A reverse flow reactor (RFR) and process having a forward reaction feed cycle, a reverse reaction feed cycle, and a reverse regeneration cycle. The heat convected in the forward feed cycle matches the heat convected in the reverse flow cycles. Compared to an RFR without the reverse feed cycle, the three-cycle RPR substantially reduces the regeneration air flow rate, associated compression requirements, and the overall reactor volume, that are required.

A process for synthesis of urea from ammonia and carbon dioxide comprising the synthesis of urea in parallel in a first urea reactor (1) at a first urea synthesis pressure and in a second urea reactor (2) at a second and lower urea synthesis pressure; a stripping step of the reaction effluent of the first reactor, which is performed in a stripper (4) operating at a stripping pressure lower than the first urea synthesis pressure; the reaction effluent (21) of the second reactor (2) and the stripper liquid effluent (11) are sent to a recovery section (13) where a carbamate-containing recycle solution (17) is produced, and said recycle solution (17) is sent partly to said first reactor and partly to said second reactor.

The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 2 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing a regeneration loop for the inert gas and at least one regeneration loop for the gas streams comprising oxygen.

Chemical production systems which allow for an optimized carbon footprint are presented. Plasma-based reforming systems may provide a viable alternative to standard chemical production techniques, such systems can reduce the carbon footprint of the chemicals produced. Example systems include the production of synthesis gas (syngas), hydrogen, synthetic hydrocarbon fuels, ammonia, and urea. Reducing the carbon footprint of chemicals such as these is of vital importance to reducing the environmental impact of industries such as transportation and agriculture. In many of the embodiments a secondary product is produced, the sale of this secondary product may make the primary low-carbon footprint chemical more economical. In many cases the secondary product is carbon, methods of sequestering this carbon via reverse mining and enhanced oil and gas recovery are presented.

A hybrid dehydrogenation reaction system includes: an acid aqueous solution tank having an acid aqueous solution; an exothermic dehydrogenation reactor including a chemical hydride of a solid state and receiving the acid aqueous solution from the acid aqueous solution tank for an exothermic dehydrogenation reaction of the chemical hydride and the acid aqueous solution to generate hydrogen; an LOHC tank including a liquid organic hydrogen carrier (LOHC); and an endothermic dehydrogenation reactor receiving the liquid organic hydrogen carrier from the LOHC tank and generating hydrogen through an endothermic dehydrogenation reaction of the liquid organic hydrogen carrier by using heat generated from the exothermic dehydrogenation reactor.

Systems and methods for direct crude oil upgrading to hydrogen and chemicals including separating an inlet hydrocarbon stream into a light fraction and a heavy fraction comprising diesel boiling point temperature range material; producing from the light fraction syngas comprising H.sub.2 and CO; reacting the CO produced; producing from the heavy fraction and separating CO.sub.2, polymer grade ethylene, polymer grade propylene, C.sub.4 compounds, cracking products, light cycle oils, and heavy cycle oils; collecting and purifying the CO.sub.2 produced from the heavy fraction; processing the C.sub.4 compounds to produce olefinic oligomerate and paraffinic raffinate; separating the cracking products; oligomerizing a light cut naphtha stream; hydrotreating an aromatic stream; hydrocracking the light cycle oils to produce a monoaromatics product stream; gasifying the heavy cycle oils; reacting the CO produced from gasifying the heavy cycle oils; collecting and purifying the CO.sub.2; and processing and separating produced aromatic compounds into benzene and paraxylene.

A feed stream including crude oil may be processed by a method that includes separating the feed stream into at least a C.sub.1 hydrocarbon fraction, a C.sub.2-C.sub.4 hydrocarbon fraction, and a C.sub.5+ hydrocarbon fraction. The method may further include methane cracking at least a portion of the C.sub.1 hydrocarbon fraction to form a methane cracked product, steam cracking at least a portion of the C.sub.2-C.sub.4 hydrocarbon fraction to form a steam cracked product, and steam enhanced catalytically cracking at least a portion of the C.sub.5+ hydrocarbon fraction to form a steam enhanced catalytically cracked product. The method may further include passing at least a portion of the steam cracked product and at least a portion of the steam enhanced catalytically cracked product to a product separator to produce one or more product streams. Systems for processing a feed stream comprising crude oil are further described herein.

The invention relates to a method of performing a chemical reaction under elevated pressure. It is suggested that the method comprises the steps of pressurizing a first vessel (3) and a second vessel (5) with reactant-containing liquid and gas to a predetermined pressure, providing reaction conditions in one of the vessels (3, 5) such that the chemical reaction is effected and a product-containing liquid is obtained, withdrawing liquid from the respective vessel (3, 5) as reaction product when a predetermined amount of reaction product has formed, preferably after the chemical reaction in the respective vessel (3, 5) has concluded, and synchronously supplying reactant-containing liquid to the respective other vessel (3, 5), wherein the first and second vessels (3, 5) are in fluid communication by way of a gas communication passage (27). The invention also relates to an apparatus and use thereof for performing said chemical reaction.

The present application provides systems and methods for upgrading an oil stream. The system includes a reactor, a phase separator, an expansion device, a cooling unit, and two separation units. The reactor receives the oil stream, ammonia, and supercritical water. The supercritical water upgrades the oil stream, and the ammonia reacts with sulfur initially present in the oil stream to produce ammonia-sulfur compounds. The phase separator receives a mixture stream comprising the upgraded oil stream, supercritical water, and the ammonia-sulfur compounds, and separates out non-dissolved components. The expansion device reduces the pressure of the mixture stream below a water critical pressure. The cooling unit reduces the temperature of the mixture stream. A first separation unit separates the mixture stream it into a hydrocarbon-rich gaseous phase, a water stream containing ammonia-sulfur compounds, and a treated oil stream. A second separation unit separates the ammonia-sulfur compounds from the water stream.

A liquid process assembly, the assembly including a length of pipework, and a reversible pump for selectively reciprocally moving liquid through the pipework.