Abstract: The invention relates to a process medium guiding apparatus for a recombination system having a recombination device for the catalytic recombination of hydrogen and oxygen created in accumulators to form water. According to the invention, a process medium guiding apparatus for a recombination system having a recombination device for the catalytic recombination of hydrogen and oxygen created in accumulators to form water is to be provided. The process medium guiding apparatus is designed such that the recombination system is limited towards the outside and comprises at least one guiding element. The guiding element is arranged above the recombination device, so that a process medium, more particular water, is guided from the process medium guiding apparatus to at least a partial region of an interior region of the recombination system.

Abstract: The present invention concerns reactors with a radial flow of process stream to be treated comprising improved internals which can be used to minimize the catalytic zones which do not receive any of the process stream which is to be treated. The invention also concerns the use of these radial flow reactors in refining or petrochemical processes.

Abstract: A process is described for increasing the hydrogen content of a synthesis gas mixture comprising hydrogen, carbon oxides and steam, comprising the steps of: (i) passing the synthesis gas mixture at an inlet temperature in the range 300-450° C. over a first water-gas shift catalyst disposed in a first shift vessel to form a first shifted gas mixture, and (ii) passing the first shifted gas mixture at an inlet temperature in the range 170-300° C. over a second water gas shift catalyst disposed in a second shift vessel to form a second shifted gas mixture, wherein the second water-gas shift catalyst comprises copper and the first shift vessel contains a sorbent material for capturing halogen contaminants disposed downstream of the first water gas shift catalyst.

Abstract: A flow connector creates a fluid connection between a port in a wall of a reactor vessel and an axial flow path of the reactor vessel. The flow connector has a wall defining a flow path of the flow connector. The flow path terminates in a first end opening and a second end opening. The first end opening is configured to connect to the axial flow path of the reactor vessel, and the second end opening is configured to connect to the port in a wall of the reactor. The flow connector includes a passageway extending through the wall of the flow connector to provide access to the flow path of the flow connector. A cover is dimensioned for sealing the passageway. The passageway may be dimensioned such that a person may traverse the passageway to access the flow path of the flow connector.

Abstract: A solvent for absorbing H2S and CO2 is regenerated using two regenerators. Rich solvent is fed to a first regenerator producing a first acid gas stream from the top, and a partially regenerated solvent from the bottom. The partially regenerated solvent is fed to a second regenerator producing an overhead vapor stream from the top and a lean solvent stream from the bottom. A portion of the second regenerator overhead vapor stream may be cascaded to the first regenerator to contact rich solvent. The first acid gas stream and the remaining second regenerator overhead vapor stream are respectively fed to the first and second reaction zones of a two-stage Claus reaction furnace. Substantially all volatile organic contaminants are stripped in the first regenerator, and thus favorably destroyed in the first reaction furnace zone by virtue of higher local combustion temperatures and closer approach to oxidizing conditions.

Abstract: Methods for controlling series or series-parallel reactions are described. Novel microchannel apparatus having mesoporous structures adjacent to bulk flow paths are described. Methods of synthesizing formaldehyde from methanol are also described.

Abstract: A solvent for absorbing H2S and CO2 is regenerated using two regenerators. Rich solvent is fed to a first regenerator producing a first acid gas stream from the top, and a partially regenerated solvent from the bottom. The partially regenerated solvent is fed to a second regenerator producing an overhead vapor stream from the top and a lean solvent stream from the bottom. A portion of the second regenerator overhead vapor stream is cascaded to the first regenerator to contact rich solvent. The first acid gas stream and the remaining second regenerator overhead vapor stream are respectively fed to the first and second reaction zones of a two-stage Claus reaction furnace. Substantially all volatile organic contaminants are stripped in the first regenerator, and thus favorably destroyed in the first reaction furnace zone by virtue of higher local combustion temperatures and closer approach to oxidizing conditions.

Abstract: An inclined baseplate for a radial bed reactor improves solids flow from the bottom of the reactor. Gas flow can be improved by utilizing an aerated baseplate or by providing a non-porous section of outer perforated cylinder in the area below the level of the bottom of the inner perforated cylinder.

Abstract: A process for the double-bond isomerization of olefins is disclosed. The process may include contacting a hydrocarbon stream including olefins with a ?-alumina-titania isomerization catalyst to convert at least a portion of the olefin to its positional isomer. The ?-alumina-titania isomerization catalysts disclosed herein may also have the activity to convert alcohol into additional olefins, while having increased resistance to oxygenate poisons.

Abstract: Compositions comprising boron chain embedded carbon nanotubes, methods of making, and methods of using are provided. Electroluminescent compositions comprising the same are also provided.

Abstract: A liquid/gas reactor includes a bulk catalyst bed and means for supplying fresh feed and recycled at least partially converted liquid product stream to the bulk catalyst bed. The reactor also includes means for collecting an at least partially converted liquid product stream from the bulk catalyst bed and recycling at least a portion thereto. A minor catalyst bed extends substantially vertically through the bulk catalyst bed. Means for supplying recycled at least partially converted product stream only to the minor catalyst bed is also provided. A separating wall is disposed between the bulk catalyst bed and the minor catalyst bed.

Abstract: A method for preparing fuel components from crude tall oil. Feedstock containing tall oil including unsaturated fatty acids is introduced to a catalytic hydrodeoxygenation to convert unsaturated fatty acids, rosin acids and sterols to fuel components. Crude tall oil is purified in a purification by washing the crude tall oil with washing liquid and separating the purified crude tall oil from the washing liquid. The purified crude tall oil is introduced directly to the catalytic hydrodeoxygenation as a purified crude tall oil feedstock. An additional feedstock may be supplied to the catalytic hydrodeoxygenation.

Abstract: A plant for preparing monosilane (SiH4) by catalytic disproportionation of trichlorosilane (SiHCl3) includes a reaction column having a feed line for trichlorosilane and a discharge line for silicon tetrachloride (SiCl4) formed, and at least one condenser via which monosilane produced can be discharged from the reaction column, wherein the reaction column has at least two reactive/distillative reaction regions operated at different temperatures and containing different catalytically active solids, at least one of the reaction regions containing a catalytically active solid based on vinylpyridine, and at least one of the reaction regions containing a catalytically active solid based on styrene.

Abstract: This disclosure relates to systems for the fast pyrolysis of organic matter. More specifically, it relates to systems for the catalytic modification of vapors created during the fast pyrolysis of organic matter to create transportation fuel or a transportation fuel component. The inventive systems either catalytically stabilize or convert at least a first portion of pyrolysis vapors, then combine them with a portion of raw, unconverted bio-derived pyrolysis vapors at a temperature and pressure sufficient for molecules of the combined vapors to react and produce hydrocarbons of increased molecular weight that are suitable for use as a hydrocarbon transportation fuel or component thereof.

Abstract: A process and apparatus are disclosed for hydrotreating a hydrocarbon feed in a hydrotreating unit and hydrocracking a second hydrocarbon stream in a hydrocracking unit. The hydrocracking unit and the hydrotreating unit may share the same recycle gas compressor. A make-up hydrogen stream may also be compressed in the recycle gas compressor. The second hydrocarbon stream may be a diesel stream from the hydrotreating unit. The diesel stream may be a diesel and heavier stream from a bottom of a hydrotreating fractionation column.

Abstract: A fuel reformulation system for an engine comprising an annular body for a flow of fluids therethrough connected to the engine, a source of fuel for flowing through at least a portion of the annular body, and a catalytic member connected to the annular body for the flow of any fluids thereacross from the annular body.

Abstract: A second stage Fischer-Tropsch reaction system to enhance a conversion ratio of a synthetic gas, includes, at least one first reactor that uses a Fe catalyst, receives a first synthetic gas extracted from a coal, biomass or natural gas, and reacts the first synthetic gas with the Fe catalyst to obtain a synthetic fuel, and a second reactor that uses a Fe.Co or Co catalyst, receives a second synthetic gas discharged from the first reactors after reaction, and reacts the second synthetic gas with the Fe.Co or Co catalyst to obtain a synthetic fuel.

Abstract: A shell which encloses an interior and has at least one first orifice for feeding at least one gas stream into the interior and at least one second orifice for withdrawing a gas stream fed to the interior beforehand via the at least one first orifice from the interior, the surface of the shell, on its side in contact with the interior, being manufactured at least partly, in a layer thickness of at least 1 mm, from a steel which has a specific elemental composition, and in the interior, a process for continuous heterogeneously catalyzed partial dehydrogenation of at least one hydrocarbon to be dehydrogenated is carried out in a reactor which is manufactured from the steel on its side in contact with the reaction gas.

Abstract: In a method by which hydrogen supplied as a combustion aid to an ammonia combustion engine is produced from ammonia, the filling amount of a decomposition catalyst in an ammonia decomposition apparatus is reduced. The method includes an ammonia decomposition apparatus that produces hydrogen as a combustion aid and an ammonia oxidation apparatus that allows a part of introduced ammonia to react with oxygen for combustion by action of an oxidation catalyst in order to supply the heat needed for the ammonia decomposition reaction, wherein the amount of ammonia and the amount of air introduced into the oxidation apparatus are controlled in accordance with the entrance temperature of an ammonia oxidation catalyst layer, so as to set the ammonia decomposition ratio in the ammonia decomposition apparatus to be 40 to 60% at all times.

Abstract: A partially digested biomass solids is converted in a fixed bed catalytic reduction reactor under hydrothermal catalytic condition with a supported metal catalyst having a high void fraction. The catalyst having high void fraction allows high permeability and extends reaction run time.

Abstract: The present invention is generally directed to methods and systems for producing biofuels via biomass, waste plastic, and/or Fischer-Tropsch product feeds. Such methods and systems are an improvement over the existing art at least in that they are feed-tolerant (i.e., allow for variability) and provide an economy of scale, while typically retaining the environmental benefits associated with such processing of such feeds.

Abstract: Disclosed is a micro-macro channel reactor comprising: a top end plate and a bottom end plate assembled on the outskirts of the micro-macro channel reactor; a heat exchanging plate by which a heat exchanging material passes through passages thereof so that heat is transferred between the heat exchanging material and such a fluid as a reactant, a product, or a mixture thereof that passes through a catalyst plate; a catalyst plate stacked and assembled together with the heat exchanging plate and including a catalyst section containing a reaction catalyst necessary to perform a catalytic reaction of the reactant while the reactant is passing through the catalyst section; and a support plate stacked and assembled together with the catalyst plate and configured to provide passages that allows the reactant to pass through the catalyst section of the catalyst plate.

Abstract: An apparatus is described which comprises at least one process microchannel having a height, width and length, the height being up to about 10 mm, the process microchannel having a base wall extending in one direction along the width of the process microchannel and in another direction along the length of the process microchannel; at least one fin projecting into the process microchannel from the base wall and extending along at least part of the length of the process microchannel; and a catalyst or sorption medium supported by the fin.

Abstract: In a process for producing xylene by transalkylation of a C9+ aromatic hydrocarbon feedstock with a C6 and/or C7 aromatic hydrocarbon, the C9+ aromatic hydrocarbon feedstock, at least one C6 and/or C7 aromatic hydrocarbon and hydrogen are contacted with a first catalyst comprising (i) a first molecular sieve having a Constraint Index in the range of about 3 to about 12 and (ii) at least first and second different metals or compounds thereof of Groups 6 to 12 of the Periodic Table of the Elements. Contacting with the first catalyst is conducted under conditions effective to dealkylate aromatic hydrocarbons in the feedstock containing C2+ alkyl groups and to saturate C2+ olefins formed so as to produce a first effluent.

Abstract: A process for the efficient capture of CO2 and sulfur from combustion flue gas streams and gasification based fuel gas mixtures using regenerable and recyclable calcium based sorbents. The regeneration of the calcium sorbent is accomplished by hydrating the sorbent at high temperatures of about 600° C. and a pressure higher than 6 bars to lower the parasitic energy consumption.

Abstract: In a process for producing xylene by transalkylation of a C9+aromatic hydrocarbon feedstock with a C6 and/or C7 aromatic hydrocarbon, the C9+aromatic hydrocarbon feedstock, at least one C6 and/or C7 aromatic hydrocarbon and hydrogen are contacted with a first catalyst under conditions effective to dealkylate aromatic hydrocarbons in the feedstock containing C2+alkyl groups and to saturate C2+olefins formed so as to produce a first effluent. At least a portion of the first effluent is then contacted with a second catalyst under conditions effective to transalkylate C9+aromatic hydrocarbons with said at least one C6-C7 aromatic hydrocarbon to form a second effluent comprising xylene.

Abstract: Reactors and methods for solar thermochemical reactions are disclosed. Embodiments of reactors include at least two distinct reactor chambers between which there is at least a pressure differential. In embodiments, reactive particles are exchanged between chambers during a reaction cycle to thermally reduce the particles at first conditions and oxidize the particles at second conditions to produce chemical work from heat. In embodiments, chambers of a reactor are coupled to a heat exchanger to pre-heat the reactive particles prior to direct exposure to thermal energy with heat transferred from reduced reactive particles as the particles are oppositely conveyed between the thermal reduction chamber and the fuel production chamber. In an embodiment, particle conveyance is in part provided by an elevator which may further function as a heat exchanger.

Abstract: Integrated Combustion Reactors (ICRs) and methods of making ICRs are described in which combustion chambers (or channels) are in direct thermal contact to reaction chambers for an endothermic reaction. Particular reactor designs are also described. Processes of conducting reactions in integrated combustion reactors are described and results presented. Some of these processes are characterized by unexpected and superior results, and/or results that can not be achieved with any prior art devices.

Abstract: A multiphase multifunctional reactor, system and method is described which has the capacity to effect extractive oxidation of sulfur and nitrogen compounds and unstable unsaturated compounds that are present in raw hydrocarbon streams, in such a way that the reaction conditions are adjusted and avoid losses of yield of the treated hydrocarbon in the stages of the extraction and/or absorption. The objective is achieved by means of the conception of a reactor which comprises a column divided into five sections which can be classified as two reaction sections (1, 2) two decantation sections (3, 4) and an inert gas section (5) under pressure.

Abstract: A reactor system for the transformation of solid, liquid, gaseous, and related hydrocarbon feedstocks into high-purity, high-pressure gas streams capable of withstanding high temperatures and high pressures. The system comprises a plurality of reactor housings and a plurality of molten-metal bath vessels within the housings, the bath vessels in fluid communication with each other via conduits, with communication facilitated by gravity and temperature/pressure differentials.

Abstract: A catalytic membrane reactor assembly for producing a hydrogen stream from a feed stream having liquid hydrocarbons, steam, and an oxygen source through the use of an autothermal reforming reaction, a water-gas-shift reaction, and a hydrogen permeable membrane.

Abstract: In a process for producing xylene by transalkylation of a C9+ aromatic hydrocarbon feedstock with a C6 and/or C7 aromatic hydrocarbon, the C9+ aromatic hydrocarbon feedstock, at least one C6 and/or C7 aromatic hydrocarbon and hydrogen are contacted with a first catalyst under conditions effective to dealkylate aromatic hydrocarbons in the feedstock containing C2+ alkyl groups and to saturate C2+ olefins formed so as to produce a first effluent. At least a portion of the first effluent is then contacted with a second catalyst under conditions effective to transalkylate C9+ aromatic hydrocarbons with said at least one C6-C7 aromatic hydrocarbon to form a second effluent comprising xylene.

Abstract: Apparatus and methods for the production of hydrogen using a reformer including a housing, a first plate having a first plurality of fin structures and a second plate having a second plurality of fin structures assembled such that the first plurality of fin structures is interleaved with the second plurality of fin structures. At least one inlet port is formed in at least one of the first plate and the second plate, and at least one outlet port is formed in at least one of the first plate and the second plate. The fin structures may be coated with a catalytic material to enhance or stimulate reactions taking place within the apparatus. A heat exchange device may also be integrated into one or both plates of the reformer.

Abstract: Disclosed are a syngas production process and a reforming exchanger 100. The process involves passing a first portion of hydrocarbon feed mixed with steam and oxidant through an autothermal catalytic steam reforming zone to form a first reformed gas of reduced hydrocarbon content, passing a second portion of the hydrocarbon feed mixed with steam through an endothermic catalytic steam reforming zone to form a second reformed gas of reduced hydrocarbon content, and mixing the first and second reformed gases and passing the resulting gas mixture through a heat exchange zone for cooling the gas mixture and thereby supplying heat to the endothermic catalytic steam reforming zone. The endothermic catalytic steam reforming zone and the heat exchange zone are respectively disposed tube side and shell side within a shell-and-tube reforming exchanger 100.

Abstract: One embodiment of the invention includes a method of treating a gas stream comprising flowing the gas stream over a hydrocarbon reduction and NOx reduction catalyst first, and thereafter flowing the gas over a perovskite and NOx trap material for NOx oxidation and storage. In one embodiment, the hydrocarbon reduction and NOx reduction catalyst may include palladium. In one embodiment, the perovskite catalyst may have the general formula ABO3, AA?BO3, ABB?O3, or AA?BB?O3. The perovskite catalyst may be the only catalyst or a second non-perovskite catalyst may include at least one of palladium, platinum, rhodium, ruthenium or a catalyst system including one or more of the same or alloys thereof. In one embodiment, the NOx trap material may include at least one of alkali metals, alkaline earth metals such as barium, calcium, potassium, or sodium.

Abstract: Steam, partial oxidation and pyrolytic fuel reformers (14 or 90) with rotating cylindrical surfaces (18, 24 or 92, 96) that generate Taylor Vortex Flows (28 or 98) and Circular Couette Flows (58, 99) for extracting hydrogen from hydrocarbon fuels such as methane (CH4), methanol (CH3OH), ethanol (C2H5OH), propane (C3H8), butane (C4H10), octane (C8H18), kerosene (C12H26) and gasoline and hydrogen-containing fuels such as ammonia (NH3) and sodium borohydride (NaBH4) are disclosed.

Abstract: Disclosed are a mixed catalyst comprising catalyst A and catalyst B mixed in a volume ratio ranging from 1:0.1 to 1:10, heavy crude oil ebullated-bed hydrotreating systems comprising at least one ebullated-bed reactor comprising the mixed catalyst, and heavy crude oil ebullated-bed hydrotreating processes comprising: introducing heavy crude oil and hydrogen into at least one ebullated-bed reactor, reacting the heavy crude oil and the hydrogen with the mixed catalyst in the at least one ebullated-bed reactor to produce reaction products; and discharging the reaction products from the top of the at least one ebullated-bed reactor.

Abstract: A reactor for converting methane, ammonia and oxygen and alkaline or alkaline earth hydroxides into alkaline or alkaline earth cyanides by two-stage reactions comprising a first stage with a gas inlet, wherein the first stage is formed by a cone with distribution plates providing an even gas distribution over the catalyst material wherein the distribution plates are located between the gas inlet of the reactor and catalyst material and the distribution plates being perforated with a number of holes, with the distribution plates spaced from each other in the flow direction of the gas, the first distribution plate(s) functioning mainly to distribute the gas, whereas the last distribution plate works as a heat radiation shield and as a distribution plate facing the catalyst material, and wherein the catalyst material is present in the form of catalyst gauze fixed by catalyst weights.

Abstract: There is disclosed a permselective membrane reactor which efficiently forms hydrogen by use of a water-gas shift reaction and which is excellent in an aspect of manufacturing cost. In a permselective membrane reactor, a permselective membrane is a Pd membrane or a Pd alloy membrane, and a catalyst layer includes a first catalyst layer on the side of the permselective membrane and a second catalyst layer disposed apart from the permselective membrane. The first catalyst layer has a noble metal-based catalyst, and the second catalyst layer has an iron-based catalyst.

Abstract: Continuous processes for monoalkylating aromatic compound with an aliphatic feedstock comprising aliphatic olefin of 8 to 18 carbon atoms per molecule are effected using at least 3 reaction zones in series, each containing solid alkylation catalyst with effluent cooling between reaction zones, each of which reaction zones is supplied a portion of the fresh aliphatic feedstock, such that the Reaction Zone Delta T in each reaction zone is less than about 15° C. The overall aromatic compound to olefin molar ratio is less than about 20:1. The alkylation product has desirable linearity and low amounts of dimers, dealkylated compounds and diaryl compounds even though a low aromatic compound to olefin molar ratio is used.

Abstract: A hydrogen generating apparatus for effectively generating hydrogen from ammonia and relates to the hydrogen generating apparatus for generating hydrogen from ammonia. The apparatus comprises an ammonia oxidation part having ammonia oxidation catalysts which oxidizes ammonia, and an ammonia decomposition part having an ammonia decomposition catalyst which decomposes ammonia to generate nitrogen and hydrogen. The decomposition part is located downstream of the oxidation part in a direction of feed gas flow.

Abstract: Methods and systems for preparing catalyst, such as chromium catalysts, are provided. The valence of at least a portion of the catalyst sent to an activator is changed from Cr(III) to Cr(VI). The catalyst is prepared or activated continuously using a fluidization bed catalyst activator.

Abstract: A unified fuel processing reactor for a solid oxide fuel cell can reform hydrocarbon-based fuel into hydrogen-rich gas, remove a sulfur component, and convert non-converted fuel and a low carbon (C2˜C5) hydrocarbon compound into hydrogen and methane in a single reactor. The reactor comprises a primary-reformer which reforms a hydrocarbon-base fuel and generates hydrogen-rich reformed gas, a desulfurizer which removes a sulfur component from the reformed gas, and a post-reformer which selectively decomposes a low carbon (C2˜C5) hydrocarbon in the desulfurized reformed gas into hydrogen and methane. The primary-reformer, desulfurizer and post-reformer are in the unified reactor and isolated, except for a fluid passage, from each other by internal partition walls. The primary-reformer is disposed at a center portion of the reactor. The post-reformer and the desulfurizer are concentrically disposed outside of the primary-reformer.

Abstract: Processes and catalyst systems are provided for dewaxing a hydrocarbon feedstock to form a lubricant base oil. A layered catalyst system of the present invention may comprise a first hydroisomerization dewaxing catalyst disposed upstream from a second hydroisomerization dewaxing catalyst. Each of the first and second hydroisomerization dewaxing catalysts may be selective for the isomerization of n-paraffins. The first hydroisomerization catalyst may have a higher level of selectivity for the isomerization of n-paraffins than the second hydroisomerization dewaxing catalyst. At least one of the first and second hydroisomerization dewaxing catalysts comprises small crystallite zeolite SSZ-32x.

Abstract: A device for carrying out exothermal chemical reactions wherein a gas phase is guided across a fixed bed and allowed to react, comprising a housing and an exchangeable unit wherein the reaction takes place.

Abstract: A reformer for a fuel cell system includes a leading segment and a trailing segment. The leading segment includes less reactive catalyst and/or more stabilizing catalyst than the trailing segment. The reformer may be used for reformation of high and low hydrocarbon fuels.

Abstract: The invention provides methods, apparatus and chemical systems for making vinyl acetate from ethylene, oxygen, and acetic acid.

Abstract: The present invention relates to a process and apparatus for the production of light olefins comprising olefins having from 2 to 3 carbon atoms per molecule from a feedstock containing heavier olefins. An intermediate cut from a fractionation column is used as olefinic feed to an olefin cracking process preferably after undergoing selective hydrogenation of diolefins. In one embodiment, a liquid side draw from a fractionation column is selectively hydrogenated and then returned to the fractionation column from which a vapor side draw containing olefins is cracked in the olefin cracking reactor.

Abstract: A fuel reforming apparatus includes a catalyst packed portion containing therein fuel reforming catalyst (I) having excellent hydrocarbon conversion rate and fuel reforming catalyst (II) having excellent H2+CO formation rate. Each of catalyst (I) and catalyst (II) especially preferably includes rhodium supported thereon. When the carrier for catalyst (I) is aluminum oxide and the carrier for catalyst (II) is cerium oxide, the hydrogen generation efficiency is excellent particularly even at start-up.

Abstract: An apparatus including storage means containing methanol and a peroxide, a housing containing a catalyst comprising at least one group 7, 8, 9, 10 or 11 transition metal, and means for introducing the methanol and the peroxide into the housing.