A method for producing a zeolite with improved Si/Al according to the present invention includes the steps of: subjecting a zeolite synthesized without using an organic structure directing agent to ion exchange, thereby obtaining a sodium-type, a proton-type, or an ammonium-type zeolite; and bringing the zeolite subjected to ion exchange into contact with an ammonium salt solution, thereby dealuminating the zeolite. It is preferable that the ammonium salt is any one of ammonium oxalate, ammonium fluoride, ammonium fluorosilicate, ammonium fluoroborate, ammonium fluorophosphate, ammonium fluorotitanate, and ammonium florozirconate. It is also preferable that the zeolite after ion exchange is exposed to water vapor, and is then brought into contact with the ammonium salt solution.

In order to specify a catalytic converter, especially SCR catalytic converter, with maximum catalytic activity, this catalytic converter has at least one catalytically active component and additionally at least one porous inorganic filler component having meso- or macroporosity. The organic porous filler component has a proportion of about 5 to 50% by weight. More particularly, a diatomaceous earth or a pillared clay material is used as the porous inorganic filler component.

The present invention relates to the use of a material B containing palladium and platinum in a weight ratio of 2:3 to 10:1 for increasing the low-temperature storage of nitrogen oxides by means of a material A containing palladium and zeolite, wherein material A and material B are present on a carrier substrate of the length L, and wherein material A and material B are different from one another.

The instant disclosure provides a composition for fluid catalytic cracking of petroleum based feedstock into useful short chain olefins. The composition comprising: 76-86% of a non-zeolitic material; and 2-30% of at least one zeolite material, the percentage being based on weight of the catalyst composition, wherein one of the zeolites has been modified with 0.1-2.5 wt % metal. The said catalyst was found to be selective in enhancing the usable propylene gas content, while reducing the undesirable dry gas content of the cracked olefinic products. The present disclosure also provides a process for the preparation of the composition. The present disclosure also provides an apparatus (100) and process (200) for fluid catalytic cracking to obtain light olefins. The apparatus comprises a second riser (33) that includes a lower dense riser (2) and upper dilute riser (3). Further, the lower dense riser (2) has a diameter that is 1.1 to 2 times that of the upper dilute riser (3).

A heterogeneous catalyst composition for para-hydrogen induced polarization includes ligand-capped nanoparticles dispersed in water. The ligand-capped nanoparticles include metal nanoparticles that are surface functionalized with organic ligands, a molecular weight of the organic ligands is no greater than 300 g/mol, and the organic ligands each includes multiple binding moieties as coordinates sites for binding to a nanoparticle surface.

A process is provided for the preparation of value added chemicals such as ethyl levulinate from a glucose or other sugars, catalyzed by a mixture of a Lewis acid catalyst and a Bronsted acid catalyst.

A process for dehydrating methanol to dimethyl ether product in the presence of a catalyst and a promoter, wherein the catalyst is at least one aluminosilicate zeolite, and the promoter is selected from one or more compounds of Formula I: (I) wherein each of X and any or all of the Y's may independently be selected from hydrogen, halide, a substituted or unsubstituted hydrocarbyl substituent, or a compound of the formula —CHO, —CO.sub.2R, —COR, or —OR, where R is hydrogen or a substituted or unsubstituted hydrocarbyl substituent, and wherein the molar ratio of promoter to methanol is maintained at less than 1.

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The present disclosure is directed to methods for upgrading a hydrocarbon feed that may include separating the hydrocarbon feed to produce at least a greater boiling point effluent and a lesser boiling point effluent. The greater boiling point effluent may have an American Petroleum Institute gravity less than 30 degrees. The method may further include contacting the greater boiling point effluent with a multicomponent catalyst, which may cause at least a portion of the greater boiling point effluent to undergo catalytic cracking and produce a first spent multicomponent catalyst and a first cracked effluent comprising one or more olefins. The multicomponent catalyst may include from 0 weight percent to 10 weight percent ZSM-5, from 10 weight percent to 40 weight percent zeolite Beta, and from 10 weight percent to 30 weight percent USY zeolite based on the total weight of the multicomponent catalyst.

Described is related to nano-structured composite materials for removing harmful chemical air pollutants and odors from the air to prevent people from breathing in disease-causing chemicals and provide them with clean indoor air. The nano-structured composite materials comprise nano-catalysts embedded in the pores of nano-structured substrate materials selected from the group consisting of nano-porous carbon, nano-porous rare earth oxide, nano-porous zeolite, nano-porous alumina and nano-porous silica. The nano-scale synergy of nano-catalysts and nano-structured substrate materials provides effective air filtration materials for the complete trapping and elimination of the full spectrum of chemical air pollutants including both organic and inorganic compounds and odors for indoor spaces, which HEPA or activated carbon filters cannot achieve.

Methods for interconverting olefins in an olefin-rich hydrocarbon stream include contacting the olefin-rich hydrocarbon stream with a catalyst system in an olefin interconversion unit to produce an interconverted effluent comprising ethylene and propylene. The contacting may be conducted at a reaction temperature from 450° C. to 750° C., a reaction pressure from 1 bar to 5 bar, and a residence time from 0.5 seconds to 1000 seconds. The catalyst system includes a framework-substituted beta zeolite. The framework-substituted beta zeolite has a *BEA aluminosilicate framework that has been modified by substituting a portion of framework aluminum atoms of the *BEA aluminosilicate framework with beta-zeolite Al-substitution atoms independently selected from the group consisting of titanium atoms, zirconium atoms, hafnium atoms, and combinations thereof.