The present invention provides an impregnated catalyst composition for production of carbon monoxide comprising: 30 wt %-50 wt % metal oxide and 50 wt %-70 wt % support material. Another aspect of the present invention is to provide a method of preparation of an impregnated catalyst for carbon monoxide production (10) and a method for producing carbon monoxide (20) according to the impregnated catalyst of the present invention. The present invention is able to reduce the reaction temperature by 1 fold and also able to reduce the usage of energy but maintain its good production quality. Besides, selectivity of the present invention is high, hence able to produce high purity of carbon monoxide.

A carbon-based solid acid catalyst, a preparation method of the catalyst, and a method to use the catalyst for hydrothermal conversion of biomass are provided. The preparation method of the carbon-based solid acid catalyst includes the following steps: S1. mixing pectin with water, adding concentrated sulfuric acid for activation, and adding a resulting mixture to an ionic resin with an aromatic ring matrix; S2. drying a material obtained in S1, crushing a dried material into a powder, and subjecting the powder to pyrolysis in a dry inert gas; S3. subjecting a solid obtained after the pyrolysis to sulfonation with concentrated sulfuric acid; S4. diluting a material obtained in S3 with water, filtering a resulting mixture, and washing a resulting filter residue with water until no sulfate ions are detected in washing water; S5. drying the filter residue.

To provide an ion exchange membrane with a catalyst layer, an ion exchange membrane and an electrolytic hydrogenation apparatus, which can lower electrolysis voltage and increase current efficiency at the time of electrolytic hydrogenation of an aromatic compound.

The ion exchange membrane with a catalyst layer of the present invention has an inorganic particle layer containing inorganic particles and a binder, a layer (Sa) containing a first fluorinated polymer having sulfonic acid type functional groups, and a layer (Sb) containing a second fluorinated polymer having sulfonic acid type functional groups, and a catalyst layer, in this order, wherein the ion exchange capacity of the above first fluorinated polymer is lower than the ion exchange capacity of the above second fluorinated polymer.

An embodiment of the present invention provides a MXene nanodot core-carbon shell multifunctional catalyst including a MXene nanodot core and a carbon shell surrounding the MXene nanodot core. By introducing the carbon shell surrounding the nanodot core, the stability of the catalyst is ensured, thereby providing effects in that the catalyst may function under various conditions.

A core-shell structure supported catalyst and a preparation method and use thereof are disclosed. The core-shell structure supported catalyst includes a core-shell structure carrier and platinum supported on the surface of the core-shell structure carrier, wherein the core-shell structure carrier includes a ferroferric oxide nanoparticle core and a nitrogen-doped carbon shell, and a molar ratio of the ferroferric oxide nanoparticle core to platinum is 1:(0.03-0.3).

Disclosed are methods for forming a supported catalyst and catalysts formed according to disclosed methods. Methods include contacting a catalyst support with a precursor solution and displacing the solvent of the precursor solution (e.g., water) with a second solvent that has a lower surface tension than the first solvent. The second solvent displaces the first solution according to the Marangoni effect. Methods also include activation of the precursor to form a catalyst, e.g., a supported platinum group metal catalyst or the like.

Disclosed are methods for forming a supported catalyst and catalysts formed according to disclosed methods. Methods include contacting a catalyst support with a precursor solution and displacing the solvent of the precursor solution (e.g., water) with a second solvent that has a lower surface tension than the first solvent. The second solvent displaces the first solution according to the Marangoni effect. Methods also include activation of the precursor to form a catalyst, e.g., a supported platinum group metal catalyst or the like.

Provided are a carbon-based noble metal-transition metal composite catalyst enabling high selective conversion of a carboxylic acid functional group into an alcohol functional group by pre-treating a carbon carrier including a predetermined ratio or more of mesopores, and a production method therefor.

Provided are a carbon-based noble metal-transition metal composite catalyst enabling high selective conversion of a carboxylic acid functional group into an alcohol functional group by pre-treating a carbon carrier including a predetermined ratio or more of mesopores, and a production method therefor.

Disclosed is a ruthenium-based catalyst for ammonia synthesis, preparation method and use thereof. The ruthenium-based catalyst comprises Ru—Ba-A core-shell structure which comprises a ruthenium nanoparticle as a core covered with a first shell and a second shell sequentially, wherein the first shell consists of a barium nanoparticle, and the second shell consists of a metal oxide. The Ru—Ba-A core-shell structure can effectively preventing agglomerations of ruthenium nanoparticles during the use of the catalyst and avoiding direct contact between the ruthenium nanoparticles and the metal oxides. In addition, barium nanoparticles have a promoting effect as an electronic promoter, which can effectively improve the stability and catalytic activity of ruthenium-based catalyst for ammonia synthesis, especially in the system for synthesizing ammonia from a coal gas.