C07C29/156

Indium-based catalysts and pre-catalysts

Embodiments of the present disclosure describe pre-catalysts comprising including one or more of indium oxide, indium hydroxide, indium oxyhydroxide, an active oxide, and a refractory oxide. Embodiments of the present disclosure also describe method of making pre-catalysts based on one or more of impregnation, precipitation or co-precipitation, ball milling, and metal-organic framework (MOF)-mediated synthesis. Embodiments of the present disclosure further describe methods of activating pre-catalysts and synthesizing one or more of methanol and olefins using catalysts obtained from the pre-catalysts.

Nanocage-confined catalyst, preparation process and use thereof
20210299644 · 2021-09-30 ·

A nanocage-confined catalyst has the formula: NC-m[M(Salen1)X]-n[M′(Salen2)]. NC is a material having a nanocage structure, and M(Salen1)X and M′ (Salen2) are active centers, respectively; each occurrence of M is independently selected from the group consisting of Co ion, Fe ion, Ga ion, Al ion, Cr ion, and a mixture thereof. Each occurrence of M′ is independently selected from Cu ion, Ni ion and a mixture thereof, m is 0 to 100; n is 0 to 100, with the proviso that at least one of m and n is not 0; each occurrence of Salen1 and Salen2 is independently a derivative of Shiff bases; X is an axial anion selected from the group consisting of substituted or unsubstituted acetate, substituted or unsubstituted benzene sulfonate, substituted or unsubstituted benzoate, F—, Cl—, Br—, I—, SbF6-, PF6-, BF4-, and a mixture thereof.

Nanocage-confined catalyst, preparation process and use thereof
20210299644 · 2021-09-30 ·

A nanocage-confined catalyst has the formula: NC-m[M(Salen1)X]-n[M′(Salen2)]. NC is a material having a nanocage structure, and M(Salen1)X and M′ (Salen2) are active centers, respectively; each occurrence of M is independently selected from the group consisting of Co ion, Fe ion, Ga ion, Al ion, Cr ion, and a mixture thereof. Each occurrence of M′ is independently selected from Cu ion, Ni ion and a mixture thereof, m is 0 to 100; n is 0 to 100, with the proviso that at least one of m and n is not 0; each occurrence of Salen1 and Salen2 is independently a derivative of Shiff bases; X is an axial anion selected from the group consisting of substituted or unsubstituted acetate, substituted or unsubstituted benzene sulfonate, substituted or unsubstituted benzoate, F—, Cl—, Br—, I—, SbF6-, PF6-, BF4-, and a mixture thereof.

CATALYSTS FOR PRODUCING ALCOHOLS AND ETHERS FROM SYNTHESIS GAS

Catalysts for the production of an alcohol and/or an ether from synthesis gas, methods of making the catalysts, and uses thereof are described. The catalyst can include catalytic Cu metal particles or oxides thereof and/or Ni metal particles or oxides thereof on an alkali metal or alkaline earth metal silicate support.

CATALYSTS FOR PRODUCING ALCOHOLS AND ETHERS FROM SYNTHESIS GAS

Catalysts for the production of an alcohol and/or an ether from synthesis gas, methods of making the catalysts, and uses thereof are described. The catalyst can include catalytic Cu metal particles or oxides thereof and/or Ni metal particles or oxides thereof on an alkali metal or alkaline earth metal silicate support.

INDIUM-BASED CATALYSTS AND PRE-CATALYSTS

Embodiments of the present disclosure describe pre-catalysts comprising including one or more of indium oxide, indium hydroxide, indium oxyhydroxide, an active oxide, and a refractory oxide. Embodiments of the present disclosure also describe method of making pre-catalysts based on one or more of impregnation, precipitation or co-precipitation, ball milling, and metal-organic framework (MOF)-mediated synthesis. Embodiments of the present disclosure further describe methods of activating pre-catalysts and synthesizing one or more of methanol and olefins using catalysts obtained from the pre-catalysts.

INDIUM-BASED CATALYSTS AND PRE-CATALYSTS

Embodiments of the present disclosure describe pre-catalysts comprising including one or more of indium oxide, indium hydroxide, indium oxyhydroxide, an active oxide, and a refractory oxide. Embodiments of the present disclosure also describe method of making pre-catalysts based on one or more of impregnation, precipitation or co-precipitation, ball milling, and metal-organic framework (MOF)-mediated synthesis. Embodiments of the present disclosure further describe methods of activating pre-catalysts and synthesizing one or more of methanol and olefins using catalysts obtained from the pre-catalysts.

INDIUM-BASED CATALYSTS AND PRE-CATALYSTS

Embodiments of the present disclosure describe pre-catalysts comprising including one or more of indium oxide, indium hydroxide, indium oxyhydroxide, an active oxide, and a refractory oxide. Embodiments of the present disclosure also describe method of making pre-catalysts based on one or more of impregnation, precipitation or co-precipitation, ball milling, and metal-organic framework (MOF)-mediated synthesis. Embodiments of the present disclosure further describe methods of activating pre-catalysts and synthesizing one or more of methanol and olefins using catalysts obtained from the pre-catalysts.

Catalytic conversion of carbon dioxide to methanol using diformate esters as intermediates

The present disclosure relates to a new catalytic process for the production of methanol from carbon dioxide, comprising: (1) the conversion of carbon dioxide and hydrogen to formic acid or formate salts; (2) converting the formic acid or formate salts to diformate esters of diols; (3) hydrogenating the diformate esters to methanol and diols. The diols produced from the hydrogenation reaction can be recovered and re-used to prepare the diformate esters.

Catalytic conversion of carbon dioxide to methanol using diformate esters as intermediates

The present disclosure relates to a new catalytic process for the production of methanol from carbon dioxide, comprising: (1) the conversion of carbon dioxide and hydrogen to formic acid or formate salts; (2) converting the formic acid or formate salts to diformate esters of diols; (3) hydrogenating the diformate esters to methanol and diols. The diols produced from the hydrogenation reaction can be recovered and re-used to prepare the diformate esters.