A supported catalyst having rhodium particles with an average diameter of less than 1 nm disposed on a support material containing magnetic iron oxide (e.g. Fe.sub.3O.sub.4). A method of producing the supported catalyst and a process of reducing nitroarenes to corresponding aromatic amines employing the supported catalyst with a high product yield are also described. The supported catalyst may be recovered with ease using an external magnet and reused.

The present invention relates to a catalytic material for the preparation of one or more of 4,4′-methylenedianiline, 2,2′-methylenedianiline, 2,4′-methylenedianiline, and oligomers of two or more thereof, the catalytic material comprising an oxidic support, wherein the oxidic support comprises an element E.sub.OS1 selected from the group consisting of Ti, Zr, Al, Si, and mixtures of two or more thereof, and further comprising a supported material supported on the oxidic support, wherein the supported material comprises an element E.sub.SM1 selected from the group consisting of Ti, Zr, V, Nb, Ta, Mo, W, Ge, Sn, Sc, Y, La, Ce, Nd, Pr, Hf, Cr, Fe, Co, Ni, Cu Zn, Pb and mixtures of two or more thereof. Further, the present invention relates in particular to a process for the preparation of a catalytic material and to a process for the preparation of one or more of 4,4′-methylenedianiline, 2,2′-methylenedianiline, 2,4′-methylenedianiline and oligomers of two or more thereof.

Catalyst compositions to perform selective alkyl-demethylation of C2+-hydrocarbyl-substituted aromatic hydrocarbon may exhibit a hydrogen chemisorption of at least 15% and comprise an oxide support material selected from the group consisting of an alkaline earth metal oxide, silica, a composite of an alkaline earth metal oxide and Al.sub.2O.sub.3, a composite of ZnO and Al.sub.2O.sub.3, a lanthanide oxide, a composite of a lanthanide oxide and Al.sub.2O.sub.3, and combinations and mixtures of two or more thereof; and a transition metal element dispersed upon the oxide support material. Alkyl-demethylation processes of a C6+ aromatic hydrocarbon-containing stream comprising C2+-hydrocarbyl-substituted aromatic hydrocarbons may comprise contacting the catalyst compositions in an alkyl-demethylation zone under alkyl-demethylation conditions to form an alkyl-demethylated aromatic hydrocarbon as an effluent exiting the alkyl-demethylation zone.

Disclosed are catalyst compositions comprising two or more metal elements with high performances for selective alkyl-demethylation of C2+-hydrocarbyl-substituted aromatics, processes for making such catalyst compositions, and alkyl-demethylation processes using same. Also disclosed are preferred processes for making alkyl-demethylation catalyst compositions including a high-temperature calcination step, and preferred alkyl-demethylation processes having a high H.sub.2/HC molar ratio.

A DLM-1 molecular sieve, a process for preparing the molecular sieve, and use thereof in treating an organic substance are provided. The DLM-1 molecular sieve is an Al-SBA-15 molecular sieve, and has a schematic chemical composition as represented by the formula “first oxide*second oxide”. The first oxide is silica, the second oxide is alumina, and the content by mass percent of alumina in the schematic chemical composition is 2% to 85%. The DLM-1 molecular sieve is suitable for the hydrodenitrogenation reaction of heavy distillate oil, and is favorable for improving the hydrodenitrogenation activity.

Disclosed herein is a fungicide, including a porous carbon material and a silver member adhered to the porous carbon material, wherein a value of a specific surface area based on a nitrogen BET, namely Brunauer, Emmett, and Teller method is equal to or larger than 10 m.sup.2/g, and a volume of a fine pore based on a BJH, namely Barrett, Joyner, and Halenda method and an MP, namely Micro Pore method is equal to or larger than 0.1 cm.sup.3/g.

A de-hydrogenation catalyst and its use in dehydrogenation of hydrocarbons. The catalyst has low cracking activity and comprises gallium or gallium and platinum on an essentially non-acidic and amorphous alumina-phosphate or silica-alumina-phosphate support with an empirical chemical composition of [Al2O3][SiO2].sub.Y[P2O5].sub.Z, wherein Y is between 0 and 0.2 and Z is between 0.01 and 1.1, with a BET surface area above 50 m.sup.2/g, as measured by N2 adsorption experiment.

Multi-metallic bulk catalysts and methods for synthesizing the same are provided. The multi-metallic bulk catalysts contain nickel, molybdenum tungsten, copper, and optionally, titanium and/or niobium. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.

The present invention provides a process to prepare middle distillates and base oils from a Fischer-Tropsch product, by (a) subjecting the Fischer-Tropsch product to a hydroprocessing step in the presence of a catalyst comprising a molecular sieve with a pore size between 5 and 7 angstrom and a SiO.sub.2/AlO.sub.3 ratio of at least 25, preferably from 50 to 180 and a group VIII metal to obtain a mixture comprising one or more middle distillate fractions and a first residual fraction and a naphtha fraction; (b) separating the mixture as obtained in step (a) by means of atmospheric distillation into one or more middle distillate fractions, a first residual fraction and a naphtha fraction; (c) separating the first residual fraction by means of vacuum distillation into at least a distillate base oil fraction and a second residual fraction.

Catalysts for the hydrogenolysis of butane are described. A supported catalyst for hydrogenolysis of butane to ethane can include a support and a catalytic crystalline bimetallic composition that can include a molybdenum-iridium (Mo—Ir) crystalline composition attached to the support. The supported catalyst has a BET specific surface area of at least 100 m.sup.2/g, preferably 100 m.sup.2/g to 500 m.sup.2/g. Method of use and methods of making the catalyst are also described.