A method for preparing a transition-metal adamantane carboxylate salt is presented. The method includes mixing a transition-metal hydroxide and a diamondoid compound having at least one carboxylic acid moiety to form a reactant mixture, where M is a transition metal. Further, the method includes hydrothermally treating the reactant mixture at a reaction temperature for a reaction time to form the transition-metal adamantane carboxylate salt.

A method for preparing a transition-metal adamantane carboxylate salt is presented. The method includes mixing a transition-metal hydroxide and a diamondoid compound having at least one carboxylic acid moiety to form a reactant mixture, where M is a transition metal. Further, the method includes hydrothermally treating the reactant mixture at a reaction temperature for a reaction time to form the transition-metal adamantane carboxylate salt.

Apparatus and processes herein provide for converting hydrocarbon feeds to light olefins and other hydrocarbons. The processes and apparatus include a conventional riser reactor in combination with a mixed flow (e.g., including both counter-current and co-current catalyst flows) fluidized bed reactor designed for maximizing light olefins production. The effluents from the riser reactor and mixed flow reactor are processed in a catalyst disengagement vessel, and the catalysts used in each reactor may be regenerated in a common catalyst regeneration vessel. Further, integration of the two-reactor scheme with a catalyst cooler provides a refinery the flexibility of switching the operation between the two-reactor flow scheme, a catalyst cooler only flow scheme, or using both simultaneously.

Apparatus and processes herein provide for converting hydrocarbon feeds to light olefins and other hydrocarbons. The processes and apparatus include a conventional riser reactor in combination with a mixed flow (e.g., including both counter-current and co-current catalyst flows) fluidized bed reactor designed for maximizing light olefins production. The effluents from the riser reactor and mixed flow reactor are processed in a catalyst disengagement vessel, and the catalysts used in each reactor may be regenerated in a common catalyst regeneration vessel. Further, integration of the two-reactor scheme with a catalyst cooler provides a refinery the flexibility of switching the operation between the two-reactor flow scheme, a catalyst cooler only flow scheme, or using both simultaneously.

The invention relates to a process of catalytic conversion by dehydro steam cracking of paraffinic and naphthenic hydrocarbons from a naphtha feedstock to propylene in presence of steam, comprising the following steps: a. providing a naphtha feedstock (1) containing one or more paraffins and/or naphthene's comprising 4 to 10 carbons atoms; b. contacting (3) said naphtha feedstock (1) with a catalyst composition in the presence of steam in a reaction zone under dehydro steam cracking conditions at a temperature of at most 650 C., resulting in the production of an effluent (5); c. recovering the effluent of step b) and separating (7) it into a converted fraction (9) and an unconverted fraction (11), wherein the unconverted fraction (11) comprises propane and one or more paraffins comprising 4 to 10 carbons atoms; and d. submitting the unconverted fraction (11) to a steam cracking step;
wherein the catalyst composition comprises one or more acid zeolite catalysts comprising at least one 10-membered ring channels, and one or more soft dehydrogenation elements containing basic compounds selected from rare-earth or alkaline earth metals oxide, salts or hydroxide.

The delayed coking method includes directing a heated secondary feedstock, which contains heated primary feedstock and recirculate, from a reaction furnace to a coking chamber. Vapor-liquid coking products formed in the coking chamber are then directed to a fractionation column, which fractionates hydrocarbon gas, gasoline, light and heavy gas oils, and bottom residues. Heavy gas oil from the fractionation column is directed to a thermal cracking furnace, the products of which are cooled by cooled light gas oil and directed to an evaporator for separation. In the evaporator, gases and light boiling products are removed by evaporation and returned to the fractionation column, and the remaining distillate cracking residue is separated and used as a component of the recirculate, along with bottom residues from the fractionation column. The resulting process produces high quality and high yield needle and anode cokes.

Processes herein may be used to thermally crack various hydrocarbon feeds, and may eliminate the refinery altogether while making the crude to chemicals process very flexible in terms of crude. In embodiments herein, crude is progressively separated into light and heavy fractions utilizing convection heat from heaters used in steam cracking. Depending on the quality of the light and heavy fractions, these are routed to one of three upgrading operations, including a fixed bed hydroconversion unit, a fluidized catalytic conversion unit, or a residue hydrocracking unit that may utilize either an ebullated bed reactor with extrudate catalysts or a slurry hydrocracking reactor using a homogeneous catalyst system, such as a molybdenum based catalysts which may optionally be promoted with nickel. Products from the upgrading operations can be finished olefins and/or aromatics, or, for heavier products from the upgrading operations, may be used as feed to the steam cracker.

Embodiments disclosed herein relate to systems and processes for producing olefins and/or dienes. The processes may include: thermally cracking a hydrocarbon containing feed to produce a cracked hydrocarbon effluent containing a mixture of olefins and paraffins; and catalytically cracking the cracked hydrocarbon effluent to produce a catalytically cracked effluent containing additional olefins and/or dienes. The systems may include a reaction zone for thermally cracking a hydrocarbon containing feed to produce a cracked hydrocarbon effluent containing a mixture of olefins and paraffins; and, a catalytic cracking reaction zone for catalytically cracking the cracked hydrocarbon effluent to produce a catalytically cracked hydrocarbon effluent containing additional olefins and/or dienes.

Embodiments disclosed herein relate to systems and processes for producing olefins and/or dienes. The processes may include: thermally cracking a hydrocarbon containing feed to produce a cracked hydrocarbon effluent containing a mixture of olefins and paraffins; and catalytically cracking the cracked hydrocarbon effluent to produce a catalytically cracked effluent containing additional olefins and/or dienes. The systems may include a reaction zone for thermally cracking a hydrocarbon containing feed to produce a cracked hydrocarbon effluent containing a mixture of olefins and paraffins; and, a catalytic cracking reaction zone for catalytically cracking the cracked hydrocarbon effluent to produce a catalytically cracked hydrocarbon effluent containing additional olefins and/or dienes.

Flash chemical ionizing pyrolysis (FCIP) at 450 C.-600 C. forms liquid ionizing pyrolyzate (LIP) that can be blended in oil feedstock for thermal processes to promote conversion of heavier hydrocarbons to reduce resid/coke yields and/or increase yields of liquid hydrocarbons and isomerates. A front-end refinery process modifies crude oil with LIP for distillation to reduce resid/coke yields and/or increase liquid oil yields. A downstream process modifies a heavy oil stream such as resid with LIP and the LIP-modified stream can be thermally processed to reduce resid/coke yields and/or increase liquid oil yields. FCIP of the LIP blends also improves quality and/or yields of the liquid pyrolyzate product. Finely divided FCIP solids can contain FeCl.sub.3 supported on NaCl-treated calcium bentonite. A process for preparing the FCIP solids treats iron with HCl and HNO.sub.3 to form acidified FeCl.sub.3 of limited solubility, loads the FeCl.sub.3 on NaCl-treated bentonite, and heat-treats the material at 400 C.-425 C.