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.

A modified Y-type molecular sieve has a rare earth content of about 4% to about 11% by weight on the basis of the oxide, a phosphorus content of about 0.05% to about 10% by weight on the basis of P.sub.2O.sub.5, a sodium content of no more than about 0.5% by weight on the basis of sodium oxide, and an active element content of about 0.1% to about 5% by weight on the basis of the oxide, with the active element being gallium and/or boron. The modified Y-type molecular sieve has a total pore volume of about 0.36 mL/g to about 0.48 mL/g, a percentage of the pore volume of secondary pores having a pore size of 2-100 nm of about 20% to about 40%; a lattice constant of about 2.440 nm to about 2.455 nm, and a lattice collapse temperature of not lower than about 1060° C.

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.

A hydrocarbon feed stream, particularly one comprising heavier hydrocarbons, may be converted to valuable products such as motor gasoline and/or lubricating oil by employing one or more large pore zeolitic catalysts, which may be prepared from a precursor zeolite. In some examples, a large pore zeolitic catalyst may be utilized to selectively reduce the endpoint of a hydrocarbon composition.

The present disclosure relates to an FCC catalyst composition and a process for its preparation. The FCC catalyst composition comprises Y type zeolite, silicon oxide, alumina, at least one clay, at least one rare earth metal, and at least one metal oxide. The FCC catalyst composition of the present disclosure provides improved yields of high value gasoline such as propylene and LPG and reduces yields of low value hydrocarbons such as CSO and LCO.

A dehydrogenation catalyst for producing propylene by a dehydrogenation reaction of propane, the dehydrogenation catalyst including a platinum element and an element M1 and may contain an element M2 as active components, wherein the element M1 is one or more elements selected from the group consisting of a gallium element, a cobalt element, a copper element, a germanium element, a tin element and an iron element, the element M2 is one or more elements selected from the group consisting of a lead element and a calcium element, and the platinum element and the element M1 form an alloy.

The moisture-resistant catalyst for air pollution remediation is a catalyst with moisture-resistant properties, and which is used for removing nitrogen compound pollutants, such as ammonia (NH.sub.3), from air. The moisture-resistant catalyst for air pollution remediation includes at least one metal oxide catalyst, at least one inorganic oxide support for supporting the at least one metal oxide catalyst, and a porous framework for immobilizing the at least one metal oxide catalyst and the at least one inorganic oxide support, where the porous framework is moisture-resistant. As non-limiting examples, the at least one metal oxide catalyst may be supported on the at least one inorganic oxide support by precipitation, impregnation, dry milling, ion-exchange or combinations thereof. The at least one metal oxide catalyst supported on the at least one inorganic oxide support may be physically embedded in the porous framework.

Metal-organic framework materials (MOFs) are highly porous entities comprising a multidentate organic ligand coordinated to multiple metal centers. MOFs having ambient condition stability may comprise a plurality of metal clusters comprising one or more M.sub.4O clusters (M is a metal), and a plurality of 4-pyrazolecarboxylate ligands coordinated to the plurality of metal clusters to define an at least partially crystalline network structure having a plurality of internal pores. The MOFs may have a Pa3 symmetry, which upon activation may convert into Fm3m symmetry. Methods for synthesizing the MOFs may comprise combining a metal source, such as a preformed metal cluster, with 4-pyrazolecarboxylic acid, and reacting the preformed metal cluster with the 4-pyrazolecarboxylic acid to form a MOF having an at least partially crystalline network structure with a plurality of internal pores defined therein and comprising a plurality of metal clusters coordinated to a multidentate organic ligand comprising 4-pyrazolecarboxylate.

A porous carbon material, wherein a half width (2θ) of a diffraction peak (10×) (38° to 49°) by X-ray diffraction is 4.2° or less, and wherein a ratio (mesopore volume/micropore volume) of a mesopore volume (cm.sup.3/g) measured by a BJH method to a micropore volume (cm.sup.3/g) measured by a HK method is 1.20 or more.

A method for degrading polyethylene terephthalate is provided. The method includes: providing polyethylene terephthalate material, providing a catalyst composite including a porous carrier having a pore size of 45 Å to 250 Å and a metal compound including at least one selected from a group consisting of zinc oxide, zinc hydroxide, zinc carbonate, magnesium oxide, calcium oxide, zirconium oxide, and titanium dioxide, in which the metal oxide is loaded on the porous carrier; and performing a degradation reaction, in which the polyethylene terephthalate material is reacted with the catalyst composite in the presence of an alcohol solvent.