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 para-xylene.

Processes for producing high biogenic concentration Fischer-Tropsch liquids derived from the organic fraction of municipal solid wastes (MSW) feedstock that contains a relatively high concentration of biogenic carbon (derived from plants) and a relatively low concentration of non-biogenic carbon (derived from fossil sources) wherein the biogenic content of the Fischer-Tropsch liquids is the same as the biogenic content of the feedstock.

The present disclosure relates to the technical field of Fischer-Tropsch synthesis reaction catalysts, and discloses a supported ε/ε′ iron carbide catalyst for Fischer-Tropsch synthesis reaction, preparation method thereof and Fischer-Tropsch synthesis process, wherein the method comprises the following steps: (1) dipping a catalyst carrier in a ferric salt aqueous solution, drying and roasting the dipped carrier to obtain a catalyst precursor; (2) subjecting the catalyst precursor and H.sub.2 to a precursor reduction at the temperature of 300-550° C.; (3) pretreating the material obtained in the step (2) with H.sub.2 and CO at the temperature of 90-185° C., wherein the molar ratio of H.sub.2/CO is 1.2-2.8:1; (4) preparing carbide with the material obtained in the step (3), H.sub.2 and CO at the temperature of 200-300° C., wherein the molar ratio of H.sub.2/CO is 1.0-3.2:1. The preparation method has the advantages of simple and easily obtained raw materials, simple and convenient operation steps, being capable of preparing the catalyst with 100% pure phase ε/ε′ iron carbide as the active phase, the catalyst has lower selectivity of CO.sub.2 and CH.sub.4 and higher selectivity of effective products.

A continuous multi-stage vertically sequenced gasification process for conversion of solid carbonaceous fuel material into clean (low tar) syngas. The process involves forming a pyrolysis residue bed having a uniform depth and width to pass raw syngas there through for an endothermic reaction, while controlling the reduction zone pressure drop, resident time and syngas flow space velocity during the endothermic reaction to form substantially tar free syngas, to reduce carbon content in the pyrolysis residue, and to reduce the temperature of raw syngas as compared to the temperature of the partial oxidation zone.

A feedstock delivery system transfers a carbonaceous material, such as municipal solid waste, into a product gas generation system. The feedstock delivery system includes a splitter for splitting bulk carbonaceous material into a plurality of carbonaceous material streams. Each stream is processed using a weighing system for gauging the quantity of carbonaceous material, a densification system for forming plugs of carbonaceous material, a de-densification system for breaking up the plugs of carbonaceous material, and a gas and carbonaceous material mixing system for forming a carbonaceous material and gas mixture. A pressure of the mixing gas is reduced prior to mixing with the carbonaceous material, and the carbonaceous material to gas weight ratio is monitored. A transport assembly conveys the carbonaceous material and gas mixture to a first reactor where at least the carbonaceous material within the mixture is subject to thermochemical reactions to form the product gas.

To encode High Dynamic Range (HDR) images, the HDR images can be converted to Low Dynamic Range (LDR) images through tone mapping operation, and the LDR images can be encoded with an LDR encoder. The present principles formulates a rate distortion minimization problem when designing the tone mapping curve. In particular, the tone mapping curve is formulated as a function of the probability distribution function of the HDR images to be encoded and a Lagrangian multiplier that depends on encoding parameters. At the decoder, based on the parameters indicative of the tone mapping function, an inverse tone mapping function can be derived to reconstruct HDR images from decoded LDR images.

The present invention provides an improved process for removing heat from an exothermic reaction. In particular, the present invention provides a process wherein heat can be removed from multiple reaction trains using a common coolant system.

Disclosed herein is a method of producing a product comprising C2-C5 hydrocarbons and C6-C18 hydrocarbons comprising the steps of: a) converting synthesis gas to the product comprising C2-C5 hydrocarbons and C6-C18 hydrocarbons in a first reactor; b) removing the product comprising C2-C5 hydrocarbons and C6-C18 hydrocarbons from the first reactor; c) reintroducing the C6-C18 hydrocarbons into the first reactor and/or introducing the C6-C18 hydrocarbons into a cooling jacket of the first reactor; and d) performing an exothermic reaction in the first reactor, thereby transferring heat from the exothermic reaction to the C6-C18 hydrocarbons, thereby storing heat in the C6-C18 hydrocarbons.

Systems and methods are provided for improving thermal management and/or efficiency of reaction systems including a reverse flow reactor for performance of at least one endothermic reaction and at least one supplemental exothermic reaction. The supplemental exothermic reaction can be performed in the recuperation zone of the reverse flow reactor system. By integrating the supplemental exothermic reaction into the recuperation zone, the heat generated from the supplemental exothermic reaction can be absorbed by heat transfer surfaces in the recuperation zone. The adsorbed heat can then be used to heat at least one of the fuel and the oxidant for the combustion reaction performed during regeneration, thus reducing the amount of combustion that is needed to achieve a desired temperature profile at the end of the regeneration step.

The invention relates to a method for treating oxygenated volatile organic compounds in Fischer-Tropsch synthesis reaction water. Fischer-Tropsch synthesis reaction water is subjected to (a) primary concentration and separation, (b) carbonyl compound hydrogenation, (c) carbonyl compound cutting, (d) mixed-alcohol dehydration, (e) solvent recovery, (f) ethyl alcohol separation, (g) methyl alcohol removal and separation, (h) isopropanol separation, (i) propyl alcohol cutting, (j) n-propyl alcohol separation, and (k) 2-butanol separation, so that basic organic chemicals such as ethyl alcohol, isopropanol, n-propyl alcohol, 2-butanol and mixed alcohols are obtained. Compared with the prior art, the method directly converts the concentrated Fischer-Tropsch synthesis water rich in alcohols, aldehydes, ketones, acids, and esters into a mixed-alcohol solution by hydrogenation, thus having the advantages of simple separation process and high product purity.