According to one or more embodiments disclosed herein, a mesoporous zeolite may be made by a method comprising contacting an initial zeolite material with ammonium hexafluorosilicate to modify the framework of the initial zeolite material, and forming mesopores in the framework-modified zeolite material. The contacting may form a framework-modified zeolite material. The mesoporous zeolites may be incorporated into catalysts.

The invention relates to the preparation of a catalyst containing: a mainly aluminum oxide calcined support; a hydro-dehydrogenating active phase containing at least one metal of group VIB,
the process including:
a) a first precipitation step of at least one basic precursor and at least one acidic precursor,
b) a heating step,
c) a second precipitation step by addition to the suspension of at least one basic precursor and at least one acidic precursor,
d) a filtration step;
e) a drying step,
f) a moulding step,
g) a heat treatment step;
h) an impregnation step of the hydro-dehydrogenating active phase on the support obtained in the step g).

Embodiments of processes for producing propylene utilize a dual catalyst system comprising a mesoporous silica catalyst impregnated with metal oxide and a mordenite framework inverted (MFI) structured silica catalyst downstream of the mesoporous silica catalyst, where the mesoporous silica catalyst includes a pore size distribution of at least 2.5 nm to 40 nm and a total pore volume of at least 0.600 cm.sup.3/g, and the MFI structured silica catalyst has a total acidity of 0.001 mmol/g to 0.1 mmol/g. The propylene is produced from the butene stream via metathesis by contacting the mesoporous silica catalyst and subsequent cracking by contacting the MFI structured silica catalyst.

Process of preparing hydroconversion catalyst comprising: a calcined, predominantly alumina, oxide support; a hydrogenating-dehydrogenating active phase comprising group VIB metal, the catalyst having: specific surface area ?100 m.sup.2/g, total pore volume ?0.75 ml/g, median mesopore diameter by volume ?18 nm, mesopore volume ?0.65 ml/g, macropore volume 15-40% of total pore volume; comprising: a) dissolving acidic aluminum precursor; b) adjusting pH with basic precursor; c) co-precipitating acidic and basic precursors, at least one containing aluminum, to form suspension of alumina gel with a targeted alumina concentration; d) filtration; e) drying to a powder; f) forming; g) thermal treatment to an alumina oxide support; h) impregnating of the hydrogenating-dehydrogenating active phase on the alumina oxide support. Catalyst prepared by this process and use thereof for hydrotreating or hydroconverting heavy hydrocarbon feedstocks.

Embodiments of the present disclosure are directed to a method of producing hierarchical mesoporous zeolite beta. The method comprises providing a parent zeolite beta with a silicon to aluminum molar ratio of 5 to 50. The method further comprises, mixing the parent zeolite beta with an aqueous metal hydroxide solution and heating the parent zeolite beta and aqueous metal hydroxide mixture to a temperatures greater than or equal to 100? C. to produce the hierarchical mesoporous beta zeolites having and average pore size greater than 8 nm. In embodiments, the hierarchical mesoporous beta zeolites are produced without a templating agent or pore-directing agent.

Methods for producing mesoporous beta zeolites from parent beta zeolites having a Si/Al molar ratio of at least 10 comprise selecting a target average mesoporous size between 2 nm and 8 nm for the parent beta zeolites, selecting a pore directing agent (PDA) based on the target average mesopore size, where a non-ionic surfactant, a small cationic surfactant has a molecular weight of greater than 100 grams/mole, or both may be selected as the PDA when the target average mesopore size is at least 5 nm, and a large cationic surfactant having a molecular weight of less than 100 grams/mole may be selected as the PDA when the target average mesopore size is less than 5 nm. The method further comprises adding the selected PDA to an alkaline solution to form a PDA-base mixture, and adding the parent beta zeolites to the PDA-base mixture to produce the mesoporous beta zeolites.

The present invention relates to a catalyst having improved selectivity and reactivity and applied to preparing olefins by dehydrogenating C9 to C13 paraffin, and particularly to a technique for preparing a catalyst, which uses a heat-treated support having controlled pores, and most of metal components contained therein are distributed evenly in a support in the form of an alloy rather than in the form of each separate metal, thereby exhibiting high a conversion rate and selectivity when used in dehydrogenation.

A catalyst composition includes a zeolite, a binder, and a Group 12 transition metal selected from the group consisting of Zn, Cd, or a combination thereof, the zeolite having a silicon to aluminum ratio of at least about 10, the catalyst composition comprising about 50 wt % or less of the binder based on a total weight of the catalyst composition, the catalyst composition having a micropore surface area of at least about 340 m.sup.2/g, a molar ratio of Group 12 transition metal to aluminum of about 0.1 to about 1.3, and at least one of (a) a mesoporosity of greater than about 20 m.sup.2/g; (b) a diffusivity for 2,2-dimethylbutane of greater than about 110.sup.2 sec.sup.1 when measured at a temperature of about 120 C. and a 2,2-dimethylbutane pressure of about 60 torr (about 8 kPa).

The invention relates to a process for preparing a shaped CuAl catalyst body for the hydrogenation of organic compounds containing a carbonyl function. More particularly, the shaped catalyst body is suitable for the hydrogenation of aldehydes, ketones and of carboxylic acids or esters thereof, specifically of fatty acids or esters thereof, such as fatty acid methyl esters, to the corresponding alcohols such as butanediol. The present invention further relates to CuAl catalysts obtainable by the preparation process.

A catalyst composition comprising a zeolite, an alumina binder, and a Group 12 transition metal selected from Zn and/or Cd, the zeolite having a Si/Al ratio of at least about 10 and a micropore surface area of at least about 340 m.sup.2/g, the catalyst composition comprising about 50 wt % or less of the binder, based on a total weight of the catalyst composition, and having a micropore surface area of at least about 290 m.sup.2/g, a molar ratio of Group 12 transition metal to aluminum of about 0.1 to about 1.3, and at least one of: a mesoporosity of about 20 m.sup.2/g to about 120 m.sup.2/g; a diffusivity for 2,2-dimethylbutane of greater than about 110.sup.2 sec.sup.1 when measured at a temperature of about 120 C. and a 2,2-dimethylbutane pressure of about 60 torr (8 kPa); and a combined micropore surface area and mesoporosity of at least about 380 m.sup.2/g.