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6611 results about "Dehydrogenation" patented technology

Dehydrogenation is a chemical reaction that involves the removal of hydrogen from an organic molecule.It is the reverse of hydrogenation. Dehydrogenation is an important reaction because it converts alkanes, which are relatively inert and thus low-valued, to olefins (including alkenes), which are reactive and thus more valuable. Alkenes are precursors to aldehydes, alcohols, polymers, and aromatics. Dehydrogenation processes are used extensively to produce aromatics and styrene in the petrochemical industry. Such processes are highly endothermic and require temperatures of 500 °C and above. Dehydrogenation also converts saturated fats to unsaturated fats. Enzymes that catalyze dehydrogenation are called dehydrogenases.

Method for improving catalyst reacting activity in the propylene producing through propane dehydrogenation

A method to promote the activity of a catalyst for dehydrogenation of propane to propylene is as follows: (1) an inorganic oxide bonding agent, a promoter and an acid solvent are added into a heat-resistant oxide; then after the oxide bonding agent, the promoter, the acid solvent and the oxide are kneaded evenly, the oxide is molded by rolling or band-extruding; (2) the catalyst carrier prepared is dried for 2 to 10 hours under the temperature of 60 centigrade degrees, and calcined under the temperature of 400 to 800 degrees; (3) the calcined carrier is immersed in a rare earth metal water solution under the temperature of 60 to 100 centigrade degrees for 2 to 10 hours; (4) the catalyst carrier modified by the rare earth is immersed in a water solution comprising platinum metal elementsand the fourteenth metal elements under the temperature of 400 to 600 centigrade degrees for 2 to 10 hours, and then the carrier is filtered, washed with distilled water, dried under the temperature of 60 to 180 centigrade degrees for 2 to 10 hours, and calcined under the temperature of 400 to 600 centigrade degrees for 2 to 10 hours; (5) the catalyst prepared is activated in the air under the temperature of 400 to 600 centigrade degrees for 3 to 10 hours, and reduced in a hydrogen flow under the temperature of 400 to 600 centigrade degrees for 2 to 10 hours; the reduced catalyst is used for catalytic reaction for dehydrogenation of propane to propylene.
Owner:SOUTHEAST UNIV

Apparatus and process for production of high purity hydrogen

The invention relates to a new and improved process and apparatus for the production of high purity hydrogen by steam reforming. The apparatus is an integrated flameless distributed combustion-membrane steam reforming (FDC-MSR) or reactor for steam reforming of a vaporizable hydrocarbon to produce H2 and CO2, with minimal CO, and minimal CO in the H2 stream. The flameless distributed combustion drives the steam reforming reaction which pro-vides great improvements in heat exchange efficiency and load following capabilities. The reactor may contain multiple flameless distributed combustion chambers and multiple hydrogen-selective, hydrogen-permeable, membrane tubes. The feed and reaction gases may flow through the reactor either radially or axially. A further embodiment of the invention involves producing high purity hydrogen by dehydrogenation using an integrated FDC-membrane de-hydrogenation reactor. A still further embodiment of the invention involves a zero emission hybrid power system wherein the produced hydrogen is used to power a high-pressure internally manifolded molten carbonate fuel cell. In addition, the design of the FDC-SMR powered fuel cell makes it possible to capture good concentrations of CO2 for sequestration or use in other processes.
Owner:SHELL OIL CO

Catalytically inactive heat generator and improved dehydrogenation process

An improved dehydrogenation catalyst bed system for olefin production utilizing classical processing techniques is disclosed. The catalyst bed system comprises a dehydrogenation catalyst comprising an active component selected from an oxide of a metal of Group 4 or Group 5 or Group 6 and combinations thereof and a support selected from aluminum oxide, aluminas, alumina monohydrate, alumina trihydrate, alumina-silica, transition aluminas, alpha-alumina, silica, silicate, aluminates, calcined hydrotalcites, zeolites and combinations thereof mixed with a first inert material selected from any material that is catalytically inactive when subjected to reaction conditions that can effect dehydrogenation of olefins and that has a high density and high heat capacity and that is not capable of producing heat during any stage of the dehydrogenation process, and the dehydrogenation catalyst plus the first inert material then being physically mixed with a secondary component comprising a heat-generating inert material and a carrier capable of supporting the heat-generating inert material, wherein the secondary component is catalytically inert with respect to dehydrogenation reactions or to cracking or to coking and generates heat after being exposed to reducing and / or to oxidizing reaction conditions.
Owner:CLARIANT INT LTD

Catalyzer used for low carbon alkane catalytic dehydrogenation and method of manufacturing propylene by paraffin hydrocarbons catalytic dehydrogenation with the same as catalyzer

InactiveCN101108362AReactiveMitigation of heightened demandMolecular sieve catalystsHydrocarbonsAlkaneReaction temperature
The invention relates to a catalyst used for catalyzing and dehydrogenation of low-carbon alkane and the method of producing propylene by alkane catalyzing and dehydrogenation with the catalyst. The former catalyst used for catalyzing and dehydrogenation of low-carbon alkane, each molecule of the hydrocarbon has about 2 to 8 carbon atom, which is characterized in that: the catalyst makes a molecular sieve the carrier, the Pt family metal is loaded on the carrier as the active component, makes the IVA family metal element and alkalinity metal element as additional agent and high temperature standing inorganic oxide as connection agent; when the catalyst is used in producing propylene by alkane catalyzing and dehydrogenation, the reaction temperature is 500 to 700 DEG C., the pressure is 0 to 0.2Mpa, the quality air speed is 2 to 5h to 1, the regenerating temperature of the catalyst is 500 to 700 DEG C., the air speed is 100 to 1000h to 1, the pressure is 0 to 1.0MPa. With adopting the invention, the reaction of producing propylene by alkane catalyzing and dehydrogenation is good, the average transforming rate is 30 per cent, the selectivity above 95 per cent can keep for 50 days.
Owner:SINOPEC JINLING PETROCHEMICAL CO LTD

Dehydrogenation catalyst for feed gas containing carbon monoxide, preparation method and application method thereof

The invention discloses a dehydrogenation catalyst for feed gas containing carbon monoxide, a preparation method and an application method thereof. The catalyst takes alumina as a carrier, palladium and / or platinum as an active component and 2 to 4 MOxes as an additive, M is sodium, potassium, magnesium, titanium, zirconium, vanadium, manganese, iron, nickel, cobalt, copper, molybdenum, tungsten or cerium, and components of the catalyst (calculated by carrier mass) are: 0.01 to 2 percent of the palladium and / or 0.01 to 1 percent of the platinum, and 1 to 2 percent of MOxes. The preparation method for the catalyst comprises the following steps that: firstly, an additive metal salt solution is used to impregnate the carrier; a palladium and / or platinum salt solution is used to impregnate the carrier after the carrier is dried and roasted; and the impregnated carrier is roasted at a temperature of between 450 and 850 DEG C to obtain the catalyst. Before the use, H2-N2 mixed gas containing more than 10 percent of hydrogen or pure hydrogen is activated by the catalyst at a temperature of between 450 and 650 DEG C. The catalyst can perform deep removal on less than 5 percent of hydrogen in the feed gas with the CO content of between 10 and 99 percent, the using temperature is between 100 and 300 DEG C, the space velocity is between 500 and 9,000h<-1>, the dehydrogenation rate is more than 99 percent, the content of outlet hydrogen is less than 100 ppm, and the loss of the carbon monoxide is less than 0.5 percent.
Owner:HAISO TECH

Process for Preparing Butadiene by Oxidative Dehydrogenation of N-Butenes with Monitoring of the Peroxide Content During Work-Up of the Product

The invention relates to a process for preparing butadiene from n-butenes, which comprises the following steps:
    • A) provision of a feed gas stream a comprising n-butenes;
    • B) introduction of the feed gas stream a comprising n-butenes and an oxygen-comprising gas into at least one dehydrogenation zone and oxidative dehydrogenation of n-butenes to butadiene, giving a product gas stream b comprising butadiene, unreacted n-butenes, water vapor, oxygen, low-boiling hydrocarbons, possibly carbon oxides and possibly inert gases;
    • C) cooling and compression of the product gas stream b in at least one cooling stage and at least one compression stage, with the product gas stream b being brought into contact with a circulated coolant to give at least one condensate stream c1 comprising water and a gas stream c2 comprising butadiene, n-butenes, water vapor, oxygen, low-boiling hydrocarbons, possibly carbon oxides and possibly inert gases;
    • D) separation of incondensable and low-boiling gas constituents comprising oxygen, low-boiling hydrocarbons, possibly carbon oxides and possibly inert gases as gas stream d2 from the gas stream c2 by absorption of the C4-hydrocarbons comprising butadiene and n-butenes in a circulated absorption medium, giving an absorption medium stream loaded with C4-hydrocarbons and the gas stream d2, and subsequent desorption of the C4-hydrocarbons from the loaded absorption medium stream to give a C4 product gas stream d1;
    • E) separation of the C4 product stream d1 by extractive distillation using a solvent which is selective for butadiene into a stream e1 comprising butadiene and the selective solvent and a stream e2 comprising n-butenes;
    • F) distillation of the stream e1 comprising butadiene and the selective solvent to give a stream f1 consisting essentially of the selective solvent and a stream f2 comprising butadiene;
    • where samples are taken from the circulated coolant in step C) and/or the circulated absorption medium in step D) and the peroxide content of the samples taken is determined by means of iodometry, differential scanning calorimetry (DSC) or microcalorimetry.
Owner:BASF AG
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