A highly active copper catalyst for the hydrogenation of carbon dioxide to formate under ambient conditions

2020 ◽  
Vol 49 (9) ◽  
pp. 2994-3000
Author(s):  
Karan Chaudhary ◽  
Manoj Trivedi ◽  
D. T. Masram ◽  
Abhinav Kumar ◽  
Girijesh Kumar ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Copper Catalyst ◽  
Catalytic Conversion ◽  
Ambient Conditions ◽  
Turnover Number ◽  
Highly Active ◽  
Tin Metal ◽  
Hydrogenation Of Carbon Dioxide

Catalytic conversion of CO2via hydrogenation using in situ gaseous H2 (granulated tin metal and concentrated HCl) to produce the formate salt (HCO2−) with turnover number (TON) values of 326 to 1.065 × 105 in 12 h to 48 h of reaction at 25 °C to 80 °C has been reported.

Efficient Carboxylation of Terminal Alkynes with Carbon Dioxide Catalyzed by Ligand‐Free Copper Catalyst under Ambient Conditions

2019 ◽  
Vol 8 (8) ◽  
pp. 1501-1505 ◽  
Author(s):  
Wan‐Hui Wang ◽  
Lihong Jia ◽  
Xiujuan Feng ◽  
Dingqiao Fang ◽  
Hongyu Guo ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Copper Catalyst ◽  
Terminal Alkynes ◽  
Ambient Conditions ◽  
Ligand Free

A phenanthroline-based porous organic polymer for the iridium-catalyzed hydrogenation of carbon dioxide to formate

2019 ◽  
Vol 7 (23) ◽  
pp. 14019-14026 ◽  
Author(s):  
Gunniya Hariyanandam Gunasekar ◽  
Sungho Yoon
Keyword(s):  
Carbon Dioxide ◽  
Functional Groups ◽  
Single Site ◽  
Organic Polymer ◽  
Selective Catalyst ◽  
Porous Organic Polymer ◽  
Highly Active ◽  
First Time ◽  
Hydrogenation Of Carbon Dioxide ◽  
Hydrogenation Of Co

A novel phenanthroline-functionalized porous organic polymer (phen-POP) has been designed, and prepared for the first time without other reactive functional groups in the polymer skeleton. Post-synthetic metalation of phen-POP with IrCl3 afforded a single-site, highly active and selective catalyst for the hydrogenation of CO2 to formate.

Transfer hydrogenation of carbon dioxide via bicarbonate promoted by bifunctional C–N chelating Cp*Ir complexes

2020 ◽  
Vol 56 (73) ◽  
pp. 10762-10765
Author(s):  
Yasuhiro Sato ◽  
Yoshihito Kayaki ◽  
Takao Ikariya
Keyword(s):  
Carbon Dioxide ◽  
Transfer Hydrogenation ◽  
Turnover Number ◽  
Mild Conditions ◽  
Carbonate Salts ◽  
Hydrogenation Of Carbon Dioxide

Metal–NH cooperative Ir complexes having a C–N chelate effectively promoted the reduction of bicarbonate and half-carbonate salts formed from CO2 in 2-propanol under mild conditions to produce formate salts with a maximum turnover number of 3200.

In Situ Formation of Ruthenium Catalysts for the Homogeneous Hydrogenation of Carbon Dioxide

2002 ◽  
Vol 41 (6) ◽  
pp. 1606-1614 ◽  
Author(s):  
Chih-Cheng Tai ◽  
Justine Pitts ◽  
John C. Linehan ◽  
A. Denise Main ◽  
Pradip Munshi ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Ruthenium Catalysts ◽  
Homogeneous Hydrogenation ◽  
In Situ Formation ◽  
Hydrogenation Of Carbon Dioxide

Development of Highly Active Ir–PNP Catalysts for Hydrogenation of Carbon Dioxide with Organic Bases

2016 ◽  
Vol 89 (1) ◽  
pp. 113-124 ◽  
Author(s):  
Wataru Aoki ◽  
Natdanai Wattanavinin ◽  
Shuhei Kusumoto ◽  
Kyoko Nozaki
Keyword(s):  
Carbon Dioxide ◽  
Organic Bases ◽  
Highly Active ◽  
Hydrogenation Of Carbon Dioxide

scholarly journals Novel Multifunctional Porous Liquid Composite for Recyclable Sequestration, Storage and In-situ Catalytic Conversion of Carbon Dioxide

2020 ◽  
Author(s):  
Archita Bhattacharjee ◽  
Raj Kumar ◽  
KAMENDRA SHARMA
Keyword(s):  
Carbon Dioxide ◽  
Light And Electron Microscopy ◽  
Enzymatic Reaction ◽  
Catalytic Conversion ◽  
Porous Solids ◽  
X Ray Diffraction ◽  
Hollow Silica ◽  
Polymer Surfactant ◽  
Silica Nanorods

<div><b>Novel Multifunctional Porous Liquid Composite for Recyclable Sequestration, Storage and In-situ Catalytic Conversion of Carbon Dioxide</b> <br></div><div><br></div><div>Archita Bhattacharjee, Raj Kumar and Prof. K. P. Sharma* Department of Chemistry, IIT Bombay, Powai, India <br></div><div>* E-mail: [email protected] <br></div><div><br></div><div>Keywords: Porous liquid composite, mesoporous liquid, hollow silica nanorods, CO<sub>2</sub> capture, CO<sub>2</sub> catalytic conversion<br></div><div><br></div><div>Abstract: Permanent pores combined with fluidity renders flow processability to porous liquids otherwise not seen in porous solids. Although, sequestration of different gases has recently been shown in porous liquids, there is still adearth of studies for deploying in-situ chemical reactionsto convert adsorbed gases into utility chemicals in this phase. Here, a facile method for the design and development of a new class of solvent-less porous liquid composite which, as shown for the first time, can catalyze the conversion of adsorbed gaseous molecules into industrially relevant product, is shown. The recyclable porous liquid composite comprising polymer-surfactant modified hollow silica nanorods and carbonic anhydrase enzyme not onlysequesters (5.5 ccg<sup>-1</sup> at 273 K and 1 atm) and stores CO<sub>2</sub>,but is also capable of driving an in-situ enzymatic reaction for hydration of CO<sub>2</sub> to HCO<sub>3</sub><sup>-</sup> ion, subsequently converting it CaCO<sub>3</sub> due to reaction with pre-dissolved Ca<sup>2+</sup>. Light and electron microscopy combined with x-ray diffraction reveals the nucleation and growth of calcite and aragonite crystals. Moreover, the liquid-like property of the porous composite material can be harnessed by executing the same reaction via diffusion ofcomplimentary Ca<sup>2+</sup> and HCO<sub>3</sub><sup>-</sup> ions through different compartments separated by an interfacial channel.<br></div><div></div>

Metal-Support Interactions and C1 Chemistry: Transforming Pt-CeO2 into a Highly Active and Stable Catalyst for the Conversion of Carbon Dioxide and Methane

2020 ◽  
Author(s):  
Feng Zhang ◽  
Ramón A. Gutiérrez ◽  
Pablo Lustemberg ◽  
Zongyuan Liu ◽  
Ning Rui ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Metal Oxide ◽  
Elevated Temperatures ◽  
Chemical Properties ◽  
Oxide Interface ◽  
Highly Active ◽  
Metal Support ◽  
Metal Support Interactions ◽  
Methane Dissociation

There is an ongoing search for materials which can accomplish the activation of two dangerous greenhouse gases like carbon dioxide and methane. In the area of C1 chemistry, the reaction between CO2 and CH4 to produce syngas, known as methane dry reforming (MDR), is attracting a lot of interest due to its green nature. On Pt(111), elevated temperatures are necessary to activate the reactants and massive deposition of carbon makes this metal surface ineffective for the MDR process. In this study, we show that strong metal-support interactions present in Pt/CeO2(111) and Pt/CeO2 powders lead to systems which can bind well CO2 and CH4 at room temperature and are excellent and stable catalysts for the MDR process at moderate temperature (500 ºC). The behaviour of these systems was studied using a combination of in-situ/operando methods which pointed to an active Pt-CeO2-x interface. In this interface, the oxide is far from being a passive spectator. It modifies the chemical properties of Pt, facilitating improved methane dissociation, and is directly involved in the adsorption and dissociation of CO2 making the MDR catalytic cycle possible. A comparison of the benefits gained by the use of an effective metal-oxide interface and those obtained by plain bimetallic bonding indicates that the former is much more important when optimizing the C1 chemistry associated with CO2 and CH4 conversion. The presence of elements with a different chemical nature at the metal-oxide interface opens the possibility for truly cooperative interactions in the activation of C-O and C-H bonds.

Sign in / Sign up

Export Citation Format

Share Document