Provided are a method and an apparatus for producing 1,2,3,4-tetrachlorobutane that are unlikely to lose 3,4-dichloro-1-butene as the material or 1,2,3,4-tetrachlorobutane as the product and can be stably and economically produce 1,2,3,4-tetrachlorobutane. A reaction liquid (1) containing 3,4-dichloro-1-butene is placed in a reaction container (11), then chlorine gas is supplied to a gas phase (2) in the reaction container (11), and the 3,4-dichloro-1-butene is reacted with the chlorine gas to give 1,2,3,4-tetrachlorobutane.

Provided are a method and an apparatus for producing 1,2,3,4-tetrachlorobutane that are unlikely to lose 3,4-dichloro-1-butene as the material or 1,2,3,4-tetrachlorobutane as the product and can be stably and economically produce 1,2,3,4-tetrachlorobutane. A reaction liquid (1) containing 3,4-dichloro-1-butene is placed in a reaction container (11), then chlorine gas is supplied to a gas phase (2) in the reaction container (11), and the 3,4-dichloro-1-butene is reacted with the chlorine gas to give 1,2,3,4-tetrachlorobutane.

Equipment for producing ethylene and/or acetylene from hydrocarbons, including the reaction chamber (13), burner (11), common or separate fuel gas inlets (12) and oxygen inlets (18), preheating tubes (14), a gas distributor (15), cracking gas inlets (16), and a reaction product outlet (17); the gas distributor (15), which has multiple gas inlets and gas outlets, is arranged on the cross section of the reaction chamber (13), where the gas inlet is connected to the cracking gas inlet (16), and the gas outlet is connected to the preheating tube (14). The cracking gas is uniformly distributed through the gas distributor (15) and passed through the preheating tubes (14), which are hollow tubes; the opening at the other end of the hollow tube is close to or inserted into the combustion area of the gaseous fuel and oxygen.

Equipment for producing ethylene and/or acetylene from hydrocarbons, including the reaction chamber (13), burner (11), common or separate fuel gas inlets (12) and oxygen inlets (18), preheating tubes (14), a gas distributor (15), cracking gas inlets (16), and a reaction product outlet (17); the gas distributor (15), which has multiple gas inlets and gas outlets, is arranged on the cross section of the reaction chamber (13), where the gas inlet is connected to the cracking gas inlet (16), and the gas outlet is connected to the preheating tube (14). The cracking gas is uniformly distributed through the gas distributor (15) and passed through the preheating tubes (14), which are hollow tubes; the opening at the other end of the hollow tube is close to or inserted into the combustion area of the gaseous fuel and oxygen.

A feed distribution apparatus and method of using such an apparatus are provided for introducing a three-phase flow into a moving bed reactor that is operated under co-current flow conditions. The feed distribution apparatus can allow for separate introduction of liquid and solids in a manner that allows for even distribution of liquid within the solids. The gas portion of the flow can be introduced in any of a variety of convenient manners for distributing gas into a liquid or solid flow.

A reactor (1) for hydrolysis of uranium hexafluoride comprises a tubular injector (9) comprising first (11), second (13) and third (15) concentric fluid circulation ducts intended to be connected respectively with a source of UF.sub.6, a source of inert gas and a source of water vapor. The tubular injector (9) is obtained by additive manufacturing.

A reactor (1) for hydrolysis of uranium hexafluoride comprises a tubular injector (9) comprising first (11), second (13) and third (15) concentric fluid circulation ducts intended to be connected respectively with a source of UF.sub.6, a source of inert gas and a source of water vapor. The tubular injector (9) is obtained by additive manufacturing.

A valve assembly wherein the inner wall of the valve body comprises at least one opening for the entry of a liquid under pressure following output of a slurry or liquid from a tube or pipe. The valve assembly is particularly useful in maintaining a semi-continuous or continuous pressurized flow of biomass from an extruder and extending the reaction zone downstream from the extruder. An advantage of having an extended reaction zone allows for a complete treatment of materials without further wear on the extruder and also allows manipulation of the upstream treatment of materials in the tube or pipe.

A method and device for producing a solution of polyphosphoric acid from a feed solution P0 by the wet method is provided. An enriched phosphoric acid solution optionally mixed with a direct feed solution is pulverised in a flame of a combustion chamber in order to form the polyphosphoric acid solution. The combustion gases from the combustion chamber are placed in contact with the feed solution in a gas-acid contactor in order to increase the temperature and the P.sub.2O.sub.5 concentration thereof and thus to form an enriched phosphoric acid solution. A portion of the enriched phosphoric acid solution is conveyed with a flow rate of Qp into the combustion chamber in order to be pulverised in the flame. The rest of the enriched phosphoric acid solution is conveyed into a recirculation loop in order to be reinjected into the gas-acid contactor with a flow rate of Q2. The ratio of Qp/(Qp+Q2) is controlled with a predefined value.

Provided is a method for preparing a sucrose-6-ester, including: preparing a reaction solution of sucrose and an organo-tin compound; atomizing the reaction solution to form droplets; thoroughly mixing and contacting the droplets with a gasified dehydration medium such that the droplets undergo a dehydration reaction to obtain an intermediate mixture containing sucrose organic tin ester droplets; separating the intermediate mixture to obtain a sucrose organic tin ester solution and a dehydrated gas-liquid mixture; recovering the sucrose organic tin ester solution obtained in the separation step and cycling to the atomization and dehydration steps several times; and subjecting an organic acid anhydride to an acylation reaction with the sucrose organic tin ester solution to obtain the sucrose-6-ester.