The invention is directed to a process for producing benzene and LPG comprising the steps of: (a) reacting a source feed stream comprising monoaromatic compounds of formula (I), wherein R1-R5 are the same or different and are chosen from hydrogen or a linear alkyl group of 1-10 carbon atoms, and methanol in an alkylation reactor comprising a basic catalyst to obtain an alkylation product stream and subsequently (b) contacting the alkylation product stream in the presence of hydrogen in a hydrocracking reactor with a hydrocracking catalyst comprising 0.01-1 wt-% hydrogenation metal in relation to the total catalyst weight and a zeolite having a pore size of 5-8 Å and a silica (SiO2) to alumina (Al2O3) molar ratio of 5-200 to produce a hydrocracking product stream comprising benzene and LPG under process conditions including a temperature of 425-580° C., a pressure of 300-5000 kPa gauge and a Weight Hourly Space Velocity of 0.1-15 h.sup.−1.

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A method of producing olefins by catalytic cracking of hydrocarbons is disclosed. The method may include catalytic cracking hydrocarbons in a feed stream that includes the hydrocarbons and the dry gas diluent. The catalytic cracking may be carried out in a process using a train of fixed bed reactors while one or more other trains of fixed bed reactors are being regenerated or are on standby after being regenerated. When the train of fixed bed reactors being used needs regenerating, it is taken out of service and the one or more other trains of fixed bed reactors put in service to carry out the catalytic cracking process. Dry gas instead of steam may be used to reduce the partial pressure of hydrocarbons.

A method of producing olefins by catalytic cracking of hydrocarbons is disclosed. The method may include catalytic cracking hydrocarbons in a feed stream that includes the hydrocarbons and the dry gas diluent. The catalytic cracking may be carried out in a process using a train of fixed bed reactors while one or more other trains of fixed bed reactors are being regenerated or are on standby after being regenerated. When the train of fixed bed reactors being used needs regenerating, it is taken out of service and the one or more other trains of fixed bed reactors put in service to carry out the catalytic cracking process. Dry gas instead of steam may be used to reduce the partial pressure of hydrocarbons.

A process for producing olefins comprising introducing butane feed (n-butane, i-butane) and hydrogen to hydrogenolysis reactor comprising hydrogenolysis catalyst to produce a hydrogenolysis product stream (hydrogen, methane, ethane, propane, i-butane, optionally n-butane, optionally C.sub.5+ hydrocarbons); and feeding the hydrogenolysis product stream and hydrogen to hydrocracking reactor comprising a hydrocracking catalyst to produce hydrocracking product stream (hydrogen, methane, ethane, propane, i-butane, optionally n-butane), wherein the amount of i-butane in the hydrocracking product stream is less than in the hydrogenolysis product stream, and wherein the amount of ethane in the hydrocracking product stream is greater than in the hydrogenolysis product stream. The hydrocracking product stream is separated into first hydrogen stream, first methane stream, first C.sub.2+ gas stream (ethane, propane), first C.sub.4s stream (i-butane, optionally n-butane), optionally C.sub.5+ stream; and the first C.sub.2+ gas stream is fed to gas steam cracker to produce a steam cracker product stream comprising olefins (ethylene, propylene).

A process plant and a process for production of a hydrocarbon suitable for use as jet fuel from a feedstock being a renewable feedstock or an oxygenate feedstock, including combining the feedstock with an amount of a liquid diluent, directing it to contact a material catalytically active in hydrodeoxygenation under hydrotreating conditions to provide a hydrodeoxygenated intermediate product, separating the hydrodeoxygenated intermediate product in at least two fractions; a vapor fraction and a liquid fraction, directing at least an amount of the liquid fraction to contact a material catalytically active in isomerization under isomerization conditions to provide an isomerized intermediate product, directing at least an amount of the isomerized intermediate product and a stream comprising sulfur to provide a hydrocracked intermediate product, and fractionating the hydrocracked intermediate product to provide at least a hydrocarbon suitable for use as jet fuel.

Disclosed are Group III base stocks comprising at least 30 wt % naphthenes, a viscosity index from 120 to 145; and a unique ratio of molecules with multi-ring naphthenes to single ring naphthenes (2R+N/1RN). A method for preparing the base stocks is also disclosed. Also disclosed is a lubricating oil having the base stock as a major component, and an additive as a minor component.

Disclosed are Group III base stocks comprising at least 30 wt % naphthenes, a viscosity index from 120 to 145; and a unique ratio of molecules with multi-ring naphthenes to single ring naphthenes (2R+N/1RN). A method for preparing the base stocks is also disclosed. Also disclosed is a lubricating oil having the base stock as a major component, and an additive as a minor component.

Provided is a novel catalyst for use in the second stage of a two-stage hydrocracking process. The present process comprises hydrocracking a hydrocarbon feed in a first stage. The catalyst in the first stage is a conventional hydrocracking catalyst. The product from the first stage can then be transferred to a second hydrocracking stage. The catalyst used in the second stage of the present hydrocracking process comprises a base impregnated with metals from Group 6 and Groups 8 through 10 of the Periodic Table, and an organic acid. The base of the catalyst used in the present second hydrocracking stage comprises alumina, an amorphous silica-alumina (ASA) material, and a USY zeolite. Improved naphtha production is achieved.

Disclosed herein are modified zeolites and methods for making modified zeolites. In one or more embodiments disclosed herein, a modified zeolite may include a microporous framework including a plurality of micropores having diameters of less than or equal to 2 nm. The microporous framework may include at least silicon atoms and oxygen atoms. The modified zeolite may further include organometallic moieties each bonded to a nitrogen atom of a secondary amine functional group including a nitrogen atom and a hydrogen atom. The organometallic moieties may include a titanium atom that is bonded to the nitrogen atom of the secondary amine functional group. The nitrogen atom of the secondary amine function group may bridge the titanium atom of the organometallic moiety and a silicon atom of the microporous framework.

Catalysts including at least one microporous material (e.g., zeolite), an organosilica material binder, and at least one catalyst metal are provided herein. Methods of making the catalysts, preferably without surfactants and processes of using the catalysts, e.g., for aromatic hydrogenation, are also provided herein.