A metal-free catalytic oxidation system, an oxygenation method and a method for producing benzoic acid derivatives. The system includes a feed device; a tubular reactor; a plurality of venturi nozzles mounted on the tubular reactor at intervals; a tubular filter; a discharge device for a solid phase product; and an intermediate tank for reaction mixture. A low-pressure zone is formed at an output end of each of the plurality of venturi nozzles, and an oxygen inlet corresponds to the low-pressure zone; the tubular filter comprises an inner tube and an outer tube connected to each other, where the inner tube is provided with small holes for solid-liquid separation; the discharge device for the solid phase product is located at an end of the inner tube; and the intermediate tank for reaction mixture is connected to the outer tube of the tubular filter through a pipeline.

An apparatus and a method for continuous solvothermal synthesis of nanoparticles, are provided. The apparatus includes an inlet section, a reactor section, a flexible quenching unit, and an outlet section. The inlet section separately receives reactants including the solvent and a precursor solution that are allowed to flow into the reactor section. The reactor section includes multiple spiral turns such that each of the spiral turns includes a helical channel followed by a counter-helical channel for enabling mixing of the reactants to cause solvothermal reactions between them. The counter-helical channel changes the direction of flow of reactants upon flow of said reactants from the helical channel to the counter-helical channel. The flexible quenching section enclosing a portion of the reactor section quenches a slurry formed as a result of the solvothermal reactions, wherein the slurry includes the nanoparticles of targeted characteristics. The outlet section facilitates withdrawal of the slurry.

An apparatus for carrying out a chemical reaction in a process fluid includes a reactor comprising one or more reaction tubes which have a number of electrically heatable tube segments which are connected to one another by an electrically conductive star bridge, and at least one power source configured to provide a multiphase alternating current with N phases to N phase lines at a predetermined voltage. N is an integer greater than or equal to 2. For each of the at least one power source, a number of power connections is provided, each of which is connected to at least one of the tube segments and to one of the phase lines of the power source. In the at least one power source, a star point is formed at which the phase lines of the power source are connected, wherein the star point is not connected to a ground connection.

A continuous acoustic chemical microreactor system is disclosed. The system includes a continuous process vessel (CPV) and an acoustic agitator coupled to the CPV and configured to agitate the CPV along an oscillation axis. The CPV includes a reactant inlet configured to receive one or more reactants into the CPV, an elongated tube coupled at a first end to the reactant inlet and configured to receive the reactants from the reactant inlet, and a product outlet coupled to a second end of the elongated tube and configured to discharge a product of a chemical reaction among the reactants from the CPV. The acoustic agitator is configured to agitate the CPV along the oscillation axis such that the inner surface of the elongated tube accelerates the one or more reactants in alternating upward and downward directions along the oscillation axis.

The present invention provided a continuous flow process for the synthesis of phenylhydrazine salts and substituted phenylhydrazine salts. Diazotization, reduction, acidic hydrolysis and salifying with acids are innovatively integrated together. Using acidic liquids of aniline or substituted aniline, diazotization reagents, reductants and acids as raw materials, phenylhydrazine derivative salts is obtained through the synthesis process, which is a three-step continuous tandem reaction including diazotization, reduction, acidic hydrolysis and salifying. The described synthesis process is a kind of integrated solutions, which is carried out in an integrated reactor. The feed inlets of the integrated reactor are continuously filled with raw materials. In the integrated reactor, diazotization, reduction, acidic hydrolysis and salifying are carried out continuously and orderly, and phenylhydrazine salts or substituted phenylhydrazine salts is obtained in the outlet of the integrated reactor without interruption. The total reaction time is no more than 20 min.

Disclosed is an LED light source photocatalytic tubular reactor and application thereof. The LED light source photocatalytic tubular reactor comprises an LED light source, a temperature control chamber and a transparent reaction pipeline; the transparent reaction pipeline is located in the temperature control chamber; at least one side of the temperature control chamber is a light-transmitting plate; the LED light source provides a light source for the transparent reaction pipeline through the light-transmitting plate; and the transparent reaction pipeline has a diameter-to-length ratio of the inner diameter to the length of 0-0.1, but not 0. The LED light source continuous photocatalytic tubular reactor of the present disclosure can eliminate the scaling up effect, increase the yield and allow continuous production with an advantage of easy to use and low cost. The tubular reaction device of the present disclosure can also realize automatic control, which can effectively reduce personnel costs and improve production safety.

A continuous flow catalytic reactor, an assembling method therefor and an application thereof includes a reaction vessel, a filler packaged in the reaction vessel and a charged catalytic component; the charged catalytic component is fixed to the filler under an action of a direct-current electric field. The continuous flow catalytic reactor may be applied to continuous flow reactions such as a monosaccharide epimerization reaction. A monosaccharide epimerization reaction method includes: providing the continuous flow catalytic reactor; electrically connecting the continuous flow catalytic reactor with a direct-current power supply, thereby to forming the direct-current electric field by electrically connecting the continuous flow catalytic reactor with the direct-current power supply; and heating a reactor container to a target temperature, and inputting a monosaccharide solution from a liquid flow inlet of the reaction vessel and then collecting a solution containing a target product from a liquid flow outlet of the reaction vessel.

A system and method including providing a feed having alkyl-bridged multi-aromatic compounds to a tubular reactor, heating the tubular reactor, and cleaving an alkyl bridge of the alkyl-bridged multi-aromatic compounds.

The present invention relates to a reactor for non-oxidative direct conversion of methane and a method of manufacturing ethylene and an aromatic compound using the same. More particularly, the present invention relates to a reactor for non-oxidative direct conversion of methane in which a catalytic reaction velocity is maximized, the production of coke is minimized, and a high conversion rate of methane and a high yield of ethylene and an aromatic compound are ensured when ethylene and the aromatic compound are manufactured from methane, and a method of manufacturing ethylene and an aromatic compound using the same.

A reactor and process for the production of bio-diesel. The reactor includes one or more coiled reaction lines. The lines are positioned within a tank containing a heat transfer media such as molten salt, maintained at about 750° F. A pump circulates the media within the tank. An emulsion of alcohol; refined feed stock, including glycerides and/or fatty acids; and preferably water is pumped through the reaction lines at temperatures and pressures sufficient to maintain the alcohol in a super-critical state. The curvature of the coils, pump pulsing, and the flow rate of the emulsion keep the emulsion in a turbulent state while in the reactor, ensuring thorough mixing of the alcohol and feed stock. The alcohol reacts with the glycerides and fatty acids to form bio-diesel. The reaction is fast, efficient with regard to energy input and waste generation, and requires minimal alcohol.