Thin-water-film-enhanced TiO2-based catalyst for CO2 hydrogenation to formic acid

2022 ◽  
Author(s):  
Shaoqin Chen ◽  
Siyuan Fang ◽  
Zongwei Sun ◽  
Zhangyang Li ◽  
Chunling Wang ◽  
...  

Carbon dioxide (CO2) hydrogenation can not only mitigate global warming, but also produce value-added chemicals. Herein, we report a novel three-phase catalytic system with an in-situ generated and dynamically updated...

Author(s):  
Dui Ma ◽  
Ting Jin ◽  
Keyu Xie ◽  
Haitao Huang

Converting CO2 into value-added fuels or chemical feedstocks through electrochemical reduction is one of the several promising avenues to reduce atmospheric carbon dioxide levels and alleviate global warming. This approach...


Author(s):  
Madhuri Santosh Bhandwalkar

To link food demand and reduction in food waste, proactive approaches should be taken. Perishable food is mainly fruits and vegetables, waste from different processing industries like pulses, meat products, oil products, dairy products, and fishery byproducts. Conventional food waste management solution is land filling which is not sustainable as it generates global warming gases like methane and carbon dioxide. To reduce food waste, the process known as “food valorization” has become another solution to landfilling, the concept which is given by European Commission in 2012, meaning food processing waste conversion to value-added products. In this chapter the study focuses on production of industrially important enzymes from food waste which could be one of the reactive solutions. Different enzymes like pectinase, peroxidase, lipase, glucoamylase, and protease can be produced from food waste.


Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 413 ◽  
Author(s):  
Silvia Mena ◽  
Iluminada Gallardo ◽  
Gonzalo Guirado

Carbon dioxide (CO2) is a known greenhouse gas, and is the most important contributor to global warming. Therefore, one of the main challenges is to either eliminate or reuse it through the synthesis of value-added products, such as carboxylated derivatives. One of the most promising approaches for activating, capturing, and valorizing CO2 is the use of electrochemical techniques. In the current manuscript, we described an electrocarboxylation route for synthesizing 4-cyanobenzoic acid by valorizing CO2 through the synergistic use of electrochemical techniques (“green technology”) and ionic liquids (ILs) (“green solvents”)—two of the major entries in the general green chemistry tool kit. Moreover, the use of silver cathodes and ILs enabled the electrochemical potential applied to be reduced by more than 0.4 V. The “green” synthesis of those derivatives would provide a suitable environmentally friendly process for the design of plasticizers based on phthalate derivatives.


2018 ◽  
Vol 20 (39) ◽  
pp. 25179-25185 ◽  
Author(s):  
Worawaran Thongnuam ◽  
Thana Maihom ◽  
Saowapak Choomwattana ◽  
Yuwanda Injongkol ◽  
Bundet Boekfa ◽  
...  

The hydrogenation of carbon dioxide (CO2) to formic acid over Lewis acidic zeolites as catalyst has been investigated by means of density functional theory (DFT) with the M06-L functional.


Catalysts ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 636 ◽  
Author(s):  
Giane B. Damas ◽  
Caetano R. Miranda ◽  
Ricardo Sgarbi ◽  
James M. Portela ◽  
Mariana R. Camilo ◽  
...  

The electrochemical reduction of carbon dioxide into carbon monoxide, hydrocarbons and formic acid has offered an interesting alternative for a sustainable energy scenario. In this context, Sn-based electrodes have attracted a great deal of attention because they present low price and toxicity, as well as high faradaic efficiency (FE) for formic acid (or formate) production at relatively low overpotentials. In this work, we investigate the role of tin oxide surfaces on Sn-based electrodes for carbon dioxide reduction into formate by means of experimental and theoretical methods. Cyclic voltammetry measurements of Sn-based electrodes, with different initial degree of oxidation, result in similar onset potentials for the CO2 reduction to formate, ca. −0.8 to −0.9 V vs. reversible hydrogen electrode (RHE), with faradaic efficiencies of about 90–92% at −1.25 V (vs. RHE). These results indicate that under in-situ conditions, the electrode surfaces might converge to very similar structures, with partially reduced or metastable Sn oxides, which serve as active sites for the CO2 reduction. The high faradaic efficiencies of the Sn electrodes brought by the etching/air exposition procedure is ascribed to the formation of a Sn oxide layer with optimized thickness, which is persistent under in situ conditions. Such oxide layer enables the CO2 “activation”, also favoring the electron transfer during the CO2 reduction reaction due to its better electric conductivity. In order to elucidate the reaction mechanism, we have performed density functional theory calculations on different slab models starting from the bulk SnO and Sn6O4(OH)4 compounds with focus on the formation of -OH groups at the water-oxide interface. We have found that the insertion of CO2 into the Sn-OH bond is thermodynamically favorable, leading to the stabilization of the tin-carbonate species, which is subsequently reduced to produce formic acid through a proton-coupled electron transfer process. The calculated potential for CO2 reduction (E = −1.09 V vs. RHE) displays good agreement with the experimental findings and, therefore, support the CO2 insertion onto Sn-oxide as a plausible mechanism for the CO2 reduction in the potential domain where metastable oxides are still present on the Sn surface. These results not only rationalize a number of literature divergent reports but also provide a guideline for the design of efficient CO2 reduction electrocatalysts.


2013 ◽  
Vol 764 ◽  
pp. 1-82 ◽  
Author(s):  
Ibram Ganesh

This article reviews the literature related to the direct uses of CO2and its conversion into various value added chemicals including high energy density liquid fuels such as methanol. The increase in the direct uses of CO2and its conversion into potential chemical commodities is very important as it directly contributes to the mitigation of CO2related global warming problem. The method being followed at present in several countries to reduce the CO2associated global warming is capturing of CO2at its major outlets using monoethanolamine based solution absorption technique followed by storing it in safe places such as, oceans, depleted coal seams, etc., (i.e., carbon dioxide capturing and storing in safe places, CCS process). This is called as CO2sequestration. Although, the CCS process is the most understood and immediate option to mitigate the global warming problem, it is considerably expensive and has become a burden for those countries, which are practicing this process. The other alternative and most beneficial way of mitigating this global warming problem is to convert the captured CO2into certain value added bulk chemicals instead of disposing it. Conversion of CO2into methanol has been identified as one of such cost effective ways of mitigating global warming problem. Further, if H2is produced from exclusively water using only solar energy instead of any fossil fuel based energy, and is used to convert CO2into methanol there are three major benefits: i) it contributes greatly to the global warming mitigation problem, ii) it greatly saves fossil fuels as methanol production from CO2could be an excellent sustainable and renewable energy resource, and iii) as on today, there is no better process than this to store energy in a more convenient and highly usable form of high energy density liquid fuel. Not only methanol, several other potential chemicals and value added chemical intermediates can be produced from CO2. In this article, i) synthesis of several commodity chemicals including poly and cyclic-carbonates, sodium carbonate and dimethyl carbonate, carbamates, urea, vicinal diamines, 2-arylsuccinic acids, dimethyl ether, methanol, various hydrocarbons, acetic acid, formaldehyde, formic acid, lower alkanes, etc., from CO2, ii) the several direct uses of CO2, and iii) the importance of producing methanol from CO2using exclusively solar energy are presented, discussed and summarized by citing all the relevant and important references.


2020 ◽  
Author(s):  
Brian Skinn ◽  
Sujat Sen ◽  
McLain Leonard ◽  
DAN WANG ◽  
Fikile R. Brushett ◽  
...  

Space programs around the globe have begun to consider the logistical demands of missions beyond the orbital neighborhood of Earth. Unlike local installations such as the International Space Station, long-range missions will not have the option to resupply critical materials from Earth. Thus, the development of capabilities for what is often termed “In-Situ Resource Utilization” (ISRU) have been a continuing focus of research through NASA and other agencies. One particular long-range mission of interest is to place human astronauts on Mars; the major component of the thin Martian atmosphere is carbon dioxide, making CO2 a natural input to ISRU technologies for production of carbon-containing materials. Production of mission consumables from in-situ Mars resources will be critical to enabling human exploration of Mars, in part by minimizing the number and size of descent/ascent vehicles. Potential ISRU products from CO2 include that seem likely to provide significant mission benefits with minimal infrastructure required are propellants (e.g., hydrocarbons), fuel cell reactants (e.g., formic acid, methanol, carbon monoxide), and life support consumables (e.g., oxygen). The first portion of this talk will comprise a high-level overview of the chemical transformations that can be imparted to CO2 via electrocatalysis on gas-diffusion electrodes (GDEs), in the form of a summary of literature reports on the catalytic performance of a wide variety of single-metallic and metal-alloy systems. The remainder will encompass an exposition of the electrocatalytic performance of tin and copper single-metal GDE electrocatalysts prepared by pulsed electrodeposition. These metals are well known for their ability to reduce carbon dioxide to formic acid and hydrocarbons/carbon monoxide, respectively, and are under active development in numerous academic research groups and industrial entities to this end. These experimental results clearly demonstrate the power and flexibility of the pulse/pulse-reverse electrodeposition approach to catalyst fabrication, as evidenced by the appreciable effects of the pulsed-waveform electrodeposition parameters on CO2 electroreduction product distribution and total current density.


2018 ◽  
Vol 11 (6) ◽  
pp. 1571-1580 ◽  
Author(s):  
M. Melchionna ◽  
M. V. Bracamonte ◽  
A. Giuliani ◽  
L. Nasi ◽  
T. Montini ◽  
...  

Direct conversion of carbon dioxide to formic acid at thermodynamic equilibrium is an advantage of enzymatic catalysis, hardly replicated by synthetic analogs, but of high priority for carbon-neutral energy schemes.


2020 ◽  
Author(s):  
Brian Skinn ◽  
McLain Leonard ◽  
DAN WANG ◽  
Fikile R. Brushett

A variety of techniques for management of carbon dioxide emissions from power generation facilities and other industrial sites have been under active investigation for decades, in an effort to mitigate the environmental impacts of these releases. Once such approach is electrochemical reduction, which treats the waste CO2 as a source material for the production of value-added materials. Currently, the most promising form factor for this electrocatalytic application appears to be a stack-based system, where catalyst is immobilized on porous media that is interfaced with a liquid or solid electrolyte, and the reactant carbon dioxide is delivered to the active region by gaseous diffusion, which is orders of magnitude faster that diffusion though aqueous media. Various carbonaceous reduction products can be created depending on the composition, size, and microstructure of the catalyst particles, including formic acid/formate, carbon monoxide, alcohols, and hydrocarbons. In general, smaller catalyst particles, ideally in the nanoparticulate (<< 1 μm) range, tend to yield superior catalytic performance, due to a combination of factors such as a higher density of exposed grain boundaries and a higher fraction of exposed crystalline facets that are uncommon in particles of micron size or larger.This talk will survey recent work illustrating the ability of pulse/pulse-reverse electrodeposition processes to tune the size of particles applied to gas-diffusion electrode substrates, with a primary focus on two single-metal catalyst materials relevant to carbon dioxide electroreduction: tin and copper. The former is a catalyst primarily for formic acid production, while the latter is unique among single-metal catalysts as the only element known to date to produce significant amounts of hydrocarbons and/or alcohols. Particle morphology and representative particle size will be discussed as a function of pulsed electrodeposition waveform parameters, with the goal of highlighting overarching trends across the waveform space.


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