A method is disclosed of purifying a recycled or renewable organic material, wherein the recycled or renewable organic material contains more than 20 ppm Cl. Exemplary methods include (a) providing the recycled or renewable organic material; (b) purifying the organic recycled or renewable organic material to obtain a purified recycled or renewable organic material, and (c) hydrotreating the purified recycled or renewable organic material in a presence of a hydrotreating catalyst at a temperature from 270 to 380° C. under pressure from 4 to 20 MPa and under continuous hydrogen flow; to obtain purified hydrotreated recycled or renewable organic material.

The disclosure provides a process to hydrodearylate the non-condensed alkyl-bridged multi-aromatics at the outlet of the clay tower where such multi-aromatics form rather than performing hydrodearylation on the reject stream of the aromatics complex. Hydrodearylation may feature combining a C.sub.8+ hydrocarbon stream from a clay treater with a hydrogen stream over a catalyst bed comprising a support and an acidic component optionally containing Group 8 and/or Group 6 metals.

In accordance with one or more embodiments of the present disclosure, a catalyst composition includes a catalyst support and at least one hydrogenative component disposed on the catalyst support. The catalyst support includes at least one USY zeolite having a framework substituted with titanium and zirconium. The framework-substituted USY zeolite comprises at least one rare earth element. Methods of making and using such a catalyst in a hydrocracking process are also disclosed.

The invention relates to a process and system arrangement to generate benzene, toluene and xylenes in a refinery. The process relies on recycling a C.sub.9+ aromatic bottoms stream from an aromatic recovery complex back to rejoining a hydrotreated naphtha stream as it enters a catalytic reformer. The aromatic bottoms can be further reacted through both the reformer and the subsequent aromatic recovery complex to transform to higher value compounds, thereby reducing waste or reducing bottoms' presence in gasoline pools.

Light olefins may be produced from hydrocarbons by a method including passing a hydrocarbon feed stream into a feed inlet of a reactor. The reactor may include an upper reactor portion defining an upper reaction zone and a lower reactor portion defining a lower reaction zone. The catalyst may move in a generally downward direction through the upper reactor portion and the lower reactor portion, and the hydrocarbon feed stream may move in a generally upward direction through the upper reactor portion and lower reactor portion such that the hydrocarbon feed stream and the catalyst move with a counter-current orientation. Contacting the catalyst with the hydrocarbon feed stream may crack one or more components of the hydrocarbon feed stream and form a hydrocarbon product stream. The method may further include passing the hydrocarbon product stream out of the upper reaction zone through the hydrocarbon product outlet.

A hydrocracking process for converting a petroleum feed to lower boiling products. The process comprises hydrotreating a petroleum feed in a pre-treating zone in the presence of hydrogen to produce a hydrotreated effluent stream comprising a liquid product. At least a portion of the hydrotreated effluent stream is then passed to an MMS catalyst zone, and then to a hydrocracking zone. In one embodiment, the MMS catalyst zone comprises a self-supported multi-metallic catalyst prepared from a precursor in the oxide or hydroxide form. The percentage work of the hydrotreating in the pre-treating zone is maintained at a level of at least 56%.

The invention relates to a process for adding an organic compound to a porous solid wherein the porous solid and the organic compound in the liquid state are brought together simultaneously, without physical contact between the solid and the organic compound in the liquid state, at a temperature below the boiling point of the organic compound and under pressure and time conditions such that a fraction of said organic compound is transferred gaseously to the porous solid.

Isobutanol may be converted into predominantly C.sub.12+ olefin oligomers under specified conditions. Such methods may comprise: contacting a feed comprising isobutanol with a zeolite solid acid catalyst having a MWW framework under conditions effective to convert the isobutanol into a product comprising C.sub.4n olefin oligomers, wherein n is an integer having a value of two or greater and about 80 wt. % or greater of the C.sub.4n olefin oligomers are larger than C.sub.8.

A process for producing light olefins and aromatics, which comprises reacting a feedstock by contacting with a catalytic cracking catalyst in at least two reaction zones, wherein the reaction temperature of at least one reaction zone among the reaction zones downstream of the first reaction zone is higher than that of the first reaction zone and its weight hourly space velocity is lower than that of the first reaction zone, separating the spent catalyst from the reaction product vapor, regenerating the separated spent catalyst and returning the regenerated catalyst to the reactor, and separating the reaction product vapor to obtain the desired products, light olefins and aromatics. This process produces maximum light olefins such as propylene, ethylene, etc from heavy feedstocks, wherein the yield of propylene exceeds 20% by weight, and produces aromatics such as toluene, xylene, etc at the same time.

The present invention relates to a catalyst for selective hydrodesulphurization of cracked naphtha streams in the form of an extrudate, which comprises a support based on an inorganic oxide and an outer layer bound to the support, wherein the outer layer comprises desulphurization metals dispersed therein forming a crown, the desulphurization metals being cobalt and molybdenum. The present invention also relates to the preparation of said catalyst by the incipient wetness impregnation method and to the process for selective hydrodesulphurization of cracked naphtha employing same.