B01J23/8872

Coprocessing of biofeeds with group VI metal catalysts

Feedstocks containing biocomponent materials are coprocessed with mineral feeds using a Group VI metal catalyst prior to hydrodesulfurization of the feedstocks. The Group VI metal catalyst is optionally a physically promoted Group VI metal catalyst.

Selective nickel based hydrogenation catalyst and the preparation thereof

A selective nickel-based hydrogenation catalyst and the preparation thereof, characterized in that: provided that the catalyst is weighed 100%, it comprises nickel oxide 14-20% as active component, lanthanum oxide and/or cerium oxide 2-8%, and VIB element oxide 1-8% as aids, 2-8% silica, 1-8% alkaline earth metal oxides, and alumina as the balance. The catalyst specific surface area is 60-150 m.sup.2/g, and the pore volume is 0.4-0.6 ml/g. The catalyst has good hydrogenation performance, especially impurity and colloid resistance and hydrogenation stability. The catalyst can be applied to the diolefin selective hydrogenation of medium or low-distillate oil, especially of the full-distillates pyrolysis gasoline.

IMPROVED CATALYST FOR DEHYDROGENATING HYDROCARBONS
20170073284 · 2017-03-16 ·

The present invention relates to a catalyst for the dehydrogenation of hydrocarbons which is based on iron oxide and a process for producing it. The catalyst comprises at least one iron compound, at least one potassium compound and from 11 to 24% by weight of at least one cerium compound, calculated as CeO.sub.2, wherein the at least one iron compound and the at least one potassium compound are at least partly present in the form of one or more K/Fe mixed oxide phases of the general formula K.sub.xFe.sub.yO.sub.z, where x is from 1 to 17; y is from 1 to 22 and z is from 2 to 34, and comprises at least 50% by weight, based on the total catalyst, of the K/Fe mixed oxide phases, and also a process for producing it.

Dual catalyst system for performing a ketonisation reaction and a hydrotreatment reaction simultaneously

The present invention provides a method for simultaneous production of components suitable for production of base oil and fuel components. In the method a feedstock comprising fatty acids and/or fatty acid esters is entered into a reaction zone and subjected to a ketonization reaction in the presence of a dual catalyst system. This system is configured to perform a ketonization reaction and a hydrotreatment reaction, under hydrogen pressure. Subsequently ketones are obtained.

Method for production of hydrocarbons by increasing hydrocarbon chain length
09533291 · 2017-01-03 · ·

The present invention provides a method for increasing hydrocarbon chain length. The method comprises providing a feedstock comprising fatty acids and/or fatty acid esters with hydrocarbon chain length below C23 into a reaction zone in which ketonization is conducted in the presence of a hydrotreatment catalyst under hydrogen pressure. The obtained ketones have a hydrocarbon chain length of from C24 to C43. The present invention further provides a method for simultaneous production of base oil components and fuel components.

Supported composite oxide catalyst and preparation and use thereof

In a supported composite oxide catalyst and preparation and use thereof, the catalyst has the general formula: FeMo.sub.aSi.sub.bX.sub.cO.sub.d, wherein X is a modified metal and is selected from alkali metals or alkaline earth metals; a=0.5-5, b=10-50, c=0.001-0.1, and d is the amount of oxygen element satisfying the chemical valence. The catalyst is prepared with the following method: (i) providing an acidic aqueous solution of a surfactant; (ii) dissolving an iron-containing compound and a complexing agent in the acidic aqueous solution, adding tetra C.sub.1-4 alkyl orthosilicate, and performing hydrolysis, crystallization and calcination to obtain a precursor; and (iii) forming a mixed liquid of the precursor, a molybdenum-containing compound and a modifying metal compound, drying same and calcinating the resultant, so as to obtain the supported composite oxide catalyst.