The invention provides for the integration of a CO-consuming process, such as a gas fermentation process, with a CO.sub.2 electrolysis process. The invention is capable of utilizing a CO.sub.2-comprising gaseous substrate generated by an industrial process and provides for one or more removal modules to remove at least one constituent from a CO.sub.2-comprising gaseous substrate prior to passage of the gaseous substrate to a CO.sub.2 electrolysis module. The invention may further comprise one or more pressure modules, one or more CO.sub.2 concentration modules, one or more O.sub.2 separation modules, and/or an H.sub.2 electrolysis module. Carbon conversion efficiency is increased by recycling CO.sub.2 produced by a CO-consuming process to the CO.sub.2 electrolysis process.

The present invention relates to a method for producing a formic acid including, a first step of allowing carbon dioxide and hydrogen to react with each other in a solution containing a solvent and a catalyst dissolved in the solvent and in the presence of an amine insoluble in the solvent, and allowing a generated formic acid to adsorb to the amine, in which the catalyst contains at least one metal element selected from the group consisting of metal elements belonging to Groups 8, 9, and 10 of a periodic table and the amine is an amine immobilized on a solid.

Disclosed herein are metal-organic frameworks and methods of making and use thereof.

A carbon dioxide reduction catalyst for hydrogenating carbon dioxide to reduce carbon dioxide to produce a hydrocarbon, containing Fe and Zr as catalytic metals. It is preferable that Ga and Na are further contained as the catalytic metals, and the content of Zr in the catalytic metals is more than 0% by mass and 15% by mass or less.

The invention provides for the integration of a CO-consuming process, such as a gas fermentation process, with a CO.sub.2 electrolysis process. The invention is capable of utilizing a CO.sub.2-comprising gaseous substrate generated by an industrial process and provides for one or more removal modules to remove at least one constituent from a CO.sub.2-comprising gaseous substrate prior to passage of the gaseous substrate to a CO.sub.2 electrolysis module. The invention may further comprise one or more pressure modules, one or more CO.sub.2 concentration modules, one or more O.sub.2 separation modules, and/or an H.sub.2 electrolysis module. Carbon conversion efficiency is increased by recycling CO.sub.2 produced by a CO-consuming process to the CO.sub.2 electrolysis process.

An efficient catalyst for the synthesis of methanol by catalytic hydrogenation of carbon dioxide is provided. A process for the preparation of the catalyst by self-combustion of a gel and a process for the synthesis of methanol by catalytic hydrogenation of carbon dioxide are also presented. The catalyst has the following formula (Cu)x(ZnO)y(ZrO2)z supported on mesoporous silica.

Disclosed are N-heterocyclic carbene (NHC) and 4-pyridinol-derived pincer ligands and metal complexes containing these ligands. These compounds can be used to photocatalyticaly reduce CO.sub.2 to CO.

Provided is a carbon dioxide reduction composite catalyst, comprising an organic-inorganic porous body, and a molecular reduction catalyst combined with the organic-inorganic porous body, wherein the organic-inorganic porous body includes metal oxide clusters, and a light-condensing organic material as linkers between the metal oxide clusters, and the linkers absorb visible light to form excitons, and move the excitons through energy transfer between the linkers to transfer the electrons of the excitons to the molecular reduction catalyst.

The present invention provides, inter alia, a multidentate ligand having the structure of: ##STR00001## Also provided are methods of preparing metal complexes from the multidentate ligand, and the metal complexes prepared by such methods. Further provided are catalysts comprising such metal complexes, and various uses of such catalysts.

The electrochemical carbon dioxide reduction reaction (CO.sub.2RR) provides opportunities to synthesize value-added products from this greenhouse gas in a sustainable manner. Efficient catalysts for this reaction are provided that selectively drive CO.sub.2 reduction over the thermodynamic and kinetically competitive hydrogen evolution reaction (HER) in organic or aqueous electrolytes. The catalysts are metal-polypyridyl coordination complexes of a redox non-innocent terpyridine-based pentapyridine ligand and a first-row transition metal. The metal-ligand cooperativity in [Fe(tpyPY2Me)].sup.2+ drives the electrochemical reduction of CO.sub.2 to CO at low overpotentials with high selectivity for CO.sub.2RR (>90%).