiochemical nature of functionalized hydrotalcite materials. This well-analyzed system was used as catalysts for CO2 hydrogenation reaction (with and without ionic liquid medium). Ru metal containing functionalized hydrotalcite materials were found highly active catalysts for formic acid synthesis via hydrogenation reaction. The concern of catalyst stability was studied via catalysts leaching and recycling experiments. We recycled the ionic liquid mediated functionalized hydrotalcite catalytic system up to 8 runs without any significant loss of catalytic activity. Surprisingly, no sign of catalyst leaching was recorded during the catalyst recycling experiment.

2020 ◽  
Vol 17 (8) ◽  
pp. 603-612
Author(s):  
Prashant Gautam ◽  
Vivek Srivastava

A series of alumina supported Ru nanoparticles (Ru γ -Al2O3-x (x=2-10 Ru wt%) was synthesized using the ethylene glycol reduction method. XRD, TEM, EDX, H2-chemisorption, XPS and H2-TPD analytical techniques were used to understand the physiochemical nature of alumina supported Ru nanoparticles. All the well-characterized Ru#Al2O3-x (x=2-10 Ru wt%) catalysts were used for high-pressure CO2 hydrogenation to formic acid synthesis. A clear correlation was recorded between the physiochemical properties of developed catalysts and the molar quantity of formic acid. Among all the developed catalysts, Ru#Al2O3-2 catalyst with or without ionic liquid reaction medium gave a good molar quantity of formic acid. Application of ionic liquid was also expanded, and ionic liquid medium appeared as a good solvent system as compared to the amine solvent system, which not only provides better solubility of reactants and catalysts but also found useful in the easy recovery of formic acid after the completion of the reaction. The catalyst recycled seven times with easy product isolation stem to make this system very useful and fulfill the requirement of sustainable chemistry.


2020 ◽  
Vol 17 (6) ◽  
pp. 443-454
Author(s):  
Prashant Gautam ◽  
Praveenkumar Ramprakash Upadhyay ◽  
Vivek Srivastava

A group of silica-ionic liquid supported Ru-based catalysts was synthesized and further utilized for CO2 hydrogenation reaction. All the materials were properly analyzed in terms of their physicochemical properties. The physiochemical impacts of different functionalized and non-functionalized ionic liquid over the synthesis, size, and stability of Ru NPs along with their effect on the rate of hydrogenation reaction were investigated. The Ru-[DAMI][NTf2] (1:10)@SiO2 furnished the best catalytic performance in CO2 conversion to formic acid under high-pressure reaction condition. The results confirmed the impact of ionic liquids as a repellent to avoid agglomeration and oxidation of the Ru nanoparticles followed by space resistance and electrostatic protection. Hence, such influence positively begins the rate of reaction as well as the selectivity of the process. Good physiochemical stability of catalyst in terms of 7-time catalyst recycling and easy product/catalyst isolation make this protocol near to the principal of sustainable chemistry.


2018 ◽  
Vol 16 (1) ◽  
pp. 853-863
Author(s):  
Vivek Srivastava

AbstractWe developed a series of new organic-inorganic hybrid hydrotalcite functionalized Ru catalytic systems. All the developed materials have been studied by FTIR, N2 physisorption, ICP-OES, XPS, NMR (1H, 13C, 29Si) and TEM analysis were performed to know the physiochemical behavior and structural morphology of functionalized hydrotalcite materials. XPS results strongly suggest that it involves the formation of N-Ru coordination bonds. We applied these well analyzed materials for CO2 hydrogenation reaction as catalyst (with and without ionic liquid medium). We found that Ru metal containing functionalized hydrotalcite materials were highly active and stable (in terms of catalyst leaching and recycling). The heterogeneous catalyst can be easily recovered and reused 8 times without significant loss of catalytic activity and selectivity, which is a better green alternative for practical applications.


RSC Advances ◽  
2016 ◽  
Vol 6 (48) ◽  
pp. 42297-42306 ◽  
Author(s):  
Praveenkumar Ramprakash Upadhyay ◽  
Vivek Srivastava

Ionic-liquid-mediated TiO2supported Ru for the selective CO2hydrogenation reaction and isolation of HCOOH.


2020 ◽  
Vol 146 ◽  
pp. 106125
Author(s):  
Rodrigo Webber ◽  
Muhammad I. Qadir ◽  
Eduardo Sola ◽  
Marta Martín ◽  
Elizabeth Suárez ◽  
...  

2021 ◽  
Vol 08 ◽  
Author(s):  
Vivek Srivastava

Background: 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. Objective: The study aims to develop a reaction protocol to achieve easy CO2 hydrogenation to formic acid using an Ionic liquid reaction medium. Methods: 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. Results: 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. Conclusion: 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.


2019 ◽  
Vol 58 (16) ◽  
pp. 6333-6339 ◽  
Author(s):  
Yunyan Wu ◽  
Yanfei Zhao ◽  
Huan Wang ◽  
Bo Yu ◽  
Xiaoxiao Yu ◽  
...  

2019 ◽  
Vol 51 (2) ◽  
pp. 289-295
Author(s):  
Y. Guo ◽  
J. Sun ◽  
F. Guo ◽  
Yu. He ◽  
P. Chen

The Friedel-Crafts acylation of 2-methoxynaphthalene (2-MN) with acetic anhydride (AA) was carried out in the ionic liquid (IL) butylpyridinium tetrafluoroborate ([BPy]BF4) using phosphotungstic acid (H3PW12O40) as the catalyst. The [BPy]BF4-mediated 2-MN acylation displays good conversion and selectivity towards 1-acyl-2-methoxynaphthalene (1-AC-2-MN), with 70.4% conversion of 2-MN and 96.4% selectivity to 1-AC-2-MN obtained under the optimal conditions. Owing to the rearrangement of 1-AC-2-MN, 6-acyl-2-methoxynaphthalene (6-AC-2-MN) can be detected after 1 h of reaction time, with the highest 6-AC-2-MN yield of 11.3% obtained under the examined reaction conditions. The system can be recycled and reused at least 6 times without significant loss of activity, indicating the good stability of the H3PW12O40/[BPy]BF4 catalytic system.


2018 ◽  
Vol 3 (9) ◽  
pp. 2631-2637 ◽  
Author(s):  
Dušan N. Sredojević ◽  
Željko Šljivančanin ◽  
Edward N. Brothers ◽  
Milivoj R. Belić

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