A method of upgrading an overflash stream from a vacuum distillation unit comprising the steps of separating the overflash stream from an atmospheric residue stream, the overflash stream comprises an overflash fraction having a T10% between 475 and 530° C. and a T90% between 600 and 700° C.; introducing the reactor feed to a supercritical reactor at a temperature between 380° C. and 500° C. and a pressure between 25 MPa and 30 MPa; maintaining upgrading reactions in the supercritical reactor to upgrade the overflash fraction such that a reactor effluent comprises upgraded hydrocarbons relative to the overflash fraction; reducing a temperature of a reactor effluent in a cooling device to produce a cooled stream; reducing a pressure of the cooled stream in a depressurizing device to produce a discharged stream; and separating the discharged stream in a gas-liquid separator to produce a liquid phase product.

A method of upgrading an overflash stream from a vacuum distillation unit comprising the steps of separating the overflash stream from an atmospheric residue stream, the overflash stream comprises an overflash fraction having a T10% between 475 and 530° C. and a T90% between 600 and 700° C.; introducing the reactor feed to a supercritical reactor at a temperature between 380° C. and 500° C. and a pressure between 25 MPa and 30 MPa; maintaining upgrading reactions in the supercritical reactor to upgrade the overflash fraction such that a reactor effluent comprises upgraded hydrocarbons relative to the overflash fraction; reducing a temperature of a reactor effluent in a cooling device to produce a cooled stream; reducing a pressure of the cooled stream in a depressurizing device to produce a discharged stream; and separating the discharged stream in a gas-liquid separator to produce a liquid phase product.

A dividing wall column is used in an alkylation process flow scheme to fractionate an alkylate reactor effluent to produce an iso-butane-rich stream as a recycle feed for the alkylation reactor while also separating iso-butane, normal butane and alkylate as separate product streams depending on the reactor effluent composition. In an optional embodiment, the scheme may contain propane.

Provided are: a method of preparing a cannabis processed product having an increased CBD content in an efficient and economic manner, through a decarboxylation reaction by continuous microwave irradiation of a cannabis extract; and use of a processed product having an increased CBD content prepared by the method, a fraction thereof, and a single ingredient of CBD, in foods, drugs, and cosmetics.

The invention relates to a process for preparing butadiene from n-butenes, comprising the steps of: A) providing an input gas stream a comprising n-butenes, B) feeding the input gas stream a comprising n-butenes and a gas containing at least oxygen into at least one oxidative dehydrogenation zone and oxidatively dehydrogenating n-butenes to butadiene, giving a product gas stream b comprising butadiene, unconverted n-butenes, water vapor, oxygen, low-boiling hydrocarbons and high-boiling secondary components, with or without carbon oxides and with or without inert gases; Ca) cooling the product gas stream b by contacting with a cooling medium in at least one cooling zone, the cooling medium being at least partly recycled and having an aqueous phase and an organic phase, Cb) compressing the cooled product gas stream b which may have been depleted of high-boiling secondary components in at least one compression stage, giving at least one aqueous condensate stream c1 and one gas stream c2 comprising butadiene, n-butenes, water vapor, oxygen and low-boiling hydrocarbons, with or without carbon oxides and with or without inert gases; D) removing uncondensable and low-boiling gas constituents comprising oxygen and low-boiling hydrocarbons, with or without carbon oxides and with or without inert gases, as gas stream d2 from the gas stream c2 by absorbing the C.sub.4 hydrocarbons comprising butadiene and n-butenes in an absorbent, giving an absorbent stream laden with C.sub.4 hydrocarbons and the gas stream d2, and then desorbing the C.sub.4 hydrocarbons from the laden absorbent stream, giving a C.sub.4 product gas stream d1, E) separating the C.sub.4 product stream d1 by extractive distillation with a butadiene-selective solvent into a stream e1 comprising butadiene and the selective solvent and a stream e2 comprising n-butenes; F) distilling the stream e1 comprising butadiene and the selective solvent into a stream f1 consisting essentially of the selective solvent and a stream f2 comprising butadiene, wherein stage Cb) comprises at least two compression stages Cba) and at least two cooling stages Cbb) configured in the form of quench columns, the cooling in the cooling stages being effected by direct contacting with a biphasic cooling medium having an aqueous phase and an organic phase.

The invention relates to a process for preparing butadiene from n-butenes, comprising the steps of: A) providing an input gas stream a comprising n-butenes, B) feeding the input gas stream a comprising n-butenes and a gas containing at least oxygen into at least one oxidative dehydrogenation zone and oxidatively dehydrogenating n-butenes to butadiene, giving a product gas stream b comprising butadiene, unconverted n-butenes, water vapor, oxygen, low-boiling hydrocarbons and high-boiling secondary components, with or without carbon oxides and with or without inert gases; Ca) cooling the product gas stream b by contacting with a cooling medium in at least one cooling zone, the cooling medium being at least partly recycled and having an aqueous phase and an organic phase, Cb) compressing the cooled product gas stream b which may have been depleted of high-boiling secondary components in at least one compression stage, giving at least one aqueous condensate stream c1 and one gas stream c2 comprising butadiene, n-butenes, water vapor, oxygen and low-boiling hydrocarbons, with or without carbon oxides and with or without inert gases; D) removing uncondensable and low-boiling gas constituents comprising oxygen and low-boiling hydrocarbons, with or without carbon oxides and with or without inert gases, as gas stream d2 from the gas stream c2 by absorbing the C.sub.4 hydrocarbons comprising butadiene and n-butenes in an absorbent, giving an absorbent stream laden with C.sub.4 hydrocarbons and the gas stream d2, and then desorbing the C.sub.4 hydrocarbons from the laden absorbent stream, giving a C.sub.4 product gas stream d1, E) separating the C.sub.4 product stream d1 by extractive distillation with a butadiene-selective solvent into a stream e1 comprising butadiene and the selective solvent and a stream e2 comprising n-butenes; F) distilling the stream e1 comprising butadiene and the selective solvent into a stream f1 consisting essentially of the selective solvent and a stream f2 comprising butadiene, wherein stage Cb) comprises at least two compression stages Cba) and at least two cooling stages Cbb) configured in the form of quench columns, the cooling in the cooling stages being effected by direct contacting with a biphasic cooling medium having an aqueous phase and an organic phase.

A solid-liquid separation device performs dehydration or deoiling from a treated object using a substance A that is a gas at normal temperature and pressure and is capable of dissolving water and oil when liquefied. The separation device includes a substance B that circulates while generating phase change in a closed system, a compressor that compresses the substance B, a first heat exchanger that condenses substance B and evaporates of the substance A, an expansion valve that decompresses the condensed substance B, a second heat exchanger that evaporates substance B and condenses substance A, and a treatment tank wherein substance A is mixed with the treated object, substance A is evaporated while separated from the liquid in the first heat exchanger, and condensed in the second heat exchanger. The center of gravity of the first heat exchanger is lower than the second heat exchanger in a vertical direction.

A process for separating or removing permanganate reducing compounds (PRC's) from a first mixture containing at least one PRC, methyl iodide, and water comprises the steps of: feeding the first mixture to a feed port of a distillation column, and distilling and separating the first mixture into an upper stream and a lower stream, wherein the distillation of the first mixture forms a second mixture at an upper position than the feed port, and the process further comprises the steps of: withdrawing the second mixture as the upper stream, and withdrawing the lower stream from a lower position than the feed port.

A process for separating or removing permanganate reducing compounds (PRC's) from a first mixture containing at least one PRC, methyl iodide, and water comprises the steps of: feeding the first mixture to a feed port of a distillation column, and distilling and separating the first mixture into an upper stream and a lower stream, wherein the distillation of the first mixture forms a second mixture at an upper position than the feed port, and the process further comprises the steps of: withdrawing the second mixture as the upper stream, and withdrawing the lower stream from a lower position than the feed port.

A method for improving heat transfer during distillation and concentration of extract with solvent includes providing a distillation vessel having a heat transfer surface and preparing the heat transfer surface with a plurality of surface features. A distillation and concentration system includes a distillation vessel having a heat transfer surface prepared with a plurality of surface features in accordance with the method.